IP Library Granted Patent US 9,187,540
Granted Patent B2
US 9,187,540 · App. 12/447,114 · Granted Nov 17, 2015

Methods of using E2F2 for the treatment of hypertension

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Quick Facts
Patent No.
US 9,187,540
App. No.
12/447,114
Granted
Nov 17, 2015
Kind
B2
Abstract

The present invention features compositions and methods of treating or preventing hypertension or a cardiac indication. In particular embodiments, the invention provides E2F2 as a new therapeutic target for the treatment of hypertension or a cardiac indication, and methods of increasing the expression and/or activity of E2F2.

Claims (20)

1. A method for ameliorating hypertension in a subject in need thereof, the method comprising;

(a) transforming an endothelial cell in vitro with an expression vector comprising a nucleic acid molecule encoding an E2F2 polypeptide fused to a protein transduction domain, wherein the protein transduction domain is selected from the group consisting of an HIV-TAT protein, a unidecapeptide protein transduction domain (YGRKKRRQRRR (SEQ ID NO: 2)), a polyarginine sequence, a VP22 domain, and a antennapedia protein transduction domain, wherein the E2F2 fusion polypeptide retains E2F2 activity;

(b) expressing the E2F2 polypeptide in the endothelial cell;

(c) isolating the E2F2 polypeptide; and

(d) administering the E2F2 polypeptide to the subject, thereby ameliorating the hypertension.

2. The method of claim 1 , wherein the endothelial cell in vitro is obtained from the subject.

3. A method for ameliorating hypertension in a subject in need thereof, the method comprising;

(a) transforming an endothelial cell in vitro with an expression vector comprising a nucleic acid molecule encoding an E2F2 polypeptide fused to a protein transduction domain selected from the group consisting of an HIV-TAT protein, a unidecapeptide protein transduction domain (YGRKKRRQRRR (SEQ ID NO: 2)), a polyarginine sequence, a VP22 domain, and a antennapedia protein transduction domain, wherein the E2F2 fusion polypeptide retains E2F2 activity;

(b) expressing the E2F2 fusion polypeptide in the endothelial cell; and

(c) administering the endothelial cell expressing the E2F2 fusion polypeptide to the subject, thereby ameliorating the hypertension.

4. The method of claim 3 , wherein the endothelial cell is a human cell.

5. The method of claim 3 , wherein the endothelial cell is a cardiac cell.

6. The method of claim 3 , wherein the endothelial cell in vitro is obtained from the subject.

7. A method of reducing hypertension in a subject in need thereof, the method comprising:

administering an effective amount of an E2F2 polypeptide having E2F2 activity to endothelial cells of the subject or

administering an effective amount of an E2F2 polypeptide fused to a protein transduction domain selected from the group consisting of an HIV-TAT protein, a unidecapeptide protein transduction domain (YGRKKRRQRRR (SEQ ID NO: 2)), a polyarginine sequence, a VP22 domain, and a antennapedia protein transduction domain to endothelial cells of the subject, wherein the E2F2 polypeptide fused to the protein transduction domain retains E2F2 activity.

8. The method of claim 7 , wherein the E2F2 activity of the E2F2 polypeptide or of the E2F2 polypeptide fused to the protein transduction domain activates an endothelial converting enzyme 1b (ECE-1b) promoter.

9. The method of claim 7 , wherein the hypertension is associated with a cardiovascular condition selected from the group consisting of cardiac hypertrophy, reduced systolic function, reduced diastolic function, maladaptive hypertrophy, heart failure with preserved systolic function, diastolic heart failure, hypertensive heart disease, aortic and mitral valve disease, pulmonary valve disease, hypertrophic cardiomyopathy, hypertrophic cardiomyopathy, post ischemic and post-infarction cardiac remodeling and cardiac failure.

10. The method of claim 7 , further comprising the step of measuring relaxation rate, cardiac contractility, cardiac ejection volume, or end-systolic volume, wherein a change in relaxation rate, cardiac contractility, cardiac ejection volume, or end-systolic volume is indicative of reducing hypertension.

11. The method of claim 7 , wherein the E2F2 polypeptide fused to the protein transduction domain is an E2F2 polypeptide fused to HIV-TAT protein that possesses E2F2 activity that activates an endothelial converting enzyme 1b (ECE-1b) promoter.

Assignments (5)
RELEASE OF SECURITY INTEREST IN PATENT COLLATERAL Recorded Aug 7, 2023
From: JPMORGAN CHASE BANK, N.A. AS COLLATERAL AGENT
To: STEWARD ST. ELIZABETH'S MEDICAL CENTER OF BOSTON, INC.
Reel/Frame 064506/0112 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2012
From: STEWARD ST. ELIZABETH'S MEDICAL CENTER OF BOSTON, INC.
To: STEWARD RESEARCH AND SPECIALTY PROJECTS CORPORATION
Reel/Frame 028801/0100 →
PATENT SECURITY AGREEMENT Recorded Jun 29, 2011
From: STEWARD ST. ELIZABETH'S MEDICAL CENTER OF BOSTON, INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 026525/0193 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 18, 2011
From: CARITAS ST. ELIZABETH'S MEDICAL CENTER OF BOSTON, INC.
To: STEWARD ST. ELIZABETH'S MEDICAL CENTER OF BOSTON, INC.
Reel/Frame 025983/0618 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 25, 2010
From: LOSORDO, DOUGLAS W.; QIN, GANGJIAN
To: CARITAS ST. ELIZABETH MEDICAL CENTER OF BOSTON, INC.
Reel/Frame 024676/0817 →