Veronika Mrázová, František Golais
Klin Onkol. 2018 Spring;31(3):178-183. doi: 10.14735/amko2018178.
Seroepidemiological studies suggest that human herpes simplex virus type 1 (HSV-1) and 2 (HSV-2) are linked with several types of cancer; however, they do not appear to play a direct role and are considered to be cofactors. The abilities of HSV-1 and -2 to transform cells in vitro can be demonstrated by suppressing their lytic ability via irradiation with a specific dose of ultraviolet light, photoinactivation in the presence of photosensitizers (e.g., neutral red or methylene blue), and culture under specific conditions. Several mechanisms have been proposed to explain the actions of these viruses. According to the hit-and-run mechanism, viral DNA initiates transformation by interacting with cellular DNA and thereby inducing mutations and epigenetic changes, but is not involved in other stages of neoplastic progression. By contrast, according to the hijacking mechanism, viral products in infected cells can activate signaling pathways and thereby cause uncontrolled proliferation. Such products include RR1PK, an oncoprotein that activates the Ras pathway and is encoded by the HSV-2 gene ICP10. Virus-encoded microRNAs may act as cofactors in tumorigenesis of serous ovarian carcinoma and some prostate tumors. Herpes virus-associated growth factors that facilitate or suppress transformation may play important roles in tumor formation. Finally, there is much evidence that HSV-2 increases the risk of cervical cancer after infection of human papilloma viruses. Key words: HSV-1 - HSV-2 - cancer - mechanisms of transformation This work was supported by APVV 0621-12. The authors declare they have no potential conflicts of interest concerning drugs, products, or services used in the study. The Editorial Board declares that the manuscript met the ICMJE recommendation for biomedical papers. Submitted: 29. 11. 2016 Accepted: 20. 3. 2018.
血清流行病学研究表明,人单纯疱疹病毒1型(HSV - 1)和2型(HSV - 2)与多种癌症相关;然而,它们似乎并不起直接作用,而是被视为辅助因素。HSV - 1和 - 2在体外转化细胞的能力可以通过用特定剂量的紫外线照射来抑制其裂解能力、在存在光敏剂(如中性红或亚甲蓝)的情况下进行光灭活以及在特定条件下培养来证明。已经提出了几种机制来解释这些病毒的作用。根据“打了就跑”机制,病毒DNA通过与细胞DNA相互作用引发转化,从而诱导突变和表观遗传变化,但不参与肿瘤进展的其他阶段。相比之下,根据“劫持”机制,受感染细胞中的病毒产物可以激活信号通路,从而导致不受控制的增殖。这些产物包括RR1PK,一种激活Ras通路并由HSV - 2基因ICP10编码的癌蛋白。病毒编码的微小RNA可能在浆液性卵巢癌和一些前列腺肿瘤的肿瘤发生中作为辅助因素起作用。促进或抑制转化的疱疹病毒相关生长因子可能在肿瘤形成中起重要作用。最后,有许多证据表明,HSV - 2在人乳头瘤病毒感染后会增加宫颈癌的风险。关键词:HSV - 1 - HSV - 2 - 癌症 - 转化机制 本研究得到了APVV 0621 - 12的支持。作者声明他们在研究中使用的药物、产品或服务方面没有潜在的利益冲突。编辑委员会声明该手稿符合ICMJE对生物医学论文的建议。提交日期:2016年11月29日 接受日期:2018年3月20日