Olivero Carlotta, Lanfredini Simone, Borgogna Cinzia, Gariglio Marisa, Patel Girish K
Virology Unit, Department of Translational Medicine, Novara Medical School, University of Eastern Piedmont, Novara, Italy.
European Cancer Stem Cell Research Institute, Cardiff School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Front Microbiol. 2018 Mar 26;9:546. doi: 10.3389/fmicb.2018.00546. eCollection 2018.
Field cancerisation was originally described as a basis for multiple head and neck squamous cell carcinoma (HNSCC) and is a pre-malignant phenomenon that is frequently attributable to oncogenic human papillomavirus (HPV) infection. Our work on β-HPV-induced cutaneous squamous cell carcinomas identified a novel Lrig1+ hair follicle junctional zone keratinocyte stem cell population as the basis for field cancerisation. Herein, we describe the ability for HPV to infect adult tissue stem cells in order to establish persistent infection and induce their proliferation and displacement resulting in field cancerisation. By review of the HPV literature, we reveal how this mechanism is conserved as the basis of field cancerisation across many tissues. New insights have identified the capacity for HPV early region genes to dysregulate adult tissue stem cell self-renewal pathways ensuring that the expanded population preserve its stem cell characteristics beyond the stem cell niche. HPV-infected cells acquire additional transforming mutations that can give rise to intraepithelial neoplasia (IEN), from environmental factors such as sunlight or tobacco induced mutations in skin and oral cavity, respectively. With establishment of IEN, HPV viral replication is sacrificed with loss of the episome, and the tissue is predisposed to multiple cancer stem cell-driven carcinomas.
场癌化最初被描述为多发性头颈部鳞状细胞癌(HNSCC)的基础,是一种癌前现象,通常归因于致癌性人乳头瘤病毒(HPV)感染。我们关于β-HPV诱导的皮肤鳞状细胞癌的研究确定了一种新的Lrig1+毛囊交界区角质形成干细胞群体作为场癌化的基础。在此,我们描述了HPV感染成人组织干细胞以建立持续感染并诱导其增殖和移位从而导致场癌化的能力。通过回顾HPV文献,我们揭示了这种机制如何作为许多组织中场癌化的基础而得以保留。新的见解已经确定HPV早期区域基因有能力失调成人组织干细胞自我更新途径,确保扩增的细胞群体在干细胞生态位之外仍保持其干细胞特征。HPV感染的细胞会获得额外的转化突变,这些突变分别可由环境因素如阳光或烟草诱导皮肤和口腔中的突变,从而引发上皮内瘤变(IEN)。随着IEN的形成,HPV病毒复制随着游离基因的丢失而牺牲,并且该组织易患多种癌症干细胞驱动的癌。