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非小细胞肺癌患者EML4-ALK融合基因突变研究

王旭洲 陈炜生 余英豪

中国肺癌杂志Issue(2):80-84,5.
中国肺癌杂志Issue(2):80-84,5.DOI:10.3779/j.issn.1009-3419.2015.02.05

非小细胞肺癌患者EML4-ALK融合基因突变研究

Analysis of EML4-ALK Gene Fusion Mutation in Patients with Non-small Cell Lung Cancer

王旭洲 1陈炜生 2余英豪1

作者信息

  • 1. 350025 福州,南京军区福州总医院病理科
  • 2. 心胸外科
  • 折叠

摘要

Abstract

Background and objective Non-small cell lung cancer (NSCLC) is the main type of lung cancer, and the related locus mutation detection research has become a hot direction of molecular targeted therapy, studying on gene mu-tation status of echinodem microtubule associated protein like 4-Anaplastic lymphoma kinase (EML4-ALK) and epidermal growth factor receptor (EGFR), detecting the sensitivity of EML4-ALK gene fusion and gene mutation of EGFR. Methods EML4-ALK gene fusion in 85 cases of paraffn embedded tumor tissue and adjacent lung tissue was detected with the applica-tion of immunohistochemistry (IHC), Scorpions ampliifcation refractory mutation system (Scorpions ARMS) lfuorescence quantitative PCR and lfuorescence in situ hybridization (FISH) technology, and EGFR gene in 18, 19, 20 and 21 exon mutation status was detected with the application of ARMS method. Results In 115 cases of NSCLC, IHC showed 32 cases with ALK (D5F3) expression, the expression rate was 27.8%;ARMS showed 27 cases with EML4-ALK fusion gene mutation, the muta-tion detection rate was 23.5%;53 cases were detected with EGFR mutation, the mutation rate was 46%. While FISH showed 23 cases with EML4-ALK fusion gene mutation, the detection rate was 20%, slightly lower than the ARMS detection results, suggesting that ARMS more sensitive. Conclusion hTe application of IHC, ARMS lfuorescence quantitative PCR and FISH technology can make a rapid and accurate evaluation of EML4-ALK gene fusion.

关键词

肺肿瘤/EML4-ALK融合基因/免疫组织化学/ARMS/荧光原位杂交

Key words

Lung neoplasms/EML4-ALK fusion gene/Immunohistochemistry/ARMS/Fluorescence in situ hybrid-ization

引用本文复制引用

王旭洲,陈炜生,余英豪..非小细胞肺癌患者EML4-ALK融合基因突变研究[J].中国肺癌杂志,2015,(2):80-84,5.

基金项目

本研究受南京军区福州总医院肺癌创新团队基金项目(No.2014CXTD06)资助 ()

中国肺癌杂志

OA北大核心CSCDCSTPCDMEDLINE

1009-3419

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