Recurrent TERT promoter mutations identified in a large-scale study of multiple tumour types are associated with increased TERT expression and telomerase activation

被引:171
作者
Huang, Dong-Sheng [1 ,2 ]
Wang, Zhaohui [3 ,4 ]
He, Xu-Jun [2 ]
Diplas, Bill H. [3 ,4 ]
Yang, Rui [3 ,4 ]
Killela, Patrick J. [3 ,4 ]
Meng, Qun [5 ]
Ye, Zai-Yuan [1 ,2 ]
Wang, Wei [5 ]
Jiang, Xiao-Ting [2 ]
Xu, Li [5 ]
He, Xiang-Lei [5 ]
Zhao, Zhong-Sheng [5 ]
Xu, Wen-Juan [5 ]
Wang, Hui-Ju [2 ]
Ma, Ying-Yu [2 ]
Xia, Ying-Jie [2 ]
Li, Li [2 ]
Zhang, Ru-Xuan [2 ]
Jin, Tao [6 ]
Zhao, Zhong-Kuo [1 ]
Xu, Ji [1 ]
Yu, Sheng [2 ]
Wu, Fang [2 ]
Liang, Junbo [7 ]
Wang, Sizhen [8 ]
Jiao, Yuchen [9 ,10 ,11 ,12 ]
Yan, Hai [3 ,4 ]
Tao, Hou-Quan [1 ,2 ]
机构
[1] Zhejiang Prov Peoples Hosp, Dept Surg, Hangzhou, Zhejiang, Peoples R China
[2] Key Lab Gastroenterol Zhejiang Prov, Hangzhou 310014, Zhejiang, Peoples R China
[3] Duke Univ, Med Ctr, Pediat Brain Tumor Fdn Inst Duke, Preston Robert Tisch Brain Tumor Ctr Duke, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[5] Zhejiang Prov Peoples Hosp, Dept Pathol, Hangzhou, Zhejiang, Peoples R China
[6] Zhejiang Prov Peoples Hosp, Dept Cardiothorac Surg, Hangzhou, Zhejiang, Peoples R China
[7] Chinese Acad Med Sci, Inst Basic Med Sci, State Key Lab Med Mol Biol, Beijing 100142, Peoples R China
[8] Genetron Hlth Beijing Technol Co Ltd, Econ & Technol Dev Area, Beijing, Peoples R China
[9] Chinese Acad Med Sci, Inst Canc, Lab Cell & Mol Biol, Beijing 100142, Peoples R China
[10] Chinese Acad Med Sci, Inst Canc, State Key Lab Mol Oncol, Beijing 100142, Peoples R China
[11] Chinese Acad Med Sci, Canc Hosp, Beijing 100142, Peoples R China
[12] Peking Union Med Coll, Beijing 100021, Peoples R China
基金
中国国家自然科学基金;
关键词
Telomerase; Promoter regions; Genetics; China; Neoplasms; Glioma; HEPATOCELLULAR-CARCINOMA; DISEASE RECURRENCE; CANCER; OCCUR; LANDSCAPE; FREQUENCY; DIAGNOSIS; MELANOMA; GLIOMAS; RISK;
D O I
10.1016/j.ejca.2015.03.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Several somatic mutation hotspots were recently identified in the telomerase reverse transcriptase (TERT) promoter region in human cancers. Large scale studies of these mutations in multiple tumour types are limited, in particular in Asian populations. This study aimed to: analyse TERT promoter mutations in multiple tumour types in a large Chinese patient cohort, investigate novel tumour types and assess the functional significance of the mutations. Methods: TERT promoter mutation status was assessed by Sanger sequencing for 13 different tumour types and 799 tumour tissues from Chinese cancer patients. Thymic epithelial tumours, gastrointestinal leiomyoma, and gastric schwannoma were included, for which the TERT promoter has not been previously sequenced. Functional studies included TERT expression by reverse-transcriptase quantitative polymerase chain reaction (RT-qPCR), telomerase activity by the telomeric repeat amplification protocol (TRAP) assay and promoter activity by the luciferase reporter assay. Results: TERT promoter mutations were highly frequent in glioblastoma (83.9%), urothelial carcinoma (64.5%), oligodendroglioma (70.0%), medulloblastoma (33.3%) and hepatocellular carcinoma (31.4%). C228T and C250T were the most common mutations. In urothelial carcinoma, several novel rare mutations were identified. TERT promoter mutations were absent in gastrointestinal stromal tumour (GIST), thymic epithelial tumours, gastrointestinal leiomyoma, gastric schwannoma, cholangiocarcinoma, gastric and pancreatic cancer. TERT promoter mutations highly correlated with upregulated TERT mRNA expression and telomerase activity in adult gliomas. These mutations differentially enhanced the transcriptional activity of the TERT core promoter. Conclusions: TERT promoter mutations are frequent in multiple tumour types and have similar distributions in Chinese cancer patients. The functional significance of these mutations reflect the importance to telomere maintenance and hence tumourigenesis, making them potential therapeutic targets. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:969 / 976
页数:8
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