TY - JOUR
T1 - A Case of Mistaken Identity? Nonductal Origins of Pancreatic "Ductal" Cancers
AU - Murtaugh, L. Charles
AU - Leach, Steven D.
N1 - Funding Information:
This work was supported by NIH grants DK61215 and DK56211 (to S.D.L.) and by Lustgarten Foundation grant RFP06-059 and Searle Scholars Program grant 06-B-116 (to L.C.M.). S.D.L. is also supported by the Paul K. Neumann Professorship at Johns Hopkins University.
PY - 2007/3/13
Y1 - 2007/3/13
N2 - In this issue of Cancer Cell, Guerra and colleagues provide important new insights regarding the ability of specific pancreatic cell types to generate invasive pancreatic cancer. First, they demonstrate that classical pancreatic "ductal" neoplasia can be induced by activation of oncogenic Kras in nonductal exocrine cells. Second, they show that, while Kras activation in immature acinar and centroacinar cells is readily able to induce ductal neoplasia, Kras-mediated tumorigenesis in mature exocrine pancreas requires the induction of chronic epithelial injury. The results shed new light on the "cell of origin" of pancreatic ductal cancer and demonstrate that chronic pancreatitis provides a permissive environment for Kras-induced pancreatic neoplasia.
AB - In this issue of Cancer Cell, Guerra and colleagues provide important new insights regarding the ability of specific pancreatic cell types to generate invasive pancreatic cancer. First, they demonstrate that classical pancreatic "ductal" neoplasia can be induced by activation of oncogenic Kras in nonductal exocrine cells. Second, they show that, while Kras activation in immature acinar and centroacinar cells is readily able to induce ductal neoplasia, Kras-mediated tumorigenesis in mature exocrine pancreas requires the induction of chronic epithelial injury. The results shed new light on the "cell of origin" of pancreatic ductal cancer and demonstrate that chronic pancreatitis provides a permissive environment for Kras-induced pancreatic neoplasia.
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U2 - 10.1016/j.ccr.2007.02.020
DO - 10.1016/j.ccr.2007.02.020
M3 - Short survey
C2 - 17349578
AN - SCOPUS:33847414390
SN - 1535-6108
VL - 11
SP - 211
EP - 213
JO - Cancer cell
JF - Cancer cell
IS - 3
ER -