A Decade of Global mRNA and miRNA Profiling of HPV-Positive Cell Lines and Clinical Specimens.

The Open Virology Journal Pub Date : 2012-01-01 Epub Date: 2012-12-28 DOI:10.2174/1874357901206010216
Bogumil Kaczkowski, Marya Morevati, Maria Rossing, Finn Cilius, Bodil Norrild
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引用次数: 7

Abstract

For more than a decade, global gene expression profiling has been extensively used to elucidate the biology of human papillomaviruses (HPV) and their role in cervical- and head-and-neck cancers. Since 2008, the expression profiling of miRNAs has been reported in multiple HPV studies. Two major strategies have been employed in the gene and miRNA profiling studies: In the first approach, HPV positive tumors were compared to normal tissues or to HPV negative tumors. The second strategy relied on analysis of cell cultures transfected with single HPV oncogenes or with HPV genomes compared to untransfected cells considered as models for the development of premalignant and malignant transformations.In this review, we summarize what we have learned from a decade of global expression profiling studies. We performed comprehensive analysis of the overlap of the lists of differentially expressed genes and microRNAs, in both tissue samples and cell culture based studies. The review focuses mainly on HPV16, however reports from other HPV species are used as references. We discuss the low degree of consensus among different studies and the limitation of differential expression analysis as well as the fragmented miRNA-mRNA target correlation evidence. Furthermore, we propose an approach for future research to include more comprehensive miRNA-mRNA target correlation analysis and to apply systems biology/gene networks methodology.

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hpv阳性细胞系和临床标本的十年全球mRNA和miRNA谱分析。
十多年来,全球基因表达谱已被广泛用于阐明人类乳头瘤病毒(HPV)的生物学及其在宫颈癌和头颈癌中的作用。自2008年以来,在多项HPV研究中报道了mirna的表达谱。基因和miRNA分析研究采用了两种主要策略:在第一种方法中,将HPV阳性肿瘤与正常组织或HPV阴性肿瘤进行比较。第二种策略依赖于对转染了单一HPV致癌基因或HPV基因组的细胞培养物与未转染的细胞进行分析,这些细胞被认为是恶性前病变和恶性转化的模型。在这篇综述中,我们总结了我们从十年来的全球表达谱研究中学到的东西。我们在组织样本和基于细胞培养的研究中对差异表达基因和microrna列表的重叠进行了全面分析。本综述主要集中于HPV16,但其他HPV品种的报道也可作为参考。我们讨论了不同研究之间的低共识程度,差异表达分析的局限性以及碎片化的miRNA-mRNA靶点相关证据。此外,我们提出了一种未来研究的方法,包括更全面的miRNA-mRNA靶点相关性分析,并应用系统生物学/基因网络方法。
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