越南肺腺癌患者的致癌驱动突变

Q3 Biochemistry, Genetics and Molecular Biology
L. Vuong, Q. Nguyen
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引用次数: 0

摘要

癌基因的突变谱在癌症治疗中起着至关重要的作用,但越南患者中肺癌致癌驱动突变的患病率数据有限。本研究旨在评估EGFR、ALK、ROS1、RET、MET的突变情况,分析基因突变与肺腺癌临床病理特征的关系。179例肺腺癌组织中,EGFR、ALK、ROS1、RET、MET的突变频率为44.6;7.9;3.0;分别为3.0%和2.0%。EGFR、ALK、ROS1和RET的改变在女性中更高。此外,ALK、ROS和RET的重排在年轻的肺腺癌中更为普遍,但外显子14 MET的跳跃在男性和老年患者中更为常见。III期和IV期似乎积累了更多的ALK、RET和MET异常。这些发现确定了具有不同临床病理特征的越南肺腺癌的频率变化,并建立了越南肺癌致癌潜水员突变的先驱数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Oncogenic driver mutations in Vietnamese patients with lung adenocarcinoma
Mutation profiles of oncogenes play essential roles in cancer therapy, but data on the prevalence of lung cancer oncogenic driver mutations in Vietnamese patients are limited. This study aims to evaluate the mutation status of EGFR, ALK, ROS1, RET and MET and analyze the association of gene mutations with clinicopathological characteristics of lung adenocarcinoma. Of the 179 lung adenocarcinoma tissues, EGFR, ALK, ROS1, RET and MET mutation frequencies were 44.6; 7.9; 3.0; 3.0 and 2.0 percent, respectively. EGFR, ALK, ROS1 and RET alterations tended to be higher in females. Moreover, rearrangements of ALK, ROS and RET were more prevalent in younger lung adenocarcinoma, but skipping at exon 14 MET was more frequent in male and older patients. Stages III and IV seem to accumulate more ALK, RET and MET abnormalities. These findings identified the variation of frequencies of Vietnamese lung adenocarcinoma with different clinicopathological characteristics and established the pioneer data for oncogenic diver mutation of lung cancer in Vietnam.
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来源期刊
Journal of Advanced Biotechnology and Experimental Therapeutics
Journal of Advanced Biotechnology and Experimental Therapeutics Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (all)
CiteScore
1.90
自引率
0.00%
发文量
41
审稿时长
8 weeks
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