IP Library Granted Patent US 9,506,061
Granted Patent B2
US 9,506,061 · App. 14/712,591 · Granted Nov 29, 2016

Methods and compositions involving miRNA and miRNA inhibitor molecules

Inventors: David Brown (Austin, TX); Lance Ford (Austin, TX); Angie Cheng (Austin, TX); Rich Jarvis (Austin, TX); Mike Byrom (Austin, TX); Dmitriy Ovcharenko (Austin, TX); Eric Devroe (Pflugerville, TX); Kevin Kelnar (Kyle, TX)
Assignee: ASURAGEN, INC.
C12N15/113A61K9/127A61K31/7088A61K31/713A61K31/7105A61K45/06A61N5/10C12N15/111C12N15/1136C12Q1/68C12N2310/14C12N2310/141C12N2310/321C12N2310/322C12N2310/33C12N2310/344C12N2310/35C12N2310/351C12N2310/3527C12N2310/3535C12N2310/533C12N2320/12C12N2320/30C12N2320/50C12N2330/10
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Quick Facts
Patent No.
US 9,506,061
App. No.
14/712,591
Granted
Nov 29, 2016
Kind
B2
Abstract

The present invention concerns methods and compositions for introducing miRNA activity or function into cells using synthetic nucleic acid molecules. Moreover, the present invention concerns methods and compositions for identifying miRNAs with specific cellular functions that are relevant to therapeutic, diagnostic, and prognostic applications wherein synthetic miRNAs and/or miRNA inhibitors are used in library screening assays.

Claims (11)

1. A method for decreasing cell viability or decreasing cell proliferation of a cancer cell in an individual in need thereof, comprising administering to the individual a therapeutically-effective amount of a pharmaceutical composition comprising:

a. a synthetic miR-101 molecule comprising:

i. an active strand comprising a sequence that is at least 90% identical to mature human miR-101; and

ii. a separate complementary strand that is at least 60% complementary to the active strand and has a 5′-terminal nucleotide that is chemically modified to comprise a lower alkylamine group, and

b. a pharmaceutically-acceptable excipient.

2. The method of claim 1 , wherein the cancer cell is a cervical cancer cell, a lung cancer cell, a cancerous T cell, a prostate cancer cell, or a skin cancer cell.

3. The method of claim 1 , wherein the active strand is 22 to 30 nucleotides in length.

4. The method of claim 1 , wherein the complementary strand is 100% complementary to the active strand.

5. The method of claim 1 , wherein the lower alkylamine group is attached to a 5′ phosphate of the 5′-terminal nucleotide of the complementary strand.

6. The method of claim 1 , wherein the active strand is 23 nucleotides in length.

7. The method of claim 1 , wherein the pharmaceutically-acceptable excipient is a carrier or a lipid.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2015
From: BROWN, DAVID; FORD, LANCE; CHENG, ANGIE; JARVIS, RICH; BYROM, MIKE; OVCHARENKO, DMITRIY; DEVROE, ERIC; KELNAR, KEVIN
To: AMBION, INC.
Reel/Frame 035973/0102 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2015
From: AMBION, INC.
To: APPLERA CORPORATION
Reel/Frame 035973/0296 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2015
From: APPLERA CORPORATION
To: ASURAGEN, INC.
Reel/Frame 035973/0380 →
Continuity (7)
Continuation 13887008 · May 3, 2013
Continuation 13299255 · Nov 17, 2011
Division 11273640 · Nov 14, 2005
Provisional Application 60683736 · May 23, 2005
Provisional Application 60649634 · Feb 3, 2005
Provisional Application 60627171 · Nov 12, 2004
Related Publication 20150344881A1 · Dec 3, 2015