US2013273178A1PendingUtilityA1
Methods and compositions for promoting activity of anti-cancer therapies
Est. expiryAug 3, 2026(~0 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 35/04A61P 37/00A61P 9/00A61P 35/00A61P 35/02A61P 27/02A61K 45/06A61P 11/00A61K 31/475A61P 15/00A61K 31/337A61K 31/7048A61P 1/00A61K 31/568A61K 31/437A61K 31/506A61K 31/58A61P 19/02A61P 17/02A61K 31/513A61K 31/704A61K 31/505A61P 19/04A61P 17/04A61P 13/08A61K 33/243A61K 33/24
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Claims
Abstract
The present invention relates to a method of inhibiting growth of a cancerous cell. The method includes the step of exposing the cancerous cell to an anti-cancer therapy and an effective amount of a steroid saponin.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . A method of inhibiting growth of a cancerous cell, the method including the step of exposing the cancerous cell to an anti-cancer agent and an effective amount of a steroid saponin, wherein the steroid saponin is selected from the group consisting of deltonin (diosgenin Rha2, [Glc4], Glc), dioscin (diosgenin Rha2, [Rha4], Glc), and prosapogenin A (diosgenin Rha2, Glc).
2 . The method according to claim 1 , wherein the anti-cancer agent is selected from one or more of the group consisting of cisplatin, taxol (paclitaxel), docetaxel, vincristine sulphate, doxorubicin, 5-fluorouracil and imatinib.
3 . The method according to claim 1 , wherein the method is used to inhibit formation and/or growth of a tumor in a subject.
4 . The method according to claim 1 , wherein the method is used to treat cancer in a subject.
5 . A method of promoting the activity of an anti-cancer agent in a subject, the method including exposing the subject to an effective amount of a steroid saponin, wherein the steroid saponin is selected from the group consisting of deltonin (diosgenin Rha2, [Glc4], Glc), dioscin (diosgenin Rha2, [Rha4], Glc), and prosapogenin A (diosgenin Rha2, Glc).
6 . The method according to claim 5 , wherein the anti-cancer agent is selected from one or more of the group consisting of cisplatin, taxol (paclitaxel), docetaxel, vincristine sulphate, doxorubicin, 5-fluorouracil and imatinib.
7 . The method according to claim 5 , wherein the method is used to reduce the amount of the anti-cancer agent provided to the subject to treat a cancer in the subject.
8 . The method according to claim 5 , wherein the method is used to treat a cancer in the subject, wherein the subject has an increased resistance to the anti-cancer agent.
9 . A method of promoting apoptosis of a cancerous cell due to exposure of the cancerous cell to an anti-cancer agent, the method including exposing the cancerous cell to an effective amount of a steroid saponin, wherein the steroid saponin is selected from the group consisting of deltonin (diosgenin Rha2, [Glc4], Glc), dioscin (diosgenin Rha2, [Rha4], Glc), and prosapogenin A (diosgenin Rha2, Glc).
10 . The method according to claim 9 , wherein the anti-cancer agent is selected from one or more of the group consisting of cisplatin, taxol (paclitaxel), docetaxel, vincristine sulphate, doxorubicin, 5-fluorouracil and imatinib.
11 . The method according to claim 9 , wherein the method reduces resistance developing to anti-cancer agent in the cancerous cell.Join the waitlist — get patent alerts
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