IP Library Granted Patent US 7,816,403
Granted Patent B2
US 7,816,403 · App. 10/437,477 · Granted Oct 19, 2010

Method of inhibiting ATF/CREB and cancer cell growth and pharmaceutical compositions for same

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,816,403
App. No.
10/437,477
Granted
Oct 19, 2010
Kind
B2
Abstract

There is provided a method for inhibiting ATF/CREB and cancer cell growth using disulfiram, administered in combination with heavy metals. It was found that disulfiram disrupts transcription factor DNA binding by forming mixed disulfides with thiols within the DNA-binding region, and that this process is facilitated by metal ions. Disulfiram administered to melanoma cells in combination with copper (II) or zinc(II) decreased expression of cyclin A, reduced proliferation in vitro, and inhibited growth of melanoma cells. The combination of oral zinc gluconate and disulfiram at currently approved doses for alcoholism stabilized tumor growth in two of three patients with Stage IV metastatic melanoma, with 12 and 17 month survivals, respectively, to date, and produced a >50% reduction in hepatic metastases in one individual.

Claims (15)

1. A method for treating established cancer in a mammal, said cancer selected from the group consisting of melanoma, lung cancer, breast cancer, hepatic cancer, colorectal cancer, and prostatic carcinoma, and said method comprising administering to said mammal in need thereof a therapeutically effective amount of disulfiram and a therapeutically effective amount of a pharmaceutically suitable source of zinc ions.

2. The method of claim 1 , wherein said pharmaceutically suitable source of zinc ions is administered as a complex with said disulfiram.

3. The method of claim 1 , wherein said disulfiram and said pharmaceutically suitable source of zinc ions are administered separately.

4. The method of claim 1 , wherein said disulfiram and said pharmaceutically suitable source of zinc ions are administered orally.

5. The method of claim 1 , wherein said disulfiram and said pharmaceutically suitable source of zinc ions are administered intravenously.

6. The method of claim 1 , wherein said disulfiram is administered at a dosage of from about 125 to about 1000 mg.

7. The method of claim 1 , wherein said pharmaceutically suitable source of zinc ions is zinc acetate.

8. The method of claim 1 , wherein said pharmaceutically suitable source of zinc ions is zinc gluconate.

9. The method of claim 1 , wherein said pharmaceutically suitable source of zinc ions is zinc chloride.

10. The method of claim 1 , wherein said cancer is melanoma.

11. The method of claim 1 , wherein said cancer is hepatic cancer.

12. The method of claim 1 , wherein said cancer is colorectal cancer.

13. The method of claim 1 , wherein said cancer is prostatic carcinoma.

14. The method of claim 1 , wherein said cancer is lung cancer.

15. The method of claim 1 , wherein said cancer is breast cancer.

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 24, 2010
From: UNIVERSITY OF UTAH
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 024585/0215 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 19, 2006
From: THE CHARLOTTE MECKLENBURG HOSPITAL AUTHORITY D/B/A CAROLINAS MEDICAL CENTER
To: THE UNIVERSITY OF UTAH
Reel/Frame 017804/0449 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2003
From: KENNEDY, THOMAS PRESTON
To: CHARLOTTE-MECKLENBURG HOSPITAL AUTHORITY
Reel/Frame 014081/0390 →