Germline EGFR mutations in lung cancer (Review)

被引:7
|
作者
Liu, Minghui [1 ]
Niu, Xiaoyu [1 ]
Liu, Hongyu [2 ]
Chen, Jun [1 ,2 ]
机构
[1] Tianjin Med Univ Gen Hosp, Dept Lung Canc Surg, Tianjin 300052, Peoples R China
[2] Tianjin Med Univ Gen Hosp, Tianjin Lung Canc Inst, Tianjin Key Lab Lung Canc Metastasis & Tumor Micro, 154 Anshan Rd, Tianjin 300052, Peoples R China
关键词
lung cancer; germline mutation; epidermal growth factor receptor; familial lung cancer; FACTOR RECEPTOR MUTATIONS; FRAGILE-X-SYNDROME; NEVER-SMOKERS; INTERGENERATIONAL INSTABILITY; T790M MUTATIONS; CTG REPEAT; V843I; LINE; SPERM; GENE;
D O I
10.3892/ol.2023.13868
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer is the leading cause of cancer-related death and familial lung cancer is a potential contributing factor. Epidermal growth factor receptor (EGFR) mutations are important events in carcinogenesis. The present study summarized the common germline mutations of EGFR, including T790M, V843I, R776H and P848L, and provided detailed information regarding each mutation site and potential treatment strategies. Individuals with germline mutations may develop lung cancer upon exposure to environmental stimuli such as smoking, air pollution or radiological contamination, or due to the occurrence of another somatic mutation. The present study recommends regular physical examinations as well as population-wide germline mutation screening for early detection and diagnosis of lung cancer.
引用
收藏
页数:11
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