Treatment of brain derived neurotrophic factor (BDNF) related diseases by inhibition of natural antisense transcript to BDNF

• US 10,519,448 B2
• Filed: 05/28/2015
• Issued: 12/31/2019
• Est. Priority Date: 02/12/2009
• Status: Active Grant

• Current Assignee: CURNA, Inc. (Opko Health, Inc.)
• Original Assignee: CURNA, Inc. (Opko Health, Inc.)
• Inventors: Collard, Joseph, Khorkova Sherman, Olga, Coito, Carlos
• Primary Examiner(s): Poliakova-Georgantas, Ekaterina
• Application Number:
  US14/723,740
• Publication Number:
  US 20160138023A1
• Time in Patent Office: 1,678 Days
• Field of Search: None
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• CPC Class Codes: A61P 29/02 : without antiinflammatory effect
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• CPC Class Codes: G01N 33/74 : involving hormones or other non-cytokine intercellular protein regulatory factors such as growth factors, including receptors to hormones and growth factors

Abstract

The present invention relates to antisense oligonucleotides that modulate the expression of and/or function of Brain derived neurotrophic factor (BDNF), in particular, by targeting natural antisense polynucleotides of Brain derived neurotrophic factor (BDNF). The invention also relates to the identification of these antisense oligonecleotides and their use in treating diseases and disorders associated with the expression of BDNF.

Claims

1. A synthetic, modified single-stranded oligonucleotide of 15 to 18 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

(i) an antisense compound which is 100% complementary to and specifically hybridizes to a 15 to 18 nucleotide target region within nucleotides 1-2535 of a natural antisense polynucleotide of a Brain derived neurotrophic factor polynucleotide having SEQ ID NO;

2 and

(ii) is specific for said natural antisense polynucleotide and upregulates the function and/or expression of a Brain derived neurotrophic factor (BDNF) gene in vivo or in vitro as compared to a mock-transfected control and wherein there is at least a 1.4 fold average increase in expression over said 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), 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), 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 specifically hybridizes to a non-overlapping region of said natural antisense polynucleotide having SEQ ID NO:

2 wherein said non-overlapping region is non-overlapping with the mRNA of the BDNF polynucleotide.

11. The oligonucleotide of claim 1, wherein the oligonucleotide has at least about 100% sequence identity to a sequence of at least about 15 consecutive nucleotides of the mRNA sense coding and/or noncoding nucleic acid sequence of the Brain derived neurotrophic factor (BDNF) polynucleotide.

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

4, 6 and 8.

13. A composition comprising one or more oligonucleotides according to claim 1 and a pharmaceutically acceptable excipient.

14. The composition of claim 13, wherein the at least one of the one or more oligonucleotides comprises one of the nucleotide sequences set forth as SEQ ID NOS:

4, 6 and 8.

15. The composition of claim 14, wherein the oligonucleotidesset forth as SEQ ID NOs:

4, 6 and 8 comprise two or more modifications or substitutions selected from a locked nucleic acid (LNA), phosphorothioate, methylphosphonate, peptide nucleicacid, and combinations thereof.