Gingras Marie-Claude, Covington Kyle R, Chang David K, Donehower Lawrence A, Gill Anthony J, Ittmann Michael M, Creighton Chad J, Johns Amber L, Shinbrot Eve, Dewal Ninad, Fisher William E, Pilarsky Christian, Grützmann Robert, Overman Michael J, Jamieson Nigel B, Van Buren George, Drummond Jennifer, Walker Kimberly, Hampton Oliver A, Xi Liu, Muzny Donna M, Doddapaneni Harsha, Lee Sandra L, Bellair Michelle, Hu Jianhong, Han Yi, Dinh Huyen H, Dahdouli Mike, Samra Jaswinder S, Bailey Peter, Waddell Nicola, Pearson John V, Harliwong Ivon, Wang Huamin, Aust Daniela, Oien Karin A, Hruban Ralph H, Hodges Sally E, McElhany Amy, Saengboonmee Charupong, Duthie Fraser R, Grimmond Sean M, Biankin Andrew V, Wheeler David A, Gibbs Richard A
Department of Molecular and Human Genetics, Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA; Michael DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX 77030, USA; Dan L. Duncan Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Department of Molecular and Human Genetics, Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX 77030, USA.
Cell Rep. 2016 Feb 2;14(4):907-919. doi: 10.1016/j.celrep.2015.12.005. Epub 2016 Jan 21.
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.
壶腹是一个复杂的细胞环境,腺癌由此产生,形成一组组织病理学上异质性的肿瘤。为了评估这些肿瘤的分子特征,对98例壶腹腺癌进行了评估,并与44例远端胆管腺癌和18例十二指肠腺癌进行了比较。基因组分析显示,一半的患者以及所有这三种腺癌(无论其起源和组织形态如何)中,WNT信号通路均存在突变。这些肿瘤的特征是ELF3失活突变频率高、微卫星不稳定性发生率高以及常见的局灶性缺失和扩增,这表明这些肿瘤在分子发病机制中存在共同的属性。WNT通路激活突变的高频率,再加上临床试验中β-连环蛋白的小分子抑制剂,表明这些患者未来的治疗决策可能由基因组分析来指导。