Bisphenol A impairs estradiol-induced protective effects against DLD-1 colon cancer cell growth

IUBMB Life. 2010 Sep;62(9):684-7. doi: 10.1002/iub.370.

Abstract

Bisphenol A (BPA), a prototype of endocrine disruptors, mimics 17β-estradiol (E2)-induced proliferation in several cancer cells by binding to estrogen receptor α (ERα). However, scarce and conflicting data are available concerning the effect of BPA on estrogen receptor β (ERβ)-mediated functions. Here, the detailed analysis of the effect of BPA, alone or in combination with E2, on ERβ-mediated cellular functions is reported in ERβ-expressing colon cancer cell line. BPA binds to ERβ without activating any receptor activities. On the other hand, BPA inhibits E2-induced genomic activity of ERβ as well as ERβ extra-nuclear activities (i.e., ERβ:p38 association and p38 activation). As a consequence, BPA impairs the E2-induced activation of the apoptotic cascade which is at the root of the protective role played by the hormone against colon cancer growth. Thus, women may be considered a highly susceptible population with an increased risk of colon cancers after BPA exposures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Benzhydryl Compounds
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Colonic Neoplasms* / physiopathology
  • Estrogen Antagonists / pharmacology*
  • Estrogen Receptor alpha / metabolism
  • Estrogens, Non-Steroidal / pharmacology*
  • Female
  • Humans
  • Phenols / pharmacology*
  • Protein Binding / drug effects

Substances

  • Benzhydryl Compounds
  • Estrogen Antagonists
  • Estrogen Receptor alpha
  • Estrogens, Non-Steroidal
  • Phenols
  • bisphenol A