Genomics Research Center, Academia Sinica, 128 Academia Road, Sect. 2, Taipei, 115, Taiwan.
School of Medicine and Big Data Research Centre, Fu-Jen Catholic University, New Taipei, Taiwan.
Recent Results Cancer Res. 2021;217:13-45. doi: 10.1007/978-3-030-57362-1_2.
Seven viruses including the Epstein-Barr virus (EBV), hepatitis B virus (HBV), hepatitis C virus (HCV), Kaposi's sarcoma herpes virus (KSHV), human immunodeficiency virus, type-1 (HIV-1), human T cell lymphotrophic virus, type-1 (HTLV-1), and human papillomavirus (HPV) have been classified as Group 1 human carcinogens by the International Agency for Research on Cancer (IARC). The conclusions are based on the findings of epidemiological and mechanistic studies. EBV, HPV, HTLV-1, and KSHV are direct carcinogens; HBV and HCV are indirect carcinogens through chronic inflammation; and HIV-1 is an indirect carcinogen through immune suppression. Some viruses may cause more than one cancer, while some cancers may be caused by more than one virus. However, only a proportion of persons infected by these oncogenic viruses will develop specific cancers. A series of studies have been carried out to assess the viral, host, and environmental cofactors of EBV-associated nasopharyngeal carcinoma, HBV/HCV-associated hepatocellular carcinoma, and HPV-associated cervical carcinoma. Persistent infection, high viral load, and viral genotype are important risk predictors of these virus-caused cancers. Risk calculators incorporating host and viral risk predictors have been developed for the prediction of long-term risk of hepatocellular carcinoma, nasopharyngeal carcinoma and cervical cancer. These risk calculators are useful for the triage and clinical management of infected patients. Both clinical trials and national programs of immunization, antiviral therapy and screening have demonstrated a significant reduction in the incidence of cancers caused by HBV, HCV, and HPV. Future research on gene-gene and gene-environment interactions of oncogenic viruses and the human host using large-scale longitudinal studies with serial measurements of biosignatures are in urgent need.
七种病毒,包括 Epstein-Barr 病毒(EBV)、乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)、卡波济肉瘤疱疹病毒(KSHV)、人类免疫缺陷病毒 1 型(HIV-1)、人类 T 细胞嗜淋巴细胞病毒 1 型(HTLV-1)和人乳头瘤病毒(HPV),已被国际癌症研究机构(IARC)归类为第 1 组人类致癌物。这些结论是基于流行病学和机制研究的发现。EBV、HPV、HTLV-1 和 KSHV 是直接致癌物;HBV 和 HCV 通过慢性炎症是间接致癌物;HIV-1 通过免疫抑制是间接致癌物。一些病毒可能导致一种以上的癌症,而一些癌症可能由一种以上的病毒引起。然而,只有一部分感染这些致癌病毒的人会患上特定的癌症。已经进行了一系列研究来评估 EBV 相关鼻咽癌、HBV/HCV 相关肝细胞癌和 HPV 相关宫颈癌的病毒、宿主和环境协同因素。持续感染、高病毒载量和病毒基因型是这些病毒引起的癌症的重要风险预测因子。已经开发了包含宿主和病毒风险预测因子的风险计算器,用于预测肝细胞癌、鼻咽癌和宫颈癌的长期风险。这些风险计算器可用于感染患者的分诊和临床管理。临床试验和国家免疫接种、抗病毒治疗和筛查计划都表明,HBV、HCV 和 HPV 引起的癌症发病率显著降低。未来需要使用具有生物标志物连续测量的大规模纵向研究来研究致癌病毒和人类宿主的基因-基因和基因-环境相互作用。