MicroRNAs as Biomarkers and Therapeutic Targets for Nonalcoholic Fatty Liver Disease: A Narrative Review

被引:8
|
作者
Sun, Yu [1 ,4 ]
Shen, Yongming [1 ]
Liang, Xiurui [2 ]
Zheng, Huilin [3 ]
Zhang, Yitong [1 ]
机构
[1] Tianjin Univ, Tianjin Childrens Hosp, Childrens Hosp, Dept Clin Lab, 238 Longyan Rd, Tianjin 300134, Peoples R China
[2] Liaoning Univ Tradit Chinese Med, Affiliated Hosp 1, Dept Cardiol, Shenyang, Peoples R China
[3] Zhejiang Univ Sci & Technol, Sch Biol & Chem Engn, Hangzhou, Zhejiang, Peoples R China
[4] Tianjin Childrens Hosp, Clin Lab, Tianjin, Peoples R China
关键词
biomarker; diagnostic; miRNA; nonal-coholic fatty liver disease; therapeutic; DIAGNOSTIC BIOMARKER; STEATOHEPATITIS; EXPRESSION; FIBROSIS; MIR-34A; AGONIST; MIR-122; MICE; PROGRESSION; HEPATOCYTES;
D O I
10.1016/j.clinthera.2023.02.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Purpose: Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in the world. However, biomarkers for NAFLD diagnosis and liver-specific drugs for treatment are lacking. This article reviews the possibility of circulating miRNAs in the diagnosis and treatment of NAFLD diseases and focuses on several well-studied miRNAs to provide preclinical data for subsequent related studies.Methods: Related articles were identified through searches of the PubMed database for literature published from 2010 to December 2022. Search terms included NAFLD, microRNA, biomarker, diagnosis, and therapy.Findings: Current research data indicate that some key circulating miRNAs may be used as diagnostic biomarkers of NAFLD and the combination of several miRNAs improves diagnostic performance. In addition, some preclinical trials using cell and mouse models provide a basis for some miRNAs as potential therapeutic targets. Implications: Current evidence suggests that circu-lating miRNAs are potential noninvasive biomarkers for clinical diagnosis of NAFLD, which needs to be validated in more heterogeneous and larger cohorts. In addition, several miRNAs regulate multiple downstream pathways related to the pathophysiology of NAFLD in a cell-and tissue-specific manner, making them attractive drug therapeutic targets for NAFLD. However, more preclinical and clinical trials are needed for these miRNAs to become therapeutic targets of NAFLD. (Clin Ther. 2023;45:234-247.) (c) 2023 Elsevier Inc.
引用
收藏
页码:234 / 247
页数:14
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