The activity of Gli transcription factors is essential for Kras-induced pancreatic tumorigenesis Journal Article


Authors: Rajurkar, M.; De Jesus-Monge, W. E.; Driscoll, D. R.; Appleman, V. A.; Huang, H.; Cotton, J. L.; Klimstra, D. S.; Zhu, L. J.; Simin, K.; Xu, L.; McMahon, A. P.; Lewis, B. C.; Mao, J.
Article Title: The activity of Gli transcription factors is essential for Kras-induced pancreatic tumorigenesis
Abstract: Pancreatic 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-κB 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-κB oncogenic activation, and provide genetic evidence supporting the therapeutic targeting of Gli activity in pancreatic cancer.
Keywords: controlled study; nonhuman; animal cell; mouse; animal tissue; cell survival; animal experiment; animal model; immunoglobulin enhancer binding protein; carcinogenesis; regulatory mechanism; cell transformation; transcription factor gli2; epithelium cell; pancreas adenocarcinoma; tumor growth; k ras protein; transcription factor gli1; transcription factor gli3; in vivo culture; i kappa b kinase epsilon; pancreas duct adenocarcinoma
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 109
Issue: 17
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2012-04-24
Start Page: E1038
End Page: E1047
Language: English
DOI: 10.1073/pnas.1114168109
PROVIDER: scopus
PMCID: PMC3340052
PUBMED: 22493246
DOI/URL:
Notes: --- - "Export Date: 4 June 2012" - "CODEN: PNASA" - "Source: Scopus"
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  1. David S Klimstra
    978 Klimstra