Treatment of refractory cancers using NA+/K+ ATPase inhibitors
The reagent, pharmaceutical formulation, kit, and methods of the invention provides a new approach to treat refractory cancers using Na + /K + -ATPase inhibitors, such as cardiac glycosides (e.g. ouabain or proscillaridin, etc.).
1 . A method of inhibiting the growth or spread of a refractory cancer in an individual, comprising administering to the individual an effective amount of a Na + /K + -ATPase inhibitor.
2 . A method for promoting treatment of an individual suffering from a refractory cancer, comprising packaging, labeling and/or marketing a Na + /K + -ATPase inhibitor to be used as part of a treatment for inhibiting the growth or spread of the refractory cancer.
3 . A method of treating multidrug resistance of refractory tumor cells in a refractory cancer patient in need of such treatment, said method comprising administering, concurrently or sequentially, an effective amount of a Na + /K + -ATPase inhibitor and an antineoplastic agent to said patient.
4 . The method of claim 1 , wherein the cancer is refractory to radiation therapy.
5 . The method of claim 1 , wherein the cancer is refractory to anti-cancer chemotherapy.
6 . The method of claim 1 , wherein the refractory cancer is a solid tumor.
7 . The method of claim 6 , wherein the solid tumor is a tumor in the pancreas, lung, kidney, ovarian, breast, prostate, gastric, colon, bladder, prostate, brain, skin, testicles, cervix, or liver.
8 . The method of claim 7 , wherein the solid tumor is a pancreatic tumor refractory to treatment by one or more of: fluorouracil, carmustine (BCNU), temozolomide (TMZ), streptozotocin, and gemcitabine.
9 . The method of claim 7 , wherein the solid tumor is a lung tumor refractory to etoposide or platinum-based therapy.
10 . The method of claim 9 , wherein the lung tumor is refractory small cell lung cancer.
11 . The method of claim 9 , wherein the lung tumor is refractory non-small cell lung cancer.
12 . The method of claim 1 , wherein the refractory cancer is a hematological cancer.
13 . The method of claim 1 , wherein the Na + /K + -ATPase inhibitor is a cardiac glycoside.
14 . The method of claim 13 , wherein the cardiac glycoside has an IC 50 for killing one or more different cancer cell lines of 500 nM or less.
15 . The method of claim 13 , wherein the cardiac glycoside is represented by the general formula:
wherein
R represents a glycoside of 1 to 6 sugar residues;
R 1 represents hydrogen, —OH or ═O;
R 2 , R 3 , R 4 , R 5 , and R 6 each independently represents hydrogen or —OH; and
R 7 represents
which cardiac glycoside has an IC 50 for killing one or more different cancer cell lines of 500 nM or less.
16 . The method of claim 13 , wherein the cardiac glycoside comprises a steroid core with either a pyrone substituent at C17 (the “bufadienolides form”) or a butyrolactone substituent at C17 (the “cardenolide” form).
17 . The method of claim 13 , wherein the cardiac glycoside is ouabain or proscillaridin.
18 . The method of claim 13 , wherein the cardiac glycoside is conjointly administered with an effective amount of one or more anti-tumor agents selected from the group consisting of: an EGF-receptor antagonist, and arsenic sulfide, adriamycin, cisplatin, carboplatin, cimetidine, carminomycin, mechlorethamine hydrochloride, pentamethylmelamine, thiotepa, teniposide, cyclophosphamide, chlorambucil, demethoxyhypocrellin A, melphalan, ifosfamide, trofosfamide, Treosulfan, podophyllotoxin or podophyllotoxin derivatives, etoposide phosphate, teniposide, etoposide, leurosidine, leurosine, vindesine, 9-aminocamptothecin, camptoirinotecan, crisnatol, Chloroambucil, megestrol, methopterin, mitomycin C, ecteinascidin 743, busulfan, carmustine (BCNU), lomustine (CCNU), lovastatin, 1-methyl-4-phenylpyridinium ion, semustine, staurosporine, streptozocin, thiotepa, phthalocyanine, dacarbazine, aminopterin, methotrexate, trimetrexate, thioguanine, mercaptopurine, fludarabine, pentastatin, cladribin, cytarabine (ara C), porfiromycin, 5-fluorouracil, 6-mercaptopurine, doxorubicin hydrochloride, leucovorin, mycophenoloc acid, daunorubicin, deferoxamine, floxuridine, doxifluridine, ratitrexed, idarubicin, epirubican, pirarubican, zorubicin, mitoxantrone, bleomycin sulfate, mitomycin C, actinomycin D, safracins, saframycins, quinocarcins, discodermolides, vincristine, vinblastine, vinorelbine tartrate, vertoporfin, paclitaxel, tamoxifen, raloxifene, tiazofuran, thioguanine, ribavirin, EICAR, estramustine, estramustine phosphate sodium, flutamide, bicalutamide, buserelin, leuprolide, pteridines, diyneses, levamisole, aflacon, interferon, interleukins, aldesleukin, filgrastim, sargramostim, rituximab, BCG, tretinoin, irinotecan hydrochloride, betamethosone, gemcitabine hydrochloride, verapamil, VP-16, altretamine, thapsigargin, and topotecan.
19 . The method of claim 13 , wherein the resistance of the refractory cancer to a therapeutic agent is mediated through tubulin.
20 . The method of claim 13 , wherein the resistance of the refractory cancer to a therapeutic agent is mediated through multidrug resistance.
21 . The method of claim 20 , wherein the multidrug resistance is caused by increased expression of ATP-binding cassette (ABC) transporters; overexpression of P-gp; or changes in topoisomerase II, protein kinase C or specific glutathione transferase enzymes.
22 . The method of claim 13 , wherein the resistance of the refractory cancer to a therapeutic agent is mediated through topoisomerase.
23 . The method of claim 13 , wherein the resistance of the refractory cancer to a therapeutic agent is mediated through Mitoxantrone.
24 . A packaged pharmaceutical comprising a Na + /K + -ATPase inhibitor formulated in a pharmaceutically acceptable excipient and suitable for use in humans, and a label or instructions for administering the Na + /K + -ATPase inhibitor as part of a treatment for inhibiting the growth or spread of a refractory cancer.