WISP3 (CCN6) Is a Secreted Tumor-Suppressor Protein that Modulates IGF Signaling in Inflammatory Breast Cancer

Celina G. Kleer, Yanhong Zhang, Quintin Pan, Sofia D. Merajver

Research output: Contribution to journalArticle

76 Scopus citations

Abstract

Inflammatory breast cancer (IBC) is the most lethal form of locally advanced breast cancer. We have found that WISP3 is lost in 80% of human IBC tumors and that it has growth- and angiogenesis-inhibitory functions in breast cancer in vitro and in vivo. WISP3 is a cysteine-rich, putatively secreted protein that belongs to the CCN family. It contains a signal peptide at the N-terminus and four highly conserved motifs. Here, for the first time, we investigate the function of WISP3 protein in relationship to its structural features. We found that WISP3 is secreted into the conditioned media and into the lumens of normal breast ducts. Once secreted, WISP3 was able to decrease, directly or through induction of other molecule(s), the IGF-1-induced activation of the IGF-IR, and two of its main downstream signaling molecules, IRS1 and ERK-1/2, in SUM149 IBC cells. Furthermore, WISP3 containing conditioned media decreased the growth rate of SUM149 cells. This work sheds light into the mechanism of WISP3 function by demonstrating that it is secreted and that, once in the extracellular media, it induces a series of molecular events that leads to modulation of IGF-IR signaling pathways and cellular growth in IBC cells.

Original languageEnglish (US)
Pages (from-to)179-185
Number of pages7
JournalNeoplasia
Volume6
Issue number2
DOIs
StatePublished - Mar 2004
Externally publishedYes

Keywords

  • Cell cycle control
  • Cell proliferation
  • ERK-1/2 phosphorylation
  • IGF-binding proteins
  • MAPK signaling

ASJC Scopus subject areas

  • Cancer Research

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