Pharmaceutical compositions and methods
Pharmaceutical compositions and kits including a tyrosine hydroxylase inhibitor; melanin, a melanin promoter, or a combination thereof a p450 3A4 promoter; and a leucine aminopeptidase inhibitor are provided. Also provided are methods of treating cancer in a subject, comprising administering an effective amount of a tyrosine hydroxylase inhibitor, a melanin promoter, a p450 3A4 promoter, and a leucine aminopeptidase inhibitor to the subject in need thereof. Also provided are methods of reducing cell proliferation in a subject comprising administering an effective amount of a tyrosine hydroxylase inhibitor, a melanin promoter, a p450 3A4 promoter, and a leucine aminopeptidase inhibitor to the subject in need thereof.
1. A method for treating cancer in a patient comprising administering to the patient an effective amount of:
a) a tyrosine hydroxylase inhibitor that is methyl (2R)-2-amino-3-(2-chloro-4hydroxyphenyl) propanoate, D-tyrosine ethyl ester hydrochloride, methyl (2R)-2-amino-3-(2,6-dichloro-3,4-dimethoxyphenyl) propanoate H-D-Tyr(TBU)-allyl ester HCl, methyl (2R)-2-amino-3-(3-chloro-4,5-dimethoxyphenyl) propanoate, methyl (2R)-2-amino-3-(2-chloro-3-hydroxy-4-methoxyphenyl) propanoate, methyl (2R)-2-amino-3-(4-[(2-chloro-6-fluorophenyl) methoxy]phenyl) propanoate, methyl (2R)-2-amino-3-(2-chloro-3,4-dimethoxyphenyl) propanoate, methyl (2R)-2-amino-3-(3-chloro-5-fluoro-4-hydroxyphenyl) propanoate, diethyl 2-(acetylamino)-2-(4-[(2-chloro-6-fluorobenzyl) oxy]benzyl malonate, methyl (2R)-2-amino-3-(3-chloro-4-methoxyphenyl) propanoate, methyl (2R)-2-amino-3-(3-chloro-4-hydroxy-5-methoxyphenyl) propanoate, methyl (2R)-2-amino-3-(2,6-dichloro-3-hydroxy-4-methoxyphenyl) propanoate, methyl (2R)-2-amino-3-(3-chloro-4-hydroxyphenyl) propanoate, H-DL-tyr-OMe HCl, H-3,5-diiodo-tyr-OMe HCl, H-D-3,5-diiodo-tyr-OMe HCl, H-D-tyr-OMe HCl, D-tyrosine methyl ester hydrochloride, D-tyrosine-OMe HCl, methyl D-tyrosinate hydrochloride, (2R)-2-amino-3-(4-hydroxyphenyl) propionic acid, (2R)-2-amino-3-(4-hydroxyphenyl) methyl ester hydrochloride, methyl (2R)-2-amino-3-(4-hydroxyphenyl) propanoate hydrochloride, methyl (2R)-2-azanyl-3(4-hydroxyphenyl) propanoate hydrochloride, 3-chloro-L-tyrosine, 3-nitro-L-tyrosine, 3-nitro-L-tyrosine ethyl ester hydrochloride, DL-m-tyrosine, DL-o-tyrosine, Boc-Tyr(3,5-I 2 )—OSu, Fmoc-tyr (3-NO 2 )—OH, and α-methyl-DL-tyrosine;
b) melanin, a melanin promoter that is methoxsalen or melanotan II, or a combination of melanin, methoxsalen and melanotan II;
c) a p450 3A4 promoter that is 5,5-diphenylhydantoin, valproic acid, or carbamazepine; and
d) a leucine aminopeptidase inhibitor that is N-[(2S,3R)-3-amino-2-hydroxy-4-phenylbutyryl]-L-leucine, or rapamycin; and
wherein said cancer is metastatic breast cancer, metastatic pancreatic cancer, metastatic prostate cancer, metastatic thyroid cancer, metastatic lung cancer, metastatic colon cancer, metastatic brain cancer, metastatic glioma, metastatic ovarian cancer, metastatic bile duct cancer, metastatic choleangiocarcinoma, metastatic sarcoma, metastatic Hodgkin's lymphoma, metastatic lymphoma, metastatic renal cancer, metastatic tonsil squamous cell carcinoma, or metastatic colorectal cancer.
2. The method of claim 1 , wherein each of said tyrosine hydroxylase inhibitor, said melanin, melanin promoter, or combination of melanin, methoxsalen and melanotan II; said p450 3Ap4 promoter; and said leucine aminopeptidase inhibitor is administered to said patient within a 24 hour period.
3. The method of claim 1 , wherein each of said tyrosine hydroxylase inhibitor, said melanin, melanin promoter, or combination of melanin, methoxsalen and melanotan II; said p450 3A4 promoter; and said leucine aminopeptidase inhibitor is administered to said patient five days per week for six weeks.
4. The method of claim 1 , wherein the tyrosine hydroxylase inhibitor is α-methyl-DL-tyrosine, α-methyl-D-tyrosine, or a-methyl-L-tyrosine.
5. The method of claim 1 , wherein the tyrosine hydroxylase inhibitor is α-methyl-DL-tyrosine.
6. The method of claim 1 , wherein said cancer is metastatic breast cancer.
7. The method of claim 1 , wherein said cancer is metastatic pancreatic cancer.
8. The method of claim 1 , wherein said cancer is metastatic prostate cancer.
9. The method of claim 1 , wherein said cancer is metastatic thyroid cancer.
10. The method of claim 1 , wherein said cancer is metastatic lung cancer.
11. The method of claim 1 , wherein said cancer is metastatic colon cancer.
12. The method of claim 1 , wherein said cancer is metastatic brain cancer.
13. The method of claim 1 , wherein said cancer is metastatic glioma.
14. The method of claim 1 , wherein said cancer is metastatic ovarian cancer.
15. The method of claim 1 , wherein said cancer is metastatic bile duct cancer.
16. The method of claim 1 , wherein said cancer is metastatic choleangiocarcinoma.
17. The method of claim 1 , wherein said cancer is metastatic sarcoma.
18. The method of claim 1 , wherein said cancer is metastatic Hodgkin's lymphoma.
19. The method of claim 1 , wherein said cancer is metastatic lymphoma.
20. The method of claim 1 , wherein said cancer is metastatic renal cancer.
21. The method of claim 1 , wherein said cancer is metastatic tonsil squamous cell carcinoma.
22. The method of claim 1 , wherein said cancer is metastatic colorectal cancer.