The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy
Open accessAbstract
Autophagy is an intracellular degradation system, by which cytoplasmic contents are degraded in lysosomes. Autophagy is dynamically induced by nutrient depletion to provide necessary amino acids within cells, thus helping them adapt to starvation. Although it has been suggested that mTOR is a major negative regulator of autophagy, how it controls autophagy has not yet been determined. Here, we report a novel mammalian autophagy factor, Atg13, which forms a stable ∼3-MDa protein complex with ULK1 and FIP200. Atg13 localizes on the autophagic isolation membrane and is essential for autophagosome formation. In contrast to yeast counterparts, formation of the ULK1–Atg13–FIP200 complex is not altered by nutrient conditions. Importantly, mTORC1 is incorporated into the ULK1–Atg13–FIP200 complex through ULK1 in a nutrient-dependent manner and mTOR phosphorylates ULK1 and Atg13. ULK1 is dephosphorylated by rapamycin treatment or starvation. These data suggest that mTORC1 suppresses autophagy through direct regulation of the ∼3-MDa ULK1–Atg13–FIP200 complex.
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
“The initiation step begins with the dissociation of MTOR (mechanistic target of rapamycin kinase) from the PAS, cued by nutrient starvation or treatment with rapamycin or its various derivatives [36,37].”
From Autophagy and ALS: mechanistic insights and therapeutic implications (2022) · cites this paper as [37]
In the citing paper
“Under starvation, mTORC1 is suppressed and dissociates from the ULK1–ULK2 complex, allowing ULK1 to be activated by AMPK to induce autophagy”
From Autophagy in kidney homeostasis and disease (2020) · cites this paper as [17]
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
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 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
Self-citationTOR 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
Autophagy: process and functionPreprint
Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104
Self-citationBjørkøy, G., Lamark, T., Brech, A., Outzen, H., Perander, M., Øvervatn, A., Stenmark, H., & Johansen, T. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200507002 · Cited by 3,276
Defining the role of mTOR in cancer
Guertin, D. A., & Sabatini, D. M. (2007) · Cancer Cell · doi:10.1016/j.ccr.2007.05.008 · Cited by 2,833
Genomic Libraries and a Host Strain Designed for Highly Efficient Two-Hybrid Selection in Yeast
James, P. M., Halladay, J. T., & Craig, E. A. (1996) · Genetics · doi:10.1093/genetics/144.4.1425 · Cited by 2,638
How to Interpret LC3 Immunoblotting
Mizushima, N., & Yoshimori, T. (2007) · Autophagy · doi:10.4161/auto.4600 · Cited by 2,595 · cited 2×
“Because LC3-II inside autophagosomes is degraded in autolysosomes, we could see accumulation of LC3-II more clearly if cells were treated with lysosome protease inhibitors (E64d and pepstatin A; Figure Vol. 20, April 1, 2009 1983 3A, lane 3; Tanida et al., 2005; Mizushima and Yoshimori, 2007).”
BackgroundMethodSelf-citationRavikumar, B., Vacher, C., Berger, Z., Davies, J. E., Luo, S., Oroz, L. G., Scaravilli, F., Easton, D. F., Duden, R., O'Kane, C. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1362 · Cited by 2,347
ULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery
Jung, C. H., Jun, C. B., Ro, S.-H., Kim, Y.-M., Otto, N. M., Cao, J., Kundu, M., & Kim, D.-H. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1249 · Cited by 2,025
Cited by
Sorted by citations
Items 901–1,000 of 1,006
Loss of Macrophage mTORC2 Drives Atherosclerosis via FoxO1 and IL-1β Signaling
Zhang, X., Evans, T. D., Chen, S., Sergin, I., Stitham, J., Jeong, S., Rodríguez-Vélez, A., Yeh, Y., Park, A. C., Jung, I., et al. (2023) · Circulation Research · doi:10.1161/circresaha.122.321542 · Cited by 50
Autophagy induction of reversine on human follicular thyroid cancer cells
Lu, C., Liu, Y., Hua, S., Yu, H.-I., Chang, Y., & Lee, Y. (2012) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2012.08.001 · Cited by 44
Molecular Machinery of Autophagy and Its Implication in Cancer
Li, Y., Zhang, J., Liu, T., Chen, Y., Zeng, X., Chen, X., & He, W. (2011) · The American Journal of the Medical Sciences · doi:10.1097/maj.0b013e31821f978d · Cited by 43
Chronic mTOR activation promotes cell survival in Merkel cell carcinoma
Lin, Z., McDermott, A., Shao, L., Kannan, A., Morgan, M., Stack, B. C., Moreno, M. A., Davis, D. A., Cornelius, L. A., & Gao, L. (2013) · Cancer Letters · doi:10.1016/j.canlet.2013.11.005 · Cited by 46
Autophagy: An Integral Component of the Mammalian Stress Response.
Ryter, S. W., & Choi, A. M. K. (2013) · PubMed · Cited by 44
To eat, or NOt to eat: S ‐nitrosylation signaling in autophagy
Montagna, C., Rizza, S., Maiani, E., Piredda, L., Filomeni, G., & Cecconi, F. (2016) · The FEBS Journal · doi:10.1111/febs.13736 · Cited by 42
mTOR Inhibition Role in Cellular Mechanisms
Zaza, G., Granata, S., Caletti, C., Signorini, L. F., Stallone, G., & Lupo, A. (2018) · Transplantation · doi:10.1097/tp.0000000000001806 · Cited by 46
Sphingolipids as Regulators of Autophagy and Endocytic Trafficking
Young, M. M., & Wang, H. (2018) · Advances in cancer research · doi:10.1016/bs.acr.2018.04.008 · Cited by 45
Hyttinen, J. M. T., Petrovski, G., Salminen, A., & Kaarniranta, K. (2011) · Rejuvenation Research · doi:10.1089/rej.2011.1220 · Cited by 44
Mafi, S., Ahmadi, E., Meehan, E. V., Chiari, C. C., Mansoori, B., Sadeghi, H., Milani, S., Jafarinia, M., Taeb, S., Bashmagh, B. M., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-3032 · Cited by 43
PRKAA2, MTOR, and TFEB in the regulation of lysosomal damage response and autophagy
Shariq, M., Khan, M. F., Raj, R., Ahsan, N., & Kumar, P. (2024) · Journal of Molecular Medicine · doi:10.1007/s00109-023-02411-7 · Cited by 42
Hegedűs, K., Nagy, P., Gáspári, Z., & Juhász, G. (2014) · BioMed Research International · doi:10.1155/2014/470482 · Cited by 47
Huan, J., Grivas, P. D., Birch, J., & Hansel, D. E. (2022) · Cancers · doi:10.3390/cancers14061555 · Cited by 45
Parkhitko, A. A., Favorova, O. O., Khabibullin, D., Anisimov, V. N., & Henske, E. P. (2014) · Biochemistry (Moscow) · doi:10.1134/s0006297914020023 · Cited by 44
Sinha, R. A., Singh, B. K., Zhou, J., Xie, S. Y., Farah, B. L., Lesmana, R., Ohba, K., Tripathi, M., Ghosh, S., Hollenberg, A. N., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1235123 · Cited by 45
Interactions between Autophagy and DNA Viruses
Yin, H., Shao, S., Jiang, X.-J., Xie, P.-Y., Sun, W.-S., & Yu, T. (2019) · Viruses · doi:10.3390/v11090776 · Cited by 44
The interplay between oxidative stress and autophagy in chronic obstructive pulmonary disease
Zhao, X., Zhang, Q., & Zheng, R. (2022) · Frontiers in Physiology · doi:10.3389/fphys.2022.1004275 · Cited by 48
Zhang, M., Wang, Z., Zhao, Q., Yang, Q., Bai, J., Yang, C., Zhang, Z.-R., & Liu, Y. (2024) · Autophagy · doi:10.1080/15548627.2024.2347103 · Cited by 42
Szymańska-Rożek, P., Martin, K. R., MacKeigan, J. P., Hlavacek, W. S., & Tomasz Lipniacki, B. (2015) · PLoS ONE · doi:10.1371/journal.pone.0116550 · Cited by 42
Phosphoinositide‐binding proteins in autophagy
Lystad, A. H., & Simonsen, A. (2016) · FEBS Letters · doi:10.1002/1873-3468.12286 · Cited by 43
Hubber, A. M., Kubori, T., Coban, C., Matsuzawa, T., Ogawa, M., Kawabata, T., Yoshimori, T., & Nagai, H. (2017) · Scientific Reports · doi:10.1038/srep44795 · Cited by 43
Inhibition of mTOR kinase as a therapeutic target for acute myeloid leukemia
Tabe, Y., Tafuri, A., Sekihara, K., Yang, H., & Konopleva, M. Y. (2017) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2017.1333600 · Cited by 44
Grasso, G., Santoro, A. M., Lanza, V., Sbardella, D., Tundo, G. R., Ciaccio, C., Marini, S., Coletta, M., & Milardi, D. (2017) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2017.06.004 · Cited by 42
Mecca, C., Giambanco, I., Bruscoli, S., Bereshchenko, O., Fioretti, B., Riccardi, C., Donato, R., & Arcuri, C. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00099 · Cited by 43
Zhang, T., Guo, J., Gu, J., Chen, K., Li, H., & Wang, J. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/7861290 · Cited by 41
Self-Eating for Muscle Fitness: Autophagy in the Control of Energy Metabolism
Sebastián, D., & Antonio Zorzano, A. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.06.030 · Cited by 43
Autophagy: A Friend or Foe in Allergic Asthma?
Theofani, E., & Xanthou, G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22126314 · Cited by 44
Liu, J., Su, H., & Qu, Q. (2016) · Neurochemical Research · doi:10.1007/s11064-016-1945-6 · Cited by 41
Unified theory of Alzheimer’s disease (UTAD): implications for prevention and curative therapy
Nehls, M. (2016) · Journal of Molecular Psychiatry · doi:10.1186/s40303-016-0018-8 · Cited by 41
Jaikumkao, K., Thongnak, L., Htun, K. T., Pengrattanachot, N., Phengpol, N., Sutthasupha, P., Promsan, S., Montha, N., Sriburee, S., Kothan, S., et al. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2023.166912 · Cited by 41
Autophagy Modulation As a Potential Therapeutic Target for Liver Diseases
Puri, P., & Chandra, A. (2014) · Journal of Clinical and Experimental Hepatology · doi:10.1016/j.jceh.2014.04.001 · Cited by 42
Gilad, Y., Shiloh, R., Ber, Y., Bialik, S., & Kimchi, A. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.06.049 · Cited by 41
The Roles of ceRNAs-Mediated Autophagy in Cancer Chemoresistance and Metastasis
Zhang, H., & Lü, B. (2020) · Cancers · doi:10.3390/cancers12102926 · Cited by 41
ANXA6 suppresses the tumorigenesis of cervical cancer through autophagy induction
Sun, X., Shu, Y., Xu, M., Jiang, J.-K., Wang, L., Wang, J., Huang, D., & Zhang, J. (2020) · Clinical and Translational Medicine · doi:10.1002/ctm2.208 · Cited by 41
Amino Acid Transporters Are a Vital Focal Point in the Control of mTORC1 Signaling and Cancer
Cormerais, Y., Vučetić, M., Parks, S. K., & Pouysségur, J. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms22010023 · Cited by 45
Najjar, R. S., & Feresin, R. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22041668 · Cited by 42
Dysregulation of mTOR Signaling after Brain Ischemia
Villa-González, M., Martín-López, G., & Pérez-Álvarez, M. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052814 · Cited by 41
Meske, V., Erz, J., Priesnitz, T., & Ohm, T. G. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2013.12.018 · Cited by 41
Phosphorylation of FAM134C by CK2 controls starvation-induced ER-phagy
Lorenzo, G. D., Iavarone, F., Maddaluno, M., Plata-Gómez, A. B., Aureli, S., Meza, C. P. Q., Cinque, L., Palma, A., Reggio, A., Cirillo, C., et al. (2022) · Science Advances · doi:10.1126/sciadv.abo1215 · Cited by 43
Takakura, Y., Machida, M., Terada, N., Katsumi, Y., Kawamura, S., Horie, K., Miyauchi, M., Ishikawa, T., Akiyama, N., Seki, T., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-45206-1 · Cited by 36
The endolysosomal system in conventional and unconventional protein secretion
Néel, E., Chiritoiu-Butnaru, M., Fargues, W., Denus, M., Colladant, M., Filaquier, A., Stewart, S. E., Lehmann, S., Zurzolo, C., Rubinsztein, D. C., et al. (2024) · Journal of Cell Biology · doi:10.1083/jcb.202404152 · Cited by 50
Pelizzaro‐Rocha, K. J., de Jesus, M. B., Ruela-de-Sousa, R. R., Nakamura, C. V., Reis, F. S., de Fátima, Â., & Ferreira‐Halder, C. V. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.07.010 · Cited by 40
Quayle, L. A., Ottewell, P. D., & Holen, I. (2015) · Current Cancer Drug Targets · doi:10.2174/1568009615666150506092443 · Cited by 40
Soma‐Nagae, T., Nada, S., Kitagawa, M., Takahashi, Y., Mori, S., Oneyama, C., & Okada, M. (2013) · Journal of Cell Science · doi:10.1242/jcs.121913 · Cited by 40
Button, R. W., Vincent, J. H., Strang, C. J., & Luo, S. (2016) · Oncotarget · doi:10.18632/oncotarget.6986 · Cited by 41
Kim, Y. H., Baek, S. H., Kim, E. K., Ha, J. M., Jin, S. Y., Lee, H. S., Ha, H. K., Song, S. H., Kim, S. J., Shin, H. K., et al. (2016) · FEBS Letters · doi:10.1002/1873-3468.12172 · Cited by 40
Allavena, G., Boyd, C. M., Oo, K. S., Maellaro, E., Zhivotovsky, B., & Kaminskyy, V. O. (2016) · Autophagy · doi:10.1080/15548627.2016.1226733 · Cited by 43
Autophagy as an Emerging Common Pathomechanism in Inherited Peripheral Neuropathies
Haidar, M., & Timmerman, V. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00143 · Cited by 40
Mitophagy in Huntington's disease
Šonský, I., Vodička, P., Kepková, K. V., & Hansíková, H. (2021) · Neurochemistry International · doi:10.1016/j.neuint.2021.105147 · Cited by 42
Mechanisms of neuronal survival safeguarded by endocytosis and autophagy
Overhoff, M., Bruyckere, E. D., & Kononenko, N. L. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15194 · Cited by 40
Golgi-associated Rab GTPases implicated in autophagy
Lu, Q., Wang, P., & Yang, L. (2021) · Cell & Bioscience · doi:10.1186/s13578-021-00543-2 · Cited by 41
Exploring the Role of Autophagy Dysfunction in Neurodegenerative Disorders
Rana, T., Behl, T., Sehgal, A., Mehta, V., Singh, S., Bhatia, S., Al‐Harrasi, A., & BUNGAU, S. G. (2021) · Molecular Neurobiology · doi:10.1007/s12035-021-02472-0 · Cited by 42
Leucine Supplementation in Cancer Cachexia: Mechanisms and a Review of the Pre-Clinical Literature
Beaudry, A. G., & Law, M. L. (2022) · Nutrients · doi:10.3390/nu14142824 · Cited by 42
Molecular Mechanism and Regulation of Autophagy and Its Potential Role in Epilepsy
Zhu, H., Wang, W., & Li, Y. (2022) · Cells · doi:10.3390/cells11172621 · Cited by 44
Autophagy, immunity and human disease
Heath, R. J. W., & Xavier, R. J. (2009) · Current Opinion in Gastroenterology · doi:10.1097/mog.0b013e32833104f1 · Cited by 39
Autophagy in Chronic Myeloid Leukaemia: Stem Cell Survival and Implication in Therapy
Helgason, G. V., Mukhopadhyay, A., Karvela, M., Salomoni, P., Calabretta, B., & Holyoake, T. L. (2013) · Current Cancer Drug Targets · doi:10.2174/15680096113139990088 · Cited by 42
Novel Insights into Osteoarthritis Joint Pathology from Studies in Mice
Moon, P. M., & Beier, F. (2015) · Current Rheumatology Reports · doi:10.1007/s11926-015-0524-1 · Cited by 41
Contribution of autophagy to antiviral immunity
Rey-Jurado, E., Riedel, C. A., González, P. A., Bueno, S. M., & Kalergis, A. M. (2015) · FEBS Letters · doi:10.1016/j.febslet.2015.07.047 · Cited by 40
Molecular cloning, characterization and expression analysis of ATG1 in the silkworm, Bombyx mori
Casati, B., Terova, G., Cattaneo, A. G., Rimoldi, S., Franzetti, E., de Eguileor, M., & Tettamanti, G. (2012) · Gene · doi:10.1016/j.gene.2012.09.086 · Cited by 39
Deubiquitinase inhibition by WP1130 leads to ULK1 aggregation and blockade of autophagy
Drießen, S., Berleth, N., Friesen, O., Löffler, A. S., Böhler, P., Hieke, N., Stuhldreier, F., Peter, C., Schink, K. O., Schultz, S. W., et al. (2015) · Autophagy · doi:10.1080/15548627.2015.1067359 · Cited by 39
Exploiting cancer vulnerabilities: mTOR, autophagy, and homeostatic imbalance
Johnson, C. E., & Tee, A. R. (2017) · Essays in Biochemistry · doi:10.1042/ebc20170056 · Cited by 40
Metformin inhibits cell proliferation in SKM-1 cells via AMPK-mediated cell cycle arrest
Zhou, X., Kuang, Y., Liang, S., & Wang, L. (2019) · Journal of Pharmacological Sciences · doi:10.1016/j.jphs.2019.10.003 · Cited by 39
The Vicious Circle of Hepatic Glucagon Resistance in Non-Alcoholic Fatty Liver Disease
Galsgaard, K. D. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9124049 · Cited by 40
Jiang, Y., Luo, W., Wang, B., Yi, Z., Gong, P., & Xiong, Y. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100287 · Cited by 39
Xuan, C., Xi, Y.-M., Zhang, Y., Tao, C.-H., Zhang, L., & Cao, W. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.624404 · Cited by 39
mTORC1 beyond anabolic metabolism: Regulation of cell death
Zhu, J., Wang, H., & Jiang, X. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202208103 · Cited by 42
Inhibition of autophagy; an opportunity for the treatment of cancer resistance
Tonkin-Reeves, A., Giuliani, C. M., & Price, J. T. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1177440 · Cited by 41
Gao, Y., & Tian, T. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241411811 · Cited by 39
Autophagy in cerebral ischemia and the effects of traditional Chinese medicine
Xiao-ping, H., Ding, H., Lu, J.-D., Tang, Y., Bing-xiang, D., & Deng, C.-Q. (2015) · Journal of Chinese Integrative Medicine · doi:10.1016/s2095-4964(15)60187-x · Cited by 38
Role of autophagy in the maintenance and function of cancer stem cells
Vitale, I., Manic, G., Dandrea, V., & Maria, R. D. (2015) · The International Journal of Developmental Biology · doi:10.1387/ijdb.150082iv · Cited by 39
Sensing the Environment Through Sestrins: Implications for Cellular Metabolism
Parmigiani, A., & Budanov, A. V. (2016) · International review of cytology · doi:10.1016/bs.ircmb.2016.05.003 · Cited by 40
Ntsapi, C., Lumkwana, D., Swart, C., du Toit, A., & Loos, B. (2017) · International review of cytology · doi:10.1016/bs.ircmb.2017.07.002 · Cited by 39
In Silico HTS and Structure Based Optimization of Indazole-Derived ULK1 Inhibitors
Wood, S. D., Grant, W. M., Adrados, I., Choi, J. Y., Alburger, J. M., Duckett, D. R., & Roush, W. R. (2017) · ACS Medicinal Chemistry Letters · doi:10.1021/acsmedchemlett.7b00344 · Cited by 38
A high-throughput screen identifies the long non-coding RNA DRAIC as a regulator of autophagy
Tiessen, I., Abildgaard, M. H., Lubas, M., Gylling, H. M., Steinhauer, C., Pietras, E. J., Diederichs, S., Frankel, L. B., & Lund, A. H. (2019) · Oncogene · doi:10.1038/s41388-019-0783-9 · Cited by 39
Acute knockdown of Depdc5 leads to synaptic defects in mTOR-related epileptogenesis
Fusco, A. D., Cerullo, M. S., Marte, A., Michetti, C., Romei, A., Castroflorio, E., Baulac, S., & Benfenati, F. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104822 · Cited by 40
mTOR pathway and DNA damage response: A therapeutic strategy in cancer therapy
Pazhooh, R. D., Farnood, P. R., Asemi, Z., Mirsafaei, L., Yousefi, B., & Mirzaei, H. (2021) · DNA repair · doi:10.1016/j.dnarep.2021.103142 · Cited by 36
Autophagy: A Key Player in Pancreatic Cancer Progression and a Potential Drug Target
Gillson, J., El-Aziz, Y. S. A., Leck, L. Y. W., Jansson, P. J., Pavlakis, N., Samra, J. S., Mittal, A., & Sahni, S. (2022) · Cancers · doi:10.3390/cancers14143528 · Cited by 38
Protein metabolism and related body function: mechanistic approaches and health consequences
Tomé, D., Benoit, S., & Azzout‐Marniche, D. (2020) · Proceedings of The Nutrition Society · doi:10.1017/s0029665120007880 · Cited by 39
Hill, C. N., Hernández‐Cáceres, M. P., Asencio, C., Torres, B. M., Solis, B., & Owen, G. I. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.605314 · Cited by 38
Gottschalk, G., Peterson, D. L., Knox, K. K., Maynard, M., Whelan, R. J., & Roy, A. (2022) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2022.103731 · Cited by 39
Role of autophagy in cancer prevention, development and therapy
Helgason, G. V., Holyoake, T. L., & Ryan, K. M. (2013) · Essays in Biochemistry · doi:10.1042/bse0550133 · Cited by 38
Targeting tissue-specific metabolic signaling pathways in aging: the promise and limitations
Hu, F., & Liu, F. (2013) · Protein & Cell · doi:10.1007/s13238-013-0002-3 · Cited by 39
Trafficking and signaling in mammalian autophagy
Tooze, S. A., Jefferies, H. B. J., Kalie, E., Longatti, A., McAlpine, F. E., McKnight, N. C., Orsi, A., Polson, H. E. J., Razi, M., Robinson, D. J., et al. (2010) · IUBMB Life · doi:10.1002/iub.334 · Cited by 37
Correa, R. J. M., Valdés, Y. R., Shepherd, T. G., & DiMattia, G. E. (2015) · Journal of Ovarian Research · doi:10.1186/s13048-015-0182-y · Cited by 38
Autophagy as a target for hematological malignancy therapy
Dong, Z., Liang, S., Hu, J., Jin, W., Zhan, Q., & Zhao, K. (2016) · Blood Reviews · doi:10.1016/j.blre.2016.04.005 · Cited by 37
Novel pharmacological modulators of autophagy: an updated patent review (2012-2015)
Ha, J., & Kim, J. (2016) · Expert Opinion on Therapeutic Patents · doi:10.1080/13543776.2016.1217996 · Cited by 37
Autophagy and Autophagy-Related Proteins in CNS Autoimmunity
Keller, C. W., & Lünemann, J. D. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00165 · Cited by 38
Wang, C., Yeo, S. K., Haas, M. A., & Guan, J. (2017) · The Journal of Cell Biology · doi:10.1083/jcb.201609093 · Cited by 40
Self-citationCanonical and Non-Canonical Autophagy in HIV-1 Replication Cycle
Leymarie, O., Lepont, L., & Berlioz‐Torrent, C. (2017) · Viruses · doi:10.3390/v9100270 · Cited by 37
Targeting mTORs by omega-3 fatty acids: A possible novel therapeutic strategy for neurodegeneration?
Shirooie, S., Nabavi, S. F., Dehpour, A. R., Belwal, T., Habtemariam, S., Argüelles, S., Sureda, A., Daglia, M., Tomczyk, M., Sobarzo‐Sánchez, E., et al. (2018) · Pharmacological Research · doi:10.1016/j.phrs.2018.07.004 · Cited by 37
Cai, J., Zhang, H., Zhang, Y. F., Zhou, Z., & Wu, S. (2018) · Experimental Cell Research · doi:10.1016/j.yexcr.2018.11.028 · Cited by 37
Vucicevic, L. M., Misirkic-Marjanovic, M., Ćirić, D., Martinović, T., Jovanović, M., Isaković, A., Marković, I., Šaponjić, J., Foretz, M., Rabanal‐Ruiz, Y., et al. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03356-2 · Cited by 37
Eating the unknown: Xenophagy and ER-phagy are cytoprotective defenses against pathogens
Reggio, A., Buonomo, V., & Grumati, P. (2020) · Experimental Cell Research · doi:10.1016/j.yexcr.2020.112276 · Cited by 38
The Interplay of HIV and Autophagy in Early Infection
Cabrera-Rodríguez, R., Pérez-Yanes, S., Estévez‐Herrera, J., Márquez-Arce, D., Cabrera, C., Espert, L., Blanco, J., & Valenzuela-Fernández, A. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.661446 · Cited by 37
Multifaceted roles of HSF1 in cell death: A state-of-the-art review
Zhang, B., Fan, Y., Cao, P., & Tan, K. (2021) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2021.188591 · Cited by 37
Autophagy in toxicology: self‐consumption in times of stress and plenty
Bolt, A. M., & Klimecki, W. T. (2012) · Journal of Applied Toxicology · doi:10.1002/jat.1787 · Cited by 36
Yuan, J., Zhao, X., Hu, Y., Sun, H., Gong, G., Huang, X., Chen, X., Xia, M., Sun, C., Huang, Q., et al. (2018) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2018.3393 · Cited by 36
Dong, Q., Majumdar, G., O’Meally, R. N., Cole, R. N., Elam, M. B., & Raghow, R. (2019) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-019-03625-5 · Cited by 36
Yang, S., Zhang, Y., Ting, C.-Y., Bettedi, L., Kim, K., Ghaniam, E., & Lilly, M. A. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.08.006 · Cited by 36
Metadata
- Authors
- Hosokawa, N., Hara, T., Kaizuka, T., Kishi, C., Takamura, A., Miura, Y., Iemura, S.-I., Natsume, T., Takehana, K., Yamada, N., Guan, J.-L., Oshiro, N., & Mizushima, N.
- Affiliations
- Tokyo Medical and Dental University (JP)
- National Institute of Advanced Industrial Science and Technology (JP)
- Exploratory Research, Pharmaceutical Research Laboratory, and
- Ajinomoto (Japan) (JP)
- University of Michigan (US)
- Biosignal Research Center, Kobe University (JP)
- Venue
- Molecular Biology of the Cell
- Published
- 2009-04
- Volume
- 20
- Issue
- 7
- Pages
- 1981-1991
- ISSN
- 1059-1524 (ISSN-L)
- 1939-4586
- PMC
- PMC2663915
- OpenAlex
- W2156144699
- Cited by
- 2,076
- References
- 54
- Citations by year
- 2026: 68 · 2025: 81 · 2024: 133 · 2023: 128 · 2022: 139 · 2021: 171 · 2020: 154 · 2019: 132 · 2018: 114 · 2017: 128 · 2016: 132 · 2015: 142 · 2014: 115 · 2013: 112 · 2012: 110
- FWCI
- 73.07
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Molecular Biology of the Cell (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Tokyo
- Tokyo Medical and Dental University
- Toray Science Foundation
- Japan Society for the Promotion of Science
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Keywords
- autophagy, mTORC1, ULK1, ATG13, FIP200, autophagosome formation, nutrient signaling, mTOR phosphorylation, rapamycin, starvation, lysosomal degradation
- MeSH terms
- Autophagy-Related Proteins, Autophagy-Related Protein-1 Homolog, Mechanistic Target of Rapamycin Complex 1, Amino Acids, Animals, Autophagy, Cell Line, Cell Membrane, Humans, Molecular Weight, Phosphorylation, Protein Binding, Protein Kinases, Proteins, Transcription Factors, Protein Serine-Threonine Kinases, Protein Transport, Multiprotein Complexes, Intracellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, Mice, TOR Serine-Threonine Kinases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review