Genetic deletion of p66 Shc adaptor protein prevents hyperglycemia-induced endothelial dysfunction and oxidative stress
Open accessAbstract
Increased production of reactive oxygen species (ROS) and loss of endothelial NO bioavailability are key features of vascular disease in diabetes mellitus. The p66 Shc adaptor protein controls cellular responses to oxidative stress. Mice lacking p66 Shc (p66 Shc−/− ) have increased resistance to ROS and prolonged life span. The present work was designed to investigate hyperglycemia-associated changes in endothelial function in a model of insulin-dependent diabetes mellitus p66 Shc−/− mouse. p66 Shc−/− and wild-type (WT) mice were injected with citrate buffer (control) or made diabetic by an i.p. injection of 200 mg of streptozotocin per kg of body weight. Streptozotocin-treated p66 Shc−/− and WT mice showed a similar increase in blood glucose. However, significant differences arose with respect to endothelial dysfunction and oxidative stress. WT diabetic mice displayed marked impairment of endothelium-dependent relaxations, increased peroxynitrite (ONOO − ) generation, nitrotyrosine expression, and lipid peroxidation as measured in the aortic tissue. In contrast, p66 Shc−/− diabetic mice did not develop these high-glucose-mediated abnormalities. Furthermore, protein expression of the antioxidant enzyme heme oxygenase 1 and endothelial NO synthase were up-regulated in p66 Shc−/− but not in WT mice. We report that p66 Shc−/− mice are resistant to hyperglycemia-induced, ROS-dependent endothelial dysfunction. These data suggest that p66 Shc adaptor protein is part of a signal transduction pathway relevant to hyperglycemia vascular damage and, hence, may represent a novel therapeutic target against diabetic vascular complications.
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
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?
p66Shc activation is involved in adipogenesis, insulin resistance, and cardiovascular complications associated with diabetes mellitus.
“Additional work has revealed that p66Shc activation is involved in adipogenesis, insulin resistance and cardiovascular complications associated with diabetes mellitus187–189.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [187]
p66Shc−/− mice are protected against streptozotocin-induced diabetic cardiomyopathy and diabetes-induced vascular endothelial dysfunction and oxidative stress.
“Consequently, work has shown that p66Shc−/− mice are protected against streptozotocin-induced diabetic cardiomyopathy191, diabetes mellitus-induced vascular endothelial dysfunction and oxidative stress187.”
From Mitochondrial and metabolic dysfunction in ageing and age-related diseases (2022) · cites this paper as [187]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Oxyl radicals, redox-sensitive signalling cascades and antioxidants
Genestra, M. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.04.009 · Cited by 4,930 · see citing works
Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage
Nishikawa, T., Edelstein, D., Du, X. L., Yamagishi, S.-I., Matsumura, T., Kaneda, Y., Yorek, M. A., Beebe, D., Oates, P. J., Hammes, H.-P., et al. (2000) · Nature · doi:10.1038/35008121 · Cited by 4,277 · see citing works
Bilirubin Is an Antioxidant of Possible Physiological Importance
Stocker, R., Yamamoto, Y., McDonagh, A. F., Glazer, A. N., & Ames, B. N. (1987) · Science · doi:10.1126/science.3029864 · Cited by 3,502 · see citing works
The clinical implications of endothelial dysfunction
Widlansky, M. E., Gokce, N., Keaney, J. F., & Vita, J. A. (2003) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(03)00994-x · Cited by 1,749 · see citing works
The p66shc adaptor protein controls oxidative stress response and life span in mammals
Migliaccio, E., Giorgio, M., Mele, S., Pelicci, G., Reboldi, P., Pandolfi, P. P., Lanfrancone, L., & Pelicci, P. G. (1999) · Nature · doi:10.1038/46311 · Cited by 1,712 · see citing works
Self-citationCreager, M. A., Lüscher, T. F., of, P. W. T. A., Cosentino, F., & Beckman, J. A. (2003) · Circulation · doi:10.1161/01.cir.0000091257.27563.32 · Cited by 1,654 · see citing works
Self-citationHofstra, L., Tordoir, J. H. M., Kitslaar, P. J. E. H. M., Hoeks, A. P. G., & Daemen, M. J. A. P. (1996) · PubMed · doi:10.1161/01.cir.94.6.1283 · Cited by 1,603 · see citing works
Oxidative stress causes enhanced endothelial cell injury in human heme oxygenase-1 deficiency
Yachie, A., Niida, Y., Wada, T., Igarashi, N., Kaneda, H., Toma, T., Ohta, K., Kasahara, Y., & Koizumi, S. (1999) · Journal of Clinical Investigation · doi:10.1172/jci4165 · Cited by 1,256 · see citing works
Giorgio, M., Migliaccio, E., Orsini, F., Paolucci, D., Moroni, M., Contursi, C., Pelliccia, G., Luzi, L., Minucci, S., Marcaccio, M., et al. (2005) · Cell · doi:10.1016/j.cell.2005.05.011 · Cited by 1,176 · see citing works
Self-citationImpaired endothelium-dependent vasodilation in patients with insulin-dependent diabetes mellitus.
Johnstone, M. T., Creager, S. J., Scales, K. M., Cusco, J. A., Lee, B. K., & Creager, M. A. (1993) · Circulation · doi:10.1161/01.cir.88.6.2510 · Cited by 1,117 · see citing works
Endothelial Function: Cardiac Events
Lerman, A., & Zeiher, A. M. (2005) · Circulation · doi:10.1161/01.cir.0000153339.27064.14 · Cited by 1,096 · see citing works
McVeigh, G. E., Brennan, G. M., Johnston, G. D., McDermott, B. J., McGrath, L. T., Henry, W. R., Andrews, J. W., & Hayes, J. R. (1992) · Diabetologia · doi:10.1007/bf00429099 · Cited by 916 · see citing works
Ting, H. H., Timimi, F. K., Boles, K., Creager, S. J., Ganz, P., & Creager, M. A. (1996) · Journal of Clinical Investigation · doi:10.1172/jci118394 · Cited by 869 · see citing works
Redox Regulation of Forkhead Proteins Through a <i>p66shc</i> -Dependent Signaling Pathway
Nemoto, S., & Finkel, T. (2002) · Science · doi:10.1126/science.1069004 · Cited by 818 · see citing works
Cosentino, F., Hishikawa, K., Katušić, Z. S., & Lüscher, T. F. (1997) · Circulation · doi:10.1161/01.cir.96.1.25 · Cited by 762 · see citing works
Self-citationSuperoxide and peroxynitrite inatherosclerosis.
White, C. R., Brock, T. A., Chang, L. Y., Crapo, J. D., BRISCOE, P. M., Ku, D. D., Bradley, W. A., Gianturco, S. H., Gore, J. Z., & Freeman, B. Α. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.3.1044 · Cited by 685 · see citing works
Enhanced Peroxynitrite Formation Is Associated with Vascular Aging
van der Loo, B., Labugger, R., Skepper, J. N., Bachschmid, M. M., Kilo, J., Powell, J. M., Palacios‐Callender, M., Erusalimsky, J. D., Quaschning, T., Maliñski, T., et al. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.12.1731 · Cited by 674 · see citing works
Self-citationTrinei, M., Giorgio, M., Cicalese, A., Barozzi, S., Ventura, A., Migliaccio, E., Milia, E., Padura, I. M., Raker, V. A., Maccarana, M., et al. (2002) · Oncogene · doi:10.1038/sj.onc.1205513 · Cited by 436 · see citing works
Self-citationCosentino, F., Eto, M., Paolis, P. D., van der Loo, B., Bachschmid, M. M., Ullrich, V., Kouroedov, A., Gatti, C., Joch, H., Volpe, M., et al. (2003) · Circulation · doi:10.1161/01.cir.0000051367.92927.07 · Cited by 419 · see citing works
Self-citationNapoli, C., Martin-Padura, I., de Nigris, F., Giorgio, M., Mansueto, G., Somma, P., Condorelli, M., Sica, G., De Rosa, G., & Pelicci, P. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0336359100 · Cited by 380 · see citing works
Self-citationProtein Nitration in Cardiovascular Diseases
Turko, I. V., & Murad, F. (2002) · Pharmacological Reviews · doi:10.1124/pr.54.4.619 · Cited by 372 · see citing works
Induction of Heme Oxygenase-1 Suppresses Venular Leukocyte Adhesion Elicited by Oxidative Stress
Hayashi, S., Takamiya, R., Yamaguchi, T., Matsumoto, K., Tojo, S. J., Tamatani, T., Kitajima, M., Makino, N., Ishimura, Y., & Suematsu, M. (1999) · Circulation Research · doi:10.1161/01.res.85.8.663 · Cited by 350 · see citing works
Deletion of p66 <sup>shc</sup> Gene Protects Against Age-Related Endothelial Dysfunction
Francia, P., delli Gatti, C., Bachschmid, M., Martin-Padura, I., Savoia, C., Migliaccio, E., Pelicci, P. G., Schiavoni, M., Lüscher, T. F., Volpe, M., et al. (2004) · Circulation · doi:10.1161/01.cir.0000147731.24444.4d · Cited by 298 · see citing works
Self-citationForesti, R., Clark, J., Green, C. J., & Motterlini, R. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.29.18411 · Cited by 294 · see citing works
Orsini, F., Migliaccio, E., Moroni, M., Contursi, C., Raker, V. A., Piccini, D., Martín-Padura, I., Pelliccia, G., Trinei, M., Bono, M., et al. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m401844200 · Cited by 293 · see citing works
Self-citationNath, K. A., Haggard, J. J., Croatt, A. J., Grande, J. P., Poss, K. D., & Alam, J. (2000) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)65024-9 · Cited by 263 · see citing works
Not all Shc's roads lead to Ras
Bonfini, L., Migliaccio, E., Pelicci, G., Lanfrancone, L., & Pelicci, P. G. (1996) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(96)10033-5 · Cited by 240 · see citing works
Self-citationMenini, S., Amadio, L., Oddi, G., Ricci, P. C., Pesce, C. M., Pugliese, F. R., Giorgio, M., Migliaccio, E., Pelicci, P. G., Iacobini, C., et al. (2006) · Diabetes · doi:10.2337/db05-1477 · Cited by 183 · see citing works
Self-citationAbraham, N. G., Kushida, T., McClung, J. A., Weiss, M. B., Quan, S., Lafaro, R., Darżynkiewicz, Z., & Wolin, M. S. (2003) · Circulation Research · doi:10.1161/01.res.0000091828.36599.34 · Cited by 150 · see citing works
Absence of Heme Oxygenase-1 Exacerbates Myocardial Ischemia/Reperfusion Injury in Diabetic Mice
Liu, X., Wei, J., Peng, D. H., Layne, M. D., & Yet, S. (2005) · Diabetes · doi:10.2337/diabetes.54.3.778 · Cited by 145 · see citing works
Pagnin, E., Fadini, G., de Toni, R., Tiengo, A., Calò, L., & Avogaro, A. (2005) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2004-1283 · Cited by 127 · see citing works
p66 ShcA Modulates Tissue Response to Hindlimb Ischemia
Zaccagnini, G., Martelli, F., Fasanaro, P., Magenta, A., Gaetano, C., Carlo, A. D., Biglioli, P., Giorgio, M., Martín-Padura, I., Pelicci, P. G., et al. (2004) · Circulation · doi:10.1161/01.cir.0000129309.58874.0f · Cited by 110 · see citing works
Self-citationKurosawa, T., Itoh, F., Nozaki, A., Nakano, Y., Katsuda, S.-I., Osakabe, N., Tsubone, H., Kondo, K. N., & Itakura, H. (2005) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2004.12.003 · Cited by 84 · see citing works
Endothelial dysfunction in a model of hyperglycemia and hyperinsulinemia
Pieper, G. M., Meier, D. A., & Hager, S. R. (1995) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1995.269.3.h845 · Cited by 83 · see citing works
Heme oxygenase-1 prevents superoxide anion-associated endothelial cell sloughing in diabetic rats
Quan, S., Kaminski, P. M., Yang, L. M., Morita, T., Inaba, M., Ikehara, S., Goodman, A. I., Wolin, M. S., & Abraham, N. G. (2004) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2004.01.086 · Cited by 78 · see citing works
Goodman, A. I., Chander, P. N., Rezzani, R., Schwartzman, M. L., Regan, R. F., Rodella, L. F., Türkseven, S., Lianos, E. A., Dennery, P. A., & Abraham, N. G. (2006) · Journal of the American Society of Nephrology · doi:10.1681/asn.2004121082 · Cited by 78 · see citing works
Contribution of apoptotic cell death to renal injury
Ortíz, A., Lorz, C., Justo, P., Catalan, M. P., & Egido, J. (2001) · Journal of Cellular and Molecular Medicine · doi:10.1111/j.1582-4934.2001.tb00135.x · Cited by 68 · see citing works
Matsuoka, T., Wada, J., Hashimoto, I., Zhang, Y., Eguchi, J., Ogawa, N., Shikata, K., Kanwar, Y. S., & Makino, H. (2005) · Diabetes · doi:10.2337/diabetes.54.10.2882 · Cited by 59 · see citing works
Postoperative sensitivity in Class I composite resin restorations in vivo.
Casselli, D. S. M., & Martins, L. R. M. (2006) · PubMed · Cited by 48 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- [8]Bonfini L, Migliaccio E, Pelicci G, Lanfrancone L, Pelicci PG. Trends Biochem Sci. 1996;21:257–261. [PubMed] [Google Scholar]
- [37]Casselli DS, Martins LR. J Adhes Dent. 2006;8:53–58. [PubMed] [Google Scholar]
Cited by
Sorted by citations
Authors Task Force Members, Rydén, L., Grant, P. J., Anker, S. D., Berne, C., Cosentino, F., Danchin, N., Deaton, C., Escaned, J., Hammes, H., et al. (2013) · European Heart Journal · doi:10.1093/eurheartj/eht108 · Cited by 1,958 · see citing works
Self-citationDiabetes and vascular disease: pathophysiology, clinical consequences, and medical therapy: part I
Paneni, F., Beckman, J. A., Creager, M. A., & Cosentino, F. (2013) · European Heart Journal · doi:10.1093/eurheartj/eht149 · Cited by 1,420 · see citing works
Self-citationManolagas, S. C. (2010) · Endocrine Reviews · doi:10.1210/er.2009-0024 · Cited by 1,210 · see citing works
Mitochondrial and metabolic dysfunction in ageing and age-related diseases
Amorim, J. A., Coppotelli, G., Rolo, A. P., Palmeira, C. M., Ross, J. M., & Sinclair, D. A. (2022) · Nature Reviews Endocrinology · doi:10.1038/s41574-021-00626-7 · Cited by 990 · see citing works
Kalogeris, T. J., Bao, Y., & Korthuis, R. J. (2014) · Redox Biology · doi:10.1016/j.redox.2014.05.006 · Cited by 719 · see citing works
Mitochondria-Ros Crosstalk in the Control of Cell Death and Aging
Marchi, S., Giorgi, C., Suski, J. M., Agnoletto, C., Bononi, A., Bonora, M., Marchi, E. D., Missiroli, S., Patergnani, S., Poletti, F., et al. (2011) · Journal of Signal Transduction · doi:10.1155/2012/329635 · Cited by 639 · see citing works
Impact of Oxidative Stress on the Heart and Vasculature
Münzel, T. F., Camici, G. G., Maack, C., Bonetti, N. R., Fuster, V., & Kovacic, J. C. (2017) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2017.05.035 · Cited by 623 · see citing works
Self-citationEelen, G., de Zeeuw, P., Treps, L., Harjes, U., Wong, B. W., & Carmeliet, P. (2017) · Physiological Reviews · doi:10.1152/physrev.00001.2017 · Cited by 591 · see citing works
Cardiovascular disease risk in type 2 diabetes mellitus: insights from mechanistic studies
Mazzone, T., Chait, A., & Plutzky, J. (2008) · The Lancet · doi:10.1016/s0140-6736(08)60768-0 · Cited by 545 · see citing works
Mitochondria and Endothelial Function
Kluge, M. A., Fetterman, J. L., & Vita, J. A. (2013) · Circulation Research · doi:10.1161/circresaha.111.300233 · Cited by 508 · see citing works
Mitochondrial oxidative stress in aging and healthspan
Dai, D., Chiao, Y. A., Marcinek, D. J., Szeto, H. H., & Rabinovitch, P. S. (2014) · Longevity & Healthspan · doi:10.1186/2046-2395-3-6 · Cited by 481 · see citing works
Ageing, metabolism and cardiovascular disease
Costantino, S., Paneni, F., & Cosentino, F. (2015) · The Journal of Physiology · doi:10.1113/jp270538 · Cited by 465 · see citing works
Self-citationMolecular Biology of Atherosclerosis
Hopkins, P. N. (2013) · Physiological Reviews · doi:10.1152/physrev.00004.2012 · Cited by 456 · see citing works
Mitochondrial Function, Biology, and Role in Disease
Murphy, E., Ardehali, H., Balaban, R. S., DiLisa, F., Dorn, G. W., Kitsis, R. N., Otsu, K., Ping, P., Rizzuto, R., Sack, M. N., et al. (2016) · Circulation Research · doi:10.1161/res.0000000000000104 · Cited by 459 · see citing works
Mitochondria and Cardiovascular Aging
Dai, D., Rabinovitch, P. S., & Ungvari, Z. I. (2012) · Circulation Research · doi:10.1161/circresaha.111.246140 · Cited by 435 · see citing works
Thomas, S. R., Witting, P. K., & Drummond, G. R. (2008) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2027 · Cited by 383 · see citing works
WNT Signaling in Cardiac and Vascular Disease
Foulquier, S., Daskalopoulos, E. P., Lluri, G., Hermans, K. C. M., Deb, A., & Blankesteijn, W. M. (2017) · Pharmacological Reviews · doi:10.1124/pr.117.013896 · Cited by 344 · see citing works
Reactive oxygen species: key regulators in vascular health and diseases
Chen, Q., Wang, Q., Zhu, J., Xiao, Q., & Zhang, L. (2017) · British Journal of Pharmacology · doi:10.1111/bph.13828 · Cited by 344 · see citing works
Manolagas, S. C., & Almeida, M. (2007) · Molecular Endocrinology · doi:10.1210/me.2007-0259 · Cited by 330 · see citing works
Giorgi, C., Missiroli, S., Patergnani, S., Duszyński, J., Wieckowski, M. R., & Pinton, P. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.6223 · Cited by 332 · see citing works
Reactive Nitrogen Species: Molecular Mechanisms and Potential Significance in Health and Disease
Martínez, M. C., & Andriantsitohaina, R. (2008) · Antioxidants and Redox Signaling · doi:10.1089/ars.2007.1993 · Cited by 329 · see citing works
Wang, C., Wu, S., Wu, Y., & Wei, Y. (2013) · Experimental Biology and Medicine · doi:10.1177/1535370213493069 · Cited by 315 · see citing works
Varga, Z. V., Giricz, Z., Liaudet, L., Haskó, G., Ferdinandy, P., & Pacher, P. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.06.030 · Cited by 288 · see citing works
Scioli, M. G., Storti, G., D’Amico, F., Rodríguez Guzmán, R., Centofanti, F., Doldo, E., Céspedes Miranda, E. M., & Orlandi, A. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9061995 · Cited by 281 · see citing works
Zhou, S., Chen, H., Wan, Y.-Z., Zhang, Q.-J., Wei, Y.-S., Huang, S., Liu, J., Lu, Y., Zhang, Z., Yang, R., et al. (2011) · Circulation Research · doi:10.1161/circresaha.111.243592 · Cited by 273 · see citing works
Targeting Age-Related Pathways in Heart Failure
Li, H., Hastings, M. H., Rhee, J., Trager, L. E., Roh, J. D., & Rosenzweig, A. (2020) · Circulation Research · doi:10.1161/circresaha.119.315889 · Cited by 270 · see citing works
Gioscia‐Ryan, R. A., LaRocca, T. J., Sindler, A. L., Zigler, M. C., Murphy, M. P., & Seals, D. R. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2013.268680 · Cited by 263 · see citing works
Mitochondrial ROS Formation in the Pathogenesis of Diabetic Cardiomyopathy
Kaludercic, N., & Lisa, F. D. (2020) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2020.00012 · Cited by 264 · see citing works
Paneni, F., Mocharla, P. S., Akhmedov, A. T., Costantino, S., Osto, E., Volpe, M., Lüscher, T. F., & Cosentino, F. (2012) · Circulation Research · doi:10.1161/circresaha.112.266593 · Cited by 256 · see citing works
Self-citationMonoamine oxidases as sources of oxidants in the heart
Kaludercic, N., Mialet‐Perez, J., Paolocci, N., Parini, A., & Lisa, F. D. (2014) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.12.032 · Cited by 251 · see citing works
Molecular mechanism of endothelial and vascular aging: implications for cardiovascular disease
Camici, G. G., Savarese, G., Akhmedov, A., & Lüscher, T. F. (2015) · European Heart Journal · doi:10.1093/eurheartj/ehv587 · Cited by 223 · see citing works
Self-citationCostantino, S., Paneni, F., Battista, R., Castello, L., Capretti, G., Chiandotto, S., Tanese, L., Russo, G., Pitocco, D., Lanza, G. A., et al. (2017) · Diabetes · doi:10.2337/db17-0294 · Cited by 188 · see citing works
Self-citationTherapeutic potential of targeting oxidative stress in diabetic cardiomyopathy
Byrne, N. J., Rajasekaran, N. S., Abel, E. D., & Bugger, H. (2021) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2021.03.046 · Cited by 175 · see citing works
Final Common Molecular Pathways of Aging and Cardiovascular Disease
Cosentino, F., Francia, P., Camici, G. G., Pelicci, P. G., Volpe, M., & Lüscher, T. F. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.156059 · Cited by 169 · see citing works
Self-citationThe Role of Oxidative Stress in Cardiovascular Aging and Cardiovascular Diseases
Izzo, C., Vitillo, P., Pietro, P. D., Visco, V., Strianese, A., Virtuoso, N., Ciccarelli, M., Galasso, G., Carrizzo, A., & Vecchione, C. (2021) · Life · doi:10.3390/life11010060 · Cited by 167 · see citing works
Insulin Resistance, Diabetes, and Cardiovascular Risk
Paneni, F., Costantino, S., & Cosentino, F. (2014) · Current Atherosclerosis Reports · doi:10.1007/s11883-014-0419-z · Cited by 160 · see citing works
Self-citationMitochondria in endothelial cells: Sensors and integrators of environmental cues
Caja, S., & Enrı́quez, J. A. (2017) · Redox Biology · doi:10.1016/j.redox.2017.04.021 · Cited by 150 · see citing works
Teodoro, J. S., Nunes, S., Rolo, A. P., Reis, F., & Palmeira, C. M. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2018.01857 · Cited by 149 · see citing works
The Promise of Cell-Based Therapies for Diabetic Complications
Jarajapu, Y. P. R., & Grant, M. B. (2010) · Circulation Research · doi:10.1161/circresaha.109.213140 · Cited by 142 · see citing works
Bock, F. M., Shahzad, K., Wang, H., Stoyanov, S., Wolter, J., Dong, W., Pelicci, P. G., Kashif, M., Ranjan, S., Schmidt, S., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1218667110 · Cited by 141 · see citing works
Self-citationOxidative stress in chronic vascular disease: From prediction to prevention
Santilli, F., D’Ardes, D., & Davı̀, G. (2015) · Vascular Pharmacology · doi:10.1016/j.vph.2015.09.003 · Cited by 140 · see citing works
D’Onofrio, N., Servillo, L., Giovane, A., Casale, R., Vitiello, M., Marfella, R., Paolisso, G., & Balestrieri, M. L. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.04.013 · Cited by 135 · see citing works
Oxidative Stress in Cardiovascular Diseases and Obesity: Role of p66Shc and Protein Kinase C
Marchi, E. D., Baldassari, F., Bononi, A., Wieckowski, M. R., & Pinton, P. (2013) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2013/564961 · Cited by 132 · see citing works
Yamagishi, S., Fukami, K., & Matsui, T. (2015) · Cardiovascular Diabetology · doi:10.1186/s12933-015-0176-5 · Cited by 125 · see citing works
The Role of Mitochondrial Reactive Oxygen Species in Cardiovascular Injury and Protective Strategies
Muntean, D. M., Sturza, A., Dănilă, M. D., Borza, C., Duicu, O., & Mornoş, C. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/8254942 · Cited by 122 · see citing works
wang, L., Quan, N., Sun, W., Chen, X., Cates, C. A., Rousselle, T. V., Zhou, X., Zhao, X., & Li, J. (2018) · Cardiovascular Research · doi:10.1093/cvr/cvy033 · Cited by 122 · see citing works
Wils, J., Favre, J., & Bellien, J. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.10.014 · Cited by 114 · see citing works
Kumar, S., Kim, Y., Vikram, A., Naqvi, A., Li, Q., Kassan, M., Kumar, V., Bachschmid, M. M., Jacobs, J. S., Kumar, A., et al. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1614112114 · Cited by 117 · see citing works
Self-citationMunasinghe, P. E., Riu, F., Dixit, P., Edamatsu, M., Saxena, P., Hamer, N. S. J., Galvin, I. F., Bunton, R. W., Lequeux, S., Jones, G. T., et al. (2015) · International Journal of Cardiology · doi:10.1016/j.ijcard.2015.08.111 · Cited by 112 · see citing works
Nitric Oxide, Oxidative Stress, and p66Shc Interplay in Diabetic Endothelial Dysfunction
Magenta, A., Greco, S., Capogrossi, M. C., Gaetano, C., & Martelli, F. (2014) · BioMed Research International · doi:10.1155/2014/193095 · Cited by 110 · see citing works
Khullar, M., Al‐Shudiefat, A. A., Lüdke, A., Binepal, G., & Singal, P. K. (2010) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y10-016 · Cited by 110 · see citing works
Mitochondria and vascular pathology
Lisa, F. D., Kaludercic, N., Carpi, A., Menabò, R., & Giorgio, M. (2009) · Pharmacological Reports · doi:10.1016/s1734-1140(09)70014-3 · Cited by 104 · see citing works
Signaling of Reactive Oxygen and Nitrogen Species in Diabetes Mellitus
Afanasʹev, I. B. (2010) · Oxidative Medicine and Cellular Longevity · doi:10.4161/oxim.3.6.14415 · Cited by 100 · see citing works
Paneni, F., Costantino, S., Castello, L., Battista, R., Capretti, G., Chiandotto, S., D’Amario, D., Scavone, G., Villano, A., Rustighi, A., et al. (2014) · European Heart Journal · doi:10.1093/eurheartj/ehu179 · Cited by 101 · see citing works
Self-citationXiong, Y., Liu, T., WANG, S., Chi, H., Chen, C., & Zheng, J. (2016) · Gene · doi:10.1016/j.gene.2016.10.011 · Cited by 99 · see citing works
Protein kinase C in enhanced vascular tone in diabetes mellitus
Kizub, I. V., Klymenko, K., & Soloviev, A. I. (2014) · International Journal of Cardiology · doi:10.1016/j.ijcard.2014.04.117 · Cited by 99 · see citing works
NADPH Oxidase Activation: A Mechanism of Hypertension-Associated Erectile Dysfunction
Jin, L., Lagoda, G. A., Leite, R., Webb, R. C., & Burnett, A. L. “. (2008) · The Journal of Sexual Medicine · doi:10.1111/j.1743-6109.2007.00733.x · Cited by 98 · see citing works
Shi, Y., Cosentino, F., Camici, G., Akhmedov, A., Vanhoutte, P., Tanner, F., & Lüscher, T. (2011) · Arteriosclerosis, Thrombosis and Vascular Biology · doi:10.1161/atvbaha.111.229260 · Cited by 79 · see citing works
Self-citationMitochondrial Injury and Protection in Ischemic Pre- and Postconditioning
Lisa, F. D., Canton, M., Carpi, A., Kaludercic, N., Menabò, R., Menazza, S., & Semenzato, M. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2010.3375 · Cited by 91 · see citing works
Epigenetics and Immunometabolism in Diabetes and Aging
Guzik, T. J., & Cosentino, F. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7299 · Cited by 93 · see citing works
Self-citationFadini, G. P., Albiero, M., Menegazzo, L., Boscaro, E., Pagnin, E., Iori, E., Cosma, C., Lapolla, A., Pengo, V., Stendardo, M., et al. (2010) · Diabetes · doi:10.2337/db09-1727 · Cited by 89 · see citing works
Self-citationTrinei, M., Berniakovich, I., Beltrami, E., Migliaccio, E., Fassina, A., Pelicci, P. G., & Giorgio, M. (2009) · Aging · doi:10.18632/aging.100057 · Cited by 88 · see citing works
Self-citationOsto, E., Matter, C. M., Kouroedov, A., Maliñski, T., Bachschmid, M. M., Camici, G. G., Kılıç, Ü., Stallmach, T., Borén, J., Iliceto, S., et al. (2008) · Circulation · doi:10.1161/circulationaha.108.765032 · Cited by 88 · see citing works
Self-citationLuo, Z., Yao, J., Wang, Z., & Xu, J. (2023) · Journal of Translational Medicine · doi:10.1186/s12967-023-04286-1 · Cited by 87 · see citing works
Targeting SIRT1 Rescues Age- and Obesity-Induced Microvascular Dysfunction in Ex Vivo Human Vessels
Mengozzi, A., Costantino, S., Paneni, F., Duranti, E., Nannipieri, M., Mancini, R., Lai, M., Rocca, V. L., Puxeddu, I., Antonioli, L., et al. (2022) · Circulation Research · doi:10.1161/circresaha.122.320888 · Cited by 87 · see citing works
Mitochondrial longevity pathways
Raffaello, A., & Rizzuto, R. (2010) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2010.10.007 · Cited by 87 · see citing works
Kaludercic, N., & Giorgio, V. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/3869610 · Cited by 88 · see citing works
Novel role of p66Shc in ROS-dependent VEGF signaling and angiogenesis in endothelial cells
Oshikawa, J., Kim, S.-J., Furuta, E., Caliceti, C., Chen, G., McKinney, R. D., Kuhr, F., Levitan, I., Fukai, T., & Ushio‐Fukai, M. (2011) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00739.2011 · Cited by 85 · see citing works
Spescha, R. D., Shi, Y., Wegener, S., Keller, S., Weber, B., Wyss, M. T., Lauinger, N. D., Tabatabai, G., Paneni, F., Cosentino, F., et al. (2012) · European Heart Journal · doi:10.1093/eurheartj/ehs331 · Cited by 83 · see citing works
Self-citationP66Shc-Induced MicroRNA-34a Causes Diabetic Endothelial Dysfunction by Downregulating Sirtuin1
Li, Q., Kim, Y., Vikram, A., Kumar, S., Kassan, M., Gabani, M. H., Lee, S. K., Jacobs, J. S., & Irani, K. (2016) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.116.308321 · Cited by 83 · see citing works
Xiao, Y., Xia, J., Cheng, J., Huang, H., Zhou, Y., Yang, X., Su, X., Ke, Y., & Ling, W. (2019) · Circulation · doi:10.1161/circulationaha.118.036336 · Cited by 82 · see citing works
P53 Impairs Endothelium-Dependent Vasomotor Function Through Transcriptional Upregulation of P66shc
Kim, C., Jung, S.-B., Naqvi, A., Hoffman, T. A., DeRicco, J. S., Yamamori, T., Cole, M. P., Jeon, B. H., & Irani, K. (2008) · Circulation Research · doi:10.1161/circresaha.108.181644 · Cited by 81 · see citing works
Zhang, S. X., Ma, J. H., Bhatta, M., Fliesler, S. J., & Wang, J. J. (2014) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2014.12.001 · Cited by 79 · see citing works
Tie, L., Yang, H., An, Y., Liu, S., Han, J., Xu, Y., Hu, M., Li, W., Chen, A. F., Lin, Z.-B., et al. (2012) · Cellular Physiology and Biochemistry · doi:10.1159/000338512 · Cited by 79 · see citing works
Maiocchi, S. L., Ku, J., Thai, T., Chan, E., Rees, M. D., & Thomas, S. R. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107711 · Cited by 75 · see citing works
Spescha, R. D., Klohs, J., Semerano, A., Giacalone, G., Derungs, R., Reiner, M. F., Rodríguez, D., Méndez‐Carmona, N., Glanzmann, M., Savarese, G., et al. (2015) · European Heart Journal · doi:10.1093/eurheartj/ehv140 · Cited by 75 · see citing works
Self-citationIntensive Glucose Lowering and Cardiovascular Disease Prevention in Diabetes
Mazzone, T. (2010) · Circulation · doi:10.1161/circulationaha.109.913350 · Cited by 75 · see citing works
Role of oxidative stress in endothelial insulin resistance
Paneni, F. (2015) · World Journal of Diabetes · doi:10.4239/wjd.v6.i2.326 · Cited by 75 · see citing works
Luo, X.-Y., Qu, S.-L., Tang, Z., Zhang, Y. E., Liu, M., Peng, J., Tang, H. R., Yu, K., Zhang, C., Ren, Z., et al. (2014) · Clinica Chimica Acta · doi:10.1016/j.cca.2014.07.019 · Cited by 72 · see citing works
Epigenetic Signatures and Vascular Risk in Type 2 Diabetes: A Clinical Perspective
Paneni, F., Costantino, S., Volpe, M., Lüscher, T. F., & Cosentino, F. (2013) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2013.07.003 · Cited by 70 · see citing works
Self-citationBoosting the pentose phosphate pathway restores cardiac progenitor cell availability in diabetes
Katare, R., Oikawa, A., Cesselli, D., Beltrami, A. P., Avolio, E., Muthukrishnan, D., Munasinghe, P. E., Angelini, G. D., Emanueli, C., & Madeddu, P. R. (2012) · Cardiovascular Research · doi:10.1093/cvr/cvs291 · Cited by 70 · see citing works
The Lifespan-regulator p66Shc in mitochondria: redox enzyme or redox sensor?
Gertz, M., & Steegborn, C. (2010) · Antioxidants & Redox Signaling · doi:10.1089/ars.2010.3147 · Cited by 75 · see citing works
Mitochondria and Oxidative Stress in the Cardiorenal Metabolic Syndrome
Aroor, A. R., Mandavia, C. H., Ren, J. T., Sowers, J. R., & Pulakat, L. (2012) · Cardiorenal Medicine · doi:10.1159/000335675 · Cited by 67 · see citing works
Mitochondrial dysfunction and oxidative stress in diabetic wound
Jiang, G., Jiang, T., Chen, J., Yao, H., Mao, R., Yang, X., Chen, Z., & Li, W. (2023) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.23407 · Cited by 64 · see citing works
Namdar, M., Gebhard, C., Studiger, R., Shi, Y., Mocharla, P. S., Schmied, C. M., Brugada, P., Lüscher, T. F., & Camici, G. G. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036373 · Cited by 64 · see citing works
Self-citationStefano, V. D., Cencioni, C., Zaccagnini, G., Magenta, A., Capogrossi, M. C., & Martelli, F. (2009) · Cardiovascular Research · doi:10.1093/cvr/cvp082 · Cited by 65 · see citing works
Torreggiani, M., Liu, H., Wu, J. C., Zheng, F., Cai, W., Striker, G. E., & Vlassara, H. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.090138 · Cited by 60 · see citing works
Structure-functional implications of longevity protein p66Shc in health and disease
Mir, H. A., Ali, R., Mushtaq, U., & Khanday, F. A. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101139 · Cited by 60 · see citing works
Conserva, F., Gesualdo, L., & Papale, M. (2015) · Journal of Diabetes Research · doi:10.1155/2016/7934504 · Cited by 59 · see citing works
Decreased Superoxide Production in Macrophages of Long-lived p66Shc Knock-out Mice
Tomilov, A. A., Bicocca, V. T., Schoenfeld, R. A., Giorgio, M., Migliaccio, E., Ramsey, J. J., Hagopian, K., Pelicci, P. G., & Cortopassi, G. A. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.017491 · Cited by 60 · see citing works
Self-citationQuintela, A. M., Jiménez, R., Gómez‐Guzmán, M., Zarzuelo-Romero, M. J., Galindo, P., Sánchez, M., Vargas, F., Cogolludo, A. L., Tamargo, J. L., Pérez‐Vizcaíno, F., et al. (2012) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2012.05.045 · Cited by 57 · see citing works
The role of p66Shcdeletion in age-associated arterial dysfunction and disease states
Camici, G. G., Cosentino, F., Tanner, F. C., & Lüscher, T. F. (2008) · Journal of Applied Physiology · doi:10.1152/japplphysiol.90579.2008 · Cited by 56 · see citing works
Self-citationHistone deacetylases and atherosclerosis
Zheng, X., Zhou, T., Wang, X., Tong, X.-H., & Ding, J. (2014) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2014.12.048 · Cited by 56 · see citing works
Actions of 17β-estradiol and testosterone in the mitochondria and their implications in aging
Vasconsuelo, A., Milanesi, L., & Boland, R. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.09.001 · Cited by 55 · see citing works
Spescha, R. D., Glanzmann, M., Simic, B., Witassek, F., Keller, S., Akhmedov, A., Tanner, F. C., Lüscher, T. F., & Camici, G. G. (2014) · Hypertension · doi:10.1161/hypertensionaha.113.02129 · Cited by 55 · see citing works
Self-citationP66shc and its role in ischemic cardiovascular diseases
Boengler, K., Bornbaum, J., Schlüter, K., & Schulz, R. (2019) · Basic Research in Cardiology · doi:10.1007/s00395-019-0738-x · Cited by 55 · see citing works
Franzeck, F. C., Hof, D., Spescha, R. D., Hasun, M., Akhmedov, A., Steffel, J., Shi, Y., Cosentino, F., Tanner, F. C., von Eckardstein, A., et al. (2012) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2011.10.035 · Cited by 54 · see citing works
Self-citationp66Shc protein, oxidative stress, and cardiovascular complications of diabetes: the missing link
Francia, P., Cosentino, F., Schiavoni, M., Huang, Y., Perna, E., Camici, G. G., Lüscher, T. F., & Volpe, M. (2009) · Journal of Molecular Medicine · doi:10.1007/s00109-009-0499-3 · Cited by 54 · see citing works
Self-citationMartin-Padura, I., de Nigris, F., Migliaccio, E., Mansueto, G., Minardi, S., Rienzo, M., Lerman, L. O., Stendardo, M., Giorgio, M., De Rosa, G., et al. (2008) · Endothelium · doi:10.1080/10623320802487791 · Cited by 52 · see citing works
Self-citationMitochondria and Oxidative Stress as a Link between Alzheimer’s Disease and Diabetes Mellitus
Veselov, I. M., Vinogradova, D. V., Maltsev, A. V., Shevtsov, P. N., Spirkova, E. A., Бачурин, С. О., & Shevtsova, E. F. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914450 · Cited by 55 · see citing works
- Authors
- Camici, G. G., Schiavoni, M., Francia, P., Bachschmid, M., Martin-Padura, I., Hersberger, M., Tanner, F. C., Pelicci, P., Volpe, M., Anversa, P., Lüscher, T. F., & Cosentino, F.
- Affiliations
- University of Zurich (CH)
- Sapienza University of Rome (IT)
- University of Konstanz (DE)
- Department of Experimental Oncology, European Institute of Oncology, 20141 Milan, Italy;
- University Hospital Zurich (CH)
- Istituto Neurologico Mediterraneo (IT)
- New York Medical College (US)
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-03-20
- Volume
- 104
- Issue
- 12
- Pages
- 5217-5222
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1829289
- OpenAlex
- W2148034645
- Cited by
- 249
- References
- 39
- Citations by year
- 2026: 4 · 2025: 7 · 2024: 2 · 2023: 8 · 2022: 5 · 2021: 5 · 2020: 11 · 2019: 15 · 2018: 14 · 2017: 15 · 2016: 16 · 2015: 14 · 2014: 29 · 2013: 19 · 2012: 20
- FWCI
- 12.02
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion)
- IRIS Research product catalog (Sapienza University of Rome) (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry › Antioxidant Activity and Oxidative Stress
- Keywords
- p66Shc, hyperglycemia, endothelial dysfunction, oxidative stress, reactive oxygen species, diabetes mellitus, streptozotocin-induced diabetes, peroxynitrite, nitrotyrosine, lipid peroxidation, heme oxygenase-1, endothelial nitric oxide synthase, diabetic vascular complications, gene deletion
- MeSH terms
- Src Homology 2 Domain-Containing, Transforming Protein 1, Animals, Aorta, Diabetes Mellitus, Experimental, Endothelium, Vascular, Hyperglycemia, Isometric Contraction, Male, Streptozocin, Vasomotor System, Free Radical Scavengers, Gene Deletion, Thiobarbituric Acid Reactive Substances, Oxidative Stress, Peroxynitrous Acid, Adaptor Proteins, Signal Transducing, Luminescence, Mice, Heme Oxygenase-1, Nitric Oxide Synthase Type III, Shc Signaling Adaptor Proteins, In Vitro Techniques
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