Department of Human Genetics, Radboud University Medical Center, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
i3S, Institute for Research and Innovation in Health of the University of Porto, Porto, Portugal.
Eur J Hum Genet. 2021 Sep;29(9):1354-1358. doi: 10.1038/s41431-021-00853-6. Epub 2021 Jun 1.
Hereditary diffuse gastric cancer (HDGC) is associated with germline deleterious variants in CDH1 and CTNNA1. The majority of HDGC-suspected patients are still genetically unresolved, raising the need for identification of novel HDGC predisposing genes. Under the collaborative environment of the SOLVE-RD consortium, re-analysis of whole-exome sequencing data from unresolved gastric cancer cases (n = 83) identified a mosaic missense variant in PIK3CA in a 25-year-old female with diffuse gastric cancer (DGC) without familial history for cancer. The variant, c.3140A>G p.(His1047Arg), a known cancer-related somatic hotspot, was present at a low variant allele frequency (18%) in leukocyte-derived DNA. Somatic variants in PIK3CA are usually associated with overgrowth, a phenotype that was not observed in this patient. This report highlights mosaicism as a potential, and understudied, mechanism in the etiology of DGC.
遗传性弥漫性胃癌 (HDGC) 与 CDH1 和 CTNNA1 种系有害变异相关。大多数 HDGC 疑似患者的遗传仍未得到解决,这就需要鉴定新的 HDGC 易感性基因。在 SOLVE-RD 联盟的协作环境下,对未解决的胃癌病例(n=83)的全外显子组测序数据进行重新分析,在一名 25 岁女性弥漫性胃癌(DGC)患者中发现了 PIK3CA 中的镶嵌错义变异,该患者无癌症家族史。该变异,c.3140A>G p.(His1047Arg),是一个已知的癌症相关体细胞热点,在白细胞衍生 DNA 中的变异等位基因频率(18%)较低。PIK3CA 的体细胞变异通常与过度生长有关,但该患者未观察到这种表型。本报告强调了镶嵌现象是 DGC 病因学中的一个潜在但研究不足的机制。