ARID1A Maintains Differentiation of Pancreatic Ductal Cells and Inhibits Development of Pancreatic Ductal Adenocarcinoma in Mice

作者：Kimura Yoshito; Fukuda Akihisa; Ogawa Satoshi; Maruno Takahisa; Takada Yutaka; Tsuda Motoyuki; Hiramatsu Yukiko; Araki Osamu; Nagao Munemasa; Yoshikawa Takaaki; Ikuta Kozo; Yoshioka Takuto; Wang Zong; Akiyama Haruhiko; Wright Christopher V; Takaori Kyoichi; Uemoto Shinji; Chiba Tsutomu; Seno Hiroshi

来源：Gastroenterology, 2018, 155(1): 194-+.

DOI：10.1053/j.gastro.2018.03.039

• Oncogene
• Pancreatic Cancer
• Transcriptional Regulator
• Tumorigenesis

BACKGROUND & AIMS: The ARID1A gene encodes a protein that is part of the large adenosine triphosphate (ATP)-dependent chromatin remodeling complex SWI/SNF and is frequently mutated in human pancreatic ductal adenocarcinomas (PDACs). We investigated the functions of ARID1A during formation of PDACs in mice. METHODS: We performed studies with Ptf1a-Cre; Kras(G12D) mice, which express activated Kras in the pancreas and develop pancreatic intraepithelial neoplasias (PanINs), as well as those with disruption of Aird1a (Ptf1a-Cre; Kras(G12D); Arid1a(f/f) mice) or disruption of Brg1 (encodes a catalytic ATPase of the SWI/SNF complex) (Ptf1a-Cre; Kras(G12D); Brg1(f/f) mice). Pancreatic ductal cells (PDCs) were isolated from Arid1a(f/f) mice and from Arid1a(f/f); SOX9OE mice, which overexpress human SOX9 upon infection with an adenovirus-expressing Cre recombinase. Pancreatic tissues were collected from all mice and analyzed by histology and immunohistochemistry; cells were isolated and grown in 2-dimensional and 3-dimensional cultures. We performed microarray analyses to compare gene expression patterns in intraductal papillary mucinous neoplasms (IPMNs) from the different strains of mice. We obtained 58 samples of IPMNs and 44 samples of PDACs from patients who underwent pancreatectomy in Japan and analyzed them by immunohistochemistry. RESULTS: Ptf1a-Cre; Kras(G12D) mice developed PanINs, whereas Ptf1a-Cre; Kras(G12D); Arid1a(f/f) mice developed IPMNs and PDACs; IPMNs originated from PDCs. ARID1A-deficient IPMNs did not express SOX9. ARID1A-deficient PDCs had reduced expression of SOX9 and dedifferentiated in culture. Overexpression of SOX9 in these cells allowed them to differentiate and prevented dilation of ducts. Among mice with pancreatic expression of activated Kras, those with disruption of Arid1a developed fewer PDACs from IPMNs than mice with disruption of Brg1. ARID1A-deficient IPMNs had reduced activity of the mTOR pathway. Human IPMN and PDAC specimens had reduced levels of ARID1A, SOX9, and phosphorylated S6 (a marker of mTOR pathway activation). Levels of ARID1A correlated with levels of SOX9 and phosphorylated S6. CONCLUSIONS: ARID1A regulates expression of SOX9, activation of the mTOR pathway, and differentiation of PDCs. ARID1A inhibits formation of PDACs from IPMNs in mice with pancreatic expression of activated KRAS and is down-regulated in IPMN and PDAC tissues from patients.

• 出版日期2018-7