Met (HGF Receptor) in Breast Cancer

Abstract

The hepatocyte growth factor (HGF)/Met signaling pathway has been shown to be important for stimulating cell proliferation, motility, invasion and metastasis. Recent work from our lab has identified a 60 kDa fragment from the carboxy-terminal domain of Met that localizes to the nucleus. Preliminary data from our also indicates that Met is translocated to the nucleus during in vitro wound healing of epithelial sheets of cells. Because several pharmaceutical companies are currently developing Metbased therapies, it becomes even more important to gain an understanding of the role of nuclear Met, especially whether or not it may be contributing to invasion and metastasis. To date, no studies have been conducted to understand this aspect of Met function. Therefore the objectives of my proposal are to assess the role of Met in a model of epithelial-mesenchymal transition (EMT), identify key residues in the Met receptor necessary for nuclear translocation, and determine the functional role of Met in the nucleus.

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Document Details

Document Type
Technical Report
Publication Date
Sep 01, 2009
Accession Number
ADA515399

Entities

People

  • Jennifer Bordeaux

Organizations

  • Yale University

Tags

DTIC Thesaurus Topics

  • Biological Staining And Labeling
  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Cell Line
  • Cells
  • Demographic Cohorts
  • Epithelial Cells
  • Growth Factors
  • Inhibition
  • Lymph Nodes
  • Metastasis
  • Neoplasms
  • Small Molecules
  • Terminals
  • Transitions
  • Wound Healing

Readers

  • Breast cancer cell signaling and growth regulation.
  • Molecular Biology and Genetics