APA
Peña, Cristina & Céspedes, María Virtudes & Bradic Lindh, Maja & Kiflemariam, Sara & Mezheyeuski, Artur & Edqvist, Per-Henrik & Hagglof, Christina & Birgisson, Helgi & Bojmar, Linda & Jirstrom, Karin & Sandstr¿om, Per & Olsson, Eleonor & Veerla, Srinivas & Gallardo, Alberto & Sjoblom, Tobias & Chang, Andy C.-M. & Reddel, Roger R. & Mangues, Ramon & Augsten, Martin & Ostman, Arne .STC1 Expression By Cancer-Associated Fibroblasts Drives Metastasis of Colorectal Cancer.
ISO 690
Peña, Cristina & Céspedes, María Virtudes & Bradic Lindh, Maja & Kiflemariam, Sara & Mezheyeuski, Artur & Edqvist, Per-Henrik & Hagglof, Christina & Birgisson, Helgi & Bojmar, Linda & Jirstrom, Karin & Sandstr¿om, Per & Olsson, Eleonor & Veerla, Srinivas & Gallardo, Alberto & Sjoblom, Tobias & Chang, Andy C.-M. & Reddel, Roger R. & Mangues, Ramon & Augsten, Martin & Ostman, Arne. STC1 Expression By Cancer-Associated Fibroblasts Drives Metastasis of Colorectal Cancer.
https://hdl.handle.net/20.500.12080/39556
Résumé:
Platelet-derived growth factor (PDGF) receptor signaling is a major functional determinant of cancerassociated
fibroblasts (CAF). Elevated expression of PDGF receptors on stromal CAFs is associated with
metastasis and poor prognosis, but mechanism(s) that underlie these connections are not understood. Here,
we report the identification of the secreted glycoprotein stanniocalcin-1 (STC1) as a mediator of metastasis by
PDGF receptor function in the setting of colorectal cancer. PDGF-stimulated fibroblasts increased migration and
invasion of cocultured colorectal cancer cells in an STC1-dependent manner. Analyses of human colorectal
cancers revealed significant associations between stromal PDGF receptor and STC1 expression. In an orthotopic
mouse model of colorectal cancer, tumors formed in the presence of STC1-deficient fibroblasts displayed reduced
intravasation of tumor cells along with fewer and smaller distant metastases formed. Our results reveal a
mechanistic basis for understanding the contribution of PDGF-activated CAFs to cancer metastasis. Cancer Res;
73(4); 1287¿97. 2012 AACR.