恶性黑色素瘤患者肿瘤组织中BRAF基因突变的分子病理检测
作者: |
1田玉旺,
2许春伟,
1张立英,
3方美玉,
4沈斌
1 陆军总医院病理科,北京 100700 2 福建省肿瘤医院病理科,福州 350014 3 浙江省肿瘤医院综合肿瘤内科,杭州 310022 4 浙江省湖州市中心医院介入放疗科,浙江 湖州 313000 |
通讯: |
许春伟
Email: xuchunweibbb@163.com 方美玉 Email: fangjade2004@icloud.com |
DOI: | 10.3978/j.issn.2095-6959.2017.03.024 |
基金: | 浙江省卫生科研计划基金, 2013KYB051 浙江省中医药局科研基金, 2013ZQ005 |
摘要
目的:探讨恶性黑色素瘤患者肿瘤组织中BRAF基因突变情况。方法:应用Taqman-ARMS方法检测164例恶性黑色素瘤患者肿瘤组织中BRAF基因突变情况。结果:恶性黑色素瘤患者肿瘤组织中BRAF基因总突变率为11.59%(19/164),均为V600E突变,BRAF基因突变在黑色素瘤亚型和临床分期Ⅰ或Ⅱ中差异有统计学意义(P<0.05)。结论:恶性黑色素瘤患者中BRAF基因存在一定的突变率,且慢性日光损伤型或非慢性日光损伤型及Ⅲ或Ⅳ期恶性黑素瘤BRAF基因突变多见。
关键词:
Taqman-ARMS方法
恶性黑色素瘤
BRAF基因
Molecular pathology detection of BRAF gene mutation in malignant melanoma
CorrespondingAuthor: XU Chunwei Email: xuchunweibbb@163.com
DOI: 10.3978/j.issn.2095-6959.2017.03.024
Abstract
Objective: To investigate the mutations of BRAF gene in malignant melanoma. Methods: Taqman-ARMS was used to detect the tissues in 164 patients of malignant melanoma with paraffin tissue BRAF gene mutation. Results: The total BRAF gene mutation rate was 11.59% (19/164) in malignant melanoma, and they were all V600E mutation. BRAF gene mutation in melanoma subtype and clinical stage were statistically significant (P<0.05). Conclusion: BRAF gene mutation has a certain mutation rate in malignant melanoma patients, especially in chronic sun damage type or non-chronic sun damage type and III or IV stage.