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微小RNA与子宫内膜异位症:区分疾病发病机制中的驱动因素与过客因素

MicroRNAs and Endometriosis: Distinguishing Drivers from Passengers in Disease Pathogenesis.

作者信息

Nothnick Warren B

机构信息

Department of Molecular and Integrative Physiology, University of Kansas Medical Center, Kansas City, Kansas.

出版信息

Semin Reprod Med. 2017 Mar;35(2):173-180. doi: 10.1055/s-0037-1599089. Epub 2017 Feb 17.

DOI:10.1055/s-0037-1599089
PMID:28212593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5815380/
Abstract

Endometriosis is a disease common in women of reproductive age, characterized by pelvic pain and infertility. Despite its prevalence, the factors and mechanisms which contribute to the development and survival of ectopic lesions remain uncertain. MicroRNAs (miRNAs) are small RNA molecules that regulate posttranscriptional gene regulation which have been proposed to contribute to the pathogenesis of many diseases including that of endometriosis. This review summarizes the results of initial studies describing differentially expressed miRNAs between endometriotic lesion tissue and eutopic endometrium. Focus then moves toward discussion of studies on examining function of differentially expressed miRNAs to determine if they play a permissive role (driver of the disease) in events conducive to endometriosis progression/survival. Included in this discussion are the potential targets of these miRNAs and how their mis-expression may contribute to the disease. Limitations and challenges faced in studying miRNAs and endometriosis pathogenesis and recommendations to overcome these hurdles are presented at the end.

摘要

子宫内膜异位症是育龄期女性的常见疾病,其特征为盆腔疼痛和不孕。尽管该病较为普遍,但导致异位病灶发展和存活的因素及机制仍不明确。微小RNA(miRNA)是一类小RNA分子,可调节转录后基因调控,有人提出其在包括子宫内膜异位症在内的多种疾病发病机制中发挥作用。本综述总结了最初一些研究的结果,这些研究描述了子宫内膜异位症病灶组织与在位内膜中差异表达的miRNA。接着重点讨论了关于检测差异表达miRNA功能的研究,以确定它们是否在有利于子宫内膜异位症进展/存活的事件中起促成作用(疾病驱动因素)。该讨论内容包括这些miRNA的潜在靶点以及它们的表达异常可能如何导致疾病。最后介绍了研究miRNA与子宫内膜异位症发病机制时面临的局限和挑战,以及克服这些障碍的建议。

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本文引用的文献

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miRNA-15a-5p regulates VEGFA in endometrial mesenchymal stem cells and contributes to the pathogenesis of endometriosis.微小RNA-15a-5p调控子宫内膜间充质干细胞中的血管内皮生长因子A,并参与子宫内膜异位症的发病机制。
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Hum Reprod. 2015 Dec;30(12):2881-91. doi: 10.1093/humrep/dev229. Epub 2015 Sep 14.
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MiR-183 Regulates ITGB1P Expression and Promotes Invasion of Endometrial Stromal Cells.微小RNA-183调节整合素β1假基因表达并促进子宫内膜基质细胞侵袭。
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MiR-199a inhibits the angiogenic potential of endometrial stromal cells under hypoxia by targeting HIF-1α/VEGF pathway.微小RNA-199a通过靶向缺氧诱导因子-1α/血管内皮生长因子途径抑制缺氧条件下子宫内膜基质细胞的血管生成潜能。
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miR-142-3p is a novel regulator of cell viability and proinflammatory signalling in endometrial stroma cells.微小RNA-142-3p是子宫内膜基质细胞中细胞活力和促炎信号传导的新型调节因子。
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The expression of microRNA-451 in human endometriotic lesions is inversely related to that of macrophage migration inhibitory factor (MIF) and regulates MIF expression and modulation of epithelial cell survival.微小RNA-451在人子宫内膜异位症病灶中的表达与巨噬细胞移动抑制因子(MIF)的表达呈负相关,并调节MIF的表达及上皮细胞存活的调控。
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miR-29c is downregulated in the ectopic endometrium and exerts its effects on endometrial cell proliferation, apoptosis and invasion by targeting c-Jun.miR-29c在异位子宫内膜中表达下调,并通过靶向c-Jun对子宫内膜细胞的增殖、凋亡和侵袭发挥作用。
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The differential expression of microRNA-143,145 in endometriosis.微小RNA-143、145在子宫内膜异位症中的差异表达。
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miR-20a contributes to endometriosis by regulating NTN4 expression.微小RNA-20a通过调节神经营养因子4的表达促成子宫内膜异位症。
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