IP Library Granted Patent US 9,056,923
Granted Patent B2
US 9,056,923 · App. 13/992,998 · Granted Jun 16, 2015

Mimetic peptides derived from collagen type IV and their use for treating angiogenesis- and lymphagiogenesis-dependent diseases

Inventors: Aleksander S. Popel (Lutherville, MD); Elena V. Rosca (Baltimore, MD); Jacob E. Koskimaki (Baltimore, MD); Corban G. Rivera (Baltimore, MD); Niranjan B. Pandey (White Marsh, MD); Amir P. Tamiz (Silver Spring, MD)
Assignee: THE JOHNS HOPKINS UNIVERSITY
C07K14/78A61K38/00
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Quick Facts
Patent No.
US 9,056,923
App. No.
13/992,998
Granted
Jun 16, 2015
Kind
B2
Abstract

Mimetic peptides having anti-angiogenic and anti-tumorigenic properties and methods of their use for treating cancer, ocular diseases, such as age-related macular degeneration, and other-angiogenesis-dependent diseases are disclosed. More particularly, active non-cysteine analogs (mimetics), which exhibit anti-angiogenic activity in endothelial cell proliferation, migration, adhesion, and tube formation assays, anti-migratory activity in human breast cancer cells in vitro, anti-angiogenic and anti-tumorigenic activity in vivo in breast cancer xenograft models, and age-related macular degeneration models are disclosed. The presently disclosed mimetic peptides also exhibit anti-lymphangiogenic and directly anti-tumorigenic properties.

Claims (29)

1. An isolated peptide comprising an amino acid sequence LRRFSTXPXXXXNINNVXNF (SEQ ID No:1), wherein X at position 7 is M, A, or G; X at position 9 is F, A, Y, or G; X at position 10 is M, A, G, dA, or Nle; X at position 11 is F, A, Y, G, or 4-ClPhe; X at position 12 and position 18 are G, V, T, I, L or AllyGly, and wherein the peptide exhibits anti-angiogenic, anti-vascular permeability, anti-tumorigenesis and/or anti-lymphangiogenic properties.

2. The non-naturally occurring peptide of claim 1 , wherein the non-naturally occurring peptide comprises at least one of the following amino acid sequences:

(SEQ ID No: 2)

LRRFSTMPFMFGNINNVGNF;

(SEQ ID No: 14)

LRRFSTMPFMFVNINNVVNF;

(SEQ ID No: 12)

LRRFSTMPFMFTNINNVTNF;

(SEQ ID No: 13)

LRRFSTMPFMFAllyGlyNINNVAllyGlyNF;

(SEQ ID No: 11)

LRRFSTMPFMFININNVINF;

(SEQ ID No: 15)

LRRFSTMPFdAFININNVINF;

(SEQ ID No: 16)

LRRFSTAPFMFNINNVINF;

and

(SEQ ID No: 17)

LRRFSTAPFAFININNVINF.

3. The non-naturally occurring peptide of claim 1 , wherein at least one C-terminal amino acid and/or at least one N-terminal amino acid of SEQ ID NO:1 is deleted, wherein the peptide inhibits the proliferation, adhesion, migration, and/or tube formation of endothelial cells, and wherein the isolated peptide comprises at least one of the following amino acid sequences:

(SEQ ID NO: 22)

LRRFSTMPFMFTNINN;

(SEQ ID NO: 23)

LRRFSTMPFMFININN;

and

(SEQ ID NO: 34)

FTNINNVTN.

4. A composition comprising a pharmaceutically acceptable substance and an effective amount of at least one isolated peptide of claim 1 .

5. A kit comprising an isolated peptide of claim 1 .

Assignments (6)
CONFIRMATORY ASSIGNMENT Recorded Aug 21, 2018
From: RIVERA, CORBAN G.
To: THE JOHNS HOPKINS UNIVERISTY
Reel/Frame 046878/0174 →
CONFIRMATORY ASSIGNMENT Recorded Aug 21, 2018
From: KOSKIMAKI, JACOB E.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 046883/0646 →
CONFIRMATORY ASSIGNMENT Recorded Aug 21, 2018
From: PANDEY, NIRANJAN B.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 046884/0390 →
CONFIRMATORY ASSIGNMENT Recorded Aug 21, 2018
From: ROSCA, ELENA V.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 046884/0395 →
CONFIRMATORY ASSIGNMENT Recorded Aug 21, 2018
From: POPEL, ALEKSANDER S.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 046884/0400 →
CONFIRMATORY ASSIGNMENT Recorded Aug 21, 2018
From: TAMIZ, AMIR P.
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 046884/0405 →
Continuity (3)
Provisional Application 61421706 · Dec 10, 2010
Provisional Application 61546314 · Oct 12, 2011
Related Publication 20130316950A1 · Nov 28, 2013