Syndecan peptides and polypeptides and uses thereof
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, or inhibiting scarring and/or pathologic neovascularization.
1. A method of inhibiting pathologic neovascularization or inhibiting scarring in a subject in need thereof, 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 of SEQ ID NO:1 (SEQ ID NO:4), whereby pathologic neovascularization or scarring is inhibited in the subject.
2. The method of claim 1 , wherein the peptide segment 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.
3. The method of claim 1 , wherein the peptide segment 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.
4. The method of claim 1 , wherein the peptide segment consists essentially of residues 87-131 of SEQ ID NO:1 (SEQ ID NO:4).
5. The method of claim 1 , wherein the peptide segment consists of residues 87-131 of SEQ ID NO:1 (SEQ ID NO:4).
6. The method of claim 1 , wherein the peptide segment consists essentially of residues 78-131 of SEQ ID NO:1 (SEQ ID NO:5).
7. The method of claim 1 , wherein said peptide segment consists of residues 78-131 of SEQ ID NO:1 (SEQ ID NO: 5).
8. The method of claim 1 , wherein the peptide segment comprises all D amino acid, all L amino acids, or a mixture of D and L amino acids.
9. The method of claim 1 , wherein pathologic neovascularization is inhibited in the subject.
10. The method of claim 9 , wherein said pathologic neovascularization involves activated vascular endothelial cells.
11. The method of claim 1 , wherein scarring is inhibited in the subject.