WO2007079128A1 - Na+, k+-atpase expression in cervical dysplasia and cancer - Google Patents
Na+, k+-atpase expression in cervical dysplasia and cancer Download PDFInfo
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- WO2007079128A1 WO2007079128A1 PCT/US2006/049392 US2006049392W WO2007079128A1 WO 2007079128 A1 WO2007079128 A1 WO 2007079128A1 US 2006049392 W US2006049392 W US 2006049392W WO 2007079128 A1 WO2007079128 A1 WO 2007079128A1
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/574—Immunoassay; Biospecific binding assay; Materials therefor for cancer
- G01N33/57407—Specifically defined cancers
- G01N33/57411—Specifically defined cancers of cervix
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/02—Drugs for genital or sexual disorders; Contraceptives for disorders of the vagina
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- This application relates to methods of diagnosing cervical dysplasia and cancer by detecting Na + , K + -ATPase expression, and to methods of treating cervical dysplasia and cancer by decreasing the biological activity of the Na + , K + -ATPaSe.
- the goal of cervical cancer prevention is to detect and treat all "committed" pre- cancer cells before the invasion of cancer cells occurs.
- Human papillomavirus (HPV) is a factor for the development of cervical cancer, and its detection in cervical tissue is currently used to diagnose cervical dysplasias and cancers.
- HPV-induced lesions are cleared by the patient's natural immune system and only a small portion of women with HPV infected cervix actually develop cervical cancer. Therefore, biomarkers are needed that facilitate detection of the group of pre-cancer cells among low and high grade clinical cases and all cancer cases. Once biomarkers for the early detection of cervical cancer are identified, those biomarkers become are candidates for the treatment of cervical dysplasia.
- Na + , K + -ATPase expression in cervical tissue differs in normal cervical tissue as compared to cervical dysplasia and cervical cancer tissue.
- increased expression of the Na + , K + -ATPase ⁇ -subunit in cervical tissue correlates with progression from low grade dysplasia to high grade dysplasia to cervical cancer.
- the ratio of expression of the Na + , K + -ATPase ⁇ -subunit to the ⁇ -subunit in cervical tissue decreased with progression from low grade dysplasia to high grade dysplasia to cervical cancer.
- the localization pattern OfNa + , K + -ATPase differed in normal and diseased cervical tissue.
- normal Na + , K + -ATPase expression was basal, while in cervical dysplasia or cancer tissue Na + , K + -ATPase expression was more localized to the cell membrane.
- methods are provided for using the Na + , K + -ATPaSe as a biomarker for cervical dysplasia and cervical cancer and as a therapeutic target for treatment of cervical dysplasia and cancer.
- the method includes detecting Na + , K + -ATPase expression (such as protein or nucleic acid molecule expression) in a cervical sample obtained from the subject.
- Na + , K + -ATPase expression such as protein or nucleic acid molecule expression
- expression of the ⁇ -subunit such as the ⁇ l-subunit
- the ⁇ -subunit or both
- the expression levels are quantitated.
- the detected Na + , K + -ATPase expression can be compared to a reference value or reference sample representing a particular disease state (such as cervical dysplasia or cervical cancer, or a particular stage thereof).
- the detected level OfNa + , K + - ATPase expression in the sample can be compared to a level OfNa + , K + -ATPase expression in one or more reference cervical tissue samples or to a reference value representing expected Na + , K + -ATPase expression in a control tissue sample.
- exemplary reference samples and values include those representing a known presence, absence, or grade of cervical dysplasia or cervical cancer.
- K + -ATPase expression (such as expression of the ⁇ subunit) is substantially similar to the level OfNa + , K + -ATPase expression (such as expression of the ⁇ subunit) in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value.
- a detected increase in Na + , K + -ATPase expression of at least 2-fold (such as at least 3- fold) relative to such a reference value indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- the disclosed method can further include detecting ⁇ -subunit of a Na + , K + -ATPase expression in a cervical tissue sample and determining the ratio of the ⁇ - and ⁇ -subunit expression.
- the determined ratio is compared to a ratio of ⁇ - and ⁇ - subunit expression observed in one or more reference values or samples having a known presence, absence or grade of cervical dysplasia or cervical cancer. For example, if the detected ratio of ⁇ - and ⁇ -subunit expression is substantially similar to the ratio of ⁇ - and ⁇ - subunit expression in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value.
- a detected decrease in the ratio of ⁇ - and ⁇ -subunit expression indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- the disclosed methods can further include detecting another marker, such as a cell cycle marker, for example a nuclear marker.
- the method can include detecting histone H3 (for example using histone H3-specific antibodies).
- additional markers can be used to further distinguish normal cervical tissue from cervical dysplasia or cervical cancer. For example, an increase in detected dividing cells-relative to normal cervical tissue (such as an increase of at least 2-fold, at least 5-fold, or at least 10- fold, such as 2-3 fold, 2-10 fold, or 2-20 fold) would indicate the presence of cervical dysplasia or cervical cancer.
- the method of detecting and grading cervical dysplasia or cervical cancer can also include determining the localization pattern of the Na + , K + -ATPase (such as the ⁇ - or ⁇ - subunit) in a cervical sample.
- the location of either or both of the ⁇ - or ⁇ -subunits in a cervical tissue sample can be compared to one or more reference values or samples having a known presence, absence or grade of cervical dysplasia or cervical cancer.
- the detected Na + , K + -ATPase localization is substantially similar to the Na + , K + -ATPase localization in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value.
- the reference value or sample is normal (non-dysplastic, non-cancerous) cervical cells, a detected Na + , K + -ATPase localization (such as increased localization in the cell membrane) relative to such a reference value indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- compositions include one or more Na + , K + -ATPase inhibitors (such as an inhibitor of the ⁇ -subunit) and a pharmaceutically acceptable carrier.
- the pharmaceutically acceptable is a carrier that permits topical application of the Na + , K + - ATPase inhibitor, for example topical application to the cervix.
- Na + , K + -ATPase inhibitors can significantly decrease the enzymatic activity of the protein (such as a cardiac glycoside) or decrease expression of a Na + , K + -ATPase (such as an inhibitory RNA molecule).
- the method includes administering to a subject having cervical dysplasia or cervical cancer a composition that includes a therapeutically effective amount of a Na + , K + - ATPase inhibitor, such as a composition provided herein.
- a subject determined to have cervical dysplasia or cervical cancer using the methods described herein can be selected to receive treatment for the cervical dysplasia.
- the diseased cervix can be contacted with a Na + , K + -ATPase inhibitor in an amount and for a time sufficient to lower Na + , K + -ATPase activity in the cervix (for example in the cervical dysplastic or cancer cells).
- FIGS. IA-H show digital images of the immunolocalization OfNa + , K + -ATPase (A, C, E, G) ⁇ and (B, D, F 5 H) ⁇ subunits in (A 5 B) normal cervical tissue, (C, D) low grade cervical dysplasia, (E, F) high grade cervical dysplasia, and (G, H) cervical cancer tissue samples.
- Normal cervical tissue expressed the Na + , K + -ATPase ⁇ subunit, but not the ⁇ l subunit.
- Cervical dysplasia and cervical cancer samples were positive for both the Na + , K + - ATPase ⁇ and ⁇ l subunits.
- FIGS. 2A-D show digital images of cervical tissue stained to reveal Na + , K + - ATPase expression in endocervical mucus glands.
- the endocervical mucus glands are rarely seen in (A and B) normal samples and are mainly observed in the stroma of (C and D) cervical dyplasia samples.
- FIGS. 3A-F show digital images comparing (A and D) centromere and (B and E) telomere in situ hybridization with (C and F) Na + , K + -ATPase ⁇ -subunit levels in cervical dysplasia tissue samples. These figures demonstrate that in cases of cervical dysplasia, the increased level OfNa + , K + -ATPase ⁇ -subunit correlates positively with telomere shortening (indicated by a low level of staining in E).
- HPV human papillomavirus
- Na + , K + -ATPaSe sodium potassium ATPase (also referred to as the sodium pump)
- an agent such as a composition that includes a Na + , K + -ATPaSe inhibitor
- routes of administration include, but are not limited to, oral, injection (such as subcutaneous, intramuscular, intradermal, intraperitoneal, and intravenous), sublingual, rectal, transdermal, intranasal, vaginal, cervical, and inhalation routes.
- administration of an agent is accomplished via vaginal or cervical administration.
- Antibody A molecule including an antigen binding site which specifically binds (immunoreacts with) an antigen. Includes immunoglobulin molecules and immunologically active portions thereof, as well as immunoglobulin-like molecules. Immunoglobulin genes include the kappa, lambda, alpha, gamma, delta, epsilon, and mu constant region genes, as well as the myriad immunoglobulin variable region genes. Light chains are classified as either kappa or lambda. Heavy chains are classified as gamma, mu, alpha, delta, or epsilon, which in turn define the immunoglobulin classes, IgG, IgM, IgA, IgD and IgE, respectively.
- a Na + , K + -ATPase-specific antibody is used to detect expression or localization of the Na + , K + - ATPase in a cell.
- Antibodies include both monoclonal and polyclonal antibody preparations.
- an antibody specifically binds to a target (such as a Na + , IC 1 - ATPase) with a binding constant that is at least 10 3 M "1 greater, 10 4 M “1 greater or 10 5 M “1 greater than a binding constant for other molecules in a sample.
- a target such as a Na + , IC 1 - ATPase
- an antibody has a Kd value for binding to an antigenic determinant (such as a hapten or epitope) that is on the order of 10 "6 M or lower, such as 10 "9 M or lower, or even 10 "12 M or lower.
- Kd values can, for example, be determined by competitive ELISA (enzyme-linked immunosorbent assay) or using a surface-plasmon resonance device such as the Biacore TlOO, which is available from Biacore, Inc., Piscataway, NJ.
- Antibody fragments include proteolytic antibody fragments [such as F(ab')2 fragments, Fab' fragments, Fab'-SH fragments and Fab fragments], recombinant antibody fragments (such as sFv fragments, dsFv fragments, bispecific sFv fragments, bispecific dsFv fragments, diabodies, and triabodies), camel id antibodies (see, for example, U.S. Patent Nos.
- Cardiac glycoside An inhibitor of the Na + , K + -ATPase, which is traditionally used to treat congestive heart failure and cardiac arrhythmia.
- Such glycosides are found as secondary metabolites in several plants, and in some animals.
- cardiac glycosides can be obtained from Strophanthus (such as ouabain g/k/e-strophanthin), Digitalis lanata and Digitalis purpurea (digoxin, digitoxin), Scilla maritima (proscillaridine A), Adonis vernalis, Adonis aestivalis, Acokanthera oblongifolia, Convallaria, and frogs (such as bufalin, marinobufagenin and bufadienolides). Additional non-limiting examples are provided in US Patent Publication 20060205679.
- Cervical cancer A malignant neoplasm of the cervix that has undergone characteristic anaplasia with loss of differentiation, increased rate of growth, invasion of surrounding tissue, and is capable of metastasis.
- cervical cancer squamous cell (epidermoid) cervical cancer and adenocarcinoma cervical cancer.
- cervical cancer is caused by infection with human papillomavirus
- Cervical cancer can be classified by the degree of spread of cancer cells, with stage I the least severe and stage IV the most severe (for example metastazied).
- Cervical dysplasia Cervical intraepithelial neoplasia (CES))- The presence of abnormal cells (cells which have not matured) on the cervix. Dysplasias are considered precancerous. The more abnormal cells found on the surface, the more serious the dysplasia. Cervical dysplasia is often classified by the degree of penetration of abnormal cells into the tissue lining (epithelium): CIN I describes the involvement of the basal third of the epithelium; CIN II involves the basal two thirds of the epithelium; and CIN III involves more than two thirds of the epithelium. When the entire cervical epithelium (the tissue that lines the cervix) is covered with primitive cells, this is referred to as cervical carcinoma in situ.
- Cervical sample A biological specimen obtained from the cervix, which can include cells from both the outside of the cervix (exocervix, or portio) and the inside of the cervix (endocervix). Exemplary methods that can be used to obtain a cervical sample include a PAP smear, colposcopy, and cone biopsy. Cervix: The lower part of the uterus that opens into the vagina. Chemotherapy: In cancer treatment, such as treatment of cervical cancer, chemotherapy refers to the administration of one or more agents to kill or slow the reproduction of rapidly multiplying cells, such as tumor or cancer cells.
- chemotherapy refers to the administration of one or more anti-neoplastic agents to significantly reduce the number of tumor cells in the subject, such as a reduction of at least 10%, at least 20%, or at least 50%.
- Cytotoxic anti-neoplastic chemotherapeutic agents include, but are not limited to: 5-fluorouraciI (5-FU), azathioprine, cyclophosphamide, antimetabolites (such as Fludarabine), and other antineoplastics such as Etoposide, Doxorubicin, methotrexate, Vincristine, carboplatin, cis-platinum and the taxanes (such as taxol).
- cisplatin such as Platinol®
- fluorouracil such as Adrucil®, Efudex®
- a therapy decreases a cervical dysplasia or cancer (such as the size of a cervical dysplasia or cancer, the number of dysplasias or tumors, the metastasis of a tumor, or combinations thereof), or one or more symptoms associated with cervical dysplasia or cancer, for example as compared to the response in the absence of the therapy.
- a therapy decreases the size of a cervical dysplasia or cancer, the number of cervical dysplasias or cancers, the metastasis of a cervical cancer, or combinations thereof, subsequent to the therapy, such as a decrease of at least 10%, at least 20%, at least 50%, or even at least 90%. Such decreases can be measured using the methods disclosed herein.
- Detect To determine if an agent is present or absent. In some examples this can further include quantification.
- antibodies specific for the Na + , K + -ATPase can be used to detect the presence or absence OfNa + , K + -ATPase (such as the ⁇ - or ⁇ -subunit) in a cervical sample, for example by detecting a label associated with the antibody.
- Diagnose The process of identifying a medical condition or disease, for example from the results of one or more diagnostic procedures.
- cervical cancer or cervical dysplasia is diagnosed by detecting Na + , K + -ATPase expression in a cervical sample, wherein increased expression of the Na + , K + -ATPase ⁇ -subunit, decreased ratio of ⁇ - to ⁇ - subunit expression, or combinations thereof, indicates the presence of cervical dysplasia or cancer.
- Digitalis A cardiac glycoside present in the foxglove plant, which significantly reduces the biological activity of the Na + , K + -ATPaSe, and thus is a Na + , K + -ATPase inhibitor.
- digitalis compounds include digoxin, digitoxin, strophanthin and ouabain.
- Expression The process by which the coded information of a gene is converted into an operational, non-operational, or structural part of a cell, such as the synthesis of a protein.
- nucleic acid molecule can be altered relative to a normal (wild type) nucleic acid molecule.
- Alterations in gene expression, such as differential expression includes but is not limited to: (1) overexpression; (2) underexpression; or (3) suppression of expression. Alternations in the expression of a nucleic acid molecule can be associated with, and in fact cause, a change in expression of the corresponding protein.
- Protein expression can also be altered in some manner to be different from the expression of the protein in a normal (wild type) situation. This includes but is not necessarily limited to: ( 1) a mutation in the protein such that one or more of the amino acid residues is different; (2) a short deletion or addition of one or a few (such as no more than 10-20) amino acid residues to the sequence of the protein; (3) a longer deletion or addition of amino acid residues (such as at least 20 residues), such that an entire protein domain or sub-domain is removed or added; (4) expression of an increased amount of the protein compared to a control or standard amount; (5) expression of a decreased amount of the protein compared to a control or standard amount; (6) alteration of the subcellular localization or targeting of the protein; (7) alteration of the temporally regulated expression of the protein (such that the protein is expressed when it normally would not be, or alternatively is not expressed when it normally would be); (8) alteration in stability of a protein through increased longevity in the time that the protein remains localized in a cell; and
- Controls or standards for comparison to a sample, for the determination of differential expression include samples believed to be normal (in that they are not altered for the desired characteristic, for example a sample from a subject who has not had cervical dysplasia or cervical cancer) as well as laboratory values, even though possibly arbitrarily set, keeping in mind that such values can vary from laboratory to laboratory.
- Laboratory standards and values may be set based on a known or determined population value and can be supplied in the format of a graph or table that permits comparison of measured, experimentally determined values.
- ⁇ -subunit protein or nucleic acid molecule in cervical dysplasia and cervical cancer cells is said to be "increased" relative to normal (non- dysplastic or non-cancer cervical cells) when the detected level of ⁇ -subunit is at least 2-fold, such as at least 3-fold, at least 4-fold, or at least 10-fold greater in a test cervical sample relative to a normal sample.
- Label An agent capable of detection, for example by ELISA, spectrophotometry, flow cytometry, or microscopy.
- a label can be attached to a protein or nucleic acid molecule, such as a subunit of the Na + ,K + -ATPAse, thereby permitting detection of the protein or nucleic acid molecule.
- labels include, but are not limited to, radioactive isotopes, enzyme substrates, co-factors, ligands, chemiluminescent agents, fluorophores, haptens, enzymes, and combinations thereof.
- Na + , K + -ATPaSe sodium, potassium-adenosine triphosphatase: Also referred to in the art as the sodium pump.
- the Na + , K + -ATPaSe is a ubiquitous membrane transport enzyme (EC 3.6.3.9) in mammalian cells that is responsible for establishing and maintaining high K + and low Na + in the cytoplasm required for normal resting membrane potentials and various cellular activities.
- the Na + , K + -ATPase includes two ⁇ and two ⁇ - subunits. There are at least four different isoforms of the ⁇ - ( ⁇ l, ⁇ 2, ⁇ 3, and ⁇ 4) and ⁇ - ( ⁇ l , ⁇ 2, ⁇ 3, and ⁇ 4) subunits.
- Na + , K + -ATPaSe inhibitor An agent capable of significantly reducing the biological activity of the Na + , K + -ATPase. Such an agent can work at the nucleic acid level (for example by decreasing expression of the Na + , K + -ATPase, such as an siRNA molecule), or at the protein level (for example by reducing the activity of the protein). Inhibitors, may, but need not reduce Na + , K + -ATPase biological activity or expression by 100%. For example, therapeutic effects may be observed when the inhibitor decreases Na + , K + -ATPase biological activity or expression by at least 20%, at least 50%, at least 75%, or at least 90%.
- Neoplasm An abnormal cellular proliferation, which includes benign and malignant tumors, as well as other proliferative disorders.
- a cervical neoplasm includes cervical dysplasia and cervical cancer.
- Pharmaceutical agent or drug A chemical compound or composition capable of inducing a desired therapeutic effect when administered to a subject, alone or in combination with another therapeutic agent(s) or pharmaceutically acceptable carriers.
- a pharmaceutical agent such as one that includes a Na + , K + -ATPase inhibitor treats a cervical dysplasia or cancer, for example by reducing the size of the dysplasia or cancer (such as the volume or reducing the number of dysplasia or cancer cells), reducing metastasis of the cancer, or combinations thereof.
- compositions and formulations suitable for pharmaceutical delivery of one or more therapeutic agents such as a Na + , K + -ATPase inhibitor.
- parenteral formulations can include injectable fluids that include pharmaceutically and physiologically acceptable fluids such as water, physiological saline, balanced salt solutions, aqueous dextrose, glycerol or the like as a vehicle.
- pharmaceutical compositions to be administered can contain minor amounts of non-toxic auxiliary substances, such as wetting or emulsifying agents, preservatives, and pH buffering agents and the like, for example sodium acetate or sorbitan monolaurate, sodium lactate, potassium chloride, calcium chloride, and triethanolamine oleate.
- exemplary topical carriers include, but are not limited to, those suitable for cervical or vaginal administration.
- Reference value A number or range of numbers representing a particular condition.
- An experimental value can be compared to the reference value, for example to make a diagnosis or prognosis.
- a reference value can be a relative or absolute amount (or range) of Na + , K + -ATPase expression (such as ⁇ - or ⁇ -subunit) expected for a particular cervical condition, such as normal cervical cells, cervical dysplasia (for example a particular stage of dysplasia), or cervical cancer (for example a particular stage of cancer).
- Sample Biological specimens such as samples containing biomolecules, such as nucleic acid molecules, proteins, or both.
- Exemplary samples are those containing cells or cell lysates from a subject, such as those present in peripheral blood (or a fraction thereof such as serum), urine, saliva, tissue biopsy, cheek swabs, surgical specimen, fine needle aspirates, cervical samples, and autopsy material.
- a sample is obtained from the cervix (for example a PAP smear), which can include cells from both the outside of the cervix (exocervix, or portio) and the inside of the cervix (endocervix).
- Subject Living multi-cellular vertebrate organisms, a category that includes human and non-human mammals (such as laboratory or veterinary subjects).
- Therapeutically effective amount An amount of an agent that alone, or together with a pharmaceutically acceptable carrier or one or more additional therapeutic agents, induces the desired response.
- a therapeutic agent such as a Na + , K + -ATPaSe inhibitor, is administered in therapeutically effective amounts that stimulate the desired response, for example treatment of cervical dysplasia or cancer.
- Effective amounts a therapeutic agent can be determined in many different ways, such as assaying for improvement of a physiological condition of a subject having cervical dysplasia or cancer. Effective amounts also can be determined through various in vitro, in vivo or in situ assays. Therapeutic agents can be administered in a single dose, or in several doses, for example weekly, monthly, or bi-monthly, during a course of treatment. However, the effective amount of can be dependent on the source applied, the subject being treated, the severity and type of the condition being treated, and the manner of administration.
- a pharmaceutical preparation can decrease one or more symptoms of the cervical dysplasia or cancer (such as the size of the dysplasia or cancer or the number of tumors), for example decrease a symptom by at least 20%, at least 50%, at least 70%, at least 90%, at least 98%, or even at least 100%, as compared to an amount in the absence of the pharmaceutical preparation.
- Treating a disease refers to a therapeutic intervention that ameliorates a sign or symptom of a disease or pathological condition, such a sign or symptom of cervical dysplasia or cervical cancer. Treatment can also induce remission or cure of a condition, such as cervical dysplasia or cervical cancer. In particular examples, treatment includes preventing a disease, for example by inhibiting the full development of a disease, such as preventing development of a cervical cancer from a cervical dysplasia or preventing metastasis of a cervical cancer. Prevention of a disease does not require a total absence of a dysplasia or cancer. For example, a decrease of at least 50% can be sufficient. Under conditions sufficient for: A phrase that is used to describe any environment that permits the desired activity.
- the method includes incubating a Na + , K + -ATPase antibody with a cervical sample under conditions that allow the antibody to specifically bind to Na + , K + -ATPase proteins in the sample.
- the desired activity is decreasing growth or multiplication of such cells, or the invasion of such cells into the cervix, or metastasis of such cells to other organs.
- Unit dose A physically discrete unit containing a predetermined quantity of an active material (such as a Na + , K + -ATPase) calculated to individually or collectively produce a desired effect such as a therapeutic effect.
- an active material such as a Na + , K + -ATPase
- a single unit dose or a plurality of unit doses can be used to provide the desired effect, such as a therapeutic effect.
- the Na + , K + -ATPaSe has two major functions for maintaining cell functions Na + ZK + pump and signal transduction. It is shown herein that the expression patterns OfNa + , K + -ATPase ⁇ - and ⁇ l-subunits differed between normal and dysplasia and cancer cervical tissues. For example, increased Na + , K + -ATPaSe ⁇ l-subunit expression was observed in the cervical dysplasia and cervical cancer tissues. In addition, the ratio of the Na + , K + -ATPase ⁇ - and ⁇ l-subunits was altered between normal and Na + , K + -ATPase ⁇ - and ⁇ l-subunits. The relative ratio OfNa + , K + -ATPase ⁇ -subunit to ⁇ l-subunit decreased in the cervical dysplasia and cervical cancer tissues relative to the normal cervical samples.
- IGF-I insulin-like growth factor I
- the inventors also observed insulin-like growth factor binding protein 3 (IGFBP-3) protein accumulation sites and Na + /K + -ATPase ⁇ l expression sites in the cervical epithelia cells and cancer cells. This indicates a paracrine regulatory mechanism between the epithelial cell layer and the stroma in the cervical tissue.
- IGFBP-3 insulin-like growth factor binding protein 3
- IGFBP-3 over- expressed IGFBP-3 in the epithelial layer of the cervix due to HPV infection enhances the IGF-I receptor sensitivity.
- IGF-I secreted from the mucus glands binds to IGF-I receptor in the epithelial layer, and IGF-I binding to the receptor causes signal transduction including an increase in Na + , K + -ATPase and KCC expression and phenotype transformation of HPV- infected cells (cancer development and progression).
- methods of detecting cervical dysplasia or cervical cancer in clinical tissue sections are provided.
- methods of treating cervical dysplasia and cervical cancer are provided.
- inhibitors of the Na + , K + -ATPase can be applied to the cervix (for example in the form of a topical ointment) to treat cervical dysplasia and cervical cancer.
- Such inhibitors can significantly reduce the expression or biological activity of the Na + , K + -ATPase.
- the Na + , K + -ATPase ⁇ l subunit is targeted.
- the present disclosure provides methods that can be used to detect a cervical neoplasm, such as a cervical dysplasia or cervical cancer. Detection can include determining whether the cervical dysplasia or cervical cancer is present, grading the cervical dysplasia or cervical cancer (for example determining if it is a CIN I, CIN II, or CIN III cervical dysplasia, or a Stage 0, Stage I (such as Stage IA, IAl, IA2, IBl, IB2), Stage II (such as IIA or IIB), Stage III (such as IHA or HIB), or Stage IV (such as IVA or IVB) or cervical cancer), determining the prognosis of a subject found to have cervical dysplasia or cervical cancer, or combinations thereof.
- Stage I such as Stage IA, IAl, IA2, IBl, IB2
- Stage II such as IIA or IIB
- Stage III such as IHA or HIB
- Stage IV such as IVA or IVB
- the method includes detecting a Na + , K + -ATPase or subunit thereof (such as an ⁇ -subunit, ⁇ -subunit, or both) in a cervical sample obtained from the subject, such as detecting Na + , K + -ATPase protein expression or nucleic acid molecule expression.
- a Na + , K + -ATPase or subunit thereof such as an ⁇ -subunit, ⁇ -subunit, or both
- expression of the ⁇ -subunit such as the ⁇ l-subunit
- the ⁇ - subunit, or both can be detected.
- the expression levels are quantitated. Methods of detecting protein or nucleic acid molecule expression are well known.
- the presence of a significant increase in expression of a Na + , K + -ATPaSe indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- detection of an at least 2-fold increase indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- Exemplary changes are provided in Table 1.
- the detected Na + , K + -ATPase expression can be compared to a reference value or reference sample representing a particular disease or disease-free state (such as normal cervical tissue, cervical dysplasia or cervical cancer, or a particular stage of dysplasia or cancer).
- a reference value or reference sample representing a particular disease or disease-free state (such as normal cervical tissue, cervical dysplasia or cervical cancer, or a particular stage of dysplasia or cancer).
- the detected level OfNa + , K + -ATPase expression in the sample can be compared to a level OfNa + , K + -ATPaSe expression in one or more reference cervical tissue samples or to a reference value representing expected Na + , K -ATPase expression in a control tissue sample.
- Exemplary reference samples and values include those representing a known presence, absence, or grade of cervical dysplasia or cervical cancer.
- K + -ATPase expression (such as expression of the ⁇ -subunit, for example the ⁇ l -subunit) is substantially similar to the level OfNa + , K + -ATPase expression (such as expression of the ⁇ -subunit, for example the ⁇ l-subunit) in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value.
- a detected increase in Na + , K + - ATPase expression of at least 2-fold (such as at least 3-fold) relative to such a reference value indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- detection of the ⁇ -subunit is performed. If the detected level of ⁇ -subunit in the test cervical sample is substantially similar to the level of ⁇ -subunit expression in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value. For example, if the detected relative value of ⁇ subunit expression is 50, and the reference value for ⁇ -subunit expression is 10 for normal cervical tissue, the reference value for ⁇ -subunit expression is 40 for cervical dysplasia, and the reference value for ⁇ -subunit expression is 100 for cervical cancer, then it is concluded that the subject has cervical dysplasia. Similar methods can be used to determine whether the subject has normal, dysplasic, or cancerous cervical cells using any Na + , K + -ATPase subunit and the appropriate reference values or samples.
- the reference value or sample is normal cervical cells (non- dysplastic, non-cancerous), and expression of the Na + , K + -ATPase ⁇ l-subunit is detected, wherein an at least 2-fold (such as at least 3-fold) increased in ⁇ l-subunit expression relative to the reference value indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- the disclosed method can include detecting both ⁇ -subunit and ⁇ -subunit Na + , K + - ATPase expression in a cervical tissue sample.
- the method can include determining the ratio of ⁇ - to ⁇ -subunit expression, wherein an at least 20% decrease relative to a level of ⁇ - to ⁇ -subunit expression in normal cervical tissue (non-cancerous and non-dysplastic), indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- detection of an at least 20%, at least 40%, at least 50%, or at least 75% decrease in ratio of ⁇ l - to ⁇ l-subunit expression, relative to such expression in normal cervical tissue indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- the determined ratio of ⁇ - to ⁇ -subunit expression is compared to a ratio of ⁇ - and ⁇ -subunit expression observed in one or more reference values or samples having a known presence, absence or grade of cervical dysplasia or cervical cancer. For example, if the detected ratio of ⁇ - and ⁇ -subunit expression is substantially similar to the ratio of ⁇ - and ⁇ -subunit expression in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value.
- a detected decrease in the ratio of ⁇ - and ⁇ -subunit expression indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- the method of detecting cervical dysplasia or cervical cancer can also include determining the localization pattern of the Na + , K + -ATPase (such as the ⁇ - or ⁇ -subunit) in a cervical sample.
- the location of either or both of the ⁇ - or ⁇ -subunits in a cervical tissue sample can be compared to one or more reference values or samples having a known presence, absence or grade of cervical dysplasia or cervical cancer. For example, if the detected Na + , K + -ATPase localization is substantially similar to the Na + , K + -ATPase localization in a particular reference sample or value, this indicates that the subject has that presence, absence or grade of cervical dysplasia or cervical cancer represented by the reference sample or value.
- a detected Na + , K + -ATPase localization indicates the presence of cervical dysplasia or cervical cancer in the cervical sample obtained from the subject.
- DNA replication status is an indication of cell growth rate, particularly in carcinogenesis.
- Na + , K + -ATPase expression in cervical tissue can indicate cellular physiological status, but does not indicate the status of cell cycle. Therefore, in some examples the method further includes detecting a cell cycle marker, such as histone H3 (for example using histone H3-specific antibodies).
- a cell cycle marker such as histone H3 (for example using histone H3-specific antibodies).
- detection can be used to provide additional information on the ability to diagnose a subject as having a cervical dysplasia or cancer. For example, increased detection of a cell cycle marker relative to normal cervical cells can indicate the presence of increased cell division, such as that occurring in cervical dysplasia or cancer.
- a detectable increase of at least 2-fold more histone H3 or other cell cycle marker (such as at least 5-fold, or at least 20-fold) relative to normal cervical tissue, coupled with one or more of increased ⁇ -subunit (such as ⁇ l) expression, decreased ratio of ⁇ - to ⁇ -subunit expression, increased cell membrane staining, or combinations thereof, indicates that the subject has cervical dysplasia or cancer.
- Methods of detecting a protein in a sample are well known in the art. For example, immunoassays and immunocytology methods can be used. However, the disclosure is not limited to particular methods of detection.
- the availability of antibodies specific for the Na + , K + -ATPase (such as antibodies specific to the ⁇ - or ⁇ -subunit, such as a particular isoform thereof), facilitate the detection and quantitation of Na + , K + -ATPase proteins. Exemplary commercially available antibodies are shown in Table 2.
- the method includes contacting a biological sample obtained from a subject (such as a sample containing cervical cells or proteins isolated from such a sample) with a Na + , K + -ATPase-specif ⁇ c antibody under conditions sufficient for the antibody to specifically bind to Na + , K + -ATPase proteins in the sample, thereby forming Na + , K + - ATPase-antibody complexes.
- the resulting Na + , K + -ATPase-antibody complexes are then detected using any standard detection system.
- the Na + , K + -ATPase-anti body can include a label, thereby permitting detection of the complexes.
- the Na + , K + -ATPase-antibody complexes are contacted with an appropriate labeled secondary antibody under conditions sufficient to permit specific binding of the secondary antibody to Na + , K + -ATPase-antibody complexes, thereby forming labeled-Na + , K + -ATPase-antibody complexes.
- the label associated with the secondary label can then be detected. Similar methods can be used to detect the Na + , K + -ATPase localization pattern in cervical cells obtained from the subject.
- labels include fluorophores, such as Cy3, FITC, BODIPY, and Cy5.
- Methods of detecting labels are known, and include detection using microscopy and flow cytometry.
- the biological sample includes cervical proteins isolated from a cervical sample.
- any standard immunoassay format such as ELISA, Western blot, or RlA assay
- Na + , K + -ATPase proteins can be detected and quantitated using antibody probe arrays, quantitative spectroscopic methods (for example mass spectrometry, such as surface-enhanced laser desorption/ionization (SELDI)-based mass spectrometry), or combinations thereof.
- SELDI surface-enhanced laser desorption/ionization
- RNA or DNA for example mRNA or cDNA
- nucleic acid amplification methods with the appropriate probes and primers
- nucleic acid arrays containing the appropriate probes
- the level OfNa + , K + - ATPase gene expression can be determined or even quantitated utilizing methods well known in the art, such as Northern-Blots, RNase protection assays, nucleic acid arrays, quantitative PCR (such as TaqMan assays), dot blot assays, in-situ hybridization, or combinations thereof.
- the method includes contacting nucleic acid molecules (which can be isolated) from a biological sample obtained from a subject (such as a sample containing cervical cells or nucleic acid molecules obtained from such a sample) with a Na + , K + - ATPase-specific nucleic acid probe (such as probe specific for the ⁇ - or ⁇ -subunit) under conditions sufficient for the probe to specifically bind to Na + , K + -ATPaSe nucleic acid molecules (such as mRNA molecule)in the sample, thereby forming Na + , K + -ATPaSe- nucleic acid molecules complexes.
- the resulting complexes are then detected using any standard detection system, for example by detecting a label on the probe.
- the method includes contacting nucleic acid molecules (which can be isolated) from a biological sample obtained from a subject (such as a sample containing cervical cells or nucleic acid molecules obtained from such a sample) with primers that permit amplification of the Na + , K + -ATPase (such as the ⁇ - or ⁇ -subunit).
- the resulting amplicons can be detected, for example by detecting a label on the amplicon.
- the amplicons are applied to a nucleic acid molecule detection array containing Na + , K + -ATPase-specif ⁇ c nucleic acid probes that can hybridize specifically to the amplicons, under suitable hybridization conditions to form a hybridization complex.
- hybridization conditions are selected to permit discrimination between matched and mismatched oligonucleotides.
- Hybridization conditions can be chosen to correspond to those known to be suitable in standard procedures for hybridization to filters and then optimized for use with the arrays.
- conditions suitable for hybridization of one type of target such as a subunit of the Na + , K + -ATPaSe
- other targets such as a control sequence
- temperature is controlled to substantially eliminate formation of duplexes between sequences other than exactly complementary Na + , K + -ATPase sequences.
- a variety of known hybridization solvents can be employed, the choice being dependent on considerations known to one of skill in the art (see U.S. Patent 5,981,185).
- detection includes detecting one or more labels present on the oligonucleotides, the sequences obtained from the subject, or both. Detection can further include treating the hybridized complex with a conjugating solution to effect conjugation or coupling of the hybridized complex with the detection label, and treating the conjugated, hybridized complex with a detection reagent. In particular examples, the method further includes quantification, for instance by determining the amount of hybridization.
- Non-radiolabels include, but are not limited to enzymes, chemiluminescent compounds, fluorophores, metal complexes, haptens, colorimetric agents, dyes, or combinations thereof.
- Radiolabels include, but are not limited to, 125 I and 35 S. Radioactive and fluorescent labeling methods, as well as other methods known in the art, are suitable for use with the present disclosure.
- the primers used to amplify the subject's nucleic acids are labeled (such as with biotin, a radiolabel, or a fluorophore).
- amplified nucleic acid samples are end-labeled to form labeled amplified material.
- amplified nucleic acid molecules can be labeled by including labeled nucleotides in the amplification reactions.
- nucleic acid molecules obtained from a subject are labeled, and applied to an array containing oligonucleotides.
- the detected Na + , K + -ATPase (such as an ⁇ - or ⁇ -subunit protein or nucleic acid) can be compared to a reference value (such as a number or range of values) or reference sample (such as an actual biological sample).
- a reference value such as a number or range of values
- reference sample such as an actual biological sample.
- a comparison to a reference sample or value representing Na + , K + -ATPase expression expected for normal cervical tissue or a particular disease state, such as cervical dysplasia or cervical cancer (or a particular stage thereof) can be used to determine if the subject from whom the sample was obtained has cervical dysplasia or cervical cancer.
- the reference value or sample represents a relative or actual amount OfNa + , K + -ATPase ⁇ - or ⁇ -subunit (or both) expression expected or routinely observed for normal (non-dysplastic, non cancerous) cervical tissue.
- the reference value or sample represents a relative or actual amount OfNa + , K + -ATPase ⁇ - or ⁇ -subunit (or both) expression expected or routinely observed for cervical dysplasia or a particular grade thereof (such as CIN I, CIN II, or CIN III).
- the reference value or sample represents a relative or actual amount OfNa + , K + -ATPase ⁇ - or ⁇ -subunit (or both) expression expected or routinely observed for cervical cancer or a particular grade thereof (such as Stage 0, Stage I, Stage II, Stage III, or Stage IV, or a substage thereof such as Stage IIA).
- one or more of such reference value or samples are used, such as at least 2, at least 5, at least 10 of such reference values or samples, for example, 1, 2, 3, 4, 5, 6, 7, ,8, 9, 10, 1 1, 12, 13, 14, 15 or 16 of such reference values or samples.
- the reference sample or value represents a Na + , K + -ATPaSe localization pattern expected for normal cervical tissue or a particular disease state, such as cervical dysplasia or cervical cancer (or a particular stage thereof).
- the reference value or sample represents a relative or actual Na + , K + -ATPase ⁇ - or ⁇ -subunit (or both) localization expected or routinely observed for normal (non-dysplastic, non cancerous) cervical tissue.
- the reference value or sample represents a relative or actual Na + , K + -ATPase ⁇ - or ⁇ -subunit (or both) localization expected or routinely observed for cervical dysplasia or a particular grade thereof (such as ClN I, CIN II, or CIN III).
- the reference value or sample represents a relative or actual Na + , K + -ATPase ⁇ - or ⁇ -subunit (or both) localization expected or routinely observed for cervical cancer or a particular grade thereof (such as Stage 0, Stage I, Stage II, Stage III, or Stage IV, or a substage thereof such as Stage IIA).
- one or more of such reference value or samples are used, such as at least 2, at least 5, at least 10 of such reference values or samples, for example, 1, 2, 3, 4, 5, 6, 7, ,8, 9, 10, 1 1, 12, 13, 14, 15 or 16 of such reference values or samples.
- reference values or samples representing Na + , K + -ATPaSe expression and reference value or samples representing Na + , K + -ATPase localization patterns are used.
- a medicament and method for treatment of cervical dysplasia and cervical cancer is provided.
- the subject is first screened to determine if they have cervical dysplasia or cancer, for example using the methods provided herein.
- Subjects having cervical dysplasia or cancer can be selected for treatment, for example using the treatment methods provided herein.
- subjects identified as having at least a 2-fold increase in Na + , K + - ATPase expression in their cervical sample relative to a reference value OfNa + , K + -ATPase expression for a cervical sample negative for cervical dysplasia or cervical cancer can be selected for treatment.
- Exemplary treatments include administration of one or more Na + , K + -ATPaSe inhibitors, for example to the diseased cervical cells.
- such subjects receive surgery to at least partially remove the cervical dysplasia or cervical cancer cells (such as loop electrosurgical excision procedure (LEEP), cone biopsy, or hysterectomy), radiation therapy, chemotherapy, treatment with one or more Na + , K + - ATPase inhibitors, or combinations thereof.
- LEEP loop electrosurgical excision procedure
- cone biopsy cone biopsy
- hysterectomy hysterectomy
- the therapeutic composition includes one or more Na + , K + -ATPase inhibitors (such as an agent that inhibits the Na + , K + -ATPase ⁇ -subunit), and pharmaceutically acceptable carrier.
- such compositions can be used to treat cervical dysplasia or cancer.
- Na + , K + -ATPase inhibitors are agents that significantly decrease the biological activity of the Na + , K + - ATPase. Although such a decrease can be a 100% reduction in biological activity, a 100% reduction is not required for the composition to be effective.
- a Na + , K + -ATPase inhibitor can be an agent that reduces the biological activity of a Na + , K + -ATPase by at least 20%, at least 50%, or at least 90%. Methods of measuring Na + , K + -ATPase biological activity are known in the art, and the disclosure is not limited to particular methods.
- the method includes measuring the uptake Of 86 Rb + as an indicator OfNa + , K + -ATPase ion transport activity.
- cells can be incubated with 1 ⁇ Ci Of 86 Rb + as the chloride salt (Amersham Biosciences) per 10 6 cells, and the reaction stopped after 30 minutes by placing cells on ice with addition of ice-cold phosphate-buffered saline followed by pelleting of the cells.
- the cell pellets were counted in a counter (Cobra Quantium, Packard), wherein the amount Of 86 Rb + detected is reflective OfNa + , K + -ATPase activity (for example greater amounts of 86 Rb + detected indicate greater Na + , K + -ATPase activity).
- a counter Cobra Quantium, Packard
- Another method that can be used to determine Na + , K + -ATPaSe activity is to measure ATPase activity in microsomes using a coupled-enzyme assay (for example see Norby, Methods Enzymol.
- a Na + , K + -ATPase inhibitor is an agent that significantly decreases the biological activity of the Na + , K + -ATPase protein.
- the Na + , K + -ATPase inhibitor can be a cardiac glycoside, such as a cardiac glycoside isolated from a plant or animal.
- cardiac glycosides examples include oubain and g/k/e-strophanthin (from Strophantus ' ), digitalis, digoxin and digitoxin (from Digitalis lanata and Digitalis purpurea), proscillaridine A (from ScMa maritima ), vitexin and rutin (from Crataegus), as well as cardiac glycosides from Adonis vernalis, Adonis aestivalis, Ammi visnaga, Acokanthera oblongifolia, and Convallaria, as well as frog (such as bufalin, marinobufagenin and bufadienolides).
- a glycolipoprotein fraction prepared from Leptospira interrogans has also been shown to have Na + , K ⁇ -ATPase inhibitory activity.
- the Na + , K + -ATPase inhibitor is a digitalis compound.
- the cardiac glycoside is present in the composition at a therapeutically effective amount, such as an amount that reduces Na + , K + -ATPase biological activity in cervical dysplasia or cancer cells.
- the cardiac glycoside can be present in the composition in an amount that reduces growth of or kills cervical dysplasia or cancer cells.
- the cardiac glycoside is present in the composition at a concentration of at least 0.01 mg per gram by weight of the composition, such as at least 0.1 mg, at least 0.25 mg, at least 0.5 mg, or at least 5 mg per gram by weight of the composition, such as 0.01 mg to 0.5 mg or 0.01 mg to 10 mg per gram by weight of the composition.
- a Na + , K + -ATPase inhibitor is an agent that significantly decreases expression of the Na + , K + -ATPase.
- Methods of inhibiting expression in vivo are known in the art, and can include inhibitory RNA (RNAi) molecules, such as siRNA, mRNA, and short hairpin (sh) RNA molecules.
- RNAi inhibitory RNA
- sh short hairpin
- the inhibitor significantly decreases expression of the Na + , K + -ATPase ⁇ -subunit.
- RNAi inhibitory RNA
- sh short hairpin
- RNAi molecules can be generated using routine methods in the art, such as RNAi molecules 20-30 nucleotides in length, such as about 27 nucleotides.
- Exemplary Na + , K + -ATPase RNAi molecules are provided in US Publication No. 20060172965 and 20060234970. Na + , K + -
- ATPase RNAi molecules are administered in therapeutically effective amounts, for example to the vagina or cervix.
- a therapeutic composition includes 0.1% to 99% by weight of the RNAi.
- a therapeutically effective amount of the RNAi results in an extracellular concentration at the surface of the target cervical cell (such as a neoplastic cells, for example a dysplastic or cancerous cell) of at least 100 pM, at least 1 nM, or at least 100 nm, for example 100 pM to 100 nM, 1 nM to 50 nM, 5 nM to 10 nM, or 100 pM to 25 nM.
- compositions provided herein can be in the form of an ointment, cream, emulsion, lotion, gel, solid, solution, suspension, foam or liposomal composition; such as a formulation suitable for vaginal or cervical delivery.
- the pH of the compositions that includes a Na + , K + -ATPase can be about pH 4-9, such as pH 4.5 to pH 7.4.
- the therapeutic composition is contained within a vaginal ring, tampon, suppository, sponge, pillow, puff, or osmotic pump system.
- Pharmaceutically acceptable carriers include agents that permit delivery of one or more therapeutic agents, such as a Na + , K + -ATPase inhibitor.
- Pharmaceutically acceptable carriers that can be used are known to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, 18th Ed. (Easton, Pa.: Mack Publishing Company, 1990).
- the pharmaceutically acceptable carrier is a topical carrier, such as a carrier that is suitable for administration of the composition to cervical tissue in vivo.
- Topical carriers are known in the art, and include any of those used as a basis for ointments., lotions, creams, salves, aerosols, suppositories, gels and the like, such as those suitable for vaginal or cervical administration.
- Suitable carriers for use herein include water, silicone, waxes, petroleum jelly, polyethylene glycol (such as polyethylene glycol-lOOO (PEG-1000)), propylene glycol, liposomes, sugars (such as mannitol and lactose), ointment bases; conventional ophthalmic vehicles; creams; and gels. Additional pharmaceutically acceptable carriers that can be used are provided in US Patent Nos: 6,699,494; 6,306,841; 5,814,338 and US Publication Nos. 2005/0129736 and 2006/0205679.
- the disclosed composition or portion thereof (such as the carrier) can be sterilized or mixed with auxiliary agents, for example thixotropes, stabilizers, wetting agents, and the like.
- auxiliary agents for example thixotropes, stabilizers, wetting agents, and the like.
- the disclosed pharmaceutical compositions can be formed by dispersing the finely divided or dissolved Na + , K + -ATPase inhibitor uniformly throughout the vehicle or base using conventional techniques, for example by a levigating the agent with a small quantity of the base to form a concentrate, which is then diluted geometrically with further base.
- a mechanical mixer can be used.
- Creams, lotions and emulsions can be formed by way of a two-phase heat system, wherein oil-phase ingredients are combined under heat to provide a liquified, uniform system.
- the aqueous-phase ingredients are separately combined using heat.
- the oil and aqueous phases are then added together with constant agitation and allowed to cool.
- concentrated agents can be added as a slurry.
- Volatile or aromatic materials can be added after the emulsion has sufficiently cooled. Preparation of such pharmaceutical compositions is within the general skill of the art.
- Two-phase gel systems generally include a suspension or network of small, discrete particles interpenetrated by a liquid to provide a dispersed phase and a liquid phase.
- Single-phase gel systems are formed by distributing organic macromolecules uniformly throughout a liquid such that there are no apparent boundaries between the dispersed and liquid phases.
- Suitable gelling agents include synthetic macromolecules (such as Carbomers, polyvinyl alcohols and polyoxyethylene- polyoxypropylene copolymers), gums such as tragacanth, as well as sodium alginate, gelatin, methylcellulose, sodium carboxymethylcellulose, methylhydroxyethyl cellulose and hydroxyethyl cellulose.
- dispersing agents such as alcohol or glycerin can be added, or the gelling agent can be dispersed by trituration, mechanical mixing or stirring, or combinations thereof.
- Liposomes can be used to prepare a composition that includes a Na + , K + -ATPase inhibitor.
- liposome formulations are used for poorly soluble or insoluble pharmaceutical agents.
- Liposomal preparations that can be used include cationic (positively charged), anionic (negatively charged) and neutral preparations.
- Cationic liposomes such as, N[l-2,3-dioleyloxy)propyl]-N,N,N-triethylammonium (“DOTMA”), available under the tradename Lipofectin (GIBCO BRJL, Grand Island, N.Y.)
- anionic and neutral liposomes are readily available or can be easily prepared using readily available materials (such as phosphatidyl choline, cholesterol phosphatidyl ethanolamine, dioleoylphosphatidyl choline (“DOPC”), dioleoylphosphatidyl glycerol (“DOPG”), and dioleoylphoshatidyl ethanolamine (“DOPE”)).
- DOPC dioleoylphosphatidyl choline
- DOPG dioleoylphosphatidyl glycerol
- DOPE dioleoylphoshatidyl ethanolamine
- the present disclosure also provides methods for treating cervical dysplasia or cervical cancer in a subject, such as a human female subject.
- the method includes administering a therapeutically effective amount of one or more Na + , K + - ATPase inhibitors to a subject having cervical dysplasia or cancer under conditions that permit treatment of the cervical dysplasia or cancer.
- Exemplary therapeutic compositions are provided above.
- the Na + , K + -ATPase inhibitor can be administered in an amount sufficient to significantly decrease Na + , K + -ATPase biological activity in cells of the cervix, such as dysplastic or cancer cells.
- Na + , K + -ATPase biological activity in cells of the cervix is decreased by at least 50%, such as at least 95%.
- administration of a therapeutically effective amount of a Na + , K + -ATPase inhibitor to the cervix reduces the number or size of diseased cervical cells by at least 20%, at least 40%, at least 50%, at least 80%, such as at least 95%.
- treatment of a cervical dysplasia prevents or delays development of cervical cancer, reduces the stage or grade of dysplasia or cancer (for example CIN III to CIN II or I, or Stage IHA to a Stage IIA or Stage I or Stage 0), or combinations thereof.
- the method can be used to treat cervical dysplasia prior to its progression to cancer.
- the therapeutic composition containing one or more Na + , K + -ATPase inhibitor is administered directly to the cervix.
- the epithelial layer of the cervix can be contacted with a therapeutically effective amount of a Na + , K + -ATPase inhibitor (such as a digitalis compound), thereby decreasing or reversing molecular changes associated progression from dypslasia to cancer or increasing the grade of dysplasia or cancer.
- a therapeutically effective amount of a Na + , K + -ATPase inhibitor such as a digitalis compound
- Higher concentrations and longer periods of contact can be used to reach and treat invading cancer cells below the epithelial layer, or to reach and treat endocervical glands located below the epithelial layer in dysplastic cervical tissues.
- the therapeutic composition containing one or more Na + , K + -ATPaSe inhibitors is administered vaginally, thereby permitting the composition to reach the diseased cervical cells.
- the therapeutic composition containing one or more Na + , K + - ATPase inhibitors is administered to the subject at a dose of at least 0.001 ⁇ g/kg of subject, for example at least 0.01 ⁇ g/kg, at least 0.1 ⁇ g/kg, such as 0.001 ⁇ g/kg to 1 ⁇ g/kg.
- the therapeutic composition can be applied in a single unit dose or multiple doses over time, such as daily, weekly, or monthly over a period of time, such as at least one month, at least 6-months, or at least 12-months.
- Na + , K + -ATPase Expression in Cervical Dysplasia and Cervical Cancer This example describes methods used to compare Na + , K + -ATPase expression in normal, cervical dysplasia, and cervical cancer samples. Although particular detection methods are provided, one skilled in the art will appreciate that other antibodies and other immunohistochemical methods can be used.
- Monoclonal anti-Na + , K + -ATPase ⁇ subunit (clone M7-PB-E9) and ⁇ l subunit (clone M17-P5-F11) antibodies were used to detect the ⁇ and ⁇ l subunits of the Na + , K + -ATPase, respectively, in cervical tissue samples (namely normal, low grade, high grade, and cancer cases), using a BenchMark XT automated slide stainer (Ventana Medical Systems, Inc., Arlington, AZ).
- the signal for Na + , K + -ATPase ⁇ and ⁇ l was visualized with /VIEW DAB (Ventana Medical Systems, Inc.) and tissue sections were counterstained with Hematoxylin II and Bluing Reagent. The specificity OfNa + , K + -ATPaSe ⁇ and ⁇ l immunostaining was confirmed with tissue microarray slides containing normal and cancer tissues (Super Bio Chips, Korea).
- tissue sections on the tissue microarray slides showed both Na + , K + - ATPase ⁇ and ⁇ l subunits in the same cell populations.
- the cell membrane staining patterns for Na + , K + -ATPase ⁇ and ⁇ l subunits were different among different tissue types.
- kidney sections showed the basal and lateral cell surface staining while the small intestine showed mainly the lateral cell surface staining.
- Na + , K + -ATPase ⁇ and ⁇ l subunits were visualized in the cervical tissue sections.
- Na + , K + -ATPase ⁇ subunit was localized at the basal layer of cervical epithelial layers of the normal cervical tissues (FIG. IA).
- the first cell layer next to the stroma tissue showed strong cytoplasmic staining Na + , K + -ATPase ⁇ subunit while adjacent a few cell layers toward epithelial surface showed cell membrane staining.
- normal cervical tissues were absent for the Na + , K + -ATPase ⁇ l subunit (FIG. IB), though the levels OfNa + , K + - ATPase ⁇ l subunit might be too low to permit immunohistochemical detection, or a different ⁇ subunit (such as ⁇ 2 and/or ⁇ 3), may be expressed.
- FIG. I D high grade dysplasia clinical samples also demonstrated expression of the Na + , K + -ATPase ⁇ l subunit in the membrane.
- This example describes methods used to visualize chromosomal DNA and compare Na + , K + -ATPase expression in cervical dysplasia samples. Although particular detection methods are provided, one skilled in the art will appreciate that other staining and detection methods can be used.
- Telomere and centromere (which serves as DNA positive control) specific oligoprobes were used for in situ hybridization to visualizing chromosomal DNA sequences in cervical tissue samples. Telomere and centromere in situ hybridization applications were optimized on a BenchMark XT instrument by modifying established HPV in situ hybridization protocols. The signal for telomeric and centromeric chromosomal DNA was detected with iVIEW Blue Plus and counterstained with Red Counterstain II. Na + , K + - ATPase ⁇ -subunit expression was detected as described in Example 1.
- FIGS. 3A-F dysplastic cervical tissue samples having different levels of telomeric shortening, and as telomeric shortening occurs, there is a corresponding increase in the level OfNa + , K + -ATPaSe ⁇ -subunit expressed in the sample.
- FIGS. 3A and 3D are positive controls indicating the presence of chromosomal DNA in the samples
- FIGS. 3B and 3E show the differing levels of telomeric DNA in two cases of dysplasia (less signal indicating shorter telomeric regions)
- FIGS. 3C and 3F show corresponding levels ofNa + , K + -ATPase ⁇ -subunit expression.
- compositions that include a Na + , K + -ATPase inhibitor, as well as methods of using such a composition to treat cervical dysplasia or cancer.
- a Na + , K + -ATPase inhibitor as well as methods of using such a composition to treat cervical dysplasia or cancer.
- Na + , K + -ATPase inhibitors and methods of administration are provided, the disclosure is not limited to such agents and methods.
- the therapeutic composition includes one or more Na + , K + -ATPase inhibitors, such as an agent that inhibits the activity or expression of the Na + , K + -ATPase ⁇ -subunit (such as the ⁇ l-subunit).
- the Na + , K + -ATPase inhibitor includes a digitalis compound and a pharmaceutically acceptable topical carrier.
- the digitalis compound is digoxin, digitoxin, or combinations thereof, for example in 0.01 digitalis mg per gram by weight of the composition, such as at least 0.1 mg, at least 0.25 mg, at least 0.5 mg, or at least 5 mg per gram by weight of the composition, such as 0.01 mg to 0.5 mg or 0.01 mg to 10 mg per gram by weight of the composition.
- the medicament and method can be used specifically for treatment of cervical dysplasia prior to its progression to cancer. By contacting the epithelial layer (where ⁇ -subunit expression levels increase first) with a digitalis compound, the molecular changes associated progression from dypslasia to cancer may be halted or reversed. Higher concentrations and longer periods of contact may be useful for reaching and treating invading cancer cells below the epithelial layer or for endocervical glands located below the epithelial layer in dysplastic cervical tissues.
- the digitalis compound can be added to any pharmaceutically acceptable topical carrier to prepare the medicament.
- the topical carrier can be any of those well-known for use in the pharmaceutical, cosmetic, and medical arts as a basis for ointments, lotions, creams, salves, aerosols, suppositories, gels and the like. If desired, these may be sterilized or mixed with auxiliary agents, e.g., thixotropes, stabilizers, wetting agents, and the like.
- auxiliary agents e.g., thixotropes, stabilizers, wetting agents, and the like.
- vehicles for non-sprayable topical preparations include ointment bases, e.g., polyethylene glycol- 1000 (PEG-1000); conventional ophthalmic vehicles; creams; and gels, as well as petroleum jelly and the like.
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- Gynecology & Obstetrics (AREA)
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
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Abstract
Description
Claims
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
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AU2006332806A AU2006332806B2 (en) | 2005-12-30 | 2006-12-27 | Na+, K+-ATPase expression in cervical dysplasia and cancer |
JP2008548712A JP4960972B2 (en) | 2005-12-30 | 2006-12-27 | Expression of Na +, K + -ATPase in cervical dysplasia and cervical cancer |
CA2634896A CA2634896C (en) | 2005-12-30 | 2006-12-27 | Na+, k+-atpase expression in cervical dysplasia and cancer |
US12/096,075 US7851145B2 (en) | 2005-12-30 | 2006-12-27 | Na+, K+-ATPase expression in cervical dysplasia and cancer |
AT06848224T ATE456053T1 (en) | 2005-12-30 | 2006-12-27 | NA+, K+-ATPASE EXPRESSION IN CERVICAL DYSPLASIA AND CANCER |
CN200680050096.6A CN101360998B (en) | 2005-12-30 | 2006-12-27 | Na+, K+ adenosine triphosphate expression of enzymes in cervical atypical hyperplasia and cervical carcinoma |
EP06848224A EP1977246B1 (en) | 2005-12-30 | 2006-12-27 | Na+, k+-atpase expression in cervical dysplasia and cancer |
DE602006011959T DE602006011959D1 (en) | 2005-12-30 | 2006-12-27 | NA +, K + -ATPASE EXPRESSION IN ZERVIX DYSPLASIA AND CANCER |
HK09102663.3A HK1124918A1 (en) | 2005-12-30 | 2009-03-19 | Na, k-atpase expression in cervical dysplasia and cancer nak |
Applications Claiming Priority (4)
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US75522305P | 2005-12-30 | 2005-12-30 | |
US60/755,223 | 2005-12-30 | ||
US76444706P | 2006-02-01 | 2006-02-01 | |
US60/764,447 | 2006-02-01 |
Publications (1)
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WO2007079128A1 true WO2007079128A1 (en) | 2007-07-12 |
Family
ID=38051860
Family Applications (1)
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PCT/US2006/049392 WO2007079128A1 (en) | 2005-12-30 | 2006-12-27 | Na+, k+-atpase expression in cervical dysplasia and cancer |
Country Status (11)
Country | Link |
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US (1) | US7851145B2 (en) |
EP (1) | EP1977246B1 (en) |
JP (1) | JP4960972B2 (en) |
CN (1) | CN101360998B (en) |
AT (1) | ATE456053T1 (en) |
AU (1) | AU2006332806B2 (en) |
CA (1) | CA2634896C (en) |
DE (1) | DE602006011959D1 (en) |
ES (1) | ES2340206T3 (en) |
HK (1) | HK1124918A1 (en) |
WO (1) | WO2007079128A1 (en) |
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WO2008055530A1 (en) * | 2006-11-09 | 2008-05-15 | Unibioscreen S.A. | Targeting of alpha-1 or alpha-3 subunit of na+, k+-atpase in the treatment of proliferative diseases |
US7695929B2 (en) | 2006-11-01 | 2010-04-13 | Ventana Medical Systems, Inc. | Haptens, hapten conjugates, compositions thereof and method for their preparation and use |
JP2011501809A (en) * | 2007-10-15 | 2011-01-13 | ケンブリッジ キャンサー ダイアグノスティクス リミテッド | Cancer diagnosis, prediction, and prognostic testing |
JP2011508184A (en) * | 2007-11-13 | 2011-03-10 | フェニックス・バイオテクノロジー・インコーポレイテッド | A method to determine the probability of therapeutic response in cancer chemotherapy using cardiac glycosides |
US9017954B2 (en) | 2007-05-23 | 2015-04-28 | Ventana Medical Systems, Inc. | Polymeric carriers for immunohistochemistry and in situ hybridization |
WO2017013637A1 (en) | 2015-07-19 | 2017-01-26 | Yeda Research And Development Co. Ltd. | Selective inhibitors of alpha2-containing isoforms of na,k-atpase and use thereof for reduction of intraocular pressure |
US10718693B2 (en) | 2008-06-05 | 2020-07-21 | Ventana Medical Systems, Inc. | Compositions comprising nanomaterials and method for using such compositions for histochemical processes |
EP3907231A1 (en) | 2015-07-19 | 2021-11-10 | Yeda Research and Development Co., Ltd. | Selective inhibitors of alpha2-containing isoforms of na,k-atpase and use thereof for reducing intraocular pressure |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
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US20130107066A1 (en) * | 2011-10-27 | 2013-05-02 | Qualcomm Incorporated | Sensor aided video stabilization |
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- 2006-12-27 CA CA2634896A patent/CA2634896C/en active Active
- 2006-12-27 US US12/096,075 patent/US7851145B2/en active Active
- 2006-12-27 AU AU2006332806A patent/AU2006332806B2/en active Active
- 2006-12-27 AT AT06848224T patent/ATE456053T1/en not_active IP Right Cessation
- 2006-12-27 ES ES06848224T patent/ES2340206T3/en active Active
- 2006-12-27 WO PCT/US2006/049392 patent/WO2007079128A1/en active Application Filing
- 2006-12-27 EP EP06848224A patent/EP1977246B1/en active Active
- 2006-12-27 CN CN200680050096.6A patent/CN101360998B/en active Active
- 2006-12-27 DE DE602006011959T patent/DE602006011959D1/en active Active
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2009
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US8846320B2 (en) | 2006-11-01 | 2014-09-30 | Ventana Medical Systems, Inc. | Haptens, hapten conjugates, compositions thereof and method for their preparation and use |
US7695929B2 (en) | 2006-11-01 | 2010-04-13 | Ventana Medical Systems, Inc. | Haptens, hapten conjugates, compositions thereof and method for their preparation and use |
US9719986B2 (en) | 2006-11-01 | 2017-08-01 | Ventana Medical Systems, Inc. | Haptens, hapten conjugates, compositions thereof preparation and method for their preparation and use |
WO2008055530A1 (en) * | 2006-11-09 | 2008-05-15 | Unibioscreen S.A. | Targeting of alpha-1 or alpha-3 subunit of na+, k+-atpase in the treatment of proliferative diseases |
US9575067B2 (en) | 2007-05-23 | 2017-02-21 | Ventana Medical Systems, Inc. | Polymeric carriers for immunohistochemistry and in situ hybridization |
US9017954B2 (en) | 2007-05-23 | 2015-04-28 | Ventana Medical Systems, Inc. | Polymeric carriers for immunohistochemistry and in situ hybridization |
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JP2011501809A (en) * | 2007-10-15 | 2011-01-13 | ケンブリッジ キャンサー ダイアグノスティクス リミテッド | Cancer diagnosis, prediction, and prognostic testing |
JP2011508184A (en) * | 2007-11-13 | 2011-03-10 | フェニックス・バイオテクノロジー・インコーポレイテッド | A method to determine the probability of therapeutic response in cancer chemotherapy using cardiac glycosides |
US10718693B2 (en) | 2008-06-05 | 2020-07-21 | Ventana Medical Systems, Inc. | Compositions comprising nanomaterials and method for using such compositions for histochemical processes |
WO2017013637A1 (en) | 2015-07-19 | 2017-01-26 | Yeda Research And Development Co. Ltd. | Selective inhibitors of alpha2-containing isoforms of na,k-atpase and use thereof for reduction of intraocular pressure |
EP3907231A1 (en) | 2015-07-19 | 2021-11-10 | Yeda Research and Development Co., Ltd. | Selective inhibitors of alpha2-containing isoforms of na,k-atpase and use thereof for reducing intraocular pressure |
Also Published As
Publication number | Publication date |
---|---|
AU2006332806A8 (en) | 2011-10-20 |
DE602006011959D1 (en) | 2010-03-11 |
CN101360998B (en) | 2015-12-02 |
EP1977246B1 (en) | 2010-01-20 |
EP1977246A1 (en) | 2008-10-08 |
AU2006332806A1 (en) | 2007-07-12 |
CA2634896C (en) | 2018-08-07 |
US7851145B2 (en) | 2010-12-14 |
HK1124918A1 (en) | 2009-07-24 |
JP2009522551A (en) | 2009-06-11 |
AU2006332806B2 (en) | 2012-03-15 |
ES2340206T3 (en) | 2010-05-31 |
CA2634896A1 (en) | 2007-07-12 |
US20080286386A1 (en) | 2008-11-20 |
ATE456053T1 (en) | 2010-02-15 |
CN101360998A (en) | 2009-02-04 |
JP4960972B2 (en) | 2012-06-27 |
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