The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Autophagy and Metabolism
Open accessAbstract
Autophagy is a process of self-cannibalization. Cells capture their own cytoplasm and organelles and consume them in lysosomes. The resulting breakdown products are inputs to cellular metabolism, through which they are used to generate energy and to build new proteins and membranes. Autophagy preserves the health of cells and tissues by replacing outdated and damaged cellular components with fresh ones. In starvation, it provides an internal source of nutrients for energy generation and, thus, survival. A powerful promoter of metabolic homeostasis at both the cellular and whole-animal level, autophagy prevents degenerative diseases. It does have a downside, however—cancer cells exploit it to survive in nutrient-poor tumors.
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
“Unsurprisingly, glutamine metabolism plays a critical role in tumor progression since it not only supports mitochondrial oxidative phosphorylation but also supplies metabolic intermediates for the TCA cycle, glutathione synthesis, and NEAA synthesis and simultaneously produces NADPH157–159.”
From Glutamine reliance in cell metabolism (2020) · cites this paper as [159]
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
Mitochondrial Autophagy Is an HIF-1-dependent Adaptive Metabolic Response to Hypoxia
Zhang, H., Bosch-Marce, M., Shimoda, L. A., Tan, Y. S., Baek, J. H., Wesley, J. B., Gonzalez, F. J., & Semenza, G. L. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m800102200 · Cited by 1,601
RetractedParkin is recruited selectively to impaired mitochondria and promotes their autophagy
Narendra, D., Tanaka, A., Suen, D.-F., & Youle, R. J. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200809125 · Cited by 4,026
Autophagy regulates lipid metabolism
Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975
Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice
Hara, T., Nakamura, K., Matsui, M., Yamamoto, A., Nakahara, Y., Suzuki-Migishima, R., Yokoyama, M., Mishima, K., Saito, I., Okano, H., et al. (2006) · Nature · doi:10.1038/nature04724 · Cited by 3,882
Loss of autophagy in the central nervous system causes neurodegeneration in mice
Komatsu, M., Waguri, S., Chiba, T., Murata, S., Iwata, J.-I., Tanida, I., Ueno, T., Koike, M., Uchiyama, Y., Kominami, E., et al. (2006) · Nature · doi:10.1038/nature04723 · Cited by 3,500
The role of autophagy during the early neonatal starvation period
Kuma, A., Hatano, M., Matsui, M., Yamamoto, A., Nakaya, H., Yoshimori, T., Ohsumi, Y., Tokuhisa, T., & Mizushima, N. (2004) · Nature · doi:10.1038/nature03029 · Cited by 2,865
PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1
Geisler, S., Holmström, K. M., Skujat, D., Fiesel, F. C., Rothfuss, O. C., Kahle, P. J., & Springer, W. (2010) · Nature Cell Biology · doi:10.1038/ncb2012 · Cited by 2,835
Impairment of starvation-induced and constitutive autophagy in Atg7 -deficient mice
Komatsu, M., Waguri, S., Ueno, T., Iwata, J., Murata, S., Tanida, I., Ezaki, J., Mizushima, N., Ohsumi, Y., Uchiyama, Y., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200412022 · Cited by 2,331
Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice.
Komatsu, M., Waguri, S., Koike, M., Sou, Y.-S., Ueno, T., Hara, T., Mizushima, N., Iwata, J.-I., Ezaki, J., Murata, S., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.035 · Cited by 2,124
Mizushima, N., Yamamoto, A., Matsui, M., Yoshimori, T., & Ohsumi, Y. (2004) · Molecular Biology of the Cell · doi:10.1091/mbc.e03-09-0704 · Cited by 2,105
Flagged first, then by citations
Cited by
Sorted by citations
Items 701–800 of 1,005
Raut, P. K., Choi, D. Y., Kim, S. H., Hong, J. T., Kwon, T. K., Jeong, J. H., & Park, P. (2017) · Oncotarget · doi:10.18632/oncotarget.22684 · Cited by 48
Tian, X., Zhang, K., Min, J., Chen, C., Cao, Y., Ding, C., Liu, W., & Li, J. (2019) · Viruses · doi:10.3390/v11111007 · Cited by 47
Macropinocytosis Renders a Subset of Pancreatic Tumor Cells Resistant to mTOR Inhibition
Michalopoulou, E., Auciello, F. R., Bulusu, V., Strachan, D., Campbell, A. D., Tait-Mulder, J., Karim, S. A., Morton, J. P., Sansom, O. J., & Kamphorst, J. J. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.01.080 · Cited by 50
Kishawy, A. T. Y., Al-Khalaifah, H. S., Nada, H. S., Roushdy, E. M., Zaglool, A. W., Ismail, T. A., Ibrahim, S. M., & Ibrahim, D. (2022) · Veterinary Sciences · doi:10.3390/vetsci9020043 · Cited by 48
Autophagy-based survival prognosis in human colorectal carcinoma
Yang, M., Zhao, H., Guo, L., Zhang, Q., Zhao, L., Bai, S., Zhang, M., Xu, S., Wang, F., Wang, X., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3054 · Cited by 47
Jutten, B., Keulers, T. G., Peeters, H. J. M., Schaaf, M. B. E., Savelkouls, K. G. M., Compter, I., Clarijs, R., Schijns, O. E. M. G., Ackermans, L. P. C. M., Teernstra, O., et al. (2018) · Autophagy · doi:10.1080/15548627.2017.1409926 · Cited by 46
Ma, Y., Chen, H., Hao, B.-M., Zhou, J., He, G., Miao, Z., Xu, Y., Gao, L., Zhou, W., & Zha, Z. (2018) · Journal of Materials Chemistry B · doi:10.1039/c8tb01987h · Cited by 47
Molecular Mechanisms and Treatment Options of Nephropathic Cystinosis
Jamalpoor, A., Othman, A., Levtchenko, E. N., Masereeuw, R., & Janssen, M. J. (2021) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2021.04.004 · Cited by 51
Dai, X., Jiang, C., Jiang, Q., Fang, L., Yu, H., Guo, J., Yan, P., Chi, F., Zhang, T., Inuzuka, H., et al. (2023) · Nature Metabolism · doi:10.1038/s42255-022-00732-4 · Cited by 48
Glycemic Targets and Approaches to Management of the Patient with Critical Illness
Mesotten, D., & den Berghe, G. V. (2011) · Current Diabetes Reports · doi:10.1007/s11892-011-0241-8 · Cited by 45
Torres, A., Luke, J. D., Kullas, A. L., Kapilashrami, K., Botbol, Y. M., Koller, A. A., Tonge, P. J., Chen, E. I., Macián, F., & van der Velden, A. W. M. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.4a0615-252r · Cited by 47
EMC6/TMEM93 suppresses glioblastoma proliferation by modulating autophagy
Shen, X., Kan, S., Hu, J., Li, M., Lu, G., Zhang, M., Zhang, S., Hou, Y., Chen, Y., & Bai, Y. (2016) · Cell Death and Disease · doi:10.1038/cddis.2015.408 · Cited by 45
Autophagic Regulation of Lipid Homeostasis in Cardiometabolic Syndrome
Yang, M., Zhang, Y., & Ren, J. T. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2018.00038 · Cited by 45
Yang, M., Fan, J., Sun, W. C., Du, J., Long, S., Shao, K., & Peng, X. (2019) · Chemical Communications · doi:10.1039/c9cc04060a · Cited by 45
Guttiferone K induces autophagy and sensitizes cancer cells to nutrient stress-induced cell death
Wu, M., Lao, Y., Xu, N., Wang, X., Tan, H., Fu, W., Lin, Z., & Xu, H. (2015) · Phytomedicine · doi:10.1016/j.phymed.2015.06.008 · Cited by 45
Combining Small-Volume Metabolomic and Transcriptomic Approaches for Assessing Brain Chemistry
Knolhoff, A. M., Nautiyal, K. M., Nemes, P., Kalachikov, S. M., Morozova, I., Silver, R., & Sweedler, J. V. (2013) · Analytical Chemistry · doi:10.1021/ac3032959 · Cited by 46
Knuppertz, L., & Osiewacz, H. D. (2016) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2016.01.003 · Cited by 44
Shared and distinct mechanisms of skeletal muscle atrophy: A narrative review
Wilburn, D. T., Ismaeel, A., Machek, S. B., Fletcher, E., & Koutakis, P. (2021) · Ageing Research Reviews · doi:10.1016/j.arr.2021.101463 · Cited by 47
The role of the Hippo pathway in autophagy in the heart
Maejima, Y., Zablocki, D., Nah, J., & Sadoshima, J. (2022) · Cardiovascular Research · doi:10.1093/cvr/cvac014 · Cited by 45
Zhang, Q., Yaoita, N., Tabuchi, A., Liu, S., Chen, S.-H., Li, Q., Hegemann, N., Li, C., Rodor, J., Timm, S., et al. (2024) · Circulation · doi:10.1161/circulationaha.124.068726 · Cited by 47
Rapino, F. A., Jung, M., & Fulda, S. (2013) · Oncogene · doi:10.1038/onc.2013.110 · Cited by 47
Matched and mismatched metabolic fuels in lymphocyte function
Caro‐Maldonado, A., Gerriets, V. A., & Rathmell, J. C. (2012) · Seminars in Immunology · doi:10.1016/j.smim.2012.12.002 · Cited by 44
You, W.-C., Chiou, S., Huang, K. C., Chiang, S., Yang, C.-L., Sudhakar, J. N., Lin, T., Chiang, I. ‐., Shen, C., Cheng, W.-Y., et al. (2013) · Neuro-Oncology · doi:10.1093/neuonc/not077 · Cited by 44
Tsai, T., Lai, K.-H., Su, J.-H., Wu, Y., & Sheu, J. (2018) · Marine Drugs · doi:10.3390/md16040104 · Cited by 44
Ringseis, R., Keller, J., & Eder, K. (2018) · Journal of Animal Physiology and Animal Nutrition · doi:10.1111/jpn.12959 · Cited by 47
Sun, Y., Li, T. Y., Song, L., Zhang, C., Li, J., Lin, Z., Lin, S., & Lin, S. (2018) · Hepatology · doi:10.1002/hep.29759 · Cited by 43
Immunometabolism of macrophages regulates skeletal muscle regeneration
Chen, Y.-F., Lee, C., Wu, H.-H., Lin, W., & Lee, O. K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.948819 · Cited by 46
Wu, J., Wang, D., Zhou, J., Li, J., Xie, R., Li, Y., Huang, J., Liu, B., & Qiu, J. (2022) · Phytotherapy Research · doi:10.1002/ptr.7614 · Cited by 44
NAD Depletion Mediates Cytotoxicity in Human Neurons With Autophagy Deficiency
Sun, C., Seranova, E., Cohen, M. A., Chipara, M., Roberts, J., Astuti, D., Palhegyi, A. M., Acharjee, A., Sedlackova, L., Kataura, T., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2023.112372 · Cited by 43
Lysosome-targeted fluorescent probes: Design mechanism and biological applications
Duan, X., Tong, Q., Fu, C., & Chen, L. (2023) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2023.106832 · 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
Lysosomes in Cancer—At the Crossroad of Good and Evil
Eriksson, I., & Öllinger, K. M. (2024) · Cells · doi:10.3390/cells13050459 · Cited by 48
Tiwari, R. V., Parajuli, P., & Sylvester, P. W. (2015) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-015-2488-x · Cited by 44
Lee, M., Cherla, R. P., Jenson, M. H., Leyva‐Illades, D., Martinez-Moczygemba, M., & Tesh, V. L. (2011) · Cellular Microbiology · doi:10.1111/j.1462-5822.2011.01634.x · Cited by 44
Zhang, L., Shamaladevi, N., Jayaprakasha, G. K., Patil, B. S., & Lokeshwar, B. L. (2015) · Oncotarget · doi:10.18632/oncotarget.3834 · Cited by 43
Mohan, N., Banik, N. L., & Ray, S. K. (2011) · Neuroscience Letters · doi:10.1016/j.neulet.2011.07.016 · Cited by 44
Autophagic program is regulated by miR-325
Bo, L., Su-Ling, D., Fang, L., Lu-Yu, Z., An, T., Stefan, D., Kun, W., & Pei-feng, L. (2014) · Cell Death and Differentiation · doi:10.1038/cdd.2014.18 · Cited by 43
Metabolic Control by Target of Rapamycin and Autophagy during Ageing - A Mini-Review
Markaki, M., & Tavernarakis, N. (2013) · Gerontology · doi:10.1159/000348599 · Cited by 42
The Regulation of the Autophagic Network and Its Implications for Human Disease
Yang, J. H., Carra, S., Zhu, W., & Kampinga, H. H. (2013) · International Journal of Biological Sciences · doi:10.7150/ijbs.6666 · Cited by 45
Analyzing Tumor Metabolism In Vivo
Faubert, B., & DeBerardinis, R. J. (2016) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-050216-121954 · Cited by 44
Angeletti, F., Fossati, G., Pattarozzi, A., Würth, R., Solari, A., Daga, A., Masiello, I., Barbieri, F., Florio, T., & Comincini, S. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00107 · Cited by 45
Metabolic PET Imaging in Oncology
Sai, K. K. S., Zachar, Z., Bingham, P. M., & Mintz, A. (2017) · American Journal of Roentgenology · doi:10.2214/ajr.17.18112 · Cited by 43
Rapamycin Reduces Podocyte Apoptosis and is Involved in Autophagy and mTOR/ P70S6K/4EBP1 Signaling
Jin, J., Hu, K. Q., Ye, M., Wu, D., & He, Q. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000491905 · Cited by 45
Tackling Cancer with Yeast-Based Technologies
Ferreira, R., Limeta, A., & Nielsen, J. (2018) · Trends in biotechnology · doi:10.1016/j.tibtech.2018.11.013 · Cited by 46
Ammonia and autophagy: An emerging relationship with implications for disorders with hyperammonemia
Soria, L. R., & Brunetti‐Pierri, N. (2019) · Journal of Inherited Metabolic Disease · doi:10.1002/jimd.12061 · Cited by 43
Autophagy-related 7 modulates tumor progression in triple-negative breast cancer
Li, M., Liu, J., Li, S., Feng, Y., Yi, F., Wang, L., Wei, S., & Cao, L. (2019) · Laboratory Investigation · doi:10.1038/s41374-019-0249-2 · Cited by 43
The Role of Autophagy in Pancreatic Cancer: From Bench to the Dark Bedside
Görgülü, K., Diakopoulos, K. N., Kaya-Aksoy, E., Ciecielski, K. J., Ai, J., Lesina, M., & Algül, H. (2020) · Cells · doi:10.3390/cells9041063 · Cited by 43
Oh, D. S., Park, J. H., Jung, H. E., Kim, H.-J., & Lee, H. K. (2020) · Autophagy · doi:10.1080/15548627.2020.1812218 · Cited by 45
Autophagy: A promising target for triple negative breast cancers
El-Aziz, Y. S. A., Gillson, J., Jansson, P. J., & Sahni, S. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.106006 · Cited by 44
McCormick, J. J., Dokładny, K., Moseley, P. L., & Kenny, G. P. (2020) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00542.2020 · Cited by 43
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, L., Liú, W., Wu, N., Wang, H., Zhang, Z., Liu, Y., & Wang, X. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011134 · Cited by 42
dos Santos, C., Cambraia, A., Shrestha, S., Cutler, M., Cottam, M. A., Perkins, G. A., Lev‐Ram, V., Roy, B., Acree, C., Keun-young Kim, A., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-53127-2 · Cited by 53
Induced proximity-based therapeutic modalities
King, E. A., Meyers, M., & Nomura, D. K. (2025) · Nature Reviews Drug Discovery · doi:10.1038/s41573-025-01316-z · Cited by 61
Wang, Z., Li, S., Ren, R., Li, J., & Cui, X. (2015) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5b02644 · Cited by 42
Yu, X., & Long, Y. C. (2014) · The FASEB Journal · doi:10.1096/fj.14-252841 · Cited by 44
Protein oxidation seems to be linked to constitutive autophagy: A sex study
Campesi, I., Straface, E., Occhioni, S., Montella, A., & Franconi, F. (2013) · Life Sciences · doi:10.1016/j.lfs.2013.06.001 · Cited by 42
Modulation of protein quality control systems by food phytochemicals
Murakami, A. (2013) · Journal of Clinical Biochemistry and Nutrition · doi:10.3164/jcbn.12-126 · Cited by 42
Long-Term Artificial Selection Reveals a Role of TCTP in Autophagy in Mammalian Cells
Chen, K., Huang, C., Yuan, J., Cheng, H., & Zhou, R. (2014) · Molecular Biology and Evolution · doi:10.1093/molbev/msu181 · 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
Lipotoxic Effects of Palmitic Acid on Astrocytes Are Associated with Autophagy Impairment
Ortiz‐Rodriguez, A., Acaz‐Fonseca, E., Boya, P., Arévalo, M., & García‐Segura, L. M. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1183-9 · Cited by 44
Lv, L.-L., Liu, B., Liu, J., Li, L.-S., Jin, F., Xu, Y.-Y., Wu, Q., Liu, J., & Shi, J.-S. (2020) · Journal of Alzheimer's Disease · doi:10.3233/jad-200308 · Cited by 40
Camps, J., Castañé, H., Rodríguez‐Tomàs, E., Baiges‐Gayà, G., Hernández‐Aguilera, A., Arenas, M., Iftimie, S. M., & Joven, J. (2021) · Biomolecules · doi:10.3390/biom11070971 · Cited by 43
14-3-3 proteins contribute to autophagy by modulating SINAT-mediated degradation of ATG13
Qi, H., Xue, L., Wang, Y., Yu, S., Liu, T., Zhou, S., Chen, J., Chen, Q., Qiu, R., Jiang, L., et al. (2022) · The Plant Cell · doi:10.1093/plcell/koac273 · Cited by 42
A prospective strategy leveraging nanomedicine for cancer therapy: Pouring ferroptosis on apoptosis
Xia, Y., Zhang, J., & Liu, G. (2022) · Nano Today · doi:10.1016/j.nantod.2022.101740 · Cited by 41
Characterization of early autophagy signaling by quantitative phosphoproteomics
Rigbolt, K. T. G., Zarei, M., Sprenger, A., Becker, A. C., Diedrich, B., Huang, X., Eiselein, S., Kristensen, A. R., Gretzmeier, C., Andersen, J., et al. (2013) · Autophagy · doi:10.4161/auto.26864 · Cited by 41
Nguyen, T. G., Honson, N. S., Arns, S., Davis, T. L., Dhe‐Paganon, S., Kovacic, S., Kumar, N. S., Pfeifer, T. A., & Young, R. N. (2014) · Assay and Drug Development Technologies · doi:10.1089/adt.2013.561 · Cited by 41
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
Agwa, M. M., Abu-Serie, M. M., Abdelmonsif, D. A., Moussa, N., Elsayed, H., Khattab, S. N., & Sabra, S. A. (2021) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2021.120965 · Cited by 41
Cui, J., Sim, T. H.-F., Gong, Z., & Shen, H. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.04.145 · Cited by 41
Williams, A. C., Hill, L. J., & Ramsden, D. B. (2012) · Current Gerontology and Geriatrics Research · doi:10.1155/2012/302875 · Cited by 42
When Cells Suffocate: Autophagy in Cancer and Immune Cells under Low Oxygen
Schlie, K., Spowart, J. E., Hughson, L. R. K., Townsend, K. N., & Lum, J. J. (2011) · International Journal of Cell Biology · doi:10.1155/2011/470597 · Cited by 45
Liu, Y. L., Lai, F., Wilmott, J. S., Yan, X. G., Liu, X. Y., Luan, Q., Guo, S. T., Jiang, C. C., Tseng, H.-Y., Scolyer, R. A., et al. (2014) · Oncotarget · doi:10.18632/oncotarget.2616 · Cited by 40
Li, T., Tong, H., Yin, H., Luo, Y., Zhu, J., Qin, Z., Yin, S., & He, W. (2021) · Cancer Cell International · doi:10.1186/s12935-021-02303-1 · Cited by 40
Ras-mutant cancers are sensitive to small molecule inhibition of V-type ATPases in mice
Tolani, B., Celli, A., Yao, Y., Tan, Y. Z., Fetter, R. D., Liem, C. R., de Smith, A. J., Vasanthakumar, T., Bisignano, P., Cotton, A. D., et al. (2022) · Nature Biotechnology · doi:10.1038/s41587-022-01386-z · Cited by 44
Yao, H., Li, J., Liu, Z., Ouyang, C., Qiu, Y., Zheng, X., Mu, J., & Xie, Z. (2022) · Autophagy · doi:10.1080/15548627.2022.2139920 · Cited by 40
Paraoxonases and Chemokine (C–C Motif) Ligand-2 in Noncommunicable Diseases
Camps, J., Rodríguez‐Gallego, E., García‐Heredia, A., Triguero, I., Riera-Borrull, M., Hernández‐Aguilera, A., Luciano‐Mateo, F., Fernández‐Arroyo, S., & Joven, J. (2013) · Advances in clinical chemistry · doi:10.1016/b978-0-12-800094-6.00007-8 · Cited by 40
Yang, D., Jiang, T., Lin, P., Chen, H., Wang, L., Wang, N., Zhao, F., Tang, K., Zhou, D., Wang, A., et al. (2016) · Reproductive Toxicology · doi:10.1016/j.reprotox.2016.12.005 · Cited by 40
Alteration of cellular metabolism in cancer cells and its therapeutic prospects
Biswal, B. N., Das, S., Das, B., & Rath, R. (2017) · Journal of Oral and Maxillofacial Pathology · doi:10.4103/jomfp.jomfp_60_17 · Cited by 42
Li, Z., Zhang, L., Gao, M., Han, M., Liu, K., Zhang, Z., Gong, Z., Xing, L., Shi, X., Lu, K., et al. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-018-1012-z · Cited by 41
RetractedThe small GTPase Rab32 resides on lysosomes to regulate mTORC1 signaling
Drizyte‐Miller, K., Chen, J., Cao, H., Schott, M. B., & McNiven, M. A. (2020) · Journal of Cell Science · doi:10.1242/jcs.236661 · Cited by 40
Kumar, A., Welch, N., Mishra, S., Bellar, A., Silva, R. N., Li, L., Singh, S. S., Sharkoff, M., Kerr, A., Chelluboyina, A. K., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.154089 · Cited by 40
Cu‐Doped Polypyrrole with Multi‐Catalytic Activities for Sono‐Enhanced Nanocatalytic Tumor Therapy
Chen, T., Zeng, W., Liu, Y., Yu, M., Huang, C., Shi, Z., Lin, C., Tang, J., Mei, L., & Wu, M. (2022) · Small · doi:10.1002/smll.202202964 · Cited by 40
Zhou, Y., Zou, J., Xu, J. B., Zhou, Y., Cen, X., & Zhao, Y. (2023) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2023.115219 · Cited by 43
Jagannathan, S., Malek, E., Vallabhapurapu, S., Vallabhapurapu, S., & Driscoll, J. J. (2014) · Oncotarget · doi:10.18632/oncotarget.2590 · Cited by 42
Autophagy and its implication in Chinese hamster ovary cell culture
Kim, Y. J., Baek, E., Lee, J. S., & Lee, G. M. (2013) · Biotechnology Letters · doi:10.1007/s10529-013-1276-5 · Cited by 40
Cardiomyocyte autophagy: metabolic profit and loss
Wang, Z. V., Ferdous, A., & Hill, J. A. (2012) · Heart Failure Reviews · doi:10.1007/s10741-012-9350-y · Cited by 39
Autophagy targets Hd1 for vacuolar degradation to regulate rice flowering
Hu, Z., Yang, Z., Zhang, Y., Zhang, A., Lu, Q., Fang, Y. R., & Lu, C. (2022) · Molecular Plant · doi:10.1016/j.molp.2022.05.006 · Cited by 38
Metformin: An Inhibitor of mTORC1 Signaling
Melnik, B. C., & Schmitz, G. (2014) · Cited by 39
Unravelling the relationship between macroautophagy and mitochondrial ROS in cancer therapy
Zhao, Y., Qu, T., Wang, P., Li, X., Qiang, J., Xia, Z., Duan, H., Huang, J., & Zhu, L. (2016) · APOPTOSIS · doi:10.1007/s10495-016-1236-3 · Cited by 40
Metabolic plasticity in heterogeneous pancreatic ductal adenocarcinoma
Liang, C., Qin, Y., Zhang, B., Ji, S., Shi, S., Xu, W., Liu, J., Xiang, J., Liang, D., Hu, Q., et al. (2016) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2016.09.001 · Cited by 39
Macropinocytosis and autophagy crosstalk in nutrient scavenging
Florey, O., & Overholtzer, M. (2018) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2018.0154 · Cited by 39
Titin truncations lead to impaired cardiomyocyte autophagy and mitochondrial function in vivo
Zhou, J., Ng, B., Ko, N. S. J., Fiedler, L. R., Khin, E. S. W., Lim, A. R., Sahib, N. B. E., Wu, Y., Chothani, S. P., Schäfer, S., et al. (2019) · Human Molecular Genetics · doi:10.1093/hmg/ddz033 · Cited by 40
Wang, F., Cao, M., Fan, M., Wu, H., Huang, W., Zhang, Y., Hu, Z., & Jin, X. (2019) · Journal of Cellular Physiology · doi:10.1002/jcp.29307 · Cited by 39
Lu, J., Liu, F., Li, H., Xu, Y., & Sun, S. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c06117 · Cited by 39
Shi, X., Xi, B., Jasbi, P., Turner, C., Jin, Y., & Gu, H. (2020) · Analytical Chemistry · doi:10.1021/acs.analchem.0c01767 · Cited by 40
The Aging Liver: Redox Biology and Liver Regeneration
Bellanti, F., & Vendemiale, G. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0048 · Cited by 40
Protein networks linking Warburg and reverse Warburg effects to cancer cell metabolism
Johar, D., Elmehrath, A. O., Khalil, R. M., Elberry, M. H., Zaky, S., Shalabi, S. A., & Bernstein, L. H. (2021) · BioFactors · doi:10.1002/biof.1768 · Cited by 42
Brain-enriched RagB isoforms regulate the dynamics of mTORC1 activity through GATOR1 inhibition
Figlia, G., Müller, S., Hagenston, A. M., Kleber, S., Roiuk, M., Quast, J.-P., ten Bosch, N., Ibañez, D. C., Mauceri, D., Martín-Villalba, A., et al. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00977-x · Cited by 41
Nutrigenomics: An inimitable interaction amid genomics, nutrition and health
Mishra, U. N., Jena, D., Sahu, C., Devi, R., Kumar, R., Jena, R., Irondi, E. A., Rout, S., Tiwari, R. K., Lal, M. K., et al. (2022) · Innovative Food Science & Emerging Technologies · doi:10.1016/j.ifset.2022.103196 · Cited by 39
Metadata
- Authors
- Rabinowitz, J. D., & White, E.
- Affiliations
- Princeton University (US)
- Rutgers, The State University of New Jersey (US)
- Venue
- Science
- Published
- 2010-12-03
- Volume
- 330
- Issue
- 6009
- Pages
- 1344-1348
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3010857
- OpenAlex
- W2039607936
- Cited by
- 1,982
- References
- 37
- Citations by year
- 2026: 54 · 2025: 82 · 2024: 97 · 2023: 110 · 2022: 165 · 2021: 175 · 2020: 172 · 2019: 128 · 2018: 108 · 2017: 144 · 2016: 143 · 2015: 132 · 2014: 123 · 2013: 151 · 2012: 120
- FWCI
- 12.58
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (R37CA053370, RC1CA147961, R01CA130893)
- 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, cellular metabolism, lysosomal degradation, metabolic homeostasis, starvation, energy production, degenerative diseases, cancer cells
- MeSH terms
- Animals, Autophagy, Cell Survival, Disease, Energy Metabolism, Homeostasis, Humans, Metabolism, Neoplasms, Phagosomes, Proteins, Starvation, Signal Transduction, 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