IP Library Granted Patent US 7,645,734
Granted Patent B2
US 7,645,734 · App. 11/267,431 · Granted Jan 12, 2010

Compositions and methods for treating and preventing heart tissue degeneration and uses thereof

Assignee: The Trustees of Columbia University in the City of New York
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Quick Facts
Patent No.
US 7,645,734
App. No.
11/267,431
Granted
Jan 12, 2010
Kind
B2
Abstract

The present invention provides compositions useful for cardiac therapy comprising a cyclin-associated agent. The present invention also provides kits for use in delivering a cyclin-associated agent to cardiac cells in a subject, comprising the composition of the present invention and a catheter. The present invention additionally provides a methods for enhancing cardiac function; promoting regeneration of cardiac tissue; inducing endogenous myocardial regeneration; and preventing or treating heart failure in a subject in need thereof by augmenting cyclin in cells.

Claims (28)

1. A method of treating a subject, the method comprising administering a composition comprising a cyclin A2 protein to the subject, wherein the cyclin A2 protein has an amino acid sequence having greater than about 85% homology to SEQ ID NO: 1 and promotes both G1/S and G2/M transitions, and wherein the subject has heart failure or heart tissue damage or degeneration.

2. The method of claim 1 wherein the cyclin A2 protein has an amino acid sequence having greater than about 90% homology to SEQ ID NO: 1.

3. The method of claim 1 , wherein the cyclin A2 protein is naturally occurring.

4. The method of claim 3 , wherein the cyclin A2 protein is a human protein.

5. The method of claim 1 , wherein the subject is a human.

6. The method of claim 1 , wherein the subject experiences cardiomyocyte hyperplasia, improved cardiac ejection fraction, and/or increased cardiac output after administration of the composition.

7. The method of claim 1 , wherein the composition is administered to the subject parenterally.

8. The method of claim 1 , wherein the composition is administered to the subject by a catheter inserted into the subject's heart tissue.

9. The method of claim 1 , wherein the composition is administered to the subject by contacting the composition with heart tissue cells or side-population progenitor cells of the subject in vivo.

10. The method of claim 1 , wherein the composition is administered to the subject by contacting the composition with cells in vitro then introducing the cells into the subject.

11. The method of claim 10 , wherein the cells are introduced into the subject through a catheter inserted into the subject's heart tissue.

12. The method of claim 10 , wherein the cells are heart tissue cells.

13. The method of claim 10 , wherein the cells are side-population progenitor cells.

14. The method of claim 10 , wherein contacting is accomplished by delivering a viral vector capable of producing said composition.

15. A method of treating a subject, the method comprising administering a composition comprising a cyclin A2 protein to the subject, wherein the cyclin A2 protein has an amino acid sequence having greater than about 85% homology to SEQ ID NO:1 and promotes both G1/S and G2/M transitions, and wherein the subject has a family history of heart failure or heart tissue damage or degeneration.

16. The method of claim 15 , wherein the cyclin A2 protein is naturally occurring.

17. The method of claim 15 , wherein the cyclin A2 protein is a human protein.

18. The method of claim 15 , wherein the subject is a human.

19. The method of claim 15 , wherein the subject experiences cardiomyocyte hyperplasia, improved cardiac ejection fraction, and/or increased cardiac output after administration of the composition.

20. The method of claim 15 , wherein the composition is administered to the subject parenterally.

21. The method of claim 15 , wherein the composition is administered to the subject by a catheter inserted into the subject's heart tissue.

22. The method of claim 15 , wherein the composition is administered to the subject by contacting the composition with heart tissue cells or side-population progenitor cells of the subject in vivo.

23. The method of claim 15 , wherein the composition is administered to the subject by contacting the composition with cells in vitro then introducing the cells into the subject.

24. The method of claim 15 , wherein the cells are introduced into the subject through a catheter inserted into the subject's heart tissue.

25. The method of claim 23 , wherein the cells are heart tissue cells.

26. The method of claim 23 , wherein the cells are side-population progenitor cells.

27. The method of claim 23 , wherein contacting is accomplished by delivering a viral vector capable of producing said composition.

28. The method of claim 15 wherein the cyclin A2 protein has an amino acid sequence having greater than about 90% homology to SEQ ID NO: 1.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 3, 2006
From: CHAUDHRY, HINA W.; WOLGERNUTH, DEBRA J
To: TRUSTEES OF COLUMBIA UNIVERSITY, THE
Reel/Frame 017428/0641 →
Continuity (2)
Provisional Application 6047195200 · May 19, 2003
Related Publication 20060160733A1 · Jul 20, 2006