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人乳头瘤病毒16型E6蛋白调节子宫颈癌细胞系中膜联蛋白1(ANXA1)的蛋白表达。

HPV16 E6 regulates annexin 1 (ANXA1) protein expression in cervical carcinoma cell lines.

作者信息

Calmon Marilia Freitas, Sichero Laura, Boccardo Enrique, Villa Luisa Lina, Rahal Paula

机构信息

Department of Biology, Institute of Bioscience, Language and Exact Science, São Paulo State University, São Jose do Rio Preto, Brazil.

Molecular Biology Laboratory, Centre for Translational Research in Oncology, Instituto do Câncer do Estado de São Paulo (ICESP), São Paulo, Brazil.

出版信息

Virology. 2016 Sep;496:35-41. doi: 10.1016/j.virol.2016.05.016. Epub 2016 May 28.

Abstract

Annexin 1 (ANXA1) is a substrate for E6AP mediated ubiquitylation. It has been hypothesized that HPV 16 E6 protein redirects E6AP away from ANXA1, increasing its stability and possibly contributing to viral pathogenesis. We analyzed ANXA1 expression in HPV-positive and negative cervical carcinoma-derived cells, in cells expressing HPV-16 oncogenes and in cells transduced with shRNA targeting E6AP. We observed that ANXA1 protein expression increased in HPV-16-positive tumor cells, in keratinocytes expressing HPV-16 E6wt (wild-type) or E6/E7 and C33 cells expressing HPV-16 E6wt. ANXA1 protein expression decreased in cells transfected with E6 Dicer-substrate RNAs (DsiRNA) and C33 cells cotransduced with HPV-16 E6wt and E6AP shRNA. Moreover, colony number and proliferation rate decreased in HPV16-positive cells transduced with ANXA1 shRNA. We observed that in cells infected with HPV16, the E6 binds to E6AP to degrade p53 and upregulate ANXA1. We suggest that ANXA1 may play a role in HPV-mediated carcinogenesis.

摘要

膜联蛋白1(ANXA1)是E6相关蛋白(E6AP)介导的泛素化作用的底物。据推测,人乳头瘤病毒16型(HPV 16)E6蛋白使E6AP不再作用于ANXA1,从而增加其稳定性,并可能在病毒致病过程中发挥作用。我们分析了HPV阳性和阴性宫颈癌衍生细胞、表达HPV - 16癌基因的细胞以及用靶向E6AP的短发夹RNA(shRNA)转导的细胞中ANXA1的表达情况。我们观察到,在HPV - 16阳性肿瘤细胞、表达HPV - 16 E6野生型(E6wt)或E6/E7的角质形成细胞以及表达HPV - 16 E6wt的C33细胞中,ANXA1蛋白表达增加。在用E6 Dicer底物RNA(DsiRNA)转染的细胞以及同时用HPV - 16 E6wt和E6AP shRNA共转导的C33细胞中,ANXA1蛋白表达降低。此外,用ANXA1 shRNA转导的HPV16阳性细胞中的集落数和增殖率降低。我们观察到,在感染HPV16的细胞中,E6与E6AP结合以降解p53并上调ANXA1。我们认为ANXA1可能在HPV介导的致癌作用中发挥作用。

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