The Role of Integrins and IGFBPs in the IGF-l Stimulated Migration of Human Breast Cancer Cells

Abstract

We have previously shown that IGF-I stimulates chemotaxis of MCF-7 and MDA-231 human breast cancer cells. We now report that PDGF is a potent stimulant of migration. FGF is less effective, and EGF has no effect. The integrins that are present on 4 additional cell lines were identified. Antibodies that bind to the Beta 3 integrin inhibited migration in 3 of the 4 cell lines. Anti-alpha 5 antibodies were also potent inhibitors. The combination of estradiol and IGF-I potently stimulated chemotaxis in MCF-7 cells, and the response to both hormones was greater than that to either hormone alone. Two IGF binding proteins were shown to alter the chemokinetic response of MDA-231 1 cells to IGF-I. IGFBP-3 inhibited the response to IGF-I. In contrast, IGFBP-5 enhanced the response to IGF-I, suggesting that different binding proteins have different effects.

Open PDF

Document Details

Document Type
Technical Report
Publication Date
Jun 01, 1998
Accession Number
ADA353342

Entities

People

  • Bo Zheng
  • David D. Clemmons

Organizations

  • University of North Carolina at Chapel Hill

Tags

DTIC Thesaurus Topics

  • Breast Cancer
  • Carrier Proteins
  • Cell Line
  • Cell Physiological Processes
  • Cells
  • Chemical Synthesis
  • Chemistry
  • Growth Factors
  • Inhibitors
  • Peptide Growth Factors
  • Peptides
  • Proteins
  • Tumor Cell Line

Fields of Study

  • Biology
  • Medicine

Readers

  • Cellular and Molecular Pathways of Apoptosis.
  • Molecular Biology and Genetics
  • Women's Health and Cancer Risk Research: African American Women and Pregnancy Outcomes.