Department of Experimental Medicine, "Sapienza" University of Rome, Viale Regina Elena 324, 00161, Rome, Italy.
Sci Rep. 2017 Oct 12;7(1):13052. doi: 10.1038/s41598-017-13533-7.
KSHV and EBV are gammaherpesviruses strictly linked to human cancers. Even if the majority of cancer cells harbor a latent infection, the few cells that undergo viral replication may contribute to the pathogenesis and maintenance of the virus-associated malignancies. Cytotoxic drugs used for the therapies of cancers harboring virus-infection often have, as side effect, the activation of viral lytic cycle. Therefore it is important to investigate whether they affect viral reactivation and understand the underlying mechanisms involved. In this study, we found that proteasome inhibitor bortezomib, a cytotoxic drug that efficiently target gammaherpesvirus-associated B cell lymphomas, triggered KSHV or EBV viral lytic cycle by activating JNK, in the course of ER stress, and inducing autophagy. These results suggest that the manipulation of these pathways could limit viral spread and improve the outcome of bortezomib treatment in patients affected by gammaherpesvirus-associated lymphomas.
KSHV 和 EBV 是与人类癌症密切相关的γ疱疹病毒。尽管大多数癌细胞都存在潜伏感染,但少数发生病毒复制的细胞可能有助于病毒相关性恶性肿瘤的发病机制和维持。用于治疗病毒感染相关癌症的细胞毒性药物通常会产生激活病毒裂解周期的副作用。因此,研究它们是否会影响病毒的重新激活以及了解相关的潜在机制非常重要。在这项研究中,我们发现蛋白酶体抑制剂硼替佐米(bortezomib),一种能够有效靶向与γ疱疹病毒相关的 B 细胞淋巴瘤的细胞毒性药物,通过在 ER 应激过程中激活 JNK 和诱导自噬,触发 KSHV 或 EBV 病毒的裂解周期。这些结果表明,对这些途径的操纵可以限制病毒的传播,并改善接受与γ疱疹病毒相关的淋巴瘤患者硼替佐米治疗的效果。