Ceramide reversal of multi-drug resistance
Based on the observation that the application of small amounts of exogenous acid sphingomyelinase to generate endogenous ceramide, or provision of exogenous long-chain natural C16-ceramide resulted in rapid translocation of vacuolar daunorubicin into the nucleus in multi-drug resistant (MDR) cells, the present invention relates to a nano-liposomal preparation that includes C16-ceramide. Exposure of MDR cells to the C16:0 ceramide-based nanoliposomes provide a mechanism to reverse MDR in chemoresistant cells and tumors, by inducing rapid translocation of chemotherapeutic agent from cytoplasmic vesicles to the nucleus.
1. A method for inducing nuclear trafficking of a therapeutic agent and reversing multi-drug resistance (MDR) in cancer cells that overexpress P-glycoprotein (P-gp) comprising contacting said cancer cells with the therapeutic agent and C16-ceramide.
2. The method of claim 1 , wherein said cancer cells are contacted with a nano-liposome comprising said C16-ceramide.
3. The method of claim 1 , wherein said therapeutic agent is an anti-cancer therapeutic agent.
4. The method of claim 1 , wherein said cancer cells are contacted with C16:0 prior to, simultaneously with, or after exposure of said tumor cells to the therapeutic agent.
5. A method for treating a P-gp-mediated MDR cancer, the method comprising administering to a subject in need thereof, a therapeutically effective amount of C16:0-ceramide.
6. The method of claim 5 , wherein the C16:0 ceramide is administered as part of a nano-liposome.
7. A nano-liposome comprising a C16-ceramide, wherein said nano-liposome induces nuclear trafficking of a therapeutic agent when applied to a cell that overexpresses P-glycoprotein (P-gp) lipid transporter and exhibits multidrug resistance (MDR).
8. The nano-liposome of claim 7 , wherein said ceramide is present in an amount between 1% to 75% of said total lipid composition of said liposome.
9. The nano-liposome of claim 7 , wherein said ceramide is present in an amount between 5% to 50% of said total lipid composition of said liposome.
10. The nano-liposome of claim 7 , wherein said ceramide is present in an amount between 10% to 25% of said total lipid composition of said liposome.
11. The nano-liposome of claim 7 , wherein said nano-liposome consists essentially of fully hydrogenated soybean phosphatidylcholine (HSPC), N-carbamyl-poly-(ethylene glycol methyl ether)-1,2-distearoyl-sn-glyco-3-phosphoethanolamine (2kPEG-DSPE), and ceramide in a mol/mol ratio of 82.5:7.5:10.
12. The nano-liposome of claim 7 , wherein said nano-liposome has a mean diameter of about 50 nM to about 200 nM.
13. The nano-liposome of claim 7 , wherein said nano-liposome has a mean diameter of about 75 nM to about 150 nM.
14. The nano-liposome of claim 7 , wherein said nano-liposome has a mean diameter of about 90 nM to about 125 nM in size.
15. The nano-liposome of claim 7 , wherein said nano-liposome further comprises a therapeutic agent.
16. The nano-liposome of claim 15 , wherein said therapeutic agent is selected from the group consisting of doxorubicin, daunorubicin, vincristine, cisplatin.
17. A method for selective treatment of a cancer associated with high lipid transporter P-glycoprotein (P-gp) levels, the method comprising administering to a subject in need thereof a ceramide-based nano-liposome of claim 7 .
18. A pharmaceutical composition comprising a nano-liposome of any of claims 7 and a pharmaceutically acceptable carrier.
19. A method for the selection of appropriate treatment for a subject with a MDR cancer, the method comprising:
(a) determining the levels of lipid transporter P-glycoprotein (P-gp) in a tumor cell from the subject;
(b) identifying the tumor as MDR if levels of lipid transporter P-glycoprotein (P-gp) in a cell from said tumor are elevated in comparison to levels from a cell that is drug sensitive.
(c) administering exogenous ceramide with an anti-cancer agent if the tumor is identified as MDR.