Ferroptosis and its role in cardiomyopathy

Biomedicine & Pharmacotherapy(2022)

引用 27|浏览16
暂无评分
摘要
Heart disease is the leading cause of death worldwide. Cardiomyopathy is a disease characterized by the heart muscle damage, resulting heart in a structurally and functionally change, as well as heart failure and sudden cardiac death. The key pathogenic factor of cardiomyopathy is the loss of cardiomyocytes, but the related molecular mechanisms remain unclear. Ferroptosis is a newly discovered regulated form of cell death, characterized by iron accumulation and lipid peroxidation during cell death. Recent studies have shown that ferroptosis plays an important regulatory roles in the occurrence and development of many heart diseases such as myocardial ischemia/reperfusion injury, cardiomyopathy and heart failure. However, the systemic association of ferroptosis and cardiomyopathy remains largely unknown and needs to be elucidated. In this review, we provide an overview of the molecular mechanisms of ferroptosis and its role in individual cardiomyopathies, highlight that targeting ferroptosis maybe a potential therapeutic strategy for cardiomyopathy therapy in the future.
更多
查看译文
关键词
AA,ABCB7,Acot1,ACR,ACSL4,AdA,Ang II,AHA,AIM2,AKI,AKT,AMI,AMR,APAF1,ARE,ATF3,ATP,Bax,Bcl-2,CaMKII,CAD,CAV,cGAS,CLP,COX2,CREB,CYP,DADs,DAMPs,DCM,DiaCM,Dcytb,DICM,DM,DMT1,DOX,DZX,EMT,Fer-1,FGF2,FOXO,FPN1,FRDA,FTH1,FTL,GPX4,GSH,GSSG,GSTA1,GSTP1,HCECest2,HCM,HIF-1,HMGB1,HMOX1/HO-1,HNC,HUVECs,IBD,ICAM-1,ICM,ICU,IGF1R,IGFBP3,IFN,IHD,IL-1β,INF3,iNOS,IOC,iPSC-CMs,IRI,ISCs,Keap1,LCN-2,LIP,LIP-1,L-OOH,LOX,LPCAT3,LPS,LTCC,LV,LVH,MAPK,MFRN,MI,MMPs,mPTP,MuRF1,mTOR,MYD88,NADPH,NCOA4,NEC-1,NETs,NFS1,NK,NLRP3,NOX4,NQO1,Nrf2,NTBI,OS,Ox-PL,P2RX7,PDGF,PEs,PGD,P-gp,PRDX1,PTCM,PTZ-K,PUFAs,RAS,RCD,Rho/ROCK,RICM,RIHD,RILF,RIPK3,ROS,RT,SIRT1,SCD,SCM,SE-P,SFXN1,SLC3A2,SLC40A1,SLC7A11,STEAP3,STING,SUDEP,T1D,T2DM,TCA,TF,TfR1,TGF-β,TIMPs,TLRs,TN‑I,TNF-α,TRIF,TTCC,TXNRD,TXNIP,VCAM-1,VEGF,WIT
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