IP Library Granted Patent US 7,816,511
Granted Patent B2
US 7,816,511 · App. 10/383,241 · Granted Oct 19, 2010

Remedies for heart failure

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Quick Facts
Patent No.
US 7,816,511
App. No.
10/383,241
Granted
Oct 19, 2010
Kind
B2
Abstract

The present invention provides methods for screening drugs inhibiting the expression of OSF-2 gene or the production or function of the protein encoded thereby and therapeutic agents for heart failure having such effects. Useful methods for diagnosing heart failure can be provided by monitoring the expression or variation of said gene or the production of the protein encoded thereby. The present invention also provides transgenic animals with forced expression of OSF-2 gene and methods for studying changes in gene expression or protein production or the functions of various genes or proteins with the progress of the pathology of heart failure using them and novel therapeutic agents for heart failure.

Claims (14)

1. An isolated nucleotide sequence consisting of SEQ ID NO: 12.

2. A pharmaceutical composition comprising an antisense nucleotide sequence comprising nucleotides complementary to 16 or more contiguous nucleotides in SEQ ID NO: 5 and a pharmacologically acceptable carrier, wherein the antisense nucleotide sequence is complementary to a nucleotide containing the initiation codon of SEQ ID NO: 5, and wherein the antisense nucleotide sequence is SEQ ID NO: 12.

3. A method of treating heart failure associated with overexpression of OSF-2 comprising, administering via injection into the heart a pharmaceutical composition comprising an effective amount of an antisense nucleotide sequence comprising nucleotides complementary to 16 or more contiguous nucleotides in SEQ ID NO: 5 to inhibit expression of OSF-2, wherein the antisense nucleotide sequence (i) does not contain three continuous guanines (triplet G), (ii) is incapable of forming a hairpin structure, and (iii) is incapable of self-annealing.

4. The method of claim 3 , wherein the antisense nucleotide sequence is SEQ ID NO: 12.

5. The method of claim 3 , wherein the antisense nucleotide sequence is complementary to a nucleotide containing the initiation codon of SEQ ID NO: 5.

6. The method of claim 3 , further comprising determining the expression level of OSF-2 prior to administering said pharmaceutical composition.

7. A method of inhibiting OSF-2 gene expression comprising, administering via injection into the heart an effective amount of an antisense nucleotide sequence comprising nucleotides complementary to 16 or more contiguous nucleotides in SEQ ID NO: 5, whereby OSF-2 gene expression is inhibited, wherein the antisense nucleotide sequence (i) does not contain three continuous guanines (triplet G), (ii) is incapable of forming a hairpin structure, and (iii) is incapable of self-annealing.

8. The method of claim 7 , wherein the antisense nucleotide sequence is SEQ ID NO: 12.

9. The method of claim 7 , wherein the antisense nucleotide sequence is complementary to a nucleotide containing the initiation codon of SEQ ID NO: 5.

10. The method of claim 7 , further comprising determining the expression level of OSF-2 prior to administering said antisense nucleotide sequence.

11. A method of inhibiting cardiac dilatation comprising, administering via injection into the heart a pharmaceutical composition comprising an effective amount of an antisense nucleotide sequence comprising nucleotides complementary to 16 or more contiguous nucleotides in SEQ ID NO: 5 to inhibit cardiac dilatation, wherein the antisense nucleotide sequence (i) does not contain three continuous guanines (triplet G), (ii) is incapable of forming a hairpin structure, and (iii) is incapable of self-annealing.

12. The method of claim 11 , wherein the antisense nucleotide sequence is SEQ ID NO: 12.

13. The method of claim 11 , wherein the antisense nucleotide sequence is complementary to a nucleotide containing the initiation codon of SEQ ID NO: 5.

14. The method of claim 11 , further comprising determining the expression level of OSF-2 prior to administering said pharmaceutical composition.

Assignments (5)
CHANGE OF NAME Recorded Apr 30, 2007
From: DAIICHI ASUBIO PHARMA CO., LTD.
To: ASUBIO PHARMA CO., LTD.
Reel/Frame 019229/0039 →
CHANGE OF NAME TO CORRECT ADDRESS OF RECEIVING PARTY TO RECITE "TOKYO" - REEL/FRAME: 017279/0094 Recorded Apr 4, 2006
From: DAIICHI SUNTORY PHARMA CO., LTD.
To: DAIICHI ASUBIO PHARMA CO., LTD.
Reel/Frame 017433/0745 →
CHANGE OF NAME Recorded Oct 31, 2005
From: DAIICHI SUNTORY PHARMA CO., LTD.
To: DAIICHI ASUBIO PHARMA CO., LTD.
Reel/Frame 017279/0094 →
MERGER Recorded Apr 29, 2005
From: DAIICHI SUNTORY BIOMEDICAL RESEARCH LTD
To: DAIICHI SUNTORY PHARMA CO., LTD.
Reel/Frame 016507/0827 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 8, 2003
From: KAWASHIMA, KAYOKO; KATSURAGI, NARUTO; SUGIMURA, KEIJIRO; FURUYA, MAYUMI; MORISHITA, RYUICHI
To: DAIICHI SUNTORY PHARMA CO., LTD.; DAIICHI SUNTORY BIOMEDICAL RESEARCH LTD.
Reel/Frame 014469/0990 →