微卫星不稳定性
肺癌
医学
PTEN公司
肿瘤科
腺癌
内科学
癌症
癌症研究
微卫星
生物
基因
遗传学
等位基因
PI3K/AKT/mTOR通路
细胞凋亡
作者
Jie Tian,Hongdan Wang,Conghua Lu,Lan Liu,Xianquan Zhang,Yunbo Xie,Rutian Li,Xin Lv,Dan Fu,Ling Zhang,Xisheng Fang,Xuming Wang,Jing Hu,Xinyi Liu,Xiao‐Chun Huang,Qian Zhao,Nuo Luo,Huan Tang,Zhaoyang Zhong,Yong He,Li Li
出处
期刊:Lung Cancer
[Elsevier]
日期:2023-05-20
卷期号:181: 107255-107255
被引量:11
标识
DOI:10.1016/j.lungcan.2023.107255
摘要
Microsatellite instability (MSI) is the first pan-cancer biomarker approved to guide immune checkpoint inhibitor therapy for MSI-high (MSI-H) solid tumors. In lung cancer, the MSI-H frequency is very low, and the genetic characteristics and prognosis of lung cancer with MSI-H were rarely reported.Next-generation sequencing and immunohistochemistry were used detect MSI status, tumor mutation burden (TMB) and PD-L1 expression.Among 12,484 lung cancer patients screened, 66 were found with MSI-H, the proportion was as low as 0.5%. Compared with Microsatellite stability (MSS), TMB was higher in MSI-H lung cancer patients, while PD-L1 expression showed no considerable difference between MSI-H and MSS. After propensity score matching, compared with MSS, the most common companion mutations in MSI-H were TP53, BRCA2, TGFBR2, PTEN and KMT2C. In MSI-H lung adenocarcinoma with EGFR mutation, TGFBR2 and ERBB2 had higher mutation frequency than in MSS.The current study reveals the genetic characteristics of MSI-H lung cancer, which advanced our understanding of MSI-H lung cancer.
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