Spectrum of LKB1, EGFR, and KRAS Mutations in Chinese Lung Adenocarcinomas

被引:80
作者
Gao, Bin [1 ]
Sun, Yihua [2 ]
Zhang, Junhua [2 ]
Ren, Yan [1 ]
Fang, Rong [1 ]
Han, Xiangkun [1 ]
Shen, Lei [3 ]
Liu, Xin-yuan [1 ]
Pao, William [4 ]
Chen, Haiquan [2 ]
Ji, Hongbin [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab, Shanghai 200031, Peoples R China
[2] Fudan Univ, Shanghai Canc Hosp, Dept Thorac Surg, Shanghai 200032, Peoples R China
[3] Fudan Univ, Shanghai Canc Hosp, Dept Pathol, Shanghai 200032, Peoples R China
[4] Vanderbilt Ingram Canc Ctr, Nashville, TN USA
基金
中国国家自然科学基金;
关键词
Chinese lung adenocarcinoma; LKB1; EGFR; KRAS; Mutation; PEUTZ-JEGHERS-SYNDROME; GROWTH-FACTOR-RECEPTOR; SOMATIC MUTATIONS; CANCER PATIENTS; GENE-MUTATIONS; CLINICOPATHOLOGICAL FEATURES; TUMOR-SUPPRESSOR; NEVER SMOKERS; GEFITINIB; INHIBITORS;
D O I
10.1097/JTO.0b013e3181e05016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Somatic LKB1 mutations are found in lung adenocarcinomas at different frequencies in Caucasian and East Asian (Japanese and Korean) populations. This study was designed to characterize the frequency of LKB1 mutations, their relationship to EGFR and KRAS mutations, and their associated clinicopathologic characteristics in Chinese patients. Methods: Two hundred thirty-nine lung adenocarcinomas consecutively collected from October 2007 to July 2009 were dissected into 3 to 4 small (3 mm) pieces for histopathological analyses of tumor content. Genomic DNA and/or cDNA from 86 samples with more than 70% tumor content were used for sequencing of LKB1 (exons 1-9), EGFR (exons 18-21), and KRAS (exon 2). LKB1 germline mutation status was determined by sequencing of genomic DNA from matched histologically distant lung tissues that are histologically normal. Results: 6.9% of lung adenocarcinomas harbored LKB1 somatic mutations. A total of 10.5% of patients had an LKB1 germline polymorphism, F354L. Interestingly, in two of these patients, tumors displayed loss of heterozygosity at this allele. EGFR kinase domain and KRAS mutations were found in 66.3% and 2.3% of Chinese lung adenocarcinomas, respectively. Concurrent LKB1 and EGFR somatic mutations were observed in one patient. Both KRAS-mutant tumors harbored LKB1 mutations. Conclusions: These data provide important clinical and molecular characteristics of lung adenocarcinomas from Chinese patients.
引用
收藏
页码:1130 / 1135
页数:6
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