IP Library Granted Patent US 11,033,570
Granted Patent B2
US 11,033,570 · App. 16/465,083 · Granted Jun 15, 2021

Modulation of Lnc05 expression

Inventors: Allen Tingjin Yu (Pleasanton, CA); David L. Spector (Cold Spring Harbor, NY); Frank Rigo (Carlsbad, CA); Susan M. Freier (San Diego, CA); Jan Bergmann (Basel, CH); Carmen Berasain (Pamploma, ES)
Assignees: Cold Spring Harbor Laboratory; Ionis Pharmaceuticals, Inc.
A61K31/713A61K9/0019A61K31/7125C12N15/113A61K45/06C12N2310/11C12N2310/113C12N2310/315C12N2310/321C12N2310/3231C12N2310/3341C12N2310/341
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Quick Facts
Patent No.
US 11,033,570
App. No.
16/465,083
Granted
Jun 15, 2021
Kind
B2
Abstract

Provided herein are methods, compounds, and compositions for reducing expression of Inc05 in a cell or individual. Such methods, compounds, and compositions are useful to treat, prevent, delay, or ameliorate a cancer in an individual.

Claims (21)

1. A method of treating cancer in an individual having cancer comprising administering a compound comprising a modified oligonucleotide having a nucleobase sequence complementary to a Inc05 nucleic acid to the individual, thereby treating the cancer in the individual.

2. The method of claim 1 , wherein the compound is single-stranded.

3. The method of claim 1 , wherein the compound is double-stranded.

4. The method of claim 1 , wherein the modified oligonucleotide is 12 to 30 linked nucleosides in length.

5. The method of claim 1 , wherein the modified oligonucleotide comprises at least one modified internucleoside linkage, at least one modified sugar moiety, or at least one modified nucleobase.

6. The method of claim 5 , wherein the at least one modified internucleoside linkage is a phosphorothioate internucleoside linkage, the at least one modified sugar is a bicyclic sugar or 2′-O-methyoxyethyl, and the at least one modified nucleobase is a 5-methylcytosine.

7. The method of claim 5 , wherein at least one modified sugar comprises a 4′-CH(CH3)-O-2′ bridge or a 4′-(CH2)n-O-2′ bridge, wherein n is 1 or 2.

8. The method of claim 1 , wherein the modified oligonucleotide comprises:

a gap segment consisting of linked deoxynucleosides;

a 5′ wing segment consisting of linked nucleosides;

a 3′ wing segment consisting of linked nucleosides;

wherein the gap segment is positioned immediately adjacent to and between the 5′ wing segment and the 3′ wing segment and wherein each nucleoside of each wing segment comprises a modified sugar.

9. The method of claim 8 , wherein the modified oligonucleotide consists of 20 linked nucleosides and has a nucleobase sequence consisting of the nucleobase sequence of SEQ ID NO: 8, wherein the modified oligonucleotide comprises:

a gap segment consisting of 10 linked deoxynucleosides;

a 5′ wing segment consisting of 5 linked nucleosides;

a 3′ wing segment consisting of 5 linked nucleosides;

wherein the gap segment is positioned immediately adjacent to and between the 5′ wing segment and the 3′ wing segment, each nucleoside of each wing segment comprises a 2′-O-methoxyethyl nucleoside, each internucleoside linkage of the modified oligonucleotide is a phosphorothioate linkage, and each cytosine of the modified oligonucleotide is a 5-methylcytosine.

10. The method of claim 1 , wherein the Inc05 nucleic acid has the sequence of any of SEQ ID NOs: 1-5.

11. The method of claim 10 , wherein the modified oligonucleotide is at least 90% complementary to the Inc05 nucleic acid.

12. The method of claim 10 , wherein the modified oligonucleotide is at least 95% complementary to the Inc05 nucleic acid.

13. The method of claim 10 , wherein the modified oligonucleotide is 100% complementary to the Inc05 nucleic acid.

Continuity (2)
Provisional Application 62429634 · Dec 2, 2016
Related Publication 20190343863A1 · Nov 14, 2019
Cited By (2)
US 12,319,913 US 12,371,693