IP Library Granted Patent US 7,838,495
Granted Patent B2
US 7,838,495 · App. 12/109,600 · Granted Nov 23, 2010

Compositions and methods of use of EPB1, and ErbB3 binding protein

Assignee: University of Maryland, Baltimore
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Quick Facts
Patent No.
US 7,838,495
App. No.
12/109,600
Granted
Nov 23, 2010
Kind
B2
Abstract

Inhibition of the proliferation of hormone refractory prostate cancer cells is achieved by administering EPB1, an ErbB3 binding protein, in combination with another anti-proliferation therapy such as administration of antiandrogens, other anticancer agents, radiation therapy, or surgery. Administration of EPB1 reverses the phenotype of hormone-resistant prostate cancer cells to hormone-sensitive prostate cancer cells.

Claims (53)

1. A method of treating hormone-independent prostate cancer in a subject in need thereof, comprising the steps of:

administering to said subject a therapeutically effective amount of EPB1; and

administering to said subject a therapeutically effective amount of at least one antiproliferation therapy.

2. The method of claim 1 , wherein said at least one antiproliferation therapy is selected from the group consisting of administration of an antiandrogen, administration of an anticancer agent, radiation therapy, and surgery.

3. The method of claim 1 , wherein the EPB1 is expressed from a viral vector.

4. The method of claim 3 , wherein the viral vector, is a lentiviral vector.

5. The method of claim 1 , wherein the EPB1 is expressed from polymer-packaged DNA.

6. The method of claim 1 , wherein said step of administering to said subject a therapeutically effective amount of EPB1 comprises administering a composition comprising EPB1 and a protein transduction domain.

7. The method of claim 6 , wherein said EPB1 is part of a fusion protein.

8. A method of inhibiting cell proliferation of a hormone-independent cancer cell, comprising:

providing, to said hormone-independent cancer cell,

a therapeutically effective amount of EPB1; and

a therapeutically effective amount of at lest one antiproliferation therapy.

9. The method of claim 8 , wherein said hormone-independent cancer cell is a hormone-refractory prostate cancer cell.

10. The method of claim 8 , wherein the EPB1 is expressed from a viral vector.

11. The method of claim 10 , wherein the viral vector is a lentiviral vector.

12. The method of claim 8 , wherein the EPB1 is expressed from polymer-packaged DNA.

13. The method of claim 8 , wherein said step of providing a therapeutically effective amount of EPB1 comprises providing a composition comprising EPB1 and a protein transduction domain.

14. The method of claim 13 , wherein said EPB1 is part of a fusion protein.

15. A method of inhibiting unregulated proliferation of a cell that can otherwise be regulated by hormone administration, comprising:

providing said cell with a therapeutically effective amount of EPB1 to convert said cell to a hormone-regulated phenotype; and

providing said cell with at least one antiproliferation therapy to reduce unregulated cell proliferation.

16. The method of claim 15 , wherein said at least one antiproliferation therapy is selected from the group consisting of administration of an antiandrogen, administration of an anticancer agent, radiation therapy, and surgery.

17. The method of claim 15 , wherein the EPB1 is expressed from a viral vector.

18. The method of claim 17 , wherein the viral vector is a lentiviral vector.

19. The method of claim 15 , wherein the EPB1 is expressed from polymer-packaged DNA.

20. The method of claim 15 , wherein said step of providing said cell with a therapeutically effective amount of EPB1 to convert said cell to a hormone-regulated phenotype comprises providing a composition comprising EPB1 and a protein transduction domain.

21. The method of claim 20 , wherein said EPB1 is part of a fusion protein.

22. A method of treating a cancer cell with an antiproliferation therapy, wherein said cancer cell is first sensitized to treatment with said antiproliferation therapy, comprising

providing to said cancer cell. EPB1, wherein said EPB1 is provided in a therapeutically effective amount so as to sensitize said cancer cell to said treatment with said antiproliferation therapy; and

treating said sensitized cancer cell with said antiproliferation therapy.

23. The method of claim 22 , wherein said antiproliferation therapy is selected from the group consisting of administration of an antiandrogen, administration of an anticancer agent, radiation therapy, and surgery.

24. The method of claim 22 , wherein said EPB1 is expressed from a viral vector.

25. The method of claim 24 , wherein the viral vector is a lentiviral vector.

26. The method of claim 22 , wherein said EPB1 is expressed from polymer-packaged DNA.

27. The method of claim 22 , wherein said step of providing comprises providing a composition comprising. EPB1 and a protein transduction domain.

28. The method of claim 27 , wherein said EPB1 is part of a fusion protein.

29. A method of reversing a phenotype of a prostate cancer cell from hormone refractory to hormone susceptible, comprising providing EPB1 to said prostate cancer cell, wherein said EPB1 is provided in a therapeutically effective amount so as to reverse said phenotype of said prostate cancer cell from hormone refractory to hormone susceptible.

30. The method of claim 29 , wherein said EPB1 is expressed from a viral vector.

31. The method of claim 30 , wherein the viral vector is a lentiviral vector.

32. The method of claim 29 , wherein said EPB1 is expressed from polymer-packaged DNA.

33. The method of claim 29 , wherein said step of providing comprises providing a composition comprising EPB1 and a protein transduction domain.

34. The method of claim 33 , wherein said EPB1 is part of a fusion protein.

35. A method of inhibiting proliferation of a cancer cell, comprising:

providing a therapeutically effective amount of EPB1 to said cancer cell; and

providing a therapeutically effective amount of at least one antiproliferation therapy to said cancer cell.

36. The method of claim 35 , wherein said cell is a prostate cancer cell.

37. A composition comprising EPB1 or an EPB1 expressing entity in combination with an antiandrogen and/or an anticancer agent.

38. The composition of claim 37 , wherein said EPB1 expressing entity is an EPB1 expressing viral vector.

39. The composition of claim 38 , wherein the viral vector is a lentiviral vector.

40. The composition of claim 37 , wherein EPB1 expressing entity is polymer-packaged EPB1 expressing DNA.

41. The composition of claim 37 , wherein said EPB1 is a protein.

42. The composition of claim 41 , wherein said EPB1 is part of a fusion protein.

Assignments (5)
CONFIRMATORY LICENSE Recorded Aug 9, 2023
From: UNIVERSITY OF MARYLAND, BALTIMORE
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 064530/0908 →
CONFIRMATORY LICENSE Recorded Jul 24, 2014
From: UNIVERSITY OF MARYLAND, BALTIMORE
To: US ARMY, SECRETARY OF THE ARMY
Reel/Frame 033378/0988 →
CONFIRMATORY LICENSE Recorded Aug 11, 2010
From: UNIVERSITY OF MARYLAND BALT PROF SCHOOL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 024825/0948 →
EXECUTIVE ORDER 9424, CONFIRMATORY LICENSE Recorded Feb 23, 2009
From: UNIVERSITY OF MARYLAND BALT PROF SCHOO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 022293/0761 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2008
From: ZHANG, YUEXING; HAMBURGER, ANNE
To: UNIVERSITY OF MARYLAND, BALTIMORE
Reel/Frame 021220/0752 →
Continuity (2)
Provisional Application 6091443000 · Apr 27, 2007
Related Publication 20080269133A1 · Oct 30, 2008