IP Library Granted Patent US 8,999,944
Granted Patent B2
US 8,999,944 · App. 11/814,442 · Granted Apr 7, 2015

Thioredoxin interacting protein (TXNIP) as regulator of vascular function

Inventor: Bradford C. Berk (Rochester, NY)
Assignee: University of Rochester
G01N33/6893G01N2500/02G01N2500/10G01N2800/32
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Quick Facts
Patent No.
US 8,999,944
App. No.
11/814,442
Granted
Apr 7, 2015
Kind
B2
Abstract

The present invention relates to screening assays for the identification of agents that can modify the interaction of thioredoxin interacting protein (TXNEP) on thioredoxin (TRX)5 preferably by inhibiting TXNIP downregulation of TXR. The use of such compounds, including the disclosed siRNA and antibodies against TXNIP, is contemplated for therapeutic or prophylactic treatment of vascular disease conditions, particularly those associated with pro-inflammatory activity of the TNF-ASK1-JNK-p38 pathways.

Claims (15)

1. A method of treating a vascular disease characterized by reduced laminar flow in a subject comprising:

selecting a subject having a vascular disease characterized by reduced laminar flow; and

administering to the selected subject a therapeutically effective amount of a nucleic acid molecule that inhibits expression of thioredoxin interacting protein (TXNIP) under conditions effective to inhibit expression of TXNIP in endothelial or vascular smooth muscle cells, thereby treating the vascular disease characterized by reduced laminar flow.

2. The method according to claim 1 , wherein said administering is carried out orally, by inhalation, by intranasal instillation, topically, transdermally, parenterally, subcutaneously, intravenous injection, intra-arterial injection, intramuscular injection, intrapleural instillation, intraperitoneally injection, intraventricularly, intralesionally, by application to mucous membranes, or by implantation of a sustained release vehicle.

3. The method according to claim 1 , wherein said treating is effective to inhibit pro-inflammatory activity of the TNF-ASK1-JNK-p38 pathways.

4. The method according to claim 1 , wherein the endothelial or vascular smooth muscle cells are associated with disease-affected vasculature.

5. The method according to claim 1 , wherein the nucleic acid molecule is an inhibitory RNA molecule.

6. The method according to claim 5 , wherein the inhibitory RNA molecule is an siRNA molecule.

7. The method according to claim 6 , wherein the siRNA molecule is targeted to SEQ ID NO: 1.

8. A method of treating a vascular disease condition in a subject comprising:

providing an siRNA molecule that is targeted to SEQ ID NO: 1 and inhibits expression of thioredoxin interacting protein (TXNIP); and

administering a therapeutically effective amount of the siRNA molecule to a subject under conditions effective to inhibit expression of TXNIP in endothelial or vascular smooth muscle cells, thereby treating the vascular disease condition.

9. A method of treating a vascular disease characterized by reduced laminar flow in a subject comprising:

selecting a subject having a vascular disease characterized by reduced laminar flow which is selected from the group consisting of atherosclerosis, coronary artery disease, cardiovascular disease, hypertension, peripheral vascular disease, diabetes, and sepsis; and

administering to the selected subject a therapeutically effective amount of a nucleic acid molecule that inhibits expression of thioredoxin interacting protein (TXNIP) under conditions effective to inhibit expression of TXNIP in endothelial or vascular smooth muscle cells, thereby treating the vascular disease characterized by reduced laminar flow.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2008
From: BERK, BRADFORD C.
To: UNIVERSITY OF ROCHESTER
Reel/Frame 021904/0495 →
CONFIRMATORY LICENSE Recorded Sep 19, 2008
From: UNIVERSITY OF ROCHESTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 021554/0899 →
Continuity (2)
Provisional Application 60645380 · Jan 20, 2005
Related Publication 20110097317A1 · Apr 28, 2011