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本文引用的文献

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Circulating microRNAs as a marker for liver injury in human immunodeficiency virus patients.循环 microRNAs 作为人类免疫缺陷病毒患者肝损伤的标志物。
Hepatology. 2015 Jan;61(1):46-55. doi: 10.1002/hep.27369. Epub 2014 Nov 20.
2
Regulation of the extrinsic apoptotic pathway by microRNA-21 in alcoholic liver injury.微小RNA-21在酒精性肝损伤中对外源性凋亡途径的调控
J Biol Chem. 2014 Oct 3;289(40):27526-39. doi: 10.1074/jbc.M114.602383. Epub 2014 Aug 12.
3
MicroRNA-200a controls Nrf2 activation by target Keap1 in hepatic stellate cell proliferation and fibrosis.微小RNA-200a通过靶向 Kelch样环氧氯丙烷相关蛋白1调控肝星状细胞增殖和纤维化过程中的核因子E2相关因子2激活。
Cell Signal. 2014 Nov;26(11):2381-9. doi: 10.1016/j.cellsig.2014.07.016. Epub 2014 Jul 15.
4
Elevated miR-122 serum levels are an independent marker of liver injury in inflammatory diseases.血清中miR-122水平升高是炎症性疾病中肝损伤的一个独立标志物。
Liver Int. 2015 Apr;35(4):1172-84. doi: 10.1111/liv.12627. Epub 2014 Jul 21.
5
Retinoid X receptor α in human liver is regulated by miR-34a.人肝中的视黄酸 X 受体 α 受 miR-34a 调控。
Biochem Pharmacol. 2014 Jul 15;90(2):179-87. doi: 10.1016/j.bcp.2014.05.002. Epub 2014 May 14.
6
MicroRNA-101 suppresses liver fibrosis by targeting the TGFβ signalling pathway.MicroRNA-101 通过靶向 TGFβ 信号通路抑制肝纤维化。
J Pathol. 2014 Sep;234(1):46-59. doi: 10.1002/path.4373. Epub 2014 Jun 17.
7
Overexpression of miR-483-5p/3p cooperate to inhibit mouse liver fibrosis by suppressing the TGF-β stimulated HSCs in transgenic mice.在转基因小鼠中,miR-483-5p/3p的过表达通过抑制转化生长因子-β刺激的肝星状细胞协同抑制小鼠肝纤维化。
J Cell Mol Med. 2014 Jun;18(6):966-74. doi: 10.1111/jcmm.12293. Epub 2014 May 6.
8
Detection and quantification of extracellular microRNAs in murine biofluids.检测和定量检测鼠类生物体液中的细胞外 microRNAs。
Biol Proced Online. 2014 Mar 14;16(1):5. doi: 10.1186/1480-9222-16-5.
9
microRNA-222 modulates liver fibrosis in a murine model of biliary atresia.miRNA-222 调节先天性胆道闭锁小鼠模型中的肝纤维化。
Biochem Biophys Res Commun. 2014 Mar 28;446(1):155-9. doi: 10.1016/j.bbrc.2014.02.065. Epub 2014 Feb 22.
10
Liver fibrosis and repair: immune regulation of wound healing in a solid organ.肝纤维化与修复:实体器官中创伤愈合的免疫调控。
Nat Rev Immunol. 2014 Mar;14(3):181-94. doi: 10.1038/nri3623.

miRNAs 在肝纤维化炎症过程调控中的作用。

The role of miRNAs in the regulation of inflammatory processes during hepatofibrogenesis.

机构信息

Department of Medicine III, University of Aachen (RWTH), Pauwelsstraße 30, 52074 Aachen, Germany.

出版信息

Hepatobiliary Surg Nutr. 2015 Feb;4(1):24-33. doi: 10.3978/j.issn.2304-3881.2015.01.05.

DOI:10.3978/j.issn.2304-3881.2015.01.05
PMID:25713802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4318955/
Abstract

Liver cirrhosis represents the end stage of most chronic inflammatory liver diseases and is a major global health burden. Despite the enormous relevance of cirrhotic disease, pharmacological strategies for prevention or treatment of hepatic fibrosis are still limited, underlining the need to establish a better understanding of the molecular mechanisms underlying the pathogenesis of hepatic cirrhosis. Recently, miRNAs have emerged as a new class of RNAs that do not withhold the information to encode for proteins but regulate whole gene expression networks during different physiological and pathological processes. Various authors demonstrated that miRNA species are functionally involved in the regulation of chronic liver damage and development of liver cirrhosis in inflamed livers. Moreover, circulating miRNA patterns were suggested to serve as blood-based biomarkers indicating liver injury and progression to hepatic cirrhosis and cancer. Here we summarize current findings on a potential role of miRNAs in the cascade leading from liver inflammation to liver fibrosis and finally hepatocellular carcinoma. We compare data from animal models with findings on miRNAs dysregulated in human patients and finally highlight a potential use of miRNAs as biomarkers for liver injury, fibrosis and cancer.

摘要

肝硬化是大多数慢性炎症性肝病的终末期阶段,是全球主要的健康负担之一。尽管肝硬化疾病具有重要意义,但预防或治疗肝纤维化的药物治疗策略仍然有限,这突显了需要更好地了解肝纤维化发病机制的分子机制。最近,miRNA 作为一类新的 RNA 出现,它们不包含编码蛋白质的信息,而是在不同的生理和病理过程中调节整个基因表达网络。许多作者证明,miRNA 物种在调节慢性肝损伤和炎症性肝脏中肝硬化的发展中具有功能作用。此外,循环 miRNA 模式被认为可以作为基于血液的生物标志物,指示肝损伤和向肝硬化和肝癌的进展。在这里,我们总结了 miRNA 在从肝炎症到肝纤维化最终到肝细胞癌的级联反应中可能发挥作用的最新发现。我们将动物模型中的数据与人类患者中失调的 miRNA 研究结果进行了比较,最后强调了 miRNA 作为肝损伤、纤维化和癌症生物标志物的潜在用途。