Genome Center, School of Medicine, University of California at Davis, Davis, CA, USA.
Genome Center, School of Medicine, University of California at Davis, Davis, CA, USA; Population Sciences and Cancer Health Disparities Program, UC Davis Comprehensive Cancer Center, School of Medicine, University of California at Davis, Davis, CA, USA; Department of Biochemistry and Molecular Medicine, School of Medicine, University of California at Davis, Davis, CA, USA.
Lancet Gastroenterol Hepatol. 2018 Dec;3(12):874-883. doi: 10.1016/S2468-1253(18)30237-1.
Every year gastric cancer accounts for nearly 1 million new cases and more than 720 000 deaths worldwide. Prognosis is dismal because most patients are diagnosed with advanced disease; as such, gastric cancer outcomes will benefit from better methods for identification of at-risk individuals that can be targeted for early detection. One approach to targeting high-risk populations is to identify individuals who are genetically predisposed to gastric cancer, as up to 15% of all patients report family history of the disease. On the basis of clinical manifestations, three gastric cancer syndromes have been described, but the diagnosis of some of these syndromes is suboptimal and could benefit from genetic information. Over the past decade, genome-wide association and next-generation sequencing studies have identified several low penetrance variants and high-risk genes, considerably increasing our understanding of inherited gastric cancer predisposition. From these studies, PALB2 has emerged as a new familial gastric cancer gene. Furthermore, genetic analyses in patients with sporadic gastric cancer suggest that more than 10% of all cases have pathogenic mutations, a finding of great importance for cancer aetiology. In this Review, we summarise the role of genetics in gastric cancer aetiology and the implications of genetics findings for the prevention of this malignancy.
每年,胃癌在全球范围内导致近 100 万例新发病例和超过 72 万例死亡。由于大多数患者被诊断为晚期疾病,因此预后较差;如果能够找到更好的方法来识别高危人群,并针对这些人群进行早期检测,那么胃癌的结局将会得到改善。针对高危人群的一种方法是识别那些遗传易患胃癌的个体,因为高达 15%的患者报告有家族病史。基于临床表现,已经描述了三种胃癌综合征,但其中一些综合征的诊断并不理想,可以从遗传信息中受益。在过去的十年中,全基因组关联和下一代测序研究已经确定了几个低外显率变异体和高风险基因,这极大地增加了我们对遗传性胃癌易感性的理解。从这些研究中,PALB2 已成为一种新的家族性胃癌基因。此外,对散发性胃癌患者的遗传分析表明,超过 10%的病例存在致病性突变,这一发现对癌症病因学具有重要意义。在这篇综述中,我们总结了遗传学在胃癌发病机制中的作用,以及遗传学研究结果对预防这种恶性肿瘤的意义。