IP Library Granted Patent US 10,517,842
Granted Patent B2
US 10,517,842 · App. 15/921,380 · Granted Dec 31, 2019

Methods of modulating miRNA levels and compositions for use in the same

Inventors: Omid Khorram (Rolling Hills, CA); Tsai-Der Chuang (Inglewood, CA)
Assignee: Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center
A61K31/196A61P35/00C12Q1/6883C12Q2600/178
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Quick Facts
Patent No.
US 10,517,842
App. No.
15/921,380
Granted
Dec 31, 2019
Kind
B2
Abstract

Methods of modulating a miRNA level, such as a miR-29c and/or miR-200c level, in a cell are provided. Aspects of the methods include contacting the cell with an anti-fibrotic miRNA modulating active agent, such as a tranilast active agent. Also provided are compositions for use in practicing the methods. The methods and compositions find use in a variety of applications, including the treatment of fibrotic disorders, such as a uterine leiomyoma.

Claims (15)

1. A method of increasing expression of miR-29c, miR-200c and combinations thereof in a cell, the method comprising:

contacting the cell with an amount of a tranilast active agent effective to increase expression of miR-29c, miR-200c and combinations thereof in the cell.

2. The method according to claim 1 , wherein the method increases a level of two or more miRNAs in a cell.

3. The method according to claim 1 , wherein the cell is in vitro.

4. The method according to claim 1 , wherein the cell is in vivo.

5. The method according to claim 1 , wherein the cell has been evaluated for expression of a miRNA.

6. The method according to claim 5 , wherein the miRNA is selected from the group consisting of miR-29c, miR-200c and combinations thereof.

7. A method of increasing a cellular miRNA level in a subject, the method comprising:

administering to the subject an effective amount of a tranilast active agent to increase the cellular miRNA level in the subject, wherein the cellular miRNA is selected from the group consisting of miR-29c, miR-200c and combinations thereof.

8. The method according to claim 7 , wherein the method increases a level of two or more cellular miRNAs in the subject.

9. The method according to claim 7 , wherein the method further comprises decreasing expression of one or more genes selected from the group consisting of: CCND1, CDK2, COL1A1, COL3A1, TGF-β3, DNMT1 and EZH2 and combinations thereof.

10. The method according to claim 7 , wherein the method is a method of treating the subject for a leiomyoma.

11. The method according to claim 10 , wherein the leiomyoma comprises a uterine leiomyoma.

12. The method according to claim 11 , wherein the subject has been diagnosed as having at least one of down regulated miR-29c and miR-200c.

13. The method according to claim 12 , wherein the method further comprises diagnosing the subject as having at least one of down regulated miR-29 c and miR-200c.

Assignments (3)
CONFIRMATORY LICENSE Recorded Dec 11, 2020
From: LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 054705/0596 →
CHANGE OF NAME Recorded Jan 30, 2020
From: LOS ANGELES BIOMEDICAL RESEARCH INSTITUTE AT HARBOR-UCLA MEDICAL CENTER
To: LUNDQUIST INSTITUTE FOR BIOMEDICAL INNOVATION AT HARBOR-UCLA MEDICAL CENTER
Reel/Frame 051758/0366 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2018
From: KHORRAM, OMID; CHUANG, TSAI-DER
To: LOS ANGELES BIOMEDICAL RESEARCH INSTITUTE AT HARBOR-UCLA MEDICAL CENTER
Reel/Frame 045332/0284 →
Continuity (2)
Provisional Application 62471744 · Mar 15, 2017
Related Publication 20180263941A1 · Sep 20, 2018