An AR-Skp2 pathway for proliferation of androgen-dependent prostate-cancer cells

J Cell Sci. 2008 Aug 1;121(Pt 15):2578-87. doi: 10.1242/jcs.030742. Epub 2008 Jul 15.

Abstract

Androgen-androgen-receptor (androgen-AR) signaling in normal prostate epithelium promotes terminal luminal epithelial cell differentiation. In androgen-dependent prostate-cancer cells, androgen-AR signaling gains the ability to promote both differentiation and proliferation. How this signaling promotes proliferation of androgen-dependent prostate-cancer cells and its relationship with the differentiation-promoting functions of the AR are important issues regarding the biology of androgen-dependent prostate-cancer cells. Herein, we report the identification of an AR-Skp2 pathway in prostate-cancer cells that depend on the AR for proliferation; in this pathway, AR is a robust upstream regulator of Skp2 through blocking the D-box-dependent degradation of this protein, and Skp2, in turn, serves as an essential downstream effector of AR in promoting proliferation independently of the differentiation-promoting function of AR. These results provide new knowledge on how AR functions in androgen-dependent prostate-cancer cells and identify strategies to specifically target the proliferation-promoting function of AR without compromising cancer-cell differentiation.

Publication types

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

MeSH terms

  • Androgens / metabolism*
  • Cell Cycle
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Proliferation
  • Gene Silencing
  • Humans
  • Male
  • Prostatic Neoplasms / metabolism*
  • RNA, Messenger / metabolism
  • Receptors, Androgen / metabolism*
  • S-Phase Kinase-Associated Proteins / genetics
  • S-Phase Kinase-Associated Proteins / metabolism*
  • Signal Transduction*

Substances

  • Androgens
  • RNA, Messenger
  • Receptors, Androgen
  • S-Phase Kinase-Associated Proteins