Usefulness of immunohistochemistry for the detection of the BRAF V600E mutation in Japanese lung adenocarcinoma

被引:43
|
作者
Sasaki, Hidefumi [1 ]
Shimizu, Shigeki [2 ]
Tani, Yoichi [3 ]
Shitara, Masayuki [1 ]
Okuda, Katsuhiro [1 ]
Hikosaka, Yu [1 ]
Moriyama, Satoru [1 ]
Yano, Motoki [1 ]
Fujii, Yoshitaka [1 ]
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Oncol Immunol & Surg, Nagoya, Aichi 4678601, Japan
[2] Natl Hosp Org, Kinki Chuo Chest Med Ctr, Dept Pathol, Sakai, Osaka, Japan
[3] Dako Japan Co, Tokyo, Japan
基金
日本学术振兴会;
关键词
BRAF; V600E expression; Lung adenocarcinoma; 599 insertion T; IHC; Linker; EnVision; METASTATIC MELANOMA; CANCER PATIENTS; FUSION GENE; OPEN-LABEL; GEFITINIB; ACTIVATION; EML4-ALK; PATHWAY; EGFR;
D O I
10.1016/j.lungcan.2013.06.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Mutations in components of the mitogen-activated protein kinase (MAPK) cascade may be a new candidate for target for lung cancer. The usefulness of immunohistochemistry (IHC) as a new approach for the detection of BRAF V600E in cancer patients has been recently reported. Methods: To increase the sensitivity, we modified BRAF V600E expression detection assay by IHC using mutation specific antibody. From the screening step, we found a novel 599 insertion T BRAF mutation in lung adenocarcinoma. In this study included 26 surgically removed cases with EGFR, Kras, erbB2,EML4-ALK and KIF5B-RET wild-type (wt) lung adenocarcinomas, including 7 BRAF mutants (5 V600E, 1 N581I, and 1 novel 599 insertion T mutation) analyzed by DNA sequencing. Detection of the BRAF V600E mutation was carried out by the Dako EnVision (TM) FLEX detection system using the VE1 clone antibody and compared with the results of direct sequencing. Results: The autostainer IHC VE1 assay was positive in 5 of 5 (100%) BRAF V600E-mutated tumors and negative in 20 of 21 (95.2%) BRAF non-V600E tumors, except for a novel 599 insertion T case. Conclusion: IHC using the VE1 clone and FLEX linker is a specific method for the detection BRAF V600E and may be an alternative to molecular biology for the detection of mutations in lung adenocarcinomas. This method might be useful for screening to use molecular target therapy for lung adenocarcinomas. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:51 / 54
页数:4
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