Materials and methods for sensitizing multidrug resistant cells
Disclosed herein are materials and methods for sensitizing multidrug resistant cancer cells that express ABCG2 and related proteins members of a family of ATP-binding transporter superfamily that mediate drug efflux found in some types of multidrug resistant cancer cells. A series of compounds, including (N-(4-chlorophenyl)-2-[(6-{[4,6-di(4-morpholinyl)-1,3,5-tri-azin-2-yl]amino}-1,3-benzothiazol-2-yl)sulfanyl]acetamide), specifically inhibits ABCG2 and can be used to boost the bio-avail-ability of one or more effective cancer killing drugs, making it possible to use certain widely used chemotherapeutic reagent to treat multidrug resistance cancers. Using these compounds in combination with chemotherapeutic drugs that are substrates for ABCG2 and related proteins may also find utility in treating cancer cells that are not currently identified as multi-drug resistant. Additionally, these compounds appear to accelerate the intercellular degradation of ABCG2 and related proteins. They are not toxic to animals at levels at which they effect the activity of ABCG2 expressed in multi-drug resistant cancer lines.
1. A method of overcoming multidrug resistance in an individual undergoing cancer chemotherapy, the method comprising the step of:
providing to the individual a pharmaceutical composition comprising a chemotherapeutic reagent and an ABCG2 inhibitor, or a pharmaceutically acceptable salt thereof, wherein the ABCG2 inhibitor has a formula of:
wherein R 1 is selected from the group consisting of:
wherein R 2 is selected from the group consisting of:
and
wherein X is a halide; wherein said chemotherapeutic reagent is selected from a group consisting of an anthracycline antibiotic, anthracenedione and topoisomerase I inhibitor.
2. The method of claim 1 , wherein the ABCG2 inhibitor is present in the pharmaceutical composition at about 45 nM or less.
3. The method of claim 1 , wherein the ABCG2 inhibitor is:
4. The method of claim 1 , wherein the ABCG2 inhibitor is:
5. The method of claim 1 , wherein the ABCG2 inhibitor is:
6. The method of claim 1 , wherein the ABCG2 inhibitor is:
7. The method of claim 1 , wherein the ABCG2 inhibitor is:
8. The method of claim 1 , wherein the ABCG2 inhibitor is:
9. The method of claim 1 , wherein the anthracycline antibiotic is Adriamycin.
10. The method of claim 1 , wherein the anthracenedione is mitoxantrone.
11. The method of claim 1 , wherein the topoisomerase I inhibitor is topotecan.
12. The method of claim 1 , wherein the topoisomerase I inhibitor is camptothecin.