|本期目录/Table of Contents|

[1]王 璇,时姗姗,马恒辉,等.非小细胞肺癌表皮生长因子受体基因突变的结果分析[J].医学研究与战创伤救治(原医学研究生学报),2012,14(05):387-389.
 WANG Xuan,SHI Shan-shan,MA Heng-hui,et al.Respective analysis of EGFR mutations in non-small cell lung cancer[J].JOURNAL OF MEDICALRESEARCH —COMBAT TRAUMA CARE,2012,14(05):387-389.
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非小细胞肺癌表皮生长因子受体基因突变的结果分析()

《医学研究与战创伤救治》(原医学研究生学报)[ISSN:1672-271X/CN:32-1713/R]

卷:
第14卷
期数:
2012年05期
页码:
387-389
栏目:
出版日期:
2012-09-20

文章信息/Info

Title:
Respective analysis of EGFR mutations in non-small cell lung cancer
文章编号:
1672-271X(2012)05-0387-03
作者:
王 璇时姗姗马恒辉周晓军王建东
210002 江苏南京,南京军区南京总医院病理科
Author(s):
WANG XuanSHI Shan-shanMA Heng-huiZHOU Xiao-junWANG Jian-dong
Department of Pathology,Nanjing General Hospital of Nanjing Military Command,PLA,Nanjing,Jiangsu 210002,China
关键词:
肺癌表皮生长因子受体突变
Keywords:
lung cancer EGFR mutation
分类号:
R574
DOI:
-
文献标志码:
A
摘要:
目的 回顾性分析301例非小细胞肺癌(NSCLC)组织表皮生长因子受体(EGFR)基因突变检测结果,比较三种实验方法检查EGFR突变的差异。探讨肺癌临床靶向个体化治疗进行EGFR分子病理检查的最佳方法。方法 应用聚合酶链反应(PCR)结合直接测序法检测171例肺癌DNA样本;TaqMan探针荧光定量PCR法检测88例肺癌DNA样本;扩增阻碍突变系统(ARMS)法检测42例肺癌DNA样本。结果 PCR直接测序法、TaqMan探针荧光定量PCR法、ARMS法的阳性总检出率分别是31.58%、27.27%、42.86%。结论 PCR直接测序法和TaqMan探针荧光定量PCR法阳性总检出率差异无统计学意义(P>0.05),ARMS法阳性总检出率高于PCR直接测序法和TaqMan探针荧光定量PCR法(P均<0.01)。对于不同来源的肺癌组织标本,不同方法检测EGFR突变具有各自的优点和不足。
Abstract:
Objective The results of epidermal growth factor receptor (EGFR) mutations in 301 tissues with non-small cell lung cancer (NSCLC) detected by three different methods were respectively analyzed.The differences among three methods were compared.The objective of this study was to explore the proper molecular method for personalized target therapy in lung cancer.Methods Polymerase chain reaction combine with direction sequencing was used to detect EGFR mutations in 171 patients.Real-time PCR with TaqMan fluorecent probe was used to detect EGFR mutations in 88 patients and amplification refractory mutation system PCR (ARMS-PCR) was used to detect EGFR mutations in 42 patients.Results The total positive rates for sequencing,TaqMan real-time PCR,and ARMS-PCR methods were 31.58%,27.27%,and 42.86% respectively.Conclusion No significant difference in total positive rate between direct sequencing and TaqMan real-time PCR (P>0.05).The total positive rate was higher in ARMS-PCR than that in direct sequencing and TaqMan real-time PCR (P<0.01).To different tissues,different methods have their superiority when used for detection of EGFR mutations in lung cancer.

参考文献/References:

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备注/Memo

备注/Memo:
国家自然科学基金(30970813;81171391)
更新日期/Last Update: 2012-09-20