IP Library Granted Patent US 7,838,505
Granted Patent B2
US 7,838,505 · App. 11/957,170 · Granted Nov 23, 2010

Hybrid hepatocyte growth factor gene having high expression efficiency of two heterotypes of hepatocyte growth factor

Assignee: ViroMed Co., Ltd.
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Quick Facts
Patent No.
US 7,838,505
App. No.
11/957,170
Granted
Nov 23, 2010
Kind
B2
Abstract

The present invention relates to a hybrid Hepatocyte Growth Factor (HGF) gene which is prepared by inserting an inherent or foreign intron between exons 4 and 5 in HGF cDNA, which has a base sequence of SEQ ID NO: 2. The gene has high expression efficiency and simultaneously expresses two heterotypes of HGF and dHGF (deleted variant HGF). Further the gene may be used for treating or preventing ischemic or liver diseases.

Claims (24)

1. A method of increasing angiogenesis in a tissue of a subject comprising administering to the tissue of said subject a hybrid Hepatocyte Growth Factor (HGF) construct comprising

(a) a first cDNA which has the same sequence as exons 1-4 of the human HGF gene wherein said exons 1-4 are arranged in sequential order without an intron therebetween, or degenerates thereof which do not alter the amino acid sequence encoded by said first cDNA,

(b) a polynucleotide that has the same sequence as intron 4 of a HGF gene or a fragment thereof, and

(c) a second cDNA which has the same sequence as exons 5-18 of the human HGF gene wherein said exons 5-18 are arranged in sequential order without an intron therebetween, or degenerates thereof which do not alter the amino acid sequence encoded by said second cDNA;

wherein (b) is located between (a) and (c); and the HGF construct simultaneously encodes two heterotypes of human HGF, wherein said administration results in increased angiogenesis in said tissue.

2. The method of claim 1 , wherein the polynucleotide of (b) has the same sequence as the full intron 4 of the human HGF gene.

3. The method of claim 2 , wherein said hybrid HGF construct comprises a nucleotide sequence comprising SEQ ID NO: 2.

4. The method of claim 1 , wherein the polynucleotide of (b) has the same sequence as a fragment of intron 4 of the human HGF gene.

5. The method of claim 4 , wherein said hybrid HGF construct comprises SEQ ID NO: 19.

6. The method of claim 4 , wherein said hybrid HGF construct comprises SEQ ID NO: 20.

7. The method of claim 4 , wherein said hybrid HGF construct comprises SEQ ID NO: 21.

8. The method of claim 1 , wherein said hybrid HGF construct is a vector.

9. The method of claim 8 , wherein said vector further comprises one or more sequences for regulating expression, a self-replication sequence, or a secretory signal.

10. The method of claim 8 , wherein said vector is selected from the group consisting of: pCK-HGF-X2, pCK-HGF-X3, pCK-HGF-X6, pCK-HGF-X7, pCK-HGF-X8, pCP-HGF-X2, pCP-HGF-X3, pCP-HGF-X6, pCP-HGF-X7 and pCP-HGF-X8.

11. The method of claim 1 , wherein said hybrid HGF construct is administered intramuscularly to said tissue.

12. The method of claim 1 , wherein said tissue is an ischemic limb.

13. A method of increasing angiogenesis in a tissue of a subject comprising administering to the tissue of said subject a hybrid Hepatocyte Growth Factor (HGF) construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO: 2, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF, wherein said administration results in increased angiogenesis in said tissue.

14. The method of claim 13 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO:2.

15. A method of increasing angiogenesis in a tissue of a subject comprising administering to the tissue of said subject a hybrid Hepatocyte Growth Factor (HGF) construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO: 19, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF, wherein said administration results in increased angiogenesis in said tissue.

16. The method of claim 15 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO: 19.

17. A method of increasing angiogenesis in a tissue of a subject comprising administering to the tissue of said subject a hybrid Hepatocyte Growth Factor (HGF) construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO: 20, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF, wherein said administration results in increased angiogenesis in said tissue.

18. The method of claim 17 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO: 20.

19. A method of increasing angiogenesis in a tissue of a subject comprising administering to the tissue of said subject a hybrid Hepatocyte Growth Factor (HGF) construct comprising a polynucleotide having a nucleotide sequence not less than 90% identical to SEQ ID NO: 21, wherein the polynucleotide having said nucleotide sequence simultaneously encodes two heterotypes of human HGF, wherein said administration results in increased angiogenesis in said tissue.

20. The method of claim 19 , wherein said nucleotide sequence is not less than 95% identical to SEQ ID NO: 21.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S NAME FROM --HELIXMITH CO., LTD PREVIOUSLY RECORDED AT REEL: 049151 FRAME: 0562. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 24, 2020
From: VIROMED CO., LTD
To: HELIXMITH CO., LTD
Reel/Frame 054511/0459 →
CHANGE OF NAME Recorded May 10, 2019
From: VIROMED CO., LTD.
To: HELIXMITH CO., LTD
Reel/Frame 049151/0562 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE'S COUNTRY FROM "KOREA, DEMOCRATIC PEOPLE'S REPUBLIC OF" TO --REPUBLIC OF KOREA-- PREVIOUSLY RECORDED ON REEL 022771 FRAME 0272. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT DOCUMENT. Recorded Jul 11, 2017
From: KIM, JONG-MOOK; HAHN, WOONG
To: VIROMED CO., LTD.
Reel/Frame 043145/0906 →
CORRECTIVE ASSIGNMENT TO CORRECT THE EXECUTION DATE OF THE SECOND INVENTOR PREVIOUSLY RECORDED AT REEL: 022771 FRAME: 0272. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT . Recorded Jul 11, 2017
From: KIM, JONG-MOOK; HAHN, WOONG
To: VIROMED CO., LTD.
Reel/Frame 043162/0441 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2009
From: KIM, JONG-MOOK; HAHN, WOONG
To: VIROMED CO., LTD.
Reel/Frame 022771/0272 →
Priority Claims (1)
KR 10-2002-0015074 · Mar 20, 2002 · national
Continuity (3)
Division 1094427700 · Sep 20, 2004
Continuation PCTKR030054800 · Mar 20, 2003
Related Publication 20090131350A1 · May 21, 2009