The oxysterol receptors LXRα and LXRβ suppress proliferation in the colon

Mol Carcinog. 2013 Nov;52(11):835-44. doi: 10.1002/mc.21924. Epub 2012 May 18.

Abstract

The oxysterol receptors LXRα and LXRβ are members of the nuclear receptor family and established transcriptional regulators of lipid metabolism with additional anti-inflammatory functions. Recent investigations have indicated an important role of LXRs in the control of proliferation. Here we further extend this knowledge to human colon cancer cells and proliferation in mouse colon. We show that activation of LXRs leads to a robust cell cycle arrest in colorectal adenocarcinoma cell lines. At the molecular level LXRs control expression of several cell cycle genes including Skp2, c-Myc, CDKs, cyclins, and p15. Furthermore, activation of LXRs causes hypo-phosphorylation of the retinoblastoma (Rb) tumor suppressor protein. Experiments performed in vivo show that the colon structure appears to be intact in LXR null mice. However, LXRαβ(-/-) mice show a significant increase of proliferation markers in colon compared to wild type mice and administration of the LXR specific agonist, GW3965 significantly reduced expression of proliferation in mouse colon. Taken together, these findings point toward a strong anti-proliferative effect of LXRs in colon revealing the potential of LXR ligands as possible anti cancer agents.

Keywords: cell cycle; liver X receptors; nuclear receptors; proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Cycle
  • Cell Line, Tumor
  • Cell Proliferation*
  • Colon / cytology
  • Colon / metabolism*
  • Colon / pathology*
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology*
  • Gene Expression Regulation
  • Humans
  • Liver X Receptors
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Orphan Nuclear Receptors / analysis
  • Orphan Nuclear Receptors / genetics
  • Orphan Nuclear Receptors / metabolism*

Substances

  • Liver X Receptors
  • NR1H3 protein, human
  • Nr1h3 protein, mouse
  • Orphan Nuclear Receptors