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 Autophagy preserves the health of cells and tissues by replacing outdated and damaged cellular components with fresh ones.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
Cited by
Sorted by citations
Items 401–500 of 1,005
Bad phosphorylation as a target of inhibition in oncology
Bui, N.-L.-C., Pandey, V., Zhu, T., Ma, L., Basappa, & Lobie, P. E. (2018) · Cancer Letters · doi:10.1016/j.canlet.2017.11.017 · Cited by 86
Liu, L., He, J., Wei, X., Wan, G., Lao, Y., Xu, W., Li, Z., Hu, H., Hu, Z., Luo, X., et al. (2017) · Oncogene · doi:10.1038/onc.2017.193 · Cited by 92
Mennigen, J. A., Panserat, S., Larquier, M., Plagnes‐Juan, E., Médale, F., Seiliez, I., & Cassy, S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038604 · Cited by 93
Dai, Z., Tian, L., Song, B., Liu, X., & Yuan, J. (2016) · Chemical Science · doi:10.1039/c6sc03667h · Cited by 90
Graphene oxide nanoarchitectures in cancer biology: Nano-modulators of autophagy and apoptosis
Taheriazam, A., Abad, G. G. Y., Hajimazdarany, S., Imani, M. H., Ziaolhagh, S., Zandieh, M. A., Bayanzadeh, S. D., Mirzaei, S., Hamblin, M. R., Entezari, M., et al. (2023) · Journal of Controlled Release · doi:10.1016/j.jconrel.2023.01.028 · Cited by 95
Zhu, L. Y., Wang, H., Wu, Y. C., He, Z., Qin, Y., & Shen, Q. (2017) · Mediators of Inflammation · doi:10.1155/2017/7623145 · Cited by 90
Enhancing autophagy in Alzheimer's disease through drug repositioning
Eshraghi, M., Ahmadi, M., Afshar, S., Lorzadeh, S., Adlimoghaddam, A., Rezvani Jalal, N., West, R., Dastghaib, S., Igder, S., Torshizi, S. R. N., et al. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108171 · Cited by 89
Emerging role of the Hippo pathway in autophagy
Wang, D., He, J., Huang, B., Liu, S., Zhu, H., & Xu, T. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03069-6 · Cited by 89
Mechanisms, pathophysiological roles and methods for analyzing mitophagy – recent insights
Williams, J. A. R., & Ding, W. (2017) · Biological Chemistry · doi:10.1515/hsz-2017-0228 · Cited by 92
Tao, J., Chen, H., Li, X., & Wang, J. (2021) · Journal of Orthopaedic Surgery and Research · doi:10.1186/s13018-020-02056-z · Cited by 90
Sun, K., Guo, X.-L., Zhao, Q.-D., Jing, Y.-Y., Kou, X.-R., Xie, X.-Q., Zhou, Y., Cai, N., Gao, L., Zhao, X., et al. (2013) · Cell Death and Disease · doi:10.1038/cddis.2013.35 · Cited by 91
Baicalin inhibits autophagy induced by influenza A virus H3N2
Zhu, H., Han, L., Shi, X., Wang, B., Huang, H. Y., Wang, X., Chen, D., Ju, D., & Feng, M. (2014) · Antiviral Research · doi:10.1016/j.antiviral.2014.11.003 · Cited by 90
Tetrandrine blocks autophagic flux and induces apoptosis via energetic impairment in cancer cells
Qiu, W., Su, M., Xie, F., Ai, J., Ren, Y., Zhang, J., Guan, R., He, W., Gong, Y., & Guo, Y. (2014) · Cell Death and Disease · doi:10.1038/cddis.2014.84 · Cited by 89
Doridot, L., Châtre, L., Ducat, A., Vilotte, J.-L., Lombès, A., Méhats, C., Barbaux, S., Calicchio, R., Ricchetti, M., & Vaiman, D. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5661 · Cited by 90
Mockler, M. B., Conroy, M. J., & Lysaght, J. (2014) · Frontiers in Oncology · doi:10.3389/fonc.2014.00107 · Cited by 89
You eat what you are: autophagy inhibition as a therapeutic strategy in leukemia
Sehgal, A. R., Koenig, H., Johnson, D. E., Tang, D., Amaravadi, R. K., Boyiadzis, M. M., & Lotze, M. T. (2014) · Leukemia · doi:10.1038/leu.2014.349 · Cited by 89
Yang, L., Zhang, Q. H., Tian, R., Wang, Q., Zhao, J. J., Iglehart, J. D., Wang, Z. C., & Richardson, A. L. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-0940 · Cited by 90
Chai, W., Ye, F., Zeng, L., Li, Y., & Yang, L. (2019) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-019-1328-3 · Cited by 87
Autophagy in adipose tissue biology
Zhang, Y., Zeng, X., & Jin, S. V. (2012) · Pharmacological Research · doi:10.1016/j.phrs.2012.09.004 · Cited by 92
Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15
Vantaggiato, C., Crimella, C., Airoldi, G., Polishchuk, R., Bonato, S., Brighina, E., Scarlato, M., Musumeci, O., Toscano, A., Martinuzzi, A., et al. (2013) · Brain · doi:10.1093/brain/awt227 · Cited by 89
Plasmonic Nanoprobes for Real‐Time Optical Monitoring of Nitric Oxide inside Living Cells
Rivera-Gil, P., Vázquez-Vázquez, C., Giannini, V., Callao, M. P., Parak, W. J., Correa‐Duarte, M. A., & Álvarez‐Puebla, R. A. (2013) · Angewandte Chemie International Edition · doi:10.1002/anie.201306390 · Cited by 87
Bae, H. R., & Guan, J. (2011) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-11-0098 · Cited by 87
Endoplasmic reticulum protein BI-1 regulates Ca2+-mediated bioenergetics to promote autophagyPreprint
Sano, R., Hou, Y.-C., Hedvat, M., Correa, R. G., Shu, C., Krajewska, M., Diaz, P. W., Tamble, C. M., Quarato, G., Gottlieb, R. A., et al. (2012) · Genes & Development · doi:10.1101/gad.184325.111 · Cited by 87
Autophagy‐related prognostic signature for breast cancer
Gu, Y., Li, P., Peng, F., Zhang, M., Zhang, Y., Liang, H., Zhao, W., Qi, L., Wang, H., Wang, C., et al. (2015) · Molecular Carcinogenesis · doi:10.1002/mc.22278 · Cited by 86
Wu, D., Zhuo, L., & Wang, X. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.11.003 · Cited by 88
Tamima, U., Santra, M., Song, C. W., Reo, Y. J., & Ahn, K. H. (2019) · Analytical Chemistry · doi:10.1021/acs.analchem.9b02384 · Cited by 86
Mammalian phospholipase D: Function, and therapeutics
McDermott, M. I., Wang, Y., Wakelam, M. J. O., & Bankaitis, V. A. (2019) · Progress in Lipid Research · doi:10.1016/j.plipres.2019.101018 · Cited by 89
Glutamine deprivation stimulates mTOR-JNK-dependent chemokine secretion
Shanware, N. P., Bray, K., Eng, C. H., Wang, F., Follettie, M. T., Myers, J. S., Fantin, V. R., & Abraham, R. T. (2014) · Nature Communications · doi:10.1038/ncomms5900 · Cited by 86
Liu, Y., & Fan, D. (2018) · Food & Function · doi:10.1039/c8fo01122b · Cited by 86
Abounit, K., Scarabelli, T. M., & McCauley, R. B. (2012) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v3.i1.1 · Cited by 92
Dichloroacetate induces autophagy in colorectal cancer cells and tumours
Lin, G., Hill, D. K., Andrejeva, G., Boult, J. K. R., Troy, H., Fong, A.-C. L. F. W. T., Orton, M. R., Panek, R., Parkes, H. G., Jafar, M. M., et al. (2014) · British Journal of Cancer · doi:10.1038/bjc.2014.281 · Cited by 84
Autophagic activity in neuronal cell death
Button, R. W., Luo, S., & Rubinsztein, D. C. (2015) · Neuroscience Bulletin · doi:10.1007/s12264-015-1528-y · Cited by 88
Autophagy in Pulmonary Diseases
Nakahira, K., Pabon Porras, M. A., & Choi, A. M. K. (2016) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201512-2468so · Cited by 78
Li, C., Zhang, K., Pan, G., Ji, H., Li, C., Wang, X., Hu, X., Liu, R., Deng, L., Wáng, Y., et al. (2021) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-021-01915-9 · Cited by 84
Role of autophagy in intervertebral disc degeneration
Kritschil, R., Scott, M. J., Sowa, G., & Vo, N. N. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30631 · Cited by 85
Teng, R., Du, J., Welak, S. R., Guan, T., Eis, A., Shi, Y., & Konduri, G. G. (2012) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00177.2011 · Cited by 85
Mitochondrial function in vascular endothelial cell in diabetes
Pangare, M., & Makino, A. (2012) · Journal of Smooth Muscle Research · doi:10.1540/jsmr.48.1 · Cited by 87
Targeting Mitochondrial Metabolism by Inhibiting Autophagy in BRAF-Driven Cancers
Strohecker, A. M., & White, E. (2014) · Cancer Discovery · doi:10.1158/2159-8290.cd-14-0196 · Cited by 83
Self-citationInteraction of caveolin-1 with ATG12-ATG5 system suppresses autophagy in lung epithelial cells
Chen, Z., Cao, J., Zhou, J.-S., Liu, H., Che, L., Mizumura, K., Li, W., Choi, A. M. K., & Shen, H. (2014) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00268.2013 · Cited by 86
Autophagy is required for PDAC glutamine metabolism
Seo, J., Choi, J., Lee, S., Sung, S., Yoo, H. J., Kang, M., Cheong, H., & Son, J. (2016) · Scientific Reports · doi:10.1038/srep37594 · Cited by 86
Pioglitazone Enhances Cytosolic Lipolysis, β-oxidation and Autophagy to Ameliorate Hepatic Steatosis
Hsiao, P., Chiou, H.-Y. C., Jiang, H., Lee, M., Hsieh, T., & Kuo, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-09702-3 · Cited by 84
Mechanisms of redox metabolism and cancer cell survival during extracellular matrix detachment
Hawk, M. A., & Schafer, Z. T. (2018) · Journal of Biological Chemistry · doi:10.1074/jbc.tm117.000260 · Cited by 82
Arabidopsis SINAT Proteins Control Autophagy by Mediating Ubiquitylation and Degradation of ATG13
Qi, H., Li, J., Xia, F., Chen, J., Xue, L., Han, M.-Q., Xie, L., Zhou, Q., & Xiao, S. (2019) · The Plant Cell · doi:10.1105/tpc.19.00413 · Cited by 83
Characteristics and requirements of basal autophagy in HEK 293 cells
Musiwaro, P., Smith, M. D., Manifava, M., Walker, S. A., & Ktistakis, N. T. (2013) · Autophagy · doi:10.4161/auto.25455 · Cited by 87
Moulder, D. E., Hatoum, D., Tay, E. S. E., Lin, Y., & McGowan, E. M. (2018) · Cancers · doi:10.3390/cancers10060189 · Cited by 87
Rojas, A., Añazco, C., González, I., & Araya, P. (2018) · Carcinogenesis · doi:10.1093/carcin/bgy012 · Cited by 82
Effects of modified LDL and HDL on retinal pigment epithelial cells: a role in diabetic retinopathy?
Du, M., Wu, M., Fu, D., Yang, S., Chen, J., Wilson, K., & Lyons, T. J. (2013) · Diabetologia · doi:10.1007/s00125-013-2986-x · Cited by 82
Huang, H., Zhu, J., Li, Y., Zhang, L., Gu, J., Xie, Q., Jin, H., Che, X., Li, J., Huang, C., et al. (2016) · Autophagy · doi:10.1080/15548627.2016.1196313 · Cited by 82
Is autophagy associated with diabetes mellitus and its complications? A review
Bhattacharya, D., Mukhopadhyay, M., Bhattacharyya, M., & Karmakar, P. (2018) · EXCLI journal · doi:10.17179/excli2018-1353 · Cited by 82
Dai, Z., Cheng, J. R., Bao, L., Zhu, X., Li, H., Cheng, X. J., Zhang, Y., Zhang, J., Chu, W., Pan, Y., et al. (2020) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2020.111051 · Cited by 82
The Role of Chaperone-Mediated Autophagy in Cell Cycle Control and Its Implications in Cancer
Andrade-Tomaz, M., de Souza, I., Rocha, C. R. R., & Gomes, L. R. (2020) · Cells · doi:10.3390/cells9092140 · Cited by 84
Class III PI3K Vps34: essential roles in autophagy, endocytosis, and heart and liver function
Jaber, N. L., & Zong, W. (2013) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12026 · Cited by 82
Chung, K. W., Kim, K. M., Choi, Y. J., An, H. J., Lee, B., Kim, D. H., Lee, E. K., Im, E., Lee, J., Im, D., et al. (2017) · Autophagy · doi:10.1080/15548627.2017.1319040 · Cited by 82
Thorburn, A. M. (2017) · Journal of Biological Chemistry · doi:10.1074/jbc.r117.810739 · Cited by 80
Varışlı, L., Çen, O., & Vlahopoulos, S. (2019) · Immunology · doi:10.1111/imm.13160 · Cited by 81
Tan, Y., Yin, L., Sun, Z., Shao, S., Chen, W., Man, X., Du, Y., & Chen, Y. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.02.282 · Cited by 81
Wang, N., Liu, H., Liu, G., Li, M., He, X., Yin, C., Tu, Q., Shen, X., Bai, W., Wang, Q., et al. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101495 · Cited by 81
RIPK1 regulates survival of human melanoma cells upon endoplasmic reticulum stress through autophagy
Luan, Q., Jin, L., Jiang, C. C., Tay, K. H., Lai, F., Liu, X., Liu, Y. L., Guo, S., Li, C. Y., Yan, X. G., et al. (2015) · Autophagy · doi:10.1080/15548627.2015.1049800 · Cited by 81
Hsieh, P. N., Zhou, G., Yuan, Y., Zhang, R., Prosdocimo, D. A., Sangwung, P., Borton, A. H., Boriushkin, E., Hamik, A., Fujioka, H., et al. (2017) · Nature Communications · doi:10.1038/s41467-017-00899-5 · Cited by 78
Autophagy is a major metabolic regulator involved in cancer therapy resistance
Poillet-Perez, L., Sarry, J., & Joffre, C. (2021) · Cell Reports · doi:10.1016/j.celrep.2021.109528 · Cited by 85
Zhou, S.-F., Ding, Y.-H., Zhou, Z.-W., Ha, C., Zhang, X.-Y., Pan, S.-T., He, Z.-X., Edelman, J. L., Wang, D., Yang, Y.-X., et al. (2015) · Drug Design Development and Therapy · doi:10.2147/dddt.s74062 · Cited by 80
RetractedThe Evolving, Multifaceted Roles of Autophagy in Cancer
Liu, J., & Debnath, J. (2016) · Advances in cancer research · doi:10.1016/bs.acr.2016.01.005 · Cited by 82
Autophagy role(s) in response to oncogenes and DNA replication stress
Vanzo, R., Bartkova, J., Merchut-Maya, J. M., Hall, A., Bouchal, J., Dyrskjøt, L., Frankel, L. B., Gorgoulis, V., Maya-Mendoza, A., Jäättelä, M., et al. (2020) · Cell Death & Differentiation · doi:10.1038/s41418-019-0403-9 · Cited by 79
Zhu, T., Yao, Q. Z., Wang, W., Yao, H., & Chao, J. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000443098 · Cited by 79
Autophagy modulation: a potential therapeutic approach in cardiac hypertrophy
Wang, X., & Cui, T. (2017) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00145.2017 · Cited by 79
Role of Autophagy in Lung Inflammation
Painter, J. D., Galle-Treger, L., & Akbari, O. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01337 · Cited by 79
Ashrafizadeh, M., Zhang, W., Zou, R., Sethi, G., Klionsky, D. J., & Zhang, X. (2023) · Pharmacological Research · doi:10.1016/j.phrs.2023.106822 · Cited by 79
Chen, Z., Teo, A. E., & McCarty, N. (2015) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-15-0987 · Cited by 81
Oestrogen Inhibits Arterial Calcification by Promoting Autophagy
Peng, Y., Xiong, D., Lin, X., Cui, R., Xu, F., Zhong, J., Zhu, T., Wu, F., Mao, M., Liao, X., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03801-x · Cited by 79
Autophagy Paradox of Cancer: Role, Regulation, and Duality
Verma, A. K., Bharti, P. S., Rafat, S., Bhatt, D., Goyal, Y., Pandey, K. K., Ranjan, S. K., Almatroodi, S. A., Alsahli, M. A., Rahmani, A. H., et al. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/8832541 · Cited by 78
Do cytotoxicity and cell death cause false positive results in the in vitro comet assay?
Azqueta, A., Stopper, H., Zegura, B., Dusinska, M., & Møller, P. (2022) · Mutation Research/Genetic Toxicology and Environmental Mutagenesis · doi:10.1016/j.mrgentox.2022.503520 · Cited by 80
CD47 Receptor Globally Regulates Metabolic Pathways That Control Resistance to Ionizing Radiation
Miller, T. W., Soto‐Pantoja, D. R., Schwartz, A. L., Sipes, J. M., DeGraff, W., Ridnour, L. A., Wink, D. A., & Roberts, D. D. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.665752 · Cited by 77
Matrix Rigidity Regulates Cancer Cell Growth by Modulating Cellular Metabolism and Protein Synthesis
Tilghman, R., Blais, E., Cowan, C., Sherman, N., Grigera, P., Jeffery, E. D., Fox, J., Blackman, B., Tschumperlin, D., Papin, J., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0037231 · Cited by 72
Autophagy in the cancer-immunity dialogue
Yamazaki, T., Pedro, J. M. B., Galluzzi, L., Kroemer, G., & Pietrocola, F. (2020) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2020.12.003 · Cited by 80
Mitochondrial-derived compartments facilitate cellular adaptation to amino acid stress
Schuler, M.-H., English, A. M., Xiao, T., Campbell, T. J., Shaw, J. M., & Hughes, A. L. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.08.021 · Cited by 77
Deja, S., Fletcher, J. A., Kim, C.-W., Kucejová, B., Fu, X., MIZERSKA, M. N., Villegas, M., Pudełko‐Malik, N., Browder, N., Iñigo, M. R., et al. (2024) · Cell Metabolism · doi:10.1016/j.cmet.2024.02.004 · Cited by 89
Quiroga, A. D., & Lehner, R. S. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2011.09.007 · Cited by 82
ROS, autophagy, mitochondria and cancer: Ras, the hidden master?
Bellot, G. L., Liu, D., & Pervaiz, S. (2012) · Mitochondrion · doi:10.1016/j.mito.2012.06.007 · Cited by 78
Targeting PDK1 with dichloroacetophenone to inhibit acute myeloid leukemia (AML) cell growth
Qin, L., Tian, Y., Yu, Z., Shi, D., Wang, J., Zhang, C., Peng, R., Chen, X., Liu, C., Chen, Y., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6366 · Cited by 80
Protein Quality Control in Neurodegenerative Disease
Gestwicki, J. E., & Garza, D. (2012) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-385883-2.00003-5 · Cited by 80
Liver Autophagy in Anorexia Nervosa and Acute Liver Injury
Kheloufi, M., Boulanger, C. M., Durand, F., & Rautou, P. (2014) · BioMed Research International · doi:10.1155/2014/701064 · Cited by 81
Chen, G., Zhang, W., Li, Y., Ren, J., Xu, N., Liu, H., Wang, F., Sun, Z., Jia, J., & Zhao, Y. (2013) · Cardiovascular Research · doi:10.1093/cvr/cvt035 · Cited by 78
Zhang, B., Hou, R., Zou, Z., Luo, T., Zhang, Y., Wang, L., & Wang, B. (2017) · Redox Biology · doi:10.1016/j.redox.2017.10.021 · Cited by 76
Mutant p53 as a Regulator and Target of Autophagy
Shi, Y., Norberg, E., & Vakifahmetoglu-Norberg, H. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2020.607149 · Cited by 77
Li, Z., Miao, Z., Ding, L., Teng, X., & Bao, J. (2021) · Ecotoxicology and Environmental Safety · doi:10.1016/j.ecoenv.2021.112219 · Cited by 76
YY1-MIR372-SQSTM1 regulatory axis in autophagy
Feng, L., Ma, Y., Sun, J., Shen, Q., Liu, L., Lu, H., Wang, F., Yue, Y., Li, J., Zhang, S., et al. (2014) · Autophagy · doi:10.4161/auto.29486 · Cited by 78
Xi, H., Barredo, J. C., Merchan, J. R., & Lampidis, T. J. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.02.037 · Cited by 78
The Multifaceted Roles of Autophagy in Tumors—Implications for Breast Cancer
Debnath, J. (2011) · Journal of Mammary Gland Biology and Neoplasia · doi:10.1007/s10911-011-9223-3 · Cited by 78
Cyclin A2: At the crossroads of cell cycle and cell invasion
Loukil, A. (2015) · World Journal of Biological Chemistry · doi:10.4331/wjbc.v6.i4.346 · Cited by 75
Zhou, S., Niu, N., Wang, Z.-L., Pan, S., Ding, H.-Q., Au, G. H. T., He, Z., Zhou, Z.-W., Xiao, G., Yang, Y., et al. (2015) · Drug Design Development and Therapy · doi:10.2147/dddt.s74197 · Cited by 73
Functions and Implications of Autophagy in Colon Cancer
Devenport, S. N., & Shah, Y. M. (2019) · Cells · doi:10.3390/cells8111349 · Cited by 76
Expanding Role of Ubiquitin in Translational Control
Dougherty, S. E., Maduka, A. O., Inada, T., & Silva, G. M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21031151 · Cited by 76
Raulien, N., Friedrich, K., Strobel, S., Rubner, S., Baumann, S., von Bergen�, M., Körner, A., Krueger, M. C., Rossol, M., & Wagner, U. G. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00609 · Cited by 76
The effects of combined selenium nanoparticles and radiation therapy on breast cancer cells in vitro
Chen, F., Zhang, X. H., Hu, X. D., Liu, P. D., & Zhang, H. Q. (2017) · Artificial Cells Nanomedicine and Biotechnology · doi:10.1080/21691401.2017.1347941 · Cited by 75
Cui, Y., Yang, M., Wang, Y., Ren, J., Lin, P., Cui, C., Song, J., He, Q., Hu, H., Wang, K., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202002247rr · Cited by 73
Yu, Y., Liu, B., Li, X., Lu, D., Yang, L., Chen, L., Li, Y., Cheng, L., Lv, F., Zhang, P., et al. (2022) · Cell Death and Disease · doi:10.1038/s41419-021-04494-x · Cited by 73
FTO levels affect RNA modification and the transcriptome
Berulava, T., Ziehe, M., Klein‐Hitpaß, L., Mladenov, E., Thomale, J., Rüther, U., & Horsthemke, B. (2012) · European Journal of Human Genetics · doi:10.1038/ejhg.2012.168 · Cited by 76
Bacterial autophagy: restriction or promotion of bacterial replication?
Mostowy, S., & Cossart, P. (2012) · Trends in Cell Biology · doi:10.1016/j.tcb.2012.03.006 · Cited by 73
Hou, X., Yang, C., Zhang, L., Hu, T., Sun, D., Cao, H., Yang, F., Guo, G. F., Gong, C., Zhang, X., et al. (2017) · Biomaterials · doi:10.1016/j.biomaterials.2016.12.032 · Cited by 75
Autophagy, Oxidative Stress and Cancer Development
Taucher, E., Mykoliuk, I., Fediuk, M., & Smolle‐Jüttner, F. (2022) · Cancers · doi:10.3390/cancers14071637 · Cited by 75
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