IP Library Granted Patent US 9,988,631
Granted Patent B2
US 9,988,631 · App. 15/334,666 · Granted Jun 5, 2018

Pharmaceutical composition comprising Nanog shRNA, and method of using Nanog shRNA to treat cancer

Inventors: John Milburn Jessup (Potomac, MD); Nikolay Korokhov (Germantown, MD)
Assignee: The United States of America, as represented by the Secretary, Dept. of Health and Human Services
C12N15/113C12N15/86C12N2310/14C12N2310/531C12N2320/32C12N2710/10032C12N2710/10043C12N2710/10045C12N2799/022C12N2799/028C12N2820/007C12N2830/008
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Quick Facts
Patent No.
US 9,988,631
App. No.
15/334,666
Granted
Jun 5, 2018
Kind
B2
Abstract

The present description relates to an inhibitory RNA molecule, comprising an oligonucleotide that selectively knocks down expression a Nanog pseudogene expressed in many human cancers, a replicating viral vector capable of encoding such inhibitory RNA molecule, pharmaceutical compositions comprising said vector, and methods of treating cancer by administration of said pharmaceutical composition.

Claims (14)

1. A method of treating colorectal cancer in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of an inhibitory RNA molecule, comprising an oligonucleotide that knocks down expression of NANOGP8 wherein the oligonucleotide comprises a sequence selected from the group consisting of

SEQ ID NO:3 (5′-GAGGCAGCAGAGACCGCTGCATGCACTTCCAGCCA-3′);

SEQ ID NO:8 (5′-TCTGACAGGAAGTGGCTGGAAGTGCATGCAG-3′); and,

SEQ ID NO:56 (CTGCATGCACTTCCAGCCG).

2. The method of claim 1 , wherein the method of treating cancer is by inhibiting cancer cells capable of metastasizing.

3. The method of claim 1 , wherein the administration is via intravenous administration or direct injection at the site of disease.

4. The method of claim 1 , wherein the inhibitory RNA molecule is a double stranded siRNA comprising

SEQ ID NO:54 (CTGCATGCACTTCCAGCCA) and

SEQ ID NO:55 (TGGCTGGAAGTGCATGCAG)

or

SEQ ID NO:56 (CTGCATGCACTTCCAGCCG) and

SEQ ID NO:57 (TGGCTGGAAGTGCATGCAG).

5. The method of claim 1 , wherein the patient is administered a conditionally replicating viral vector comprising the inhibitory RNA molecule.

6. The method of claim 5 , wherein the conditionally replicating viral vector is a conditionally replicating adenovirus with a 5/3 fiber (CRAd5/3).

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 18, 2019
From: GENEVA FOUNDATION
To: THE GOVERNMENT OF THE UNITED STATES, AS REPRESENTED BY THE SECRETARY OF THE ARMY
Reel/Frame 051044/0401 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2017
From: JESSUP, JOHN M.; KOROKHOV, NIKOLAY
To: THE USA, AS REPRESENTED BY THE SECRETARY, DEPT. OF HEALTH AND HUMAN SERVICES
Reel/Frame 041969/0946 →
Continuity (4)
Continuation 14886970 · Oct 19, 2015
Continuation In Part 13991989
Provisional Application 61420214 · Dec 6, 2010
Related Publication 20170037406A1 · Feb 9, 2017