Chiantore Maria Vincenza, Mangino Giorgio, Iuliano Marco, Zangrillo Maria Simona, De Lillis Ilaria, Vaccari Gabriele, Accardi Rosita, Tommasino Massimo, Fiorucci Gianna, Romeo Giovanna
Department of Infectious, Parasitic and Immune-mediated Diseases, Istituto Superiore di Sanità, 00161 Rome, Italy.
Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University of Rome, 04100 Latina, Italy.
Cytokine. 2017 Jan;89:235-238. doi: 10.1016/j.cyto.2015.12.014. Epub 2015 Dec 31.
Human Papilloma Viruses (HPVs) are the causative agents of cervical cancer although other types of cancers are associated with HPV infection. Type I Interferons can interfere with HPV E6- and/or E7-dependent transformation and can affect microRNA (miRNA) expression. Cancer cells show a specific pattern of miRNA expression and HPVs are able to modulate miRNAs expressed in infected cells. Keratinocytes transduced with E6 and E7 from mucosal HPV-16 or cutaneous HPV-38 (K16 and K38) were studied to analyze the involvement of HPV oncoproteins in the anti-proliferative activity of IFN-β. In view of our previous data showing senescence induction by the cytokine in K38 cells, we observe that IFN-β treatment leads to p53-indipendent apoptosis in K16 cells whereas induces senescence in K16 cells if E6 is silenced and p53 expression is restored. The levels of selected miRNAs, deregulated in K16 and K38 cells, can be modulated by IFN-β when E6 and E7 proteins of HPV-16, but not HPV-38, are expressed.
人乳头瘤病毒(HPV)是宫颈癌的致病因子,尽管其他类型的癌症也与HPV感染有关。I型干扰素可干扰HPV E6和/或E7依赖性转化,并能影响微小RNA(miRNA)的表达。癌细胞呈现出特定的miRNA表达模式,HPV能够调节感染细胞中表达的miRNA。研究了用黏膜型HPV-16或皮肤型HPV-38的E6和E7转导的角质形成细胞(K16和K38),以分析HPV癌蛋白在IFN-β抗增殖活性中的作用。鉴于我们之前的数据显示细胞因子在K38细胞中诱导衰老,我们观察到IFN-β处理导致K16细胞中p53非依赖性凋亡,而如果E6沉默且p53表达恢复,则在K16细胞中诱导衰老。当HPV-16而非HPV-38的E6和E7蛋白表达时,IFN-β可调节K16和K38细胞中失调的所选miRNA的水平。