A Genetic Model for the Breast Cancer Microenvironment

Abstract

Despite improved treatments, metastatic breast cancer kills more than 40,000 women each year in the US. Little is known about what factors in the host contribute to the establishment of metastases. To understand how the host microenvironment affects the behavior of cancer cells, we have used the zebrafish, a powerful, genetically tractable vertebrate model system with cancer biology very similar to human. Our studies focus on the interaction of the chemokine receptor CXCR4b, expressed in breast cancer cells, with its ligand sdf-1, expressed in the microenvironment. This interaction is a key determinant of metastatic potential. We have selected breast cancer lines with varying expression levels of CXCR4b and sdf-1. We have selectively altered the expression of sdf-1 in zebrafish embryos using knockdown and targeted expression techniques. As proof-of-principle, we shown that perturbing embryo sdf-1 directly affects the migration of endogenous primordial germ cells, which also depend on CXCR4b. In subsequent work, we will assess the effect of these manipulations on survival and spread of breast cancer xenografts. The goal of this study is to understand how the host microenvironment influences the development of breast cancer metastasis.

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Document Details

Document Type
Technical Report
Publication Date
Sep 30, 2008
Accession Number
ADA495343

Entities

People

  • James F. Amatruda

Organizations

  • University of Texas Southwestern Medical Center

Tags

DTIC Thesaurus Topics

  • Angiogenesis
  • Biomedical Research
  • Breast Cancer
  • Cancer
  • Cell Line
  • Cell Movement
  • Cells
  • Embryos
  • Endothelial Cells
  • Fish
  • Germ Cells
  • Metastasis
  • Migration
  • Neoplasms
  • Transplants
  • Xenografts

Fields of Study

  • Biology

Readers

  • Molecular and Cellular Biochemistry
  • Oncology (Cancer Research).

Technology Areas

  • Biotechnology
  • Biotechnology - Cancer Biotech