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Reactive oxygen species, cellular redox systems, and apoptosis
Open accessAbstract
Reactive oxygen species (ROS) are products of normal metabolism and xenobiotic exposure, and depending on their concentration, ROS can be beneficial or harmful to cells and tissues. At physiological low levels, ROS function as "redox messengers" in intracellular signaling and regulation, whereas excess ROS induce oxidative modification of cellular macromolecules, inhibit protein function, and promote cell death. Additionally, various redox systems, such as the glutathione, thioredoxin, and pyridine nucleotide redox couples, participate in cell signaling and modulation of cell function, including apoptotic cell death. Cell apoptosis is initiated by extracellular and intracellular signals via two main pathways, the death receptor- and the mitochondria-mediated pathways. Various pathologies can result from oxidative stress-induced apoptotic signaling that is consequent to ROS increases and/or antioxidant decreases, disruption of intracellular redox homeostasis, and irreversible oxidative modifications of lipid, protein, or DNA. In this review, we focus on several key aspects of ROS and redox mechanisms in apoptotic signaling and highlight the gaps in knowledge and potential avenues for further investigation. A full understanding of the redox control of apoptotic initiation and execution could underpin the development of therapeutic interventions targeted at oxidative stress-associated disorders.
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“ROS are highly chemically reactive molecules, derived from the deficient reduction in molecular oxygen (O2) and playing a critical role as signaling molecules in tumorigenesis [68], including asbestos-mediated carcinogenesis [15,66,69].”
From Chronic Inflammation, Oxidative Stress and Metabolic Plasticity: Three Players Driving the Pro-Tumorigenic Microenvironment in Malignant Mesothelioma (2023) · cites this paper as [69]
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Cites
The NOX Family of ROS-Generating NADPH Oxidases: Physiology and Pathophysiology
Bedard, K., & Krause, K.-H. (2007) · Physiological Reviews · doi:10.1152/physrev.00044.2005 · Cited by 6,989
Oxidants, antioxidants, and the degenerative diseases of aging.
Ames, B. N., Shigenaga, M. K., & Hagen, T. M. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.17.7915 · Cited by 5,958
Meister, A., & Anderson, M. E. (1983) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.52.070183.003431 · Cited by 5,694
Mitochondrial formation of reactive oxygen species
Turrens, J. F. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049478 · Cited by 5,084
Schafer, F. Q., & Buettner, G. R. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00480-4 · Cited by 4,587
Molecular characterization of mitochondrial apoptosis-inducing factor
Susin, S. A., Lorenzo, H. K., Zamzami, N., Marzo, I., Snow, B. E., Brothers, G. M., Mangion, J., Jacotot, E., Costantini, P., Loeffler, M., et al. (1999) · Nature · doi:10.1038/17135 · Cited by 4,060
Du, C., Fang, M., Li, Y., Li, L., & Wang, X. (2000) · Cell · doi:10.1016/s0092-8674(00)00008-8 · Cited by 3,513
Stress-dependent regulation of FOXO transcription factors by the SIRT1 deacetylase
Brunet, A., Sweeney, L. B., Sturgill, J. F., Chua, K. F., Greer, P. L., Lin, Y., Tran, H., Ross, S. E., Mostoslavsky, R., Cohen, H. Y., et al. (2004) · Science · doi:10.1126/science.1094637 · Cited by 3,239
Induction of TNF receptor I-mediated apoptosis via two sequential signaling complexes
Micheau, O., & Tschopp, J. (2003) · Cell · doi:10.1016/s0092-8674(03)00521-x · Cited by 2,738
Structure, mechanism and regulation of peroxiredoxins
Wood, Z. A., Schröder, E., Harris, J. R., & Poole, L. B. (2003) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(02)00003-8 · Cited by 2,546
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Feng, H., Zou, S., Chen, M., Xiong, F., Lee, M., Fang, L., & Tang, B. Z. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.0c02434 · Cited by 98
Maryam, A., Mehmood, T., Zhang, H., Li, Y., Khan, M. N., & Ma, T. (2017) · Scientific Reports · doi:10.1038/s41598-017-06535-y · Cited by 101
Pang, Q., Li, Y., Meng, L., Li, G., Luo, Z., & Fan, R. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.03.177 · Cited by 96
Magnetic nanoparticles for ferroptosis cancer therapy with diagnostic imaging
Ko, M. J., Min, S., Hong, H., Yoo, W., Joo, J., Zhang, Y. S., Kang, H., & Kim, D. (2023) · Bioactive Materials · doi:10.1016/j.bioactmat.2023.09.015 · Cited by 101
Bax Inhibitor 1 in apoptosis and disease
Robinson, K. S., Clements, A., Williams, A. C., Berger, C. N., & Frankel, G. M. (2011) · Oncogene · doi:10.1038/onc.2010.636 · Cited by 99
Sun, B., Sun, G., Xiao, J., Chen, R., Wang, X., Wu, Y., Cao, L., Yang, Z., & Sun, X. (2011) · Journal of Cellular Biochemistry · doi:10.1002/jcb.23371 · Cited by 99
Huang, Y., Zhu, D., Chen, X., Chen, Q.-K., Luo, Z., Chang-chun, L., Wang, G., Zhang, W., & Liao, N.-Z. (2017) · Oncotarget · doi:10.18632/oncotarget.16828 · Cited by 100
Mukherjee, A. K., Saviola, A. J., Burns, P. D., & Mackessy, S. P. (2015) · APOPTOSIS · doi:10.1007/s10495-015-1157-6 · Cited by 97
Zhong, D., Wang, H., Liu, M., Li, X., Huang, M., Zhou, H., Lin, S., Lin, Z., & Yang, B. (2015) · Scientific Reports · doi:10.1038/srep16910 · Cited by 97
Novel method for rapid toxicity screening of magnetic nanoparticles
Erofeev, A. S., Gorelkin, P. V., Garanina, A. S., Alova, A. V., Efremova, M. V., Vorobyeva, N. S., Edwards, C., Korchev, Y. E., & Majouga, A. G. (2018) · Scientific Reports · doi:10.1038/s41598-018-25852-4 · Cited by 101
Targeting of AML1-ETO in t(8;21) Leukemia by Oridonin Generates a Tumor Suppressor–Like Protein
Zhen, T., Wu, C., Liu, P., Wu, H., Zhou, G., Lu, Y., Liu, J., Liang, Y., Li, K. K., Wang, Y., et al. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3003562 · Cited by 97
Factors Affecting the Formation and Treatment of Thrombosis by Natural and Synthetic Compounds
Lichota, A., Szewczyk, E. M., & Gwoździński, K. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217975 · Cited by 108
Chattopadhyay, M., Kodela, R., Nath, N., Barsegian, A., Boring, D. L., & Kashfi, K. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2011.12.019 · Cited by 96
Mesenchymal stem cells restore CCl4‐induced liver injury by an antioxidative process
Cho, K., Woo, S., Seoh, J., Han, H., & Ryu, K. (2012) · Cell Biology International · doi:10.1042/cbi20110634 · Cited by 96
Martinez, R. M., Pinho-Ribeiro, F. A., Steffen, V. S., Silva, T. C. C., Caviglione, C. V., Bottura, C., Fonseca, M. J. V., Vicentini, F. T. M. C., Vignoli, J. A., Baracat, M. M., et al. (2016) · PLoS ONE · doi:10.1371/journal.pone.0146296 · Cited by 96
Jin, Y., Liu, F., Yin, P., Zhao, H., Luan, W., Hou, X., Zhong, Y., Jia, D. T., Zan, J., Ma, W., et al. (2012) · Stress · doi:10.3109/10253890.2012.680526 · Cited by 98
Jia, Y., Lin, J., Mi, Y., & Zhang, C. (2011) · Reproductive Toxicology · doi:10.1016/j.reprotox.2010.12.057 · Cited by 95
Sharma, P., Reddy, T. S., Kumar, N. P., Senwar, K. R., Bhargava, S. K., & Shankaraiah, N. (2017) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2017.06.035 · Cited by 94
Eldehna, W. M., Abo-Ashour, M. F., Ibrahim, H. S., Al-Ansary, G. H., Ghabbour, H. A., Elaasser, M. M., Ahmed, H. Y., & Safwat, N. A. (2018) · Journal of Enzyme Inhibition and Medicinal Chemistry · doi:10.1080/14756366.2017.1421181 · Cited by 95
Selective anticancer copper( ii )-mixed ligand complexes: targeting of ROS and proteasomes
Ng, C. H., Kong, S. M., Tiong, Y. L., Maah, M. J., Sukram, N., Ahmad, M., & Khoo, A. S. B. (2014) · Metallomics · doi:10.1039/c3mt00276d · Cited by 93
Feng, Z., Xia, Y., Gao, T., Xu, F., Lei, Q., Peng, C., Yang, Y., Xue, Q., Hu, X., Wang, Q., et al. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-1046-3 · Cited by 93
Wu, D., Hu, Q., Liu, X., Pan, L., Xiong, Q., & Zhu, Y. Z. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.11.006 · Cited by 92
Song, Y., Li, X., Li, Y., Li, N., Shi, X., Ding, H., Zhang, Y., Liu, G., Liu, G., & Wang, Z. (2014) · APOPTOSIS · doi:10.1007/s10495-014-0982-3 · Cited by 92
Bone Marrow Injury Induced via Oxidative Stress in Mice by Inhalation Exposure to Formaldehyde
Zhang, Y., Liu, X., McHale, C. M., Li, R., Zhang, L., Wu, Y., Ye, X., Yang, X., & Ding, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0074974 · Cited by 92
Burraco, P., & Gómez-Mestre, I. (2016) · Physiological and Biochemical Zoology · doi:10.1086/688737 · Cited by 92
Cardiac metabolism — A promising therapeutic target for heart failure
Noordali, H., Loudon, B. L., Frenneaux, M. P., & Madhani, M. (2017) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2017.08.001 · Cited by 94
Dua, K., Rapalli, V. K., Shukla, S. D., Singhvi, G., Shastri, M. D., Chellappan, D. K., Satija, S., Mehta, M., Gulati, M., Pinto, T. D. J. A., et al. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.08.101 · Cited by 92
Intracellular Transport and Cytotoxicity of the Protein Toxin Ricin
Sowa-Rogozińska, N., Sominka, H., Nowakowska-Gołacka, J., Sandvig, K., & Słomińska-Wojewódzka, M. (2019) · Toxins · doi:10.3390/toxins11060350 · Cited by 91
Ahamed, M., Akhtar, M. J., Khan, M. A. M., Alaizeri, Z. M., & Alhadlaq, H. A. (2021) · ACS Omega · doi:10.1021/acsomega.1c01467 · Cited by 92
Scott, M. B., Styring, A., & McCullagh, J. (2022) · Pathogens · doi:10.3390/pathogens11070770 · Cited by 98
Chae, H.-D., & Broxmeyer, H. E. (2010) · Stem Cells and Development · doi:10.1089/scd.2010.0465 · Cited by 93
Huang, Y., Zhu, M., Li, Z., Sa, R., Chu, Q., Zhang, Q., Zhang, H., Tang, W. Y., Zhang, M., & Yin, H. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.02.024 · Cited by 93
Ruskovska, T., & Bernlohr, D. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2013.04.002 · Cited by 92
Georgiev, M. I., Alipieva, K. I., Orhan, İ. E., Abrashev, R., Denev, P. N., & Angelova, M. (2011) · Food Chemistry · doi:10.1016/j.foodchem.2011.02.083 · Cited by 92
Hsiao, Y., Peng, S., Lai, K., Liao, C., Huang, Y., Lin, C., Lin, M., Liu, K.-C., Tsai, C., Ma, Y., et al. (2019) · Environmental Toxicology · doi:10.1002/tox.22698 · Cited by 91
Karkhanei, B., Ghane, E. T., & Mehri, F. (2021) · New Microbes and New Infections · doi:10.1016/j.nmni.2021.100897 · Cited by 92
Dual-Site Chemosensor for Monitoring ·OH-Cysteine Redox in Cells and In Vivo
Kang, Z., Jiang, J., Tu, Q., Liu, S., Zhang, Y., Wang, D., Wang, J., & Yuan, M. (2022) · Journal of the American Chemical Society · doi:10.1021/jacs.2c10855 · Cited by 90
Üremiş, N., & Üremi̇ş, M. M. (2025) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70133 · Cited by 103
Nox4 and redox signaling mediate TGF-β-induced endothelial cell apoptosis and phenotypic switch
Yan, F., Wang, Y., Wu, X., Peshavariya, H., Dusting, G. J., Zhang, M., & Jiang, F. (2014) · Cell Death and Disease · doi:10.1038/cddis.2013.551 · Cited by 90
Avolio, R., Matassa, D. S., Criscuolo, D., Landriscina, M., & Esposito, F. (2020) · Biomolecules · doi:10.3390/biom10010135 · Cited by 90
Jiao, Z., Huo, Q., Lin, X., Chu, X., Deng, Z., Guo, H., Peng, Y., Lu, S. T., Zhou, X., Wang, X., et al. (2022) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2022.119314 · Cited by 90
Dirican, N., Dirican, A., Sen, O., Aynalı, A., Atalay, S., Bircan, A., Öztürk, Ö., Erdoğan, S., Çakır, M., & Akkaya, A. (2015) · Redox Report · doi:10.1179/1351000215y.0000000027 · Cited by 90
Mitochondrial ion channels as oncological targets
Leanza, L., Zoratti, M., Gulbins, E., & Szabó, I. (2014) · Oncogene · doi:10.1038/onc.2013.578 · Cited by 93
The Induction of Apoptosis by Shiga Toxins and Ricin
Tesh, V. L. (2011) · Current topics in microbiology and immunology · doi:10.1007/82_2011_155 · Cited by 89
Momordin Ic induces HepG2 cell apoptosis through MAPK and PI3K/Akt-mediated mitochondrial pathways
Wang, J., Li, Y., Xiao, H., Xiao, C., Wang, Y., & Liu, X. (2013) · APOPTOSIS · doi:10.1007/s10495-013-0820-z · Cited by 89
In Vitro Photodynamic Effect of Phycocyanin against Breast Cancer Cells
Bharathiraja, S., Seo, H., Manivasagan, P., Santhamoorthy, M., Park, S. H., & Oh, J. (2016) · Molecules · doi:10.3390/molecules21111470 · Cited by 89
Molecular mechanisms of oxidative stress in stroke and cancer
Chavda, V. K., Chaurasia, B. K., Garg, K., Deora, H., Umana, G. E., Palmisciano, P., Scalia, G., & Lu, B. (2021) · Brain Disorders · doi:10.1016/j.dscb.2021.100029 · Cited by 98
Oxidative stress modulating nanomaterials and their biochemical roles in nanomedicine
Patel, K. D., Keskin‐Erdogan, Z., Sawadkar, P., Sharifulden, N. S. A. N., Shannon, M. R., Patel, M., Silva, L. V. B., Patel, R., Chau, D. Y. S., Knowles, J. C., et al. (2024) · Nanoscale Horizons · doi:10.1039/d4nh00171k · Cited by 92
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Krueger, T., Becker, S., Pontasch, S., Dove, S., Hoegh‐Guldberg, O., Leggat, W. P., Fisher, P. L., & Davy, S. K. (2014) · Journal of Phycology · doi:10.1111/jpy.12232 · Cited by 89
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Kashfi, K. (2013) · Antioxidants and Redox Signaling · doi:10.1089/ars.2013.5308 · Cited by 89
Fontani, F., Marcucci, G., Iantomasi, T., Brandi, M. L., & VINCENZINI, M. T. (2015) · Calcified Tissue International · doi:10.1007/s00223-015-9961-0 · Cited by 89
Liu, B., Tan, X., Liang, J., Wu, S., Liu, J., Zhang, Q., & Zhu, R. (2014) · Scientific Reports · doi:10.1038/srep07041 · Cited by 90
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Zinovkin, R. A., Romaschenko, V. P., Galkin, I. I., Zakharova, V., Pletjushkina, O. Y., Chernyak, B. V., & Popova, E. N. (2014) · Aging · doi:10.18632/aging.100685 · Cited by 89
Tuli, H. S., Kaur, J., Vashishth, K., Sak, K., Sharma, U., Choudhary, R., Behl, T., Singh, T., Sharma, S., Saini, A. K., et al. (2022) · Archives of Toxicology · doi:10.1007/s00204-022-03421-z · Cited by 91
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Yang, T., Peleli, M., Zollbrecht, C., Giulietti, A., Terrando, N., Lundberg, J. O., Weitzberg, E., & Carlström, M. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.02.016 · Cited by 88
Hydrogen sulfide, reactive sulfur species and coping with reactive oxygen species
Olson, K. R. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2019.01.020 · Cited by 88
Fernando, W., Rupasinghe, H. P. V., & Hoskin, D. W. (2019) · Cancer Letters · doi:10.1016/j.canlet.2019.03.022 · Cited by 88
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Nagai-Singer, M. A., Morrison, H. A., & Allen, I. C. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02419 · Cited by 87
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Yang, L., Zhang, X., Wang, Z., Li, B., & Zhu, H. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1156538 · Cited by 96
Redox signaling in the pancreas in health and disease
Sastre, J., Pérez, S., Sabater-Orti, L., & Rius‐Pérez, S. (2024) · Physiological Reviews · doi:10.1152/physrev.00044.2023 · Cited by 101
Fluorescent probes for visualizing ROS-associated proteins in disease
Wang, H., Wang, X., Li, P., Dong, M., Yao, S. Q., & Tang, B. (2021) · Chemical Science · doi:10.1039/d1sc02165f · Cited by 87
Oshi, M., Gandhi, S., Yan, L., Tokumaru, Y., Wu, R., Yamada, A., Matsuyama, R., Endo, I., & Takabe, K. (2022) · Breast Cancer Research and Treatment · doi:10.1007/s10549-022-06633-0 · Cited by 88
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Chen, D., Guo, Z., Yao, L., Sun, Y., Dian, Y., Zhao, D., Ke, Y., Zeng, F., Zhang, C., Deng, G., et al. (2025) · Redox Biology · doi:10.1016/j.redox.2025.103686 · Cited by 95
Brechbuhl, H. M., Kachadourian, R., Min, E., Chan, D. C. F., & Day, B. J. (2011) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2011.08.004 · Cited by 86
Li, H., Wang, J., Xu, H., Xing, R., Pan, Y., Li, W., Cui, J., Zhang, H., & Lu, Y. (2013) · Molecular Cancer · doi:10.1186/1476-4598-12-110 · Cited by 86
Autoxidation of gallic acid induces ROS-dependent death in human prostate cancer LNCaP cells.
Russell, L. H., MAZZIO, E. A., Badisa, R. B., Zhu, Z.-P., Agharahimi, M., Oriaku, E. T., & Goodman, C. B. (2012) · PubMed · Cited by 86
Shen, R., Liu, P., Zhang, Y., Yu, Z., Chen, X., Zhou, L., Nie, B., Zaczek, A. J., Chen, J., & Liu, J. (2018) · Analytical Chemistry · doi:10.1021/acs.analchem.7b04798 · Cited by 85
Zhang, Y., Li, Z., Kholodkevich, S. V., Sharov, A. N., Feng, Y., Ren, N., & Sun, K. (2019) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2019.134549 · Cited by 85
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Das, A., Ranadive, N., Kinra, M., Nampoothiri, M., Arora, D. S., & Mudgal, J. (2020) · Current Neuropharmacology · doi:10.2174/1570159x18666200221113842 · Cited by 87
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Han, S., Bi, S., Guo, T., Sun, D., Zou, Y., Wang, L., Song, L., Chu, D., Liao, A., Song, X., et al. (2022) · Journal of Controlled Release · doi:10.1016/j.jconrel.2022.05.057 · Cited by 88
Fan, L., Wang, A., & Wu, Y. (2013) · Journal of Proteomics · doi:10.1016/j.jprot.2012.12.017 · Cited by 85
Zhang, X., Chen, M., Zou, P., Kanchana, K., Weng, Q., Chen, W., Zhong, P., Ji, J., Zhou, H., He, L., et al. (2015) · BMC Cancer · doi:10.1186/s12885-015-1851-3 · Cited by 86
Hekimi, S., Wang, Y., & Noë, A. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00161 · Cited by 83
Mitochondria-Targeting Anticancer Metal Complexes
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Coppolino, G., Leonardi, G., Andreucci, M., & Bolignano, D. (2019) · Current Pharmaceutical Design · doi:10.2174/1381612825666190112165206 · Cited by 84
Zhang, M., Harashima, N., Moritani, T., Huang, W., & Harada, M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127386 · Cited by 86
Pgc-1α overexpression Via local transfection attenuates mitophagy pathway in muscle disuse atrophy
Kang, C., & Ji, L. L. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.12.032 · Cited by 83
Wei, Y., Zhang, J., Xu, S., Peng, X., Xia, Y., Li, X., Wang, H., Chang, H., & Gao, Y. (2018) · Open Biology · doi:10.1098/rsob.180068 · Cited by 82
Wang, L., Huang, H., Yang, F., Kong, B., Hu, H., Hu, K., Guo, J., Mei, Y., & Liu, W. (2014) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2014/960362 · Cited by 83
Liu, J., Wang, C., Liu, F., Lu, Y., & Cheng, J. (2015) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-015-8481-0 · Cited by 83
Lim, J. B., Huang, B. K., Deen, W. M., & Sikes, H. D. (2015) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2015.07.009 · Cited by 86
Respiratory chain complex II as general sensor for apoptosis
Grimm, S. (2013) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2012.09.009 · Cited by 82
ROS homeostasis in cell fate, pathophysiology, and therapeutic interventions
Chen, Y.-S., Tian, H., Rong, D., Wang, L., Chen, S., Zeng, J., Xu, H., Mei, J., Wang, L.-Y., Liou, Y., et al. (2025) · Molecular Biomedicine · doi:10.1186/s43556-025-00338-8 · Cited by 96
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Hu, Y. H., Deng, H., Xu, S., & Zhang, J. (2015) · International Journal of Molecular Sciences · doi:10.3390/ijms161024895 · Cited by 81
Shadab, M., Jha, B., Asad, M., Deepthi, M., Kamran, M., & Ali, N. (2017) · PLoS ONE · doi:10.1371/journal.pone.0171306 · Cited by 82
Cao, R., Wang, G., Qian, K., Chen, L., Ju, L., Qian, G., Wu, C., Dan, H. C., Jiang, W., Wu, M., et al. (2017) · Cancer Letters · doi:10.1016/j.canlet.2017.11.015 · Cited by 82
Albendazole as a promising molecule for tumor control
Castro, L. S. E. P. W., Kviecinski, M. R., Ourique, F., Parisotto, E. B., Grinevicius, V. M. A. S., Correia, J. F. G., Wilhelm Filho, D., & Pedrosa, R. C. (2016) · Redox Biology · doi:10.1016/j.redox.2016.09.013 · Cited by 81
On the epigenetic role of guanosine oxidation
Giorgio, M., Dellino, G. I., Gambino, V., Roda, N., & Pelicci, P. G. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101398 · Cited by 82
Development of Cerium Oxide Nanoparticles and Its Cytotoxicity in Prostate Cancer Cells
Renu, G., Rani, V. V. D., Nair, S. V., Subramanian, K. R. V., & Lakshmanan, V. (2012) · Advanced Science Letters · doi:10.1166/asl.2012.3312 · Cited by 81
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Metadata
- Authors
- Circu, M. L., & Aw, T. Y.
- Affiliations
- Louisiana State University Health Sciences Center Shreveport (US)
- Corresponding author
- Aw, Tak Yee
- ORCID
- Circu, Magdalena L.
- Venue
- Free Radical Biology and Medicine
- Publisher
- Elsevier BV
- Published
- 2010-03
- Volume
- 48
- Issue
- 6
- Pages
- 749-762
- ISSN
- 0891-5849 (ISSN-L)
- PMC
- PMC2823977
- OpenAlex
- W1977178308
- Cited by
- 3,340
- References
- 224
- Citations by year
- 2026: 116 · 2025: 134 · 2024: 154 · 2023: 190 · 2022: 262 · 2021: 243 · 2020: 243 · 2019: 298 · 2018: 264 · 2017: 287 · 2016: 240 · 2015: 217 · 2014: 210 · 2013: 163 · 2012: 152
- FWCI
- 13.45
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Free Radical Biology and Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK044510, DK 44510)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- reactive oxygen species, apoptosis, oxidative stress, redox signaling, glutathione, thioredoxin, pyridine nucleotides, death receptor signaling, mitochondrial apoptosis, antioxidant deficiency, redox homeostasis
- MeSH terms
- Animals, Humans, Oxidation-Reduction, Signal Transduction, Apoptosis, Reactive Oxygen Species
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