TY - JOUR
T1 - Netrin-1 up-regulation in inflammatory bowel diseases is required for colorectal cancer progression
AU - Paradisi, Andrea
AU - Maisse, Carine
AU - Coissieux, Marie May
AU - Gadot, Nicolas
AU - Lépinasse, Florian
AU - Delloye-Bourgeois, Céline
AU - Delcros, Jean Guy
AU - Svrcek, Magali
AU - Neufert, Clemens
AU - Fléjou, Jean François
AU - Scoazec, Jean Yves
AU - Mehlen, Patrick
PY - 2009/10/6
Y1 - 2009/10/6
N2 - Chronic inflammation and cancer are intimately associated. This is particularly true for inflammatory bowel diseases (IBD), such as ulcerative colitis and Crohn's disease, which show a major increased risk for colorectal cancer. While the understanding of the molecular pathogenesis of IBD has recently improved, the mechanisms that link these chronic inflammatory states to colorectal cancer development are in large part unknown. One of these mechanisms is NF-κB pathway activation which in turn may contribute to tumor formation by providing anti-apoptotic survival signals to the epithelial cells. Based on the observation that netrin-1, the anti-apoptotic ligand for the dependence receptors DCC and UNC5H is up-regulated in colonic crypts in response to NF-κB, we show here that colorectal cancers from inflammatory bowel diseases patients have selected up-regulation of netrin-1. Moreover, we demonstrate that this inflammation-driven netrin-1 up-regulation is causal for colorectal cancer development as interference with netrin-1 autocrine loop in a mouse model for ulcerative colitis-associated colorectal cancer, while showing no effect on inflammation, inhibits colorectal cancer progression.
AB - Chronic inflammation and cancer are intimately associated. This is particularly true for inflammatory bowel diseases (IBD), such as ulcerative colitis and Crohn's disease, which show a major increased risk for colorectal cancer. While the understanding of the molecular pathogenesis of IBD has recently improved, the mechanisms that link these chronic inflammatory states to colorectal cancer development are in large part unknown. One of these mechanisms is NF-κB pathway activation which in turn may contribute to tumor formation by providing anti-apoptotic survival signals to the epithelial cells. Based on the observation that netrin-1, the anti-apoptotic ligand for the dependence receptors DCC and UNC5H is up-regulated in colonic crypts in response to NF-κB, we show here that colorectal cancers from inflammatory bowel diseases patients have selected up-regulation of netrin-1. Moreover, we demonstrate that this inflammation-driven netrin-1 up-regulation is causal for colorectal cancer development as interference with netrin-1 autocrine loop in a mouse model for ulcerative colitis-associated colorectal cancer, while showing no effect on inflammation, inhibits colorectal cancer progression.
UR - http://www.scopus.com/inward/record.url?scp=70350129898&partnerID=8YFLogxK
U2 - 10.1073/pnas.0901767106
DO - 10.1073/pnas.0901767106
M3 - Article
C2 - 19721007
AN - SCOPUS:70350129898
SN - 0027-8424
VL - 106
SP - 17146
EP - 17151
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 40
ER -