EGFR and KRAS mutations and altered c-Met gene copy numbers in primary non-small cell lung cancer and associated stage N2 lymph node-metastasis

被引:30
作者
Han, Cheng-Bo [1 ]
Ma, Jie-Tao [1 ]
Li, Fan [2 ]
Zhao, Jian-Zhu [1 ]
Jing, Wei [1 ]
Zhou, Yang [1 ]
Zou, Hua-Wei [1 ]
机构
[1] China Med Univ, Shengjing Hosp, Dept Oncol 1, Shenyang 110022, Peoples R China
[2] China Med Univ, Coll Basic Sci, Shenyang 110001, Peoples R China
基金
中国国家自然科学基金;
关键词
Non-small cell lung cancer; Epidermal growth factor receptor; KRAS; MET; Mutation; Gene copy number; TYROSINE KINASE INHIBITORS; CLINICAL-IMPLICATIONS; ACQUIRED-RESISTANCE; PRIMARY TUMORS; GEFITINIB; HETEROGENEITY; AMPLIFICATION; EXPRESSION; BIOMARKERS;
D O I
10.1016/j.canlet.2011.09.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study aimed to detect mutations in EGFR and KRAS and alterations of c-Met gene copy number (GCN) changes in primary and lymph node-metastatic NSCLCs. The data showed the concordant rate of EGFR genotype in primary and stage N2 lymph node-metastatic tumors was 95.45%. c-Met GCN in stage N2 lymph nodes was significantly higher than that of the primary tumors (P = 0.038). The results suggest both primary and lymph-node metastases have relatively consistent EGFR mutations and EGFR mutations are not relevant to changes in c-Met GCN. c-Met GCN was increased significantly in EGFR TKI-naive patients with lymph node-metastatic tumors. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:63 / 72
页数:10
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