Role of WISP-2/CCN5 in the maintenance of a differentiated and noninvasive phenotype in human breast cancer cells

Mol Cell Biol. 2008 Feb;28(3):1114-23. doi: 10.1128/MCB.01335-07. Epub 2007 Dec 10.

Abstract

WISP-2/CCN5 is an estrogen-regulated member of the "connective tissue growth factor/cysteine-rich 61/nephroblastoma overexpressed" (CCN) family of the cell growth and differentiation regulators. The WISP-2/CCN5 mRNA transcript is undetectable in normal human mammary cells, as well as in highly aggressive breast cancer cell lines, in contrast with its higher level in the breast cancer cell lines characterized by a more differentiated phenotype. We report here that knockdown of WISP-2/CCN5 by RNA interference in estrogen receptor alpha (ERalpha)-positive MCF-7 breast cancer cells induced an estradiol-independent growth linked to a loss of ERalpha expression and promoted epithelial-to-mesenchymal transdifferentiation. In contrast, forced expression of WISP-2/CCN5 directed MCF-7 cells toward a more differentiated phenotype. When introduced into the poorly differentiated, estrogen-independent, and invasive MDA-MB-231 breast cancer cells, WISP-2/CCN5 was able to reduce their proliferative and invasive phenotypes. In a series of ERalpha-positive tumor biopsies, we found a positive correlation between the expression of WISP-2/CCN5 and ID2, a transcriptional regulator of differentiation in normal and transformed breast cells. We propose that WISP-2/CCN5 is an important regulator involved in the maintenance of a differentiated phenotype in breast tumor epithelial cells and may play a role in tumor cell invasion and metastasis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / etiology
  • Breast Neoplasms / pathology*
  • CCN Intercellular Signaling Proteins
  • Cell Differentiation
  • Cell Line, Tumor
  • Cell Proliferation
  • Estrogen Receptor alpha
  • Female
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / physiology*
  • Neoplasm Invasiveness
  • Neoplasm Metastasis
  • Phenotype
  • RNA Interference
  • RNA, Small Interfering / pharmacology
  • Repressor Proteins
  • Transcription Factors / genetics
  • Transcription Factors / physiology*

Substances

  • CCN Intercellular Signaling Proteins
  • CCN5 protein, human
  • Estrogen Receptor alpha
  • Intercellular Signaling Peptides and Proteins
  • RNA, Small Interfering
  • Repressor Proteins
  • Transcription Factors