Regulation of the human catalytic subunit of telomerase (hTERT)

被引:214
作者
Daniel, Michael [1 ]
Peek, Gregory W. [1 ]
Tollefsbol, Trygve O. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Univ Alabama Birmingham, Dept Biol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Ctr Aging, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Ctr Comprehens Canc, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Nutr Obes Res Ctr, Birmingham, AL 35294 USA
[5] Univ Alabama Birmingham, Comprehens Diabet Ctr, Birmingham, AL 35294 USA
关键词
Telomerase; Cancer; Gene regulation; Telomeres; REVERSE-TRANSCRIPTASE HTERT; PROSTATE-CANCER CELLS; HUMAN BREAST-CANCER; NF-KAPPA-B; ESTROGEN-RECEPTOR-ALPHA; TUMOR-SUPPRESSOR GENES; HUMAN LUNG-CANCER; C-MYC EXPRESSION; TGF-BETA; DOWN-REGULATION;
D O I
10.1016/j.gene.2012.01.095
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Over the past decade, there has been much interest in the regulation of telomerase, the enzyme responsible for maintaining the integrity of chromosomal ends, and its crucial role in cellular immortalization, tumorigenesis, and the progression of cancer. Telomerase activity is characterized by the expression of the telomerase reverse transcriptase (TERT) gene, suggesting that TERT serves as the major limiting agent for telomerase activity. Recent discoveries have led to characterization of various interactants that aid in the regulation of human TERT (hTERT), including numerous transcription factors; further supporting the pivotal role that transcription plays in both the expression and repression of telomerase. Several studies have suggested that epigenetic modulation of the hTERT core promoter region may provide an additional level of regulation. Although these studies have provided essential information on the regulation of hTERT, there has been ambiguity of the role of methylation within the core promoter region and the subsequent binding of various activating and repressive agents. As a result, we found it necessary to consolidate and summarize these recent developments and elucidate these discrepancies. In this review, we focus on the co-regulation of hTERT via transcriptional regulation, the presence or absence of various activators and repressors, as well as the epigenetic pathways of DNA methylation and histone modifications. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 146
页数:12
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