Compositions and methods including celecoxib and plumbagin relating to treatment of cancer
The present invention relates to compositions and methods for treatment of proliferative disease. In specific aspects, the present invention relates to compositions including celecoxib and plumbagin in combination; methods for treatment of a proliferative disease including administration of celecoxib and plumbagin in a subject in need thereof; and particularly methods for treatment of skin cancer including administration of celecoxib and plumbagin in a subject in need thereof.
1. A pharmaceutical composition, comprising: plumbagin and celecoxib in a synergistic ratio in the range of 1:7.5-1:20 effective to decrease viability of melanoma cells; and a pharmaceutically acceptable carrier.
2. The pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable carrier comprises liposomes.
3. The pharmaceutical composition of claim 2 , wherein the liposomes have an average particle size in the range of 1 nm-500 nm.
4. The pharmaceutical composition of claim 1 , wherein the plumbagin is present in a concentration in the range of 0.1 micromolar-100 millimolar and the celecoxib is present in a concentration in the range of 0.1 micromolar-100 millimolar.
5. The pharmaceutical composition of claim 2 , wherein the liposomes comprise at least one polyethylene glycol modified neutral lipid, wherein the amount of polyethylene glycol modified neutral lipid is an amount in the range of 2.5-30 molar percent, inclusive, of total lipids in the liposomes; and one or more anionic, cationic or neutral lipids in an amount in the range of 70-97.5, inclusive, molar percent of total lipids in the liposomes.
6. The pharmaceutical composition of claim 2 , wherein the liposomes comprise at least one polyethylene glycol modified neutral lipid, wherein the amount of polyethylene glycol modified neutral lipid is an amount in the range of 5-20 molar percent, inclusive, of total lipids in the liposomes; and one or more anionic, cationic or neutral lipids in an amount in the range of 80-95, inclusive, molar percent of total lipids in the liposomes.
7. A method of treating melanoma in a subject in need thereof, comprising: administering, concurrently or sequentially, a therapeutically effective amount of plumbagin and celecoxib in a synergistic ratio in the range of 1:7.5-1:20 to the subject.
8. The method of treating melanoma of claim 7 , wherein administering the therapeutically effective amount of plumbagin and celecoxib to the subject comprises administering liposomes containing plumbagin and/or liposomes containing celecoxib.
9. The method of treating melanoma of claim 8 , wherein the liposomes have an average particle size in the range of 1 nm-500 nm.
10. The method of treating melanoma of claim 7 , wherein the plumbagin is administered in a concentration in the range of 0.1 micromolar-100 millimolar and the celecoxib is administered in a concentration in the range of 0.1 micromolar-100 millimolar.
11. The method of treating melanoma of claim 7 , wherein the subject is human.
12. The method of treating melanoma of claim 7 , wherein the subject has malignant melanoma.
13. The method of treating melanoma of claim 7 , wherein the melanoma is characterized by abnormal activation of COX-2 and STAT3.
14. The method of treating melanoma of claim 7 , further comprising assay of COX-2 and/or STAT3 to detect abnormal activation of COX-2 and/or STAT3 in a sample obtained from the subject containing melanoma cells.
15. The method of treating melanoma of claim 7 , further comprising administration of an adjunct anti-cancer treatment.
16. A commercial package, comprising: a pharmaceutical composition comprising: plumbagin and celecoxib in a synergistic ratio in the range of 1:7.5-1:20 effective to decrease viability of melanoma cells; and a pharmaceutically acceptable carrier.