Inhibitors of multidrug resistance transporter P-glycoprotein
The present disclosure provides a method of treating a subject that is resistant to one or more drugs by identifying a subject having one or more drug resistant cells; administering to the subject a pharmaceutically effective amount of an inhibitor compound, and contacting one or more drug resistant cells with the inhibitor compound to reduce the export of the inhibitor compound from the one or more drug resistant tumor cells and to block the transport of drug(s) from the one or more drug resistant cells.
1. A method of treating a subject having prostate cancer or liver cancer that is resistant to one or more chemotherapeutic drugs comprising the steps of:
identifying a subject having one or more drug resistant prostate or liver cancer cells that express a P-glycoprotein;
administering to the subject a pharmaceutically effective amount of an inhibitor compound having the following structural formula:
and
contacting one or more drug resistant cancer cells with the inhibitor compound to reduce the drug resistance of the prostate or liver cancer cells.
2. The method of claim 1 , wherein the inhibitor compound interacts with an exporter protein.
3. The method of claim 1 , wherein the inhibitor compound is a P-glycoprotein inhibitor.
4. The method of claim 1 , wherein the inhibitor compound interacts with drug-toxin pumping structures of a P-glycoprotein.
5. The method of claim 1 , wherein the inhibitor compound interacts with ATP binding domain(s) of a P-glycoprotein and the inhibitor compound does not bind to drug binding site(s) on the P-glycoprotein.
6. The method of claim 1 , wherein the inhibitor compound is transported by a P-glycoprotein.
7. The method of claim 1 , wherein the one or more drug resistant prostate or liver cancer cells are one or more multidrug resistant prostate or liver tumor cells.