Estrogen receptor beta as target for colorectal cancer prevention

Cancer Lett. 2016 Mar 1;372(1):48-56. doi: 10.1016/j.canlet.2015.12.009. Epub 2015 Dec 18.

Abstract

Colorectal cancer (CRC) is a leading cause of death in the United States. Despite its slow development and the capacity for early diagnosis, current preventive approaches are not sufficient. However, a role for estrogen has been demonstrated in multiple epidemiologic studies, which may benefit CRC prevention. A large body of evidence from preclinical studies indicates that expression of the estrogen receptor beta (ERβ/ESR2) demonstrates an inverse relationship with the presence of colorectal polyps and stage of tumors, and can mediate a protective response. Natural compounds, including phytoestrogens, or synthetic ERβ selective agonists, can activate or upregulate ERβ in the colon and promote apoptosis in preclinical models and in clinical experience. Importantly, this activity has been associated with a reduction in polyp formation and, in rodent models of CRC, has been shown to lower incidence of colon adenocarcinoma. Collectively, these findings indicate that targeted activation of ERβ may represent a novel clinical approach for management of colorectal adenomatous polyps and prevention of colorectal carcinoma in patients at risk for this condition. In this review, we discuss the potential of new chemopreventive or dietary approaches based on estrogen signaling.

Keywords: Colorectal cancer; Estrogen; Estrogen receptor beta; Gene expression; Phytoestrogens; Prevention.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenocarcinoma / epidemiology
  • Adenocarcinoma / genetics
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Adenocarcinoma / prevention & control*
  • Adenomatous Polyps / drug therapy*
  • Adenomatous Polyps / epidemiology
  • Adenomatous Polyps / genetics
  • Adenomatous Polyps / metabolism
  • Adenomatous Polyps / pathology
  • Animals
  • Anticarcinogenic Agents / therapeutic use*
  • Cell Transformation, Neoplastic / drug effects
  • Cell Transformation, Neoplastic / metabolism
  • Colon / drug effects
  • Colon / metabolism
  • Colon / pathology
  • Colonic Polyps / drug therapy*
  • Colonic Polyps / epidemiology
  • Colonic Polyps / genetics
  • Colonic Polyps / metabolism
  • Colonic Polyps / pathology
  • Colorectal Neoplasms / epidemiology
  • Colorectal Neoplasms / genetics
  • Colorectal Neoplasms / metabolism
  • Colorectal Neoplasms / pathology
  • Colorectal Neoplasms / prevention & control*
  • Estrogen Receptor Antagonists / therapeutic use*
  • Estrogen Receptor beta / antagonists & inhibitors*
  • Estrogen Receptor beta / metabolism
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Molecular Targeted Therapy / methods*
  • Risk Factors
  • Signal Transduction / drug effects

Substances

  • Anticarcinogenic Agents
  • Estrogen Receptor Antagonists
  • Estrogen Receptor beta