Evans Michael R, James Claire D, Loughran Oonagh, Nulton Tara J, Wang Xu, Bristol Molly L, Windle Brad, Morgan Iain M
Department of Oral and Craniofacial Molecular Biology, VCU Philips Institute for Oral Health Research, Virginia Commonwealth University School of Dentistry, Richmond, VA, USA.
VCU Massey Cancer Center, Richmond, VA, USA.
Oncotarget. 2017 Jun 1;8(47):81892-81909. doi: 10.18632/oncotarget.18328. eCollection 2017 Oct 10.
Many aspects of the HPV life cycle have been characterized in cervical cell lines (W12, CIN612) and in HPV immortalized primary foreskin keratinocytes. There is now an epidemic of HPV positive oropharyngeal cancers (HPV16 is responsible for 80-90% of these); therefore increased understanding of the HPV16 life cycle in oral keratinocytes is a priority. To date there have been limited reports characterizing the HPV16 life cycle in oral keratinocytes. Using TERT immortalized "normal" oral keratinocytes (NOKs) we generated clonal cell lines maintaining the HPV16 genome as an episome, NOKs+HPV16. Organotypic raft cultures demonstrated appropriate expression of differentiation markers, E1^E4 and E2 expression along with amplification of the viral genome in the upper layers of the epithelium. Using this unique system RNA-seq analysis revealed extensive gene regulation of the host genome by HPV16; many of the changes have not been observed for HPV16 before. The RNA-seq data was validated on a key set of anti-viral innate immune response genes repressed by HPV16 in NOKs+HPV16. We show that the behavior of these NOKs+HPV16 lines is identical to HPV16 immortalized human tonsil keratinocytes with regards innate gene regulation. Finally, using The Cancer Genome Atlas (TCGA) data we examined gene expression patterns from HPV positive and negative head and neck cancers and demonstrate this innate immune gene signature set is also downregulated in HPV positive cancers versus negative. Our system provides a model for understanding HPV16 transcriptional regulation of oral keratinocytes that is directly relevant to HPV positive head and neck cancer.
人乳头瘤病毒(HPV)生命周期的许多方面已在宫颈细胞系(W12、CIN612)以及HPV永生化的原代包皮角质形成细胞中得到了表征。目前,HPV阳性口咽癌呈流行态势(其中80 - 90%由HPV16引起);因此,深入了解HPV16在口腔角质形成细胞中的生命周期成为当务之急。迄今为止,关于HPV16在口腔角质形成细胞中生命周期的报道有限。我们利用端粒酶逆转录酶(TERT)永生化的“正常”口腔角质形成细胞(NOKs),构建了以附加体形式维持HPV16基因组的克隆细胞系,即NOKs + HPV16。器官型筏式培养显示,分化标志物、E1^E4和E2表达以及病毒基因组在上皮上层的扩增均表达正常。利用这一独特系统,RNA测序分析揭示了HPV16对宿主基因组的广泛基因调控;其中许多变化在之前的HPV16研究中尚未观察到。RNA测序数据在一组由HPV16在NOKs + HPV16中抑制的关键抗病毒先天免疫反应基因上得到了验证。我们发现,就先天基因调控而言,这些NOKs + HPV16细胞系的行为与HPV16永生化的人扁桃体角质形成细胞相同。最后,我们利用癌症基因组图谱(TCGA)数据,研究了HPV阳性和阴性头颈癌的基因表达模式,并证明与阴性癌相比,该先天免疫基因特征集在HPV阳性癌中也下调。我们的系统为理解HPV16对口腔角质形成细胞的转录调控提供了一个模型,这与HPV阳性头颈癌直接相关。