IP Library Granted Patent US 9,034,828
Granted Patent B2
US 9,034,828 · App. 13/936,872 · Granted May 19, 2015

Syndecan peptides and polypeptides as inhibitors of cancer

Inventor: Alan Rapraeger (Stoughton, WI)
Assignee: Wisconsin Alumni Research Foundation
C07K14/4703
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Quick Facts
Patent No.
US 9,034,828
App. No.
13/936,872
Granted
May 19, 2015
Kind
B2
Abstract

The invention provides for peptides from syndecan 4 and methods of use therefor. These peptides can inhibit α6β4 integrin interaction with EGFR, thereby preventing tumor cell growth and tissue invasion.

Claims (16)

1. A method of inhibiting the interaction of α6β 4 integrin on the surface of a cancer cell with EGFR in a subject comprising administering to said subject a peptide segment consisting of between 45 and 100 amino acid residues and comprising about 45 residues of SEQ ID NO:1 including residues 87-131 (SEQ ID NO: 4) such that said cancer cells are contacted by said peptide.

2. The method of claim 1 , wherein said cancer cell is a carcinoma, a melanoma or a glioma.

3. A method of treating a subject with a cancer, cancer cells of which express α6β 4 integrin and EGFR, comprising administering to said subject a peptide segment consisting of between 45 and 100 amino acid residues and comprising about 45 residues of SEQ ID NO:1 including residues 87-131 (SEQ ID NO: 4) such that said cancer cells are contacted by said peptide.

4. The method of claim 3 , wherein said cancer is a carcinoma, a myeloma, a melanoma or a glioma.

5. The method of claim 1 , wherein said peptide or polypeptide is 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 60, 65, 70, 75, 80, 85, 90, 95 or 100 amino acid residues in length.

6. The method of claim 1 , wherein peptide is between 45 and 54 amino acid residues in length, between 45 and 65 amino acid residues in length, or between 45 and 75 amino acid residues in length.

7. The method of claim 1 , wherein said peptide consists essentially of residues 87-131 (SEQ ID NO: 4).

8. The method of claim 1 , wherein said peptide consists of residues 87-131 (SEQ ID NO: 4).

9. The method of claim 1 , wherein said peptide consists essentially of residues 78-131 (SEQ ID NO: 5).

10. The method of claim 1 , wherein said peptide consists of residues 78-131 (SEQ ID NO: 5).

11. The method of claim 1 , wherein said peptide comprises all D amino acid, all L amino acids, or a mixture of D and L amino acids.

12. The method of claim 1 , wherein said peptide is between 45-54 residues in length.

13. The method of claim 2 , wherein said cancer cell is a schwannoma, or a malignant peripheral nerve sheath tumor cell.

14. The method of claim 2 , further comprising contacting said cancer cell with a second cancer inhibitory agent.

15. The method of claim 2 , wherein said cancer cell is a metastatic cancer cell or a tumor stem cell.

16. The method of claim 2 , wherein administering comprises providing to said cell an expression construct comprising a nucleic acid encoding said peptide segment operably linked to a promoter active in said cell.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2013
From: RAPRAEGER, ALAN
To: WISCONSIN ALUMNI RESEARCH FOUNDATION
Reel/Frame 031586/0577 →
CONFIRMATORY LICENSE Recorded Aug 8, 2013
From: WISCONSIN ALUMNI RESEARCH FOUNDATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 030993/0902 →
Continuity (3)
Provisional Application 61669551 · Jul 9, 2012
Provisional Application 61784930 · Mar 14, 2013
Related Publication 20140011747A1 · Jan 9, 2014