Vascular Endothelial Growth Factor and Receptors in Breast Cancer

Abstract

Experiments completed in the past year were designed to characterize the modifications in mammary gland and tumor vascular endothelium. Studies included analysis of VEGF isoform expression and vascular morphology in mammary gland tumors, mammary glands from ovariectomized (implanted with estrogen or placebo pellets), pregnant, lactating and involuting mice. Our findings demonstrate that estrogen alone can up-regulate the expression of VEGF 120, 164, and 188 isoforms and induce continuous vascular endothelium to become fenestrated. In all cases, where estrogen was present, VEGF was up- regulated, vessels were proliferating, vascular endothelium was fenestrated and caveolae were clustered and fused. Moreover in situations, where estrogen was lacking or decreasing, vascular endothelium had no fenestrations or clustered, fused caveolae. It is known that microvascular permeability is increased with the presence of fenestrae and clustered, fused caveolae.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1998
Accession Number
ADA361569

Entities

People

  • Walter Roberts

Organizations

  • University of California, San Diego

Tags

DTIC Thesaurus Topics

  • Biological Factors
  • Blood Vessels
  • Breast Cancer
  • Cancer
  • Cell Physiological Processes
  • Cells
  • Cellular Structures
  • Chemistry
  • Diseases And Disorders
  • Gene Expression
  • Growth Factors
  • Neoplasms
  • Nervous System Neoplasms
  • Oncology
  • Proteins
  • Rodents
  • Vascular Endothelium

Fields of Study

  • Biology

Readers

  • Molecular Biology and Genetics
  • Oncology (Cancer Research).
  • Women's Health and Cancer Risk Research: African American Women and Pregnancy Outcomes.