Decreased expression of microRNAs targeting type-2 diabetes susceptibility genes in peripheral blood of patients and predisposed individuals

被引:48
作者
Kokkinopoulou, Ioanna [1 ]
Maratou, Eirini [2 ,3 ]
Mitrou, Panayota [4 ]
Boutati, Eleni [2 ,3 ]
Sideris, Diamantis C. [1 ]
Fragoulis, Emmanuel G. [1 ]
Christodoulou, Maria-Ioanna [1 ,5 ]
机构
[1] Natl & Kapodistrian Univ Athens, Fac Biol, Dept Biochem & Mol Biol, Athens, Greece
[2] Natl & Kapodistrian Univ Athens, Attikon Univ Hosp, Dept Internal Med 2, Athens, Greece
[3] Natl & Kapodistrian Univ Athens, Attikon Univ Hosp, Res Inst, Sch Med, Athens, Greece
[4] Minist Hlth, Athens, Greece
[5] Univ Glasgow, Inst Infect Immun & Inflammat, Glasgow, Lanark, Scotland
关键词
MicroRNA (miRNA); Type-2 diabetes mellitus (T2D); T2D-susceptibility genes; Peripheral blood; PAP-RT-qPCR; CIRCULATING MICRORNAS; BIOMARKERS; ASSOCIATION; CHOLESTEROL; DIAGNOSIS; MIR-24; LOCUS; PANEL;
D O I
10.1007/s12020-019-02062-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim Certain microRNA molecules (miRNAs) that target genes involved in beta-cell growth and insulin resistance are found deregulated in patients with type-2 diabetes mellitus (T2D) and correlate with its complications. However, the expression profile of miRNAs that regulate genes bearing T2D-related single-nucleotide polymorphisms has been hardly studied. We recently reported that the mRNA patterns of specific T2D-susceptibility genes are impaired in patients, and associate with disease parameters and risk factors. The aim of this study was to explore the levels of miRNAs that target those genes, in peripheral blood of patients versus controls. Methods A panel of 14 miRNAs validated to target the CDKN2A, CDK5, IGF2BP2, KCNQ1, and TSPAN8 genes, was developed upon combined search throughout the DIANNA TarBase v7.0, miRTarBase, miRSearch v3.0-Exiqon, miRGator v3.0, and miRTarget Link Human algorithms. Specifically developed poly(A)polyadenylation(PAP)-reverse transcription (RT)-qPCR protocols were applied in peripheral blood RNA samples from patients and controls. Possible correlations with the disease, clinicopathological parameters and/or risk factors were evaluated. Results T2D patients expressed decreased levels of let-7b-5p, miR-1-3p, miR-24-3p, miR-34a-5p, miR-98-5p, and miR-133a-3p, compared with controls. Moreover, these levels correlated with certain disease features including insulin and % HbA1c levels in patients, as well as BMI, triglycerides' levels and family history in controls. Conclusions A T2D-specific expression profile of miRNAs that target disease-susceptibility genes is for the first time described. Future studies are needed to elucidate the associated transcription-regulatory mechanisms, perchance involved in T2D pathogenesis, and to evaluate the potential of these molecules as possible biomarkers for this disorder. Highlights Let-7b-5p, miR-1-3p, miR-24-3p, miR-34a-5p, miR-98-5p, and miR-133a-3p, which target certain T2D-susceptibility genes, are decreased in peripheral blood samples of patients compared with controls. The expression levels of let-7b-5p, miR-1-3p, miR-24-3p, miR-34a-5p, miR-98-5p, and miR-133a-3p correlate with the mRNA levels of their target T2D-susceptibility genes. The levels of these miRNAs correlate with certain disease parameters, including insulin, % HbA1c levels, BMI, triglycerides' levels, and family history.
引用
收藏
页码:226 / 239
页数:14
相关论文
共 39 条
  • [31] Plasma Exosome MicroRNA Profiling Unravels a New Potential Modulator of Adiponectin Pathway in Diabetes: Effect of Glycemic Control
    Santovito, Donato
    De Nardis, Velia
    Marcantonio, Pamela
    Mandolini, Claudia
    Paganelli, Camilla
    Vitale, Elita
    Buttitta, Fiamma
    Bucci, Marco
    Mezzetti, Andrea
    Consoli, Agostino
    Cipollone, Francesco
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2014, 99 (09) : E1681 - E1685
  • [32] STRING v10: protein-protein interaction networks, integrated over the tree of life
    Szklarczyk, Damian
    Franceschini, Andrea
    Wyder, Stefan
    Forslund, Kristoffer
    Heller, Davide
    Huerta-Cepas, Jaime
    Simonovic, Milan
    Roth, Alexander
    Santos, Alberto
    Tsafou, Kalliopi P.
    Kuhn, Michael
    Bork, Peer
    Jensen, Lars J.
    von Mering, Christian
    [J]. NUCLEIC ACIDS RESEARCH, 2015, 43 (D1) : D447 - D452
  • [33] DIANA-TarBase v7.0: indexing more than half a million experimentally supported miRNA:mRNA interactions
    Vlachos, Ioannis S.
    Paraskevopoulou, Maria D.
    Karagkouni, Dimitra
    Georgakilas, Georgios
    Vergoulis, Thanasis
    Kanellos, Ilias
    Anastasopoulos, Ioannis-Laertis
    Maniou, Sofia
    Karathanou, Konstantina
    Kalfakakou, Despina
    Fevgas, Athanasios
    Dalamagas, Theodore
    Hatzigeorgiou, Artemis G.
    [J]. NUCLEIC ACIDS RESEARCH, 2015, 43 (D1) : D153 - D159
  • [34] miR-24 in diabetes
    Xiang, Yaozu
    [J]. ONCOTARGET, 2015, 6 (19) : 16816 - 16817
  • [35] Hyperglycemia repression of miR-24 coordinately upregulates endothelial cell expression and secretion of von Willebrand factor
    Xiang, Yaozu
    Cheng, Jijun
    Wang, Dandan
    Hu, Xiaoyue
    Xie, Yi
    Stitham, Jeremiah
    Atteya, Gourg
    Du, Jing
    Tang, Wai Ho
    Lee, Seung Hee
    Leslie, Kristen
    Spollett, Geralyn
    Liu, Zejian
    Herzog, Erica
    Herzog, Raimund I.
    Lu, Jun
    Martin, Kathleen A.
    Hwa, John
    [J]. BLOOD, 2015, 125 (22) : 3377 - 3387
  • [36] RETRACTED: The muscle-specific microRNAs miR-1 and miR-133 produce opposing effects on apoptosis by targeting HSP60, HSP70 and caspase-9 in cardiomyocytes (Retracted article. See vol. 124, pg. 3187, 2011)
    Xu, Chaoqian
    Lu, Yanjie
    Pan, Zhenwei
    Chu, Wenfeng
    Luo, Xiaobin
    Lin, Huixian
    Xiao, Jiening
    Shan, Hongli
    Wang, Zhiguo
    Yang, Baofeng
    [J]. JOURNAL OF CELL SCIENCE, 2007, 120 (17) : 3045 - 3052
  • [37] Serum miR-23a, a potential biomarker for diagnosis of pre-diabetes and type 2 diabetes
    Yang, Zhangping
    Chen, Haimin
    Si, Hongqiang
    Li, Xuan
    Ding, Xianfeng
    Sheng, Qing
    Chen, Ping
    Zhang, Hongqiang
    [J]. ACTA DIABETOLOGICA, 2014, 51 (05) : 823 - 831
  • [38] MicroRNAs and regenerative medicine
    Yang, Zhaojuan
    Wu, Ji
    [J]. DNA AND CELL BIOLOGY, 2007, 26 (04) : 257 - 264
  • [39] Plasma MicroRNA Profiling Reveals Loss of Endothelial MiR-126 and Other MicroRNAs in Type 2 Diabetes
    Zampetaki, Anna
    Kiechl, Stefan
    Drozdov, Ignat
    Willeit, Peter
    Mayr, Ursula
    Prokopi, Marianna
    Mayr, Agnes
    Weger, Siegfried
    Oberhollenzer, Friedrich
    Bonora, Enzo
    Shah, Ajay
    Willeit, Johann
    Mayr, Manuel
    [J]. CIRCULATION RESEARCH, 2010, 107 (06) : 810 - U359