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具有胚系突变的中国肺癌患者的临床和基因组特征

Clinical and genomic features of Chinese lung cancer patients with germline mutations.

作者信息

Peng Wenying, Li Bin, Li Jin, Chang Lianpeng, Bai Jing, Yi Yuting, Chen Rongrong, Zhang Yanyan, Chen Chen, Pu Xingxiang, Jiang Meilin, Li Jia, Zhong Rui, Xu Fang, Chen Bolin, Xu Li, Wang Ning, Huan Jiaojiao, Dai Pingping, Guan Yanfang, Yang Ling, Xia Xuefeng, Yi Xin, Wang Jiayin, Yu Fenglei, Wu Lin

机构信息

The Second Department of Thoracic Oncology, Hunan Cancer Hospital/the Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, 410000, Changsha, China.

The second department of Oncology, Yunnan Cancer Hospital & The Third Affiliated Hospital of Kunming Medical University & Yunnan Cancer Center, 650000, Kunming, China.

出版信息

Nat Commun. 2022 Mar 10;13(1):1268. doi: 10.1038/s41467-022-28840-5.

Abstract

The germline mutation landscape in Chinese lung cancer patients has not been well defined. In this study, sequencing data of 1,021 cancer genes of 1,794 Chinese lung cancer patients was analyzed. A total of 111 pathogenic or likely pathogenic germline mutations were identified, significantly higher than non-cancer individuals (111/1794 vs. 84/10,588, p < 2.2e-16). BRCA1/2 germline mutations are associated with earlier onset age (median 52.5 vs 60 years-old, p = 0.008). Among 29 cancer disposition genes with germline mutations detected in Chinese cohort and/or TCGA lung cancer cohort, Only 11 from 29 genes are identified in both cohorts and BRCA2 mutations are significantly more common in Chinese cohort (p = 0.015). Chinese patients with germline mutations have different prevalence of somatic KRAS, MET exon 14 skipping and TP53 mutations compared to those without. Our findings suggest potential ethnic and etiologic differences between Western and Asian lung cancer patients.

摘要

中国肺癌患者的种系突变图谱尚未明确界定。在本研究中,分析了1794例中国肺癌患者的1021个癌症基因的测序数据。共鉴定出111个致病性或可能致病性种系突变,显著高于非癌症个体(111/1794对84/10588,p < 2.2e-16)。BRCA1/2种系突变与发病年龄较早相关(中位年龄52.5岁对60岁,p = 0.008)。在中国队列和/或TCGA肺癌队列中检测到种系突变的29个癌症易感性基因中,两个队列中仅鉴定出29个基因中的11个,且BRCA2突变在中国队列中更为常见(p = 0.015)。与无种系突变的患者相比,有种系突变的中国患者体细胞KRAS、MET外显子14跳跃和TP53突变发生率不同。我们的研究结果表明,西方和亚洲肺癌患者之间存在潜在的种族和病因差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c5b6/8913621/ffe16dfe4423/41467_2022_28840_Fig1_HTML.jpg

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