TY - JOUR
T1 - Expression of connective tissue growth factor (CTGF/CCN2) in breast cancer cells is associated with increased migration and angiogenesis
AU - Chien, Wenwen
AU - O'Kelly, James
AU - Lu, Daning
AU - Leiter, Amanda
AU - Sohn, Julia
AU - Yin, Dong
AU - Karlan, Beth
AU - Vadgama, Jay
AU - Lyons, Karen M.
AU - Koeffler, H. Phillip
PY - 2011/6
Y1 - 2011/6
N2 - 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.
AB - 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.
KW - Angiogenesis
KW - Breast cancer
KW - Connective tissue growth factor
KW - Migration
UR - https://www.scopus.com/pages/publications/79955825522
U2 - 10.3892/ijo.2011.985
DO - 10.3892/ijo.2011.985
M3 - Article
C2 - 21455569
AN - SCOPUS:79955825522
SN - 1019-6439
VL - 38
SP - 1741
EP - 1747
JO - International Journal of Oncology
JF - International Journal of Oncology
IS - 6
ER -