MicroRNAs and the regulation of fibrosis.

MicroRNAs and the regulation of fibrosis.
复制标题

DOI:
10.1111/j.1742-4658.2010.07632.x
复制
发表时间:
2010-05
期刊:
The FEBS journal
影响因子:
--
通讯作者:
Lindsay MA
Lindsay MA
中科院分区:
其他
文献类型:
--
作者:
Jiang X;Tsitsiou E;Herrick SE;Lindsay MA

文献摘要

参考文献

被引文献

相似文献

MicroRNA(miRNAs)是一类长度为18-25个核苷酸的非编码小RNA,通常被认为可以阻断靶mRNA的翻译或诱导其降解。miRNAs在细胞增殖、分化、凋亡和癌变等多种生物学和病理学过程中发挥重要作用。纤维化由细胞外基质分子周转的不平衡引起,并且是最终可导致器官功能障碍的高度衰弱过程。越来越多的证据表明,miRNA参与了许多器官的纤维化过程,包括心脏、肾脏、肝脏和肺。本文就miRNAs在组织纤维化发生发展中的作用及其作为新型药物靶点的潜力作一综述。
MicroRNAs (miRNAs) are small non-coding RNAs of 18–25 nucleotides that are generally believed to either block the translation or induce the degradation of target mRNA. miRNAs have been shown to play fundamental roles in diverse biological and pathological processes including cell proliferation, differentiation, apoptosis and carcinogenesis. Fibrosis results from an imbalance in the turnover of extracellular matrix molecules and is a highly debilitating process that can eventually lead to organ dysfunction. A growing body of evidence suggests that miRNAs participate in the fibrotic process in a number of organs including the heart, kidney, liver and lung. In this review, we summarize our current understanding of the role of miRNAs in the development of tissue fibrosis and their potential as novel drug targets.
DOI: 10.1126/science.1121158
发表时间: 2005-12-16
期刊: SCIENCE
影响因子: 56.9
作者:
Farh, KKH;Grimson, A;Bartel, DP
通讯作者: Bartel, DP
DOI: 10.1038/nsmb1226
发表时间: 2007-04-01
影响因子: 16.8
作者:
Long, Dang;Lee, Rosalind;Ding, Ye
通讯作者: Ding, Ye
DOI: 10.1016/s0092-8674(03)01018-3
发表时间: 2003-12-26
期刊: CELL
影响因子: 64.5
作者:
Lewis, BP;Shih, IH;Burge, CB
通讯作者: Burge, CB
对糖尿病性肾病中纤维化和硬化症机制的新见解。
DOI: 10.1007/s11154-008-9100-6
发表时间: 2008-12
影响因子: 8.2
作者:
Brosius, Frank C., III
通讯作者: Brosius, Frank C., III
DOI: 10.1111/j.1582-4934.2009.00744.x
发表时间: 2009-04
影响因子: 5.3
作者:
Mishra PK;Tyagi N;Kumar M;Tyagi SC
通讯作者: Tyagi SC