Stromal Influence on Breast Cancer Progression.

Abstract

Metastatic estrogen receptor positive breast carcinoma may be treatable with tamoxifen, an antiestrogen, but the tumor may subsequently become refractory to treatment, growing in the absence of estrogenic stimulation. We have developed a model of breast cancer progression by transfecting MCF-7 breast carcinoma cells, which are estrogen-dependent for growth in ovariectornized nude mice, with cDNAs for FGF-l or FGF-4. he transfected cell lines are able to form tumors in ovariectomized nude mice. Since FGFs are angiogenic actors, this project investigates the importance of angiogenesis in the phenotypic transition of the transfected cells by looking for differences in the angiogenesis in tumors produced by the parental MCF-7 or the FGF- transfected cells. Our model is validated by a positive correlation of tumor microvessel density and tumor size. We have defined temporal and spatial events in the process of tumor-induced angiogenesis by identifing sprouting or proliferating endothelial cells. We have identified patterns of angiogenesis which are associated with regressing parental cell tumors and growing FGF-transfected cell tumors. (AN)

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Document Details

Document Type
Technical Report
Publication Date
Jul 14, 1995
Accession Number
ADA298413

Entities

People

  • Sandra W. Mcleskey

Organizations

  • Georgetown University

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Biological Factors
  • Blood
  • Blood Vessels
  • Breast Cancer
  • Cancer
  • Carcinoma
  • Cell Physiological Processes
  • Cells
  • Chemistry
  • Endothelial Cells
  • Growth Factors
  • Neoplasms
  • Peptide Growth Factors
  • Peptides
  • Proteins
  • Statistical Analysis

Fields of Study

  • Biology

Readers

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