Department of Interventional Therapy, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Anesthesiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cell Death Dis. 2024 Oct 10;15(10):738. doi: 10.1038/s41419-024-07129-z.
The occurrence of multiple primary lung cancer (MPLC) has witnessed a significant surge in recent years within the Chinese population. MPLC is distinguished by its potential genetic susceptibility and notable genetic heterogeneity. Investigating the etiology of MPLC holds substantial clinical importance.The whole genome sequencing (WGS) and genome-wide linkage analysis were performed in a family affected by a dominant form of lung abnormalities. Specifically, five family members were diagnosed with MPLC, while nine members had pulmonary nodules and one normal member. To confirm the potential pathogenic germline mutations sites, Sanger sequencing was performed in an additional 162 MPLC family patients. Furthermore, molecular biology experiments were conducted to investigate the function and the mechanism of the identified pathogenic mutation site in lung cancer A549 and H322, both in vitro and in vivo. Linkage analysis revealed the presence of shared genomic regions among affected family members. Subsequent exome sequencing identified a deleterious variant within these linkage intervals, specifically a heterozygous mutation in ETS-oncogene transcription factors 4 (ETV4). This particular variant was found in affected family members at a rate of 13 out of 15 individuals. Furthermore, ETV4 P433L mutation could be detected in an additional MPLC family patients and mutation frequency was 3.7% (6 out of 162). The ETV4 P433L mutations site was introduced into lung cancer cell lines, resulting in altered migration and stem-like properties of the cancer cells. Further investigation revealed that the activation of the Wnt/β-catenin signaling pathway, which is associated with stemness, could be attributed to the presence of the ETV4 P433L mutation, suggesting its involvement in tumor promotion. A novel pathogenic germline mutation, ETV4 P433L, was identified in a dominant MPLC family, with a mutation rate of 3.7% among MPLC family patients. The ETV4 P433L mutation was found to impact the stem-like properties and migration of tumors through Wnt/β-catenin signaling pathway.
近年来,中国人群中多原发性肺癌(MPLC)的发生率显著上升。MPLC 的特点是潜在的遗传易感性和显著的遗传异质性。研究 MPLC 的病因具有重要的临床意义。对一个受显性肺异常影响的家族进行了全基因组测序(WGS)和全基因组连锁分析。具体来说,有 5 名家族成员被诊断为 MPLC,9 名家族成员有肺结节,1 名家族成员正常。为了确认潜在的致病性种系突变位点,对 162 名 MPLC 家族患者进行了 Sanger 测序。此外,还进行了分子生物学实验,以研究鉴定的肺癌 A549 和 H322 中致病性突变位点的功能和机制,包括在体外和体内。连锁分析显示受影响的家族成员之间存在共享的基因组区域。随后的外显子组测序在这些连锁区间内发现了一个有害的变异,即 ETS-oncogene 转录因子 4(ETV4)的杂合突变。在 15 名受影响的家族成员中有 13 人发现了这种特定的变异。此外,还在另一个 MPLC 家族患者中检测到 ETV4 P433L 突变,突变频率为 3.7%(162 人中 6 人)。将 ETV4 P433L 突变引入肺癌细胞系,导致癌细胞的迁移和干细胞样特性发生改变。进一步研究表明,与干细胞特性相关的 Wnt/β-catenin 信号通路的激活可能归因于 ETV4 P433L 突变的存在,表明其参与了肿瘤的促进。在一个显性 MPLC 家族中发现了一种新的致病性种系突变 ETV4 P433L,在 MPLC 家族患者中的突变率为 3.7%。ETV4 P433L 突变通过 Wnt/β-catenin 信号通路影响肿瘤的干细胞样特性和迁移。