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|本期目录/Table of Contents|

microRNA Let-7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:
2016年第4期
页码:
476-478,487
栏目:
综述
出版日期:
2016-04-01

文章信息/Info

Title:
Research progress of microRNA let-7 in cardiovascular diseases
作者:
刘向兰吴 健朱静怡迟 迪孙 勇
(哈尔滨医科大学附属第二临床医学院心内科,教育部心肌缺血重点实验室,黑龙江 哈尔滨 150081)
Author(s):
LIU Xiang-lan WU Jian ZHU Jing-yi CHI Di SUN Yong
(Department of Cardiology, Second Affiliated Hospital of Harbin Medical & Key Laboratory of Myocardial Ischemia, Chinese Ministry of Education, Harbin 150081, Heilongjiang, China)
关键词:
microRNA let-7 心脏发育心血管疾病循环标志物
Keywords:
microRNA let-7 heart development cardiovascular diseases circulation biomarker
分类号:
R541
DOI:
-
文献标识码:
A
摘要:
microRNA let-7家族是在秀丽隐杆线虫中发现的长度21nt的microRNA之一。最近的研究发现它在心血管系统起到重要的调控作用。Let-7成员在心血管组织中特异性表达使其在心脏发育及心脏疾病的发生发展中发挥重要作用。目前, let-7的靶向基因主要是TLR4、LOX-1、Bcl-xl和AGO1,确定let-7靶基因和信号通路在心脏疾病的临床诊断和治疗上具有重要的应用前景。Let-7可能为一个潜在的治疗心血管疾病的目标。本文对 let-7在心血管疾病中的研究进展进行综述。
Abstract:
Let-7 family is one of the microRNAs that consists of 21 nucleotides found in C. elegans. Recent research has shown that it plays an important role in regulating the cardiovascular system. Let-7 members are important in the development of heart disease because let-7 is specifically expressed in cardiovascular tissue. So far, TLR4, LOX-1, Bcl-xl and AGO1 are the identified target genes of let-7. Let-7 may be a potential therapeutic target for cardiovascular diseases. This article reviews research progress of microRNA let-7 in cardiovascular diseases.

参考文献/References

[1]Barh D,Malhotra R,Ravi B,et al.MicroRNA let-7:an emerging next-generation cancer therapeutic[J].Curr Oncol,2010,17(1):70-80.
[2]Song H,Xu W,Song J,et al.Overexpression of Lin28 inhibits the proliferation, migration and cell cycle progression and induces apoptosis of BGC-823 gastric cancer cells[J].Oncol Rep,2015,33(2):997-1003.
[3]Cao L,Kong LP,Yu ZB,et al.microRNA expression profiling of the developing mouse heart[J].Int J Mol Med,2012,30(5):1095-1104.
[4]Fu J,Peng C,Wang W,et al.Let-7 g is involved in doxorubicin induced myocardial injury[J].Environ Toxicol Pharmacol,2012,33(2):312-317.
[5]Melton C,Judson RL,Blelloch R.Opposing microRNA families regulate self-renewal in mouse embryonic stem cells[J].Nature,2010,463(7281):621-626.
[6]Yang J,Nie Y,Wang F,et al.Reciprocal regulation of miR-23a and lysophosphatidic acid receptor signaling in cardiomyocyte hypertrophy[J].Biochim Biophys Acta,2013,1831(8):1386-1394.
[7]Yang Y,Ago T,Zhai P,et al.Thioredoxin 1 negatively regulates angiotensin II-induced cardiac hypertrophy through upregulation of miR-98/let-7[J].Circ Res,2011,108(3):305-313.
[8]Arciniegas E,Frid MG,Douglas IS,et al.Perspectives on endothelial-to-mesenchymal transition: potential contribution to vascular remodeling in chronic pulmonary hypertension[J].Am J Physiol Lung Cell Mol Physiol,2007,293(1):L1-L8.
[9]Chen XM,Splinter PL,O'Hara SP,et al.A cellular micro-RNA,let-7i, regulates Toll-like receptor 4 expression and contributes to cholangiocyte immune responses against Cryptosporidium parvum infection[J].J Biol Chem,2007,282(39):28929-28938.
[10]Chen KC,Hsieh IC,Hsi E,et al.Negative feedback regulation between microRNA let-7g and the oxLDL receptor LOX-1[J].J Cell Sci,2011,124(Pt 23):4115-4124.
[11]Satoh M,Tabuchi T,Minami Y,et al.Expression of let-7i is associated with Toll-like receptor 4 signal in coronary artery disease:effect of statins on let-7i and Toll-like receptor 4 signal[J].Immunobiology,2012,217(5):533-539.
[12]Kin K,Miyagawa S,Fukushima S,et al.Tissue- and plasma-specific MicroRNA signatures for atherosclerotic abdominal aortic aneurysm[J].J Am Heart Assoc,2012,1(5):e000745.
[13]Luo X,Zhang H,Xiao J,et al.Regulation of human cardiac ion channel genes by microRNAs:theoretical perspective and pathophysiological implications[J].Cell Physiol Biochem,2010,25(6):571-586.
[14]Ikeda S,Kong SW,Lu J,et al.Altered microRNA expression in human heart disease[J].Physiol Genomics,2007,31(3):367-373.
[15]Li S,Zhu J,Zhang W,et al.Signature microRNA expression profile of essential hypertension and its novel link to human cytomegalovirus infection[J].Circulation,2011,124(2):175-184.
[16]Chen X,Liang H,Zhang J,et al.Secreted microRNAs:a new form of intercellular communication[J].Trends Cell Biol,2012,22(3):125-132.
[17]Ahmed RP,Haider HK,Buccini S,et al.Reprogramming of skeletal myoblasts for induction of pluripotency for tumor-free cardiomyogenesis in the infarcted heart[J].Circ Res,2011,109(1):60-70.
[18]Deddens JC,Colijn JM,Oerlemans MI,et al.Circulating microRNAs as novel biomarkers for the early diagnosis of acute coronary syndrome[J].J Cardiovasc Transl Res,2013,6(6):884-898.
[19]Synetos A,Toutouzas K,Stathogiannis K,et al. MicroRNAs in arterial hypertension[J].Curr Top Med Chem,2013,13(13):1527-32.
[20]Eskildsen TV,Jeppesen PL,Schneider M,et al.Angiotensin II regulates microRNA-132/-212 in hypertensive rats and humans[J].IntJ Mol Sci,2013,14(6):11190-111207.
[21]Deddens JC,Colijn JM,Oerlemans MI,et al.Circulating microRNAs as novel biomarkers for the early diagnosis of acute coronary syndrome[J].J Cardiovasc Transl Res,2013,6(6):884-898.

备注/Memo

备注/Memo:
收稿日期:2015-03-18.
基金项目:国家自然基金青年基金项目资助(81200240),教育部重点实验室开放基金资助(KF201405)
通讯作者:孙勇,主任医师,主要从事先天性心脏病及冠脉血管介入治疗研究 Email:ssunyyong@126.com
作者简介:刘向兰,硕士生 Email:liuxianglan09061@126.com
更新日期/Last Update: 2016-04-01