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. 2022 Sep 20;8:394. doi: 10.1038/s41420-022-01183-2

Table 2.

The role of ferroptosis in CVDs.

Disease Factors Mechanism Role Reference
MI miR-23a-3p Inhibit DMT1 expression Inhibit ferroptosis and reduce myocardial injury [47]
BACH1 Adjust the threshold of iron ion induction Inhibit ferroptosis [48]
Reperfusion injury C3G Decreased Fe2+, downregulated TfR1 expression, upregulated Fth1 and GPX4 expression Inhibit ferroptosis and reduce myocardial injury [57]
Res Decreased Fe2+, downregulated TfR1 expression, upregulated Fth1 and GPX4 expression Inhibit ferroptosis and reduce myocardial injury [58]
Lip-1 Reduce VDAC1 level and increase GPX4 level Reduce I/R injury [126]
Eto Induced Nrf2 nuclear translocation Inhibit I/R-induced ferroptosis, improve fibrosis [127]
AS SIRT1 Reduce IL-1β and IL-18 levels Inhibit ferroptosis and limit AS development [64]
PDSS2 Activate Nrf2, inhibit ROS release and reduce iron levels Promote the proliferation of HCAECs and limit AS development [65]
miR-17-92 Targeting zinc lipoprotein A20 reduces Acsl4 expression and ROS accumulation Inhibit ferroptosis [66]
CD98hc Unknown Promote VSMCs proliferation and prevent atherosclerotic thrombosis [34]
Hypertension Monocrotaline (MCT) Activate the the HMGB1/TLR4/NLRP3 inflammatory pathway Promote ferroptosis [73]
Celastrol Increase HO-1 expression and decrease ROS production Reduce inflammation and oxidative stress in VSMCs caused by hypertension [74]
CA Regulate iron metabolism Improve PAH [76]
Elabela Regulate the IL-6/STAT3/GPX4 signalling pathway Inhibit AngII-induced ferroptosis in poor myocardial remodelling, fibrosis and cardiac dysfunction [79]
Myocardial hypertrophy DHA Increase IRF3-SLC7A11, decrease ALOX12 and iron levels Inhibit ferroptosis [128]
miR-351 Regulate the JNK/p53 signalling pathway Inhibit ferroptosis and improve fibrosis [84]
LncRNA AAB Sponge miR-30b-5p, induced imbalance of MMP9/TIMP1 and enhanced TfR-1 Promote ferroptosis [86]
HF CD147 Activate TRAF2-TAK1 signalling pathway Promote cardiac remodelling and dysfunction [91]
TLR4 and NOX4 Unknown Inhibit cardiac autophagy and ferroptosis in HF rats [129]
DCM TRIM46 Promote GPX4 ubiquitination Resist cell damage caused by high glucose [37]
PA Reduce HSF1 and GPX4 Promote ferroptosis and enhance endoplasmic reticulum stress [39]
DIC EMPA Participate in NLRP3- and MYD88-related pathways Inhibit ferroptosis, fibrosis, apoptosis and inflammation [99]
AsIV Activate Nrf2 signalling pathway and increase GPX4 expression Inhibit ferroptosis and improve fibrosis [100]
Sepsis LPS Activate NCOA4 and SFXN1, increase free iron Cause mitochondrial damage and promote ferroptosis [108]
Dexmedetomidine Reduce HO-1 expression, increase GPX4 expression Reduce sepsis-induced myocardial cell damage [107]
Stroke NCOA4 USP14 upregulates NCOA4 through deubiquitination Silencing NCOA4 can eliminate the ferritinophagy induced by I/R injury [102]
CDKN1A C9orf106/C9orf139-miR-22-3p-CDKN1A axes Regulate ferroptosis during IS progression [104]
JUN GAS5-miR-139-5p/miR-429-JUN axes
HIF-1α Inhibits ACSL4 expression in early IS Against ferroptosis [105]