US2009163405A1PendingUtilityA1
Angiogenic peptides and uses thereof
Est. expiryOct 29, 2023(expired)· nominal 20-yr term from priority
A61P 43/00A61P 9/10A61P 9/00G01N 2333/4709A61K 47/64C07K 14/52G01N 33/6896A61P 17/02G01N 33/5064A61K 38/10A61K 38/08
55
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Claims
Abstract
A peptide comprising an amino acid sequence as set forth in SEQ ID NO: 2, 4, 6, 8, 10 or 12 is provided. The peptide being at least 6 and no more than 50 amino acid residues in length. Also provided are therapeutic applications using such peptides.
Claims
exact text as granted — not AI-modified1 .- 69 . (canceled)
70 . A method of promoting angiogenesis in a tissue of a subject, the method comprising providing to the subject a therapeutically effective amount of a peptide comprising the amino acid sequence set forth in SEQ ID NO:2, 6, 10 or 12, said peptide is no more than 50 amino acids in length, thereby promoting angiogenesis in the subject.
71 . A method of promoting angiogenesis in a tissue of a subject, the method comprising providing to the subject a therapeutically effective amount of a peptide consisting of the amino acid sequence set forth in SEQ ID NO:2, 6, 10 or 12, thereby promoting angiogenesis in the subject.
72 . A method of promoting angiogenesis in a tissue of a subject, the method comprising providing to the subject a therapeutically effective amount of at least two peptides each independently selected from the group consisting of SEQ ID NO:2, 4, 6, 10 and 12, thereby promoting angiogenesis in the subject.
73 . A method of promoting angiogenesis in a tissue of a subject, the method comprising providing to the subject a therapeutically effective amount of at least two peptides each independently selected from the group consisting of SEQ ID NO:2, 6, 8, 10 and 12, thereby promoting angiogenesis in the subject.
74 . The method of claim 70 , wherein said peptide is a cyclic peptide and whereas said amino acid sequence is selected from the group consisting of SEQ ID NOs:2, 6, 10 and 12.
75 . The method of claim 70 , wherein the subject suffers from delayed wound-healing, delayed ulcer healing, reproduction associated disorders, coronary artery disease, arteriosclerosis, myocardial ischemia, peripheral ischemia, cerebral ischemia, retinopathy, remodeling disorder, von Hippel-Lindau syndrome, diabetes and/or hereditary hemorrhagic telengiectasia.
76 . The method of claim 71 , wherein the subject suffers from delayed wound-healing, delayed ulcer healing, reproduction associated disorders, coronary artery disease, arteriosclerosis, myocardial ischemia, peripheral ischemia, cerebral ischemia, retinopathy, remodeling disorder, von Hippel-Lindau syndrome, diabetes and/or hereditary hemorrhagic telengiectasia.
77 . The method of claim 72 , wherein the subject suffers from delayed wound-healing, delayed ulcer healing, reproduction associated disorders, coronary artery disease, arteriosclerosis, myocardial ischemia, peripheral ischemia, cerebral ischemia, retinopathy, remodeling disorder, von Hippel-Lindau syndrome, diabetes and/or hereditary hemorrhagic telengiectasia.
78 . The method of claim 70 , wherein the tissue is vascular tissue.
79 . The method of claim 71 , wherein the tissue is vascular tissue.
80 . The method of claim 72 , wherein the tissue is vascular tissue.
81 . A nucleic acid construct comprising a polynucleotide sequence encoding a peptide comprising the amino acid sequence selected from the group consisting of SEQ ID NOs: 6 and 10.
82 . The nucleic acid construct of claim 81 , further comprising a promoter.
83 . A nucleic acid construct comprising a polynucleotide sequence encoding a peptide comprising the amino acid sequence as set forth in SEQ ID NO:13, 27 or 32, the peptide being at least 6 and no more than 50 amino acid residues in length.
84 . The nucleic acid construct of claim 83 , further comprising a promoter.
85 . A method of identifying putative angiogenic molecules, the method comprising:
(a) providing endothelial cells having peptides bound thereto, each of said peptides having an amino acid sequence selected from the group consisting of SEQ ID NOs: 2, 4, 6, 8, 10 and 12, said peptide being no more than 50 amino acid residues in length; and (b) identifying a molecule capable of displacing said peptides from said endothelial cells, to thereby identify putative angiogenic molecules.
86 . A cyclic peptide comprising the amino acid sequence selected from the group consisting of SEQ ID NOs:2 and 12, the peptide being no more than 50 amino acid residues in length.
87 . A composition for targeting a drug to endothelial cells, the composition comprising the drug fused to the cyclic peptide of claim 86 .
88 . A pharmaceutical composition comprising as an active ingredient the cyclic peptide of claim 86 and a pharmaceutically acceptable carrier or diluent.
89 . A peptide comprising the amino acid sequence as set forth in SEQ ID NO:27 or 32, wherein the peptide being at least 6 and no more than 50 amino acid residues in length.
90 . The peptide of claim 89 , being cyclic.
91 . The cyclic peptide of claim 90 , wherein the amino acid sequence is set forth by SEQ ID NO:2 or 12.
92 . A composition for targeting a drug to endothelial cells, the composition comprising the drug fused to the peptide of claim 89 .
93 . A pharmaceutical composition comprising as an active ingredient the peptide of claim 89 and a pharmaceutically acceptable carrier or diluent.Cited by (0)
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