端粒酶
端粒酶逆转录酶
癌变
癌症研究
尿路上皮
端粒
膀胱癌
癌症
恶性转化
医学
生物
基因
遗传学
膀胱
内科学
作者
Çagatay Güneş,Felix Wezel,Jennifer Southgate,Christian Bolenz
标识
DOI:10.1038/s41585-018-0001-5
摘要
Telomerase activity imparts eukaryotic cells with unlimited proliferation capacity, one of the cancer hallmarks. Over 90% of human urothelial carcinoma of the bladder (UCB) tumours are positive for telomerase activity. Telomerase activation can occur through several mechanisms. Mutations in the core promoter region of the human telomerase reverse transcriptase gene (TERT) cause telomerase reactivation in 60–80% of UCBs, whereas the prevalence of these mutations is lower in urothelial cancers of other origins. TERT promoter mutations are the most frequent genetic alteration across all stages of UCB, indicating a strong selection pressure during neoplastic transformation. TERT promoter mutations could arise during regeneration of normal urothelium and, owing to consequential telomerase reactivation, might be the basis of UCB initiation, which represents a new model of urothelial cancer origination. In the future, TERT promoter mutations and telomerase activity might have diagnostic and therapeutic applications in UCB. In this Perspectives, the authors present a new model of urothelial carcinogenesis that incorporates the role of telomerase activation. They also highlight the potential of targeting telomerase as a therapeutic approach for bladder cancer.
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