Expression of connective tissue growth factor (CTGF/CCN2) in breast cancer cells is associated with increased migration and angiogenesis

Wenwen Chien, James O'Kelly, Daning Lu, Amanda Leiter, Julia Sohn, Dong Yin, Beth Karlan, Jay Vadgama, Karen M. Lyons, H. Phillip Koeffler

Research output: Contribution to journalArticlepeer-review

65 Scopus citations

Abstract

Connective tissue growth factor (CTGF/CCN2) belongs to the CCN family of matricellular proteins, comprising Cyr61, CTGF, NovH and WISP1-3. The CCN proteins contain an N-terminal signal peptide followed by four conserved domains sharing sequence similarities with the insulin-like growth factor binding proteins, von Willebrand factor type C repeat, thrombospondin type 1 repeat, and a C-terminal growth factor cysteine knot domain. To investigate the role of CCN2 in breast cancer, we transfected MCF-7 cells with full-length CCN2, and with four mutant constructs in which one of the domains had been deleted. MCF-7 cells stably expressing full-length CCN2 demonstrated reduced cell proliferation, increased migration in Boyden chamber assays and promoted angiogenesis in chorioallantoic membrane assays compared to control cells. Deletion of the C-terminal cysteine knot domain, but not of any other domain-deleted mutants, abolished activities mediated by full-length CCN2. We have dissected the role of CCN2 in breast tumorigenesis on a structural basis.

Original languageEnglish
Pages (from-to)1741-1747
Number of pages7
JournalInternational Journal of Oncology
Volume38
Issue number6
DOIs
StatePublished - Jun 2011
Externally publishedYes

Keywords

  • Angiogenesis
  • Breast cancer
  • Connective tissue growth factor
  • Migration

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