Advances in understanding effects of miRNAs on apoptosis, autophagy, and pyroptosis in knee osteoarthritis

被引:6
|
作者
An, Fangyu [1 ]
Sun, Bai [2 ]
Liu, Ying [3 ]
Wang, Chunmei [3 ]
Wang, Xiaxia [2 ]
Wang, Jiayu [2 ]
Liu, Yongqi [3 ]
Yan, Chunlu [2 ,4 ]
机构
[1] Gansu Univ Chinese Med, Teaching Expt Training Ctr, Lanzhou 730000, Gansu, Peoples R China
[2] Gansu Univ Chinese Med, Sch Tradit Chinese & Western Med, Lanzhou 730000, Gansu, Peoples R China
[3] Gansu Univ Chinese Med, Sch Basic Med, Lanzhou 730000, Gansu, Peoples R China
[4] Gansu Univ Chinese Med, Res Ctr Tradit Chinese Med Gansu, Lanzhou 730000, Gansu, Peoples R China
关键词
Knee osteoarthritis; Apoptosis; Autophagy; Pyroptosis; miRNA; PI3K/AKT/MTOR SIGNALING PATHWAY; CHONDROCYTE APOPTOSIS; ALLEVIATES OSTEOARTHRITIS; CARTILAGE DEGRADATION; NONCODING RNA; PROMOTES; PROLIFERATION; DEGENERATION; PROGRESSION; MECHANISM;
D O I
10.1007/s00438-023-02077-3
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
MicroRNAs (miRNAs) are a class of endogenous small non-coding RNAs. MicroRNAs-mediated signaling pathways play a critical regulatory role in inducing apoptosis, autophagy, and pyroptosis in developing knee osteoarthritis (KOA). Given this, we searched databases, such as PubMed, using keywords including "miRNA," "knee osteoarthritis," "apoptosis," "autophagy," "pyroptosis", and their combinations. Through an extensive literature review, we conclude that miRNAs can be modulated through various signaling pathways, such as Wnt/beta-catenin, TGF-beta, PI3K/AKT/mTOR, and NLRP3/Caspase-1, to regulate apoptosis, autophagy, and pyroptosis in KOA. Furthermore, we note that P2X7R and HMGB1 may be crucial regulatory molecules involved in the interconnected regulation of apoptosis, autophagy, and pyroptosis in KOA. Additionally, we describe that miR-140-5p and miR-107 can modulate the advancement of KOA chondrocytes by targeting distinct molecules involved in apoptosis, autophagy, and pyroptosis, respectively. Therefore, we conclude that miRNAs may be potential biomarkers and therapeutic targets for the early prediction, diagnosis, and effective therapeutic approaches of KOA.
引用
收藏
页码:1261 / 1278
页数:18
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