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Regulation of Ferroptotic Cancer Cell Death by GPX4

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

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DEPDC5 protects CD8+ T cells from ferroptosis by limiting mTORC1-mediated purine catabolism

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Cysteine is a limiting factor for glioma proliferation and survival

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Ferroptosis mechanisms and its novel potential therapeutic targets for DLBCL

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Regulatory mechanisms of amino acids in ferroptosis

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NINJ1 regulates ferroptosis via xCT antiporter interaction and CoA modulation

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Ferroptosis and renal fibrosis: mechanistic insights and emerging therapeutic targets

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Cysteine Metabolism in Tumor Redox Homeostasis

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Ferroptosis: a potential therapeutic target for Alzheimer’s disease

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NIR-AIEgens nanospheres featuring high-fidelity dynamic lipid droplet targeting, expediting ferroptosis to annihilating tumor in hypoxia

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Cathepsin B serves as a potential prognostic biomarker and correlates with ferroptosis in rheumatoid arthritis

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A Ferroptosis‐Inducing Arsenene‐Iridium Nanoplatform for Synergistic Immunotherapy in Pancreatic Cancer

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An iron-containing nanomedicine for inducing deep tumor penetration and synergistic ferroptosis in enhanced pancreatic cancer therapy

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Metabolic and immune crosstalk between cancer-associated fibroblasts and pancreatic cancer cells

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Differences in cell death in methionine versus cysteine depletion

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Opportunities for Ferroptosis in Cancer Therapy

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CARS senses cysteine deprivation to activate AMPK for cell survival

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The Art of War: Ferroptosis and Pancreatic Cancer

Liu, J., Kang, R., & Tang, D. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.773909 · Cited by 27

MicroRNAs in doxorubicin-induced cardiotoxicity: The DNA damage response

Kawano, I., & Adamcová, M. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1055911 · Cited by 26

Reprogramming of iron metabolism confers ferroptosis resistance in ECM-detached cells

He, J., Abikoye, A. M., McLaughlin, B. P., Middleton, R. S., Sheldon, R. D., Jones, R. G., & Schafer, Z. T. (2023) · iScience · doi:10.1016/j.isci.2023.106827 · Cited by 25

c-Myc protects hepatocellular carcinoma cell from ferroptosis induced by glutamine deprivation via upregulating GOT1 and Nrf2

Zhao, Y., Wang, Y., Miao, Z., Liu, Y., & Yang, Q. (2023) · Molecular Biology Reports · doi:10.1007/s11033-023-08495-1 · Cited by 26

Regulation of m6A modification on ferroptosis and its potential significance in radiosensitization

Chen, X., Zhang, L., He, Y., Huang, S., Chen, S., Zhao, W., & Yu, D. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01645-1 · Cited by 32

LINC01133 can induce acquired ferroptosis resistance by enhancing the FSP1 mRNA stability through forming the LINC01133-FUS-FSP1 complex

Wang, S., Chen, J., Li, P., & Chen, Y. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06311-z · Cited by 26

Gestational exposure to 1-NP induces ferroptosis in placental trophoblasts via CYP1B1/ERK signaling pathway leading to fetal growth restriction

Yu, S., Mu, Y., Wang, K., Wang, L., Wang, C., Yang, Z., Liu, Y., Li, S., & Zhang, M. (2023) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2023.110812 · Cited by 25

Metabolic plasticity of T cell fate decision

Pan, X., Wang, J., Zhang, L., Li, G., & Huang, B. (2023) · Chinese Medical Journal · doi:10.1097/cm9.0000000000002989 · Cited by 26

Frontier knowledge and future directions of programmed cell death in clear cell renal cell carcinoma

Cao, F., Xu, Z., Zhang, S., & Pang, J. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-01880-0 · Cited by 28

Targeting ferroptosis as a potential strategy to overcome the resistance of cisplatin in oral squamous cell carcinoma

Chen, R., Zhu, S., Zhao, R., Liu, W., Jin, L., Ren, X., & He, H. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1402514 · Cited by 28

Copper overload exacerbates testicular aging mediated by lncRNA:CR43306 deficiency through ferroptosis in Drosophila

Huang, Q., Li, J., Qi, Y., He, X., Shen, C., Wang, C., Wang, X., Xia, Q., Zhang, Y., Pan, Z., et al. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103315 · Cited by 25

Metabolic reprogramming in lung cancer and its clinical implication

Huang, Q., Fan, L., Gong, M., Ren, J. T., Chen, C., & Xie, S. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1516650 · Cited by 29

Iron and ferroptosis in kidney disease: molecular and metabolic mechanisms

Wang, W., Chen, J., Zhan, L., Zou, H., Wang, L., Guo, M., Gao, H., Xu, J., & Wu, W. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1531577 · Cited by 28

Synergistic Disruption of Metabolic Homeostasis through Hyperbranched Poly(ethylene glycol) Conjugates as Nanotherapeutics to Constrain Cancer Growth

Pan, D., Zheng, X., Zhang, L., Li, X., Zhu, G., Gong, M., Kopytynski, M., Zhou, L., Yi, Y., Zhu, H., et al. (2022) · Advanced Materials · doi:10.1002/adma.202109036 · Cited by 25

Role of ferroptosis in periodontitis: An animal study in rats

Fu, E., Kuo, C., Hsia, Y., Huang, Y., Tseng, H., Fu, M., & Shih, K. (2023) · Journal of Periodontal Research · doi:10.1111/jre.13165 · Cited by 25

Cystine/glutamate antiporter xCT deficiency reduces metastasis without impairing immune system function in breast cancer mouse models

Ruiu, R., Cossu, C., Iacoviello, A., Conti, L., Bolli, E., Ponzone, L., Magri, J., Rumandla, A., Calautti, E., & Cavallo, F. (2023) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-023-02830-x · Cited by 25

Implanted, Wireless, Self‐Powered Photodynamic Therapeutic Tablet Synergizes with Ferroptosis Inducer for Effective Cancer Treatment

Zou, P., Lin, R., Fang, Z., Chen, J., Guan, H., Yin, J., Chang, Z., Xing, L., Lang, J., Xue, X., et al. (2023) · Advanced Science · doi:10.1002/advs.202302731 · Cited by 24

E3 ubiquitin ligase RBCK1 confers ferroptosis resistance in pancreatic cancer by facilitating MFN2 degradation

Su, D., Ding, C., Wang, R., Qiu, J., Liu, Y., Tao, J., Luo, W., Weng, G., Yang, G., & Zhang, T. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.05.031 · Cited by 27

Ferroptosis regulation by Cap’n’collar family transcription factors

Murray, M. B., & Dixon, S. J. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107583 · Cited by 26

Improving understanding of ferroptosis: Molecular mechanisms, connection with cellular senescence and implications for aging

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Combined Methylome and Transcriptome Analyses Reveals Potential Therapeutic Targets for EGFR Wild Type Lung Cancers with Low PD-L1 Expression

Hu, W., Wang, G., Yarmus, L. B., & Wan, Y. (2020) · Cancers · doi:10.3390/cancers12092496 · Cited by 24

A Cystine-Cysteine Intercellular Shuttle Prevents Ferroptosis in xCTKO Pancreatic Ductal Adenocarcinoma Cells

Meira, W., Daher, B., Parks, S. K., Cormerais, Y., Durivault, J., Tambutté, É., Pouysségur, J., & Vučetić, M. (2021) · Cancers · doi:10.3390/cancers13061434 · Cited by 24

Targeting Nutrient Dependency in Cancer Treatment

Fan, K., Liu, Z., Gao, M., Tu, K., Xu, Q., & Zhang, Y. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.820173 · Cited by 26

Ferroptosis at the crossroads of tumor-host interactions, metastasis, and therapy response

Yao, Y., Shi, Y., Gao, Z., Sun, Y., Yao, F., & Ma, L. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00148.2022 · Cited by 23

Ferroptosis-Related Gene GCLC Is a Novel Prognostic Molecular and Correlates with Immune Infiltrates in Lung Adenocarcinoma

Luo, L., Zhang, Z., Weng, Y., & Zeng, J. (2022) · Cells · doi:10.3390/cells11213371 · Cited by 26

Metabolic Rewiring toward Oxidative Phosphorylation Disrupts Intrinsic Resistance to Ferroptosis of the Colon Adenocarcinoma Cells

Gotorbe, C., Durivault, J., Meira, W., Cassim, S., Ždralević, M., Pouysségur, J., & Vučetić, M. (2022) · Antioxidants · doi:10.3390/antiox11122412 · Cited by 24

Dietary Manipulation of Amino Acids for Cancer Therapy

Jiménez‐Alonso, J. J., & López‐Lázaro, M. (2023) · Nutrients · doi:10.3390/nu15132879 · Cited by 26

Recent advances of ferroptosis in tumor: From biological function to clinical application

Hu, S., Chu, Y., Zhou, X., & Wang, X. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115419 · Cited by 24

Depletion of Igfbp7 alleviates zebrafish NAFLD progression through inhibiting hepatic ferroptosis

Wang, Y., Bo, J., Zhao, Z., Han, Y., Zhang, Q., & Liu, L. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122086 · Cited by 24

SLC7A11, a potential immunotherapeutic target in lung adenocarcinoma

Shan, Q., Zhang, C., Li, Y., Li, Q., Zhang, Y., Li, X., Shi, J., & Hu, F. (2023) · Scientific Reports · doi:10.1038/s41598-023-45284-z · Cited by 25

Co-exposure of decabromodiphenyl ethane and polystyrene nanoplastics damages grass carp (Ctenopharyngodon idella) hepatocytes: Focus on the role of oxidative stress, ferroptosis, and inflammatory reaction

Shi, B., Xu, T., Chen, T., Xu, S., & Yao, Y. (2024) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2024.173575 · Cited by 24

Self‐Assembled Aza‐Boron‐Dipyrromethene‐Based H2S Prodrug for Synergistic Ferroptosis‐Enabled Gas and Sonodynamic Tumor Therapies

Zhao, J., Bian, E., Zhang, R., Xu, T., Nie, Y., Wang, L., Jin, G., Xie, H., Xiang, H., Chen, Y., et al. (2024) · Advanced Science · doi:10.1002/advs.202309542 · Cited by 22

Advancements in programmed cell death research in antitumor therapy: a comprehensive overview

Wei, S., Han, C., Mo, S., Huang, H., & Luo, X. (2024) · APOPTOSIS · doi:10.1007/s10495-024-02038-0 · Cited by 29

ACSL3 is an unfavorable prognostic marker in cholangiocarcinoma patients and confers ferroptosis resistance in cholangiocarcinoma cells

Sae-Fung, A., Vinayavekhin, N., Fadeel, B., & Jitkaew, S. (2024) · npj Precision Oncology · doi:10.1038/s41698-024-00783-8 · Cited by 23

Ferroptosis induced by environmental pollutants and its health implications

Gong, F., Liu, L., Wang, X., Xiang, Q., Yi, X., & Jiang, D. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02305-2 · Cited by 23

SIK1 promotes ferroptosis resistance in pancreatic cancer via HDAC5-STAT6-SLC7A11 axis

Zhang, H., Ma, T., Wen, X., Jiang, J., Chen, J., Jiang, J., Xie, J., Mo, T., Li, R., Xie, H., et al. (2025) · Cancer Letters · doi:10.1016/j.canlet.2025.217726 · Cited by 25

The mist of ferroptosis: The Orpheus journey of mitochondria - Exploring the symphony of cell fate

Jiang, Y., Liu, X., & Sun, M. (2025) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2025.145472 · Cited by 27

Pharmacologic approaches to amino acid depletion for cancer therapy

Wilder, C. S., Chen, Z., & DiGiovanni, J. (2021) · Molecular Carcinogenesis · doi:10.1002/mc.23349 · Cited by 23

Upstream stimulatory factor 2 inhibits erastin-induced ferroptosis in pancreatic cancer through transcriptional regulation of pyruvate kinase M2

Chen, M., Li, X., Du, B., Chen, S., & Li, Y. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.115255 · Cited by 23

A Self‐Assembly Combined Nano‐Prodrug to Overcome Gemcitabine Chemo‐Resistance of Pancreatic Tumors

Yao, Z., Hu, Q., Jin, P., Li, B., Huang, Y. X., Zhang, F., Wang, M., Huang, J., Huang, J., Shao, S., et al. (2023) · Advanced Functional Materials · doi:10.1002/adfm.202214598 · Cited by 23

DNA methylation of RUNX3 promotes the progression of gallbladder cancer through repressing SLC7A11-mediated ferroptosis

Cai, C., Zhu, Y., Mu, J., Liu, S., Yang, Z., Wu, Z.-Y., Zhao, C., Song, X., Ye, Y., Gu, J., et al. (2023) · Cellular Signalling · doi:10.1016/j.cellsig.2023.110710 · Cited by 24

Pancreatic acinar cell fate relies on system xC- to prevent ferroptosis during stress

Pan, Z., den Bossche, J.-L. V., Rodríguez-Aznar, E., Janssen, P., Lara, O., Ates, G., Massie, A., Paep, D. L. D., Houbracken, I., Mambretti, M., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06063-w · Cited by 26

SNHG15 ‐mediated feedback loop interplays with HNRNPA1 / SLC7A11 / GPX4 pathway to promote gastric cancer progression

Duan, Y., Yan, Y., Fu, H., Dong, Y., Li, K., Ye, Z., Dou, Y., Huang, B., Kang, W., Wei, G., et al. (2024) · Cancer Science · doi:10.1111/cas.16181 · Cited by 23

Mutually reinforced cancer treatment based on phototherapy combined with ferroptosis

Chen, G., Gan, L., Tian, L.-Y., Huang, B.-X., Xiao, Q., Zhang, Y., Xiao, M., Zheng, B.-D., & Ye, J. (2024) · Chemical Engineering Journal · doi:10.1016/j.cej.2024.152397 · Cited by 23

A two-pronged approach to inhibit ferroptosis of MSCs caused by the iron overload in postmenopausal osteoporosis and promote osseointegration of titanium implant

Yang, Y., Zhang, X., Yang, Y., Gao, P., Fan, W., Zheng, T., Yang, W., Tang, Y. J., & Cai, K. (2024) · Bioactive Materials · doi:10.1016/j.bioactmat.2024.07.024 · Cited by 23

Role of amino acids in regulation of ROS balance in cancer

Jaune, E., & Vasseur, S. (2020) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2020.108438 · Cited by 23

Ferroptosis as a Potential Therapeutic Target for Reducing Inflammation and Corneal Scarring in Bacterial Keratitis

Chen, Q., Wang, L., Wei, Y., Xu, X., Guo, X., & Liang, Q. (2024) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.65.2.29 · Cited by 24

Ferroptosis is an effective strategy for cancer therapy

Khan, A., Huo, Y., Guo, Y., Shi, J., & Hou, Y. (2024) · Medical Oncology · doi:10.1007/s12032-024-02317-5 · Cited by 24

Intrinsic temperature increase drives lipid metabolism towards ferroptosis evasion and chemotherapy resistance in pancreatic cancer

de Laat, V., Topal, H., Spotbeen, X., Talebi, A., Dehairs, J., Idkowiak, J., Vanderhoydonc, F., Ostyn, T., Zhao, P., Jacquemyn, M., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-52978-z · Cited by 22

Targeting novel regulated cell death: disulfidptosis in cancer immunotherapy with immune checkpoint inhibitors

Du, F., Wang, G., Dai, Q., Huang, J. H., Li, J., Liu, C., Du, K., Tian, H., Deng, Q., Xie, L., et al. (2025) · Biomarker Research · doi:10.1186/s40364-025-00748-4 · Cited by 25

Molecular signatures of disulfidptosis: interplay with programmed cell death pathways and therapeutic implications in oncology

Liu, Y., Li, S., Wu, Y., Zhang, P., Yu, Y., Chen, X., Yu, L., Yang, X., Li, Y., Wu, C., et al. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00743-5 · Cited by 34

Mitochondrial Redox Vulnerabilities in Triple-Negative Breast Cancer: Integrative Perspectives and Emerging Therapeutic Strategies

Cruz‐Gregorio, A. (2026) · Metabolites · doi:10.3390/metabo16010060 · Cited by 24

Targeting ferroptosis in cancer: from mechanistic insights to therapeutic approaches

Wang, J., Guo, D., Jiang, S., Wu, W., & Gao, X. (2026) · Molecular Biomedicine · doi:10.1186/s43556-026-00416-5 · Cited by 27

Combinatorial Approaches to Enhance DNA Damage following Enzyme-Mediated Depletion of L-Cys for Treatment of Pancreatic Cancer

Saha, A., Zhao, S., Chen, Z., Georgiou, G., Stone, E. M., Kidane, D., & DiGiovanni, J. (2020) · Molecular Therapy · doi:10.1016/j.ymthe.2020.10.016 · Cited by 24

Mitophagy in Pancreatic Cancer

Xie, Y., Liu, J., Kang, R., & Tang, D. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.616079 · Cited by 22

Identification of the Roles of a Stemness Index Based on mRNA Expression in the Prognosis and Metabolic Reprograming of Pancreatic Ductal Adenocarcinoma

Tang, R., Liu, X., Wang, W., Hua, J., Xu, J., Liang, C., Meng, Q., Liu, J., Zhang, B., Yu, X., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.643465 · Cited by 22

Potential Role of APEX1 During Ferroptosis

Guo, N., Chen, Y., Zhang, Y., Deng, Y., Zeng, F., & Li, X. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.798304 · Cited by 20

Clinical Significance and Immune Infiltration Analyses of the Cuproptosis-Related Human Copper Proteome in Gastric Cancer

Tang, X., Guo, T., Wu, X., Gan, X., Wang, Y., Jia, F., Zhang, Y., Xing, X., Gao, X., & Li, Z. (2022) · Biomolecules · doi:10.3390/biom12101459 · Cited by 22

Emerging Potential Mechanism and Therapeutic Target of Ferroptosis in PDAC: A Promising Future

Li, C., Yin, X., Liu, Z., & Wang, J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232315031 · Cited by 24

Melanin precursors mediated adaption to temperature changes in fungus and animal via inhibition of lipid-mediated ferroptosis

Yang, X., Chen, Y., Zhang, L., He, J., Wu, Q., Li, S., Wang, D., Gou, J., Wu, Z., Zhang, K., et al. (2023) · Science China Life Sciences · doi:10.1007/s11427-022-2265-6 · Cited by 22

Ferroptosis model system by the re-expression of BACH1

Irikura, R., Nishizawa, H., Nakajima, K., Yamanaka, M., Chen, G., Tanaka, K., Onodera, M., Matsumoto, M., & Igarashi, K. (2023) · The Journal of Biochemistry · doi:10.1093/jb/mvad036 · Cited by 22

Molecular subtyping of acute myeloid leukemia through ferroptosis signatures predicts prognosis and deciphers the immune microenvironment

Fu, D., Zhang, B., Wu, S., Feng, J., & Jiang, H. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1207642 · Cited by 22

Ferroptosis of epithelial ovarian cancer: genetic determinants and therapeutic potential

Lin, C., & Chi, J. (2020) · Oncotarget · doi:10.18632/oncotarget.27749 · Cited by 24

Ferroptosis: a new target for hepatic ischemia-reperfusion injury?

Guo, S., Li, Z., Liu, Y., Cheng, Y., & Jia, D. (2024) · Free Radical Research · doi:10.1080/10715762.2024.2386075 · Cited by 23

A Robust ROS Generation and Ferroptotic Lipid Modulation Nanosystem for Mutual Reinforcement of Ferroptosis and Cancer Immunotherapy

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Organomolecular Ferroelectric Nanocatalyst Augments Tumor Immunotherapy by Inducing Apoptosis and Ferroptosis

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Expression Profiles of tRNA-Derived Small RNAs and Their Potential Roles in Primary Nasopharyngeal Carcinoma

Lu, Z., Su, K., Wang, X., Zhang, M., Ma, S., Li, H., & Qiu, Y. (2021) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2021.780621 · Cited by 21

Bibliometric Evaluation of 2012–2020 Publications on Ferroptosis in Cancer Treatment

Zhou, Q., Wu, F., Zhao, M., & Yang, M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.793347 · Cited by 21

A Novel Ferroptosis-Related lncRNAs Signature Predicts Clinical Prognosis and Is Associated With Immune Landscape in Pancreatic Cancer

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Metallopolysaccharide-Based Smart Nanotheranostic for Imaging-Guided Precise Phototherapy and Sequential Enzyme-Activated Ferroptosis

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Post-Translational Modifications of p53 in Ferroptosis: Novel Pharmacological Targets for Cancer Therapy

Zhang, L., Hou, N., Chen, B., Kan, C., Han, F., Zhang, J., & Sun, X. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.908772 · Cited by 21

CDGSH iron sulfur domain 2 over‐expression alleviates neuronal ferroptosis and brain injury by inhibiting lipid peroxidation via AKT / mTOR pathway following intracerebral hemorrhage in mice

Li, R., Zhang, X., Gu, L., Yuan, Y., Luo, X., Shen, W., & Xie, Z. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.15785 · Cited by 21

Bioinformatics analysis of ferroptosis-related gene AKR1C3 as a potential biomarker of asthma and its identification in BEAS-2B cells

Wang, Y., Fan, J., Yu, T., Wang, L., Wang, L., Weng, C., Lai, C., Song, J., & Zhang, W. (2023) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2023.106740 · Cited by 21

Single Component Organic Photosensitizer with NIR‐I Emission Realizing Type‐I Photodynamic and GSH‐Depletion Caused Ferroptosis Synergistic Theranostics

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Epigenetic modulation of ferroptosis in cancer: Identifying epigenetic targets for novel anticancer therapy

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Dietary approaches for exploiting metabolic vulnerabilities in cancer

Menyhárt, O., & Győrffy, B. (2023) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2023.189062 · Cited by 23

Exploiting the metabolic vulnerability of circulating tumour cells

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Ferroptosis contributes to the progression of female-specific neoplasms, from breast cancer to gynecological malignancies in a manner regulated by non-coding RNAs: Mechanistic implications

Hushmandi, K., Klionsky, D. J., Aref, A. R., Bonyadi, M., Reiter, R. J., Nabavi, N., Salimimoghadam, S., & Saadat, S. H. (2024) · Non-coding RNA Research · doi:10.1016/j.ncrna.2024.05.008 · Cited by 21

BACH1 inhibits senescence, obesity, and short lifespan by ferroptotic FGF21 secretion

Nishizawa, H., Matsumoto, M., Yamanaka, M., Irikura, R., Nakajima, K., Tada, K., Nakayama, Y., Konishi, M., Itoh, N., Funayama, R., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114403 · Cited by 21

Cytoplasmic Vacuolization: A Fascinating Morphological Alteration From Cellular Stress to Cell Death

Wen, X., & Ma, H. (2025) · Cancer Science · doi:10.1111/cas.70013 · Cited by 22

Targeting ferroptosis for the treatment of female reproductive system disorders

Ye, R., Mao, Y., Fei, Y.-R., Shang, Y., Zhang, T., Zhang, Z.-Z., Liu, Y., Li, J. F., Chen, S., & He, Y. (2025) · Journal of Molecular Medicine · doi:10.1007/s00109-025-02528-x · Cited by 20

The metabolic underpinnings of sebaceous lipogenesis

Schmidt, M., Binder, H., & Schneider, M. R. (2025) · Communications Biology · doi:10.1038/s42003-025-08105-9 · Cited by 24

Copper deposited metal-phenolic networks enabled crosstalk between cuproptosis and ferroptosis for triple-negative breast cancer immunotherapy

Yin, W., Chang, J., Zhi, H., Chen, S., Xue, L., Zhang, X., Dong, H., & Li, Y. (2025) · Chemical Engineering Journal · doi:10.1016/j.cej.2025.163577 · Cited by 20

Ferroptotic cell death and cancer

Kiberstis, P. A. (2020) · Science · doi:10.1126/science.368.6486.42-m · Cited by 1

Cysteine Is Required for Preventing Ferroptosis in Pancreatic Cancer

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“Induction of pancreatic tumor-selective ferroptosis through modulation of cystine import”Preprint

Badgley, M. A., Kremer, D. M., Maurer, H. C., DelGiorno, K. E., Lee, H., Purohit, V., Sagalovskiy, I. R., Ma, A., Kapilian, J., Firl, C. E. M., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/827972 · Cited by 2

Abstract 5711: Therapeutic induction of tumor-selective ferroptosis in models of pancreatic cancer

Badgley, M. A., DelGiorno, K. E., Wahl, G. M., Lyssiotis, C. A., & Olive, K. P. (2020) · Cancer Research · doi:10.1158/1538-7445.am2020-5711

The critical role of cysteine import and metabolism in pancreatic cancer

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