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|

微小RNA-缺血性心脏病治疗新的靶点

《心脏杂志》[ISSN:1009-7236/CN:61-1268/R]

期数:
2012年第4期
页码:
517-520
栏目:
综述
出版日期:
2012-08-25

文章信息/Info

Title:
miRNAs: A novel therapeutic target in ischemic heart disease
作者:
涂应锋王晓云卜丽红闫雪峰杨丽丽申宝忠
(哈尔滨医科大学附属第四医院分子影像中心,黑龙江 哈尔滨 150001)
Author(s):
TU Ying-feng WANG Xiao-yun BU Li-hong YAN Xue-feng YANG Li-li SHEN Bao-zhong
(Molecular Imaging Center, Fourth Affiliated Hospital, Harbin Medical University, Harbin150001, Heilongjiang, China)
关键词:
微小RNA缺血性心脏病治疗
Keywords:
microRNA ischemic heart disease therapy
分类号:
R541.4
DOI:
-
文献标识码:
A
摘要:
当前,缺血性心脏病(IHD)是世界主要死亡原因之一。IHD是指因冠状动脉不同程度的受阻引起冠状血流和心肌耗氧需求之间不平衡而导致的心肌损害,最终形成充血性心力衰竭。心脏缺血损伤后,非缺血部位的心肌出现心肌重构,如心肌间质纤维化和心肌肥厚。心肌的重构过程可使心脏功能进一步恶化,更容易诱发心律失常。微小RNA(microRNAs,miRNAs)是一类长约22个核苷酸的非编码小分子RNA,通过与靶蛋白 mRNA 3′端非编码区的不完全互补结合,抑制靶 mRNA 转录后的表达。最近大量研究显示,miRNA 在心脏病理、生理过程中发挥着重要的调控作用,尤其与心肌梗死和梗死后心脏重构的发生、发展密切相关。本文将从miRNAs在IHD中的调控作用进行阐述,并探讨以miRNAs为靶点改善IHD患者的临床转归。
Abstract:
Ischemic heart disease (IHD) is one of the leading causes of mortality worldwide. IHD is a form of congestive heart failure resulting from the imbalance between myocardial blood supply and oxygen demand, which is caused by different degrees of coronary artery obstruction. In response to the injury, nonischemic myocardium displays signs of secondary remodeling such as interstitial fibrosis and hypertrophy of cardiac myocytes. This remodeling process further deteriorates the pump function and increases susceptibility to arrhythmias. MicroRNAs (miRNAs) are small, noncoding RNAs that primarily function posttranscriptionally by interacting with the 3’untranslated region (UTR) of specific target mRNAs in a sequence-specific manner and regulate gene expression in a sequence-dependent manner. Recent research shows that miRNAs play important roles in the physiological and pathological processes of the heart, especially being involved in the occurrence and progress of myocardial infarction (MI) and post-MI remodeling. In this review we discuss how modulation of these miRNAs represents a promising new therapeutic strategy to improve the clinical outcome in IHD.

参考文献/References

[1]Brodersen P,Voinnet O.Revisiting the principles of microRNA target recognition and mode of action[J].Nat Rev Mol Cell Biol,2009,10(2):141-148.

[2]Belevych AE,Sansom SE,Terentyeva R, et al.MicroRNA-1 and -133 increase arrhythmogenesis in heart failure by dissociating phosphatase activity from RyR2 complex[J].PLoS One,2011,6(12):e28324.

[3]van Almen GC,Verhesen W,van Leeuwen RE,et al.MicroRNA-18 and microRNA-19 regulate CTGF and TSP-1 expression in age-related heart failure[J].Aging Cell,2011,10(5):769-779.

[4]Wang GK,Zhu JQ,Zhang JT,et al.Circulating microRNA:a novel potential biomarker for early diagnosis of acute myocardial infarction in humans[J].Eur Heart J,2010,31(6):659-666.

[5]Ren XP,Wu J,Wang X,et al.MicroRNA-320 is involved in the regulation of cardiac ischemia/reperfusion injury by targeting heat-shock protein 20[J].Circulation,2009,119(17):2357-2366.

[6]Cheng Y,Zhang C:MicroRNA-21 in cardiovascular disease[J].J Cardiovasc Transl Res,2010,3(3):251-255.

[7]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.

[8]Rane S,He M,Sayed D,et al.Downregulation of miR-199a derepresses hypoxia-inducible factor-1alpha and Sirtuin 1 and recapitulates hypoxia preconditioning in cardiac myocytes[J].Circ Res,2009,104(7):879-886.

[9]Xu C,Lu Y,Pan Z,et al.The muscle-specific microRNAs miR-1 and miR-133 produce opposing effects on apoptosis by targeting HSP60, HSP70 and caspase-9 in cardiomyocytes[J].J Cell Sci,2011,124(Pt 18):3187.

[10]Li J,Donath S,Li Y,et al.miR-30 regulates mitochondrial fission through targeting p53 and the dynamin-related protein-1 pathway[J].PLoS Genet,2010,6(1):e1000795.

[11]van Rooij E,Sutherland LB, Thatcher JE, et al. Dysregulation of microRNAs after myocardial infarction reveals a role of miR-29 in cardiac fibrosis[J].Proc Natl Acad Sci U S A,2008,105(35):13027-13032.

[12]van Rooij E, Olson EN.Searching for miR-acles in cardiac fibrosis[J].Circ Res,2009,104(2):138-140.

[13]Duisters RF,Tijsen AJ,Schroen B,et al.miR-133 and miR-30 regulate connective tissue growth factor:implications for a role of microRNAs in myocardial matrix remodeling[J].Circ Res,2009, 104(2):170-178.

[14]Wang J,Huang W,Xu R,et al.MicroRNA-24 Regulates Cardiac Fibrosis after Myocardial Infarction[J].J Cell Mol Med,2012.doi:10.1111/j.1582-4934.2012.01523.x.

[15]Hullinger TG,Montgomery RL,Seto AG,et al.Inhibition of miR-15 protects against cardiac ischemic injury[J].Circ Res,2012,110(1):71-81.

[16]Yang B,Lin H,Xiao J,et al.The muscle-specific microRNA miR-1 regulates cardiac arrhythmogenic potential by targeting GJA1 and KCNJ2[J]. Nat Med,2007,13(4):486-491.

[17]Salloum FN,Yin C,Kukreja RC.Role of microRNAs in cardiac preconditioning[J].J Cardiovasc Pharmacol,2010,56(6):581-588.

[18]Schipper ME,van Kuik J,de Jonge N,et al.Changes in regulatory microRNA expression in myocardium of heart failure patients on left ventricular assist device support[J].J Heart Lung Transplant,2008,27(12):1282-1285.

[19]Voellenkle C,van Rooij J,Cappuzzello C,et al.MicroRNA signatures in peripheral blood mononuclear cells of chronic heart failure patients[J].Physiol Genomics,2010,42(3):420-426.

[20]Seto AG,van Rooij E.Circulating microRNAs to identify human heart failure[J].Eur J Heart Fail,2012,14(2):118-119.

[21]Bonauer A,Carmona G,Iwasaki M,et al.MicroRNA-92a controls angiogenesis and functional recovery of ischemic tissues in mice[J].Science,2009,324(5935):1710-1713.

[22]Fleissner F,Jazbutyte V,Fiedler J,et al.Short communication: asymmetric dimethylarginine impairs angiogenic progenitor cell function in patients with coronary artery disease through a microRNA-21-dependent mechanism[J].Circ Res,2010,107(1):138-143.

备注/Memo

备注/Memo:
收稿日期:2012-03-02.作者简介: 涂应锋,博士生Email:tydoctor@163.com
更新日期/Last Update: 2012-07-20