The DOI matches its Crossref record; 141 of the 141 references it cites were found in a registry or an index.
p53 in ferroptosis regulation: the new weapon for the old guardian
Open accessAbstract
Although the conventional activities of p53 such as cell cycle arrest, senescence, and apoptosis are well accepted as the major checkpoints in stress responses, accumulating evidence implicates the importance of other tumor suppression mechanisms. Among these unconventional activities, an iron-dependent form of non-apoptotic cell death, termed ferroptosis, attracts great interest. Unlike apoptotic cell death, activation of p53 alone is not sufficient to induce ferroptosis directly; instead, through its metabolic targets, p53 is able to modulate the ferroptosis response in the presence of ferroptosis inducers such as GPX4 inhibitors or high levels of ROS. Here, we review the role of ferroptosis in p53-mediated tumor suppression, with a focus on what cellular factors are critical for p53-dependent ferroptosis during tumor suppression and how p53 modulates both the canonical (GPX4-dependent) and the non-canonical (GPX4-independent) ferroptosis pathways. We also discuss the possibility of targeting p53-mediated ferroptotic responses for the treatment of human cancers and potentially, other diseases.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“It is known that p53 modulates ferroptosis, an iron-dependent, nonapoptotic form of cell death induced by lipid peroxidation in response to high levels of ROS [ 71 ].”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
Ma, S., Sun, L., Wu, W., Jiang-li, W., Sun, Z., & Ren, J. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.551318 · Cited by 202
RetractedFerroptosis: 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
Ferroptosis: mechanisms, biology and role in disease
Jiang, X., Stockwell, B. R., & Conrad, M. (2021) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00324-8 · Cited by 7,973
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
Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680
Lane, D. P. (1992) · Nature · doi:10.1038/358015a0 · Cited by 5,138
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
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
Ferroptosis as a p53-mediated activity during tumour suppression
Jiang, L., Kon, N., Li, T., Wang, S.-J., Su, T., Hibshoosh, H., Baer, R., & Gu, W. (2015) · Nature · doi:10.1038/nature14344 · Cited by 3,398
Self-citationFSP1 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
Research works printed but not linked: 1
- Jiang L, Kon N, Li T, Wang SJ, Su T, Hibshoosh H, et al. Ferroptosis as a p53-mediated activity during tumour suppression. Nature. 2015;520:57–62. · DOI · Paper page
Cited by
Sorted by citations
Items 501–540 of 540
Lieke, T., & Steinberg, C. E. W. (2026) · Springer eBooks · doi:10.1007/978-3-032-18380-4_2
Liu, J., Su, S., Lu, W., & Guo, P. (2026) · Pathology - Research and Practice · doi:10.1016/j.prp.2026.156472
Chen, Y.-C., Li, Y.-H., Chen, P., Chen, H.-H., & Su, M.-T. (2026) · Toxicology in Vitro · doi:10.1016/j.tiv.2026.106245
Ferroptosis as a potential therapeutic target for obesity-related metabolic diseases: A review
Qadir, A. M., & Omer, R. A. (2026) · Obesity Medicine · doi:10.1016/j.obmed.2026.100710
Jiang, X., Wang, Y., Wang, Y., Wu, Y., Si, J., 刘馨莲, Cao, H., Jia, C., Zeng, Y., & Zhang, L. (2026) · Scientific Reports · doi:10.1038/s41598-026-52662-w
Li, L., Xi, Y., Li, J., Feng, S., Chen, C., Liu, Q., Wu, S., Zhang, Y., Sun, Y., He, M., et al. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.05.333
Medicinal Cannabis in Cancer Therapy: Targeting Ferroptosis as a Novel and Promising Axis
Ateş, F. B. (2026) · Hacettepe University Journal of the Faculty of Pharmacy · doi:10.52794/hujpharm.1932122
Ceramidase in the Diagnosis of Lymphoproliferative Disorders: an Updated Overview
Sahakyan, L. S., Shaljyan, A. L., Sahakyan, A. S., Voskanyan, A., & Saharyan, A. V. (2026) · Medical Science of Armenia · doi:10.54503/0514-7484-2026-66.2-26
Cao, Y.-Y., Wei, Y., Peng, T., Li, Q., Ai, C. M., Ding, Q.-L., Li, T., Dai, X.-G., Chen, Z., & Wang, X. (2026) · World Journal of Traditional Chinese Medicine · doi:10.4103/wjtcm.wjtcm_85_26
Mechanistic insights into lipoprotein(a)-induced cardiomyocyte ferroptosis via ROS/p38/p53 signaling
Li, Y., Chen, X., He, C., Zhang, Y., & Jiang, T. (2026) · Frontiers in Medicine · doi:10.3389/fmed.2026.1858249
Zhang, X., Huang, X., Kang, R., & Hu, X. (2026) · Letters in Drug Design & Discovery · doi:10.1016/j.lddd.2026.100482
Metabolic control of ferroptosis in cancer: lipid dependencies as therapeutic vulnerabilities
Dio, A. D., Smaldone, G., Napolitano, V., Bertamino, A., & Gomez-Monterrey, I. M. (2026) · Frontiers in Oncology · doi:10.3389/fonc.2026.1872103
Ferroptosis in skeletal muscle: from molecular mechanisms to therapeutic interventions
Ren, K., An, Y., Zhou, K., Cheng, X., Meng, T., Li, C., Xu, H., Zhang, P., & Xu, Y. (2026) · Journal of Orthopaedic Translation · doi:10.1016/j.jot.2026.101189
Yang, S., Liu, Y., Zhang, X., Jiang, H., Hua, Q., Zhang, J., Tian, Y., Cai, Q., & Chen, Q. (2026) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2026.07.054
Self-citationBlood and lymphatic vascular remodeling in intervertebral disc degeneration
Huang, F., Lin, M., Zhang, Q., Yan, S., Li, R., Li, S., Jia, Y., Zhao, Q., Song, P., & 周海宇 (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1862921
Zhang, L., Qian, Y., Jin, J., Zhang, Y., Wang, Z., & Li, Q. (2026) · Antioxidants · doi:10.3390/antiox15081014
Impact of oxidative stress on malignant tumor progression and emerging therapeutic strategies
Feng, X.-D., Liang, G.-C., Sun, J.-J., Wang, Z.-Q., Li, T., Fu, Y., Deng, W.-W., Li, X.-Y., Luo, J., Jin, P., et al. (2026) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2026.1916698
Wang, C., Yan, B., Wu, W., Luo, D., Yu, H., Liu, D., Wang, W., & Ma, L. (2026) · Regenerative medicine reports . · doi:10.4103/regenmed.regenmed-d-25-00041
Unveiling the role of p53 in the pathogenesis and treatment of autoimmune rheumatic diseases
Akbarzadeh, F., Farhadi, E., Vodjgani, M., Jamshidi, A., & Mahmoudi, M. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12666-1
Ferro-aging: a potential driver of degenerative bone and joint diseases
Liang, S., Gao, S., Wang, F., Qu, X., Kong, L., Wang, C., & Li, N. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-03194-3
Wu, Y., Tao, Y., Wei, L., Liu, Q., Liu, J., Jiang, W., Shi, W., Cao, P., Fu, X., & Cheng, C. (2026) · Smart Medicine · doi:10.1002/smmd.70054
Yu, H., Wang, Y., Fang, Y., Yuan, W., Zhou, Z., Zhang, X., Lin, J., & Li, Y. (2026) · Biochemical Pharmacology · doi:10.1016/j.bcp.2026.118448
The Emerging Role of Ferroptosis in Pediatric Cancer Biology and Therapy
Paola, A. D., Marrapodi, M. M., Feo, G. D., Martino, M. D., Pinto, D. D., Argenziano, L., Domenico, O. D., Rossi, F., & Pota, E. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27188067
Chen, W., Wang, J., Jin, C., & Gong, L. (2026) · Research Square · doi:10.21203/rs.3.rs-10314337/v1
Zhao, H., Gao, X., Xie, R., & Zhao, M. (2026) · Cancer Letters · doi:10.1016/j.canlet.2026.218808
Kong, D., Duan, R., Wang, X., Wang, X., & Zhao, J. (2026) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2026.102798
Zdanowicz, A., Pradhan, B., Pyrzyńska, B., Otto‐Ślusarczyk, D., & Struga, M. (2026) · Pharmacological Reports · doi:10.1007/s43440-026-00910-1
Zhao, L.-J., Yu, R., Liu, Y., Yin, J.-Y., Jin, H., Zhang, J., Liu, C.-J., Lu, G., Li, Y., Wang, N., et al. (2026) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6c01218
Self-citationMandlik, D. S., & Mandlik, S. K. (2026) · Ageing Research Reviews · doi:10.1016/j.arr.2026.103384
Research Progress on Mechanisms and Pharmacological Interventions of Coronary Artery Calcification
Wang, Y., & Duan, N. (2026) · Angiology · doi:10.1177/00033197261492091
Antal, S., Anshu, T., Goswami, P., Kumar, D., Choudhary, N., & Kadam, A. (2026) · APOPTOSIS · doi:10.1007/s10495-026-02451-7
SIRT3 regulates GLS1 K311 acetylation to restrain glutamate-driven ferroptosis in renal fibrosis
MiaoYan, Hu, H., Chen, C., Hu, J., Yang, Q., Chen, W., Fan, Y., Liang, W., Ding, G., & Jian, Y. (2026) · Cellular Signalling · doi:10.1016/j.cellsig.2026.112930
Amirahmadi, Z., Raeisi, A., Koohpeyma, F., Moghadam, D., Kiani, R., Jamshidi, S., Shams, F., Naeimi, S., & Dastghaib, S. (2026) · Molecular Biology Reports · doi:10.1007/s11033-026-12804-9
Targeting ferroptosis in cancer: molecular mechanisms and emerging therapeutic strategies
Khaledi, M., Ahani, H., Tohid, F. R., Kazemi, F., Amirkhani, E., Daliri, Z., Yadegari, S., Moarefvand, K., Poureslamfar, B., Sameni, F., et al. (2026) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2026.102825
Peng, J., Hu, J., Wu, M., & Xu, H. (2026) · Aging · doi:10.18632/aging.206429
Haojun, Y., Liu, A., Sheng, M., Zhang, S., & Tang, L. (2026) · Journal of Molecular Histology · doi:10.1007/s10735-026-11009-5
Yuan, Q., Tang, X., Yang, Z., Xiao, Y., Dong, J., Cai, X., Gao, W., Wang, Y., Zeng, W., 张才乔, et al. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104444
Ugwu, O. P.-C., Ugwu, C. N., Anyanwu, G. E., Basajja, M., & Ebuoh, M. C. (2026) · Frontiers in Pharmacology · doi:10.3389/fphar.2026.1890015
Zhang, Y., Sun, Y., Cui, Y., Cheng, L., Wang, Y., Fan, K., & Wang, X. (2026) · Chemical Engineering Journal · doi:10.1016/j.cej.2026.183382
Gao, Y., Zhao, W., Chai, Q., & Ye, C.-X. (2026) · Journal of Diabetes Investigation · doi:10.1111/jdi.70467
Metadata
- Authors
- Liu, Y., & Gu, W.
- Affiliations
- Herbert Irving Comprehensive Cancer Center (US)
- Corresponding author
- Gu, Wei
- ORCID
- Venue
- Cell Death & Differentiation
- Published
- 2022-01-27
- Volume
- 29
- Issue
- 5
- Pages
- 895-910
- ISSN
- 1350-9047 (ISSN-L)
- 1476-5403
- PMC
- PMC9091200
- OpenAlex
- W4210576858
- Cited by
- 540
- References
- 141
- Citations by year
- 2026: 88 · 2025: 153 · 2024: 128 · 2023: 110 · 2022: 60
- FWCI
- 19.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Cell Death and Differentiation (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Health & Human Services | NIH | National Cancer Institute (R35CA253059, R01CA254970)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Ferroptosis and cancer prognosis
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- p53, ferroptosis, tumor suppression, GPX4, iron metabolism, reactive oxygen species, non-apoptotic cell death, cancer therapy
- MeSH terms
- Ferroptosis, Humans, Neoplasms, Tumor Suppressor Protein p53, Apoptosis, Reactive Oxygen Species
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review