Targeting proteostasis network in osteoporosis: Pathological mechanisms and therapeutic implications

Ageing research reviews(2023)

引用 0|浏览11
暂无评分
摘要
As the most common bone disease, osteoporosis (OP) increases bone fragility and makes patients more vulnerable to the threat of osteoporotic fractures. With the ageing population in today's society, OP has become a huge and growing public health problem. Unfortunately, the clear pathogenesis of OP is still under exploration, and effective interventions are still scarce. Therefore, exploring new targets for pharmacological interventions to develop promising therapeutic drugs for OP is of great clinical value. Previous studies have shown that normal bone remodeling depends on proteostasis, whereas loss of proteostasis during ageing leads to the dysfunctional proteostasis network (PN) that fails to maintain bone homeostasis. Nevertheless, only a few studies have revealed the pathophysiological relationship between bone metabolism and a single component of PN, yet the role of PN as a whole in the pathogenesis of OP is still under investigation. This review comprehensively summarized the role of PN in the pathogenesis of OP and further discussed the potential of PN as innovative drug targets for the therapy of OP.
更多
查看译文
关键词
OP,PN,PQC,UPS,RANK,RANKL,OPG,MSCs,BMSCs,Runx2,Col1α1,OCN,HSR,ER,HSP,DCs,M-CSF,IL-1β,TNF-α,HSCs,TLR2,MyD88,TIR,TIRAP,TRIF,TRAM,MNSFβ,17-AAG,HSF1,MITF,pHSP27,PGF2α,VEGF,ALP,SOST,DKK-1,MMP-2,SDF-1/CXCR4,VCAM-1,PDGF,T3,TBR-II,17-DMAG,ET-1,TRAF6,SQSTM1,DUBs,CYLD,IκB,IKK,NFATc1,CHIP,Cbl,PIs,PSME1/2,CFZ,PTH,HDAC4,Smurf1,Fbw7,SCF,LRP5/6,Dvl,TCF,β-TrCP,VDR,trGli3,CTSK,TRAP,ATGs,MCPIP,ULK1,HIF-1α,BNIP3,MAP1LC3,OVX,KO,CDC42,HDAC9,FIP200,GFP,Pyk2,3-MA,4-PBA,TRiC,Ub,mTORC1,PI3KC3,PI3KC3-CI,BMMs,MECs
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要