Objective:To observe the relationship between microRNA-30c(miR-30c) and renal interstitial fibrosis in patients with diabetic nephropathy(DN). Methods:60 patients with Type 2 diabetes(T2DM)and 60 patients with DN were selected in this study, Another 40 healthy people were used as control. The expression of miR-30c was determined by fluorescent quantitative polymerase chain reaction analysis. The TGF-β expression was detected by ELISA analysis. The HA, PC Ⅲ, and Ⅳ-C expression was detected by chemiluminescence analysis.Results: The 2-ΔΔCt values of miR-30c in control group, T2DM group, mild DN group and moderate to severe DN group was 0.62±0.11, 0.47±0.08, 0.32±0.06, and 0.25±0.04. The 2-ΔΔCt values in DN group was lower than that in control and T2DM group(P<0.01), and in moderate to severe DN group was lower than that in mild DN group(P<0.05). The expression of TGF-β, HA, PC Ⅲ, and Ⅳ-C in DN group was higher than that in control and T2DM group(P<0.01), and in moderate to severe DN group was higher than that in mild DN group(P<0.05). The 2-ΔΔCt values of miR-30c was negatively related with TGF-β, HA, PC Ⅲ, and Ⅳ-C expression(P<0.05). ROCanalysis showed that miR-30c expression had predictive value for DN.Conclusion: The low expression of miR-30c is involved in the process of renal interstitial fibrosis in DN. It may be a molecular target for DN diagnosis, disease assessment and clinical treatment. |
[1] GENTIL G,MASTROLUCA D,RUGGENTI P,et al.Novel effective drugs for diabetic kidney disease? or not?[J].Expert Opin Emerg Drugs,2014,7(1):1-31.
[2] LIU B C,TANG T T,LV L L.How tubular epithelial cell injury contributes to renal fibrosis[J].Adv Exp Med Biol,2019,1165(1):233-252.
[3] 秦凤,张惠莉.糖尿病肾病患者外周血微小RNA-21表达与肾间质损伤的关系及意义[J].中国免疫学杂志,2019,35(14):1743-1748.
[4] IRANI S,IQBAL J,ANTONI W J,et al.microRNA-30c reduces plasma cholesterol in homozygous familial hypercholesterolemic and type 2 diabetic mouse models[J].J Lipid Res,2018,59(1):144-154.
[5] 李肖肖.miR-26a和miR-30c在调节TGFβ1诱导的糖尿病肾病上皮-间充质转化中的协同作用[J].中国病理生理杂志,2017,33(05):816.
[6] TERVAERT T W,MOOYARTT A L,AMANN K,et al.Pathologic classification of diabetic nephropathy[J].J Am Soc Nephrol,2010,21(4):556-563.
[7] 纪立农,陈莉明,郭晓蕙,等.中国慢性疾病防治基层医生诊疗手册(糖尿病分册)2015年版[J].中国糖尿病杂志,2015,23(8):673-701.
[8] 敬剑英,喻雪琴,陈芳,等.microRNA在糖尿病肾病发病机制中的研究进展[J].海南医学,2019,30(11):1455-1458.
[9] ZOU Y F,LIAO W T,FU Z J,et al.MicroRNA-30c-5p ameliorates hypoxia-reoxygenation-induced tubular epithelial cell injury via HIF1α stabilization by targeting SOCS3[J].Oncotarget,2017,8(54):92801-92814.
[10] 朱彩凤,陈琪,朱斌,等.MiR-30c-2-3p对足细胞Nephrin、Podocin保护作用及雷公藤甲素干预作用研究[J].中国中西医结合肾病杂志,2016,17(11):952-955.
[11] 庄丽华,胡家才,王道春,等.威草胶囊对尿酸性肾病大鼠肾组织miR-29a和miR-30c的影响和机制[J].现代中西医结合杂志,2017,26(17):1825-1830,1931.
[12] ZHAO Y,YIN Z,LI H,et al.MiR-30c protects diabetic nephropathy by suppressing epithelial-to-mesenchymal transition in db/db mice[J].Aging Cell,2017,16(2):387-400. |