The DOI matches its Crossref record; 135 of the 135 references it cites were found in a registry or an index.
Mechanisms and Implications of Reactive Oxygen Species Generation During the Unfolded Protein Response: Roles of Endoplasmic Reticulum Oxidoreductases, Mitochondrial Electron Transport, and NADPH Oxidase
Abstract
Cellular mechanisms governing redox homeostasis likely involve their integration with other stresses. Endoplasmic reticulum (ER) stress triggers complex adaptive or proapoptotic signaling defined as the unfolded protein response (UPR), involved in several pathophysiological processes. Since protein folding is highly redox-dependent, convergence between ER stress and oxidative stress has attracted interest. Evidence suggests that ROS production and oxidative stress are not only coincidental to ER stress, but are integral UPR components, being triggered by distinct types of ER stressors and contributing to support proapoptotic, as well as proadaptive UPR signaling. Thus, ROS generation can be upstream or downstream UPR targets and may display a UPR-specific plus a nonspecific component. Enzymatic mechanisms of ROS generation during UPR include: (a) Multiple thiol-disulfide exchanges involving ER oxidoreductases including flavooxidase Ero1 and protein disulfide isomerase (PDI); (b) Mitochondrial electron transport; (c) Nox4 NADPH oxidase complex, particularly Nox4. Understanding the roles of such mechanisms and how they interconnect with the UPR requires more investigation. Integration among such ROS sources may depend on Ca(2+) levels, ROS themselves, and PDI, which associates with NADPH oxidase and regulates its function. Oxidative stress may frequently integrate with a background of ER stress/UPR in several diseases; here we discuss a focus in the vascular system.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“The signaling mechanisms of hydrogen peroxide in ECs (941) lead to the increased activity of eNOS and other enzymes (121, 141, 193, 251, 815, 940).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [815]
In the citing paper
“Reactive oxygen species are produced by the Maillard reaction [20], [21], damaging pancreatic beta cells, and leading to a subcellular stress response (the “unfolded protein response” in the endoplasmic reticulum) that drives insulin inadequacy [22], [23].”
From The relationship of sugar to population-level diabetes prevalence: an econometric analysis of repeated cross-sectional data (2013) · cites this paper as [22]
Citations
Cites
1 retracted
Proapoptotic BAX and BAK Modulate the Unfolded Protein Response by a Direct Interaction with IRE1α
Hetz, C. A., Bernasconi, P., Fisher, J. K., Lee, A., Bassik, M. C., Antonsson, B. E., Brandt, G. S., Iwakoshi, N. N., Schinzel, A. C., Glimcher, L. H., et al. (2006) · Science · doi:10.1126/science.1123480 · Cited by 688
RetractedThe 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
Signal integration in the endoplasmic reticulum unfolded protein response
Ron, D., & Walter, P. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2199 · Cited by 6,431
An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress
Harding, H. P., Zhang, Y., Zeng, H., Novoa, I., Lu, P. D., Calfon, M. A., Sadri, N., Yun, C., Popko, B., Paules, R. S., et al. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00105-9 · Cited by 3,336
THE MAMMALIAN UNFOLDED PROTEIN RESPONSE
Schröder, M., & Kaufman, R. J. (2005) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.73.011303.074134 · Cited by 3,099
Marciniak, S. J., Yun, C. Y., Oyadomari, S., Novoa, I., Zhang, Y., Jungreis, R., Nagata, K., Harding, H. P., & Ron, D. (2004) · Genes & Development · doi:10.1101/gad.1250704 · Cited by 2,066
From endoplasmic-reticulum stress to the inflammatory response
Zhang, K., & Kaufman, R. J. (2008) · Nature · doi:10.1038/nature07203 · Cited by 2,010
Oxidized Redox State of Glutathione in the Endoplasmic Reticulum
Hwang, C., Sinskey, A. J., & Lodish, H. F. (1992) · Science · doi:10.1126/science.1523409 · Cited by 1,968
Pathophysiology of coronary artery disease
Libby, P., & Theroux, P. (2005) · Circulation · doi:10.1161/circulationaha.105.537878 · Cited by 1,965
McCullough, K. D., Martindale, J. L., Klotz, L., Aw, T. Y., & Holbrook, N. J. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.4.1249-1259.2001 · Cited by 1,945
Research works printed but not linked: 1
- Diwan A, 2009, J Clin Invest, 119, 203
Cited by
Sorted by citations
Items 501–569 of 569
Stress Oxidative and Effect of Herbal Antioxidant in Animal Reproduction: Future and Perspective
Kebria, M. M., Zangiabadi, I., Ghantabpour, T., & Heydari, M. (2021) · Plant Biotechnology Persa · doi:10.52547/pbp.3.2.82 · Cited by 1
Sofiullah, S. S. M., Murugan, D. D., Muid, S. A., Wu, Y. S., Zamakshshari, N. H., Gan, Q. F., Patrick, M., Azis, N. A., Sirasanagandla, S. R., & Choy, K. W. (2024) · Sains Malaysiana · doi:10.17576/jsm-2024-5303-09 · Cited by 1
Raj, C. T. D., Palaninathan, V., Kandaswamy, S., Kumar, V., & James, R. A. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e41132 · Cited by 1
The Growing Clinical Relevance of Cellular Stress Responses and Regulated Cell Death
Land, W. G. (2020) · Springer eBooks · doi:10.1007/978-3-030-53868-2_4 · Cited by 1
Proibitina e a resposta a mecanismos de estresse em melanoma e sua relação com a via E2F1
Tortelli, T. C. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2013.tde-14082013-150136 · Cited by 1
Pescatore-Alves, L. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2012.tde-25042012-165242 · Cited by 1
Oxidative Stress - a Key Player in Periodontal Disease
Aboodi, G. M. (2015) · TSpace (University of Toronto) · Cited by 1
Matrix stiffness regulates oxidative stress response of human dermal fibroblasts
Yao, X. (2018) · doi:10.32657/10220/46707 · Cited by 1
Cordell, W. (2020) · SSRN Electronic Journal · doi:10.2139/ssrn.3721693 · Cited by 1
M. tuberculosis invades and disrupts the blood brain barrier directly to initiate meningitisPreprint
Proust, A. M., Wilkinson, K. A., & Wilkinson, R. J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.08.30.610462 · Cited by 1
Oxidative Stress and the Unfolded Protein Response in the Liver
Hudson, W. M., & Pagliassotti, M. J. (2015) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-3-319-15539-5_5
Kuwabara, W. M. T. (2013) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2013.tde-23052014-101531
Role of NADPH Oxidase in b Cell Dysfunction 34
Weaver, J. R., & Taylor, D. (2015)
Amanso, A. M. (2009) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2009.tde-25042011-110602
Duffield, J. S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-800102-8.00023-0
Marcadores urinarios de predisposición al fracaso renal agudo inducida por nefrotóxicos
Vicente, R. L. V. (2011) · Gredos (University of Salamanca) · doi:10.14201/gredos.115620
OVERCOMING SELF-REACTIVITY THROUGH IMMUNOLOGICAL AND METABOLIC REDOX MODULATION
Delmastro-Greenwood, M. M. (2012) · D-Scholarship@Pitt (University of Pittsburgh)
Tanaka, L. Y. (2014) · doi:10.11606/t.5.2014.tde-08042014-092611
Self-citationImmune Modulators of HIV Infection: The Role of Reactive Oxygen
Berrueta, L. (2012)
A influência da poluição atmosférica no remodelamento miocárdico
Ramires, F. J. A. (2014)
Diabetic Nephropathy- Recent Trends and Future Prospective in its Management
Sharma, O. P. (2025) · Int Jour of Pharmamedix India · doi:10.71152/6aycen66
Paulo, S., & Humana, F. (2013)
Santos, T. M. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2014.tde-25112014-111305
Queliconi, B. B. (2014) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.46.2014.tde-19012015-143431
Melo, T. Q. (2017) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2017.tde-01032017-131637
Interactions of L. monocytogenes with Host Cellular Defenses
Lam, G. Y. (2012) · TSpace (University of Toronto)
Examining the Role of Endoplasmic Reticulum Stress in Pancreatic Beta-cell Biology
Teodoro, T. (2012) · TSpace (University of Toronto)
The Antiviral Properties of Melaleuca alternifolia concentrate (MAC) against West Nile virus
Zamora, A. C. P. (2015) · Griffith Research Online · doi:10.25904/1912/2151
Bessa, T. C. D. (2018) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2018.tde-03072018-090616
Developing potential biomarkers through bedside-to-bench translation
Bromage, D. I., Santos, C. X. C., & Shah, A. M. (2018) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2018.07.254
Self-citationDoig, C. L., Zielinska, A. E., Fletcher, R. S., Oakey, L. A., Elhassan, Y., Garten, A., Cartwright, D., Heising, S., Alsheri, A., Watson, D. G., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/567297
Endoplasmic Reticulum Stress: Importance in Pathogenesis of Mycobacterium tuberculosis
Sharma, T., Grover, S., Ehtesham, N., & Hasnain, S. (2019) · Mycobacterium Tuberculosis: Molecular Infection Biology, Pathogenesis, Diagnostics and New Interventions · doi:10.1007/978-981-32-9413-4_14
Mullick, M., & Nayak, S. (2019) · Regenerative Engineering and Translational Medicine · doi:10.1007/s40883-019-00143-0
Mechanisms of Polyunsaturated Fatty Acid Alterations in Cystic Fibrosis
Njoroge, S. W. (2013)
Novel roles for peroxisome-linked genes in Drosophila
Pridie, C. (2020) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-wv4x-sx86
Carnosine supplementation and retina oxidative parameters in diet-induced obesity modelPreprint
Torres, R. J. D. A., Moreto, F., Luchini, A., Torres, R. J. D. A., Longo, S. P., Pinho, R. A., Nagashima, S., de Noronha, L., Ferron, A. J. T., Silva, C. V. D. A., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-2006617/v1
Sofiullah, S. S. M., Murugan, D. D., Muid, S. A., Wu, Y. S., Zamakshshari, N. H., Quan, F. G., Patrick, M., & Choy, K. W. (2023) · Research Square · doi:10.21203/rs.3.rs-2964177/v1
de Almeida, D. C. (2022) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.42.2022.tde-18082023-142552
Mitochondrial Dysfunction and Parkinson’s Disease
刘, 洋. (2023) · Advances in Clinical Medicine · doi:10.12677/acm.2023.13102203
Molina-Pelayo, F. A., García-Carrillo, R., Zárate-López, D., Cabrera-Aguilar, A., Ortega-Domínguez, B., Domı́nguez, M., Chiquete‐Félix, N., Dagnino-Acosta, A., Velasco-Loyden, G., Chávez, E., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3429206/v1
Le, H. T., Yu, J., Hong, J. Y., Ahn, H., Kim, Y. H., Kim, M., Chae, I. G., Cho, H.-N., Nam, S., Hyun, S. H., et al. (2023) · SSRN Electronic Journal · doi:10.2139/ssrn.4648361
[Research Progress of Granulocytic Myeloid-derived Suppressor Cells in Non-small Cell Lung Cancer].
Yang, C., Zhu, R., Zhang, Y., Ying, L., Wang, J., Liu, P., & Su, D. (2024) · PubMed Central · doi:10.3779/j.issn.1009-3419.2023.106.28
Almendra‐Pegueros, R., Barros-Membrilla, A. J., Pérez-Marlasca, E., Julve, J., Martínez‐González, J., Rodrı́guez, C., & Galán, M. (2024) · Clínica e Investigación en Arteriosclerosis · doi:10.1016/j.arteri.2024.09.002
Almendra‐Pegueros, R., Barros-Membrilla, A. J., Pérez-Marlasca, E., Julve, J., Martínez‐González, J., Rodrı́guez, C., & Galán, M. (2025) · Clínica e Investigación en Arteriosclerosis (English Edition) · doi:10.1016/j.artere.2025.100740
Andrade, M. R., Yun, X., Croglio, M. P., Niedermeyer, S. E., Jiang, H., Philip, N. M., Murray, S., Munson, M., Suresh, K. S., Damarla, M., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.06.687041
da Silva, C. P. V. (2014) · Aleph UCLA Undergraduate Research Journal for the Humanities and Social Sciences
Chen, X., Pan, B., Yu, L., Wang, B., & Pan, L. (2024) · Figshare · doi:10.6084/m9.figshare.26741408
Oxidative Stress and Pathophysiology of Chronic Disease
Balaji, S., Pandian, M. S., Ganesamoorthy, R., Parameswari, R., & Babujanarthanam, R. (2026) · Springer eBooks · doi:10.1007/978-981-96-9670-3_3 · Cited by 1
Arikawa, L. M., Mota, L. F. M., Fonseca, L. F. S., Júnior, G. A. F., Salatta, B. M., Frezarim, G. B., Schmidt, P. I., Nasner, S. L. C., Valente, J. P. S., Pelaez, A. M., et al. (2026) · Journal of Animal Science and Biotechnology/Journal of animal science and biotechnology · doi:10.1186/s40104-025-01341-3
ROS-Mediated Cellular Signaling Pathways in Metabolic Disorders
Gunasekaran, S. K., Gobinath, M., Roychowdhury, P., Maideen, N. M. P., & Kuppusamy, G. (2026) · Springer eBooks · doi:10.1007/978-3-032-11752-6_4
Implication de FGF9 et de FGF19 dans la fibrose pulmonaire idiopathique
Justet, A. (2020) · theses.fr (ABES) · doi:10.70675/6e72f095z0cb6z4dd3zb204z88d1b08b9910
Yu, H., Guo, Y., Wang, X., Guo, W., & Zhang, Y. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1700811
Stojiljković, M., Tepavčević, S., Kostić, M., Jakovljevic, J., Ćulafić, T., Romić, S., Ivković, T., Pantelić, M., & Korićanac, G. (2026) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2026.07.005
de Souza, J. M. F., Bessa, T. C. D., Silva, A. D. A., Fernandes, C., Tanaka, L. Y., & Laurindo, F. R. M. (2026) · Physiological Reports · doi:10.14814/phy2.71088
Self-citationChromosomal instability in cancer: sources, consequences and new therapeutic opportunities
Serpico, A. F., & Grieco, D. (2026) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-026-02940-w
Gelsolin Counteracts ER Stress-Driven Inflammatory Circuits in Psoriasis-like DermatitisPreprint
Ori, D., Okude, H., Konishi, R., Murase, M., Hiroki, S., Takahara, S., Tanaka, T., Toyodome, R., Kano, N., Kawasaki, T., et al. (2026) · eLife · doi:10.7554/elife.109970.2
Metadata
- Authors
- Santos, C. X. C., Tanaka, L. Y., Wosniak, J., & Laurindo, F. R. M.
- Affiliations
- Universidade de São Paulo (BR)
- Venue
- Antioxidants & Redox Signaling
- Publisher
- SAGE Publications
- Published
- 2009-10
- Volume
- 11
- Issue
- 10
- Pages
- 2409-2427
- ISSN
- 1523-0864 (ISSN-L)
- 1557-7716
- OpenAlex
- W2064194224
- Cited by
- 572
- References
- 135
- Citations by year
- 2026: 10 · 2025: 20 · 2024: 22 · 2023: 25 · 2022: 27 · 2021: 31 · 2020: 43 · 2019: 36 · 2018: 40 · 2017: 37 · 2016: 36 · 2015: 44 · 2014: 46 · 2013: 40 · 2012: 41
- FWCI
- 2.86
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Antioxidants and Redox Signaling (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Endoplasmic Reticulum Stress and Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Keywords
- unfolded protein response, endoplasmic reticulum stress, reactive oxygen species, oxidative stress, redox homeostasis, Ero1, protein disulfide isomerase, mitochondrial electron transport chain, NADPH oxidase, NOX4, thiol-disulfide exchange, calcium signaling, vascular disease
- MeSH terms
- Electron Transport, Endoplasmic Reticulum, Enzyme Activation, Homeostasis, Isoenzymes, Mitochondria, Oxidation-Reduction, Oxidoreductases, Stress, Physiological, Vascular Diseases, Signal Transduction, Apoptosis, Reactive Oxygen Species, NADPH Oxidases, Protein Disulfide-Isomerases
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