The DOI matches its Crossref record; 150 of the 150 references it cites were found in a registry or an index.
Crosstalk between apoptosis.; necrosis and autophagy
Open accessAbstract
Apoptosis and necrosis are the two major modes of cell death, the molecular mechanisms of which have been extensively studied. Although initially thought to constitute mutually exclusive cellular states, recent findings reveal cellular contexts that require a balanced interplay between these two modes of cellular demise. Several death initiator and effector molecules, signaling pathways and subcellular sites have been identified as key mediators in both processes, either by constituting common modules or alternatively by functioning as a switch allowing cells to decide which route to take, depending on the specific situation. Importantly, autophagy, which is a predominantly cytoprotective process, has been linked to both types of cell death, serving either a pro-survival or pro-death function. Here we review the recent literature that highlights the intricate interplay between apoptosis, necrosis and autophagy, focusing on the relevance and impact of this crosstalk in normal development and in pathology. This article is part of a Special Section entitled: Cell Death Pathways.
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?
In the citing paper
“While autophagy is implicated in several paradigms of life extension and is generally considered an antiaging mechanism, autophagy is also a well-defined mechanism of cell death, autophagy-dependent cell death, ADCD [153,154,155].”
From The mitochondrial permeability transition: Nexus of aging, disease and longevity (2021) · cites this paper as [153]
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
The NAD-dependent deacetylase SIRT2 is required for programmed necrosis
Narayan, N., Lee, I. H., Borenstein, R., Sun, J., Wong, R. P., Tong, G., Fergusson, M. M., Liu, J., Rovira, I. I., Cheng, H.-L., et al. (2012) · Nature · doi:10.1038/nature11700 · Cited by 136 · cited 2×
“Recent fi ndings indicate that SIRT2 is also involved in the regulation of necroptosis [130].”
BackgroundRetractedApoptosis: 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
p53, the cellular gatekeeper for growth and division
Levine, A. J. (1997) · Cell · doi:10.1016/s0092-8674(00)81871-1 · Cited by 7,693
AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1
Kim, J., Kundu, M., Viollet, B., & Guan, K.-L. (2011) · Nature Cell Biology · doi:10.1038/ncb2152 · Cited by 7,227 · cited 1×
“3; [135,136]), or through activation of theULK1complex[137,138].”
Cell Death: The Significance of Apoptosis
Wyllie, A. H., Kerr, J. F. R., & Currie, A. R. (1980) · International review of cytology · doi:10.1016/s0074-7696(08)62312-8 · Cited by 7,151 · cited 1×
“Mechanistically, necrosis is typically not associated with activation of caspases, and it is thought that it mediates cell demise in response to damage, or in pathology [10,11], but not during normal development.”
BackgroundAutophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069 · cited 1×
“Completion of the autophagosome is followed by fusion with a lysosome to form an autolysosome, where the captured material is degraded by specific acidic hydrolases [12].”
BackgroundAutophagy fights disease through cellular self-digestion
Mizushima, N., Levine, B., Cuervo, A. M., & Klionsky, D. J. (2008) · Nature · doi:10.1038/nature06639 · Cited by 6,452 · cited 1×
“Although it is primarily considered to have a cytoprotective function, autophagy can also promote cell death during normal development (reviewed in [13]), as well as, in disease (reviewed in [14]).”
BackgroundTOR signaling in growth and metabolism
Wullschleger, S., Loewith, R., & Hall, M. N. (2006) · Cell · doi:10.1016/j.cell.2006.01.016 · Cited by 5,787 · cited 1×
“Low insulin – IGF1 signaling, nutrient or energy limitation and stress converge to downregulate the activity of TOR [83].”
BackgroundCellular survival: a play in three Akts
Datta, S. R., Brunet, A., & Greenberg, M. E. (1999) · Genes & Development · doi:10.1101/gad.13.22.2905 · Cited by 4,216 · cited 1×
“AKT ability to prevent apoptosis in some cells is established through phosphorylation and inhibition of pro-apoptotic mediators such as Bad and caspase-9 [44].”
BackgroundTSC2 Mediates Cellular Energy Response to Control Cell Growth and Survival
Inoki, K., Zhu, T., & Guan, K.-L. (2003) · Cell · doi:10.1016/s0092-8674(03)00929-2 · Cited by 3,914 · cited 1×
“3; [135,136]), or through activation of theULK1complex[137,138].”
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 1,001
Hojo, T., Skarzynski, D. J., & Okuda, K. (2022) · Journal of Reproduction and Development · doi:10.1262/jrd.2022-097 · Cited by 23
Targeting of non-apoptotic cancer cell death mechanisms by quercetin: Implications in cancer therapy
Yang, H., Xu, S., Tang, L., Gong, J., Fang, H., Wei, J., & Su, D. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1043056 · Cited by 24
Chen, B., Liu, X., Wu, S., Hou, J., Shang, P., Chamba, Y., Mehmood, K., Fouad, D., Li, Y., & Zhang, H. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.169036 · Cited by 22
Swindell, E. C., Yuan, Q., Maili, L., Tandon, B., Wagner, D. S., & Hecht, J. T. (2015) · genesis · doi:10.1002/dvg.22897 · Cited by 22
“…death pathway genes, in crispld2 knockdown embryos using real-time quantitative PCR. Caspase 8 is a known mediator of both apoptosis and necrosis and has been shown to act in both p53-dependent and -independent cell death pathways (Blander, 2014; Nikoletopoulou et al., 2013; Shalini et al., 2015).”
MethodWinter, J., Klumpe, I., Heger, J., Rauch, U., Schultheiß, H., Landmesser, U., & Dörner, A. (2015) · Cellular Signalling · doi:10.1016/j.cellsig.2015.11.002 · Cited by 22
Costa, A. F., Gomes, S. Z., Lorenzon, A. R., Martucci, M. F., Faria, M. F. D. O., Júnior, D. D. S. P., de Oliveira, S. F., Ietta, F., Paulesu, L. R., & Bevilacqua, E. M. A. F. (2016) · Placenta · doi:10.1016/j.placenta.2016.03.001 · Cited by 22
Kwak, B. K., & Lee, S.-H. (2013) · Development & Reproduction · doi:10.12717/dr.2013.17.4.435 · Cited by 22
“On the other hand, apoptosis, another type of cell death, has been widely accepted as a major mechanism of regulated cell death, employed not only upon accidental cell damage or stress but also during normal development (Nikoletopoulou et al., 2013).”
BackgroundDoustvandi, M. A., Mohammadnejad, F., Mansoori, B., Mohammadi, A., Navaeipour, F., Baradaran, B., & Tajalli, H. (2017) · Journal of Photochemistry and Photobiology B Biology · doi:10.1016/j.jphotobiol.2017.09.020 · Cited by 22
Martínez‐Torres, A. C., Reyes‐Ruiz, A., Londoña, M. B., Franco-Molina, M. Á., & Rodrı́guez-Padilla, C. (2018) · BMC Cancer · doi:10.1186/s12885-017-3954-5 · Cited by 27
“These findings also suggest that multiple cell death modalities can engage common subcellular sites and organelles, and even share initiator and effector molecules [40, 41].”
BackgroundCao, W., Zhang, J., Wang, G., Lu, J., Wang, T., & Chen, X. (2018) · The Anatomical Record · doi:10.1002/ar.23798 · Cited by 22
“The organelles and cytoplasm are destroyed throughout the autophagy process, especially in the mitochondria and endoplasmic reticulum (Kroemer et al., 2009; Nikoletopoulou et al., 2013).”
BackgroundJembrek, M. J., Vlainić, J., Čadež, V., & Šegota, S. (2018) · PLoS ONE · doi:10.1371/journal.pone.0200119 · Cited by 22
Son, J. Y., Yoon, S., Tae, I. H., Park, Y. J., De, U., Jeon, Y., Park, Y. J., Rhyu, I. J., Lee, B. M., Chung, K., et al. (2018) · Cancer Medicine · doi:10.1002/cam4.1748 · Cited by 21
Gallorini, M., Maccallini, C., Ammazzalorso, A., Amoia, P., Filippis, B. D., Fantacuzzi, M., Giampietro, L., Cataldi, A., & Amoroso, R. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20030495 · Cited by 22
“In normal cellular conditions, Nrf-2 has anti-cancerous effects due to the induction of ARE-dependent cytoprotective genes expression that protect the cells from oxidative and electrophilic stress [14].”
BackgroundKhazaei, M., Pazhouhi, M., & Khazaei, S. (2018) · Europe PMC (PubMed Central) · doi:10.22074/cellj.2018.5380 · Cited by 23
“P53 induces autophagy through TOR inhibition and also through transcriptional activation of DRAM (24).”
BackgroundMorphological and ultrastructural examination of senescence in Morchella elata
He, P., Cai, Y., Liu, S., Han, L., Huang, L., & Liu, W. (2015) · Micron · doi:10.1016/j.micron.2015.07.010 · Cited by 22
Chen, Y., Tian, P., Li, Y., Tang, Z., & Zhang, H. (2024) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2024.106010 · Cited by 21
Role of Autophagy in Photoreceptor Cell Survival and Death
Bo, Q., Ma, S., Han, Q., Wang, F. E., Li, X., & Zhang, Y. (2015) · Critical Reviews in Eukaryotic Gene Expression · doi:10.1615/critreveukaryotgeneexpr.2015012376 · Cited by 23
TRAIL reduces impaired glucose tolerance and NAFLD in the high-fat diet fed mouse
Bernardi, S., Toffoli, B., Tisato, V., Bossi, F., Biffi, S., Lorenzon, A., Zauli, G., Secchiero, P., & Fabris, B. (2017) · Clinical Science · doi:10.1042/cs20171221 · Cited by 21
“19 In addition, based on our in vitro studies, where TRAIL increased ATG7, a possible unifying 363 hypothesis explaining TRAIL effects on liver steatosis and PGC-1α is that they might be due to 364 TRAIL-induced liver autophagy (50).”
BackgroundDu, Y., Li, K., Wang, X., Kaushik, A. C., Junaid, M., & Wei, D. (2019) · FEBS Journal · doi:10.1111/febs.15102 · Cited by 21
Grambow, F., Rutkowski, R., Podmelle, F., Schmoeckel, K., Siegerist, F., Domanski, G., Schuster, M., & Domańska, G. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21082869 · Cited by 21
“In contrast, necrosis involves cell swelling, membrane perforation, and phagocytosis with inflammation [43].”
BackgroundChan, W., & Ham, Y.-H. (2021) · Chemical Research in Toxicology · doi:10.1021/acs.chemrestox.1c00175 · Cited by 21
At the Crossroads: Mechanisms of Apoptosis and Autophagy in Cell Life and Death
Shliapina, V. L., Yurtaeva, S. V., Rubtsova, M. P., & Dontsova, O. А. (2021) · Acta Naturae · doi:10.32607/actanaturae.11208 · Cited by 22
Deng, Z., Yang, Z., & Peng, J. (2021) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2021.1992606 · Cited by 21
The role of PFKFB3 in maintaining colorectal cancer cell proliferation and stemness
Yan, S., Li, Q., Li, S., Ai, Z., & Yuan, D. (2022) · Molecular Biology Reports · doi:10.1007/s11033-022-07513-y · Cited by 21
“1 3 deprivation commonly aggravates the occurrence of cell death [66, 67].”
BackgroundXiao, H., Long, J., Chen, X., & Tan, M. (2022) · Experimental Cell Research · doi:10.1016/j.yexcr.2022.113234 · Cited by 21
Lai, H.-T., Naumova, N., Marchais, A., Gaspar, N., Geoerger, B., & Brenner, C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.948097 · Cited by 23
“It has been established that mitochondria are central initiators of the apoptotic intrinsic pathways, but they may also participate in other forms of RCD such as necroptosis, and ferroptosis (Nikoletopoulou et al., 2013).”
BackgroundLima, B. S. A., Rocha, F. A. D., Plata‐Rueda, A., Zanuncio, J. C., Cossolin, J. F. S., Martínez, L. C., & Serrão, J. É. (2023) · Journal of Pest Science · doi:10.1007/s10340-023-01642-4 · Cited by 21
Zhang, Y., Cui, J., Li, K., Xu, S., Yin, H., Li, S., & Gao, X. (2023) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2023.115628 · Cited by 21
Sereemaspun, A., Sooklert, K., Chattong, S., Manotham, K., Boonwong, C., Klaharn, I.-Y., & Jindatip, D. (2016) · International Journal of Nanomedicine · doi:10.2147/ijn.s95654 · Cited by 21
“In addition, it has been revealed that the mechanism underlying the switch in the pattern of cell death is related to inhibition of caspases.(37,38) Based on these findings, we propose that GEPO reduces cell death not only by increasing expression of the anti-apoptotic protein Bcl2 but also by inhibition of caspases i…”
BackgroundThe role of estradiol metabolism in urogenital schistosomiasis-induced bladder cancer
Vale, N., Gouveia, M. J., Rinaldi, G., Santos, J., Santos, L. L., Brindley, P. J., & da Costa, J. M. C. (2017) · Tumor Biology · doi:10.1177/1010428317692247 · Cited by 21
Adefegha, S. A., Leal, D. B. R., de Oliveira, J. S., Manzoni, A. G., & Bremm, J. M. (2017) · Food & Function · doi:10.1039/c7fo01008g · Cited by 21
Hong, L., Wei, S., Zhang, L., Yuan, C., Duan, Y., & Wang, Q. (2018) · Pathology & Oncology Research · doi:10.1007/s12253-018-0504-7 · Cited by 21
Shan, C., Gong, Y., Zhuang, Q.-Q., Hou, Y., Wang, S., Zhu, Q., Huang, G., Tao, B., Sun, L., Zhao, H., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.109670 · Cited by 21
Abbruzzese, G., Morón-Oset, J., Díaz-Castroverde, S., García-Font, N., Roncero, C., Lopez-Munoz, F. J., Marco, J. L., & Oset‐Gasque, M. J. (2020) · Antioxidants · doi:10.3390/antiox9060545 · Cited by 22
“More recently, autophagy has also been seen to crosstalk with other nonapoptotic or regulated necrotic death pathways such as necroptosis and pyroptosis [59], which have also been reported in brain ischemia [60].”
BackgroundNumb ameliorates necrosis and inflammation in acute kidney injury induced by cisplatin
Liu, Z., Li, Z., Chen, Z., Li, C., Lei, L., Wu, X., & Li, Y. (2020) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2020.109251 · Cited by 21
Denamur, S., Boland, L., Beyaert, M., Verstraeten, S. L., Fillet, M., Tulkens, P. M., Bontemps, F., & Mingeot‐Leclercq, M. (2016) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2016.08.020 · Cited by 23
Cheng, M.-F., Lin, S., Tseng, F.-J., Huang, Y., Tsai, M., Fu, Y., & Weng, C. (2017) · Oncotarget · doi:10.18632/oncotarget.18987 · Cited by 22
“In addition, Beclin-1-independent signal pathway is associated with PI3K-ClassIII and induces p62 activity [31], suggesting that Beclin-1-independent signal pathway is also involved in the activation of autophagy.”
BackgroundBaumann, A., Jorge-Finnigan, A., Jung-KC, K., Sauter, A., Horvath, I., Morozova-Roche, L. A., & Martinez, A. (2016) · Scientific Reports · doi:10.1038/srep39488 · Cited by 20
Autophagy regulatory molecule, TMEM74, interacts with BIK and inhibits BIK-induced apoptosis.
Sun, Y., Li, Q., Zhang, J., Chen, Z., He, Q.-H., Liu, X., Zhao, N., Yin, A., Huang, H., He, M., et al. (2017) · Cellular Signalling · doi:10.1016/j.cellsig.2017.04.005 · Cited by 21
mTOR inhibitor Everolimus-induced apoptosis in melanoma cells
Ciołczyk-Wierzbicka, D., Zarzycka, M., Gil, D., & Laidler, P. M. (2019) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-019-00510-0 · Cited by 20
Torres-Martínez, A., Bedrina, B., Falomir, E., Marín, M. J., Angulo‐Pachón, C. A., Galindo, F., & Miravet, J. F. (2021) · ACS Applied Bio Materials · doi:10.1021/acsabm.1c00139 · Cited by 20
Evaluation of toxicological effects of organophosphorus pesticide metabolites on human HepG2 cells
Zhang, N., Zhu, L., Zhang, R., Zhang, C., Cheng, J., Tao, L., Zhang, Y., & Xu, W. (2021) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2021.103741 · Cited by 20
Al-Botaty, B. M., Elkhoely, A. A., El-Sayed, E. K., & Ahmed, A. A. E. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.108495 · Cited by 21
Wei, L., Fu, J., Li, H., Wang, H., Ruan, J., Li, F., & Wu, H. (2022) · Toxicology in Vitro · doi:10.1016/j.tiv.2022.105520 · Cited by 21
Gut microbiota in ischemic stroke: Where we stand and challenges ahead
Long, J.-X., Wang, J., Li, Y., & Chen, D. (2022) · Frontiers in Nutrition · doi:10.3389/fnut.2022.1008514 · Cited by 22
“tBID interacts with the Bad-Bax for opening the mitochondrial transition pore (MTP) and promoting the release of mitochondrial Cytc, endonuclease G, and apoptosis-inducing factors (AIFs) (45, 46).”
BackgroundAnti‐Apoptotic and Pro‐Apoptotic Bcl‐2 Family Proteins in Peri‐Implant Diseases
Yılmaz, D., Gürsoy, M., & Gürsoy, U. K. (2023) · Clinical Oral Implants Research · doi:10.1111/clr.14067 · Cited by 20
Wang, S., Chang, Y., Liu, T., Huang, K., Fang, W., Li, A. F., Yeh, T., Hung, G., & Lee, H. (2023) · FEBS Journal · doi:10.1111/febs.16992 · Cited by 20
Zhu, X., Wang, L., Wang, K., Yao, Y., & Zhou, F. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.07.002 · Cited by 20
Shu, C., Chang, H., Wu, C., Chen, C., Wu, S., Chang, H., Kuo, S., Fu, E., Liu, P., & Hsieh, Y. (2016) · PLoS ONE · doi:10.1371/journal.pone.0160586 · Cited by 20
“Other genes, such as p27, mTOR and death-associated protein kinas, have also been shown to be related to the crosstalk between autophagy and apoptosis [45].”
BackgroundOlugbami, J. O., Damoiseaux, R. D., France, B., Gbadegesin, M. A., Stieg, A. Z., Sharma, S., Odunola, O. A., & Gimzewski, J. K. (2017) · Journal of Chinese Integrative Medicine · doi:10.1016/s2095-4964(17)60337-6 · Cited by 20
Mou, Q., & Leung, P. H. M. (2017) · Virulence · doi:10.1080/21505594.2017.1373925 · Cited by 20
“Growth in nutrient-deprived conditions causes starving mammalian cells to induce autophagy,(38,39) which in turn induces mitochondrial dysfunction and activates apoptosis or inflammatory pyroptosis.(37,38) The high rate of cell death among uninfected THP-1 cells might therefore be a result of nutrient deprivation.”
BackgroundDawar, F. U., Hu, X., Zhao, L., Dong, X., Xiong, Y., Zhou, M., Liang, R., Babu, V. S., Li, J., Mei, J., et al. (2017) · Fish & Shellfish Immunology · doi:10.1016/j.fsi.2017.09.070 · Cited by 20
Wang, S., & Gu, K. (2017) · Molecular Medicine Reports · doi:10.3892/mmr.2017.8272 · Cited by 20
“Atg and Becn1 are important markers of autophagy (19-24).”
BackgroundPark, H.-S., Han, J., Jung, S., Lee, D., Heo, K., & Myung, C. (2018) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2018.22.3.349 · Cited by 20
Zhuo, F., Zhang, C., Zhang, H., Xia, Y., Xue, G., Yang, L., & Kong, L. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27991 · Cited by 20
Alexander-Floyd, J., Haroon, S., Ying, M., Entezari, A. A., Jaeger, C., Vermulst, M., & Gidalevitz, T. (2020) · BMC Biology · doi:10.1186/s12915-020-0750-5 · Cited by 19
Aznar, M. A., Lasa-Saracíbar, B., & Blanco‐Prieto, M. J. (2014) · Molecular Pharmaceutics · doi:10.1021/mp5000696 · Cited by 20
Evaluation of Caco-2 cells response to Listeria monocytogenes virulence factors by RT-PCR.
Xie, M.-M., Ding, C.-C., Guo, L., Chen, G.-W., Zeng, H.-J., & Liu, Q. (2018) · Microbial Pathogenesis · doi:10.1016/j.micpath.2018.04.059 · Cited by 18
Sayyadi, M., Safaroghli‐Azar, A., Pourbagheri‐Sigaroodi, A., Abolghasemi, H., Anoushirvani, A. A., & Bashash, D. (2020) · Archives of Medical Research · doi:10.1016/j.arcmed.2020.06.002 · Cited by 19
HO-3867 Induces ROS-Dependent Stress Response and Apoptotic Cell Death in Leishmania donovani
Das, A., Kamran, M., & Ali, N. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.774899 · Cited by 19
Seth, E., & Chopra, M. (2022) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2022.155292 · Cited by 20
Zheng, H., Sun, H., Zhang, Z., Qian, Y., Zhu, X., & Qu, J. (2023) · Microchemical Journal · doi:10.1016/j.microc.2023.109036 · Cited by 19
He, H., Wei, Y., Chen, Y., Zhao, X., Shen, X., Zhu, Q. C., & Yin, H. (2024) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-024-01003-w · Cited by 19
“PARP1 is a ribozyme that is activated upon DNA damage and balances apoptosis and necrosis by regulating cellular ATP levels [34].”
BackgroundWang, M., Wang, Z., Li, Z., Qu, Y., Zhao, J., Wang, L., Zhou, X., Xu, Z., Zhang, D., Jiang, P., et al. (2024) · Phytotherapy Research · doi:10.1002/ptr.8216 · Cited by 20
“Upon stimulation by TNF-α , both apoptosis and necroptosis may be activated simultaneously (Nikoletopoulou et al., 2013), influenced by cell type and environmental factors.”
Fabrizi, C., Pompili, E., Somma, F., Vito, S. D., Ciraci, V., Artico, M., Lenzi, P., Fornai, F., & Fumagalli, L. (2016) · Journal of Applied Toxicology · doi:10.1002/jat.3344 · Cited by 19
“This evolutionary conserved catabolic pathway aims to remove damaged organelles and misfolded proteins and generally displays a cytoprotective function (Nikoletopoulou et al., 2013).”
BackgroundAl-Abboodi, A. S., AL-QUBAISI, M. S., Abdullah, R., Abdul, A. B., Taufiq‐Yap, Y. H., & Yeap, S. K. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17101653 · Cited by 19
“This result supports the idea that caspase-mediated apoptosis takes place at low concentrations and, at higher concentrations, treated cells undergo secondary apoptosis associated with proteolysis [41].”
BackgroundIn vitro cytotoxicity of chemical preservatives on human fibroblast cells
Spíndola, D. G., Hinsberger, A., Antunes, V. M. D. S., Michelin, L. F. G., Bincoletto, C., & Oliveira, C. R. (2018) · Brazilian Journal of Pharmaceutical Sciences · doi:10.1590/s2175-97902018000100031 · Cited by 19
“Finally, the investigated preservatives did not induce a significant increase in the Annexin V−/PI+ population, which is a fraction of cells with permeabilized membranes, suggesting the induction of necrotic cell death (Nikoletopoulou et al., 2013).”
BackgroundCui, Y., Zhang, Z., Zhang, B., Zhao, L., Hou, C., Zeng, Q., Nie, J., Yu, J., Zhao, Y., Gao, T., et al. (2018) · Toxicology Letters · doi:10.1016/j.toxlet.2018.08.020 · Cited by 19
Gendy, A. M., Amin, M. M., Al‐Mokaddem, A. K., & Abd‐Ellah, M. F. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118882 · Cited by 19
Autophagy signals orchestrate chemoresistance of gynecological cancers
Tam, C., Rao, S., Waye, M. M. Y., Ng, T. B., & Wang, C. C. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188525 · Cited by 19
Chen, B., Jia, Y., Lu, D., & Sun, Z. (2021) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2021.10120 · Cited by 19
“Studies have demonstrated that oxidative stress can cause inflamma‐ tion, but no inflammation occurs during cell apoptosis (41,42).”
BackgroundCopper impair autophagy on zebrafish (Danio rerio) gill epithelium
Luzio, A., Parra, S., da Costa, B. K., Santos, D., Álvaro, A. R., & Monteiro, S. M. (2021) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2021.103674 · Cited by 19
Autophagy mediates phase transitions from cell death to life
Han, K., Kim, J., & Choi, M. Y. (2015) · Heliyon · doi:10.1016/j.heliyon.2015.e00027 · Cited by 19
“This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).”
BackgroundInfluentialFunction of SLC7A7 in T-Cell Acute Lymphoblastic Leukemia
Ji, X., Yang, X., Wang, N., Kang, M., Wang, Y., Rong, L., Fang, Y., & Xue, Y. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000491899 · Cited by 18
Chen, L., Liu, L., Xie, Z., Wang, F., Zhu, L., Zhang, C., Fan, P., Sinkemani, A., Hong, X., & Wu, X. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27820 · Cited by 18
NLRP3 Inflammasome Activation in Hemodialysis and Hypertensive Patients with Intact Kidney Function
Ulrich, C., Wildgrube, S., Fiedler, R., Seibert, E., Kneser, L., Fick, S., Schäfer, C., Markau, S., Trojanowicz, B., & Girndt, M. (2020) · Toxins · doi:10.3390/toxins12110675 · Cited by 18
“There are several lines of evidence in the literature that ATP is involved in the regulation of inflammasome activation and programmed cell death in particular [26,27].”
BackgroundTremble, L. F., Heffron, C. C. B. B., & Forde, P. F. (2020) · Scientific Reports · doi:10.1038/s41598-020-77743-2 · Cited by 19
Xu, L., Gao, X., Pu, Y., Sang, W., Jiao, J., Niu, M., Liu, M., Qin, Y., Yan, D., Song, X., et al. (2020) · Journal of Cancer · doi:10.7150/jca.48310 · Cited by 18
“In some cases, autophagy is the cell survival pathway and inhibits apoptosis; while in other cases, autophagy itself also induces cell death, cooperates with apoptosis [32-34].”
BackgroundPoprawa, I., Chajec, Ł., Chachulska-Żymełka, A., Wilczek, G., Student, S., Leśniewska, M., & Rost-Roszkowska, M. M. (2022) · Scientific Reports · doi:10.1038/s41598-022-10664-4 · Cited by 18
Knowledge mapping of autophagy in osteoarthritis from 2004 to 2022: A bibliometric analysis
Liao, J., Yu, X., Chen, J., Wu, Z., He, Q., Zhang, Y., Song, W., Luo, J., & Tao, Q. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1063018 · Cited by 19
“Frontiers in Immunology 10 response can reduce chondrocyte death in the early stages of OA, but excessive autophagy may also lead to chondrocyte death as OA progresses (75).”
BackgroundTherapeutic potential of hesperidin: Apoptosis induction in breast cancer cell lines
Önder, G. Ö., Göktepe, Ö., Baran, M., Bıtgen, N., Aydin, F. A., & Arzu Hanım, Y. A. Y. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113791 · Cited by 18
Nosálová, N., Kešeľáková, A., Kello, M., Martinková, M., Fábianová, D., & Pilátová, M. B. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411696 · Cited by 20
“Furthermore, mitochondrial membrane permeabilization, the externalization of phosphatidylserine and the activation of caspases are hallmarks of apoptosis [35].”
BackgroundPANoptosis is a compound death in periodontitis: A systematic review of ex vivo and in vivo studies
Zhang, A., Zhang, C., Zhang, Y., Hu, T., & Cheng, R. (2023) · Oral Diseases · doi:10.1111/odi.14726 · Cited by 18
Liu, Z., Lu, T., Qian, R., Wang, Z., Qi, R., & Zhang, Z. (2024) · International Journal of Nanomedicine · doi:10.2147/ijn.s455407 · Cited by 18
Liu, W., Liu, H., Zhang, S., Hao, H., Meng, F., Ma, W., Guo, Z., Jiang, S., & Shang, X. (2024) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2024.117049 · Cited by 18
Globuli osseiin the long limb bones of Pleurodeles waltl( Amphibia , Urodela , Salamandridae )
Quilhac, A., de Ricqlès, A. J., Lamrous, H., & Zylberberg, L. (2014) · Journal of Morphology · doi:10.1002/jmor.20296 · Cited by 18
Fan, R., Zhu, B., Huang, C., Sheng, Z.-G., Mao, L., & Li, M. (2015) · Environmental Toxicology · doi:10.1002/tox.22197 · Cited by 18
Impairment of the autophagic flux in astrocytes intoxicated by trimethyltin
Fabrizi, C., Pompili, E., Vito, S. D., Somma, F., Catizone, A., Ricci, G., Lenzi, P., Fornai, F., & Fumagalli, L. (2015) · NeuroToxicology · doi:10.1016/j.neuro.2015.10.004 · Cited by 18
“Although autophagy is primarily considered to have a cytoprotective function, it can also promote cell death through a sort of self-cannibalism (Nikoletopoulou et al., 2013).”
BackgroundChrysophanic Acid Induces Necrosis but not Necroptosis in Human Renal Cell Carcinoma Caki-2 Cells
Choi, J. (2016) · Journal of Cancer Prevention · doi:10.15430/jcp.2016.21.2.81 · Cited by 18
“with cell shrinkage, the formation of an apoptotic body, and DNA fragmentation.(14) Apoptosis is induced by two different pathways: one is the intrinsic pathway mediated by the mitochondria, the other is the death receptor (DR)-mediated extrinsic pathway.”
BackgroundCell death mechanisms in human chronic liver diseases: a far cry from clinical applicability
Mazzolini, G. D., Sowa, J., & Canbay, A. E. (2016) · Clinical Science · doi:10.1042/cs20160035 · Cited by 18
Erukainure, O. L., Narainpersad, N., Singh, M., Sanni, O., & Islam, M. S. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.07.013 · Cited by 18
Shroff, A., & Reddy, K. V. R. (2018) · American Journal of Reproductive Immunology · doi:10.1111/aji.13056 · Cited by 18
Li, J., Zheng, L., Wang, X., Yao, K., Shi, L., Sun, X., Yang, G., Jiang, L., Zhang, C., Wang, Y., et al. (2019) · Toxicology Mechanisms and Methods · doi:10.1080/15376516.2019.1588931 · Cited by 18
“Interactions among components of the two pathways suggest that they have a complex cross-talk, which is often caused by similar stimuli (Nikoletopoulou et al. 2013).”
BackgroundRamos-Hryb, A. B., Platt, N., Freitas, A. E., Heinrich, I. A., López, M. G., Leal, R. B., Kaster, M. P., & Rodrigues, A. L. S. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02906-1 · Cited by 18
Yu, B., Yuan, B., Li, J., Kiyomi, A., Kikuchi, H., Hayashi, H., Hu, X., Okazaki, M., Sugiura, M., Hirano, T., et al. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01087 · Cited by 18
“org 9 (Nikoletopoulou et al., 2013; Yoshida, 2017; Chen et al., 2019), our experimental results demonstrated that the addition of either 3-MA or wortmannin, two autophagy inhibitors, successfully corrected the combined regimen-triggered S-phase arrest, however, had little effect on the apoptosis/necrosis induction (Fi…”
ResultMolecular probes for selective detection of cysteine cathepsins
Schleyer, K. A., & Cui, L. (2021) · Organic & Biomolecular Chemistry · doi:10.1039/d1ob00225b · Cited by 18
Ding, H., Yang, J., Yang, J. M., Guo, X., Tang, Y., Huang, Y., Chen, Z., Fan, Z., & Huang, C. (2021) · Molecular Biology Reports · doi:10.1007/s11033-021-06326-9 · Cited by 18
Hydrogen peroxide toxicity on auditory cells: An in vitro study
Gentilin, E., Cani, A., Simoni, E., Chicca, M. C., Paolo, M. L. D., Martini, A., & Astolfi, L. (2021) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2021.109575 · Cited by 18
Yang, J., Guo, A., Li, Q., & Wu, J. (2021) · Tissue and Cell · doi:10.1016/j.tice.2021.101646 · Cited by 18
Li, X., Wen, Y., Sheng, L., Guo, R., Zhang, Y., & Shao, L. (2021) · Bioengineered · doi:10.1080/21655979.2021.2011637 · Cited by 18
“A lack of autophagy may lead to adverse cellular outcomes, such as apoptosis [5].”
BackgroundRetracted
Metadata
- Authors
- Nikoletopoulou, V., Markaki, M., Palikaras, K., & Tavernarakis, N.
- Affiliations
- Foundation for Research and Technology Hellas (GR)
- Corresponding author
- Tavernarakis, Nektarios
- Venue
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 1833
- Issue
- 12
- Pages
- 3448-3459
- ISSN
- 0167-4889 (ISSN-L)
- OpenAlex
- W2059738518
- Cited by
- 1,366
- References
- 150
- Citations by year
- 2026: 43 · 2025: 58 · 2024: 80 · 2023: 91 · 2022: 113 · 2021: 147 · 2020: 133 · 2019: 146 · 2018: 136 · 2017: 141 · 2016: 122 · 2015: 107 · 2014: 43 · 2013: 5
- FWCI
- 8.50
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (publishedVersion)
- PubMed (publishedVersion)
- IRIS (submittedVersion)
- SERVAL (Université de Lausanne) (submittedVersion)
- Funders
- European Research Council
- Ministry of National Education and Religious Affairs
- European Molecular Biology Organization
- Seventh Framework Programme
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Social Sciences › Anthropology › Death, Funerary Practices, and Mourning
- Keywords
- apoptosis, necrosis, autophagy, cell death crosstalk, cell death pathways, cell fate determination, development (biology), disease pathology
- MeSH terms
- Autophagy, Humans, Models, Biological, Necrosis, Signal Transduction, Apoptosis
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