Methods of using RARγ agonists for cancer treatment
The invention discloses novel RAR gamma selective agonists used in the treatment of cancer. The invention also discloses administration of RAR gamma selective agonists to mammals, including humans for the purpose of selectively activating RAR gamma receptor and treat cancer by way of activating tumor infiltrating lymphocytes.
1. A method of treating cancer comprising administering to a patient in need thereof an effective amount of an RARγ-selective agonist of the structure:
or a pharmaceutically acceptable salt thereof, wherein R is H or C 1-6 alkyl; R 7 to R 12 are independently C 1-6 alkyl, a hydrogen atom, an alkoxy group, a halogen atom, a nitro group, a hydroxy group, OCF 3 , or COR 13 , wherein R 13 is C 1-6 alkyl or CF; Y is oxygen, sulfur, or NR 14 , wherein R 14 is C 1-6 alkyl; and the crossed double bond to the ═N—OH group indicates that stereochemistry is not specified.
2. The method of claim 1 , wherein the cancer is breast cancer or lung cancer.
3. The method of claim 2 , wherein the breast cancer is triple negative breast cancer.
4. The method of claim 3 , wherein the breast cancer is Her2 + breast cancer.
5. The method of claim 1 , wherein the effective amount is about 1 to about 100 mg/day.
6. The method of claim 1 , further comprising administration of a CAR-T cell or an immune checkpoint inhibitor.
7. The method of claim 1 , comprising administering the RARγ selective agonist periodically throughout an interval of treatment or in repeated cycles throughout an interval of treatment.
8. The method of claim 7 , wherein periodically is daily, twice daily, or ever other day.
9. A method of treating cancer, comprising infusing tumor infiltrating lymphocytes (TIL) generated or expanded, wherein the TIL are generated or expanded by contacting the TIL with an RARγ selective agonist of the structure:
or a pharmaceutically acceptable salt thereof, wherein R is H or C 1-6 alkyl; R 7 to R 12 are independently C 1-6 alkyl, a hydrogen atom, an alkoxy group, a halogen atom, a nitro group, a hydroxy group, OCF 3 , or COR 13 , wherein R 13 is C 1-6 alkyl or CF; Y is oxygen, sulfur, or NR 14 , wherein R 14 is C 1-6 alkyl; and the crossed double bond to the ═N—OH group indicates that stereochemistry is not specified.
10. The method of claim 9 , wherein the TIL are cultured in vitro in a media supplemented with the RARγ selective agonist.
11. The method of claim 9 , comprising isolating TIL from a tumor explant.
12. The method of claim 9 , comprising culturing peripheral blood mononuclear cells (PBMC) in vitro, in the presence of irradiated tumor cells, in a media supplemented with the RARγ selective agonist.
13. The method of claim 12 , wherein the PBMC and the irradiated tumor cells are obtained from the same individual.
14. The method of claim 1 , wherein R is H, methyl, or ethyl.
15. The method of claim 1 , wherein Y is O.
16. The method of claim 1 , wherein the ═N—OH group is in the E configuration.
17. The method of claim 1 , wherein the RARγ selective agonist is 4-((1E,3E)-3-(3-(tert-butyl)-2-ethyl-benzofuran-5-yl)-3-(hydroxyimino)prop-1-en-1-yl)-3-fluorobenzoic acid