The activity of Gli transcription factors is essential for Kras-induced pancreatic tumorigenesis
De Jesus-Monge, Wilfredo E.
Driscoll, David R.
Appleman, Victoria A.
Cotton, Jennifer L.
Klimstra, David S.
Zhu, Lihua Julie
McMahon, Andrew P.
Lewis, Brian C.
UMass Chan AffiliationsDepartment of Cancer Biology
Program in Molecular Medicine
Program in Gene Function and Expression
Carcinoma, Pancreatic Ductal
I-kappa B Proteins
Genetics and Genomics
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AbstractPancreatic ductal adenocarcinoma (PDAC), one of the most aggressive human malignancies, is thought to be initiated by KRAS activation. Here we find that transcriptional activation mediated by the Gli family of transcription factors, although dispensable for pancreatic development, is required for Kras-induced proliferation and survival in primary pancreatic epithelial cells in culture and for Kras-driven pancreatic intraepithelial neoplasia and PDAC formation in vivo. Further, ectopic Gli1 activation in the mouse pancreas accelerates Kras-driven tumor formation, underscoring the importance of Gli transcription factors in pancreatic tumorigenesis. Interestingly, we demonstrate Gli-regulated I-kappa-B kinase epsilon (IKBKE) and NF-kappaB activity in pancreatic cancer cells and show that this activity is a critical downstream mediator for Gli-dependent PDAC cell transformation and survival. Together, these studies demonstrate the requirement for Gli in Kras-dependent pancreatic epithelial transformation, suggest a mechanism of Gli-NF-kappaB oncogenic activation, and provide genetic evidence supporting the therapeutic targeting of Gli activity in pancreatic cancer.
SourceProc Natl Acad Sci U S A. 2012 Apr 24;109(17):E1038-47. Epub 2012 Apr 9. Link to article on publisher's site
Permanent Link to this Itemhttp://hdl.handle.net/20.500.14038/43995
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