The emerging role of ferroptosis in inflammation

Ferroptosis: An Iron-Dependent Form of Nonapoptotic Cell Death

Dixon, S. J., Lemberg, K. M., Lamprecht, M. R., Skouta, R., Zaitsev, E. M., Gleason, C. E., Patel, D. N., Bauer, A. J., Cantley, A. M., Yang, W. S., et al. (2012) · Cell · doi:10.1016/j.cell.2012.03.042 · Cited by 18,691

Regulation of Ferroptotic Cancer Cell Death by GPX4

Yang, W. S., SriRamaratnam, R., Welsch, M. E., Shimada, K., Skouta, R., Viswanathan, V. S., Cheah, J. H., Clemons, P. A., Shamji, A. F., Clish, C. B., et al. (2014) · Cell · doi:10.1016/j.cell.2013.12.010 · Cited by 7,713

Ferroptosis: A Regulated Cell Death Nexus Linking Metabolism, Redox Biology, and Disease

Stockwell, B. R., Friedmann Angeli, J. P., Bayir, H., Bush, A. I., Conrad, M., Dixon, S. J., Fulda, S., Gascón, S., Hatzios, S. K., Kagan, V. E., et al. (2017) · Cell · doi:10.1016/j.cell.2017.09.021 · Cited by 7,695

ACSL4 dictates ferroptosis sensitivity by shaping cellular lipid composition

Doll, S., Proneth, B., Tyurina, Y. Y., Panzilius, E., Kobayashi, S., Ingold, I., Irmler, M., Beckers, J., Aichler, M., Walch, A., et al. (2017) · Nature Chemical Biology · doi:10.1038/nchembio.2239 · Cited by 4,293

Inactivation of the ferroptosis regulator Gpx4 triggers acute renal failure in mice

Friedmann Angeli, J. P., Schneider, M., Proneth, B., Tyurina, Y. Y., Tyurin, V. A., Hammond, V. J., Herbach, N., Aichler, M., Walch, A., Eggenhofer, E., et al. (2014) · Nature Cell Biology · doi:10.1038/ncb3064 · Cited by 3,732

The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis

Bersuker, K., Hendricks, J. M., Li, Z., Magtanong, L., Ford, B., Tang, P. H., Roberts, M. A., Tong, B., Maimone, T. J., Zoncu, R., et al. (2019) · Nature · doi:10.1038/s41586-019-1705-2 · Cited by 3,703

Caspase-11 cleaves gasdermin D for non-canonical inflammasome signalling

Kayagaki, N., Stowe, I. B., Lee, B. L., O’Rourke, K., Anderson, K., Warming, S., Cuellar, T., Haley, B., Roose-Girma, M., Phung, Q. T., et al. (2015) · Nature · doi:10.1038/nature15541 · Cited by 3,686

FSP1 is a glutathione-independent ferroptosis suppressor

Doll, S., Freitas, F. P., Shah, R., Aldrovandi, M., da Silva, M. C., Ingold, I., Goya Grocin, A., Xavier da Silva, T. N., Panzilius, E., Scheel, C. H., et al. (2019) · Nature · doi:10.1038/s41586-019-1707-0 · Cited by 3,341

Chemotherapy drugs induce pyroptosis through caspase-3 cleavage of a gasdermin

Wang, Y., Gao, W., Shi, X., Ding, J., Liu, W., He, H., Wang, K., & Shao, F. (2017) · Nature · doi:10.1038/nature22393 · Cited by 3,199

Oxidized arachidonic and adrenic PEs navigate cells to ferroptosis

Kagan, V. E., Mao, G., Qu, F., Angeli, J. P. F., Doll, S., Croix, C. S., Dar, H. H., Liu, B., Tyurin, V. A., Ritov, V. B., et al. (2017) · Nature Chemical Biology · doi:10.1038/nchembio.2238 · Cited by 3,029

SAT1 promotes the progression of OA by regulating TRIM33-mediated p53 acetylation to enhance ferroptosis

Yang, J., Jiang, J., Wang, J., & Luo, L. (2025) · PLoS ONE · doi:10.1371/journal.pone.0332761 · Cited by 5

Sestrin2 Exerts a Novel Protective Effect Against LPS ‐Induced Ferroptosis via the Nrf2– SLC7A11 – GPX4 Signaling Axis

Zhang, X., Yin, J., Yang, Y., Peng, J., Xu, Y., Zhang, W., Xiao, H., Lu, Z., Liu, H., Wen, Y., et al. (2025) · The FASEB Journal · doi:10.1096/fj.202501348rrr · Cited by 5

The dual roles of ferroptosis in digestive tract tumors: mechanisms, microenvironment regulation, and therapeutic integration with emphasis on immune interactions

Guo, J., Wang, Z., Zhang, Y., Xie, C., Chen, Y., Ma, L., Guo, Z., & Zhang, C. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1737847 · Cited by 5

Ferroptosis in microglial activation: a systematic review and multidata comparison

Pesämaa, I., Koutarapu, S., Zetterberg, H., & Fruhwürth, S. (2026) · Brain Communications · doi:10.1093/braincomms/fcag109 · Cited by 6

Bioinformatics analysis of signature genes related to cell death in keratoconus

Liu, J., Gao, J., Xing, S., Yan, Y., Yan, X., Jing, Y., & Li, X. (2024) · Scientific Reports · doi:10.1038/s41598-024-63109-5 · Cited by 5

An Overview on Immunity Booster Foods in Coronavirus Disease (COVID-19)

Sahiba, N., Sethiya, A., Agarwal, D. K., & Agarwal, S. (2022) · Combinatorial Chemistry & High Throughput Screening · doi:10.2174/1386207325666220629161828 · Cited by 6

Early increase of serum ferritin among COVID-19 patients is associated with need of invasive mechanical ventilation and with in-hospital death

Ramonfaur, D., Aguirre-García, G. M., Díaz-Garza, C. A., Torre‐Amione, G., Nava, V. M. S., Lara-Medrano, R., Ramírez-Elizondo, M. T., Esparza-Sandoval, A. C., Ortega-Hernández, F. J., & Martínez‐Reséndez, M. F. (2022) · Scandinavian Journal of Infectious Diseases · doi:10.1080/23744235.2022.2101691 · Cited by 5

Construction of mPEI/pGPX4 gene therapeutic system for the effective treatment of acute lung injury

Wan, Y.-H., Huan, M., Yun, C.-X., Han, T., Zhou, S., Song, X., & Zhang, B. (2023) · Nanotechnology · doi:10.1088/1361-6528/acd198 · Cited by 5

Ferrous Ion Alleviates Lipid Deposition and Inflammatory Responses Caused by a High Cottonseed Meal Diet by Modulating Hepatic Iron Transport Homeostasis and Controlling Ferroptosis in Juvenile Ctenopharyngodon idellus

Liu, H., Chen, S., Lin, Y., Jiang, W. J., Zhao, Y., Lu, S., Miao, L., & Ge, X. (2023) · Antioxidants · doi:10.3390/antiox12111968 · Cited by 5

Unique lipid composition maintained by extracellular blockade leads to prooncogenicity

Kudo, K., Yanagiya, R., Hasegawa, M., Carreras, J., Miki, Y., Nakayama, S., Nagashima, E., Miyatake, Y., Torii, K., Ando, K., et al. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-01971-y · Cited by 5

Alpha-lipoic acid upregulates the PPARγ/NRF2/GPX4 signal pathway to inhibit ferroptosis in the pathogenesis of unexplained recurrent pregnancy loss

Zhao, Y., Zhao, X., & Feng, X. (2024) · Open Medicine · doi:10.1515/med-2024-0963 · Cited by 5

Unveiling the protective role of sevoflurane in video-assisted thoracoscopic surgery associated-acute lung injury: Inhibition of ferroptosis

Zhang, Y., Zha, T., Song, G., Abudurousuli, G., Che, J., Zhao, F., Zhang, L., Zhang, X., Gui, B., & Zhu, L. (2024) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2024.102312 · Cited by 5

Brozopine ameliorates cognitive impairment via upregulating Nrf2, antioxidation and anti-inflammation activities

Fu, Z., Wang, X., Fan, Y., Shang, D., Zhang, J., Xiao, T., Guo, J., Wang, Y., Wang, Z., Zhang, Z., et al. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1428455 · Cited by 5

Injectable thermosensitive hydrogel system based on hyaluronic acid and methylcellulose for the synergistic therapy of traumatic spinal cord injury

Zhao, J., Wang, W., Zhao, Y., Hou, L., Zhang, Y., Cai, Z., Guan, Y., Wang, J., & Zhang, B. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.144629 · Cited by 4

CuATSM Enhances Wound Repair Without Scarring via Hippo/ YAP Signalling Pathway to Reduce Ferroptosis and Macrophage Polarisation

Tang, Y., Ye, J., Xu, T., Sun, Y., Meng, W., Zhu, L., Jia, Z., Wu, Q., Chen, D., & Wu, F. (2025) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.70590 · Cited by 5

Epigenetics and Herbs: Potential Therapeutic Strategies for Osteoarthritis of the Knee

Zheng, Y., Wang, J., Wang, L., Zheng, Y., & Qi, W. (2025) · Journal of Pain Research · doi:10.2147/jpr.s517224 · Cited by 4

Advances in Ferroptosis in Chronic Inflammatory Diseases of the Upper and Lower Airways

Li, J., Li, J., Gao, Y., Zhang, L., & Zhang, Y. (2025) · International Archives of Allergy and Immunology · doi:10.1159/000547363 · Cited by 4

Mechanistic and therapeutic insights into the function of different cell death modalities in rheumatoid arthritis: emphasis on the crosstalk with non-coding RNAs

Wen, J., Liu, J., Wan, L., & Wang, F. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1620209 · Cited by 4

Targeting ferroptosis and ferritinophagy improves tooth extraction socket healing in type 2 diabetes mellitus via human bone marrow mesenchymal stem cells modulation

Bian, Y., Li, J., Yu, Y., Yu, Y., Guo, F., Cheng, Z., Chen, Z., Qin, R., Yuan, H., Wang, Y., et al. (2025) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2025.10.010 · Cited by 4

A review: Bacterial hemolysin-mediated iron dysregulation and immune cell damage synergistically drive ferroptosis

Wang, J., Jiang, Q., Wu, S., Fan, W., Peng, K., Zhou, K., Xu, L., Chen, D., Huang, X., Ouyang, P., et al. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.108130 · Cited by 4

Programmed cell death of keratinocytes: an active driver in psoriasis

Yuwen, T., Tian, J., Chen, Y., Zhou, Z., Lian, N., & Chen, X. (2026) · APOPTOSIS · doi:10.1007/s10495-025-02207-9 · Cited by 4

Yangjing Zhongyu decoction ameliorates polycystic ovary syndrome via multi-organ ferroptosis inhibition: A mechanistic study

Lu, L., Huang, X., Zhou, Y., Zhao, Y., Zou, Y., Huang, W., Ma, H., & Hu, M. (2026) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2026.121186 · Cited by 4

Integrated bioinformatic analysis reveals NOS2 as a novel ferroptosis-related biomarker for pre-eclampsia

Cai, S., Huang, S., Zhang, W., Xiao, H., Yu, D., Zhong, X., Tao, P., & Luo, Y. (2023) · BMC Pregnancy and Childbirth · doi:10.1186/s12884-023-06051-0 · Cited by 4

Effect of 2 weeks rest-pause on oxidative stress and inflammation in female basketball players

Cichoń-Woźniak, J., Ostapiuk–Karolczuk, J., Cieślicka, M., Dziewiecka, H., Basta, P., Maciejewski, D., & Skarpańska-Stejnborn, A. (2024) · Scientific Reports · doi:10.1038/s41598-024-65309-5 · Cited by 4

IL6ST: A Novel Therapeutic Target for Managing and Treating Colorectal Cancer Via Ferroptosis

Zhao, K., He, B., Xue, K., Cao, B., Ren, K., Jin, Y., Rong, S., Wei, L.-Z., & Wei, H. (2024) · The Turkish Journal of Gastroenterology · doi:10.5152/tjg.2024.23353 · Cited by 4

Comprehensive review of perioperative factors influencing ferroptosis

Fan, C.-H., Zeng, X., Feng, R.-M., Yi, H.-W., & Xia, R. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.117375 · Cited by 4

Influence of Mesalazine on Ferroptosis-Related Gene Expression in In Vitro Colorectal Cancer Culture

Słoka, J., Strzałka‐Mrozik, B., Kubica, S., Nowak, I., & Kruszniewska‐Rajs, C. (2025) · Biomedicines · doi:10.3390/biomedicines13010219 · Cited by 4

NSUN2 inhibits NCOA4 expression to alleviate ferroptosis and inflammation in sepsis-induced myocardial injury in a m5C manner

Bayinchahan, B., Lv, X., & Xiao, D. (2025) · Journal of Cardiothoracic Surgery · doi:10.1186/s13019-025-03554-z · Cited by 4

Isolation of phytochemicals and exploration the mechanism of Dolichandrone spathacea in the treatment of chronic bronchitis by integrating network pharmacology, molecular docking, and experimental validation

Nguyen, D.-K., Liu, T.-W., Chu, M.-H., Huynh, Q.-D. T., Duong, T.-L. T., Phan, T.-T. T., Huynh, D. T. M., Wang, Y., Wang, S., Hsu, S.-J., et al. (2025) · Botanical studies · doi:10.1186/s40529-025-00464-0 · Cited by 4

Ferroptosis: Oxidative stress and pathophysiology

Ahsan, H., Hasan, M. Y., & Ahmad, R. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-90905-1.00002-x · Cited by 4

α-Solanine induces ferroptosis in nasopharyngeal carcinoma via targeting HSP90α/p53 axis

Cui, X., Gong, Y., Ge, J., Feng, X., Xiong, X., Shi, Z., Zheng, Q., Li, D., & Bi, S. (2023) · Journal of Functional Foods · doi:10.1016/j.jff.2023.105517 · Cited by 5

Role of epinephrine in attenuating cytokine storm, decreasing ferritin, and inhibiting ferroptosis in SARS-CoV-2

EL-Molla, A. M., Fetouh, F. A., Bawazir, S. M., Ali, Y., Alwahby, Y. A., Bahadeg, M., Gotah, Y., Badahdah, F. A., Alsaeed, A. H., & Basseet, A. A. (2024) · The Egyptian Heart Journal · doi:10.1186/s43044-024-00455-9 · Cited by 4

Mitochondria-localizing triphenylphosphine-8-hydroxyquinoline Ru complexes induce ferroptosis and their antitumor evaluation

Meng, T., Xu, Z., Wang, H., Huang, J. L., Wen, J.-L., Huang, M.-P., Zhou, C.-Y., & Zhong, J.-P. (2024) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2024.112585 · Cited by 4

MiR-224-3p regulates ferroptosis and inflammation in lens epithelial cells by targeting ACSL4

Sun, F., Li, N., Liu, Y., Han, Y., Che, X., Che, X., Li, J., & Wang, J. (2025) · Experimental Eye Research · doi:10.1016/j.exer.2025.110306 · Cited by 4

Salidroside attenuates sepsis-induced acute kidney injury by inhibiting ferroptosis

Zhen, L., Hou, M.-T., & Wang, S. (2025) · Journal of Asian Natural Products Research · doi:10.1080/10286020.2025.2481291 · Cited by 4

Palygorskite-based antibacterial composites induced intracellular S. aureus ferroptosis through SSTR2

Wang, L., Li, G., Hui, A., Li, Y., Leng, W., Cui, H., & Liu, X. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.143897 · Cited by 4

COVID-19 and Iron Metabolism: Traditional Review

Yılmaz, N., Eren, E., ÖZ, C., Kalayci, Z., & Saribek, F. (2021) · Turkiye Klinikleri Journal of Medical Sciences · doi:10.5336/medsci.2021-81574 · Cited by 4

Ferroptosis in the pathogenesis of brain tumors

Nikolaev, A. A., & Викторович, Б. В. (2022) · Journal of clinical practice · doi:10.17816/clinpract114787 · Cited by 4

Identification of ferroptosis-related genes and predicted overall survival in patients with burns

Zhao, M., Zhang, Y., & Zhao, H. (2023) · Frontiers in Surgery · doi:10.3389/fsurg.2022.1060036 · Cited by 4

The Biological Processes of Ferroptosis Involved in Pathogenesis of COVID-19 and Core Ferroptoic Genes Related With the Occurrence and Severity of This Disease

Zhang, Z., Pang, T., Qi, M., & Sun, G. (2023) · Evolutionary Bioinformatics · doi:10.1177/11769343231153293 · Cited by 4

Hepcidin expression in the trigeminal ganglion and the oral mucosa in an oral ulcerative mucositis rat model

Hitomi, S., Nodai, T., Kokabu, S., Shikayama, T., Sago-Ito, M., Nakatomi, C., Terawaki, K., Omiya, Y., Shinoda, M., & Ono, K. (2023) · PLoS ONE · doi:10.1371/journal.pone.0284617 · Cited by 4

1,2‐Dioxetane‐based Chemiluminescence Probes for Tumor Optical Molecular Imaging

Zhou, B., Xian, M., Lu, Y., Tang, W., & Zhou, J. (2023) · ChemistrySelect · doi:10.1002/slct.202301826 · Cited by 4

Construction of a ferroptosis and hypoxia-related gene signature in cervical cancer to assess tumour immune microenvironment and predict prognosis

Wu, H., Fan, Y., Bao, Y., Zhou, Q., Xu, L., & Xu, Y. (2024) · Journal of Obstetrics and Gynaecology · doi:10.1080/01443615.2024.2321323 · Cited by 4

Screening strategy identified idebenone loaded ROS-responsive nano-polyphenolic vesicle for spinal cord injury therapy

Wu, C., Chen, X., Zhao, X., Chen, Y., Zhou, H., Deng, Y., Li, C., Huang, Y., Gao, W., Zhang, D., et al. (2024) · Materials & Design · doi:10.1016/j.matdes.2024.112972 · Cited by 4

New insights into ovarian regression-related mitochondrial dysfunction in the late-laying period

Gu, T., Liu, J., Zeng, T., Chen, L., Tian, Y., Xu, W., & Lu, L. (2025) · Poultry Science · doi:10.1016/j.psj.2025.104938 · Cited by 4

Ferroptosis and cellular senescence -Related Genes in Cervical Cancer: Mechanistic Insights from Multi-Omics and Clinical Sample Analysis

Luo, Y., Tang, L., Zeng, Z., Trang, D., Mo, D., & Yang, Y. (2025) · Translational Oncology · doi:10.1016/j.tranon.2025.102487 · Cited by 3

Assessing the Function of Porcine A Kinase-Interacting Protein 1 (AKIP1) In Vitro—A Central Regulator of Oxidative Stress and Mitochondrial Functions

Bak, A., Hinrichs, A., Schwaiger, A., Fromme, T., Fischer, A., Kurome, M., Zakhartchenko, V., Keßler, B., Klingenspor, M., Wolf, E., et al. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26167759 · Cited by 3

A Novel Peculiarity of TXNIP Reversing the Radioresistance of NPC and Inducing Ferroptosis by xCT ‐ GSH ‐ GPX4 ‐ ROS Axis

Zhou, J. L., Zhou, Q., Mo, Y., Zhang, H., Dang, R., Lin, M., Xiao, R., Chen, Y., Deng, X., Wang, S., et al. (2025) · Head & Neck · doi:10.1002/hed.70004 · Cited by 3

The protective effect and mechanism of dexmedetomidine in inhibiting ferroptosis

Ren, X., & Wang, R. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1605363 · Cited by 3

Brucine Inhibits Gastric Cancer via Activation of Ferroptosis Through Regulating the NF‐κB Signaling Pathway

Zhang, B., Yu, C., Zhang, S., & Zhang, M. (2025) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70479 · Cited by 3

High‐intensity interval training attenuates cardiac injury by targeting ferroptosis and endoplasmic reticulum‐stress in male rats with heart failure

Sabouri, A., Gaeini, A. A., Adeli, S., & Afousi, A. G. (2025) · Physiological Reports · doi:10.14814/phy2.70580 · Cited by 3

Sodium acetate and sodium butyrate ameliorate postoperative cognitive dysfunction in aged rats by suppressing inflammation and ferroptosis via inhibition of the cGAS-STING signaling pathway

Zeng, K.-H., Yu, L.-P., Chen, Z., & Li, X. (2025) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2025.111677 · Cited by 3

Ruminal microbial dysbiosis induces the development of gastrointestinal inflammation through the activation of ferritinophagy–ferroptosis via the NOCA4/FTH pathway

Peng, C., Xie, H., Su, N., He, Y., Yuan, C., Zhao, C., Zhang, W., Liu, B., Zhang, S., Fu, Y., et al. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.115816 · Cited by 4

Crosstalk between ferroptosis and extracellular vesicles in cancer: from interaction to clinical application

Liu, J., Wang, K., Hao, Z., Fan, Q., Ma, S., & Xu, L. (2026) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00736-2 · Cited by 3

Ferroptosis-Centered Mitochondria–ROS Loop Drives PFOS-Induced Renal Dysfunction, from Epidemiological Evidence to Mechanistic Insights with Mice Model

Lin, D., Liu, T., Hang, X., Yu, X., Liu, X., Xu, Y., Gui, Z., Liu, J., Kuang, Z., Li, T., et al. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c14271 · Cited by 3

JAK2/STAT3-dependent regulation of MDM4/MDM2-p53 signaling in methotrexate-induced ferroptosis and nephrotoxicity

Cheng, Y., Zhao, M., Zhang, Y., Liu, M., & Zhao, L. (2026) · Archives of Pharmacal Research · doi:10.1007/s12272-026-01599-9 · Cited by 3

Scutellarein Attenuates Intervertebral Disc Degeneration by Promoting PINK1 /Parkin‐Mediated Mitophagy to Alleviate Inflammation, Ferroptosis, and Mitochondrial Dysfunction in Nucleus Pulposus Cells

Liu, S., Zhao, J., Dong, S., Zhang, Y., Zhao, Y., Ran, N., Yang, G., Peng, C., Yang, X., Song, G., et al. (2026) · Phytotherapy Research · doi:10.1002/ptr.70291 · Cited by 3

Ethanolamine phosphate phospholyase drives non-alcoholic fatty liver disease via hepatocyte ferroptosis and ferroptosis-mediated macrophage reprogramming.

Gui, R.-L., Li, Y., Zhang, L., Jin, J., Shi, Y.-Q., Wang, J.-X., Guo, J., Qian, L., & Xiong, Y.-Y. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.151608 · Cited by 3

Mechanistic Networks, Cellular Specificity, and Therapeutic Opportunities of Ferroptosis in Ulcerative Colitis

Yi, J.-L., Zhu, J.-X., Huang, W.-F., & Yi, L. (2026) · Pharmaceuticals · doi:10.3390/ph19060858 · Cited by 3

The role of ferroptosis in the side effects of dexamethasone

Zhao, H., & Shang, H. (2022) · All Life · doi:10.1080/26895293.2022.2156623 · Cited by 3

Single-cell transcriptomes reveal heterogeneity of chlorine-induced mice acute lung injury and the inhibitory effect of pentoxifylline on ferroptosis

Zhao, C.-Q., Wang, C., Liu, M.-M., Cao, M., Peng, J., Kong, D., Ren, X.-T., Liu, R., Hai, C., & Zhang, X.-D. (2023) · Scientific Reports · doi:10.1038/s41598-023-32093-7 · Cited by 3

Recent Advances in the Nutritional Value, Chemical Compositions, Pharmacological Activity, and Application Value of Orychophragmus violaceus: A Comprehensive Review

Chen, X., Zhang, G., Cui, W., Ge, C., Li, B., Li, M., Liu, S., & wang, L. (2024) · Molecules · doi:10.3390/molecules29061314 · Cited by 4

Integrated bioinformatics and validation reveal PTGS2 and its related molecules to alleviate TNF-α-induced endothelial senescence

Xu, H., Wang, H., Ning, X., Xu, Z., & Zhang, G. (2024) · In Vitro Cellular & Developmental Biology - Animal · doi:10.1007/s11626-024-00931-1 · Cited by 3

Hub genes identification and validation of ferroptosis in SARS-CoV-2 induced ARDS: perspective from transcriptome analysis

Li, Y., Tang, L., Wang, F., Gao, C., Yang, Q., Luo, L., Wei, J., Tang, Q., & Qi, M. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1407924 · Cited by 3

Experimental Evidence of the Benefits of Acupuncture/ Electroacupuncture for Acute Lung Injury/ Acute Respiratory Distress Syndrome: A Literature Review of Rodent Studies

Zeng, L., & Yan, J. (2025) · Current Molecular Medicine · doi:10.2174/0115665240334516241123130753 · Cited by 3

Mapping oxylipin signatures in human diseases using LC-MS/MS

Diniz, L. R., Santos, R. S., Oreliana, H., Zucão, A. C. A., Yukuyama, M. N., Resende, G. R. S., Iijima, T. S., Viviani, L. G., & Miyamoto, S. (2025) · Redox Biochemistry and Chemistry · doi:10.1016/j.rbc.2025.100063 · Cited by 3

HP1 induces ferroptosis of renal tubular epithelial cells through NRF2 pathway in diabetic nephropathy

Zhou, C., Wu, M. Y., Liu, G., & Zhou, L. (2023) · Open Life Sciences · doi:10.1515/biol-2022-0678 · Cited by 3

Extracellular Vesicles and Vascular Inflammation

Yu, P., Deng, S., Yuan, X., Pan, J., & Xu, J. (2023) · Advances in experimental medicine and biology · doi:10.1007/978-981-99-1443-2_7 · Cited by 3

Anti‐Inflammatory Phomalones from the Deep‐Sea‐Derived Fungus Trichobotrys effuse FS522

Huang, H., Chen, Y., Wen, T., Li, S., Liu, Z., Zhang, W., & Gao, X. (2023) · Chemistry & Biodiversity · doi:10.1002/cbdv.202301512 · Cited by 3

Apoptosis and inflammatory forms of cell death

Elkon, K. B., & Oberst, A. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-93232-5.00027-7 · Cited by 3

In vitro assessment of ferroptosis of cells exposed to cigarette smoke aerosol using a self-designed on-chip evaluation system based on gas–liquid dual-dimensional exposure

Li, Z., Li, X., Li, X., Zhao, J., Shang, P., Hua, C., Guo, J., Xie, F., & Xie, J. (2024) · Talanta · doi:10.1016/j.talanta.2024.126352 · Cited by 3

LINC01004/hsa-mir-125b-2-3p axis restrains ferroptosis in hepatocellular carcinoma by targeting HSPA4 via ceRNA mechanism

Gao, H., Fan, L., Gai, X., Fu, R., Li, G., Jing, K., Xu, J., & Sun, S. (2024) · Technology and Health Care · doi:10.1177/09287329241291430 · Cited by 3

Potential Metabolic Markers in the Tongue Coating of Chronic Gastritis Patients for Distinguishing Between Cold Dampness Pattern and Damp Heat Pattern in Traditional Chinese Medicine Diagnosis

Yuan, S., Zhang, R., Zhu, Z., Zhou, X., Zhang, H., Li, X., & Hao, Y. (2025) · Journal of Inflammation Research · doi:10.2147/jir.s480405 · Cited by 3

[Role of interaction between reactive oxygen species and ferroptosis pathway in methylglyoxal-induced injury in mouse embryonic osteoblasts].

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