Katzenellenbogen Rachel A
Center for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA, USA; Department of Pediatrics, Division of Adolescent Medicine, University of Washington, Seattle, WA, USA.
Virus Res. 2017 Mar 2;231:50-55. doi: 10.1016/j.virusres.2016.11.003. Epub 2016 Nov 15.
Telomerase extends the ends of linear chromosomes, and its expression leads to cellular immortalization. In HPV-associated cancers, telomerase is universally detected, and this occurs by activation of the catalytic subunit of telomerase, hTERT. The expression of hTERT is affected by both high-risk HPV E6 and E7. Seminal studies over the last two decades have identified the transcriptional, epigenetic, and post-transcriptional roles high-risk E6 and E7 have in telomerase regulation. This review will summarize these findings and highlight the importance of telomerase activation as an oncogenic pathway in HPV-associated cancer development and progression.
端粒酶可延长线性染色体的末端,其表达会导致细胞永生化。在与人乳头瘤病毒(HPV)相关的癌症中,普遍可检测到端粒酶,这是通过激活端粒酶的催化亚基hTERT实现的。hTERT的表达受高危型HPV E6和E7的影响。过去二十年的开创性研究已确定高危型E6和E7在端粒酶调控中的转录、表观遗传和转录后作用。本综述将总结这些发现,并强调端粒酶激活作为HPV相关癌症发生和发展过程中的致癌途径的重要性。