MicroRNAs in diabetic nephropathy: From molecular mechanisms to new therapeutic targets of treatment

被引:26
|
作者
Yarahmadi, Amir [1 ,2 ]
Shahrokhi, Seyedeh Zahra [3 ]
Mostafavi-Pour, Zohreh [4 ]
Azarpira, Negar [2 ]
机构
[1] Mashhad Univ Med Sci, Dept Clin Biochem, Fac Med, Mashhad, Razavi Khorasan, Iran
[2] Shiraz Univ Med Sci, Transplant Res Ctr, Shiraz 713451978, Iran
[3] Shahid Beheshti Univ Med Sci, Dept Lab Med, Sch Allied Med Sci, Tehran, Iran
[4] Shiraz Univ Med Sci, Dept Biochem, Sch Med, Shiraz, Iran
关键词
MicroRNAs; Diabetic nephropathy; End-stage renal disease; Therapeutic targets; TGF-0 signaling pathway; PROMOTES RENAL FIBROSIS; TO-MESENCHYMAL TRANSITION; GROWTH-FACTOR-BETA; UBIQUITIN-PROTEASOME SYSTEM; INDUCED COLLAGEN EXPRESSION; GLUCOSE-INDUCED APOPTOSIS; GLYCATION END-PRODUCTS; TGF-BETA; DOWN-REGULATION; TRANSFORMING GROWTH-FACTOR-BETA-1;
D O I
10.1016/j.bcp.2020.114301
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite considerable investigation in diabetic nephropathy (DN) pathogenesis and possible treatments, current therapies still do not provide competent prevention from disease progression to end-stage renal disease (ESRD) in most patients. Therefore, investigating exact molecular mechanisms and important mediators underlying DN may help design better therapeutic approaches for proper treatment. MicroRNAs (MiRNAs) are a class of small non-coding RNAs that play a crucial role in post-transcriptional regulation of many gene expression within the cells and present an excellent opportunity for new therapeutic approaches because their profile is often changed during many diseases, including DN. This review discusses the most important signaling pathways involved in DN and changes in miRNAs profile in each signaling pathway. We also suggest possible approaches for miRNA derived interventions for designing better treatment of DN.
引用
收藏
页数:12
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