Tornesello Maria Lina, Cerasuolo Andrea, Starita Noemy, Tornesello Anna Lucia, Bonelli Patrizia, Tuccillo Franca Maria, Buonaguro Luigi, Isaguliants Maria G, Buonaguro Franco M
Molecular Biology and Viral Oncology Unit, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Via Mariano Semmola, 80131 Napoli, Italy.
Cancer Immunoregulation Unit, Istituto Nazionale Tumori IRCCS "Fondazione G. Pascale", Via Mariano Semmola, 80131 Napoli, Italy.
Cancers (Basel). 2022 Oct 26;14(21):5257. doi: 10.3390/cancers14215257.
Human oncoviruses are able to subvert telomerase function in cancer cells through multiple strategies. The activity of the catalytic subunit of telomerase (TERT) is universally enhanced in virus-related cancers. Viral oncoproteins, such as high-risk human papillomavirus (HPV) E6, Epstein-Barr virus (EBV) LMP1, Kaposi's sarcoma-associated herpesvirus (HHV-8) LANA, hepatitis B virus (HBV) HBVx, hepatitis C virus (HCV) core protein and human T-cell leukemia virus-1 (HTLV-1) Tax protein, interact with regulatory elements in the infected cells and contribute to the transcriptional activation of TERT gene. Specifically, viral oncoproteins have been shown to bind TERT promoter, to induce post-transcriptional alterations of TERT mRNA and to cause epigenetic modifications, which have important effects on the regulation of telomeric and extra-telomeric functions of the telomerase. Other viruses, such as herpesviruses, operate by integrating their genomes within the telomeres or by inducing alternative lengthening of telomeres (ALT) in non-ALT cells. In this review, we recapitulate on recent findings on virus-telomerase/telomeres interplay and the importance of TERT-related oncogenic pathways activated by cancer-causing viruses.
人类致癌病毒能够通过多种策略破坏癌细胞中的端粒酶功能。在病毒相关癌症中,端粒酶催化亚基(TERT)的活性普遍增强。病毒癌蛋白,如高危型人乳头瘤病毒(HPV)E6、爱泼斯坦-巴尔病毒(EBV)LMP1、卡波西肉瘤相关疱疹病毒(HHV-8)LANA、乙型肝炎病毒(HBV)HBVx、丙型肝炎病毒(HCV)核心蛋白和人类T细胞白血病病毒1型(HTLV-1)Tax蛋白,与受感染细胞中的调控元件相互作用,并促进TERT基因的转录激活。具体而言,病毒癌蛋白已被证明可结合TERT启动子,诱导TERT mRNA的转录后改变,并引起表观遗传修饰,这些对端粒酶的端粒和端粒外功能的调节具有重要影响。其他病毒,如疱疹病毒,通过将其基因组整合到端粒内或在非ALT细胞中诱导端粒替代延长(ALT)来发挥作用。在本综述中,我们总结了关于病毒-端粒酶/端粒相互作用的最新发现以及致癌病毒激活的TERT相关致癌途径的重要性。