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长链非编码RNA GAS5通过PTEN/MMP-2信号通路靶向miR-21来控制心脏成纤维细胞的激活和纤维化。

LncRNA GAS5 controls cardiac fibroblast activation and fibrosis by targeting miR-21 via PTEN/MMP-2 signaling pathway.

作者信息

Tao Hui, Zhang Jia-Gui, Qin Run-He, Dai Chen, Shi Peng, Yang Jing-Jing, Deng Zi-Yu, Shi Kai-Hu

机构信息

Department of Cardiothoracic Surgery, The Second Hospital of Anhui Medical University, Hefei, 230601, China.

Department of Pharmacology, The Second Hospital of Anhui Medical University, Hefei, 230601, China, China.

出版信息

Toxicology. 2017 Jul 1;386:11-18. doi: 10.1016/j.tox.2017.05.007. Epub 2017 May 17.

Abstract

Long noncoding RNAs (LncRNAs) are aberrantly expressed in many diseases including cardiac fibrosis. LncRNA growth arrest-specific 5 (GAS5) is reported as a significant mediator in the control of cell proliferation and growth; however, the role and function in cardiac fibrosis remain unknown. In this study, we confirmed that GAS5 was lowly expressed in cardiac fibrosis tissues as well as activated cardiac fibroblast. Overexpression of GAS5 inhibited the proliferation of cardiac fibroblast. Moreover, microRNA-21 (miR-21) has been reported to be overexpressed in cardiac fibrosis tissues as well as activated cardiac fibroblast, which is responsible for the progression of cardiac fibrosis. We found that up-regulated GAS5 decreased the expression of miR-21 significantly. Furthermore, GAS5 that upregulated or downregulated the expression of PTEN through miR-21 in cardiac fibroblasts. Taken together, GAS5 plays a suppressive role in cardiac fibrosis via negative regulation of miR-21. These results indicated that GAS5 may be a novel therapeutic target for further research of cardiac fibrosis.

摘要

长链非编码RNA(LncRNAs)在包括心脏纤维化在内的多种疾病中表达异常。据报道,长链非编码RNA生长停滞特异性5(GAS5)是控制细胞增殖和生长的重要调节因子;然而,其在心脏纤维化中的作用和功能仍不清楚。在本研究中,我们证实GAS5在心脏纤维化组织以及活化的心脏成纤维细胞中低表达。GAS5的过表达抑制了心脏成纤维细胞的增殖。此外,据报道,微小RNA-21(miR-21)在心脏纤维化组织以及活化的心脏成纤维细胞中过表达,其与心脏纤维化的进展有关。我们发现上调的GAS5显著降低了miR-21的表达。此外,GAS5通过miR-21上调或下调心脏成纤维细胞中PTEN的表达。综上所述,GAS5通过对miR-21的负调控在心脏纤维化中发挥抑制作用。这些结果表明,GAS5可能是进一步研究心脏纤维化的新型治疗靶点。

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