Barthel Floris P, Wei Wei, Tang Ming, Martinez-Ledesma Emmanuel, Hu Xin, Amin Samirkumar B, Akdemir Kadir C, Seth Sahil, Song Xingzhi, Wang Qianghu, Lichtenberg Tara, Hu Jian, Zhang Jianhua, Zheng Siyuan, Verhaak Roel G W
The Jackson Laboratory for Genomic Medicine, Farmington, Connecticut, USA.
Oncology Graduate School Amsterdam, VU University Medical Center, Amsterdam, the Netherlands.
Nat Genet. 2017 Mar;49(3):349-357. doi: 10.1038/ng.3781. Epub 2017 Jan 30.
Cancer cells survive cellular crisis through telomere maintenance mechanisms. We report telomere lengths in 18,430 samples, including tumors and non-neoplastic samples, across 31 cancer types. Telomeres were shorter in tumors than in normal tissues and longer in sarcomas and gliomas than in other cancers. Among 6,835 cancers, 73% expressed telomerase reverse transcriptase (TERT), which was associated with TERT point mutations, rearrangements, DNA amplifications and transcript fusions and predictive of telomerase activity. TERT promoter methylation provided an additional deregulatory TERT expression mechanism. Five percent of cases, characterized by undetectable TERT expression and alterations in ATRX or DAXX, demonstrated elongated telomeres and increased telomeric repeat-containing RNA (TERRA). The remaining 22% of tumors neither expressed TERT nor harbored alterations in ATRX or DAXX. In this group, telomere length positively correlated with TP53 and RB1 mutations. Our analysis integrates TERT abnormalities, telomerase activity and genomic alterations with telomere length in cancer.
癌细胞通过端粒维持机制在细胞危机中存活。我们报告了31种癌症类型中18430个样本(包括肿瘤样本和非肿瘤样本)的端粒长度。肿瘤中的端粒比正常组织中的短,肉瘤和神经胶质瘤中的端粒比其他癌症中的长。在6835例癌症中,73%表达端粒酶逆转录酶(TERT),这与TERT点突变、重排、DNA扩增和转录融合相关,并可预测端粒酶活性。TERT启动子甲基化提供了另一种TERT表达失调机制。5%的病例表现为TERT表达不可检测以及ATRX或DAXX改变,其端粒延长且含端粒重复序列的RNA(TERRA)增加。其余22%的肿瘤既不表达TERT,也没有ATRX或DAXX改变。在这一组中,端粒长度与TP53和RB1突变呈正相关。我们的分析将TERT异常、端粒酶活性和基因组改变与癌症中的端粒长度整合在一起。