Circulating microRNAs as novel biomarkers for diabetes mellitus

被引:471
作者
Guay, Claudiane [1 ]
Regazzi, Romano [1 ]
机构
[1] Univ Lausanne, Dept Fundamental Neurosci, CH-1005 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
BETA-CELL DEATH; EXPRESSION CONTRIBUTE; TRANSFERRIN RECEPTOR; ELEVATED LEVELS; SERUM; PLASMA; MICROALBUMINURIA; DIAGNOSIS; PROFILES; VESICLES;
D O I
10.1038/nrendo.2013.86
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Diabetes mellitus is characterized by insulin secretion from pancreatic beta cells that is insufficient to maintain blood glucose homeostasis. Autoimmune destruction of beta cells results in type 1 diabetes mellitus, whereas conditions that reduce insulin sensitivity and negatively affect beta-cell activities result in type 2 diabetes mellitus. Without proper management, patients with diabetes mellitus develop serious complications that reduce their quality of life and life expectancy. Biomarkers for early detection of the disease and identification of individuals at risk of developing complications would greatly improve the care of these patients. Small non-coding RNAs called microRNAs (miRNAs) control gene expression and participate in many physiopathological processes. Hundreds of miRNAs are actively or passively released in the circulation and can be used to evaluate health status and disease progression. Both type 1 diabetes mellitus and type 2 diabetes mellitus are associated with distinct modifications in the profile of miRNAs in the blood, which are sometimes detectable several years before the disease manifests. Moreover, circulating levels of certain miRNAs seem to be predictive of long-term complications. Technical and scientific obstacles still exist that need to be overcome, but circulating miRNAs might soon become part of the diagnostic arsenal to identify individuals at risk of developing diabetes mellitus and its devastating complications.
引用
收藏
页码:513 / 521
页数:9
相关论文
共 102 条
[21]
Multivesicular bodies associate with components of miRNA effector complexes and modulate miRNA activity [J].
Gibbings, Derrick J. ;
Ciaudo, Constance ;
Erhardt, Mathieu ;
Voinnet, Olivier .
NATURE CELL BIOLOGY, 2009, 11 (09) :1143-U223
[22]
Serum MicroRNAs Are Promising Novel Biomarkers [J].
Gilad, Shlomit ;
Meiri, Eti ;
Yogev, Yariv ;
Benjamin, Sima ;
Lebanony, Danit ;
Yerushalmi, Noga ;
Benjamin, Hila ;
Kushnir, Michal ;
Cholakh, Hila ;
Melamed, Nir ;
Bentwich, Zvi ;
Hod, Moshe ;
Goren, Yaron ;
Chajut, Ayelet .
PLOS ONE, 2008, 3 (09)
[23]
The microRNA Signature in Response to Insulin Reveals Its Implication in the Transcriptional Action of Insulin in Human Skeletal Muscle and the Role of a Sterol Regulatory Element-Binding Protein-1c/Myocyte Enhancer Factor 2C Pathway [J].
Granjon, Aurelie ;
Gustin, Marie-Paule ;
Rieusset, Jennifer ;
Lefai, Etienne ;
Meugnier, Emmanuelle ;
Gueller, Isabelle ;
Cerutti, Catherine ;
Paultre, Christian ;
Disse, Emmanuel ;
Rabasa-Lhoret, Remi ;
Laville, Martine ;
Vidal, Hubert ;
Rome, Sophie .
DIABETES, 2009, 58 (11) :2555-2564
[24]
Guay C, 2012, DIABETOLOGIA, V55, pS95
[25]
Diabetes mellitus, a microRNA-related disease? [J].
Guay, Claudiane ;
Roggli, Elodie ;
Nesca, Valeria ;
Jacovetti, Cecile ;
Regazzi, Romano .
TRANSLATIONAL RESEARCH, 2011, 157 (04) :253-264
[26]
RECEPTOR-MEDIATED ENDOCYTOSIS OF TRANSFERRIN AND RECYCLING OF THE TRANSFERRIN RECEPTOR IN RAT RETICULOCYTES [J].
HARDING, C ;
HEUSER, J ;
STAHL, P .
JOURNAL OF CELL BIOLOGY, 1983, 97 (02) :329-339
[27]
Global microRNA expression profiles in insulin target tissues in a spontaneous rat model of type 2 diabetes [J].
Herrera, B. M. ;
Lockstone, H. E. ;
Taylor, J. M. ;
Ria, M. ;
Barrett, A. ;
Collins, S. ;
Kaisaki, P. ;
Argoud, K. ;
Fernandez, C. ;
Travers, M. E. ;
Grew, J. P. ;
Randall, J. C. ;
Gloyn, A. L. ;
Gauguier, D. ;
McCarthy, M. I. ;
Lindgren, C. M. .
DIABETOLOGIA, 2010, 53 (06) :1099-1109
[28]
JOHNSTONE RM, 1987, J BIOL CHEM, V262, P9412
[29]
Obesity-induced over expression of miRNA-143 inhibits insulin-stimulated AKT activation and impairs glucose metabolism [J].
Jordan, Sabine D. ;
Krueger, Markus ;
Willmes, Diana M. ;
Redemann, Nora ;
Wunderlich, F. Thomas ;
Broenneke, Hella S. ;
Merkwirth, Carsten ;
Kashkar, Hamid ;
Olkkonen, Vesa M. ;
Boettger, Thomas ;
Braun, Thomas ;
Seibler, Jost ;
Bruening, Jens C. .
NATURE CELL BIOLOGY, 2011, 13 (04) :434-U208
[30]
Diabetes Complications: The MicroRNA Perspective [J].
Kantharidis, Phillip ;
Wang, Bo ;
Carew, Rosemarie M. ;
Lan, Hui Yao .
DIABETES, 2011, 60 (07) :1832-1837