Genome-Wide Approaches to Detecting Stromal-Epithelial Interactions in Breast Cancer

Abstract

The work done to date has helped to better characterize the breast cancer microenvironment. We have confirmed that the expression normal adjacent tissue is not distinct from healthy breast reduction tissue. The genes specific to normal epithelium also identify basal-like breast tumors, potentially explaining their resistance to treatment. The interactions involving the tumor immune cells have the strongest detectable signals using the methods developed by this project. We are the first group to characterize the expression of the blood vessels in breast cancer. We have confirmed the presence of low-density mature vessels and high-density immature vessels. Surprisingly, the expression from those mature tumor vessels more closely match the characteristics of tumor vessels in other cancers. This will open new roads for a better understanding of neo-vascularization in breast cancer as well as helping to target treatment more effectively. Our work in mouse models has also identified osteoactivin as a potential effector of bone metastasis.

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Document Details

Document Type
Technical Report
Publication Date
Mar 01, 2007
Accession Number
ADA469651

Entities

People

  • Francois Pepin

Organizations

  • McGill University

Tags

Communities of Interest

  • Biomedical

DTIC Thesaurus Topics

  • Abstracts
  • Biomedical Research
  • Blood Vessels
  • Breast Cancer
  • Cancer
  • Department Of Defense
  • High Density
  • Information Operations
  • Low Density
  • Neoplasms

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics
  • Oncology (Cancer Research).
  • Theoretical Analysis.