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微小RNA家族在肝纤维化中的作用。

The roles of microRNA families in hepatic fibrosis.

作者信息

Jiang Xue-Ping, Ai Wen-Bing, Wan Lin-Yan, Zhang Yan-Qiong, Wu Jiang-Feng

机构信息

Institute of Organ Fibrosis and Targeted Drug Delivery, China Three Gorges University, 8 Daxue Road, Xiling District, Yichang, 443002 China.

The Yiling Hospital of Yichang, 31 Donghu Road, Yi Ling District, Yichang, 443100 Hubei China.

出版信息

Cell Biosci. 2017 Jul 4;7:34. doi: 10.1186/s13578-017-0161-7. eCollection 2017.

Abstract

When hepatocytes are damaged severely, a variety of signaling pathways will be triggered by inflammatory factors and cytokines involving in the process of hepatic fibrosis. The microRNA (miRNA) family consists of several miRNAs which have the potential for synergistic regulation of these signaling pathways. However, it is poor to understand the roles of miRNA family as a whole in hepatic fibrosis. Increasing studies have suggested several miRNA families are related with activation of hepatic stellate cells and hepatic fibrosis through cooperatively regulating certain signaling pathways. During the process of hepatic fibrosis, miR-29 family primarily induces cell apoptosis by modulating phosphatidylinositol 3-kinase/AKT signaling pathway and regulates extracellular matrix accumulation. miR-34 family promotes the progression of hepatic fibrosis by inducing activation of hepatic stellate cells, while miR-378 family suppresses the process in Glis dependent manner. miR-15 family mainly promotes cell proliferation and induces apoptosis. The miR-199 family and miR-200 family are responsible for extracellular matrix deposition and the release of pro-fibrotic cytokines. These miRNA family members play pro-fibrotic or anti-fibrotic roles by targeting genes collectively or respectively which involve in hepatic fibrosis related signaling pathways and hepatic stellate cell activation. Thus, good understandings of molecular mechanisms which are based on miRNA families may provide new ideas for the molecular targeted therapy of hepatic fibrosis in the future.

摘要

当肝细胞受到严重损伤时,炎症因子和细胞因子会触发多种信号通路,参与肝纤维化过程。微小RNA(miRNA)家族由几种miRNA组成,它们有可能对这些信号通路进行协同调节。然而,目前对miRNA家族作为一个整体在肝纤维化中的作用了解甚少。越来越多的研究表明,几个miRNA家族通过协同调节某些信号通路与肝星状细胞的激活和肝纤维化相关。在肝纤维化过程中,miR-29家族主要通过调节磷脂酰肌醇3激酶/AKT信号通路诱导细胞凋亡,并调节细胞外基质的积累。miR-34家族通过诱导肝星状细胞的激活促进肝纤维化的进展,而miR-378家族以Gli依赖的方式抑制这一过程。miR-15家族主要促进细胞增殖并诱导细胞凋亡。miR-199家族和miR-200家族负责细胞外基质的沉积和促纤维化细胞因子的释放。这些miRNA家族成员通过共同或分别靶向参与肝纤维化相关信号通路和肝星状细胞激活的基因,发挥促纤维化或抗纤维化作用。因此,深入了解基于miRNA家族的分子机制可能为未来肝纤维化的分子靶向治疗提供新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd1/5496266/e170e80e09ec/13578_2017_161_Fig9_HTML.jpg

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