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巴雷特干细胞的突变谱揭示了癌前病变起始的途径。

Mutational spectrum of Barrett's stem cells suggests paths to initiation of a precancerous lesion.

作者信息

Yamamoto Yusuke, Wang Xia, Bertrand Denis, Kern Florian, Zhang Ting, Duleba Marcin, Srivastava Supriya, Khor Chiea Chuen, Hu Yuanyu, Wilson Lane H, Blaszyk Hagen, Rolshud Daniil, Teh Ming, Liu Jianjun, Howitt Brooke E, Vincent Matthew, Crum Christopher P, Nagarajan Niranjan, Ho Khek Yu, McKeon Frank, Xian Wa

机构信息

Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo 104-0045, Japan.

Department of Biology and Biochemistry, University of Houston, Houston, Texas 77204, USA.

出版信息

Nat Commun. 2016 Jan 19;7:10380. doi: 10.1038/ncomms10380.

Abstract

The precancerous lesion known as Barrett's oesophagus can evolve to oesophageal adenocarcinoma in decades-long processes of regenerative growth. Here we report the isolation and propagation of distinct, patient-matched stem cells of Barrett's, gastric and oesophageal epithelia that yield divergent tumour types following in vitro transformation and xenografting. Genomic analyses reveal a broad mutational spectrum unique to Barrett's stem cells that likely reflects their risk for oncogenesis. Remarkably, 25% of cases show no cancer-related genomic changes, suggesting that Barrett's initiates without driver mutations. Most cases, however, sustain patterns of deletions almost identical to adenocarcinoma though tumour-associated gene amplifications were absent. Notably, those suspected of low-grade dysplasia have p53 mutations or undergo amplifications of proto-oncogenes and receptor tyrosine kinases, implicating these events in lethal transitions. Our findings suggest paths for the initiation and progression of Barrett's and define a discrete stem cell underlying its regenerative growth whose eradication could prevent oesophageal adenocarcinoma.

摘要

被称为巴雷特食管的癌前病变可在数十年的再生生长过程中演变为食管腺癌。在此,我们报告了巴雷特食管、胃和食管上皮中分离出的与患者匹配的不同干细胞的分离和增殖,这些干细胞在体外转化和异种移植后会产生不同类型的肿瘤。基因组分析揭示了巴雷特干细胞特有的广泛突变谱,这可能反映了它们的肿瘤发生风险。值得注意的是,25%的病例未显示与癌症相关的基因组变化,这表明巴雷特食管的起始无驱动突变。然而,大多数病例虽然没有肿瘤相关基因扩增,但维持着与腺癌几乎相同的缺失模式。值得注意的是,那些疑似低度发育异常的病例存在p53突变或原癌基因和受体酪氨酸激酶的扩增,表明这些事件与致死性转变有关。我们的研究结果提示了巴雷特食管起始和进展的途径,并确定了其再生生长背后的离散干细胞,根除这些干细胞可能预防食管腺癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/094f/4735693/9c54c13f39eb/ncomms10380-f1.jpg

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