Circular RNAs in non-alcoholic fatty liver disease: Functions and clinical significance

被引:6
作者
Zeng, Qingmin [1 ]
Liu, Chang-Hai [1 ]
Ampuero, Javier [2 ]
Wu, Dongbo [1 ,3 ,4 ]
Jiang, Wei [1 ,3 ,4 ]
Zhou, Lingyun [1 ,3 ,4 ]
Li, Hong [1 ,3 ,4 ]
Bai, Lang [1 ,3 ,4 ]
Romero-Gomez, Manuel [2 ]
Tang, Hong [1 ,3 ,4 ]
机构
[1] Sichuan Univ, West China Hosp, Ctr Infect Dis, 37 Guoxue Alley, Chengdu 610041, Peoples R China
[2] Univ Seville, Virgen del Rocio Univ Hosp, Digest Dis Unit, SeLiver Grp,Inst Biomed Seville IBIS HUVRocio,CSI, Seville, Spain
[3] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Div Infect Dis, Chengdu, Peoples R China
[4] Sichuan Univ, West China Hosp, Ctr Infect Dis, Chengdu, Peoples R China
基金
中国国家自然科学基金;
关键词
Nonalcoholic fatty liver disease; circular RNAs; function; sorting mechanism; exosomal circRNA; HEPATOCELLULAR-CARCINOMA; HEPATIC-FIBROSIS; OXIDATIVE STRESS; STEATOHEPATITIS; CIRCRNA; MECHANISMS; PATHOGENESIS; EXOSOMES; PROMOTES; CANCER;
D O I
10.1080/15476286.2023.2290769
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nonalcoholic fatty liver disease (NAFLD), which affects approximately 25% of the global population, is an urgent health issue leading to various metabolic comorbidities. Circular RNAs (circRNAs), covalently closed RNA molecules, are characterized by ubiquity, diversity, stability, and conservatism. Indeed, they participate in various biological processes via distinct mechanisms that could modify the natural history of NAFLD. In this review, we briefly introduce the biogenesis, characteristics, and biological functions of circRNAs. Furthermore, we summarize circRNAs expression profiles in NAFLD by intersecting seven sequencing data sets and describe the cellular roles of circRNAs and their potential advantages as biomarkers of NAFLD. In addition, we emphatically discuss the exosomal non-coding RNA sorting mechanisms and possible functions in recipient cells. Finally, we extensively discuss the potential application of targeting disease-related circRNAs and competing endogenous RNA networks through gain-of-function and loss-of-function approaches in targeted therapy of NAFLD.
引用
收藏
页码:1 / 15
页数:15
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