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Ampullary Cancers Harbor ELF3 Tumor Suppressor Gene Mutations and Exhibit Frequent WNT Dysregulation

Authors :
Marie-Claude Gingras
Kyle R. Covington
David K. Chang
Lawrence A. Donehower
Anthony J. Gill
Michael M. Ittmann
Chad J. Creighton
Amber L. Johns
Eve Shinbrot
Ninad Dewal
William E. Fisher
Christian Pilarsky
Robert Grützmann
Michael J. Overman
Nigel B. Jamieson
George Van Buren II
Jennifer Drummond
Kimberly Walker
Oliver A. Hampton
Liu Xi
Donna M. Muzny
Harsha Doddapaneni
Sandra L. Lee
Michelle Bellair
Jianhong Hu
Yi Han
Huyen H. Dinh
Mike Dahdouli
Jaswinder S. Samra
Peter Bailey
Nicola Waddell
John V. Pearson
Ivon Harliwong
Huamin Wang
Daniela Aust
Karin A. Oien
Ralph H. Hruban
Sally E. Hodges
Amy McElhany
Charupong Saengboonmee
Fraser R. Duthie
Sean M. Grimmond
Andrew V. Biankin
David A. Wheeler
Richard A. Gibbs
Source :
Cell Reports, Vol 14, Iss 4, Pp 907-919 (2016)
Publication Year :
2016
Publisher :
Elsevier, 2016.

Abstract

The ampulla of Vater is a complex cellular environment from which adenocarcinomas arise to form a group of histopathologically heterogenous tumors. To evaluate the molecular features of these tumors, 98 ampullary adenocarcinomas were evaluated and compared to 44 distal bile duct and 18 duodenal adenocarcinomas. Genomic analyses revealed mutations in the WNT signaling pathway among half of the patients and in all three adenocarcinomas irrespective of their origin and histological morphology. These tumors were characterized by a high frequency of inactivating mutations of ELF3, a high rate of microsatellite instability, and common focal deletions and amplifications, suggesting common attributes in the molecular pathogenesis are at play in these tumors. The high frequency of WNT pathway activating mutation, coupled with small-molecule inhibitors of β-catenin in clinical trials, suggests future treatment decisions for these patients may be guided by genomic analysis.

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
22111247
Volume :
14
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.03ea58619548d2aee7acfa83a8cd5c
Document Type :
article
Full Text :
https://doi.org/10.1016/j.celrep.2015.12.005