The DOI matches its Crossref record; 118 of the 118 references it cites were found in a registry or an index.
Eaten alive: novel insights into autophagy from multicellular model systems
Open accessAbstract
Autophagy delivers cytoplasmic material to lysosomes for degradation. First identified in yeast, the core genes that control this process are conserved in higher organisms. Studies of mammalian cell cultures have expanded our understanding of the core autophagy pathway, but cannot reveal the unique animal-specific mechanisms for the regulation and function of autophagy. Multicellular organisms have different types of cells that possess distinct composition, morphology, and organization of intracellular organelles. In addition, the autophagic machinery integrates signals from other cells and environmental conditions to maintain cell, tissue and organism homeostasis. Here, we highlight how studies of autophagy in flies and worms have identified novel core autophagy genes and mechanisms, and provided insight into the context-specific regulation and function of autophagy.
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
“Of note, the apoptotic and autophagic machineries are highly interconnected during developmental cell death [796].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [796]
In the citing paper
“In this context, the autophagic apparatus also drives the developmental clearance of apoptotic cells [796].”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [796]
Citations
Cites
1 retracted
Martinez, J., Almendinger, J., Oberst, A., Ness, R., Dillon, C. P., Fitzgerald, P., Hengartner, M. O., & Green, D. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1113421108 · Cited by 655
RetractedRepertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351
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
Autophagy in the Pathogenesis of Disease
Levine, B., & Kroemer, G. (2008) · Cell · doi:10.1016/j.cell.2007.12.018 · Cited by 7,069
Autophagy: Renovation of Cells and Tissues
Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615
Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, R. C., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,214
Pankiv, S., Clausen, T. H., Lamark, T., Brech, A., Bruun, J.-A., Outzen, H., Øvervatn, A., Bjørkøy, G., & Johansen, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702824200 · Cited by 4,578
Autophagy and Viruses: Adversaries or Allies?
Dong, X., & Levine, B. (2013) · Journal of Innate Immunity · doi:10.1159/000346388 · Cited by 4,444
Antimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila
Moy, R. H., & Cherry, S. R. (2013) · Journal of Innate Immunity · doi:10.1159/000350326 · Cited by 3,551
Post-embryonic cell lineages of the nematode, Caenorhabditis elegans
Sulston, J. E., & Horvitz, H. R. (1977) · Developmental Biology · doi:10.1016/0012-1606(77)90158-0 · Cited by 3,479
Cited by
Sorted by citations
Galluzzi, L., Vitale, I., Aaronson, S. A., Abrams, J. M., Adam, D., Agostinis, P., Alnemri, E. S., Altucci, L., Amelio, I., Andrews, D. W., et al. (2018) · Cell Death & Differentiation · doi:10.1038/s41418-017-0012-4 · Cited by 6,680
“Of note, the apoptotic and autophagic machineries are highly interconnected during developmental cell death [796].”
BackgroundSelf-citationDoherty, J., & Baehrecke, E. H. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0201-5 · Cited by 636
Self-citationAutophagy: machinery and regulation
Yin, Z., Pascual, C., & Klionsky, D. J. (2016) · Microbial Cell · doi:10.15698/mic2016.12.546 · Cited by 582
“During ovary development, caspases are needed for autophagy induction under stress conditions, whereas nurse cell apoptosis requires autophagic clearance of its inhibitor, Bruce [21].”
Autophagosome maturation: An epic journey from the ER to lysosomes
Zhao, Y. G., & Zhang, H. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201810099 · Cited by 375
“…with the ER and is also linked to the ER by tubular membrane extensions, collectively referred to as ER–IM contacts (Hayashi-Nishino et al., 2009; Ylä-Anttila et al., 2009), at which lipid transfer between the ER and IMs may occur (Prinz, 2014; Phillips and Voeltz, 2016; Zhang and Hu, 2016).”
BackgroundSelf-citationRegulation of Liver Metabolism by Autophagy
Madrigal‐Matute, J., & Cuervo, A. M. (2015) · Gastroenterology · doi:10.1053/j.gastro.2015.09.042 · Cited by 319
Autophagy in bone homeostasis and the onset of osteoporosis
Yin, X., Zhou, C., Li, J., Liu, R., Shi, B., Yuan, Q., & Zou, S. (2019) · Bone Research · doi:10.1038/s41413-019-0058-7 · Cited by 235
Autophagy in the eye: Development, degeneration, and aging
Boya, P., Esteban‐Martínez, L., Serrano‐Puebla, A., Gómez‐Sintes, R., & Villarejo‐Zori, B. (2016) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2016.08.001 · Cited by 236
KIF1A/UNC-104 Transports ATG-9 to Regulate Neurodevelopment and Autophagy at Synapses
Stavoe, A. K. H., Kargbo-Hill, S. E., Hall, D. H., & Colón-Ramos, D. A. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.06.012 · Cited by 211
Lysosomal cell death mechanisms in aging
Gómez-Sintes, R., Ledesma, M. D., & Boya, P. (2016) · Ageing Research Reviews · doi:10.1016/j.arr.2016.02.009 · Cited by 216
Mechanisms of Selective Autophagy in Normal Physiology and Cancer
Mancias, J. D., & Kimmelman, A. C. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.02.027 · Cited by 196
“Likewise, the field will continue to learn from studying selective autophagy pathways using in vivo models[121,197].”
BackgroundGuidelines and recommendations on yeast cell death nomenclature
Carmona‐Gutiérrez, D., Bauer, M. A., Zimmermann, A., Aguilera, A., Austriaco, N. P. G., Ayscough, K. R., Balzan, R., Bar‐Nun, S., Barrientos, A., Belenky, P. A., et al. (2017) · Microbial Cell · doi:10.15698/mic2018.01.607 · Cited by 193
Liquid–liquid phase separation in autophagy
Noda, N. N., Wang, Z., & Zhang, H. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.202004062 · Cited by 175
“P granule proteins in somatic blastomeres are quickly disassembled and removed, resulting in exclusive localization of P granules in the germline blastomeres and eventually in the germline precursor cells Z2 and Z3 (Fig. 3 B; Strome, 2005; Zhang and Baehrecke, 2015).”
BackgroundSelf-citationResearch progress on morphology and mechanism of programmed cell death
Chen, Y., Li, X., Yang, M., & Liu, S. (2024) · Cell Death and Disease · doi:10.1038/s41419-024-06712-8 · Cited by 168
“…[1, 42], and its morphological feature is the observation of double-membrane phagocytic components containing vesicles, namely, autophagosomes; the expansion and fragmentation of the endoplasmic reticulum, mitochondria and other organelles; and the slight agglutination of chromatin [43, 44] (Fig.”
BackgroundIssa, A.-R., Sun, J., Petitgas, C., Mesquita, A., Dulac, A., Robin, M., Mollereau, B., Jenny, A., Chérif‐Zahar, B., & Birman, S. (2018) · Autophagy · doi:10.1080/15548627.2018.1491489 · Cited by 156
Revuelta, M., & Matheu, A. (2017) · Aging Cell · doi:10.1111/acel.12655 · Cited by 149
“…process implies the incorporation of proteins, organelles, and cytoplasm in a structure called the autophagosome, which once formed fuses with the lysosome to form autolysosomes and then releasing its content in the lysosomal lumen where it is degraded via acid hydrolases (Zhang & Baehrecke, 2015).”
BackgroundStringer, J. M., Alesi, L. R., Winship, A., & Hutt, K. J. (2023) · Human Reproduction Update · doi:10.1093/humupd/dmad005 · Cited by 157
Role of chaperone‐mediated autophagy in metabolism
Tasset, I., & Cuervo, A. M. (2016) · FEBS Journal · doi:10.1111/febs.13677 · Cited by 154
Phase Separation, Transition, and Autophagic Degradation of Proteins in Development and Pathogenesis
Wang, Z., & Zhang, H. (2019) · Trends in Cell Biology · doi:10.1016/j.tcb.2019.01.008 · Cited by 118
Self-citationProtease signaling in animal and plant‐regulated cell death
Salvesen, G. S., Hempel, A., & Coll, N. S. (2015) · FEBS Journal · doi:10.1111/febs.13616 · Cited by 109
Wu, F., Watanabe, Y., Guo, X., Qi, X., Wang, P., Zhao, H., Wang, Z., Fujioka, Y., Hui, Z., Jin-Qi, R. E. N., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.11.019 · Cited by 104
“It has been largely assumed that during multicellular organism development, an autophagy gene is equally employed for removal of distinct cargo at different developmental stages (Zhang and Baehrecke, 2015).”
Self-citationCai, Y. C., Yang, L., Hu, G., Chen, X., Niu, F., Yuan, L., Liu, H., Xiong, H., Arikkath, J., & Buch, S. J. (2016) · The Journal of Cell Biology · doi:10.1083/jcb.201605065 · Cited by 100
“The role of autophagy in morphinemediated regulation of excitatory and inhibitory synapses Autophagy is an intracellular process that delivers cellular organelles and misfolded proteins from the autophagosomes to the lysosomes for degradation (Zhang and Baehrecke, 2015).”
BackgroundGenes associated with Parkinson's disease: regulation of autophagy and beyond
Beilina, A. G., & Cookson, M. (2015) · Journal of Neurochemistry · doi:10.1111/jnc.13266 · Cited by 98
Autophagy and primary cilia: dual interplay
Pampliega, O., & Cuervo, A. M. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.01.008 · Cited by 86
“Introduction Autophagy is a highly conserved intracellular process for the degradation of proteins and organelles in lysosomes [1].”
BackgroundMechanisms and Pathophysiological Roles of the ATG8 Conjugation Machinery
Lystad, A. H., & Simonsen, A. (2019) · Cells · doi:10.3390/cells8090973 · Cited by 89
Expression of WIPI2B counteracts age-related decline in autophagosome biogenesis in neurons
Stavoe, A. K., Gopal, P. P., Gubas, A., Tooze, S. A., & Holzbaur, E. L. (2019) · eLife · doi:10.7554/elife.44219 · Cited by 82
Thuwajit, C., Ferraresi, A., Titone, R., Thuwajit, P., & Isidoro, C. (2017) · Medicinal Research Reviews · doi:10.1002/med.21473 · Cited by 83
Formation and maturation of autophagosomes in higher eukaryotes: a social network
Zhao, Y. G., & Zhang, H. (2018) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2018.04.003 · Cited by 71
Self-citationDevelopment of LC3/GABARAP sensors containing a LIR and a hydrophobic domain to monitor autophagy
Lee, Y., Jun, Y., Choi, H., Huh, Y. H., Kaang, B., Jang, D., & Lee, J. (2017) · The EMBO Journal · doi:10.15252/embj.201696315 · Cited by 66
“Extensive genetic studies in yeast and mammals have identified several autophagy-related genes ( ~ 40 genes in yeast) with specific roles in the autophagy pathway (Feng et al , 2014; Zhang & Baehrecke, 2015).”
Mitochondrial protein import regulates cytosolic protein homeostasis and neuronal integrity
Liu, W., Duan, X., Fang, X., Shang, W., & Tong, C. (2018) · Autophagy · doi:10.1080/15548627.2018.1474991 · Cited by 68
“To understand how autophagy processes are misregulated in Tom40 RNAi tissues, we carried out single and double-RNAi experiments to knockdown the expression of various core molecules of the autophagy pathway [40], alone or together with Tom40, and analyzed the patterns of ubiquitinated aggregates and Atg8a.”
BackgroundReciprocal Crosstalk Between Autophagic and Endocrine Signaling in Metabolic Homeostasis
Sinha, R. A., Singh, B. K., & Yen, P. M. (2016) · Endocrine Reviews · doi:10.1210/er.2016-1103 · Cited by 64
“autophagy in mammals, however, there has been much work on the endocrine regulation of autophagy in invertebrates and have been well described elsewhere (85, 86).”
BackgroundCurrent questions and possible controversies in autophagy
Lindqvist, L., Simon, A. K., & Baehrecke, E. H. (2015) · Cell Death Discovery · doi:10.1038/cddiscovery.2015.36 · Cited by 62
Self-citationZhao, X., Di, Q., Yu, J., Quan, J., Xiao, Y., Zhu, H., Li, H., Jing, L., & Chen, W. (2021) · Autophagy · doi:10.1080/15548627.2021.1963155 · Cited by 61
“mode of cargo delivery to the lysosome [6,7].”
BackgroundCore autophagy genes and human diseases
Zhao, Y. G., & Zhang, H. (2019) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2019.08.003 · Cited by 55
Self-citationThe interplay of autophagy and non-apoptotic cell death pathways
(2020) · International Review of Cell and Molecular Biology · doi:10.1016/bs.ircmb.2019.12.004 · Cited by 50
Osteoporosis and autophagy: What is the relationship?
Florencio‐Silva, R., Sasso, G. R. D. S., Simões, M. D. J., Simões, R. S., Baracat, M. C. P., Sasso‐Cerri, E., & Cerri, P. S. (2017) · Revista da Associação Médica Brasileira · doi:10.1590/1806-9282.63.02.173 · Cited by 53
Castets, P., Frank, S., Sinnreich, M., & Rüegg, M. A. (2016) · Journal of Neuromuscular Diseases · doi:10.3233/jnd-160153 · Cited by 49
“1).”
Icariin alleviates osteoarthritis through PI3K/Akt/mTOR/ULK1 signaling pathway
Chen, Y., Pan, X., Zhao, J., Li, C., Lin, Y., Wang, Y., Liu, X., & Tian, M. (2022) · European journal of medical research · doi:10.1186/s40001-022-00820-x · Cited by 53
“Under stress conditions, the inactivation of mTOR can promote the formation of the ULK complex, and the ULK1/FIP200/Atg13 complex is essential for the formation of autophagosomes [33, 34].”
BackgroundAsperuloside alleviates osteoporosis by promoting autophagy and regulating Nrf2 activation
Huang, F., Wang, Y., Liu, J., Cheng, Y., Zhang, X., & Jiang, H. (2024) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-024-05320-8 · Cited by 46
Wang, X., Zhou, R., Zhang, N., & Zhao, J. (2019) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2019.02.023 · Cited by 45
USP8 maintains embryonic stem cell stemness via deubiquitination of EPG5
Gu, H., Shi, X.-X., Liu, C., Wang, C., Sui, N., Zhao, Y., Gong, J., Wang, F., Zhang, H., Li, W., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09430-4 · Cited by 45
Self-citationFeng, Q., Rycke, R. M. D., Dagdas, Y., & Nowack, M. K. (2022) · Current Biology · doi:10.1016/j.cub.2022.03.053 · Cited by 44
Ojha, R., Jha, V., & Singh, S. K. (2015) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2015.12.002 · Cited by 41
Gao, H., Khawar, M. B., & Li, W. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-15-0602-4_21 · Cited by 39
Lana, D., Ugolini, F., Melani, A., Nosi, D., Pedata, F., & Giovannini, M. G. (2017) · Experimental Gerontology · doi:10.1016/j.exger.2017.06.006 · Cited by 36
Differential activation of eMI by distinct forms of cellular stress
Mesquita, A., Glenn, J., & Jenny, A. (2020) · Autophagy · doi:10.1080/15548627.2020.1783833 · Cited by 38
The Proton-Coupled Monocarboxylate Transporter Hermes Is Necessary for Autophagy during Cell Death
Velentzas, P. D., Zhang, L., Das, G., Chang, T.-K., Nelson, C., Kobertz, W. R., & Baehrecke, E. H. (2018) · Developmental Cell · doi:10.1016/j.devcel.2018.09.015 · Cited by 31
“, 2013) and hormones (Baehrecke, 2000), and studies in animals indicate that autophagy has complex regulation and functions in different cell contexts (Zhang and Baehrecke, 2015).”
BackgroundSelf-citationAas, S. N., Hamarsland, H., Cumming, K. T., Rognlien, S. H., Aase, O. J., Nordseth, M., Karsrud, S., Godager, S., Tømmerbakke, D., Handegard, V., et al. (2019) · Experimental Gerontology · doi:10.1016/j.exger.2019.110687 · Cited by 34
Peña-Ramos, O., Chiao, L. J., Liu, X., Yu, X., Yao, T., He, H., & Zhou, Z. (2022) · eLife · doi:10.7554/elife.72466 · Cited by 35
Calcium ions trigger the exposure of phosphatidylserine on the surface of necrotic cells
Furuta, Y., Peña-Ramos, O., Li, Z., Chiao, L. J., & Zhou, Z. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009066 · Cited by 33
“homolog of yeast ATG1 and mammalian ULK1 (UNC-51-like autophagy activating kinase), an important component of the autophagy pathway [57].”
BackgroundA conserved myotubularin-related phosphatase regulates autophagy by maintaining autophagic flux
Allen, E. A., Amato, C., Fortier, T. M., Velentzas, P. D., Wood, W., & Baehrecke, E. H. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201909073 · Cited by 32
Self-citationDo Fungi Undergo Apoptosis-Like Programmed Cell Death?
Hardwick, J. M. (2018) · mBio · doi:10.1128/mbio.00948-18 · Cited by 31
“Deletion of any of 16 conserved autophagy genes causes conidia to remain alive, blocking both appressorium formation and pathogenicity (85), raising the possibility of autophagy-dependent cell death (ADCD) (86, 87).”
BackgroundRoles for RAB24 in autophagy and disease
Ylä‐Anttila, P., & Eskelinen, E. (2017) · Small GTPases · doi:10.1080/21541248.2017.1317699 · Cited by 36
“thetic reactions, degrading misfolded and aggregated proteins and unnecessary organelles, and fighting against intracellular pathogens.(9,10) There are 3 ways to transport cytoplasmic material to lysosomes, called macroautophagy (or simply autophagy), microautophagy and”
BackgroundThe nuclear receptor NR4A1 is regulated by SUMO modification to induce autophagic cell death
Zárraga-Granados, G., Muciño-Hernández, G., Sánchez‐Carbente, M. D. R., Villamizar-Gálvez, W., Peñas-Rincón, A., Arredondo, C., Andrés, M. E., Wood, C. D., Covarrubias, L., & Castro‐Obregón, S. (2020) · PLoS ONE · doi:10.1371/journal.pone.0222072 · Cited by 28
Macroautophagy and Mitophagy in Neurodegenerative Disorders: Focus on Therapeutic Interventions
Magalhães, J. D., Fão, L., Vilaça, R., Cardoso, S. M., & Rego, A. C. (2021) · Biomedicines · doi:10.3390/biomedicines9111625 · Cited by 29
“Much of the current knowledge about autophagy was discovered in the yeast model or in non-polarized cells [2].”
BackgroundImpaired autophagy in amyloid-beta pathology: A traditional review of recent Alzheimer's research
Yuan, M., Wang, Y., Huang, Z., Jing, F., Qiao, P., Zou, Q., Li, J., & Cai, Z. (2022) · Journal of Biomedical Research · doi:10.7555/jbr.36.20220145 · Cited by 26
Mice deficient in the Vici syndrome gene Epg5 exhibit features of retinitis pigmentosa
Miao, G., Zhao, Y. G., Zhao, H., Ji, C., Sun, H., Chen, Y., & Zhang, H. (2016) · Autophagy · doi:10.1080/15548627.2016.1238554 · Cited by 25
“Constitutive basal autophagy acts as a quality control system by removing misfolded or aggregation-prone proteins and damaged organelles to maintain cellular homeostasis.(4,5) Mice with neural-specific deficiency in genes essential for autophagosome formation, including Atg5, Atg7 and Ei24, exhibit accumulation of ubi…”
BackgroundSelf-citationO’Keefe, L. V., & Denton, D. (2018) · BioMed Research International · doi:10.1155/2018/5195416 · Cited by 25
Autophagy Regulation Influences β-Amyloid Toxicity in Transgenic Caenorhabditis elegans
Lin, H., Gao, Y., Zhang, C., Ma, B., Wu, M., Cui, X., & Wang, H. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.885145 · Cited by 24
Huang, L., Fu, Q., Dai, J.-M., Yan, B., Wang, D., Puno, P., & Yue, J. (2021) · Cell Biology and Toxicology · doi:10.1007/s10565-021-09580-6 · Cited by 22
The Genetics of Autophagy in Multicellular Organisms
Zhang, H. (2022) · Annual Review of Genetics · doi:10.1146/annurev-genet-022422-095608 · Cited by 23
Self-citationTong, X., Yu, G., Fu, X., Song, R., Gu, J., & Liu, Z. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179846 · Cited by 23
“Class III PI3K combines with Beclin1 to form a complex that initiates autophagy, thereby affecting the regulation of downstream signaling [22,23].”
BackgroundConvergence of secretory, endosomal, and autophagic routes in trans-Golgi–associated lysosomes
Zhou, L., Xue, X., Yang, K. L., Feng, Z. J., Liu, M., & Pastor-Pareja, J. C. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202203045 · Cited by 22
Has-miR-30a regulates autophagic activity in cervical cancer upon hydroxycamptothecin exposure
Cheng, Y., Chen, G., Hu, M. S., Huang, J., Li, B.-S., Zhou, L., & Li, H. (2015) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2015.08.034 · Cited by 20
Functions of nuclear receptors SUMOylation
Liu, W., Min De, Z. E. N. G., & Fu, N. (2021) · Clinica Chimica Acta · doi:10.1016/j.cca.2021.01.007 · Cited by 19
Thongrod, S., Wanichanon, C., Kankuan, W., Siangcham, T., Phadngam, S., Morani, F., Isidoro, C., & Sobhon, P. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00613 · Cited by 17
“Eventually, the digested products are transported back to the cytoplasm for reuse in biosynthesis or production of energy to meet the needs of the cell (Ravikumar et al., 2010; Zhang and Baehrecke, 2015).”
BackgroundThe emerging role of oxidative stress in regulating autophagy: applications of cancer therapy
Zhang, W., Wan, X., Liu, Z., Xiao, L., Huang, H., & Liu, X. (2017) · Cellular and Molecular Biology · doi:10.14715/cmb/2017.63.4.11 · Cited by 17
“3) Non-protective autophagy, which exerts rare influence on cancer therapies either inhibited or promoted by chemical agents (117,118).”
BackgroundThe roles of phosphoinositides in mammalian autophagy
Jang, D., & Lee, J. (2016) · Archives of Pharmacal Research · doi:10.1007/s12272-016-0777-x · Cited by 16
Hydroxycamptothecin mediates antiproliferative effects through apoptosis and autophagy in A549 cells
Wei, Y., Li, C., Zhang, Y., He, H., Zhang, G., Hao, X., Liu, H., Wang, H., & Tian, W. (2018) · Oncology Letters · doi:10.3892/ol.2018.8107 · Cited by 16
“Subsequently, the cytosolic protein light chain 3 (LC3)I is conjugated to phosphatidylethanolamine, forms LC3II and participates in membrane elongation (12-15).”
BackgroundThe tissue- and developmental stage-specific involvement of autophagy genes in aggrephagy
Zheng, H., Yuan, C., Zhang, H., Chen, Y., & Zhang, H. (2019) · Autophagy · doi:10.1080/15548627.2019.1632121 · Cited by 15
“these core autophagy genes are not equally employed under different autophagy induction conditions [5].”
BackgroundSelf-citationLee, T. V., Kaya, H. E. K., Simin, R. T., Baehrecke, E. H., & Bergmann, A. (2016) · Cell Death and Differentiation · doi:10.1038/cdd.2016.40 · Cited by 15
“Autophagy is characterized by the formation of doublemembrane vesicles termed autophagosomes.(14,15) During autophagosome maturation, cytosolic proteins and entire”
BackgroundSelf-citationZhou, H., Ma, J., Shan, Y., Xia, Q., Wang, H., & Li, J. (2019) · Food & Function · doi:10.1039/c8fo01734d · Cited by 14
Zhao, J., Li, Z., & Li, J. (2021) · FEBS Open Bio · doi:10.1002/2211-5463.13340 · Cited by 12
Paiardi, C., Mirzoyan, Z., Zola, S., Parisi, F., Vingiani, A., Pasini, M. E., & Bellosta, P. (2017) · Genes · doi:10.3390/genes8050131 · Cited by 13
“Autophagy is a physiological process present in all organisms that uses catabolic processes to balance cellular energy in response to nutrient starvation and is also important for eliminating dysfunctional organelles or toxic proteins to preserve cellular homeostasis [20].”
BackgroundMethodCharacterization of Autophagic Responses in Drosophila melanogaster
Xu, T., Kumar, S., & Denton, D. (2017) · Methods in Enzymology · doi:10.1016/bs.mie.2016.09.089 · Cited by 12
Genes and SNPs Involved with Scrotal and Umbilical Hernia in Pigs
Rodrigues, A. F. G., Ibelli, A. M. G., Peixoto, J. D. O., Cantão, M. E., de Oliveira, H. C., Savoldi, I. R., Souza, M. R., Morés, M. A. Z., Carreño, L. O. D., & Ledur, M. C. (2021) · Genes · doi:10.3390/genes12020166 · Cited by 12
Conserved components of the macroautophagy machinery in Caenorhabditis elegans
Zhang, H., & Meléndez, A. (2025) · Genetics · doi:10.1093/genetics/iyaf007 · Cited by 11
“The physiological function of autophagy during C. elegans development has been extensively reviewed recently (Yang and Zhang 2014; Zhang and Baehrecke 2015; Hansen et al. 2018; Palmisano and Meléndez 2019), and thus we will present only the most recent advances.”
Self-citationPhase-separated Condensates in Autophagosome Formation and Autophagy Regulation
Wang, Z., & Zhang, H. (2025) · Journal of Molecular Biology · doi:10.1016/j.jmb.2025.168964 · Cited by 9
Self-citationThe Incredible ULKs: Autophagy and Beyond
Zhao, Y. G., & Zhang, H. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.05.005 · Cited by 9
“Autophagy genes also act in autophagy-independent processes, such as Atg5 and Atg7 in unconventional secretion, Epg5 in endocytic trafficking, and Atg1/Ulk1 in axon structure and guidance and in COPII vesicle transport, as demonstrated here (Zhang and Baehrecke, 2015).”
BackgroundSelf-citationWear particles enhance autophagy through up-regulation of CD147 to promote osteoclastogenesis.
Su, B., Li, D., Xu, J., Zhang, Y., Cai, Z., Kauther, M. D., & Ma, R. (2018) · Europe PMC (PubMed Central) · doi:10.22038/ijbms.2018.29347.7093 · Cited by 7
“Factors that induce cellular stress, such as hypoxia, accumulation of oxidative stress and caloric restriction, can induce autophagy (24, 25).”
BackgroundCrosstalk between Dpp and Tor signaling coordinates autophagy-dependent midgut degradation
Denton, D., Xu, T., Dayan, S., Nicolson, S., & Kumar, S. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1368-9 · Cited by 7
Zou, S., Luo, Y., Jin, Y., Jing, W., Huang, Y., Liang, Y., Li, Y., Hao, Z., Xu, Y., & Wang, H. (2025) · Advanced Science · doi:10.1002/advs.202504664 · Cited by 6
Anusha, S., & Negi, P. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.136610 · Cited by 7
Archetypal autophagic players through new lenses for bone marrow stem/mature cells regulation
Agas, D., & Sabbieti, M. G. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30296 · Cited by 6
“The ULK1/Atg1 and VPS34 complex regulates the initial phase of autophagosome formation, and the Ambra1‐TRAF6 interaction stabilizes the neo‐formed membranes or phagophores (Zhang & Baehrecke, 2015).”
BackgroundAutophagic Mediators in Bone Marrow Niche Homeostasis
Agas, D., & Sabbieti, M. G. (2021) · Advances in experimental medicine and biology · doi:10.1007/5584_2021_666 · Cited by 6
Apoptosis and Efferocytosis in Inflammatory Diseases
Purnama, C. A., Meiliana, A., Barliana, M. I., Dandan, K. L., & Wijaya, A. (2021) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v13i3.1608 · Cited by 5
Yao, X., Shen, X., Fan, Y., & Wang, H. (2025) · npj Breast Cancer · doi:10.1038/s41523-025-00779-y · Cited by 6
Li, Z., Yang, X., Mao, J., Zeng, P., Qi, Y., Shi, Y., Guo, J., Zhou, J., Wang, D., Liu, J., et al. (2026) · Autophagy · doi:10.1080/15548627.2025.2610449 · Cited by 5
“Macroautophagy relies on autophagosome-lysosome fusion [61], a process dependent on ATG5 for vesicle formation [46].”
Chávez, E., Velasco-Loyden, G., Lozano-Rosas, M. G., Aguilar-Maldonado, B., Muciño-Hernández, G., Castro‐Obregón, S., & de Sánchez, V. C. (2020) · PubMed Central · Cited by 5
Autophagy in Drosophila and Zebrafish
Duan, X., & Tong, C. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-16-2830-6_15 · Cited by 3
Liu, H., Yu, J., Ye, G., Gao, J., Huang, L., Zhang, Z., & Liu, H. (2026) · Cell Death and Differentiation · doi:10.1038/s41418-026-01716-7 · Cited by 2
Yi, Z., Wen, C., Du, H., Wang, Y., Chen, S., Liu, J., Zhang, S., Wang, J., Xiao, X., Li, S., et al. (2025) · Advanced Science · doi:10.1002/advs.202512305 · Cited by 2
Alive failures behind the windows of cancer therapy
Islam, M. T. (2017) · International Journal of Medicine · doi:10.14419/ijm.v5i2.7035 · Cited by 1
The Relationship Between Postmenopausal Osteoporosis and Autophagic Gene Polymorphisms
Turgay, T., Pala, E., Özbas‐Gerçeker, F., Gürsoy, S., Altındağ, Ö., & Aydeniz, A. (2020) · Turkish Journal of Osteoporosis · doi:10.4274/tod.galenos.2020.58234 · Cited by 1
Sengul, G. F., Celik, F. S., & Pisiren, G. (2024) · Interdisciplinary cancer research · doi:10.1007/16833_2024_479 · Cited by 2
Peña-Ramos, O., Chiao, L., Liu, X., Yu, X., Yao, T., He, H., & Zhou, Z. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.07.16.452694 · Cited by 1
“atg-7 encodes a 219 homolog of mammalian ATG7, a protein essential for conjugating a phospholipid tail onto the LC3 220 family proteins and thus for the biogenesis of both autophagosomes and LAP vesicles [10,35].”
InfluentialRegulation of Autophagy by microRNAs: Implications in Cancer Therapy
Zhu, H., & Yang, J. (2016) · Current cancer research · doi:10.1007/978-3-319-42740-9_4
Kargbo-Hill, S. E., & Colón‐Ramos, D. A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/287144
“Autophagy is well conserved from yeast to mammalian cells, and is best known for its roles in cellular homeostasis (Yin et al., 2016; Zhang and Baehrecke, 2015).”
BackgroundResearch Progress of Hepatotoxicity Induced by Tripterygium wilfordii through Autophagy
周, 捷. (2021) · Pharmacy Information · doi:10.12677/pi.2021.106041
Tissenbaum, H. A. (2022) · CABI eBooks · doi:10.1079/9781789248814.0002
Model systems in cell death-grand challenge
Schwartz, L. M. (2022) · Frontiers in Cell Death · doi:10.3389/fceld.2022.1087903
Metadata
- Authors
- Zhang, H., & Baehrecke, E. H.
- Affiliations
- Chinese Academy of Sciences (CN)
- University of Massachusetts Chan Medical School (US)
- Corresponding author
- Zhang, Hong
- Baehrecke, Eric H.
- Venue
- Trends in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2015-07
- Volume
- 25
- Issue
- 7
- Pages
- 376-387
- ISSN
- 0962-8924 (ISSN-L)
- PMC
- PMC4475674
- OpenAlex
- W2067636508
- Cited by
- 102
- References
- 118
- Citations by year
- 2026: 3 · 2025: 5 · 2024: 4 · 2023: 1 · 2022: 11 · 2021: 13 · 2020: 7 · 2019: 12 · 2018: 13 · 2017: 10 · 2016: 16 · 2015: 7
- FWCI
- 1.99
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- Funders
- National Cancer Institute (R01CA159314, CA159314)
- National Institute of General Medical Sciences (GM111658, GM079431, R01GM079431, R01GM111658)
- National Institute of Allergy and Infectious Diseases (AI099708, R01AI099708)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- autophagy, multicellular organisms, Drosophila, Caenorhabditis elegans, autophagy-related genes, lysosomal degradation, tissue homeostasis, cell-to-cell communication, autophagy regulation
- MeSH terms
- Animals, Autophagy, Drosophila melanogaster, Gene Expression Regulation, Homeostasis, Humans, Lysosomes, Models, Biological, Organ Specificity, Protein Kinases, Saccharomyces cerevisiae, Species Specificity, Ubiquitins, Signal Transduction, Caenorhabditis elegans
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