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IL2RG, identified as overexpressed by RNA-seq profiling of pancreatic intraepithelial neoplasia, mediates pancreatic cancer growth
Author(s) -
Michael Ayars,
Eileen O’Sullivan,
Anne M. MacgregorDas,
Koji Shindo,
Haeryoung Kim,
Michael Borges,
Jun Yu,
Ralph H. Hruban,
Michael Goggins
Publication year - 2017
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.19848
Subject(s) - pancreatic intraepithelial neoplasia , pancreatic cancer , cancer research , pancreatic duct , ca19 9 , medicine , pathology , biology , pancreas , cancer , pancreatic ductal adenocarcinoma
Pancreatic ductal adenocarcinoma evolves from precursor lesions, the most common of which is pancreatic intraepithelial neoplasia (PanIN). We performed RNA-sequencing analysis of laser capture microdissected PanINs and normal pancreatic duct cells to identify differentially expressed genes between PanINs and normal pancreatic duct, and between low-grade and high-grade PanINs. One of the most highly overexpressed transcripts identified in PanIN is interleukin-2 receptor subunit gamma ( IL2RG ) encoding the common gamma chain, IL2Rγ. CRISPR-mediated knockout of IL2RG in orthotopically implanted pancreatic cancer cells resulted in attenuated tumor growth in mice and reduced JAK3 expression in orthotopic tumors. These results indicate that IL2Rγ/JAK3 signaling contributes to pancreatic cancer cell growth in vivo .

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