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分析中国肝细胞癌患者 DNA 损伤修复途径基因的突变。

Analysis of mutations in DNA damage repair pathway gene in Chinese patients with hepatocellular carcinoma.

机构信息

Department of General Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, 410008, China.

出版信息

Sci Rep. 2022 Jul 19;12(1):12330. doi: 10.1038/s41598-022-16604-6.

Abstract

The incidence of hepatocellular carcinoma (HCC) has increased in these years. DNA damage repair (DDR) pathway is required in response to DNA damage Gene mutations in DDR pathway play an important role in different stages of tumorigenesis and development. Based on the importance of DDR pathway in precision therapy of multiple cancers, we analyzed DDR gene mutations in Chinese patients with HCC. The results showed that (tumor mutation burden) TMB was significantly higher in HCC patients who carried somatic mutations in DDR than in non-carriers, and TMB in patients with DS, MMR mutations and DDR genes mutations such as RAD50, MLH1, MSH2, CHEK2 was significantly higher than that in wild-type patients. Based on the results of next-generation sequencing (NGS) testing, we are trying to provide clues for targeted therapy and provide feasible basis for PD-1/PD-L1 immune checkpoint inhibitor therapy.

摘要

近年来,肝细胞癌(HCC)的发病率有所增加。DNA 损伤修复(DDR)途径是应对 DNA 损伤所必需的。DDR 途径中的基因突变在肿瘤发生和发展的不同阶段发挥着重要作用。基于 DDR 途径在多种癌症精准治疗中的重要性,我们分析了中国 HCC 患者的 DDR 基因突变。结果表明,携带 DDR 体细胞突变的 HCC 患者的肿瘤突变负荷(TMB)显著高于非携带者,并且 DS、MMR 突变以及 DDR 基因 RAD50、MLH1、MSH2、CHEK2 等突变患者的 TMB 显著高于野生型患者。基于下一代测序(NGS)检测的结果,我们正试图为靶向治疗提供线索,并为 PD-1/PD-L1 免疫检查点抑制剂治疗提供可行的依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f49b/9296649/48909c618784/41598_2022_16604_Fig1_HTML.jpg

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