IP Library Granted Patent US 8,153,778
Granted Patent B2
US 8,153,778 · App. 12/693,787 · Granted Apr 10, 2012

RNA interference mediated inhibition of vascular cell adhesion molecule (VCAM) gene expression using short interfering nucleic acid (siNA)

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Quick Facts
Patent No.
US 8,153,778
App. No.
12/693,787
Granted
Apr 10, 2012
Kind
B2
Abstract

This invention relates to compounds, compositions, and methods useful for modulating vascular cell adhesion molecule gene expression using short interfering nucleic acid (siNA) molecules. This invention also relates to compounds, compositions, and methods useful for modulating the expression and activity of other genes involved in pathways of vascular cell adhesion molecule gene expression and/or activity by RNA interference (RNAi) using small nucleic acid molecules. In particular, the instant invention features small nucleic acid molecules, such as short interfering nucleic acid (siNA), short interfering RNA (siRNA), double stranded RNA (dsRNA), micro-RNA (miRNA), and short hairpin RNA (shRNA) molecules and methods used to modulate the expression of vascular cell adhesion molecule genes, such as vascular cell adhesion molecule-1 (VCAM-1).

Claims (10)

1. A chemically modified short interfering nucleic acid (siNA) molecule, wherein:

(a) the siNA molecule comprises a sense strand and a separate antisense strand, each strand having one or more pyrimidine nucleotides and one or more purine nucleotides;

(b) each strand is independently 18 to 27 nucleotides in length, and together comprise a duplex having between 17 and 23 base pairs;

(c) the antisense strand is complementary to a human VCAM-1 RNA sequence comprising SEQ ID NO: 471;

(d) a plurality of the pyrimidine nucleotides present in the sense strand are 2′-deoxy-2′-fluoro pyrimidine nucleotides and a plurality of the purine nucleotides present in the sense strand are 2′-deoxy purine nucleotides; and,

(e) a plurality of the pyrimidine nucleotides in the antisense strand are 2′-deoxy-2′-fluoro pyrimidine nucleotides and a plurality of the purine nucleotides present in the antisense strand are 2′-O-methyl purine nucleotides.

2. The siNA molecule of claim 1 , wherein the sense strand includes a terminal cap moiety at both 5′- and 3′-ends.

3. The siNA molecule of claim 1 , wherein the antisense strand has a phosphorothioate internucleotide linkages at the 3′-end.

4. The siNA molecule of claim 1 , wherein the sense strand, the antisense strand, or both the sense strand and the antisense strand include a 3′-overhang.

5. A composition comprising the siNA molecule of claim 1 , in a pharmaceutically acceptable carrier or diluent.

Assignments (4)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
CHANGE OF NAME Recorded Aug 29, 2012
From: SCHERING CORPORATION
To: MERCK SHARP & DOHME CORP.
Reel/Frame 028866/0511 →
MERGER Recorded Aug 27, 2012
From: MERCK SHARP & DOHME CORP.
To: SCHERING CORPORATION
Reel/Frame 028850/0515 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2012
From: MCSWIGGEN, JAMES; BEIGELMAN, LEONID
To: MERCK SHARP & DOHME CORP.
Reel/Frame 027756/0520 →