Non-Coding RNAs as Biomarkers and Therapeutic Targets for Diabetic Kidney Disease.

作者信息

Gu Yue-Yu, Lu Fu-Hua, Huang Xiao-Ru, Zhang Lei, Mao Wei, Yu Xue-Qing, Liu Xu-Sheng, Lan Hui-Yao

机构信息

Department of Nephrology and State Key Laboratory of Dampness Syndrome of Chinese Medicine, Guangdong Provincial Hospital of Chinese Medicine, The Second Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou, China.

Department of Medicine and Therapeutics, Li Ka Shing Institute of Health Sciences, The Chinese University of Hong Kong, Hong Kong, China.

出版信息

Front Pharmacol. 2021 Jan 26;11:583528. doi: 10.3389/fphar.2020.583528. eCollection 2020.

Abstract

Diabetic kidney disease (DKD) is the most common diabetic complication and is a leading cause of end-stage kidney disease. Increasing evidence shows that DKD is regulated not only by many classical signaling pathways but also by epigenetic mechanisms involving chromatin histone modifications, DNA methylation, and non-coding RNA (ncRNAs). In this review, we focus on our current understanding of the role and mechanisms of ncRNAs, including microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) in the pathogenesis of DKD. Of them, the regulatory role of TGF-β/Smad3-dependent miRNAs and lncRNAs in DKD is highlighted. Importantly, miRNAs and lncRNAs as biomarkers and therapeutic targets for DKD are also described, and the perspective of ncRNAs as a novel therapeutic approach for combating diabetic nephropathy is also discussed.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1b2/7870688/24af2b302e87/fphar-11-583528-g001.jpg

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