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miRNA与糖尿病心肌病 被引量:7

Study progress of miRNA in diabetic cardiomyopathy
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摘要 miRNA是一类长约18~25个核苷酸大小的内源性非编码RNA,参与调节转录和转录后基因表达,并调控糖尿病心肌病(DCM)的生理过程.DCM是糖尿病患者慢性不可逆的心脏并发症,主要表现心肌纤维化、心肌细胞肥大、凋亡及微血管病变等,发病机制仍不明确.近年来发现氧化应激、炎症反应与DCM密切相关.本文对miRNA在DCM中的异常表达、发病机制及治疗靶点进行评述,为临床诊治DCM提供依据. miRNAs are a class of endogenous non-coding RNAs of about 18 to 25 nucleotides in length that regulate transcription and post-transcriptional gene expression and are involved in the regulation of the physiological processes of diabetic cardiomyopathy(DCM).DCM is a chronic irreversible cardiac complication in diabetic patients.The main manifestations include myocardial fibrosis,cardiomyocyte hypertrophy,apoptosis and microvascular disease.The mechanism leading to DCM remains unclear.In recent years,it has been found that oxidative stress and inflammatory response are closely related to DCM.This article intends to provide a new way for the diagnosis and treatment of DCM by briefly describing the new study progress of miRNAs in the abnormal expression,pathogenesis and therapeutic targets of DCM.
作者 刘洁婷 肖阳 初彦辉 冯彪 LIU Jieting;XIAO Yang;CHU Yanhui(Department of Medical Research Center,Mudanjiang Medical University,Mudanjiang 157011,China)
出处 《中国糖尿病杂志》 CAS CSCD 北大核心 2020年第3期233-236,共4页 Chinese Journal of Diabetes
基金 国家自然科学基金(81770828) 黑龙江省卫生厅项目(2016-367).
关键词 糖尿病心肌病 MIRNA 心肌纤维化 Diabetic cardiomyopathy miRNA Myocardial fibrosis
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  • 1Rubler S, Dlugash J, Yuceoglu YZ, et al. New type of cardiomyopathy associated with diabetic glomeruloscle- rosis. Am J Cardiol, 1972,30(6):595-602.
  • 2Fein FS. Diabetic cardiomyopathy. Diabetes Care, 1990,13(11):1169-1179.
  • 3Regan T J, Ahmed S, Haider B, et al. Diabetic cardio- myopathy: experimental and clinical observations. N J Med, 1994,91(11):776-778.
  • 4Asbun J, Villarreal FJ. The pathogenesis of myocardial fibrosis in the setting of diabetic cardiomyopathy. J Am Coll Cardiol, 2006,47(4):693-700.
  • 5Rota M, LeCapitaine N, Hosoda T, et al. Diabetes pro- motes cardiac stem cell aging and heart failure, which are prevented by deletion of the p66shc gene. Circ Res, 2006,99(1):42-52.
  • 6Yoon YS, Uchida S, Masuo O, et al. Progressive attenua- tion of myocardial vascular endothelial growth factor ex- pression is a seminal event in diabetic cardiomyopathy: restoration of microvascular homeostasis and recovery of cardiac fimction in diabetic cardiomyopathy after replen- ishment of local vascular endothelial growth factor. Cir- culation, 2005,111 (6):2073-2085.
  • 7Bartel DP. MicroRNAs: genomics, biogenesis, mecha- nism, and function. Cell, 2004,116(2):281-297.
  • 8Rooij EV, Sutherland L, Qi X, et al. Control of stress-dependent cardiac growth and gene expression by a microRNA. Science, 2007,316(5824):575-579.
  • 9Miranda KC, Huynh T, Tay Y, et al. A pattern-based method for the identification of microRNA binding sites and their corresponding heteroduplexes. Cell, 2006,126 (6):1203-1217.
  • 10RooijEV, Sutherland LB, Liu N, etal. A signature pattem of stress-responsive microRNAs that can evoke cardiac hypertrophy and heart failure. Proc Natl Acad Sci USA, 2006,103(48):18 255-18 260.

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