IP Library Granted Patent US 7,229,960
Granted Patent B2
US 7,229,960 · App. 10/013,815 · Granted Jun 12, 2007

Methods and compositions for inhibiting GRB7

Assignee: University of Vermont and State Agricultural College
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Quick Facts
Patent No.
US 7,229,960
App. No.
10/013,815
Granted
Jun 12, 2007
Kind
B2
Abstract

The invention provides methods and compositions for treating subjects using Grb7 antagonists. Specifically disclosed are Grb7 antagonists that bind selectively to Grb7 and interfere with the ability of Grb7 to bind to its native ligands. These compositions are useful in the prevention and treatment of disorders characterized by abnormal interaction of Grb7 with its native ligands (e.g., ErbB2).

Claims (5)

1. A method for treating a subject having a cancer characterized by overexpression of Grb7 comprising administering to a subject in need of such treatment a compound consisting of a non-phosphorylated Grb7 binding peptide consisting of the amino acid sequence set forth as SEQ ID NO:4, 5, 35, 42, 50, or 51, in an amount effective to inhibit metastasis, wherein the binding peptide is attached to a translocation agent capable of transporting the peptide into cell cytoplasm or the nucleus of a cell, binds to the SH2 domain of Grb7 and does not specifically bind the SH2 domain of Grb2 or Grb14, and wherein the peptide is administered locally to the cancer.

2. The method of claim 1 , wherein the peptide is cyclic.

3. The method of claim 1 wherein the cancer is a metastasis.

4. The method of claim 1 , wherein the Grb7 binding peptide is administered with a pharmaceutically acceptable carrier.

5. The method of claim 1 , wherein the translocation agent has the amino acid sequence RQIKIWFQNRRMKWKK (SEQ ID NO:19).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 29, 2002
From: KRAG, DAVID N.; PERO, STEPHANIE C.
To: UNIVERSITY OF VERMONT AND STATE AGRICULTURAL COLLEGE
Reel/Frame 012756/0581 →
Continuity (2)
Provisional Application 6024575500 · Nov 3, 2000
Related Publication 20030105000A1 · Jun 5, 2003