Circulating microRNAs as novel biomarkers for diabetes mellitus

Claudiane Guay, Romano Regazzi, Claudiane Guay, Romano Regazzi

Abstract

Diabetes mellitus is characterized by insulin secretion from pancreatic β cells that is insufficient to maintain blood glucose homeostasis. Autoimmune destruction of β cells results in type 1 diabetes mellitus, whereas conditions that reduce insulin sensitivity and negatively affect β-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.

References

    1. J Clin Endocrinol Metab. 2012 Dec;97(12):E2271-6
    1. Dev Cell. 2008 Aug;15(2):272-84
    1. Int J Clin Exp Med. 2008;1(2):98-116
    1. Br J Cancer. 2012 Feb 14;106(4):768-74
    1. Kidney Int. 2010 Jul;78(2):191-9
    1. J Am Soc Nephrol. 2007 Apr;18(4):1353-61
    1. Biochem Soc Trans. 2012 Aug;40(4):875-9
    1. Lancet. 2005 Apr 9-15;365(9467):1333-46
    1. PLoS One. 2011;6(8):e23925
    1. Nat Rev Rheumatol. 2010 Jul;6(7):391-8
    1. Clin Chem. 2010 Nov;56(11):1733-41
    1. Endocrinology. 2013 Feb;154(2):603-8
    1. Diabetes Care. 2009 Nov;32(11):2116-9
    1. PLoS One. 2008 Sep 05;3(9):e3148
    1. Nat Cell Biol. 2009 Sep;11(9):1143-9
    1. Circ Res. 2010 Sep 3;107(5):677-84
    1. Dis Markers. 2011;30(4):171-9
    1. Diabetologia. 2010 Jun;53(6):1099-109
    1. Clin Chem. 2008 Mar;54(3):482-90
    1. Kidney Int. 2011 Dec;80(11):1138-45
    1. Nat Cell Biol. 2011 Apr;13(4):434-46
    1. Diabetes Metab Res Rev. 2011 Nov;27(8):862-6
    1. Nat Rev Genet. 2008 Nov;9(11):831-42
    1. Circulation. 2011 Jan 25;123(3):282-91
    1. Cardiovasc Res. 2012 Mar 15;93(4):583-93
    1. Nat Cell Biol. 2011 Apr;13(4):423-33
    1. Nature. 2007 Jul 5;448(7149):83-6
    1. J Clin Pharmacol. 2004 Apr;44(4):397-405
    1. Proc Natl Acad Sci U S A. 2011 Mar 22;108(12):5003-8
    1. Arq Bras Endocrinol Metabol. 2008 Mar;52(2):156-65
    1. Kidney Int. 2006 Jun;69(11):2057-63
    1. Nature. 2011 Jun 08;474(7353):649-53
    1. Biochim Biophys Acta. 1981 Jul 6;645(1):63-70
    1. Protein Cell. 2012 Oct;3(10):726-38
    1. J Biol Chem. 2010 Jun 4;285(23):17442-52
    1. Transl Res. 2011 Apr;157(4):253-64
    1. J Biol Chem. 1987 Jul 5;262(19):9412-20
    1. Curr Opin Nephrol Hypertens. 2012 Mar;21(2):195-202
    1. Curr Opin Nephrol Hypertens. 2011 May;20(3):246-57
    1. Nat Methods. 2011 Sep 04;8(10):841-3
    1. Diabetes. 2011 Jul;60(7):1832-7
    1. Diabetes. 2009 Nov;58(11):2555-64
    1. Proc Natl Acad Sci U S A. 2009 Apr 7;106(14):5813-8
    1. PLoS One. 2012;7(6):e38269
    1. J Cardiovasc Transl Res. 2012 Aug;5(4):413-22
    1. Circ Res. 2012 Feb 3;110(3):483-95
    1. Biochem Biophys Res Commun. 2010 Mar 26;394(1):184-8
    1. Nature. 2004 Nov 11;432(7014):226-30
    1. Genes Dev. 2004 Mar 1;18(5):504-11
    1. Cell. 1993 Dec 3;75(5):843-54
    1. Cell. 1993 Dec 3;75(5):855-62
    1. Genome Res. 2004 Oct;14(10A):1902-10
    1. Diabetes Res Clin Pract. 2013 Jan;99(1):1-11
    1. Science. 2010 Jun 25;328(5986):1694-8
    1. Curr Hypertens Rep. 2012 Dec;14(6):498-509
    1. Br J Haematol. 2008 May;141(5):672-5
    1. Exp Diabetes Res. 2012;2012:896362
    1. Nature. 2013 Feb 7;494(7435):111-5
    1. J Cell Biol. 1983 Aug;97(2):329-39
    1. Dev Cell. 2008 Aug;15(2):261-71
    1. Diabetes Res Clin Pract. 2011 Dec;94(3):311-21
    1. Diabetes Metab Syndr Obes. 2012;5:247-82
    1. Biochim Biophys Acta. 2012 Jul;1820(7):940-8
    1. PLoS One. 2013;8(1):e54662
    1. J Cell Biol. 1985 Sep;101(3):942-8
    1. Mol Cell Proteomics. 2012 Aug;11(8):230-43
    1. Nat Cell Biol. 2007 Jun;9(6):654-9
    1. Biochem Biophys Res Commun. 2009 Dec 4;390(1):1-4
    1. Br J Cancer. 2011 Jun 28;105(1):104-11
    1. EMBO J. 2004 Oct 13;23(20):4051-60
    1. Genome Med. 2010 Feb 01;2(2):9
    1. Diabetes. 2006 May;55(5):1463-9
    1. Methods. 2010 Apr;50(4):298-301
    1. Acta Diabetol. 2011 Mar;48(1):61-9
    1. Lancet. 2011 Aug 6;378(9790):487-97
    1. Cell Res. 2008 Oct;18(10):997-1006
    1. Mamm Genome. 2009 Aug;20(8):476-85
    1. Immunobiology. 2013 May;218(5):733-7
    1. Diabetes. 2010 Apr;59(4):978-86
    1. Diabetes Care. 2009 Jul;32(7):1207-12
    1. Circ Res. 2010 Sep 17;107(6):810-7
    1. J Proteome Res. 2009 Jun;8(6):2851-62
    1. J Clin Invest. 2006 Jul;116(7):1802-12
    1. Clin Cancer Res. 2012 Nov 1;18(21):5972-82
    1. Nephrol Dial Transplant. 2011 Nov;26(11):3794-802
    1. Clin Chem. 2011 Jun;57(6):833-40
    1. Diabetes. 2008 Oct;57(10):2728-36
    1. Proc Natl Acad Sci U S A. 2008 Jul 29;105(30):10513-8
    1. Diabetes Care. 2005 Jan;28 Suppl 1:S37-42
    1. Cell. 2004 Jan 23;116(2):281-97
    1. Diabetes Care. 2010 Aug;33(8):1872-94
    1. N Engl J Med. 2003 Jun 5;348(23):2285-93
    1. Cancer Res. 2010 Dec 1;70(23):9798-807
    1. Mol Cell. 2010 Jul 9;39(1):133-44
    1. J Immunol. 2011 Aug 15;187(4):1591-600
    1. Lancet. 2011 Jul 30;378(9789):412-9
    1. PLoS One. 2012;7(12):e51140
    1. Diabetes Technol Ther. 2002;4(6):817-39
    1. Diabetes. 2012 Jul;61(7):1742-51

Source: PubMed

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