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微小 RNA 作为宫颈癌进展的标志物:系统评价。

MicroRNAs as markers of progression in cervical cancer: a systematic review.

机构信息

Italian Institute for Genomic Medicine (IIGM), Via Nizza 52, 10126, Turin, Italy.

Department of Medical Sciences, University of Turin, Via Santena 19, 10126, Turin, Italy.

出版信息

BMC Cancer. 2018 Jun 27;18(1):696. doi: 10.1186/s12885-018-4590-4.

Abstract

BACKGROUND

Invasive cervical cancer (ICC) is caused by high-risk human papillomavirus types (HR-HPVs) and is usually preceded by a long phase of intraepithelial neoplasia (CIN). Before invasion, (epi) genetic changes, potentially applicable as molecular markers within cervical screening, occur in HPV host cells. Epigenetic alterations, such as dysregulation of microRNA (miRNA) expression, are frequently observed in ICC. The mechanisms and role of miRNA dysregulation in cervical carcinogenesis are still largely unknown.

METHODS

We provide an overview of the studies investigating miRNA expression in relation to ICC progression, highlighting their common outcomes and their weaknesses/strengths. To achieve this, we systematically searched through Pubmed database all articles between January 2010 and December 2017.

RESULTS

From the 24 studies retrieved, miR-29a and miR-21 are the most frequently down- and up-regulated in ICC progression, respectively. Microarray-based studies show a small overlap, with miR-10a, miR-20b, miR-9, miR-16 and miR-106 found repeatedly dysregulated. miR-34a, miR-125 and miR-375 were also found dysregulated in cervical exfoliated cells in relation to cancer progression.

CONCLUSIONS

The pivotal role of miRNAs in ICC progression and initial development is becoming more and more relevant. Available studies are essentially based on convenience material, entailing possible selection bias, and frequently of small size: all these points still represent a limitation to a wide comprehension of miRNAs relevant for ICC. The targeted approach instead of a genome-wide investigation still precludes the identification of all the relevant miRNAs in the process. The implementation of deep sequencing on large scale population-based studies will help to discover and validate the relation between altered miRNA expression and CC progression for the identification of biomarkers. Optimally, once explored on a miRNome scale, small specific miRNA signatures maybe used in the context of screening.

摘要

背景

浸润性宫颈癌(ICC)由高危型人乳头瘤病毒(HR-HPV)引起,通常发生在上皮内瘤变(CIN)的很长一段时间之前。在侵袭之前,HPV 宿主细胞中会发生(上皮)遗传改变,这些改变可能作为宫颈筛查中的分子标志物。ICC 中经常观察到表观遗传改变,如 microRNA(miRNA)表达失调。miRNA 失调在宫颈癌发生中的机制和作用仍在很大程度上未知。

方法

我们提供了一项关于 miRNA 表达与 ICC 进展相关的研究综述,强调了它们的常见结果及其优缺点。为此,我们通过 Pubmed 数据库系统地搜索了 2010 年 1 月至 2017 年 12 月期间的所有文章。

结果

从检索到的 24 项研究中,miR-29a 和 miR-21 分别是 ICC 进展中下调和上调最频繁的两种 miRNA。基于微阵列的研究显示出很小的重叠性,miR-10a、miR-20b、miR-9、miR-16 和 miR-106 被反复发现失调。miR-34a、miR-125 和 miR-375 在与癌症进展相关的宫颈脱落细胞中也被发现失调。

结论

miRNA 在 ICC 进展和早期发展中的关键作用变得越来越重要。现有的研究基本上基于方便的材料,可能存在选择偏倚,而且通常规模较小:所有这些仍然是对与 ICC 相关的 miRNA 有更广泛理解的一个限制。靶向方法而不是全基因组研究仍然无法确定该过程中所有相关的 miRNA。在基于人群的大型研究中实施深度测序将有助于发现和验证 miRNA 表达改变与 CC 进展之间的关系,从而识别生物标志物。最佳情况下,一旦在 miRNA 组范围内进行探索,特定的小 miRNA 特征也许可以用于筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cfc7/6020348/c6022b7d0125/12885_2018_4590_Fig1_HTML.jpg

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