|
|
Research progress on the mechanism of ferroptosis and its application in myocardial ischemia-reperfusion injury |
ZHOU Dongcheng1 YANG Yuhui1 HE Jianfeng1 XIA Zhengyuan2 |
1.The First Clinical Medical College, Guangdong Medical University, Guangdong Province, Zhanjiang 524000, China;
2.Department of Anesthesiology, Affiliated Hospital of Guangdong Medical University, Guangdong Province, Zhanjiang 524000, China
|
|
|
Abstract Ferroptosis is a new type of cell death discovered in recent years, which is usually accompanied by a large amount of iron accumulation and lipid peroxidation during the cell death process. The factors that induce ferroptosis can directly or indirectly affect glutathione peroxidase through different pathways, leading to the decline of cellular antioxidant capacity and the accumulation of lipid reactive oxygen species, and ultimately lead to cellular oxidative death. Studies have shown that ferroptosis is closely related to pathophysiological processes of many diseases, such as tumors and ischemia-reperfusion injury. How to intervene in the occurrence and development of related diseases by regulating cell ferroptosis has become a hotspot and focus of etiological research and treatment, but the functional changes and specific molecular mechanisms of ferroptosis still need to be further explored. This article systematically summarizes the latest progress in the study of ferroptosis, providing reference for further understanding of its pathogenesis, and proposing new targets for treatment of related diseases.
|
|
|
|
|
[1] Dong W,Dong C,Zhu J,et al. HIF-1alpha-induced upregulated miR-322 forms a feedback loop by targeting Smurf2 and Smad7 to activate Smad3/beta-catenin/HIF-1alpha,ther- eby improving myocardial ischemia-reperfusion injury [J]. Cell Biol Int,2023,47(5):894-906
[2] Su RY,Tai WY,Yin HS,et al. miR-432 exerts a protective effect against myocardial ischemia/reperfusion injury by activating the beta-catenin/HIF-1alpha pathway and augmenting NRF2- mediated anti-oxidative stress [J]. Am J Transl Res,2023, 15(1):392-406.
[3] Dixon SJ,Lemberg KM,Lamprecht MR,et al. Ferroptosis:an iron-dependent form of nonapoptotic cell death [J]. Cell,2012,149(5):1060-1072.
[4] Xu S,Wu B,Zhong B,et al. Naringenin alleviates myocardial ischemia/reperfusion injury by regulating the nuclear factor-erythroid factor 2-related factor 2(Nrf2)/System xc-/ glutathione peroxidase 4(GPX4)axis to inhibit ferroptosis [J]. Bioengineered,2021,12(2):10924-10934.
[5] Dolma S,Lessnick SL,Hahn WC,et al. Identification of genotype-selective antitumor agents using synthetic lethal chemical screening in engineered human tumor cells [J]. Cancer Cell,2003,3(3):285-296.
[6] Galluzzi L,Vitale I,Aaronson SA,et al. Molecular mechanisms of cell death:recommendations of the Nomenclature Committee on Cell Death 2018 [J]. Cell Death Differ,2018, 25(3):486-541.
[7] Wu H,Liu Q,Shan X,et al. ATM orchestrates ferritinophagy and ferroptosis by phosphorylating NCOA4 [J]. Autophagy,2023,19(7):2062-2077.
[8] Liu X,Qi K,Gong Y,et al. Ferulic Acid Alleviates Myocardial Ischemia Reperfusion Injury Via Upregulating AMPKalpha2 Expression-Mediated Ferroptosis Depression [J]. J Cardiovasc Pharmacol,2021,79(4):489-500.
[9] Ding Y,Li W,Peng S,et al. Puerarin Protects against Myocardial Ischemia/Reperfusion Injury by Inhibiting Ferroptosis [J]. Biol Pharm Bull,2023,46(4):524-532.
[10] Wu ZF,Yan BJ,Luo W,et al. Ferroptosis and Hydrogen Sulfide in Cardiovascular Disease [J]. Curr Med Chem,2023, 30(16):1848-1859.
[11] Miyamoto HD,Ikeda M,Ide T,et al. Iron Overload via Heme Degradation in the Endoplasmic Reticulum Triggers Ferroptosis in Myocardial Ischemia-Reperfusion Injury [J]. JACC Basic Transl Sci,2022,7(8):800-819.
[12] Wang IC,Lin JH,Lee WS,et al. Baicalein and luteolin inhibit ischemia/reperfusion-induced ferroptosis in rat cardiomyocytes [J]. Int J Cardiol,2023,375:74-86.
[13] Yang WS,Kim KJ,Gaschler MM,et al. Peroxidation of poly- unsaturated fatty acids by lipoxygenases drives ferroptosis [J]. Proc Natl Acad Sci U S A,2016,113(34):E4966- E4975.
[14] Yu P,Zhang J,Ding Y,et al. Dexmedetomidine post-conditioning alleviates myocardial ischemia-reperfusion injury in rats by ferroptosis inhibition via SLC7A11/GPX4 axis activation [J]. Hum Cell,2022,35(3):836-848.
[15] Tian H,Xiong Y,Zhang Y,et al. Activation of NRF2/FPN1 pathway attenuates myocardial ischemia-reperfusion injury in diabetic rats by regulating iron homeostasis and ferroptosis [J]. Cell Stress Chaperones,2021,27(2):149-164.
[16] Ursini F,Maiorino M. Lipid peroxidation and ferroptosis:The role of GSH and GPx4 [J]. Free Radic Biol Med,2020, 152:175-185.
[17] Lv Z,Wang F,Zhang X,et al. Etomidate Attenuates the Ferroptosis in Myocardial Ischemia/Reperfusion Rat Model via Nrf2/HO-1 Pathway [J]. Shock,2021,56(3):440-449.
[18] Wang X,Chen X,Zhou W,et al. Ferroptosis is essential for diabetic cardiomyopathy and is prevented by sulforaphane via AMPK/NRF2 pathways [J]. Acta Pharm Sin B,2022,12(2):708-722.
[19] Qian W,Liu D,Han Y,et al. Cyclosporine A-loaded apoferritin alleviates myocardial ischemia-reperfusion injury by simultaneously blocking ferroptosis and apoptosis of cardiomyocytes [J]. Acta Biomater,2023,160:265-280.
[20] Li C,Wang T,Xiao Y,et al. COMMD1 upregulation is involved in copper efflux from ischemic hearts [J]. Exp Biol Med (Maywood),2021,246(5):607-616.
[21] Baba Y,Higa JK,Shimada BK,et al. Protective effects of the mechanistic target of rapamycin against excess iron and ferroptosis in cardiomyocytes [J]. Am J Physiol Heart Circ Physiol,2018,314(3):H659-H668.
[22] Yue H,Zhan Y,Zhang Z,et al. The emerging role of ferroptosis in myocardial fibrosis of atrial fibrillation [J]. Arch Med Sci,2023,19(2):507-512.
[23] Shen H,Xie K,Tian Y,et al. N6-methyladenosine writer METTL3 accelerates the sepsis-induced myocardial injury by regulating m6A-dependent ferroptosis [J]. Apoptosis,2023,28(3/4):514-524.
[24] Zou HX,Hu T,Zhao JY,et al. Exploring Dysregulated Ferroptosis-Related Genes in Septic Myocardial Injury Based on Human Heart Transcriptomes:Evidence and New Insights [J]. J Inflamm Res,2023,16:995-1015.
[25] Chopra VK,Anker SD. Anaemia,iron deficiency and heart failure in 2020:facts and numbers [J]. ESC Heart Fail,2020, 7(5):2007-2011.
[26] Rush CJ,Berry C,Oldroyd KG,et al. Prevalence of Coronary Artery Disease and Coronary Microvascular Dysfunction in Patients With Heart Failure With Preserved Ejection Fraction [J]. JAMA Cardiol,2021,6(10):1130-1143.
[27] Cao Y,Luo F,Peng J,et al. KMT2B-dependent RFK transcription activates the TNF-alpha/NOX2 pathway and enhances ferroptosis caused by myocardial ischemia-reperfusion [J]. J Mol Cell Cardiol,2022,173:75-91.
[28] Han X,Zhang J,Liu J,et al. Targeting ferroptosis:a novel insight against myocardial infarction and ischemia-reperfusion injuries [J]. Apoptosis,2023,28(1/2):108-123.
[29] Sheng H,Xiong J,Yang D. Protective Effect of Sevoflurane Preconditioning on Cardiomyocytes Against Hypoxia/Reoxygenation Injury by Modulating Iron Homeostasis and Ferroptosis [J]. Cardiovasc Toxicol,2023,23(2):86-92.
[30] Mei SL,Xia ZY,Qiu Z,et al. Shenmai Injection Attenuates Myocardial Ischemia/Reperfusion Injury by Targeting Nrf2/ GPX4 Signalling-Mediated Ferroptosis [J]. Chin J Integr Med,2022,28(11):983-991.
[31] Li W,Li W,Leng Y,et al. Ferroptosis Is Involved in Diabetes Myocardial Ischemia/Reperfusion Injury Through Endoplasmic Reticulum Stress [J]. DNA Cell Biol,2020,39(2):210-225.
[32] Chen QM. Nrf2 for protection against oxidant generation and mitochondrial damage in cardiac injury [J]. Free Radic Biol Med,2022,179:133-143
[33] Wang C,Zhu L,Yuan W,et al. Diabetes aggravates myocardial ischaemia reperfusion injury via activating Nox2- related programmed cell death in an AMPK-dependent manner [J]. J Cell Mol Med,2020,24(12):6670-6679.
[34] Wang C,Yuan W,Hu A,et al. Dexmedetomidine alleviated sepsis-induced myocardial ferroptosis and septic heart injury [J]. Mol Med Rep,2020,22(1):175-184. |
|
|
|