The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.
Receptor Interacting Protein Kinase-3 Determines Cellular Necrotic Response to TNF-α
Open accessAbstract
Smac mimetics induce apoptosis synergistically with TNF-alpha by triggering the formation of a caspase-8-activating complex containing receptor interacting protein kinase-1 (RIPK1). Caspase inhibitors block this form of apoptosis in many types of cells. However, in several other cell lines, caspase inhibitors switch the apoptotic response to necrosis. A genome wide siRNA screen revealed another member of the RIP kinase family, RIP3, to be required for necrosis. The expression of RIP3 in different cell lines correlates with their responsiveness to necrosis induction. The kinase activity of RIP3 is essential for necrosis execution. Upon induction of necrosis, RIP3 is recruited to RIPK1 to form a necrosis-inducing complex. Embryonic fibroblasts from RIP3 knockout mice are resistant to necrosis and RIP3 knockout animals are devoid of inflammation inflicted tissue damage in an acute pancreatitis model. These data indicate RIP3 as the determinant for cellular necrosis in response to TNF-alpha family of death-inducing cytokines.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“However, excess TNF-α may have the opposite effect by inducing apoptosis and necrosis of infected macrophages via stimulation of receptor-interacting serine-threonine kinases 1 and 3 (RIP1 and RIP3) and excessive radical formation (64–66).”
From Macrophage defense mechanisms against intracellular bacteria (2015) · cites this paper as [64]
Citations
Cites
Apoptosis: A Basic Biological Phenomenon with Wideranging Implications in Tissue Kinetics
Kerr, J. F. R., Wyllie, A. H., & Currie, A. R. (1972) · British Journal of Cancer · doi:10.1038/bjc.1972.33 · Cited by 15,673
Li, P., Nijhawan, D., Budihardjo, I., Srinivasula, S. M., Ahmad, M., Alnemri, E. S., & Wang, X. (1997) · Cell · doi:10.1016/s0092-8674(00)80434-1 · Cited by 7,289
Self-citationThornberry, N. A., & Lazebnik, Y. A. (1998) · Science · doi:10.1126/science.281.5381.1312 · Cited by 6,857
Cleavage of BID by Caspase 8 Mediates the Mitochondrial Damage in the Fas Pathway of Apoptosis
Li, H., Zhu, H., Xu, C.-J., & Yuan, J. (1998) · Cell · doi:10.1016/s0092-8674(00)81590-1 · Cited by 4,445
Luo, X., Budihardjo, I., Zou, H., Slaughter, C., & Wang, X. (1998) · Cell · doi:10.1016/s0092-8674(00)81589-5 · Cited by 3,626
Self-citationDu, C., Fang, M., Li, Y., Li, L., & Wang, X. (2000) · Cell · doi:10.1016/s0092-8674(00)00008-8 · Cited by 3,513
Self-citationChemical inhibitor of nonapoptotic cell death with therapeutic potential for ischemic brain injury
Degterev, A., Huang, Z., Boyce, M., Li, Y., Jagtap, P., Mizushima, N., Cuny, G. D., Mitchison, T. J., Moskowitz, M. A., & Yuan, J. (2005) · Nature Chemical Biology · doi:10.1038/nchembio711 · Cited by 3,068
Verhagen, A. M., Ekert, P. G., Pakusch, M., Silke, J., Connolly, L. M., Reid, G. E., Moritz, R. L., Simpson, R. J., & Vaux, D. L. (2000) · Cell · doi:10.1016/s0092-8674(00)00009-x · Cited by 2,372
Identification of RIP1 kinase as a specific cellular target of necrostatins
Degterev, A., Hitomi, J., Germscheid, M., Ch'en, I. L., Korkina, O., Teng, X., Abbott, D., Cuny, G. D., Yuan, C., Wagner, G., et al. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.83 · Cited by 2,059
Holler, N., Zaru, R., Micheau, O., Thome, M., Attinger, A., Valitutti, S., Bodmer, J.-L., Schneider, P., Seed, B., & Tschopp, J. (2000) · Nature Immunology · doi:10.1038/82732 · Cited by 1,987
Cited by
Sorted by citations
Items 601–700 of 1,002
Liu, X., Li, Y., Peng, S., Yu, X., Li, W., Shi, F., Luo, X., Tang, M., Tan, Z., Bode, A. M., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-017-0081-9 · Cited by 91
Mechanism of Ferroptosis: A Potential Target for Cardiovascular Diseases Treatment
Ju, J., Song, Y., & Wang, K. (2021) · Aging and Disease · doi:10.14336/ad.2020.0323 · Cited by 88
Innate immune sensing of cell death in disease and therapeutics
Man, S. M., & Kanneganti, T. (2024) · Nature Cell Biology · doi:10.1038/s41556-024-01491-y · Cited by 94
Redox signaling in the pancreas in health and disease
Sastre, J., Pérez, S., Sabater-Orti, L., & Rius‐Pérez, S. (2024) · Physiological Reviews · doi:10.1152/physrev.00044.2023 · Cited by 101
Liedtke, C., & Trautwein, C. (2011) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2011.10.001 · Cited by 87
Necroptosis: A Novel Cell Death Modality and Its Potential Relevance for Critical Care Medicine
Moreno‐González, G., Vandenabeele, P., & Krysko, D. V. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201510-2106ci · Cited by 90
Neutrophil Necroptosis Is Triggered by Ligation of Adhesion Molecules following GM-CSF Priming
Wang, X., He, Z., Liu, H., Yousefi, S., & Simon, H. (2016) · The Journal of Immunology · doi:10.4049/jimmunol.1600051 · Cited by 88
Self-citationNecroptosis: A new way of dying?
Hanson, B. (2016) · Cancer Biology & Therapy · doi:10.1080/15384047.2016.1210732 · Cited by 93
High-Fat Diet Aggravates Acute Pancreatitis via TLR4-Mediated Necroptosis and Inflammation in Rats
Hong, Y.-P., Yu, J., Su, Y.-R., Mei, F., Li, M., Zhao, K., Zhao, L., Deng, W., Chen, C., & Wang, W. (2020) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2020/8172714 · Cited by 86
Self-citationBRAF and AXL oncogenes drive RIPK3 expression loss in cancer
Najafov, A., Zervantonakis, I. K., Mookhtiar, A. K., Greninger, P., March, R. J., Egan, R. K., Luu, H. S., Stover, D. G., Matulonis, U. A., Benes, C. H., et al. (2018) · PLoS Biology · doi:10.1371/journal.pbio.2005756 · Cited by 89
Inflammasomes in Respiratory Disease
Brusselle, G., Provoost, S., Bracke, K. R., Kuchmiy, A. A., & Lamkanfi, M. (2014) · CHEST Journal · doi:10.1378/chest.13-1885 · Cited by 87
TAK1 mediates convergence of cellular signals for death and survival
Aashaq, S., Batool, A., & Andrabi, K. I. (2018) · APOPTOSIS · doi:10.1007/s10495-018-1490-7 · Cited by 86
Reovirus Activates a Caspase-Independent Cell Death Pathway
Berger, A. K., & Danthi, P. (2013) · mBio · doi:10.1128/mbio.00178-13 · Cited by 84
Cell death–mediated cytokine release and its therapeutic implications
Place, D. E., & Kanneganti, T. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20181892 · Cited by 84
Necroptosis and its role in infectious diseases
Xia, X., Lei, L., Wang, S., Hu, J., & Zhang, G. (2020) · APOPTOSIS · doi:10.1007/s10495-019-01589-x · Cited by 83
The circRNA CNEACR regulates necroptosis of cardiomyocytes through Foxa2 suppression
Gao, X., Liu, C.-Y., Zhang, Y.-H., Wang, Y.-H., Zhou, L., Li, X., Wang, K., Chen, X., Wang, T., Ju, J., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-021-00872-2 · Cited by 84
Self-citationZhang, M., Harashima, N., Moritani, T., Huang, W., & Harada, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127386 · Cited by 86
MLKL polymerization-induced lysosomal membrane permeabilization promotes necroptosis
Liu, S., Perez, P., Sun, X. F., Chen, K., Fatirkhorani, R., Mammadova, J., & Wang, Z. (2023) · Cell Death and Differentiation · doi:10.1038/s41418-023-01237-7 · Cited by 91
Organellar Dysfunction in the Pathogenesis of Pancreatitis
Gukovsky, I., Pandol, S. J., & Gukovskaya, A. S. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4068 · Cited by 87
FTY720 induces autophagy-related apoptosis and necroptosis in human glioblastoma cells
Zhang, L., Wang, H., Ding, K., & Xu, J. (2015) · Toxicology Letters · doi:10.1016/j.toxlet.2015.04.015 · Cited by 84
Necrosis-dependent and independent signaling of the RIP kinases in inflammation
Moriwaki, K., & Chan, F. K.-M. (2013) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2013.12.013 · Cited by 84
Necroptosis is a key mediator of enterocytes loss in intestinal ischaemia/reperfusion injury
Wen, S., Ling, Y., Yang, W., Shen, J., Li, C., Deng, W., Liu, W., & Liu, K. (2016) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.12987 · Cited by 85
Necroptosis in cardiovascular disease - a new therapeutic target
Gupta, K., Phan, N., Wang, Q., & Liu, B. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.03.003 · Cited by 86
The Killer Pseudokinase Mixed Lineage Kinase Domain-Like Protein (MLKL)Preprint
Murphy, J. M. (2019) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a036376 · Cited by 87
TRIM24-RIP3 axis perturbation accelerates osteoarthritis pathogenesis
Jeon, J., Noh, H.-J., Lee, H., Park, H.-H., Ha, Y., Park, S. H., Lee, H., Kim, S.-J., Kang, H. C., Eyun, S., et al. (2020) · Annals of the Rheumatic Diseases · doi:10.1136/annrheumdis-2020-217904 · Cited by 83
Metabolic tricks of cancer cells
Hönigová, K., Navrátil, J., Peltanová, B., Polanska, H. H., Raudenská, M., & Masařík, M. (2022) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2022.188705 · Cited by 84
MLKL activates the cGAS-STING pathway by releasing mitochondrial DNA upon necroptosis induction
Ding, Z., Wang, R., Li, Y., & Wang, X. (2025) · Molecular Cell · doi:10.1016/j.molcel.2025.06.005 · Cited by 91
Self-citationCritical function of the necroptosis adaptor RIPK3 in protecting from intestinal tumorigenesis
Bozec, D., Iuga, A. C., Roda, G., Dahan, S., & Yeretssian, G. (2016) · Oncotarget · doi:10.18632/oncotarget.10135 · Cited by 85
Very Long Chain Fatty Acids Are Functionally Involved in Necroptosis
Parisi, L. R., Li, N., & Atilla‐Gokcumen, G. E. (2017) · Cell chemical biology · doi:10.1016/j.chembiol.2017.08.026 · Cited by 82
Protective Effects of Necrostatin-1 against Concanavalin A-Induced Acute Hepatic Injury in Mice
Zhou, Y., Dai, W., Lin, C., Wang, F., He, L., Shen, M., Chen, P., Wang, C., Lu, J., Xu, L., et al. (2013) · Mediators of Inflammation · doi:10.1155/2013/706156 · Cited by 82
Khan, M. R., Xiang, S., Song, Z., & Wu, M. (2017) · The EMBO Journal · doi:10.15252/embj.201696239 · Cited by 82
Complex roles of necroptosis in cancer
Zhu, F., Zhang, W., Yang, T., & He, S. (2019) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b1900160 · Cited by 82
Self-citationKilling by Degradation: Regulation of Apoptosis by the Ubiquitin-Proteasome-System
Abbas, R., & Larisch, S. (2021) · Cells · doi:10.3390/cells10123465 · Cited by 91
The pathogenesis and potential therapeutic targets in sepsis
Zhang, W., Jiang, H., Wu, G., Huang, P., Wang, H., An, H., Liu, S., & Zhang, W. (2023) · MedComm · doi:10.1002/mco2.418 · Cited by 85
Critical contribution of oxidative stress to TNFα-induced necroptosis downstream of RIPK1 activation
Shindo, R., Kakehashi, H., Okumura, K., Kumagai, Y., & Nakano, H. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.05.075 · Cited by 81
Insane in the membrane: a structural perspective of MLKL function in necroptosis
Petrie, E. J., Hildebrand, J. M., & Murphy, J. M. (2016) · Immunology and Cell Biology · doi:10.1038/icb.2016.125 · Cited by 86
Ni, Y., Gu, W.-W., Liu, Z.-H., Zhu, Y.-M., Rong, J., Kent, T. A., Li, M., Qiao, S.-G., An, J.-Z., & Zhang, H.-L. (2017) · Neuroscience · doi:10.1016/j.neuroscience.2017.10.038 · Cited by 84
Therapeutic applications of TRAIL receptor agonists in cancer and beyond
Amarante-Mendes, G. P., & Griffith, T. S. (2015) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2015.09.001 · Cited by 83
Programmed necrosis and autophagy in immune function
Lu, J. V., & Walsh, C. M. (2012) · Immunological Reviews · doi:10.1111/j.1600-065x.2012.01147.x · Cited by 82
Therapeutic effects of mesenchymal stem cell-derived exosomes on retinal detachment
Ma, M., Li, B., Zhang, M., Zhou, L., Yang, F., Ma, F., Shao, H., Li, Q., Li, X., & Zhang, X. (2019) · Experimental Eye Research · doi:10.1016/j.exer.2019.107899 · Cited by 83
Viral Z-RNA triggers ZBP1-dependent cell death
Balachandran, S., & Mocarski, E. S. (2021) · Current Opinion in Virology · doi:10.1016/j.coviro.2021.10.004 · Cited by 80
Salvadores, N., Moreno‐González, I., Gamez, N., Quiroz, G., Vegas‐Gomez, L., Escandón, M., Jiménez, S., Vitórica, J., Gutiérrez, A., Soto, C. A., et al. (2022) · Acta Neuropathologica Communications · doi:10.1186/s40478-022-01332-9 · Cited by 87
Engineering micro oxygen factories to slow tumour progression via hyperoxic microenvironments
Wang, W., Zheng, H., Jiang, J., Li, Z., Jiang, D., Shi, X., Wang, H., Jiang, J., Xie, Q., Gao, M., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32066-w · Cited by 81
Shi, F., Yuan, L.-S., Wong, T.-S., Li, Q., Li, Y., Xu, R., You, Y.-P., Yuan, T., Zhang, H., Shi, Z., et al. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106697 · Cited by 82
RIPK3-Mediated Necroptosis Regulates Cardiac Allograft Rejection
Pavlosky, A., Lau, A., Su, Y., Lian, D., Huang, X., Yin, Z., Haig, A. R., Jevnikar, A. M., & Zhang, Z.-X. (2014) · American Journal of Transplantation · doi:10.1111/ajt.12779 · Cited by 82
Necroptotic cell death in failing heart: relevance and proposed mechanisms
Adameová, A., Gonçalvesová, E., Szobi, A., & Dhalla, N. S. (2016) · Heart Failure Reviews · doi:10.1007/s10741-016-9537-8 · Cited by 82
c-FLIP Maintains Tissue Homeostasis by Preventing Apoptosis and Programmed Necrosis
Piao, X., Komazawa‐Sakon, S., Nishina, T., Koike, M., Piao, J., Ehlken, H., Kurihara, H., Hara, M., van Rooijen, N., Schütz, G., et al. (2012) · Science Signaling · doi:10.1126/scisignal.2003558 · Cited by 78
RIPK1 can function as an inhibitor rather than an initiator of RIPK3‐dependent necroptosis
Kearney, C. J., Cullen, S. P., Clancy, D. M., & Martin, S. J. (2014) · FEBS Journal · doi:10.1111/febs.13034 · Cited by 85
Young, J. A., Sermwittayawong, D., Kim, H., Nandu, S., An, N., Erdjument‐Bromage, H., Tempst, P., Coscoy, L., & Winoto, A. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.172288 · Cited by 78
The Paradoxical Role of Inflammation in Cardiac Repair and Regeneration
Jiang, B., & Liao, R. (2010) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-010-9193-7 · Cited by 79
Melatonin attenuates carbon tetrachloride–induced liver fibrosis via inhibition of necroptosis
Choi, H., Kang, J., & Lee, S. (2015) · Translational research · doi:10.1016/j.trsl.2015.04.002 · Cited by 79
Autophagy is a survival force via suppression of necrotic cell death
Shen, H., & Codogno, P. (2012) · Experimental Cell Research · doi:10.1016/j.yexcr.2012.02.006 · Cited by 82
Mechanisms of action of amyloid-beta and its precursor protein in neuronal cell death
Leong, Y. Q., Ng, K. Y., Chye, S. M., Ling, A. P. K., & Koh, R. Y. (2019) · Metabolic Brain Disease · doi:10.1007/s11011-019-00516-y · Cited by 80
Glaubitz, J., Asgarbeik, S., Lange, R., Mazloum, H., Elsheikh, H., Weiß, F. U., & Sendler, M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1279539 · Cited by 81
Role of the TNF pathway in the progression of diabetic nephropathy in KK-Aymice
Omote, K., Gohda, T., Murakoshi, M., Sasaki, Y., Kazuno, S., Fujimura, T., Ishizaka, M., Sonoda, Y., & Tomino, Y. (2014) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00509.2013 · Cited by 78
Wang, L., Wang, T., Li, H., Liu, Q. L., Zhang, Z., Xie, W., Feng, Y., Socorburam, T., Wu, G., Xia, Z., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0155723 · Cited by 80
Self-citationKanak, M. A., Shahbazov, R., Yoshimatsu, G., Levy, M. F., Lawrence, M. C., & Naziruddin, B. (2016) · Journal of Gastroenterology · doi:10.1007/s00535-016-1238-5 · Cited by 80
Hänggi, K., Vasilikos, L., Valls, A. F., Yerbes, R., Knop, J., Spilgies, L. M., Rieck, K., Misra, T., Bertin, J., Gough, P. J., et al. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.20 · Cited by 76
p16Ink4A, not only a G1inhibitor?
Dulić, V. (2010) · Cell Cycle · doi:10.4161/cc.9.16.12887 · Cited by 78
Liu, T., Zhao, D.-X., Cui, H., Chen, L., Bao, Y., Wang, Y., & Jiang, J. (2016) · Scientific Reports · doi:10.1038/srep24547 · Cited by 77
USP22 controls necroptosis by regulating receptor-interacting protein kinase 3 ubiquitination
Roedig, J., Kowald, L., Juretschke, T., Karlowitz, R., Abhari, B. A., Roedig, H., Fulda, S., Beli, P., & van Wijk, S. J. L. (2020) · EMBO Reports · doi:10.15252/embr.202050163 · Cited by 72
Role for membrane remodeling in cell death: Implication for health and disease
Tekpli, X., Holme, J. A., Sergent, O., & Lagadic‐Gossmann, D. (2012) · Toxicology · doi:10.1016/j.tox.2012.12.014 · Cited by 81
AIF-independent parthanatos in the pathogenesis of dry age-related macular degeneration
Jang, K.-H., Do, Y., Son, D., Son, E., Choi, J., & Kim, E. (2017) · Cell Death and Disease · doi:10.1038/cddis.2016.437 · Cited by 77
True Grit: Programmed Necrosis in Antiviral Host Defense, Inflammation, and Immunogenicity
Mocarski, E. S., Kaiser, W. J., Livingston‐Rosanoff, D., Upton, J. W., & Daley‐Bauer, L. P. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302426 · Cited by 75
Cancer and necroptosis: friend or foe?
Philipp, S., Sosna, J., & Adam, D. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2193-2 · Cited by 77
Fakharnia, F., Khodagholi, F., Dargahi, L., & Ahmadiani, A. (2016) · Journal of Molecular Neuroscience · doi:10.1007/s12031-016-0843-3 · Cited by 76
Autophagy and Inflammatory Response in the Tumor Microenvironment
Ngabire, D., & Kim, G. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18092016 · Cited by 76
The Autophagy-Initiating Kinase ULK1 Controls RIPK1-Mediated Cell Death
Wu, W., Wang, X., Berleth, N., Deitersen, J., Wallot-Hieke, N., Böhler, P., Schlütermann, D., Stuhldreier, F., Cox, J., Schmitz, K., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107547 · Cited by 72
Self-citationDying to Defend: Neutrophil Death Pathways and their Implications in Immunity
Tu, H., Ren, H., Jiang, J., Shao, C., Shi, Y., & Li, P. (2023) · Advanced Science · doi:10.1002/advs.202306457 · Cited by 80
Role of the Mitochondrion in Programmed Necrosis
Baines, C. P. (2010) · Frontiers in Physiology · doi:10.3389/fphys.2010.00156 · Cited by 82
James, R., Schalks, R., Browne, E., Eleftheriadou, I., Muñoz, C. P., Mazarakis, N. D., & Reynolds, R. (2020) · Acta Neuropathologica Communications · doi:10.1186/s40478-020-00938-1 · Cited by 77
Zhang, Y., Li, M., Li, X., Zhang, H., Wang, L., Wu, X., Zhang, H., & Luo, Y. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-02770-w · Cited by 77
Self-citationSpeir, M., & Lawlor, K. E. (2020) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2020.07.011 · Cited by 78
A toolbox for imaging RIPK1, RIPK3, and MLKL in mouse and human cells
Samson, A. L., Fitzgibbon, C., Patel, K. M., Hildebrand, J. M., Whitehead, L. W., Rimes, J. S., Jacobsen, A. V., Horne, C. R., Gavin, X. J., Young, S. N., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-021-00742-x · Cited by 76
Necroptosis Takes Place in Human Immunodeficiency Virus Type-1 (HIV-1)-Infected CD4+ T Lymphocytes
Pan, T. S., Wu, S., He, X., Luo, H., Zhang, Y., Fan, M., Geng, G., Ruiz, V. C., Zhang, J., Mills, L., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0093944 · Cited by 73
New components of the necroptotic pathway
Zhou, Z., Han, V. K. M., & Han, J. (2012) · Protein & Cell · doi:10.1007/s13238-012-2083-9 · Cited by 75
Life and death in the thymus—cell death signaling during T cell development
Hernandez, J. B., Newton, R. H., & Walsh, C. M. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.08.003 · Cited by 77
Yang, C., Li, J., Yu, L., Zhang, Z., Xu, F., Jiang, L., Zhou, X., & He, S. (2017) · Cell Death and Disease · doi:10.1038/cddis.2017.483 · Cited by 76
Self-citationLiu, Z.-M., Chen, Q., Chen, Z., Tian, D., Li, M., Wang, J., Wang, L., Liu, B., Zhang, S., Li, F., et al. (2018) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2018.02.150 · Cited by 78
Self-citationChaudhary, G. R., Yadav, P. K., Yadav, A. K., Tiwari, M., Gupta, A., Sharma, A., Pandey, A. N., Pandey, A. K., & Chaube, S. K. (2019) · Journal of Biomedical Science · doi:10.1186/s12929-019-0504-2 · Cited by 78
Coupienne, I., Bontems, S., Dewaele, M., Rubio, N., Habraken, Y., Fulda, S., Agostinis, P., & Piette, J. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2010.12.015 · Cited by 83
Genetic Regulation of RIPK1 and Necroptosis
Xu, D., Zou, C., & Yuan, J. (2021) · Annual Review of Genetics · doi:10.1146/annurev-genet-071719-022748 · Cited by 80
GSK-3β promotes cell survival by modulating Bif-1-dependent autophagy and cell death
Yang, J., Takahashi, Y., Cheng, E., Liu, J., Terranova, P. F., Zhao, B., Thrasher, J. B., Wang, H., & Li, B. (2010) · Journal of Cell Science · doi:10.1242/jcs.060475 · Cited by 74
Kataoka, K., Matsumoto, H., Kaneko, H., Notomi, S., Takeuchi, K., Sweigard, J. H., Atik, A., Murakami, Y., Connor, K. M., Terasaki, H., et al. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.73 · Cited by 75
The role of the IAP E3 ubiquitin ligases in regulating pattern-recognition receptor signalling
Vandenabeele, P., & Bertrand, M. J. M. (2012) · Nature reviews. Immunology · doi:10.1038/nri3325 · Cited by 75
Die Another Day: Inhibition of Cell Death Pathways by Cytomegalovirus
Brune, W., & Andoniou, C. E. (2017) · Viruses · doi:10.3390/v9090249 · Cited by 77
Yu, X., Deng, Q., Li, W., Xiao, L., Luo, X., Liu, X., Yang, L., Peng, S., Ding, Z., Feng, T., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.3038 · Cited by 76
Generation of small molecules to interfere with regulated necrosis
Degterev, A., & Linkermann, A. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2198-x · Cited by 72
Regression of apoptosis-resistant colorectal tumors by induction of necroptosis in mice
He, G.-W., Günther, C., Thonn, V., Yu, Y., Martini, E., Buchen, B., Neurath, M. F., Stürzl, M., & Becker, C. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20160442 · Cited by 76
Zhou, M., He, J., Shi, Y., Liu, X., Luo, S., Cheng, C., Ge, W., Qu, C.-Y., Du, P., & Chen, Y. (2020) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjaa131 · Cited by 73
The role of regulated necrosis in endocrine diseases
Tonnus, W., Belavgeni, A., Beuschlein, F., Eisenhofer, G., Faßnacht, M., Kroiß, M., Krone, N. P., Reincke, M., Bornstein, S. R., & Linkermann, A. (2021) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00499-w · Cited by 74
RIP3-dependent necroptosis contributes to the pathogenesis of chronic obstructive pulmonary disease
Chen, D., Gregory, A. D., Li, X., Wei, J., Burton, C. L., Gibson, G. A., Scott, S., Croix, C. M. S., Zhang, Y., & Shapiro, S. D. (2021) · JCI Insight · doi:10.1172/jci.insight.144689 · Cited by 72
Knowledge Mapping of Necroptosis From 2012 to 2021: A Bibliometric Analysis
Zhang, J., Song, L., Jia, J., Tian, W., Lai, R., Zhang, Z., Li, J., Ju, J., & Xu, H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.917155 · Cited by 73
Regulated necrosis, a proinflammatory cell death, potentially counteracts pathogenic infections
Zhang, G., Wang, J., Zhao, Z., Xin, T., Fan, X., Shen, Q., Raheem, A., Lee, C. R., Jiang, H., & Ding, J. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05066-3 · Cited by 75
Etemadi, N., Holien, J. K., Chau, D., Dewson, G., Murphy, J. M., Alexander, W. S., Parker, M. W., Silke, J., & Nachbur, U. (2013) · FEBS Journal · doi:10.1111/febs.12419 · Cited by 73
Hou, X., Yang, C., Zhang, L., Hu, T., Sun, D., Cao, H., Yang, F., Guo, G. F., Gong, C., Zhang, X., et al. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2016.12.032 · Cited by 75
Sendtner, N., Seitz, R., Brandl, N., Müller, M., & Gülow, K. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262010240 · Cited by 81
To fight or die — inhibitor of apoptosis proteins at the crossroad of innate immunity and death
Lopez, J. S., & Meier, P. (2010) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2010.08.025 · Cited by 71
Necroptosis in cancer: An angel or a demon?
Wang, T., Jin, Y., Yang, W., Zhang, L., Jin, X., Liu, X., He, Y., & Li, X. (2017) · Tumor Biology · doi:10.1177/1010428317711539 · Cited by 72
Self-citationLi, Y., Tian, X., Liu, X., & Gong, P. (2018) · Carcinogenesis · doi:10.1093/carcin/bgy039 · Cited by 71
Metadata
- Authors
- He, S., Wang, L., Miao, L., Wang, T., Du, F., Zhao, L., & Wang, X.
- Affiliations
- Chinese Academy of Medical Sciences & Peking Union Medical College (CN)
- Howard Hughes Medical Institute (US)
- National Institute of Biological Sciences, Beijing (CN)
- Corresponding author
- Wang, Xiaodong
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2009-06
- Volume
- 137
- Issue
- 6
- Pages
- 1100-1111
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2052605153
- Cited by
- 2,214
- References
- 35
- Citations by year
- 2026: 82 · 2025: 118 · 2024: 114 · 2023: 124 · 2022: 158 · 2021: 168 · 2020: 147 · 2019: 136 · 2018: 143 · 2017: 147 · 2016: 171 · 2015: 155 · 2014: 179 · 2013: 101 · 2012: 106
- FWCI
- 36.20
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Bristol Research (University of Bristol) (submittedVersion)
- Funders
- National Institutes of Health (5p01ca095471-10)
- National Cancer Institute (P01 CA95471)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Social Sciences › Anthropology › Death, Funerary Practices, and Mourning
- Keywords
- RIPK3, receptor-interacting protein kinase, necrosis, TNF-α, RIPK1, IAP antagonists, caspase-8, kinase activity, acute pancreatitis, inflammation, siRNA screen
- MeSH terms
- Animals, Ceruletide, Humans, Mutation, Necrosis, Pancreatitis, Tumor Necrosis Factor-alpha, Protein Structure, Tertiary, RNA, Small Interfering, Cell Line, Tumor, Mice, Receptor-Interacting Protein Serine-Threonine Kinases
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