Abstract | BACKGROUND & AIMS: METHODS: We disrupted Acvr1b specifically in pancreata of mice (Acvr1b(flox/flox);Pdx1-Cre mice) and crossed them with LSL-KRAS(G12D) mice, which express an activated form of KRAS and develop spontaneous pancreatic tumors. The resulting Acvr1b(flox/flox);LSL-KRAS(G12D);Pdx1-Cre mice were monitored; pancreatic tissues were collected and analyzed by histology and immunohistochemical analyses. We also analyzed p16(flox/flox);LSL-Kras(G12D);Pdx1-Cre mice and Cre-negative littermates (controls). Genomic DNA, total RNA, and protein were isolated from mouse tissues and primary pancreatic tumor cell lines and analyzed by reverse-transcription polymerase chain reaction, sequencing, and immunoblot analyses. Human intraductal papillary mucinous neoplasm (IPMN) specimens were analyzed by immunohistochemistry. RESULTS: Loss of ACVR1B from pancreata of mice increased the proliferation of pancreatic epithelial cells, led to formation of acinar to ductal metaplasia, and induced focal inflammatory changes compared with control mice. Disruption of Acvr1b in LSL-KRAS(G12D);Pdx1-Cre mice accelerated the growth of pancreatic IPMNs compared with LSL-KRAS(G12D);Pdx1-Cre mice, but did not alter growth of pancreatic intraepithelial neoplasias. We associated perinuclear localization of the activated NOTCH4 intracellular domain to the apical cytoplasm of neoplastic cells with the expansion of IPMN lesions in Acvr1b(flox/flox);LSL-KRAS(G12D);Pdx1-Cre mice. Loss of the gene that encodes p16 (Cdkn2a) was required for progression of IPMNs to pancreatic ductal adenocarcinomas in Acvr1b(flox/flox);LSL-Kras(G12D);Pdx1-Cre mice. We also observed progressive loss of p16 in human IPMNs of increasing grades. CONCLUSIONS: Loss of ACVR1B accelerates growth of mutant KRAS-induced pancreatic IPMNs in mice; this process appears to involve NOTCH4 and loss of p16. ACVR1B suppresses early stages of pancreatic tumorigenesis; the activin signaling pathway therefore might be a therapeutic target for pancreatic cancer.
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Authors | Wanglong Qiu, Sophia M Tang, Sohyae Lee, Andrew T Turk, Anthony N Sireci, Anne Qiu, Christian Rose, Chuangao Xie, Jan Kitajewski, Hui-Ju Wen, Howard C Crawford, Peter A Sims, Ralph H Hruban, Helen E Remotti, Gloria H Su |
Journal | Gastroenterology
(Gastroenterology)
Vol. 150
Issue 1
Pg. 218-228.e12
(Jan 2016)
ISSN: 1528-0012 [Electronic] United States |
PMID | 26408346
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Copyright | Copyright © 2016 AGA Institute. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Acrv1 protein, mouse
- Membrane Proteins
- Hras protein, mouse
- Proto-Oncogene Proteins p21(ras)
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Topics |
- Adenocarcinoma, Mucinous
(genetics, mortality, pathology)
- Animals
- Carcinogenesis
(genetics)
- Carcinoma, Pancreatic Ductal
(genetics, mortality, pathology)
- Disease Models, Animal
- Disease Progression
- Gene Deletion
- Genes, Tumor Suppressor
- Genetic Predisposition to Disease
- Humans
- Immunohistochemistry
- Male
- Membrane Proteins
(genetics)
- Mice
- Mice, Knockout
- Pancreatic Neoplasms
(genetics, mortality, pathology)
- Proto-Oncogene Proteins p21(ras)
(genetics)
- Random Allocation
- Real-Time Polymerase Chain Reaction
- Signal Transduction
- Survival Rate
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