IP Library Granted Patent US 10,487,327
Granted Patent B2
US 10,487,327 · App. 15/918,645 · Granted Nov 26, 2019

Treatment of reprogramming factor related diseases by inhibition of natural antisense transcript to a reprogramming factor

Inventors: Joseph Collard (Delray Beach, FL); Olga Khorkova Sherman (Tequesta, FL)
Assignee: CuRNA, Inc.
C12N15/113A61K31/713C12N15/111C12N2310/11C12N2310/113C12N2310/14C12N2310/31C12N2310/312C12N2310/313C12N2310/314C12N2310/315C12N2310/316C12N2310/3181C12N2310/32C12N2310/321C12N2310/322C12N2310/3231C12N2320/30
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Quick Facts
Patent No.
US 10,487,327
App. No.
15/918,645
Granted
Nov 26, 2019
Kind
B2
Abstract

The present invention relates to antisense oligonucleotides that modulate the expression of and/or function of a Reprogramming factor, in particular, by targeting natural antisense polynucleotides of a Reprogramming factor. The invention also relates to the identification of these antisense oligonucleotides and their use in treating diseases and disorders associated with the expression of Reprogramming factors.

Claims (12)

1. A synthetic, modified oligonucleotide of 10 to 30 nucleotides in length comprising at least one modification wherein the at least one modification is selected from: at least one modified sugar moiety; at least one modified internucleotide linkage; at least one modified nucleotide, and combinations thereof; wherein said oligonucleotide is an antisense compound which specifically hybridizes to a reprogramming factor gene natural antisense polynucleotide having SEQ ID NOS: 4, 5 or 6 and upregulates the function and/or expression of a Reprogramming factor gene in vivo or in vitro as compared to a normal control.

2. The oligonucleotide of claim 1 , wherein the at least one modification comprises an internucleotide linkage selected from the group consisting of phosphorothioate, alkylphosphonate, phosphorodithioate, alkylphosphonothioate, phosphoramidate, carbamate, carbonate, phosphate triester, acetamidate, carboxymethyl ester, and combinations thereof.

3. The oligonucleotide of claim 1 , wherein said oligonucleotide comprises at least one phosphorothioate internucleotide linkage.

4. The oligonucleotide of claim 1 , wherein said oligonucleotide comprises a backbone of phosphorothioate internucleotide linkages.

5. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises at least one modified nucleotide, said modified nucleotide selected from: a peptide nucleic acid, a locked nucleic acid (LNA), analogue, derivative, and a combination thereof.

6. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises a plurality of modifications, wherein said modifications comprise modified nucleotides selected from: phosphorothioate, alkylphosphonate, phosphorodithioate, alkylphosphonothioate, phosphoramidate, carbamate, carbonate, phosphate triester, acetamidate, carboxymethyl ester, and a combination thereof.

7. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises a plurality of modifications, wherein said modifications comprise modified nucleotides selected from: peptide nucleic acids, locked nucleic acids (LNA), analogues, derivatives, and a combination thereof.

8. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises at least one modified sugar moiety selected from: a 2′-O-methoxyethyl modified sugar moiety, a 2′-methoxy modified sugar moiety, a 2′-O-alkyl modified sugar moiety, a bicyclic sugar moiety, and a combination thereof.

9. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises a plurality of modifications, wherein said modifications comprise modified sugar moieties selected from: a 2′-O-methoxyethyl modified sugar moiety, a 2′-methoxy modified sugar moiety, a 2′-O-alkyl modified sugar moiety, a bicyclic sugar moiety, and a combination thereof.

10. The oligonucleotide of claim 1 , wherein the oligonucleotide is of at least about 5 to 30 nucleotides in length and hybridizes to an antisense and/or sense strand of a Reprogramming factor polynucleotide wherein said oligonucleotide has at least about 90% sequence identity to a complementary sequence of at least about ten consecutive nucleic acids of the antisense and/or sense coding and/or noncoding nucleic acid sequences of the Reprogramming factor polynucleotide.

11. The oligonucleotide of claim 1 , wherein the oligonucleotide has 100% sequence identity to a complementary sequence of at least about ten consecutive nucleic acids of the antisense and/or sense coding and/or noncoding nucleic acid sequence of the Reprogramming factor polynucleotide.

12. The oligonucleotide of claim 1 , wherein the oligonucleotide comprises the sequences set forth as SEQ ID NOS: 7 to 17.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2018
From: COLLARD, JOSEPH; KHORKOVA SHERMAN, OLGA
To: CURNA, INC.
Reel/Frame 046237/0537 →
Continuity (6)
Division 14588442 · Jan 1, 2015
Division 13320637
Provisional Application 61286852 · Dec 16, 2009
Provisional Application 61233996 · Aug 14, 2009
Provisional Application 61179056 · May 18, 2009
Related Publication 20180208929A1 · Jul 26, 2018
Cited By (2)
US 12,319,913 US 12,371,693