我们的网站为什么显示成这样?

可能因为您的浏览器不支持样式,您可以更新您的浏览器到最新版本,以获取对此功能的支持,访问下面的网站,获取关于浏览器的信息:

|本期目录/Table of Contents|

microRNA-21及相关技术在心血管疾病中的研究进展

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2011年第2期
页码:
255-259,265
栏目:
综述
出版日期:
2010-12-10

文章信息/Info

Title:
-
作者:
苗裔 综述臧伟进 审校
西安交通大学医学院心血管生理药理研究室,陕西 西安710061
Author(s):
-
关键词:
microRNAsmicroRNA-21心血管疾病
Keywords:
-
分类号:
R54
DOI:
-
文献标识码:
A
摘要:
microRNAs(miRNAs)是近年发现的一类保守单链非编码RNA分子,由约19~24个核苷酸组成,在转录后水平调控基因的表达。miRNAs参与多种细胞进程,在疾病发生发展中也起重要作用。microRNA-21(miR-21)在多种类型肿瘤及心血管系统中均有表达,在心血管疾病的发生发展过程中发挥重要作用。本文从miRNAs的功能机制、研究方法,miR-21与心血管疾病的关系,靶基因预测及其表达干预手段等方面综述了miRNAs及miR-21现阶段的研究进展。
Abstract:
-

参考文献/References

[1]Faraoni I, Antonetti FR, Cardone J, et al. miR-155 gene: a typical multifunctional microRNA[J]. Biochim Biophys Acta, 2009, 1792(6):497-505.

[2]梁卓,姚天明,刘丽凤,等. miRNA与血小板[J]. 心脏杂志, 2011, 23(1):132-135.

[3]Perron M P, Provost P. Protein interactions and complexes in human microRNA biogenesis and function[J]. Front Biosci, 2008, 13:2537-2547.

[4]Jazbutyte V, Thum T. MicroRNA-21: from cancer to cardiovascular disease[J]. Curr Drug Targets, 2010, 11(8):926-935.

[5]Landgraf P, Rusu M, Sheridan R, et al. A mammalian microRNA expression atlas based on small RNA library sequencing[J]. Cell, 2007, 129(7):1401-1414.

[6]Kuehbacher A, Urbich C, Zeiher AM, et al. Role of Dicer and Drosha for endothelial microRNA expression and angiogenesis[J]. Circ Res, 2007, 101(1):59-68.

[7]Thum T, Gross C, Fiedler J, et al. MicroRNA-21 contributes to myocardial disease by stimulating MAP kinase signalling in fibroblasts[J]. Nature, 2008, 456(7224):980-984.

[8]Roy S, Khanna S, Hussain SR, et al. MicroRNA expression in response to murine myocardial infarction: miR-21 regulates fibroblast metalloprotease-2 via phosphatase and tensin homologue[J]. Cardiovasc Res, 2009, 82(1):21-29.

[9]Cheng Y, Liu X, Zhang S, et al. MicroRNA-21 protects against the H(2)O(2)-induced injury on cardiac myocytes via its target gene PDCD4[J]. J Mol Cell Cardiol, 2009, 47(1): 5-14.

[10]Cheng Y, Zhu P, Yang J, et al. Ischemic preconditioning-regulated miR-21 protects the heart from ischemia/reperfusion injury via anti-apoptosis through its target PDCD4[J]. Cardiovasc Res, 2010, 87(3):431-439.

[11]Sayed D, He M, Hong C, et al. MicroRNA-21 is a downstream effector of AKT that mediates its antiapoptotic effects via suppression of Fas ligand[J]. J Biol Chem, 2010, 285(26):20281-2090.

[12]Dong S, Cheng Y, Yang J, et al. MicroRNA expression signature and the role of microRNA-21 in the early phase of acute myocardial infarction[J]. J Biol Chem, 2009, 284(43):29514-29525.

[13]Lin Y, Liu X, Cheng Y, et al. Involvement of MicroRNAs in hydrogen peroxide-mediated gene regulation and cellular injury response in vascular smooth muscle cells[J]. J Biol Chem, 2009, 284(12):7903-7913.

[14]Ji R, Cheng Y, Yue J, et al. MicroRNA expression signature and antisense-mediated depletion reveal an essential role of MicroRNA in vascular neointimal lesion formation[J]. Circ Res, 2007, 100(11):1579-1588.

[15]Ebert MS, Neilson JR, Sharp PA. MicroRNA sponges: competitive inhibitors of small RNAs in mammalian cells[J]. Nat Methods, 2007, 4(9):721-726.

[16]Xiao J, Yang B, Lin H, et al. Novel approaches for gene-specific interference via manipulating actions of microRNAs: examination on the pacemaker channel genes HCN2 and HCN4[J]. J Cell Physiol, 2007, 212(2):285-292.

[17]Yin C, Salloum FN, Kukreja RC. A novel role of microRNA in late preconditioning: upregulation of endothelial nitric oxide synthase and heat shock protein 70[J]. Circ Res, 2009, 104(5):572-575.

[18]Kota J, Chivukula RR, O'Donnell KA, et al. Therapeutic microRNA delivery suppresses tumorigenesis in a murine liver cancer model[J]. Cell, 2009, 137(6):1005-1017.

[19]Ye Y, Hu Z, Lin Y, et al. Downregulation of microRNA-29 by antisense inhibitors and a PPAR-{gamma} agonist protects against myocardial ischaemia-reperfusion injury[J]. Cardiovasc Res, 2010, 87(3):535-544.

备注/Memo

备注/Memo:
收稿日期:2010-07-10.基金项目:本研究工作受国家自然科学基金(重点项目No.30930105;面上项目No.30873058、30770785),国家重点基础研究973发展计划(2007CB512005)和中华医学基金会杰出教授奖项目资助(F510000/G16916404) 通讯作者:臧伟进,教授,主要从事心血管生理药理学研究Email:zwj@mail.xjtu.edu.cn 作者简介:苗裔,博士生Email:miaoyi.xjtu@stu.xjtu.edu.cn
更新日期/Last Update: 2010-12-10