The DOI matches its Crossref record; 80 of the 82 references it cites were found in a registry or an index.
The role of reactive oxygen species in homeostasis and degradation of cartilage
Open accessAbstract
Objectives The metabolism of cells in articular joint tissues in normal and pathological conditions is subject to a complex environmental control. In addition to soluble mediators such as cytokines and growth factors, as well as mechanical stimuli, reactive oxygen species (ROS) emerge as major factors in this regulation. ROS production has been found to increase in joint diseases, such as osteoarthritis and rheumatoid arthritis, but their role in joint diseases initiation and progression remains questionable.Method This review is focused on the role of ROS, mainly nitric oxide, peroxynitrite and superoxide anion radicals, in the signaling mechanisms implied in the main cellular functions, including synthesis and degradation of matrix components. The direct effects of ROS on cartilage matrix components as well as their inflammatory and immunomodulatory effects are also considered.Results Some intracellular signaling pathways are redox sensitive and ROS are involved in the regulation of the production of some biochemical factors involved in cartilage degradation and joint inflammation. Further, ROS may cause damage to all matrix components, either by a direct attack or indirectly by reducing matrix components synthesis, by inducing apoptosis or by activating latent metalloproteinases. Finally, we have highlighted the uncoupling effect of ROS on tissue remodeling and synovium inflammation, suggesting that antioxidant therapy could be helpful to treat structural changes but not to relieve symptoms.Conclusions This review of the literature supports the concept that ROS are not only deleterious agents involved in cartilage degradation, but that they also act as integral factors of intracellular signaling mechanisms. Further investigation is required to support the concept of antioxidant therapy in the management of joint diseases.
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
“One disease whose aetiology is well known to be bound up with ROSs is rheumatoid arthritis (RA) [36,1241-1246].”
From Iron behaving badly: inappropriate iron chelation as a major contributor to the aetiology of vascular and other progressive inflammatory and degenerative diseases (2009) · cites this paper as [1245]
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
Redox Regulation of Fos and Jun DNA-Binding Activity in Vitro
Abate, C., Patel, L., Rauscher, F. J., & Curran, T. (1990) · Science · doi:10.1126/science.2118682 · Cited by 1,573
Reactive Oxygen Species as Intracellular Messengers During Cell Growth and Differentiation
Sauer, H., Wartenberg, M., & Hescheler, J. (2001) · Cellular Physiology and Biochemistry · doi:10.1159/000047804 · Cited by 1,118
Xanthoudakis, S., & Curran, T. (1992) · The EMBO Journal · doi:10.1002/j.1460-2075.1992.tb05097.x · Cited by 708
Clancy, R. M., Leszczynska-Piziak, J., & Abramson, S. B. (1992) · Journal of Clinical Investigation · doi:10.1172/jci115929 · Cited by 686
Siwik, D. A., Pagano, P. J., & Colucci, W. S. (2001) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.2001.280.1.c53 · Cited by 674
Chondrocyte apoptosis induced by nitric oxide.
Blanco, F. J., Ochs, R., Schwarz, H., & Lotz, M. (1995) · PubMed Central · Cited by 623
Lo, Y. Y. C., & Cruz, T. F. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.20.11727 · Cited by 530
Articular chondrocytes synthesize nitric oxide in response to cytokines and lipopolysaccharide
Stadler, J., Stefanović-Račić, M., Billiar, T. R., CURRAN, R. D., McIntyre, L. A., Georgescu, H. I., Simmons, R. L., & Evans, C. H. (1991) · The Journal of Immunology · doi:10.4049/jimmunol.147.11.3915 · Cited by 438
Landino, L. M., Crews, B. C., Timmons, M. D., Morrow, J. D., & Marnett, L. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15069 · Cited by 423
Nitric Oxide Activates Metalloprotease Enzymes in Articular Cartilage
Murrell, G. A. C., Jang, D., & Williams, R. J. (1995) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1995.1003 · Cited by 407
Research works printed but not linked: 1
- Henrotin, 2002, Type II collagen derived fragment (Coll2-1) is a new marker predictive of osteoarthritic progression, Osteoporos Int, 13, S17
Cited by
Sorted by citations
Nitric Oxide and Peroxynitrite in Health and Disease
Pacher, P., Beckman, J. S., & Liaudet, L. (2007) · Physiological Reviews · doi:10.1152/physrev.00029.2006 · Cited by 6,390
ROS/oxidative stress signaling in osteoarthritis
Lepetsos, P., & Papavassiliou, A. G. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2016.01.003 · Cited by 832
The role of metabolism in the pathogenesis of osteoarthritis
Mobasheri, A., Rayman, M. P., Gualillo, O., Sellam, J., van der Kraan, P., & Fearon, U. (2017) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2017.50 · Cited by 742
Why is osteoarthritis an age-related disease?
Anderson, A. S., & Loeser, R. F. (2010) · Best Practice & Research Clinical Rheumatology · doi:10.1016/j.berh.2009.08.006 · Cited by 719
Reactive oxygen species, aging and articular cartilage homeostasis
Bolduc, J. A., Collins, J. A., & Loeser, R. F. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.08.038 · Cited by 671
Reactive oxygen species and superoxide dismutases: Role in joint diseases
Afonso, V., Champy, R., Mitrovic, D. R., Collin, P., & Lomri, A. (2007) · Joint Bone Spine · doi:10.1016/j.jbspin.2007.02.002 · Cited by 640
Metabolic syndrome meets osteoarthritis
Zhuo, Q., Yang, W. P., Chen, J., & Wang, Y. (2012) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2012.135 · Cited by 599
Oxidation in rheumatoid arthritis.
Hitchon, C. A., & El-Gabalawy, H. S. (2004) · Arthritis Research · doi:10.1186/ar1447 · Cited by 597
Kell, D. B. (2009) · BMC Medical Genomics · doi:10.1186/1755-8794-2-2 · Cited by 554
Oxygen and reactive oxygen species in cartilage degradation: friends or foes?
Henrotin, Y. E., Kurz, B., & Aigner, T. G. (2005) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2005.04.002 · Cited by 496
Self-citationOxidative stress, consequences and ROS mediated cellular signaling in rheumatoid arthritis
Phull, A. R., Nasir, B., Haq, I. U., & Kim, S. J. (2017) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2017.12.024 · Cited by 465
Age-Related Changes in the Musculoskeletal System and the Development of Osteoarthritis
Loeser, R. F. (2010) · Clinics in Geriatric Medicine · doi:10.1016/j.cger.2010.03.002 · Cited by 465
Hypoxia, mitochondrial dysfunction and synovial invasiveness in rheumatoid arthritis
Fearon, U., Canavan, M., Biniecka, M., & Veale, D. J. (2016) · Nature Reviews Rheumatology · doi:10.1038/nrrheum.2016.69 · Cited by 455
The many ways to cleave hyaluronan
Stern, R., Kogan, G., Jedrzejas, M. J., & Šoltés, L. (2007) · Biotechnology Advances · doi:10.1016/j.biotechadv.2007.07.001 · Cited by 420
Advanced application of stimuli-responsive drug delivery system for inflammatory arthritis treatment
Zhang, M., Hu, W., Cai, C., Wu, Y. Q., Li, J., & Dong, S. (2022) · Materials Today Bio · doi:10.1016/j.mtbio.2022.100223 · Cited by 405
Redox and NF-κB signaling in osteoarthritis
Lepetsos, P., Papavassiliou, K. A., & Papavassiliou, A. G. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.09.025 · Cited by 412
A current review of molecular mechanisms regarding osteoarthritis and pain
Lee, A. S., Ellman, M. B., Yan, D., Kroin, J. S., Cole, B. J., van Wijnen, A. J., & Im, H. (2013) · Gene · doi:10.1016/j.gene.2013.05.069 · Cited by 403
Rosenstein, E. D., Greenwald, R. A., Kushner, L. J., & Weissmann, G. (2004) · Inflammation · doi:10.1007/s10753-004-6641-z · Cited by 375
The Pathophysiology of Patellofemoral Pain
Dye, S. F. (2005) · Clinical Orthopaedics and Related Research · doi:10.1097/01.blo.0000172303.74414.7d · Cited by 359
Diabetes Is an Independent Predictor for Severe Osteoarthritis
Schett, G. A., Kleyer, A., Perricone, C., Sahinbegovic, E., Iagnocco, A., Zwerina, J., Lorenzini, R., Aschenbrenner, F., Berenbaum, F., D’Agostino, M. A., et al. (2012) · Diabetes Care · doi:10.2337/dc12-0924 · Cited by 357
Apoptosis signaling pathways in osteoarthritis and possible protective role of melatonin
Hosseinzadeh, A., Kamrava, S. K., Joghataei, M. T., Darabi, R., Shakeri‐Zadeh, A., Shahriari, M., Reiter, R. J., Ghaznavi, H., & Mehrzadi, S. (2016) · Journal of Pineal Research · doi:10.1111/jpi.12362 · Cited by 345
Degradative Action of Reactive Oxygen Species on Hyaluronan
Šoltés, L., Mendichi, R., Kogan, G., Schiller, J., Stankovská, M., & Arnhold, J. (2006) · Biomacromolecules · doi:10.1021/bm050867v · Cited by 329
Redox signalling and the inflammatory response in rheumatoid arthritis
Filippin, L. I., Vercelino, R., Marroni, N. P., & Xavier, R. M. (2008) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2008.03634.x · Cited by 328
Molecular mechanisms of cartilage destruction: Mechanics, inflammatory mediators, and aging collide
Loeser, R. F. (2006) · Arthritis & Rheumatism · doi:10.1002/art.21813 · Cited by 320
Wang, Y., Zhao, X., Lotz, M., Terkeltaub, R. A., & Liu‐Bryan, R. (2015) · Arthritis & Rheumatology · doi:10.1002/art.39182 · Cited by 309
Role, Metabolism, Chemical Modifications and Applications of Hyaluronan
Volpi, N., Schiller, J., Stern, R., & Šoltés, L. (2009) · Current Medicinal Chemistry · doi:10.2174/092986709788186138 · Cited by 279
Autophagy modulates osteoarthritis‐related gene expression in human chondrocytes
Sasaki, H., Takayama, K., Matsushita, T., Ishida, K., Kubo, S., Matsumoto, T., Fujita, N., Oka, S., Kurosaka, M., & Kuroda, R. (2012) · Arthritis & Rheumatism · doi:10.1002/art.34323 · Cited by 266
Superoxide dismutase downregulation in osteoarthritis progression and end-stage disease
Scott, J. L., Gabrielides, C., Davidson, R. K., Swingler, T. E., Clark, I. M., Wallis, G. A., Boot-Handford, R., Kirkwood, T. B. L., Talyor, R. W., & Young, D. A. (2010) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2009.119966 · Cited by 258
Regulation of chondrogenesis and chondrocyte differentiation by stress
Zuscik, M. J., Hilton, M. J., Zhang, X., Chen, D., & O’Keefe, R. J. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34174 · Cited by 254
Metabolic stress-induced joint inflammation and osteoarthritis
Courties, A., Gualillo, O., Berenbaum, F., & Sellam, J. (2015) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2015.05.016 · Cited by 249
Failure of cartilage regeneration: emerging hypotheses and related therapeutic strategies
Muthu, S., Korpershoek, J. V., Novais, E. J., Tawy, G., Hollander, A. P., & Martín, I. (2023) · Nature Reviews Rheumatology · doi:10.1038/s41584-023-00979-5 · Cited by 253
Liu‐Bryan, R., Pritzker, K. P. H., Firestein, G. S., & Terkeltaub, R. A. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.8.5016 · Cited by 242
The evaluation of oxidative stress in osteoarthritis
Zahan, O.-M., Şerban, O., Gherman, C. D., & Fodor, D. (2020) · Medicine and Pharmacy Reports · doi:10.15386/mpr-1422 · Cited by 245
Panahi, Y., Alishiri, G. H., Parvin, S., & Sahebkar, A. (2015) · Journal of Dietary Supplements · doi:10.3109/19390211.2015.1008611 · Cited by 229
The protective role of ROS in autoimmune disease
Hultqvist, M. H., Olsson, L. M., Gelderman, K. A., & Holmdahl, R. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.03.004 · Cited by 228
Reactive oxygen species induce chondrocyte hypertrophy in endochondral ossification
Morita, K., Miyamoto, T. K., Fujita, N., Kubota, Y., Ito, K., Takubo, K., Miyamoto, K., Ninomiya, K., Suzuki, T., Iwasaki, R., et al. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20062525 · Cited by 219
Chondrosenescence: Definition, hallmarks and potential role in the pathogenesis of osteoarthritis
Mobasheri, A., Matta, C., Zákány, R., & Musumeci, G. (2014) · Maturitas · doi:10.1016/j.maturitas.2014.12.003 · Cited by 225
Chondrocyte Senescence, Joint Loading and Osteoarthritis
Martin, J. A., Brown, T. D., Heiner, A. D., & Buckwalter, J. A. (2004) · Clinical Orthopaedics and Related Research · doi:10.1097/01.blo.0000143818.74887.b1 · Cited by 215
Increased oxidative stress and its relation with collagen metabolism in knee osteoarthritis
Altındağ, Ö., Erel, Ö., Aksoy, N., Selek, Ş., Çelık, H., & Karaoğlanoğlu, M. (2006) · Rheumatology International · doi:10.1007/s00296-006-0247-8 · Cited by 209
Mitochondrial Dysregulation of Osteoarthritic Human Articular Chondrocytes Analyzed by Proteomics
Ruíz‐Romero, C., Calamia, V., Mateos, J., Carreira, V., Martiénez-Gomariz, M., Fernaéndez, M., & Blanco, F. J. (2008) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m800292-mcp200 · Cited by 208
Oxidative damage to extracellular matrix and its role in human pathologies
Rees, M. D., Kennett, E. C., Whitelock, J. M., & Davies, M. J. (2008) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2008.03.016 · Cited by 207
Rosa, S. C., Gonçalves, J., Judas, F., Mobasheri, A., Lopes, C., & Mendes, A. F. (2009) · Arthritis Research & Therapy · doi:10.1186/ar2713 · Cited by 204
Jerosch, J. (2011) · International Journal of Rheumatology · doi:10.1155/2011/969012 · Cited by 209
Mitochondrial DNA variation and the pathogenesis of osteoarthritis phenotypes
Blanco, F. J., Valdes, A. M., & Rego‐Pérez, I. (2018) · Nature Reviews Rheumatology · doi:10.1038/s41584-018-0001-0 · Cited by 199
Regulation of inflammation signalling by resveratrol in human chondrocytes in vitro
Buhrmann, C., Keshishzadeh, N., Fischer, K., & Shakibaei, M. (2007) · Biochemical Pharmacology · doi:10.1016/j.bcp.2007.09.014 · Cited by 203
Diabetes-induced osteoarthritis: from a new paradigm to a new phenotype
Berenbaum, F. (2011) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2010.146399 · Cited by 197
The role of selenium metabolism and selenoproteins in cartilage homeostasis and arthropathies
Kang, D., Lee, J., Wu, C., Guo, X., Lee, B. J., Chun, J., & Kim, J. (2020) · Experimental & Molecular Medicine · doi:10.1038/s12276-020-0408-y · Cited by 192
Qiu, L.-N., Luo, Y., & Chen, X. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.05.003 · Cited by 191
Biological actions of curcumin on articular chondrocytes
Henrotin, Y. E., Clutterbuck, A. L., Allaway, D., Lodwig, E. M., Harris, P., Mathy-Hartert, M., Shakibaei, M., & Mobasheri, A. (2009) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2009.10.002 · Cited by 189
Self-citationBiochemical properties and regulation of cathepsin K activity
Lecaille, F., Brömme, D., & Lalmanach, G. (2007) · Biochimie · doi:10.1016/j.biochi.2007.08.011 · Cited by 183
Ramadan, G., Al-Kahtani, M. A., & El-Sayed, W. M. (2010) · Inflammation · doi:10.1007/s10753-010-9278-0 · Cited by 183
Yin, W., Park, J., & Loeser, R. F. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.056838 · Cited by 181
Knudson, C. B., & Knudson, W. (2004) · Clinical Orthopaedics and Related Research · doi:10.1097/01.blo.0000143804.26638.82 · Cited by 180
The Signaling Pathways Involved in Chondrocyte Differentiation and Hypertrophic Differentiation
Li, J., & Dong, S. (2016) · Stem Cells International · doi:10.1155/2016/2470351 · Cited by 170
Portal‐Núñez, S., Esbrit, P., Alcaraz, M. J., & Largo, R. (2015) · Biochemical Pharmacology · doi:10.1016/j.bcp.2015.12.012 · Cited by 170
Terkeltaub, R. A., Yang, B., Lotz, M., & Liu‐Bryan, R. (2011) · Arthritis & Rheumatism · doi:10.1002/art.30333 · Cited by 168
Biomechanical Influence of Cartilage Homeostasis in Health and Disease
Bader, D. L., Salter, D. M., & Chowdhury, T. T. (2011) · Arthritis · doi:10.1155/2011/979032 · Cited by 162
Lu, Y., & Wahl, L. M. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.8.5423 · Cited by 161
The role of reactive oxygen species in immunopathogenesis of rheumatoid arthritis.
Mirshafiey, A., & Mohsenzadegan, M. (2008) · PubMed · Cited by 158
Ostałowska, A., Birkner, E., Wiecha, M., Kasperczyk, S., Kasperczyk, A., Kapołka, D., & Zon-Giebel, A. (2005) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2005.08.009 · Cited by 157
Angiogenesis and blood vessel stability in inflammatory arthritis
Kennedy, A., Ng, C. T., Biniecka, M., Saber, T., Taylor, C. T., O'Sullivan, J. N., Veale, D. J., & Fearon, U. (2010) · Arthritis & Rheumatism · doi:10.1002/art.27287 · Cited by 159
Autologous liquid platelet rich fibrin: A novel drug delivery system
Miron, R. J., & Zhang, Y. (2018) · Acta Biomaterialia · doi:10.1016/j.actbio.2018.05.021 · Cited by 159
Kang, D., Shin, J., Cho, Y., Kim, H.-S., Gu, Y.-R., Kim, H., You, K. T., Chang, M. J., Chang, C. B., Kang, S., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aar6659 · Cited by 148
Radical-Scavenging and Subchondral Bone-Regenerating Nanomedicine for Osteoarthritis Treatment
Lu, H., Wei, J., Liu, K., Li, Z., Xu, T., Yang, D., Gao, Q., Xiang, H., Li, G., & Chen, Y. (2023) · ACS Nano · doi:10.1021/acsnano.3c01789 · Cited by 148
Laiguillon, M.-C., Courties, A., Houard, X., Auclair, M., Sautet, A., Capeau, J., Fève, B., Berenbaum, F., & Sellam, J. (2015) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2015.04.026 · Cited by 150
A New Arthritis Therapy with Oxidative Burst Inducers
Hultqvist, M. H., Olofsson, P., Gelderman, K. A., Holmberg, J., & Holmdahl, R. (2006) · PLoS Medicine · doi:10.1371/journal.pmed.0030348 · Cited by 146
Oxygen, nitric oxide and articular cartilage
Fermor, B., Christensen, S. E., Youn, I., Cernanec, J., Davies, C., & Weinberg, J. B. (2007) · European Cells and Materials · doi:10.22203/ecm.v013a06 · Cited by 145
Signaling transduction: target in osteoarthritis
Berenbaum, F. (2004) · Current Opinion in Rheumatology · doi:10.1097/01.bor.0000133663.37352.4a · Cited by 144
Kan, S., Duan, M., Liu, Y., Wang, C., & Xie, J. (2021) · Cartilage · doi:10.1177/19476035211063858 · Cited by 145
Shin, H., Hwang, H. J., Kang, K., & Lee, B. H. (2006) · Archives of Pharmacal Research · doi:10.1007/bf02974279 · Cited by 142
Reactive oxygen species induce Cox‐2 expression via TAK1 activation in synovial fibroblast cells
Onodera, Y., Teramura, T., Takehara, T., Shigi, K., & Fukuda, K. (2015) · FEBS Open Bio · doi:10.1016/j.fob.2015.06.001 · Cited by 140
Zhong, G., Yang, X., Jiang, X., Kumar, A., Long, H., Xie, J., Zheng, L. X., & Zhao, J. (2019) · Nanoscale · doi:10.1039/c9nr03060c · Cited by 138
Mathy-Hartert, M., Hogge, L., Sanchez, C., Deby-Dupont, G. P., Crielaard, J. M., & Henrotin, Y. E. (2008) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2007.10.009 · Cited by 138
Self-citationNutrition for Aging Cats and Dogs and the Importance of Body Condition
Laflamme, D. P. (2005) · Veterinary Clinics of North America Small Animal Practice · doi:10.1016/j.cvsm.2004.12.011 · Cited by 148
Anti-Inflammatory Properties of Drugs from saffron crocus
Poma, A. M., Fontecchio, G., Carlucci, G., & Chichiriccò, G. (2012) · Anti-Inflammatory & Anti-Allergy Agents in Medicinal Chemistry · doi:10.2174/187152312803476282 · Cited by 136
Henrotin, Y. E., Sanchez, C., & Balligand, M. H. (2004) · The Veterinary Journal · doi:10.1016/j.tvjl.2004.08.014 · Cited by 135
Self-citationDiminished mitochondrial DNA integrity and repair capacity in OA chondrocytes
Grishko, V. I., Ho, R., Wilson, G. L., & Pearsall, A. W. (2008) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2008.05.009 · Cited by 134
Biochemical basis of the effect of chondroitin sulphate on osteoarthritis articular tissues
Monfort, J., Pelletier, J.-P., García‐Giralt, N., & Pelletier, J. (2007) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2006.068882 · Cited by 129
Kemppainen, J. M., & Hollister, S. J. (2009) · Biomaterials · doi:10.1016/j.biomaterials.2009.09.041 · Cited by 126
Rotenone prevents impact‐induced chondrocyte death
Goodwin, W., Mccabe, D. J., Sauter, E., Reese, E., Walter, M., Buckwalter, J. A., & Martin, J. A. (2010) · Journal of Orthopaedic Research® · doi:10.1002/jor.21091 · Cited by 133
Wu, Y., Li, J., Zeng, Y., Pu, W., Mu, X., Sun, K., Peng, Y., & Shen, B. (2022) · International Journal of Oral Science · doi:10.1038/s41368-022-00187-z · Cited by 126
Peripheral blood neutrophil cytokine hyper-reactivity in chronic periodontitis
Ling, M. R., Chapple, I., & Matthews, J. B. (2015) · Innate Immunity · doi:10.1177/1753425915589387 · Cited by 121
Rosa, S. C., Rufino, A. T., Judas, F., Tenreiro, C., Lopes, M. C., & Mendes, A. F. (2011) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2011.02.004 · Cited by 118
Manoto, S. L., Maepa, M., & Motaung, K. S. (2016) · Saudi Journal of Biological Sciences · doi:10.1016/j.sjbs.2016.02.002 · Cited by 115
Targeting nitric oxide as a key modulator of sepsis, arthritis and pain
Spiller, F., Formiga, R. D. O., Coimbra, J. F. D. S., Alves-Filho, J. C., Cunha, T. M., & Cunha, F. Q. (2019) · Nitric Oxide · doi:10.1016/j.niox.2019.04.011 · Cited by 115
Liao, F., Li, Z., Wang, Y., Shi, B., Gong, Z., & Cheng, X. (2009) · Medical Hypotheses · doi:10.1016/j.mehy.2008.12.040 · Cited by 115
Zhao, X., Petursson, F., Viollet, B., Lotz, M., Terkeltaub, R. A., & Liu‐Bryan, R. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38791 · Cited by 117
Inflammation and intracellular metabolism: new targets in OA
Liu‐Bryan, R. (2015) · Osteoarthritis and Cartilage · doi:10.1016/j.joca.2014.12.016 · Cited by 116
Pathophysiological landscape of osteoarthritis
Kulkarni, P., Märtson, A., Vidya, R., Chitnavis, S., & Harsulkar, A. (2020) · Advances in clinical chemistry · doi:10.1016/bs.acc.2020.04.002 · Cited by 118
Munroe, M. E., Arbiser, J. L., & Bishop, G. A. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.179.2.753 · Cited by 112
Ruíz‐Romero, C., López-Armada, M. J., & Blanco, F. J. (2005) · PROTEOMICS · doi:10.1002/pmic.200402106 · Cited by 112
Kogan, G., Staško, A., Bauerová, K., Polovka, M., Šoltés, L., Brezová, V., Navarová, J., & Mihalová, D. (2005) · Carbohydrate Polymers · doi:10.1016/j.carbpol.2005.02.010 · Cited by 111
Zhao, W., Wang, H., Han, Y., Wang, H., Sun, Y., & Zhang, H. (2020) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.0c14805 · Cited by 109
The role of nitric oxide in osteoarthritis
Vuolteenaho, K., Moilanen, T. P. S., Knowles, R. G., & Moilanen, E. (2007) · Scandinavian Journal of Rheumatology · doi:10.1080/03009740701483014 · Cited by 112
Oxidative damage in synovial tissue is associated with in vivo hypoxic status in the arthritic joint
Biniecka, M., Kennedy, A., Fearon, U., Ng, C. T., Veale, D. J., & O'Sullivan, J. N. (2009) · Annals of the Rheumatic Diseases · doi:10.1136/ard.2009.111211 · Cited by 108
The role of SIRT3-mediated mitochondrial homeostasis in osteoarthritis
He, Y., Wu, Z., Xu, L., Xu, K., Chen, Z., Ran, J., & Wu, L. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03497-9 · Cited by 106
Oxidative status in rheumatoid arthritis
Özkan, Y., Yardým-Akaydýn, S., Sepici, A., Keskin, E., Sepici, V., & Şimşek, B. (2006) · Clinical Rheumatology · doi:10.1007/s10067-006-0244-z · Cited by 106
Reactive oxygen species and NADPH oxidase 4 involvement in osteoarthritis
Drevet, S., Gavazzi, G., Grange, L., Dupuy, C., & Lardy, B. (2018) · Experimental Gerontology · doi:10.1016/j.exger.2018.07.007 · Cited by 107
Innate Immune Responses and Osteoarthritis
Kalaitzoglou, E., Griffin, T. M., & Humphrey, M. (2017) · Current Rheumatology Reports · doi:10.1007/s11926-017-0672-6 · Cited by 98
Loeser, R. F., Gandhi, U., Long, D. L., Yin, W., & Chubinskaya, S. (2014) · Arthritis & Rheumatology · doi:10.1002/art.38641 · Cited by 104
Metadata
- Authors
- Henrotin, Y. E., Bruckner, P., & Pujol, J.-P. L.
- Affiliations
- University of Liège (BE)
- Université de Caen Normandie (FR)
- Corresponding author
- Henrotin, Y.E
- ORCID
- Henrotin, Y.E
- Venue
- Osteoarthritis and Cartilage
- Publisher
- Elsevier BV
- Published
- 2003-10
- Volume
- 11
- Issue
- 10
- Pages
- 747-755
- ISSN
- 1063-4584 (ISSN-L)
- OpenAlex
- W2044924856
- Cited by
- 740
- References
- 82
- Citations by year
- 2026: 15 · 2025: 29 · 2024: 30 · 2023: 35 · 2022: 34 · 2021: 37 · 2020: 39 · 2019: 35 · 2018: 45 · 2017: 36 · 2016: 32 · 2015: 33 · 2014: 35 · 2013: 34 · 2012: 45
- FWCI
- 3.61
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Osteoarthritis and Cartilage (publishedVersion)
- PubMed (publishedVersion)
- ORBi (University of Liège) (submittedVersion)
- Funders
- UCB Pharma
- Topics
- Health Sciences › Medicine › Rheumatology › Osteoarthritis Treatment and Mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- reactive oxygen species, cartilage degeneration, cartilage homeostasis, nitric oxide, peroxynitrite, superoxide, redox signaling, joint inflammation, synovium, matrix metalloproteinases, apoptosis, antioxidant therapy, osteoarthritis, rheumatoid arthritis
- MeSH terms
- Cartilage, Articular, Extracellular Matrix, Homeostasis, Humans, Osteoarthritis, Oxidation-Reduction, Synovial Membrane, Signal Transduction, Cytokines, Apoptosis, Reactive Oxygen Species, Chondrocytes, Metalloproteases
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