IP Library Granted Patent US 8,691,783
Granted Patent B2
US 8,691,783 · App. 13/384,228 · Granted Apr 8, 2014

MicroRNA-24

Inventors: Thomas Thum (Hannover, DE); Jan Fiedler (Hannover, DE)
Assignee: Julius-Maximilians-Universitaet Wuerzburg
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 8,691,783
App. No.
13/384,228
Granted
Apr 8, 2014
Kind
B2
Abstract

The present invention relates to a modulator, in particular an inhibitor, of microRNA-24 (miR-24) and to direct and indirect miR-24 targets for use in a method of treatment and/or prevention of ischemia, in a method of prevention of endothelial apoptosis or in a method of induction of angiogenesis. The present invention further relates to a precursor of miR-24 and to siRNAs or shRNAs against direct or indirect miR-24 targets for use in a method of treatment of angiogenesis associated with cancer. The present invention also relates to an in vitro method for diagnosing ischemia or prevalence or disposition for ischemia, and to a method for identifying a modulator of miR-24 and/or direct or indirect miR-24 targets. In addition, the present invention relates to pharmaceutical compositions or kits comprising any of the above agents, to endothelial cells devoid of expressing functional miR-24, and to a non-human, transgenic animal comprising these endothelial cells.

Claims (4)

1. A method for treatment of ischemia or endothelial apoptosis, and/or for inducing angiogenesis, wherein said method comprises administering, to a subject in need of such treatment or induction, an inhibitor of microRNA-24 (miR-24), wherein said inhibitor is a nucleic acid.

2. The method, according to claim 1 , wherein the ischemia is associated with at least one of the group consisting of acute and/or chronic myocardial infarction, chronic heart failure, peripheral vascular occlusive disease, liver and/or kidney ischemia, stroke, bowel ischemia and chronic ulcers of the skin and/or the mucosa.

3. The method, according to claim 1 , wherein the inhibitor is an antagomir or an antisense oligonucleotide.

4. The method, according to claim 3 , wherein the antagomir or the antisense oligonucleotide is essentially complementary to SEQ ID NO: 1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 28, 2019
From: JULIUS-MAXIMILIANS-UNIVERSITÄT WÜRZBURG
To: CARDIOR PHARMACEUTICALS GMBH
Reel/Frame 049289/0888 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2012
From: THUM, THOMAS; FIEDLER, JAN
To: JULIUS-MAXIMILIANS-UNIVERSITAET WUERZBURG
Reel/Frame 027951/0989 →
Priority Claims (1)
EP 09075314 · Jul 16, 2009 · regional
Continuity (1)
Related Publication 20120180147A1 · Jul 12, 2012