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Die another way – non-apoptotic mechanisms of cell death
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Regulated, programmed cell death is crucial for all multicellular organisms. Cell death is essential in many processes, including tissue sculpting during embryogenesis, development of the immune system and destruction of damaged cells. The best-studied form of programmed cell death is apoptosis, a process that requires activation of caspase proteases. Recently it has been appreciated that various non-apoptotic forms of cell death also exist, such as necroptosis and pyroptosis. These non-apoptotic cell death modalities can be either triggered independently of apoptosis or are engaged should apoptosis fail to execute. In this Commentary, we discuss several regulated non-apoptotic forms of cell death including necroptosis, autophagic cell death, pyroptosis and caspase-independent cell death. We outline what we know about their mechanism, potential roles in vivo and define outstanding questions. Finally, we review data arguing that the means by which a cell dies actually matters, focusing our discussion on inflammatory aspects of cell death.
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“In contrast to the highly pro-inflammatory necrotic types of cell death, such as necroptosis and pyroptosis, apoptosis and autophagy do not tend to trigger an inflammatory response166.”
From Inflammation and its resolution in atherosclerosis: mediators and therapeutic opportunities (2019) · cites this paper as [166]
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Cites
Parkin is recruited selectively to impaired mitochondria and promotes their autophagy
Narendra, D., Tanaka, A., Suen, D.-F., & Youle, R. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200809125 · Cited by 4,026
Proapoptotic BAX and BAK: A Requisite Gateway to Mitochondrial Dysfunction and Death
Wei, M. C., Zong, W.-X., Cheng, E. H.-Y., Lindsten, T., Panoutsakopoulou, V., Ross, A. J., Roth, K. A., MacGregor, G. R., Thompson, C. B., & Korsmeyer, S. J. (2001) · Science · doi:10.1126/science.1059108 · Cited by 3,988
Bcl-2 Antiapoptotic Proteins Inhibit Beclin 1-Dependent Autophagy
Pattingre, S., Tassa, A., Qu, X., Garuti, R., Liang, X. H., Mizushima, N., Packer, M., Schneider, M. D., & Levine, B. (2005) · Cell · doi:10.1016/j.cell.2005.07.002 · Cited by 3,536
Pyroptosis: host cell death and inflammation
Bergsbaken, T., Fink, S. L., & Cookson, B. T. (2009) · Nature Reviews Microbiology · doi:10.1038/nrmicro2070 · Cited by 3,288
Calreticulin exposure dictates the immunogenicity of cancer cell death
Obeid, M., Tesniere, A., Ghiringhelli, F., Fimia, G. M., Apetoh, L., Perfettini, J.-L., Castedo, M., Mignot, G., Panaretakis, T., Casares, N., et al. (2007) · Nature Medicine · doi:10.1038/nm1523 · Cited by 3,216
Chemical 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
Apoptosis: controlled demolition at the cellular level
Taylor, R. C., Cullen, S. P., & Martin, S. J. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2312 · Cited by 2,708
Caspase Functions in Cell Death and DiseasePreprint
McIlwain, D. R., Berger, T., & Mak, T. W. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008656 · Cited by 2,702
Mixed Lineage Kinase Domain-like Protein Mediates Necrosis Signaling Downstream of RIP3 Kinase
Sun, L., Wang, H., Wang, Z., He, S., Chen, S., Liao, D., Wang, L., Yan, J., Liu, W., Lei, X., et al. (2012) · Cell · doi:10.1016/j.cell.2011.11.031 · Cited by 2,698
Autophagy in Human Health and Disease
Choi, A. M. K., Ryter, S. W., & Levine, B. (2013) · New England Journal of Medicine · doi:10.1056/nejmra1205406 · Cited by 2,583
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Inflammation and its resolution in atherosclerosis: mediators and therapeutic opportunities
Bäck, M., Yurdagul, A., Tabas, I., Öörni, K., & Kovanen, P. T. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-019-0169-2 · Cited by 1,341
Essential versus accessory aspects of cell death: recommendations of the NCCD 2015
Galluzzi, L., Bravo-San Pedro, J. M., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Alnemri, E. S., Altucci, L., Andrews, D., Annicchiarico-Petruzzelli, M., et al. (2015) · Cell Death & Differentiation · doi:10.1038/cdd.2014.137 · Cited by 1,002
“Taken together with the notion that the absence of either Ripk3, Casp8 or Fadd fails to rescue Ripk1 / mice from neonatal lethality,(180,185) these results pointed to the existence of a switch mechanism that regulates cell fate upon TNFR1 ligation.(204,205) Intriguingly, such switch may not operate in all cell types,…”
BackgroundSelf-citationApoptotic Caspases Prevent the Induction of Type I Interferons by Mitochondrial DNA
Rongvaux, A., Jackson, R., Harman, C. C. D., Li, T., West, A. P., de Zoete, M. R., Wu, Y., Yordy, B., Lakhani, S. A., Kuan, C.-Y., et al. (2014) · Cell · doi:10.1016/j.cell.2014.11.037 · Cited by 847
“2008; Callus and Vaux, 2007; Tait et al., 2014).”
BackgroundInfluentialMitochondrial apoptosis: killing cancer using the enemy within
Lopez, J., & Tait, S. W. G. (2015) · British Journal of Cancer · doi:10.1038/bjc.2015.85 · Cited by 817
“Importantly, MOMP often leads to cell death irrespective of caspase activity (Tait et al, 2014).”
BackgroundSelf-citationHSPB1 as a novel regulator of ferroptotic cancer cell death
Sun, X., Ou, Z., Xie, M., Kang, R., Fan, Y., Niu, X., Wang, H., Cao, L., & Tang, D. (2015) · Oncogene · doi:10.1038/onc.2015.32 · Cited by 666
Mitochondrial inner membrane permeabilisation enables mtDNA release during apoptosis
Riley, J. S., Quarato, G., Cloix, C., Lopez, J., O'Prey, J., Pearson, M., Chapman, J., Sesaki, H., Carlin, L. M., Passos, J. F., et al. (2018) · The EMBO Journal · doi:10.15252/embj.201899238 · Cited by 551
Self-citationIchim, G., Lopez, J., Ahmed, S. U., Muthalagu, N., Giampazolias, E., Delgado, M. E., Haller, M., Riley, J. S., Mason, S. M., Athineos, D., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.01.018 · Cited by 479
“However, even in the absence of caspase activity, cells typically die onceMOMP has occurred, most likely due to progressive mitochondrial dysfunction (Lartigue et al., 2009; Tait et al., 2014).”
Self-citationA fate worse than death: apoptosis as an oncogenic process
Ichim, G., & Tait, S. W. G. (2016) · Nature Reviews Cancer · doi:10.1038/nrc.2016.58 · Cited by 451
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Gupta, S., & Kaplan, M. J. (2016) · Nature Reviews Nephrology · doi:10.1038/nrneph.2016.71 · Cited by 443
JNK-signaling: A multiplexing hub in programmed cell death
Dhanasekaran, D. N., & Reddy, E. P. (2017) · Genes & Cancer · doi:10.18632/genesandcancer.155 · Cited by 369
“In contrast to necroptosis, pyroptosis is a caspase-dependent programmed cell death pathway involving caspase 1 and/ or caspase 5 [25, 30].”
BackgroundInfluentialCell death mechanisms of plant-derived anticancer drugs: beyond apoptosis
Gali‐Muhtasib, H. U., Hmadi, R., Kareh, M., Tohmé, R., & Darwiche, N. (2015) · APOPTOSIS · doi:10.1007/s10495-015-1169-2 · Cited by 298
Overcoming chemotherapy drug resistance by targeting inhibitors of apoptosis proteins (IAPs)
Rathore, R., McCallum, J. E., Varghese, E., Florea, A.-M., & Büsselberg, D. (2017) · APOPTOSIS · doi:10.1007/s10495-017-1375-1 · Cited by 288
“However, the mechanisms governing the initiation of necroptosis mediated cell death are so far unexplored in vivo and the repercussions of its potential pro-inflammatory nature have not been fully elucidated [34, 35].”
BackgroundWang, Y., Ning, X., Gao, P., Wu, S., Sha, M., Lv, M., Zhou, X., Gao, J., Fang, R., Meng, G., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.011 · Cited by 279
“Caspase-dependent apoptosis is unique in its capacity to induce a noninflammatory type of cell death (Tait et al., 2014).”
BackgroundMechanisms for Modulating Anoikis Resistance in Cancer and the Relevance of Metabolic Reprogramming
Adeshakin, F. O., Adeshakin, A. O., Afolabi, L. O., Yan, D., Zhang, G., & Wan, X. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.626577 · Cited by 277
“Furthermore, non-apoptotic cell death includes entosis, methuosis, paraptosis, mitotopsis, parthanatos, ferroptosis, pyroptosis, netosis, necrosis, and autophagic cell death as mentioned in the previous studies (9, 10).”
BackgroundMitochondrial permeabilization engages NF-κB-dependent anti-tumour activity under caspase deficiency
Giampazolias, E., Zunino, B., Dhayade, S., Bock, F., Cloix, C., Cao, K., Roca, A., Lopez, J., Ichim, G., Proïcs, E., et al. (2017) · Nature Cell Biology · doi:10.1038/ncb3596 · Cited by 258
Self-citationRole of Mitochondria in Radiation Responses: Epigenetic, Metabolic, and Signaling Impacts
Averbeck, D., & Rodriguez‐Lafrasse, C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011047 · Cited by 262
Caspase-8 as an Effector and Regulator of NLRP3 Inflammasome Signaling
Antonopoulos, C. H., Russo, H. M., Sanadi, C. E. E., Martin, B. N., Li, X., Kaiser, W. J., Mocarski, E. S., & Dubyak, G. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.652321 · Cited by 232
“Given its ubiquitous expression, caspase-8 contributes to the apoptosis or necroptosis of myeloid leukocytes in diverse models of microbial infection or pro-inflammatory stress (67, 68).”
BackgroundMechanisms of Action and Cell Death Associated with Clostridium perfringens Toxins
Navarro, M. A., McClane, B. A., & Uzal, F. A. (2018) · Toxins · doi:10.3390/toxins10050212 · Cited by 225
The Mitochondrion as an Emerging Therapeutic Target in Cancer
Roth, K. G., Mambetsariev, I., Kulkarni, P., & Salgia, R. (2019) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2019.06.009 · Cited by 219
Thompson, J. E. (2018) · Journal of Occupational and Environmental Medicine · doi:10.1097/jom.0000000000001277 · Cited by 217
“Several mechanisms of cellular death have been identified that include apoptosis, necroptosis, pyroptosis, necrosis, and autophagic cell death.(239) Understanding the cell-death mechanism is important to design intervention strategies to ameliorate the detrimental effects of PM on human health.”
BackgroundParaptosis in the anti-cancer arsenal of natural products
Lee, D., Kim, I. Y., Saha, S., & Choi, K. S. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.01.003 · Cited by 216
Pyroptosis Plays a Role in Osteoarthritis
An, S., Hu, H., Li, Y., & Hu, Y. (2020) · Aging and Disease · doi:10.14336/ad.2019.1127 · Cited by 209
“Cell death is also a characteristic of abnormal pathological responses to harmful stimuli, such as physical damage and pathogens [1].”
BackgroundJung, S., Choe, S., Woo, H., Jeong, H., An, H.-K., Moon, H., Ryu, H. Y., Yeo, B. K., Lee, Y. W., Choi, H., et al. (2020) · Autophagy · doi:10.1080/15548627.2019.1630222 · Cited by 183
“Recent progress in the field of cell death indicates the importance of the modes of programmed cell death (PCD) other than apoptosis, such as autophagic cell death (ACD) or necroptosis in human physiology and diseases [3].”
BackgroundRoles of neutrophil granule proteins in orchestrating inflammation and immunity
Othman, A., Sekheri, M., & Filep, J. G. (2021) · FEBS Journal · doi:10.1111/febs.15803 · Cited by 200
Recent insights into cell death and autophagy
Fitzwalter, B. E., & Thorburn, A. M. (2015) · FEBS Journal · doi:10.1111/febs.13515 · Cited by 177
Bacterial Pathogens versus Autophagy: Implications for Therapeutic Interventions
Kimmey, J. M., & Stallings, C. L. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.10.008 · Cited by 167
“Themechanism bywhich an infected cell dies can have amajor impact on immune responses because DAMPs released from dying cells will trigger inflammation [137].”
BackgroundCell Death in the Developing Brain after Hypoxia-Ischemia
Thornton, C., Leaw, B., Mallard, C. E., Nair, S., Jinnai, M., & Hagberg, H. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00248 · Cited by 166
Apoptosis, Necrosis, and Necroptosis in the Gut and IntestinalHomeostasis
Negroni, A., Cucchiara, S., & Stronati, L. (2015) · Mediators of Inflammation · doi:10.1155/2015/250762 · Cited by 169
“Apoptosis has long been considered the only form of regulated cell death, while the existence of additional forms of controlled cell death is now well established [24, 25].”
BackgroundTargeting Ferroptosis against Ischemia/Reperfusion Cardiac Injury
Lillo‐Moya, J., Rojas-Solé, C., Muñoz-Salamanca, D., Panieri, E., Saso, L., & Rodrigo, R. (2021) · Antioxidants · doi:10.3390/antiox10050667 · Cited by 166
“This cell death pathway, unlike other cell death pathways such as apoptosis, does not present a silent inflammatory response [91].”
BackgroundEndoplasmic reticulum stress induces ligand-independent TNFR1-mediated necroptosis in L929 cells
Saveljeva, S., Laughlin, S. L. M., Vandenabeele, P., Samali, A., & Bertrand, M. J. M. (2015) · Cell Death and Disease · doi:10.1038/cddis.2014.548 · Cited by 150
“the only form of regulated cell death, but existence of additional forms of controlled cell death is nowwell established.(32,33) These can be triggered independently of apoptosis induction or as back-up safety mechanisms in situations where the apoptotic machinery does not operate properly, such as a result of genetic…”
BackgroundZielinska, E., Zauszkiewicz–Pawlak, A., Wójcik, M., & Inkielewicz‐Stępniak, I. (2017) · Oncotarget · doi:10.18632/oncotarget.22563 · Cited by 145
Necroptosis Execution Is Mediated by Plasma Membrane Nanopores Independent of Calcium
Ros, U., Peña‐Blanco, A., Hänggi, K., Kunzendorf, U., Krautwald, S., Wong, W. W.-L., & García‐Sáez, A. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.024 · Cited by 141
“Experimentally, it is induced by a combination of TNF-a treatment with molecules that sensitize its activity such as second mitochondria-derived activator of caspases (Smac) mimetics, inhibitors of RNA, or protein synthesis and caspase inhibitors (Tait et al., 2014; Wallach et al., 2016).”
Implication of ferroptosis in aging
Mazhar, M., Din, A. U., Ali, H., Yang, G., Ren, W., Wang, L., Fan, X., & Yang, S. (2021) · Cell Death Discovery · doi:10.1038/s41420-021-00553-6 · Cited by 138
“Besides these modes of cell death, non-apoptotic mechanisms also exist [22] and that is ferroptosis.”
BackgroundPathophysiological role of different tubular epithelial cell death modes in acute kidney injury
Sancho-Martínez, S. M., López-Novoa, J. M., & López-Hernández, F. J. (2015) · Clinical Kidney Journal · doi:10.1093/ckj/sfv069 · Cited by 130
Carotenoids in Cancer Apoptosis—The Road from Bench to Bedside and Back
Koklesová, L., Líšková, A., Samec, M., Buhrmann, C., Samuel, S. M., Varghese, E., Ashrafizadeh, M., Najafi, M., Shakibaei, M., Büsselberg, D., et al. (2020) · Cancers · doi:10.3390/cancers12092425 · Cited by 128
“Programmed cell death (PCD) represents an important concept, which is defined as a genetically regulated cascade leading to controlled cell removal.”
BackgroundInfluentialMitochondria and Inflammation: Cell Death Heats Up
Vringer, E., & Tait, S. W. G. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00100 · Cited by 124
“Nevertheless, cells usually die irrespective of caspase activation upon MOMP, demarcating it as a point of no return (Tait et al., 2014).”
BackgroundSelf-citationHe, B., Shi, Y., Liang, Y., Yang, A., Fan, Z., Yuan, L., Zou, X., Chang, X. Y., Zhang, H., Wang, X., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-04700-z · Cited by 122
Oxidants, Antioxidants and Thiol Redox Switches in the Control of Regulated Cell Death Pathways
Benhar, M. (2020) · Antioxidants · doi:10.3390/antiox9040309 · Cited by 122
“In the last two decades, additional forms of RCD have been discovered and characterized [15,16].”
BackgroundInfluentialZhao, J., Dar, H. H., Deng, Y., Croix, C. M. S., Li, Z., Minami, Y., Shrivastava, I. H., Tyurina, Y. Y., Etling, E. B., Rosenbaum, J. C., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1921618117 · Cited by 121
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Yanguas, S. C., Willebrords, J., Johnstone, S. R., Maes, M., Decrock, E., Bock, M. D., Leybaert, L., Cogliati, B., & Vinken, M. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.10.006 · Cited by 122
Paraptosis: a unique cell death mode for targeting cancer
Hanson, S., Dharan, A., Jinsha, P. V., Pal, S., Nair, B. G., Kar, R., & Mishra, N. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1159409 · Cited by 124
“An alternate death pathway is activated in the cell only when its apoptosis machinery is non-functional (Chipuk and Green, 2005; Elmore, 2007; Tait et al., 2014).”
BackgroundTse, S., McKinney, K. M., Walker, W., Nguyen, M., Iacovelli, J., Small, C. G., Hopson, K., Zaks, T. Z., & Huang, E. (2021) · Molecular Therapy · doi:10.1016/j.ymthe.2021.03.002 · Cited by 114
“As an alternative to inducing constitutively active innate immune sensor signaling pathways as genetic adjuvants, we also attempted to induce two forms of programmed cell death: necroptosis and pyroptosis.(44) Both mechanisms result in loss of cell membrane integrity and subsequent release of DAMPs such as high mobili…”
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Wei, J., Zhao, Y., Liang, H., Du, W., & Wang, L. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.08.026 · Cited by 108
Cell death at the intestinal epithelial front line
Delgado, M. E., Grabinger, T., & Brunner, T. (2015) · FEBS Journal · doi:10.1111/febs.13575 · Cited by 107
Non-apoptotic cell death in malignant tumor cells and natural compounds
Ye, J., Zhang, R., Wu, F., Zhai, L., Wang, K., Xiao, M., Xie, T., & Sui, X. (2018) · Cancer Letters · doi:10.1016/j.canlet.2018.01.061 · Cited by 103
Ferritinophagy drives uropathogenic Escherichia coli persistence in bladder epithelial cells
Bauckman, K. A., & Mysorekar, I. U. (2016) · Autophagy · doi:10.1080/15548627.2016.1160176 · Cited by 100
“We first considered apoptosis and inflammatory-mediated apoptosis, pyroptosis.(38) To assess apoptosis, we used western blots to Figure 3.”
MethodRole of mitochondria in apoptotic and necroptotic cell death in the developing brain
Thornton, C., & Hagberg, H. (2015) · Clinica Chimica Acta · doi:10.1016/j.cca.2015.01.026 · Cited by 102
“In addition, RIP3 may also play a role in the decision of the cell to follow an apoptotic or necroptotic route although the mechanism is unclear [34,35].”
BackgroundThe innate immune response to allotransplants: mechanisms and therapeutic potentials
Ochando, J., Ordikhani, F., Boros, P., & Jordan, S. (2019) · Cellular and Molecular Immunology · doi:10.1038/s41423-019-0216-2 · Cited by 108
In Vitro Cell Death Determination for Drug Discovery: A Landscape Review of Real Issues
Méry, B., Guy, J., Vallard, A., Espenel, S., Ardail, D., Rodriguez‐Lafrasse, C., Rancoule, C., & Magné, N. (2017) · Journal of Cell Death · doi:10.1177/1179670717691251 · Cited by 104
Recent Advances in Cancer Therapeutic Copper-Based Nanomaterials for Antitumor Therapy
Aishajiang, R., Liu, Z., Wang, T., Zhou, L. Y., & Yu, D. N. (2023) · Molecules · doi:10.3390/molecules28052303 · Cited by 99
Programmed cell death in aortic aneurysm and dissection: A potential therapeutic target
Chakraborty, A., Yang, L., Zhang, C., Li, Y., LeMaire, S. A., & Shen, Y. H. (2021) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2021.09.010 · Cited by 95
“Many other types of non-apoptotic programmed cell death have been characterized, including necroptosis, ferroptosis, pyroptosis, parthanatos, entotic cell death, neutrophil extracellular traps–mediated (NETotic) cell death, lysosome-dependent cell death, autophagy-dependent cell death, immunogenic cell death, cellular…”
BackgroundChemical warfare agents. Classes and targets
Schwenk, M. (2017) · Toxicology Letters · doi:10.1016/j.toxlet.2017.11.040 · Cited by 90
Ferroptosis and Senescence: A Systematic Review
Coradduzza, D., Congiargiu, A., Chen, Z., Zinellu, A., Carru, C., & Medici, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043658 · Cited by 93
“Ferroptosis was first reported in 2012 [1,2], as an iron-dependent mechanism of nonapoptotic cell death [3], which has attracted the researchers’ interest due to its implications in the pathogenesis of various age-related disorders.”
BackgroundJang, Y., Lee, A. Y., Jeong, S., Park, K.-H., Paik, M.-K., Cho, N.-J., Kim, J., & Cho, M. (2015) · Toxicology · doi:10.1016/j.tox.2015.09.006 · Cited by 88
Bacteriocyte cell death in the pea aphid/ Buchnera symbiotic system
Simonet, P., Gaget, K., Balmand, S., Lopes, M. R., Parisot, N., Buhler, K., Duport, G., Vulsteke, V., Febvay, G., Heddi, A., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1720237115 · Cited by 94
Xia, Y., Xu, F., Xiong, M., Yang, H., Lin, W., Xie, Y., Xi, H., Xue, Q., Ye, T., & Yu, L. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105295 · Cited by 82
Rechter, S. D., Decuypere, J.-P., Ivanova, E., van den Heuvel, L. P., SMEDT, H. D., Levtchenko, E. N., & Mekahli, D. (2015) · Pediatric Nephrology · doi:10.1007/s00467-015-3134-2 · Cited by 80
“Unconjugated Atg12 can induce apoptosis by inhibiting Bcl-2 [26].”
BackgroundThe hidden side of SERPINB1/Leukocyte Elastase Inhibitor
Torriglia, A., Martin, E., & Jaadane, I. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.07.010 · Cited by 82
The DNA-damage response and nuclear events as regulators of nonapoptotic forms of cell death
Prokhorova, E. A., Egorshina, A. Y., Zhivotovsky, B., & Kopeina, G. S. (2019) · Oncogene · doi:10.1038/s41388-019-0980-6 · Cited by 80
SENP3-mediated deSUMOylation of Drp1 facilitates interaction with Mff to promote cell death
Guo, C., Wilkinson, K. A., Evans, A. J., Rubin, P. P., & Henley, J. M. (2017) · Scientific Reports · doi:10.1038/srep43811 · Cited by 77
Acid sphingomyelinase promotes mitochondrial dysfunction due to glutamate-induced regulated necrosis
Novgorodov, S. A., Voltin, J. R., Gooz, M. A., Li, L., Lemasters, J. J., & Gudz, T. I. (2017) · Journal of Lipid Research · doi:10.1194/jlr.m080374 · Cited by 77
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BackgroundInfluentialPopulation Dynamics in Cell Death: Mechanisms of Propagation
Riegman, M., Bradbury, M. S., & Overholtzer, M. (2019) · Trends in cancer · doi:10.1016/j.trecan.2019.07.008 · Cited by 75
“It was once thought that apoptosis, a form of cell suicide, was the only regulated form of cell death, but recent findings have uncovered numerous additional regulated death mechanisms, including several forms of necrosis [3], a program called entosis [5], and others.”
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Lazzarin, T., Tonon, C. R., Martins, D., Fávero, E. L., Baumgratz, T. D., Pereira, F. W. L., Pinheiro, V. R., Ballarin, R. S., Queiróz, D. A. R., Azevedo, P. S., et al. (2022) · Journal of Clinical Medicine · doi:10.3390/jcm12010259 · Cited by 87
“Each of these mechanisms is activated by distinct signaling pathways, culminating in different modes of cell death and different consequences for the organism [35].”
BackgroundLee, W., Probst, S., Santoyo-Sánchez, M. P., Al-Hamdani, W., Diebels, I., von Sivers, J.-K., Kerek, E. M., Prenner, E. J., & Thévenod, F. (2017) · Archives of Toxicology · doi:10.1007/s00204-017-1942-9 · Cited by 76
“Meanwhile, a plethora of additional apoptotic and non-apoptotic death modes have been characterized (Fuchs and Steller 2015; Tait et al. 2014).”
BackgroundJarman, P. J., Noakes, F. F., Fairbanks, S. D., Smitten, K. L., Griffiths, I. K., Saeed, H. K., Thomas, J. A., & Smythe, C. (2018) · Journal of the American Chemical Society · doi:10.1021/jacs.8b09999 · Cited by 72
Natural Products as Inducers of Non-Canonical Cell Death: A Weapon against Cancer
Greco, G., Catanzaro, E., & Fimognari, C. (2021) · Cancers · doi:10.3390/cancers13020304 · Cited by 70
Bonney, E. A. (2017) · American Journal of Reproductive Immunology · doi:10.1111/aji.12652 · Cited by 67
Selvi, A. M., Palanisamy, S., Jeyanthi, S., Vinosha, M., Mohandoss, S., Tabarsa, M., You, S., Ethiraj, K., & Prabhu, N. M. (2020) · Process Biochemistry · doi:10.1016/j.procbio.2020.07.008 · Cited by 66
Unconjugated bilirubin induces pyroptosis in cultured rat cortical astrocytes
Feng, J., Li, M., Wei, Q., Sheng-jun, L., Song, S., & Hua, Z. (2018) · Journal of Neuroinflammation · doi:10.1186/s12974-018-1064-1 · Cited by 65
“and cell survival in nervous system pathologies [21, 23, 37].”
Sharifi, M., Hosseinali, S. H., Saboury, A. A., Szegezdi, É., & Falahati, M. (2019) · Journal of Controlled Release · doi:10.1016/j.jconrel.2019.02.007 · Cited by 62
Green Synthesis of Platinum Nanoparticles for Biomedical Applications
Михайлова, Е. О. (2022) · Journal of Functional Biomaterials · doi:10.3390/jfb13040260 · Cited by 67
Functional Foods: An Approach to Modulate Molecular Mechanisms of Alzheimer’s Disease
Atlante, A., Amadoro, G., Bobba, A., & Latina, V. (2020) · Cells · doi:10.3390/cells9112347 · Cited by 67
Mito-priming as a method to engineer Bcl-2 addiction
Lopez, J., Bessou, M., Riley, J. S., Giampazolias, E., Todt, F., Rochegüe, T., Oberst, A., Green, D. R., Edlich, F., Ichim, G., et al. (2016) · Nature Communications · doi:10.1038/ncomms10538 · Cited by 58
“5b,c) and (2) BIM, which displays an anti-apoptotic Bcl-2 binding profile similar to tBID and PUMA5,21,29, failed to display any selectivity for BAK or BAX.”
BackgroundSelf-citationSerna, N., Álamo, P., Ramesh, P., Vinokurova, D., Sánchez‐García, L., Unzueta, U., Gallardo, A., Céspedes, M. V., Vázquez, E., Villaverde, A., et al. (2020) · Journal of Controlled Release · doi:10.1016/j.jconrel.2020.01.019 · Cited by 62
Naso, L. G., Martínez, V. R., Lezama, L. M., Salado, C., Valcárcel, M., Ferrer, E. G., & Williams, P. A. M. (2016) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2016.06.053 · Cited by 60
Depletion of mitochondria in mammalian cells through enforced mitophagy
Correia‐Melo, C., Ichim, G., Tait, S. W. G., & Passos, J. F. (2016) · Nature Protocols · doi:10.1038/nprot.2016.159 · Cited by 63
Self-citationAnticancer Agents Targeted to Sirtuins
Kozako, T., Suzuki, T., Yoshimitsu, M., Arima, N., Honda, S., & Soeda, S. (2014) · Molecules · doi:10.3390/molecules191220295 · Cited by 61
“For the maintenance of homeostasis, regulated cell death plays a key role in a variety of biological processes including tissue sculpting during embryogenesis, development of immunity, and destruction of damaged cells and tumors [53].”
BackgroundDED or alive: assembly and regulation of the death effector domain complexes
Riley, J. S., Malik, A., Holohan, C., & Longley, D. B. (2015) · Cell Death and Disease · doi:10.1038/cddis.2015.213 · Cited by 60
“cell death have emerged, including necroptosis, pyroptosis and ferroptosis, which have been comprehensively reviewed elsewhere.(2,3) Here, we focus on those mechanisms of cell”
BackgroundMitochondria orchestrate macrophage effector functions in atherosclerosis
Dumont, A., Lee, M., Barouillet, T., Murphy, A. J., & Yvan‐Charvet, L. (2020) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2020.100922 · Cited by 60
Zhan, Y., Chow, K. V., Soo, P., Xu, Z., Brady, J. L., Lawlor, K. E., Masters, S. L., O’Keeffe, M. A., Shortman, K., Zhang, J., et al. (2016) · Scientific Reports · doi:10.1038/srep25060 · Cited by 56
Edwardsiella tarda-Induced Inhibition of Apoptosis: A Strategy for Intracellular Survival
Zhou, Z., & Sun, L. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00076 · Cited by 57
Wu, C., Hong, C., Klauck, S. M., Lin, Y., & Efferth, T. (2015) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2015.10.020 · Cited by 57
Anticancer metallohelices: nanomolar potency and high selectivity
Kaner, R. A., Allison, S. J., Faulkner, A. D., Phillips, R. M., Roper, D. I., Shepherd, S. L., Simpson, D. H., Waterfield, N. R., & Scott, P. (2015) · Chemical Science · doi:10.1039/c5sc03677a · Cited by 55
Stefanović, M., Tutusaus, A., Martínez-Nieto, G., Bárcena, C., de Gregorio, E., Moutinho, C., Barbero‐Camps, E., Villanueva, A., Colell, A., Marı́, M., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.6982 · Cited by 55
“Release of mitochondrial intermembrane proteins such as cytochrome c induces a rapid loss of activity in respiratory complexes jeopardizing mitochondrial functionality, and leading to bioenergetic crisis and cell death [34].”
6-Shogaol induces caspase-independent paraptosis in cancer cells via proteasomal inhibition
Nedungadi, D., Binoy, A., Nanjan, P., Pal, S., Nair, B. G., & Mishra, N. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.02.018 · Cited by 55
The Complex Mechanisms by Which Neurons Die Following DNA Damage in Neurodegenerative Diseases
Shadfar, S., Brocardo, M. G., & Atkin, J. D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052484 · Cited by 60
“Furthermore, depending on the stimulus and cellular context, in some circumstances, autophagy may antagonize or delay apoptosis, or if these two processes act exclusively, they serve as reciprocal backup mechanisms [87].”
BackgroundMiller, R. A., Betteken, M. I., Guo, X., Altier, C., Duhamel, G. E., & Wiedmann, M. (2018) · mBio · doi:10.1128/mbio.00467-18 · Cited by 54
“Because other, nonapoptotic cell death pathways exist (32), we also quantified the number of PI-positive cells (used as a live/dead stain).”
Caspase selective reagents for diagnosing apoptotic mechanisms
Poręba, M., Groborz, K. M., Navarro, M., Snipas, S. J., Drąg, M., & Salvesen, G. S. (2018) · Cell Death and Differentiation · doi:10.1038/s41418-018-0110-y · Cited by 54
Bedient, L., Pokharel, S. M., Chiok, K. L., Mohanty, I. P., Beach, S. S., Miura, T. A., & Bose, S. (2020) · Viruses · doi:10.3390/v12090932 · Cited by 56
“Lytic cell death is an inflammatory cell death caused primarily by two cellular mechanisms: pyroptosis and necroptosis [12,13,18].”
BackgroundThe Janus Face of Death Receptor Signaling during Tumor Immunoediting
Reilly, E. O., Tirincsi, A., Logue, S. E., & Szegezdi, É. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00446 · Cited by 51
“In the absence of caspase-8 activation, the cell can either undergo death via necroptosis (134) or induce NF-κB activity and survival signaling (135) with the outcome dependent on the ubiquitination status of RIPK1 (Figure 2D).”
BackgroundKishino, A., Hayashi, K., Maeda, M., Jike, T., Hidai, C., Nomura, Y., & Oshima, T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20235896 · Cited by 53
“Recently, it has been appreciated that various types of non-apoptotic cell deaths, like necroptosis, exist [19].”
BackgroundTang, Y., Wa, Q., Peng, L., Zheng, Y., Chen, J., Chen, X., Zou, X., Shen, H., & Huang, S. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/8332825 · Cited by 52
“Activated caspase-1, meanwhile, can promote caspase-1-dependent pyroptosis [16].”
Flamme, M., Cressey, P., Lü, C., Bruno, P. M., Eskandari, A., Hemann, M. T., Hogarth, G., & Suntharalingam, K. (2017) · Chemistry - A European Journal · doi:10.1002/chem.201701837 · Cited by 53
Necroptosis in amyotrophic lateral sclerosis and other neurological disorders
Morrice, J. R., Gregory, C. Y., & Shaw, C. A. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.11.025 · Cited by 54
Carneiro, M. B. H., Roma, E. H., Ranson, A. J., Doria, N. A., Debrabant, A., Sacks, D. L., Vieira, L. Q., & Peters, N. C. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1700899 · Cited by 50
“necroptosis, pyroptosis, or some other caspase-independent form of cell death (67).”
BackgroundFibronectin has multifunctional roles in posterior capsular opacification (PCO)
Shihan, M. H., Kanwar, M., Wang, Y., Jackson, E., Faranda, A. P., & Duncan, M. K. (2020) · Matrix Biology · doi:10.1016/j.matbio.2020.02.004 · Cited by 54
Yang, L., Liu, Y., Wang, M., Qian, Y., Dai, X., Zhu, Y., Chen, J., Guo, S., & Hisamitsu, T. (2016) · Oncology Letters · doi:10.3892/ol.2016.5213 · Cited by 49
Cui, Y., Liu, Y., & Zhang, F. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.12.144 · Cited by 48
Glutathione peroxidase 7 suppresses cancer cell growth and is hypermethylated in gastric cancer
Chen, Z., Hu, T., Zhu, S., Mukaisho, K., El-Rifai, W. M., & Peng, D. (2017) · Oncotarget · doi:10.18632/oncotarget.17527 · Cited by 47
“However, there are multiple forms of non-apoptotic cell death [30, 31] that may also contribute to the net outcome and functions of GPX7 in cellular homeostasis.”
Background
Metadata
- Authors
- Tait, S. W. G., Ichim, G., & Green, D. R.
- Affiliations
- Cancer Research UK Scotland Institute (GB)
- St. Jude Children's Research Hospital (US)
- Venue
- Journal of Cell Science
- Publisher
- The Company of Biologists
- Published
- 2014-05-15
- Volume
- 127
- Issue
- 10
- Pages
- 2135-2144
- ISSN
- 0021-9533 (ISSN-L)
- 1477-9137
- PMC
- PMC4021468
- OpenAlex
- W2021358525
- Cited by
- 366
- References
- 130
- Citations by year
- 2026: 11 · 2025: 16 · 2024: 21 · 2023: 14 · 2022: 26 · 2021: 34 · 2020: 41 · 2019: 48 · 2018: 40 · 2017: 43 · 2016: 35 · 2015: 30 · 2014: 5
- FWCI
- 3.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Cell Science (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- ENLIGHTEN (Jurnal Bimbingan dan Konseling Islam) (submittedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Biotechnology and Biological Sciences Research Council (BB/K008374/1)
- National Institute of General Medical Sciences (R01GM096208)
- National Institute of Allergy and Infectious Diseases (R01AI044828)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Inflammasome and immune disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Keywords
- non-apoptotic cell death, programmed cell death, necroptosis, pyroptosis, autophagic cell death, caspase-independent cell death, apoptosis, inflammation, immune system development
- MeSH terms
- Animals, Autophagy, Humans, Cell Death, Apoptosis
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