MicroRNAs: The Underlying Mediators of Pathogenetic Processes in Vascular Complications of Diabetes

被引:24
作者
Ruiz, Michael Anthony [1 ]
Chakrabarti, Subrata [1 ]
机构
[1] Univ Western Ontario, Dept Pathol, London, ON N6A 5C1, Canada
关键词
diabetic cardiomyopathy; diabetic nephropathy; diabetic retinopathy; microRNA; pathogenesis; vascular complications of diabetes; GROWTH-FACTOR; CARDIOMYOCYTE HYPERTROPHY; MESENCHYMAL TRANSITION; TARGETING ZEB1; MIR-200; FAMILY; EXPRESSION; FIBROGENESIS; RETINOPATHY; MECHANISMS; REGULATOR;
D O I
10.1016/j.jcjd.2013.07.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes mellitus causes chronic complications primarily affecting the vasculature of various organs, risking patients for renal failure, vision loss and heart failure. A newly discovered class of molecules, microRNAs, may be important in the genesis of these pathologic processes. microRNAs regulate gene expression at the post-transcriptional level by inhibiting target messenger RNA translation. In disease states, however, the expression of microRNAs often is altered, resulting in further altered expression (mostly overexpression) of downstream target genes. Interestingly, restoring microRNA expression to normal levels can correct downstream effects and prevent diabetes-associated changes. Investigations into microRNA involved in various pathogenetic processes mediating diabetic nephropathy, retinopathy and cardiomyopathy are highlighted in this review. Future directions of microRNA in therapeutics and diagnostics are also discussed. It is our intent to help the reader appreciate the diverse interactions microRNAs have in cellular signalling and how understanding epigenetic elements, such as microRNAs, potentially can yield new therapeutic strategies. (C) 2013 Canadian Diabetes Association
引用
收藏
页码:339 / 344
页数:6
相关论文
共 52 条
[11]   High Glucose-induced Altered Basement Membrane Composition and Structure Increases Trans-endothelial Permeability: Implications for Diabetic Retinopathy [J].
Chronopoulos, Argyrios ;
Trudeau, Kyle ;
Roy, Sumon ;
Huang, Hu ;
Vinores, Stanley A. ;
Roy, Sayon .
CURRENT EYE RESEARCH, 2011, 36 (08) :747-753
[12]   How the diabetic eye loses vision [J].
Davidson, Jaime A. ;
Ciulla, Thomas A. ;
McGill, Janet B. ;
Kles, Keri A. ;
Anderson, Pamela W. .
ENDOCRINE, 2007, 32 (01) :107-116
[13]   Differentially expressed microRNAs and their target genes in the hearts of streptozotocin-induced diabetic mice [J].
Diao, Xuehong ;
Shen, E. ;
Wang, Xiaoxia ;
Hu, Bing .
MOLECULAR MEDICINE REPORTS, 2011, 4 (04) :633-640
[14]   Microparticles: major transport vehicles for distinct microRNAs in circulation [J].
Diehl, Philipp ;
Fricke, Alba ;
Sander, Laura ;
Stamm, Johannes ;
Bassler, Nicole ;
Htun, Nay ;
Ziemann, Mark ;
Helbing, Thomas ;
El-Osta, Assam ;
Jowett, Jeremy B. M. ;
Peter, Karlheinz .
CARDIOVASCULAR RESEARCH, 2012, 93 (04) :633-644
[15]   High glucose down-regulates miR-29a to increase collagen IV production in HK-2 cells [J].
Du, Bin ;
Ma, Li-Ming ;
Huang, Mian-Bo ;
Zhou, Hui ;
Huang, Hui-Lin ;
Shao, Peng ;
Chen, Yue-Qin ;
Qu, Liang-Hu .
FEBS LETTERS, 2010, 584 (04) :811-816
[16]   Regulation of cardiomyocyte hypertrophy in diabetes at the transcriptional level [J].
Feng, Biao ;
Chen, Shali ;
Chiu, Jane ;
George, Biju ;
Chakrabarti, Subrata .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2008, 294 (06) :E1119-E1126
[17]  
Feng Biao, 2012, ISRN Endocrinol, V2012, P549875, DOI 10.5402/2012/549875
[18]   miR-146a-Mediated Extracellular Matrix Protein Production in Chronic Diabetes Complications [J].
Feng, Biao ;
Chen, Shali ;
McArthur, Kara ;
Wu, Yuexiu ;
Sen, Subhrojit ;
Ding, Qingming ;
Feldman, Ross D. ;
Chakrabarti, Subrata .
DIABETES, 2011, 60 (11) :2975-2984
[19]   miR133a regulates cardiomyocyte hypertrophy in diabetes [J].
Feng, Biao ;
Chen, Shali ;
George, Biju ;
Feng, Qingping ;
Chakrabarti, Subrata .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2010, 26 (01) :40-49
[20]  
Schoof CRG, 2012, AM J CANCER RES, V2, P414