Cancer Bio-Immunotherapy Unit, CRO Aviano, National Cancer Institute, Aviano, PN, Italy.
Infect Agent Cancer. 2014 Feb 26;9(1):8. doi: 10.1186/1750-9378-9-8.
Overcoming cellular senescence is strictly required for virus-driven tumors, including those associated with Epstein-Barr virus (EBV). This critical step is successfully accomplished by EBV through TERT expression and telomerase activation in infected cells. We herein review the complex interplay between EBV and TERT/telomerase in EBV-driven tumorigenesis. Evidence accumulated so far clearly indicates that elucidation of this issue may offer promising opportunities for the design of innovative treatment modalities for EBV-associated malignancies. Indeed, several therapeutic strategies for telomerase inhibition have been developed and are being investigated in clinical trials. In this respect, our recent finding that TERT inhibition sensitizes EBV+ lymphoma cells to antivirals through activation of EBV lytic replication is particularly promising and provides a rationale for the activation of clinical studies aimed at assessing the effects of combination therapies with TERT inhibitors and antivirals for the treatment of EBV-associated malignancies.
克服细胞衰老对于病毒驱动的肿瘤是严格必需的,包括与 Epstein-Barr 病毒(EBV)相关的肿瘤。EBV 通过在感染细胞中表达 TERT 和激活端粒酶来成功完成这一关键步骤。本文综述了 EBV 在 EBV 驱动的肿瘤发生中与 TERT/端粒酶的复杂相互作用。迄今为止积累的证据清楚地表明,阐明这一问题可能为设计针对 EBV 相关恶性肿瘤的创新治疗方法提供有希望的机会。事实上,已经开发了几种针对端粒酶抑制的治疗策略,并正在临床试验中进行研究。在这方面,我们最近发现 TERT 抑制通过激活 EBV 裂解复制使 EBV+淋巴瘤细胞对抗病毒药物敏感,这特别有希望,并为旨在评估 TERT 抑制剂和抗病毒药物联合治疗用于治疗 EBV 相关恶性肿瘤的组合疗法效果的临床研究提供了依据。