Mitophagy: mechanisms, pathophysiological roles, and analysis

Autophagy: Renovation of Cells and Tissues

Mizushima, N., & Komatsu, M. (2011) · Cell · doi:10.1016/j.cell.2011.10.026 · Cited by 6,615

A role for mitochondria in nlrp3 inflammasome activation

Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602

Autophagy: process and functionPreprint

Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104

Resveratrol Improves Mitochondrial Function and Protects against Metabolic Disease by Activating SIRT1 and PGC-1α

Lagouge, M., Argmann, C., Gerhart-Hines, Z., Meziane, H., Lerin, C., Daussin, F., Messadeq, N., Milne, J., Lambert, P., Elliott, P., et al. (2006) · Cell · doi:10.1016/j.cell.2006.11.013 · Cited by 4,057

Parkin 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

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

Fission and selective fusion govern mitochondrial segregation and elimination by autophagy

Twig, G., Elorza, A., Molina, A. J. A., Mohamed, H., Wikstrom, J. D., Walzer, G., Stiles, L., Haigh, S. E., Katz, S., Las, G., et al. (2008) · The EMBO Journal · doi:10.1038/sj.emboj.7601963 · Cited by 3,082

Autophagy proteins regulate innate immune responses by inhibiting the release of mitochondrial DNA mediated by the NALP3 inflammasome

Nakahira, K., Haspel, J. A., Rathinam, V. A. K., Lee, S.-J., Dolinay, T., Lam, H. C., Englert, J. A., Rabinovitch, M., Cernadas, M., Kim, H. P., et al. (2011) · Nature Immunology · doi:10.1038/ni.1980 · Cited by 3,049

ERdj8 governs the size of autophagosomes during the formation process

Yamamoto, Y.-H., Kasai, A., Omori, H., Takino, T., Sugihara, M., Umemoto, T., Hamasaki, M., Hatta, T., Natsume, T., Morimoto, R. I., et al. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201903127 · Cited by 34

Mitophagy regulation in aging and neurodegenerative disease

Banarase, T. A., Sammeta, S. S., Wankhede, N. L., Mangrulkar, S. V., Rahangdale, S. R., Aglawe, M. M., Taksande, B. G., Upaganlawar, A. B., Umekar, M. J., & Kale, M. B. (2023) · Biophysical Reviews · doi:10.1007/s12551-023-01057-6 · Cited by 35

Induction of mitophagy by green tea extracts and tea polyphenols: A potential anti-aging mechanism of tea

Auguste, S., Yan, B., & Guo, M. (2023) · Food Bioscience · doi:10.1016/j.fbio.2023.102983 · Cited by 33

Mitochondrial dynamics, quality control, and mtDNA in alcohol-associated liver disease and liver cancer

Ma, X., Niu, M., Ni, H., & Ding, W. (2024) · Hepatology · doi:10.1097/hep.0000000000000910 · Cited by 37

Two-photon fluorescence visualization of lysosomal pH changes during mitophagy and cell apoptosis

Dong, Y., Xiao, H., Xing, L., Wu, C., Zhou, J. P., Zhou, Z., Liu, Y., Zhuo, S., & Li, P. (2019) · Talanta · doi:10.1016/j.talanta.2019.120549 · Cited by 33

Aryl hydrocarbon receptor maintains hepatic mitochondrial homeostasis in mice

Heo, M. J., Suh, J. H., Lee, S. H., Poulsen, K. L., An, Y., Moorthy, B., Hartig, S. M., Moore, D. D., & Kim, K. H. (2023) · Molecular Metabolism · doi:10.1016/j.molmet.2023.101717 · Cited by 32

Essential Protein PHB2 and Its Regulatory Mechanisms in Cancer

Qi, A., Lamont, L., Liu, E., Murray, S., Meng, X., & Yang, S. (2023) · Cells · doi:10.3390/cells12081211 · Cited by 32

Role of Mitochondria–ER Contact Sites in Mitophagy

Rühmkorf, A., & Harbauer, A. B. (2023) · Biomolecules · doi:10.3390/biom13081198 · Cited by 35

Quercetin: A Promising Candidate for the Management of Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD)

Markowska, J., Kasprzak‐Drozd, K., Niziński, P., Dragan, M., Kondracka, A., Gondek, E., Oniszczuk, T., & Oniszczuk, A. (2024) · Molecules · doi:10.3390/molecules29225245 · Cited by 32

Defective autophagy through epg5 mutation results in failure to reduce germ plasm and mitochondria

Herpin, A., Englberger, E., Zehner, M., Wacker, R., Gessler, M., & Schard, M. (2015) · The FASEB Journal · doi:10.1096/fj.14-265462 · Cited by 32

When Would Immunologists Consider a Nanomaterial to be Safe? Recommendations for Planning Studies on Nanosafety

Himly, M., Geppert, M., Hofer, S. E., Hofstätter, N., Horejs‐Hoeck, J., & Duschl, A. (2020) · Small · doi:10.1002/smll.201907483 · Cited by 32

Cystathionine beta synthase regulates mitochondrial dynamics and function in endothelial cells

Rao, G., Murphy, B., Dey, A., Dwivedi, S. K. D., Zhang, Y., Roy, R. V., Chakraborty, P. K., Bhattacharya, R., & Mukherjee, P. (2020) · The FASEB Journal · doi:10.1096/fj.202000173r · Cited by 33

Cerebroventricular Microinjections of MPTP on Adult Zebrafish Induces Dopaminergic Neuronal Death, Mitochondrial Fragmentation, and Sensorimotor Impairments

Kalyn, M., & Ekker, M. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.718244 · Cited by 34

TNF-α Induces Mitophagy in Rheumatoid Arthritis Synovial Fibroblasts, and Mitophagy Inhibition Alleviates Synovitis in Collagen Antibody-Induced Arthritis

Nam, J.-H., Lee, J., Choi, H., Choi, S.-Y., Noh, K.-E., Jung, N.-C., Song, J. Y., Choi, J., Seo, H. G., Jung, Y., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23105650 · Cited by 32

Mitophagy in Ischaemia/Reperfusion Induced Cerebral Injury

Liu, K., Sun, Y., Gu, Z., Shi, N., Zhang, T., & Sun, X. (2013) · Neurochemical Research · doi:10.1007/s11064-013-1033-0 · Cited by 32

Controlling quality and amount of mitochondria by mitophagy: insights into the role of ubiquitination and deubiquitination

Tan, T., Zimmermann, M., & Reichert, A. S. (2016) · Biological Chemistry · doi:10.1515/hsz-2016-0125 · Cited by 33

High-content analysis for mitophagy response to nanoparticles: A potential sensitive biomarker for nanosafety assessment

He, C., Jiang, S., Yao, H., Zhang, L., Yang, C., Jiang, S., Ruan, F., Zhan, D.-L., Liu, G., Lin, Z., et al. (2018) · Nanomedicine Nanotechnology Biology and Medicine · doi:10.1016/j.nano.2018.09.003 · Cited by 32

Autophagy in glioblastoma: A mechanistic perspective

Meena, D., & Jha, S. (2024) · International Journal of Cancer · doi:10.1002/ijc.34991 · Cited by 31

Mitochondrial BMI1 maintains bioenergetic homeostasis in cells

Mustafi, S. B., Aznar, N., Dwivedi, S. K. D., Chakraborty, P. K., Basak, R., Mukherjee, P., Ghosh, P., & Bhattacharya, R. (2016) · The FASEB Journal · doi:10.1096/fj.201600321r · Cited by 32

Essential role for autophagy protein VMP1 in maintaining neuronal homeostasis and preventing axonal degeneration

Wang, P., Chen, X., Wang, Y., Jia, C., Liu, X., Wang, Y., Wu, H., Cai, H., Shen, H., & Le, W. (2021) · Cell Death and Disease · doi:10.1038/s41419-021-03412-5 · Cited by 31

Hidden phenotypes of PINK1/Parkin knockout mice

Paul, S., & Pickrell, A. M. (2021) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2021.129871 · Cited by 31

HIV-associated neurotoxicity and cognitive decline: Therapeutic implications

Wallace, D. R. (2021) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2021.108047 · Cited by 33

Investigating complex I deficiency in P urkinje cells and synapses in patients with mitochondrial disease

Chrysostomou, A., Grady, J. P., Laude, A., Taylor, R. W., Turnbull, D. M., & Lax, N. Z. (2015) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12282 · Cited by 31

Parkin Mediates Mitophagy to Participate in Cardioprotection Induced by Late Exercise Preconditioning but Bnip3 Does Not

Yuan, Y., & Pan, S.-S. (2018) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000000572 · Cited by 30

Potential targets for intervention against doxorubicin-induced cardiotoxicity based on genetic studies: a systematic review of the literature

Chen, Y., Huang, T., Shi, W., Fang, J., Deng, H., & Cui, G. (2019) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2019.11.150 · Cited by 31

Research Progress on the Mechanism of Mitochondrial Autophagy in Cerebral Stroke

Li, L., Yang, S., Lu, X., Zhang, Y., & Li, T. (2021) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2021.698601 · Cited by 31

Dichotomy in hypoxia-induced mitochondrial fission in placental mesenchymal cells during development and preeclampsia: consequences for trophoblast mitochondrial homeostasis

Gillmore, T., Farrell, A., Alahari, S., Sallais, J., Kurt, M., Park, C., Ausman, J., Litvack, M. L., Post, M., & Caniggia, I. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-04641-y · Cited by 31

Complex Interplay between Autophagy and Oxidative Stress in the Development of Endometriosis

D’Amico, R., Impellizzeri, D., Cordaro, M., Siracusa, R., Interdonato, L., Marino, Y., Crupi, R., Gugliandolo, E., Macrı̀, F., Paola, D. D., et al. (2022) · Antioxidants · doi:10.3390/antiox11122484 · Cited by 30

Mapping Topoisomerase Sites in Mitochondrial DNA with a Poisonous Mitochondrial Topoisomerase I (Top1mt)

Rosa, I. D., Huang, S.-Y. N., Agama, K., Khiati, S., Zhang, H., & Pommier, Y. G. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.555367 · Cited by 30

Defective Expression of the Mitochondrial-tRNA Modifying Enzyme GTPBP3 Triggers AMPK-Mediated Adaptive Responses Involving Complex I Assembly Factors, Uncoupling Protein 2, and the Mitochondrial Pyruvate Carrier

Martínez-Zamora, A., Meseguer, S., Esteve, J. M., Villarroya, M., Aguado, C., Enrı́quez, J. A., Knecht, E., & Armengod, M. ‐. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144273 · Cited by 31

Oxidative Stress Resistance in Metastatic Prostate Cancer: Renewal by Self-Eating

Balvan, J., Gumulec, J., Raudenská, M., Křížová, A., Štěpka, P., Babula, P., Kizek, R., Adam, V., & Masařík, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0145016 · Cited by 30

Apoptosis, Autophagy, and Pyroptosis: Immune Escape Strategies for Persistent Infection and Pathogenesis of Classical Swine Fever Virus

Ma, S., Mao, Q., Yi, L., Zhao, M., & Chen, J. (2019) · Pathogens · doi:10.3390/pathogens8040239 · Cited by 30

Temperature- and chemical-induced neurotoxicity in zebrafish

Toni, M., Arena, C., Cioni, C., & Tedeschi, G. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1276941 · Cited by 29

Relationship between serum β-hydroxybutyrate and hepatic fatty acid oxidation in individuals with obesity and NAFLD

Moore, M. P., Shryack, G. E., Alessi, I. G., Wieschhaus, N., Meers, G. M.-E., Johnson, S. A., Wheeler, A. A., Ibdah, J. A., Parks, E. J., & Rector, R. S. (2024) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00336.2023 · Cited by 29

Metabolic Syndrome Modulates Protein Import into the Mitochondria of Porcine Mesenchymal Stem Cells

Nargesi, A. A., Zhu, X.-Y., Hickson, L. J., Conley, S. M., van Wijnen, A. J., Lerman, L. O., & Eirin, A. (2018) · Stem Cell Reviews and Reports · doi:10.1007/s12015-018-9855-4 · Cited by 29

A fluorescence imaging based-assay to monitor mitophagy in cultured hepatocytes and mouse liver

Ma, X., & Ding, W. (2021) · Liver Research · doi:10.1016/j.livres.2020.12.002 · Cited by 29

Mitochondrial dysfunction and mitochondrion-targeted therapeutics in liver diseases

Xiang, L., Shao, Y., & Chen, Y. (2021) · Journal of drug targeting · doi:10.1080/1061186x.2021.1909051 · Cited by 29

ACEA Attenuates Oxidative Stress by Promoting Mitophagy via CB1R/Nrf1/PINK1 Pathway after Subarachnoid Hemorrhage in Rats

Liu, B., Tian, Y., Li, Y., Wu, P., Zhang, Y., Zheng, J., & Shi, H. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/1024279 · Cited by 29

Alternative macroautophagy and mitophagy

Shimizu, S., Honda, S., Arakawa, S., & Yamaguchi, H. (2014) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2014.02.016 · Cited by 29

Possible Antioxidant Mechanism of Melanoidins Extract from Shanxi Aged Vinegar in Mitophagy-Dependent and Mitophagy-Independent Pathways

Yang, L. X., Wang, X., & Yang, X. (2014) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf501690e · Cited by 29

Phylogenetic and Molecular Evolutionary Analysis of Mitophagy Receptors under Hypoxic Conditions

Wu, X., Wu, F.-H., Wu, Q.-R., Zhang, S., Chen, S., & Sima, M. W. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00539 · Cited by 30

PINK1/Parkin-Mediated Mitophagy Promotes Resistance to Sonodynamic Therapy

Song, L., Huang, Y., Hou, X., Yang, Y., Kala, S., Qiu, Z., Zhang, R., & Sun, L. (2018) · Cellular Physiology and Biochemistry · doi:10.1159/000493629 · Cited by 29

Augmenter of Liver Regeneration Protects against Ethanol-Induced Acute Liver Injury by Promoting Autophagy

Liu, L., Xie, P., Li, W., Wu, Y., & An, W. (2018) · American Journal Of Pathology · doi:10.1016/j.ajpath.2018.11.006 · Cited by 29

TRIM28 promotes porcine epidemic diarrhea virus replication by mitophagy-mediated inhibition of the JAK-STAT1 pathway

Li, X., Yan, Z., Ma, J., Li, G., Liu, X., Peng, Z., Zhang, Y., Huang, S., Luo, J., & Guo, X. (2023) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2023.127722 · Cited by 28

Dysregulation of autophagy during photoaging reduce oxidative stress and inflammatory damage caused by UV

Zhang, Z., Tan, R., Xiong, Z., Feng, Y., & Chen, L. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1562845 · Cited by 31

Immunomodulatory Properties of Adipose-Derived Stem Cells Treated with 5-Azacytydine and Resveratrol on Peripheral Blood Mononuclear Cells and Macrophages in Metabolic Syndrome Animals

Kornicka, K., Śmieszek, A., Węgrzyn, A., Röcken, M., & Marycz, K. (2018) · Journal of Clinical Medicine · doi:10.3390/jcm7110383 · Cited by 28

Autophagic dysfunction of β cell dysfunction in type 2 diabetes, a double-edged sword

Ding, Y., GangYi, Y., & Qi-nan, W. (2020) · Genes & Diseases · doi:10.1016/j.gendis.2020.03.003 · Cited by 29

The Secrets of Alternative Autophagy

Urbańska, K., & Orzechowski, A. (2021) · Cells · doi:10.3390/cells10113241 · Cited by 30

Fighting metallodrug resistance through alteration of drug metabolism and blockage of autophagic flux by mitochondria-targeting AIEgens

Su, Y., Lin, H. L., Tu, Y., Wang, M., Zhang, G., Yang, J., Liu, H., & Su, Z. (2022) · Chemical Science · doi:10.1039/d1sc06722b · Cited by 28

ROCK2 inhibition: A futuristic approach for the management of Alzheimer’s disease

Mani, S., Jindal, D., Chopra, H., Jha, S. K., Singh, S. K., Ashraf, G. M., Kamal, M., Iqbal, D., Chellappan, D. K., Dey, A., et al. (2022) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2022.104871 · Cited by 29

Effects of hyperbaric oxygen therapy on neuropathic pain via mitophagy in microglia

Han, G., Liu, K., Li, L., Li, X., & Zhao, P. (2017) · Molecular Pain · doi:10.1177/1744806917710862 · Cited by 28

Autophagy in macrophages regulates the inflammasome and protects against liver injury

Ding, W., & Jaeschke, H. (2015) · Journal of Hepatology · doi:10.1016/j.jhep.2015.10.003 · Cited by 28

Energy Metabolism and Metabolic Sensors in Stem Cells: The Metabostem Crossroads of Aging and Cancer

Menéndez, J. A., & Joven, J. (2014) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-07320-0_10 · Cited by 27

H2O2 Signaling‐Triggered PI3K Mediates Mitochondrial Protection to Participate in Early Cardioprotection by Exercise Preconditioning

Yuan, Y., Pan, S.-S., Wan, D.-F., Lu, J., & Huang, Y. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1916841 · Cited by 27

Extracellular Vesicles, Apoptotic Bodies and Mitochondria: Stem Cell Bioproducts for Organ Regeneration

Gebara, N., Rossi, A., Škovroňová, R., Aziz, J. M., Asthana, A., & Bussolati, B. (2020) · Current Transplantation Reports · doi:10.1007/s40472-020-00282-2 · Cited by 27

Inner mitochondrial membrane protein Prohibitin 1 mediates Nix-induced, Parkin-independent mitophagy

Alula, K. M., Delgado‐Deida, Y., Callahan, R. C., Till, A., Underwood, L., Thompson, W. E., Souza, R. F., Dassopoulos, T., Onyiah, J. C., Venuprasad, K., et al. (2023) · Scientific Reports · doi:10.1038/s41598-022-26775-x · Cited by 28

African swine fever virus protein p17 promotes mitophagy by facilitating the interaction of SQSTM1 with TOMM70

Hu, B., Zhong, G., Ding, S., Xu, K., Peng, X., Dong, W.-R., & Zhou, J. (2023) · Virulence · doi:10.1080/21505594.2023.2232707 · Cited by 29

Changes to mitochondrial ultrastructure in optic nerve vulnerable to secondary degeneration in vivo are limited by irradiation at 670 nm

Cummins, N., Bartlett, C. A., Archer, M. A., Bartlett, E., Hemmi, J. M., Harvey, A. R., Dunlop, S. A., & Fitzgerald, M. (2013) · BMC Neuroscience · doi:10.1186/1471-2202-14-98 · Cited by 27

Mesenchymal stem cells desensitize castration-resistant prostate cancer to docetaxel chemotherapy via inducing TGF-β1-mediated cell autophagy

Yu, Y., Yang, F., Zhang, W., Guo, Y., Lin, Y., & Yao, X. (2021) · Cell & Bioscience · doi:10.1186/s13578-020-00494-0 · Cited by 27

Cell death in the pathogenesis and progression of heart failure

Marı́n-Garcı́a, J. (2016) · Heart Failure Reviews · doi:10.1007/s10741-016-9538-7 · Cited by 29

The impact of HBx protein on mitochondrial dynamics and associated signaling pathways strongly depends on the hepatitis B virus genotype

Schollmeier, A., Basic, M., Glitscher, M., & Hildt, E. (2024) · Journal of Virology · doi:10.1128/jvi.00424-24 · Cited by 26

Mitochondrial Acetylation and Genetic Models of Parkinson's Disease

Auburger, G. W. J., Gispert, S., & Jendrach, M. (2014) · Progress in molecular biology and translational science · doi:10.1016/b978-0-12-394625-6.00006-4 · Cited by 27

The Role of Autophagy and lncRNAs in the Maintenance of Cancer Stem Cells

Jahangiri, L., Ishola, T., Pucci, P., Trigg, R. M., Pereira, J. D., Williams, J. A., Cavanagh, M. L., Gkoutos, G. V., Tsaprouni, L., & Turner, S. D. (2021) · Cancers · doi:10.3390/cancers13061239 · Cited by 26

Supplementation of mitochondria from endometrial mesenchymal stem cells improves oocyte quality in aged mice

Zhang, Q., Hao, J., Liu, B., Ouyang, Y., Guo, J., Dong, M., Wang, Z., Gao, F., & Yao, Y. (2022) · Cell Proliferation · doi:10.1111/cpr.13372 · Cited by 27

Mitophagy and Traumatic Brain Injury: Regulatory Mechanisms and Therapeutic Potentials

Luan, Y., Jiang, L., Luan, Y., Xie, Y., Yang, Y., & Ren, K. (2023) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2023/1649842 · Cited by 28

Mitochondria–Melanocyte cellular interactions: An emerging mechanism of vitiligo pathogenesis

Kaushik, H., Kumar, V., & Parsad, D. (2023) · Journal of the European Academy of Dermatology and Venereology · doi:10.1111/jdv.19019 · Cited by 26

Adverse effects of anti-tuberculosis drugs on HepG2 cell bioenergetics

Elmorsy, E. M., Attalla, S. M., Fikry, E., Kocoń, A., Turner, R., Christie, D., Warren, A. Y., Nwidu, L. L., & Carter, W. G. (2016) · Human & Experimental Toxicology · doi:10.1177/0960327116660751 · Cited by 26

Mechanistic Insights into Recognitions of Ubiquitin and Myosin VI by Autophagy Receptor TAX1BP1

Hu, S., Wang, Y., Gong, Y., Liu, J., Li, Y., & Pan, L. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.06.030 · Cited by 27

The NRF2 activator RTA-408 ameliorates chronic alcohol exposure-induced cognitive impairment and NLRP3 inflammasome activation by modulating impaired mitophagy initiation

Lin, X., Wang, H., Zou, L., Yang, B., Chen, W., Rong, X., Zhang, X., He, L., Li, X., & Peng, Y. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.04.236 · Cited by 26

From cells to power cells: harnessing bacterial electron transport for microbial fuel cells (MFCs)

Garimella, S. S. S., Rachakonda, S. V., Pratapa, S. S., Mannem, G. D., & Mahidhara, G. (2024) · Annals of Microbiology · doi:10.1186/s13213-024-01761-y · Cited by 27

Parkin ubiquitinates mTOR to regulate mTORC1 activity under mitochondrial stress

Park, D., Lee, M. N., Jeong, H., Koh, A., Yang, Y. R., Suh, P.-G., & Ryu, S. H. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.06.010 · Cited by 25

Further the liquid biopsy: Gathering pieces of the puzzle of genometastasis theory

García‐Casas, A., Garcı́a-Olmo, D. C., & García‐Olmo, D. (2017) · World Journal of Clinical Oncology · doi:10.5306/wjco.v8.i5.378 · Cited by 25

Magnetic Nanoparticles in Human Cervical Skin

Murros, K. E., Wasiljeff, J., Macías‐Sánchez, E., Faivre, D., Soinne, L., Valtonen, J., Pohja, M., Saari, P., PESONEN, L. J., & Salminen, J. (2019) · Frontiers in Medicine · doi:10.3389/fmed.2019.00123 · Cited by 25

Transcription factor MoMsn2 targets the putative 3‐methylglutaconyl‐CoA hydratase‐encoding gene MoAUH1 to govern infectious growth via mitochondrial fusion/fission balance in Magnaporthe oryzae

Xiao, Y., Liu, L., Zhang, T., Zhou, R., Ren, Y., Li, X., Shu, H., Ye, W., Zheng, X., Zhang, Z., et al. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.15088 · Cited by 25

EBF1 promotes triple-negative breast cancer progression by surveillance of the HIF1α pathway

Qiu, Z., Guo, W., Dong, B., Wang, Y., Deng, P., Wang, C., Liu, J., Zhang, Q. H., Grosschedl, R., Yu, Z., et al. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2119518119 · Cited by 25

The progress and prospect of natural components in rhubarb (Rheum ribes L.) in the treatment of renal fibrosis

Wang, Y., Yu, F., Li, A., He, Z., Qu, C., He, C., Ma, X., & Zhan, H. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.919967 · Cited by 26

GPD1L inhibits renal cell carcinoma progression by regulating PINK1/Parkin‐mediated mitophagy

Liu, T., Zhu, H., Ge, M., Pan, Z., Zeng, Y., Leng, Y., Yang, K., & Fan, C. (2023) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17813 · Cited by 25

IL-4 Protects the Mitochondria Against TNFα and IFNγ Induced Insult During Clearance of Infection with Citrobacter rodentium and Escherichia coli

Maiti, A. K., Sharba, S., Navabi, N., Forsman, H., Fernandez, H. R., & Lindén, S. K. (2015) · Scientific Reports · doi:10.1038/srep15434 · Cited by 25

Energy Shortage in Human and Mouse Models of SLC4A11 -Associated Corneal Endothelial Dystrophies

Zhang, W., Frausto, R. F., Chung, D. D., Griffis, K. G., Kao, L., Chen, A. C., Azimov, R., Sampath, A. P., Kurtz, I., & Aldave, A. J. (2020) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.61.8.39 · Cited by 25

Increased mitochondrial turnover in the skeletal muscle of fasted, castrated mice is related to the magnitude of autophagy activation and muscle atrophy

Rossetti, M. L., Steiner, J. L., & Gordon, B. S. (2018) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2018.01.017 · Cited by 24

FUN14 Domain Containing 1 (FUNDC1): A Promising Mitophagy Receptor Regulating Mitochondrial Homeostasis in Cardiovascular Diseases

Mao, Y., Ren, J. T., & Yang, L. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.887045 · Cited by 25

Structural and functional alterations of cellular components as revealed by electron microscopy

Condello, M., Caraglia, M., Castellano, M., Arancia, G., & Meschini, S. (2013) · Microscopy Research and Technique · doi:10.1002/jemt.22266 · Cited by 24

The Apoptotic Effect of HIF-1α Inhibition Combined with Glucose plus Insulin Treatment on Gastric Cancer under Hypoxic Conditions

Tanaka, T., Kitajima, Y., MIYAKE, S., Yanagihara, K., Hara, H., Nishijima‐Matsunobu, A., Baba, K., Shida, M., Wakiyama, K., Nakamura, J., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0137257 · Cited by 25

Metabolic, autophagic, and mitophagic activities in cancer initiation and progression

Hjelmeland, A. B., & Zhang, J. (2016) · Biomedical Journal · doi:10.1016/j.bj.2015.10.002 · Cited by 24

Oxidative Stress and Cell Death in Cardiovascular Disease

Marı́n-Garcı́a, J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-404599-6.00014-7 · Cited by 26

Mitochondrial protein E2F3d, a distinctive E2F3 product, mediates hypoxia-induced mitophagy in cancer cells

Araki, K., Kawauchi, K., Sugimoto, W., Tsuda, D., Oda, H., Yoshida, R., & Ohtani, K. (2018) · Communications Biology · doi:10.1038/s42003-018-0246-9 · Cited by 28

The roles of resveratrol on cardiac mitochondrial function in cardiac diseases

Arinno, A., Apaijai, N., Chattipakorn, S. C., & Chattipakorn, N. (2020) · European Journal of Nutrition · doi:10.1007/s00394-020-02256-7 · Cited by 24

Mitochondrial ferritin affects mitochondria by stabilizing HIF-1α in retinal pigment epithelium: implications for the pathophysiology of age-related macular degeneration

Wang, X., Yang, H., Yanagisawa, D., Bellier, J., Morino, K., Zhao, S., Liu, P., Vigers, P. N., & Tooyama, I. (2016) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2016.07.025 · Cited by 24

Mitochondria at the Crossroads of Physiology and Pathology

Moro, L. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9061971 · Cited by 25

The Progress of Mitophagy and Related Pathogenic Mechanisms of the Neurodegenerative Diseases and Tumor

Song, Y., Ding, W., Xiao, Y. C., & Lu, K.-J. (2015) · Neuroscience Journal · doi:10.1155/2015/543758 · Cited by 23

CaMKIV regulates mitochondrial dynamics during sepsis

Zhang, X., Griepentrog, J. E., Zou, B., Xu, L., Cyr, A. R., Chambers, L., Zuckerbraun, B. S., Shiva, S., & Rosengart, M. R. (2020) · Cell Calcium · doi:10.1016/j.ceca.2020.102286 · Cited by 23

Lysosomal dysfunction impairs mitochondrial quality control and is associated with neurodegeneration in TBCK encephaloneuronopathy

Tintos-Hernández, J. A., Santana, A., Keller, K. N., & Ortiz-Gonzalez, X. R. (2021) · Brain Communications · doi:10.1093/braincomms/fcab215 · Cited by 23

Extra-nuclear histones: origin, significance and perspectives

Singh, A., Verma, S., Modak, S. B., Chaturvedi, M. M., & Purohit, J. S. (2021) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-021-04300-4 · Cited by 23

Polyamines and Physical Activity in Musculoskeletal Diseases: A Potential Therapeutic Challenge

Galasso, L., Cappella, A., Mulè, A., Castelli, L., Ciorciari, A. M., Stacchiotti, A., & Montaruli, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24129798 · Cited by 25

Adipose tissue autophagy and homeostasis in alcohol-induced liver injury

Li, Y., & Ding, W. (2017) · Liver Research · doi:10.1016/j.livres.2017.03.004 · Cited by 23

Acute increases in O-GlcNAc indirectly impair mitochondrial bioenergetics through dysregulation of LonP1-mediated mitochondrial protein complex turnover

Wright, J. N., Benavides, G. A., Johnson, M. S., Wani, W. Y., Ouyang, X., Zou, L., Collins, H. E., Zhang, J., Darley-Usmar, V. M., & Chatham, J. C. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00491.2018 · Cited by 23

Ginsenoside Rg3 protects heart against isoproterenol-induced myocardial infarction by activating AMPK mediated autophagy

Sun, G., Meng, F., Cai, H., Diao, X.-B., Zhang, B., & Xiu-ping, B. (2020) · Cardiovascular Diagnosis and Therapy · doi:10.21037/cdt.2020.01.02 · Cited by 23

Inositol hexakisphosphate kinase-2 non-catalytically regulates mitophagy by attenuating PINK1 signaling

Nagpal, L., Kornberg, M. D., & Snyder, S. H. (2022) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2121946119 · Cited by 22

Increased Systemic Antioxidant Power Ameliorates the Aging-Related Reduction in Oocyte Competence in Mice

Lane, S. L., Parks, J. C., Russ, J. E., Khan, S. A., Schoolcraft, W. B., Yuan, Y., & Katz‐Jaffe, M. G. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222313019 · Cited by 22

Mitophagy: A Complex Mechanism of Mitochondrial Removal

Novak, I. (2011) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4407 · Cited by 213

Induction and Detection of Mitophagy

Yapryntseva, M. A., Zhivotovsky, B., & Gogvadze, V. G. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2071-7_14 · Cited by 5

Mitophagy

Mijaljica, D., Prescott, M., & Devenish, R. J. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-405528-5.00005-5 · Cited by 3

Mitochondria removal by autophagy

Wang, K., & Klionsky, D. J. (2011) · Autophagy · doi:10.4161/auto.7.3.14502 · Cited by 380

Editorial: Mitophagy in health and disease, volume II

Fang, E. F., Tavernarakis, N., & Palikaras, K. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1242664