Divisions of Bone Marrow Transplantation and Immune Deficiency, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Divisions of Asthma Research, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229, USA.
Viruses. 2018 Jan 20;10(1):47. doi: 10.3390/v10010047.
Human papillomavirus (HPV) infections cause a significant proportion of cancers worldwide, predominantly squamous cell carcinomas (SCC) of the mucosas and skin. High-risk HPV types are associated with SCCs of the anogenital and oropharyngeal tract. HPV oncogene activities and the biology of SCCs have been intensely studied in laboratory models and humans. What remains largely unknown are host tissue and immune-related factors that determine an individual's susceptibility to infection and/or carcinogenesis. Such susceptibility factors could serve to identify those at greatest risk and spark individually tailored HPV and SCC prevention efforts. Fanconi anemia (FA) is an inherited DNA repair disorder that is in part characterized by extreme susceptibility to SCCs. An increased prevalence of HPV has been reported in affected individuals, and molecular and functional connections between FA, SCC, and HPV were established in laboratory models. However, the presence of HPV in some human FA tumors is controversial, and the extent of the etiological connections remains to be established. Herein, we discuss cellular, immunological, and phenotypic features of FA, placed into the context of HPV pathogenesis. The goal is to highlight this orphan disease as a unique model system to uncover host genetic and molecular HPV features, as well as SCC susceptibility factors.
人乳头瘤病毒(HPV)感染导致了全球范围内相当大比例的癌症,主要是黏膜和皮肤的鳞状细胞癌(SCC)。高危 HPV 型与肛门生殖器和口咽道的 SCC 有关。HPV 癌基因活性和 SCC 的生物学在实验室模型和人类中得到了深入研究。在很大程度上仍然未知的是决定个体易感染和/或致癌的宿主组织和免疫相关因素。这些易感因素可以用来识别那些风险最大的人,并引发针对 HPV 和 SCC 的个体化预防措施。范可尼贫血(FA)是一种遗传性 DNA 修复障碍,其部分特征是对 SCC 具有极高的易感性。有报道称,受影响个体的 HPV 患病率增加,并且在实验室模型中建立了 FA、SCC 和 HPV 之间的分子和功能联系。然而,一些人类 FA 肿瘤中 HPV 的存在存在争议,病因联系的程度仍有待确定。本文讨论了 FA 的细胞、免疫和表型特征,并将其置于 HPV 发病机制的背景下。目的是强调这种孤儿病作为一个独特的模型系统,以揭示宿主遗传和分子 HPV 特征以及 SCC 易感性因素。