Potential therapeutic effects of the MTOR inhibitors for preventing ageing and progeria-related disorders
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The mammalian target of rapamycin (mTOR) pathway is an highly conserved signal transduction axis involved in many cellular processes, such as cell growth, survival, transcription, translation, apoptosis, metabolism, motility and autophagy. Recently, this signalling pathway has come to the attention of the scientific community owing to the unexpected finding that inhibition of mTOR by rapamycin, an antibiotic with immunosuppressant and chemotherapeutic properties, extends lifespan in diverse animal models. Moreover, rapamycin has been reported to rescue the cellular phenotype in a progeroid syndrome [Hutchinson–Gilford Progeria syndrome (HGPS)] that recapitulates most of the traits of physiological ageing. The promising perspectives raised by these results warrant a better understanding of mTOR signalling and the potential applications of mTOR inhibitors to counteract ageing‐associated diseases and increase longevity. This review is focused on these issues.
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Inhibition of mTOR complex 1 by rapamycin prolonged the healthy lifespan of mice and exerted anti-senescence and anti-atherosclerotic effects.
“Inhibition of mTOR complex 1 by rapamycin prolonged the healthy lifespan of mice and exerted anti-senescence and anti-atherosclerotic effects.152,153”
From Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis (2020) · cites this paper as [153]
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López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013) · Cell · doi:10.1016/j.cell.2013.05.039 · Cited by 14,982 · see citing works
mTOR Signaling in Growth Control and Disease
Laplante, M., & Sabatini, D. M. (2012) · Cell · doi:10.1016/j.cell.2012.03.017 · Cited by 8,509 · see citing works
Cellular senescence: when bad things happen to good cells
Campisi, J., & d'Adda di Fagagna, F. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2233 · Cited by 4,441 · see citing works
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891 · see citing works
Rapamycin fed late in life extends lifespan in genetically heterogeneous mice
Harrison, D. E., Strong, R., Sharp, Z. D., Nelson, J. F., Astle, C. M., Flurkey, K., Nadon, N. L., Wilkinson, J. E., Frenkel, K., Carter, C. S., et al. (2009) · Nature · doi:10.1038/nature08221 · Cited by 3,766 · see citing works
Temsirolimus, Interferon Alfa, or Both for Advanced Renal-Cell Carcinoma
Hudes, G. R., Carducci, M. A., Tomczak, P., Dutcher, J. P., Figlin, R. A., Kapoor, A., Starosławska, E., Sosman, J. A., McDermott, D. F., Bodrogi, I., et al. (2007) · New England Journal of Medicine · doi:10.1056/nejmoa066838 · Cited by 3,645 · see citing works
Protein aggregation and neurodegenerative disease
Ross, C. A., & Poirier, M. A. (2004) · Nature Medicine · doi:10.1038/nm1066 · Cited by 3,454 · see citing works
Motzer, R. J., Escudier, B., Oudard, S., Hutson, T. E., Porta, C., Bracarda, S., Grünwald, V., Thompson, J. A., Figlin, R. A., Hollaender, N., et al. (2008) · The Lancet · doi:10.1016/s0140-6736(08)61039-9 · Cited by 3,019 · see citing works
Everolimus for Advanced Pancreatic Neuroendocrine Tumors
Yao, J. C., Shah, M. H., Ito, T., Lombard‐Bohas, C., Wolin, E. M., Cutsem, E. V., Hobday, T. J., Okusaka, T., Capdevila, J., de Vries, E. G. E., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1009290 · Cited by 2,879 · see citing works
Prolonged Rapamycin Treatment Inhibits mTORC2 Assembly and Akt/PKB
Sarbassov, D. D., Ali, S. M., Sengupta, S., Sheen, J.-H., Hsu, P. P., Bagley, A. F., Markhard, A. L., & Sabatini, D. M. (2006) · Molecular Cell · doi:10.1016/j.molcel.2006.03.029 · Cited by 2,659 · see citing works
Giovannucci, E., Harlan, D. M., Archer, M. C., Bergenstal, R. M., Gapstur, S. M., Habel, L. A., Pollak, M., Regensteiner, J. G., & Yee, D. (2010) · Diabetes Care · doi:10.2337/dc10-0666 · Cited by 2,366 · see citing works
Ravikumar, B., Vacher, C., Berger, Z., Davies, J. E., Luo, S., Oroz, L. G., Scaravilli, F., Easton, D. F., Duden, R., O'Kane, C. J., et al. (2004) · Nature Genetics · doi:10.1038/ng1362 · Cited by 2,347 · see citing works
Hoeijmakers, J. H. J. (2009) · New England Journal of Medicine · doi:10.1056/nejmra0804615 · Cited by 2,239 · see citing works
Rubinsztein, D. C., Mariño, G., & Kroemer, G. (2011) · Cell · doi:10.1016/j.cell.2011.07.030 · Cited by 2,107 · see citing works
Targets for Cell Cycle Arrest by the Immunosuppressant Rapamycin in Yeast
Heitman, J., Movva, N. R., & Hall, M. N. (1991) · Science · doi:10.1126/science.1715094 · Cited by 2,010 · see citing works
ULK1 induces autophagy by phosphorylating Beclin-1 and activating VPS34 lipid kinase
Russell, R. C., Tian, Y., Yuan, H., Park, H. W., Chang, Y.-Y., Kim, J., Kim, H., Neufeld, T. P., Dillin, A. G., & Guan, K. (2013) · Nature Cell Biology · doi:10.1038/ncb2757 · Cited by 1,586 · see citing works
A unifying model for mTORC1-mediated regulation of mRNA translation
Thoreen, C. C., Chantranupong, L., Keys, H. R., Wang, T., Gray, N. S., & Sabatini, D. M. (2012) · Nature · doi:10.1038/nature11083 · Cited by 1,477 · see citing works
Metformin improves healthspan and lifespan in mice
Martin-Montalvo, A., Mercken, E. M., Mitchell, S. J., Palacios, H. H., Mote, P. L., Scheibye-Knudsen, M., Gomes, A. P., Ward, T. M., Minor, R. K., Blouin, M.-J., et al. (2013) · Nature Communications · doi:10.1038/ncomms3192 · Cited by 1,445 · see citing works
Fasting: molecular mechanisms and clinical applications
Longo, V. D., & Mattson, M. P. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2013.12.008 · Cited by 1,425 · see citing works
α-Synuclein Blocks ER-Golgi Traffic and Rab1 Rescues Neuron Loss in Parkinson's Models
Cooper, A. A., Gitler, A. D., Cashikar, A. G., Haynes, C. M., Hill, K. J., Bhullar, B., Liu, K., Xu, K., Strathearn, K. E., Liu, F., et al. (2006) · Science · doi:10.1126/science.1129462 · Cited by 1,377 · see citing works
Loss of Huntingtin-Mediated BDNF Gene Transcription in Huntington's Disease
Zuccato, C., Ciammola, A., Rigamonti, D., Leavitt, B. R., Goffredo, D., Conti, L., MacDonald, M. E., Friedlander, R. M., Silani, V., Hayden, M. R., et al. (2001) · Science · doi:10.1126/science.1059581 · Cited by 1,319 · see citing works
Regulation of Yeast Replicative Life Span by TOR and Sch9 in Response to Nutrients
Kaeberlein, M., Powers, R. W., Steffen, K. K., Westman, E. A., Hu, D., Dang, N., Kerr, E. O., Kirkland, K. T., Fields, S., & Kennedy, B. K. (2005) · Science · doi:10.1126/science.1115535 · Cited by 1,293 · see citing works
Rapamycin: one drug, many effects
Li, J., Kim, S. G., & Blenis, J. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.01.001 · Cited by 1,287 · see citing works
Autophagy Genes Are Essential for Dauer Development and Life-Span Extension in <i>C. elegans</i>
Meléndez, A., Tallóczy, Z., Seaman, M., Eskelinen, E.-L., Hall, D. H., & Levine, B. (2003) · Science · doi:10.1126/science.1087782 · Cited by 1,270 · see citing works
Nakatogawa, H., Ichimura, Y., & Ohsumi, Y. (2007) · Cell · doi:10.1016/j.cell.2007.05.021 · Cited by 1,215 · see citing works
Rapamycin-Induced Insulin Resistance Is Mediated by mTORC2 Loss and Uncoupled from Longevity
Lamming, D. W., Ye, L., Katajisto, P., Goncalves, M. D., Saitoh, M., Stevens, D. M., Davis, J. G., Salmon, A. B., Richardson, A., Ahima, R. S., et al. (2012) · Science · doi:10.1126/science.1215135 · Cited by 1,199 · see citing works
Gauthier, L. R., Charrin, B. C., Borrell-Pagès, M., Dompierre, J. P., Rangone, H., Cordelières, F. P., De Mey, J., MacDonald, M. E., Leßmann, V., Humbert, S., et al. (2004) · Cell · doi:10.1016/j.cell.2004.06.018 · Cited by 1,178 · see citing works
Laberge, R.-M., Sun, Y., Orjalo, A. V., Patil, C. K., Freund, A., Zhou, L., Curran, S. C., Davalos, A. R., Wilson-Edell, K. A., Liu, S., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3195 · Cited by 1,160 · see citing works
Ribosomal Protein S6 Kinase 1 Signaling Regulates Mammalian Life Span
Selman, C., Tullet, J. M. A., Wieser, D., Irvine, E., Lingard, S. J., Choudhury, A. I., Claret, M., Al-Qassab, H., Carmignac, D., Ramadani, F., et al. (2009) · Science · doi:10.1126/science.1177221 · Cited by 1,120 · see citing works
Efficacy and safety of sirolimus in lymphangioleiomyomatosis
McCormack, F. X., Inoue, Y., Moss, J., Singer, L. G., Strange, C., Nakata, K., Barker, A. F., Chapman, J. T., Brantly, M. L., Stocks, J. M., et al. (2011) · New England Journal of Medicine · doi:10.1056/nejmoa1100391 · Cited by 1,099 · see citing works
Influence of TOR kinase on lifespan in C. elegans
Vellai, T., Takacs-Vellai, K., Zhang, Y., Kovacs, A. L., Orosz, L., & Müller, F. (2003) · Nature · doi:10.1038/426620a · Cited by 1,057 · see citing works
Mechanisms of Life Span Extension by Rapamycin in the Fruit Fly Drosophila Melanogaster
Bjedov, I., Toivonen, J. M., Kerr, F., Slack, C., Jacobson, J., Foley, A., & Partridge, L. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2009.11.010 · Cited by 1,057 · see citing works
Making new contacts: the mTOR network in metabolism and signalling crosstalk
Shimobayashi, M., & Hall, M. N. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3757 · Cited by 1,053 · see citing works
Spilman, P., Podlutskaya, N., Hart, M. J., Debnath, J., Gorostiza, O., Bredesen, D., Richardson, A., Strong, R., & Galvan, V. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009979 · Cited by 1,033 · see citing works
Everolimus for Subependymal Giant-Cell Astrocytomas in Tuberous Sclerosis
Krueger, D. A., Caré, M. M., Holland, K. D., Agricola, K. D., Tudor, C., Mangeshkar, P., Wilson, K. A., Byars, A. W., Sahmoud, T., & Franz, D. N. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa1001671 · Cited by 1,003 · see citing works
New Users of Metformin Are at Low Risk of Incident Cancer
Libby, G., Donnelly, L. A., Donnan, P. T., Alessi, D. R., Morris, A. D., & Evans, J. M. M. (2009) · Diabetes Care · doi:10.2337/dc08-2175 · Cited by 996 · see citing works
Dowling, R. J. O., Zakikhani, M., Fantus, I. G., Pollak, M., & Sonenberg, N. (2007) · Cancer Research · doi:10.1158/0008-5472.can-07-2310 · Cited by 933 · see citing works
Lifespan extension by conditions that inhibit translation in Caenorhabditis elegans
Hansen, M., Taubert, S., Crawford, D., Libina, N., Lee, S.-J., & Kenyon, C. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2006.00267.x · Cited by 918 · see citing works
Rapamycin, But Not Resveratrol or Simvastatin, Extends Life Span of Genetically Heterogeneous Mice
Miller, R. A., Harrison, D. E., Astle, C. M., Baur, J. A., Boyd, A. R., de Cabo, R., Fernandez, E., Flurkey, K., Javors, M. A., Nelson, J. F., et al. (2011) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glq178 · Cited by 896 · see citing works
Metformin, independent of AMPK, inhibits mTORC1 in a rag GTPase-dependent manner
Kalender, A., Selvaraj, A., Kim, S. Y., Gulati, P., Brûlé, S., Viollet, B., Kemp, B. E., Bardeesy, N., Dennis, P., Schlager, J. J., et al. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.03.014 · Cited by 889 · see citing works
Molecular Interplay between Mammalian Target of Rapamycin (mTOR), Amyloid-β, and Tau
Caccamo, A., Majumder, S., Richardson, A., Strong, R., & Oddo, S. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.100420 · Cited by 881 · see citing works
Regulation of innate immune cell function by mTOR
Weichhart, T., Hengstschläger, M., & Linke, M. (2015) · Nature reviews. Immunology · doi:10.1038/nri3901 · Cited by 836 · see citing works
Pathogenic Lysosomal Depletion in Parkinson's Disease
Dehay, B., Bové, J., Rodríguez-Muela, N., Perier, C., Recasens, A., Boya, P., & Vila, M. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.1920-10.2010 · Cited by 825 · see citing works
Serruys, P. W. J. C., Kutryk, M. J. B., & Ong, A. T. L. (2006) · New England Journal of Medicine · doi:10.1056/nejmra051091 · Cited by 764 · see citing works
mTOR Regulation and Therapeutic Rejuvenation of Aging Hematopoietic Stem Cells
Chen, C., Liu, Y., Liu, Y., & Zheng, P. (2009) · Science Signaling · doi:10.1126/scisignal.2000559 · Cited by 680 · see citing works
Onken, B., & Driscoll, M. (2010) · PLoS ONE · doi:10.1371/journal.pone.0008758 · Cited by 671 · see citing works
With TOR, Less Is More: A Key Role for the Conserved Nutrient-Sensing TOR Pathway in Aging
Kapahi, P., Chen, D., Rogers, A. N., Katewa, S. D., Li, P. W.-L., Thomas, E., & Kockel, L. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.05.001 · Cited by 663 · see citing works
Activation of mTORC2 by Association with the Ribosome
Zinzalla, V., Stracka, D., Oppliger, W., & Hall, M. N. (2011) · Cell · doi:10.1016/j.cell.2011.02.014 · Cited by 648 · see citing works
Heß, G., Herbrecht, R., Romaguera, J. E., Verhoef, G. E. G., Crump, M., Gisselbrecht, C., Laurell, A., Offner, F. C., Strahs, A. L., Berkenblit, A., et al. (2009) · Journal of Clinical Oncology · doi:10.1200/jco.2008.20.7977 · Cited by 641 · see citing works
Metformin, independent of AMPK, induces mTOR inhibition and cell-cycle arrest through REDD1
Ben Sahra, I., Regazzetti, C., Robert, G., Laurent, K., Le Marchand-Brustel, Y., Auberger, P., Tanti, J.-F., Giorgetti-Peraldi, S., & Bost, F. (2011) · Cancer Research · doi:10.1158/0008-5472.can-10-1769 · Cited by 616 · see citing works
A dual PI3 kinase/mTOR inhibitor reveals emergent efficacy in glioma
Fan, Q.-W., Knight, Z. A., Goldenberg, D., Yu, W., Mostov, K. E., Stokoe, D., Shokat, K. M., & Weiss, W. A. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.03.029 · Cited by 584 · see citing works
mTOR complex 2 signaling and functions
Oh, W. J., & Jacinto, E. (2011) · Cell Cycle · doi:10.4161/cc.10.14.16586 · Cited by 561 · see citing works
SDZ RAD, A NEW RAPAMYCIN DERIVATIVE
Schüler, W., Sedrani, R. C., Cottens, S., berlin, B. H., Schulz, M., Schuurman, H., Zenke, G., Zerwes, H., & Schreier, M. H. (1997) · Transplantation · doi:10.1097/00007890-199707150-00008 · Cited by 534 · see citing works
Fighting neurodegeneration with rapamycin: mechanistic insights
Bové, J., Martínez‐Vicente, M., & Vila, M. (2011) · Nature reviews. Neuroscience · doi:10.1038/nrn3068 · Cited by 525 · see citing works
Cheng, C., Adams, G. B., Perin, L., Wei, M., Zhou, X., Lam, B. S., Sacco, S. D., Mirisola, M. G., Quinn, D. I., Dorff, T. B., et al. (2014) · Cell stem cell · doi:10.1016/j.stem.2014.04.014 · Cited by 484 · see citing works
Yeast Life Span Extension by Depletion of 60S Ribosomal Subunits Is Mediated by Gcn4
Steffen, K. K., MacKay, V. L., Kerr, E. O., Tsuchiya, M., Hu, D., Fox, L. A., Dang, N., Johnston, E. D., Oakes, J. A., Tchao, B. N., et al. (2008) · Cell · doi:10.1016/j.cell.2008.02.037 · Cited by 465 · see citing works
Picking the Point of Inhibition: A Comparative Review of PI3K/AKT/mTOR Pathway Inhibitors
Dienstmann, R., Rodon, J. A., Serra, V., & Tabernero, J. M. (2014) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-13-0639 · Cited by 464 · see citing works
Rapamycin Protects against Neuron Death inIn VitroandIn VivoModels of Parkinson's Disease
Malagelada, C., Jin, Z. H., Jackson-Lewis, V. R., Przedborski, S., & Greene, L. A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3944-09.2010 · Cited by 458 · see citing works
Wei, M., Fabrizio, P., Hu, J. H., Ge, H., Cheng, C., Li, L., & Longo, V. D. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.0040013 · Cited by 454 · see citing works
Targeted polypharmacology: discovery of dual inhibitors of tyrosine and phosphoinositide kinases
Apsel, B., Blair, J. A., González, B., Nazif, T. M., Feldman, M. E., Aizenstein, B., Hoffman, R., Williams, R. L., Shokat, K. M., & Knight, Z. A. (2008) · Nature Chemical Biology · doi:10.1038/nchembio.117 · Cited by 452 · see citing works
Kraemer, K. H., Patronas, N. J., Schiffmann, R., Brooks, B. P., Tamura, D., & DiGiovanna, J. J. (2007) · Neuroscience · doi:10.1016/j.neuroscience.2006.12.020 · Cited by 443 · see citing works
mTOR and autophagy: a dynamic relationship governed by nutrients and energy.
Dunlop, E., & Tee, A. (2014) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2014.08.006 · Cited by 428 · see citing works
Understanding the benefit of metformin use in cancer treatment
Dowling, R. J. O., Goodwin, P. J., & Stambolic, V. (2011) · BMC Medicine · doi:10.1186/1741-7015-9-33 · Cited by 410 · see citing works
Anisimov, V. N., Berstein, L. M., Egormin, P. A., Piskunova, T. S., Popovich, I. G., Zabezhinski, M. A., Kovalenko, I. G., Poroshina, T. E., Semenchenko, A. V., Provinciali, M., et al. (2005) · Experimental Gerontology · doi:10.1016/j.exger.2005.07.007 · Cited by 402 · see citing works
Majumder, S., Richardson, A. G., Strong, R., & Oddo, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025416 · Cited by 401 · see citing works
Rapamycin decelerates cellular senescence
Demidenko, Z. N., Zubova, S. G., Bukreeva, E. I., Pospelov, V. A., Pospelova, T. V., & Blagosklonny, M. V. (2009) · Cell Cycle · doi:10.4161/cc.8.12.8606 · Cited by 391 · see citing works
Recurrent turnover of senescent cells during regeneration of a complex structure
Yun, M. H., Davaapil, H., & Brockes, J. P. (2015) · eLife · doi:10.7554/elife.05505 · Cited by 385 · see citing works
Aβ inhibits the proteasome and enhances amyloid and tau accumulation
Tseng, B. P., Green, K. N., Chan, J. L., Blurton-Jones, M., & LaFerla, F. M. (2008) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2007.04.014 · Cited by 384 · see citing works
Akt-dependent and -independent mechanisms of mTOR regulation in cancer
Memmott, R. M., & Dennis, P. A. (2009) · Cellular Signalling · doi:10.1016/j.cellsig.2009.01.004 · Cited by 383 · see citing works
Growth stimulation leads to cellular senescence when the cell cycle is blocked
Demidenko, Z. N., & Blagosklonny, M. V. (2008) · Cell Cycle · doi:10.4161/cc.7.21.6919 · Cited by 377 · see citing works
Rapamycin extends murine lifespan but has limited effects on aging
Neff, F., Flores-Dominguez, D., Ryan, D. P., Horsch, M., Schröder, S., Adler, T., Afonso, L. C., Aguilar-Pimentel, J. A., Becker, L., Garrett, L., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci67674 · Cited by 374 · see citing works
RecQ helicases: suppressors of tumorigenesis and premature aging
Bachrati, C. Z., & Hickson, I. D. (2003) · Biochemical Journal · doi:10.1042/bj20030491 · Cited by 372 · see citing works
Cao, K., Graziotto, J. J., Blair, C. D., Mazzulli, J. R., Erdos, M. R., Krainc, D., & Collins, F. S. (2011) · Science Translational Medicine · doi:10.1126/scitranslmed.3002346 · Cited by 350 · see citing works
Metformin slows down aging and extends life span of female SHR mice
Anisimov, V. N., Berstein, L. M., Egormin, P. A., Piskunova, T. S., Popovich, I. G., Zabezhinski, M. A., Tyndyk, M. L., Yurova, M. V., Kovalenko, I. G., Poroshina, T. E., et al. (2008) · Cell Cycle · doi:10.4161/cc.7.17.6625 · Cited by 348 · see citing works
Lehmann, A. R., McGibbon, D., & Stefanini, M. (2011) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-6-70 · Cited by 343 · see citing works
Wu, J., Liu, J., Chen, E. B., Wang, J., Cao, L., Narayan, N., Fergusson, M. M., Rovira, I. I., Allen, M. D., Springer, D., et al. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.07.030 · Cited by 333 · see citing works
Bregman, D. B., Halaban, R., van Gool, A. J., Henning, K. A., Friedberg, E. C., & Warren, S. L. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11586 · Cited by 331 · see citing works
Resveratrol as a Therapeutic Agent for Neurodegenerative Diseases
Sun, A. Y., Wang, Q., Simonyi, Á., & Sun, G. Y. (2010) · Molecular Neurobiology · doi:10.1007/s12035-010-8111-y · Cited by 330 · see citing works
Trichothiodystrophy: Update on the sulfur-deficient brittle hair syndromes
Itin, P. H., Sarasin, A. R., & Pittelkow, M. R. (2001) · Journal of the American Academy of Dermatology · doi:10.1067/mjd.2001.114294 · Cited by 292 · see citing works
Kahan, B. D., Podbielski, J. M., Napoli, K. L., Katz, S. M., Meier‐Kriesche, H., & Buren, C. T. V. (1998) · Transplantation · doi:10.1097/00007890-199810270-00013 · Cited by 288 · see citing works
Ribosomal protein S6 kinase activity controls the ribosome biogenesis transcriptional program
Chauvin, C., Koka, V., Nouschi, A., Mieulet, V., Hoareau‐Aveilla, C., Dreazen, A., Cagnard, N., Carpentier, W., Kiss, T., Meyuhas, O., et al. (2013) · Oncogene · doi:10.1038/onc.2012.606 · Cited by 279 · see citing works
Increased expression of BubR1 protects against aneuploidy and cancer and extends healthy lifespan
Baker, D. J., Dawlaty, M. M., Wijshake, T., Jeganathan, K. B., Malureanu, L. A., van Ree, J. H., Crespo‐Diaz, R. J., Reyes, S., Seaburg, L., Shapiro, V. S., et al. (2012) · Nature Cell Biology · doi:10.1038/ncb2643 · Cited by 272 · see citing works
The serine/threonine kinase ULK1 is a target of multiple phosphorylation events
Bach, M., Larance, M., James, D. E., & Ramm, G. (2011) · Biochemical Journal · doi:10.1042/bj20101894 · Cited by 253 · see citing works
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy
Capanni, C., Mattioli, E., Columbaro, M., Lucarelli, E., Parnaik, V. K., Novelli, G., Wehnert, M. S., Cenni, V., Maraldi, N. M., Squarzoni, S., et al. (2005) · Human Molecular Genetics · doi:10.1093/hmg/ddi158 · Cited by 226 · see citing works
Self-citationHalloran, J. J., Hussong, S. A., Burbank, R. R., Podlutskaya, N., Fischer, K. E., Sloane, L. B., Austad, S. N., Strong, R., Richardson, A. G., Hart, M. J., et al. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.06.054 · Cited by 221 · see citing works
Komatsu, D. E., & Hadjiargyrou, M. (2004) · Bone · doi:10.1016/j.bone.2003.12.024 · Cited by 212 · see citing works
Growth and aging: a common molecular mechanism
Blagosklonny, M. V., & Hall, M. N. (2009) · Aging · doi:10.18632/aging.100040 · Cited by 212 · see citing works
Liu, B., Ghosh, S., Yang, X., Zheng, H., Liu, X., Wang, Z., Jin, G., Zheng, B., Kennedy, B. K., Suh, Y., et al. (2012) · Cell Metabolism · doi:10.1016/j.cmet.2012.11.007 · Cited by 211 · see citing works
Huntington’s disease: degradation of mutant huntingtin by autophagy
Sarkar, S., & Rubinsztein, D. C. (2008) · FEBS Journal · doi:10.1111/j.1742-4658.2008.06562.x · Cited by 207 · see citing works
Scheibye‐Knudsen, M., Ramamoorthy, M., Sýkora, P., Maynard, S., Lin, P., Minor, R. K., Wilson, D. M., Cooper, M. P., Spencer, R. G. S., de Cabo, R., et al. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20111721 · Cited by 203 · see citing works
Majumder, S., Caccamo, A., Medina, D. X., Benavides, A. D., Javors, M. A., Kraig, E., Strong, R., Richardson, A. G., & Oddo, S. (2011) · Aging Cell · doi:10.1111/j.1474-9726.2011.00791.x · Cited by 202 · see citing works
Molecular bases of progeroid syndromes
Navarro, C. L., Cau, P., & Lévy, N. (2006) · Human Molecular Genetics · doi:10.1093/hmg/ddl214 · Cited by 189 · see citing works
Weedon, M. N., Ellard, S., Prindle, M. J., Caswell, R. C., Allen, H. L., Oram, R. A., Godbole, K., Yajnik, C. S., Sbraccia, P., Novelli, G., et al. (2013) · Nature Genetics · doi:10.1038/ng.2670 · Cited by 185 · see citing works
Kamenisch, Y., Fousteri, M. I., Knoch, J., von Thaler, A., Fehrenbacher, B., Kato, H., Becker, T., Dollé, M. E. T., Kuiper, R., Majora, M., et al. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20091834 · Cited by 182 · see citing works
Zhou, H., Luo, Y., & Huang, S. (2010) · Anti-Cancer Agents in Medicinal Chemistry · doi:10.2174/187152010793498663 · Cited by 181 · see citing works
Resveratrol Inhibits mTOR Signaling by Promoting the Interaction between mTOR and DEPTOR
Liu, M., Wilk, S. A., Wang, A., Zhou, L., Wang, R.-H., Ogawa, W., Deng, C., Dong, L., & Liu, F. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.169284 · Cited by 177 · see citing works
Mammalian Target of Rapamycin (mTOR) Pathways in Neurological Diseases
Wong, M. (2013) · Biomedical Journal · doi:10.4103/2319-4170.110365 · Cited by 169 · see citing works
Resveratrol Levels and All-Cause Mortality in Older Community-Dwelling Adults
Semba, R. D., Ferrucci, L., Bartali, B., Urpí-Sardà, M., Zamora‐Ros, R., Sun, K., Cherubini, A., Bandinelli, S., & Andrés‐Lacueva, C. (2014) · JAMA Internal Medicine · doi:10.1001/jamainternmed.2014.1582 · Cited by 168 · see citing works
Nissan, X., Blondel, S., Navarro, C. L., Maury, Y., Denis, C., Girard, M., Martinat, C., Sandre‐Giovannoli, A. D., Lévy, N., & Peschanski, M. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.05.015 · Cited by 168 · see citing works
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
Columbaro, M., Capanni, C., Mattioli, E., Novelli, G., Parnaik, V. K., Squarzoni, S., Maraldi, N. M., & Lattanzi, G. (2005) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-005-5318-6 · Cited by 160 · see citing works
Self-citationAamann, M. D., Sorensen, M. M., Hvitby, C., Berquist, B. R., Müftüoğlu, M., Tian, J., de Souza-Pinto, N. C., Scheibye‐Knudsen, M., Wilson, D. M., Stevnsner, T., et al. (2010) · The FASEB Journal · doi:10.1096/fj.09-147991 · Cited by 142 · see citing works
Metformin for aging and cancer prevention
Anisimov, V. N. (2010) · Aging · doi:10.18632/aging.100230 · Cited by 140 · see citing works
Geroconversion: irreversible step to cellular senescence
Blagosklonny, M. V. (2014) · Cell Cycle · doi:10.4161/15384101.2014.985507 · Cited by 138 · see citing works
Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
Garg, A., Subramanyam, L., Agarwal, A. K., Simha, V., Levine, B. D., D’Apice, M. R., Novelli, G., & Crow, Y. J. (2009) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jc.2009-0472 · Cited by 134 · see citing works
The kinase triad, AMPK, mTORC1 and ULK1, maintains energy and nutrient homoeostasis
Dunlop, E. A., & Tee, A. R. (2013) · Biochemical Society Transactions · doi:10.1042/bst20130030 · Cited by 122 · see citing works
Filesi, I., Gullotta, F., Lattanzi, G., D’Apice, M. R., Capanni, C., Nardone, A. M., Columbaro, M., Scarano, G., Mattioli, E., Sabatelli, P., et al. (2005) · Physiological Genomics · doi:10.1152/physiolgenomics.00060.2005 · Cited by 122 · see citing works
Self-citationTrichothiodystrophy: From basic mechanisms to clinical implications
Stefanini, M., Botta, E., Lanzafame, M., & Orioli, D. (2009) · DNA repair · doi:10.1016/j.dnarep.2009.10.005 · Cited by 119 · see citing works
Therapeutic Effects of Rapamycin on MPTP-Induced Parkinsonism in Mice
Liu, K., Shi, N., Sun, Y., Zhang, T., & Sun, X. (2012) · Neurochemical Research · doi:10.1007/s11064-012-0909-8 · Cited by 114 · see citing works
Woods, T. C., & Marks, A. R. (2004) · Annual Review of Medicine · doi:10.1146/annurev.med.55.091902.105243 · Cited by 114 · see citing works
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria
Cenni, V., Capanni, C., Columbaro, M., Ortolani, M., D’Apice, M. R., Novelli, G., Fini, M., Marmiroli, S., Scarano, E., Maraldi, N. M., et al. (2011) · European Journal of Histochemistry · doi:10.4081/ejh.2011.e36 · Cited by 101 · see citing works
Self-citationMolecular Mechanism of Global Genome Nucleotide Excision Repair
Petruseva, I. O., Evdokimov, A. N., & Lavrik, O. I. (2014) · Acta Naturae · doi:10.32607/20758251-2014-6-1-23-34 · Cited by 92 · see citing works
Lamin A Ser404 Is a Nuclear Target of Akt Phosphorylation in C2C12 Cells
Cenni, V., Bertacchini, J., Beretti, F., Lattanzi, G., Bavelloni, A., Riccio, M., Ruzzene, M., Marin, O., Arrigoni, G., Parnaik, V. K., et al. (2008) · Journal of Proteome Research · doi:10.1021/pr800262g · Cited by 89 · see citing works
Self-citationFK506 and rapamycin: novel pharmacological probes of the immune response
CHANG, J. Y., Sehgal, S. N., & Bansbach, C. C. (1991) · Trends in Pharmacological Sciences · doi:10.1016/0165-6147(91)90555-7 · Cited by 85 · see citing works
Clinical features of Bloom syndrome and function of the causative gene, BLM helicase
Kaneko, H., & Kondo, N. (2004) · Expert Review of Molecular Diagnostics · doi:10.1586/14737159.4.3.393 · Cited by 84 · see citing works
Richard, D. J., Cubeddu, L., Urquhart, A. J., Bain, A. L., Bolderson, E., Menon, D. R., White, M. F., & Khanna, K. K. (2011) · Nucleic Acids Research · doi:10.1093/nar/gkq1340 · Cited by 84 · see citing works
The protein kinase Akt/PKB regulates both prelamin A degradation and Lmna gene expression
Bertacchini, J., Beretti, F., Cenni, V., Guida, M., Gibellini, F., Mediani, L., Marin, O., Maraldi, N. M., Pol, A. D., Lattanzi, G., et al. (2013) · The FASEB Journal · doi:10.1096/fj.12-218214 · Cited by 83 · see citing works
Self-citationAll-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype
Pellegrini, C., Columbaro, M., Capanni, C., D’Apice, M. R., Cavallo, C., Murdocca, M., Lattanzi, G., & Squarzoni, S. (2015) · Oncotarget · doi:10.18632/oncotarget.4939 · Cited by 80 · see citing works
Self-citationFischer, K. E., Gelfond, J., Soto, V. Y., Han, C. J., Someya, S., Richardson, A., & Austad, S. N. (2015) · PLoS ONE · doi:10.1371/journal.pone.0126644 · Cited by 76 · see citing works
Prelamin A causes progeria through cell-extrinsic mechanisms and prevents cancer invasion
Rosa, J. D. L., Freije, J. M. P., Cabanillas, R., Osorio, F. G., Fraga, M. F., Fernández-García, M. S., Rad, R., Fanjul, V., Ugalde, A. P., Liang, Q., et al. (2013) · Nature Communications · doi:10.1038/ncomms3268 · Cited by 76 · see citing works
Nesprin-2 giant safeguards nuclear envelope architecture in LMNA S143F progeria cells
Kandert, S., Lüke, Y., Kleinhenz, T., Neumann, S., Lu, W., Jaeger, V. M., Munck, M., Wehnert, M. S., Müller, C. R., Zhou, Z., et al. (2007) · Human Molecular Genetics · doi:10.1093/hmg/ddm255 · Cited by 72 · see citing works
Improving survival with metformin: the evidence base today
Scarpello, J. H. B. (2003) · Diabetes & Metabolism · doi:10.1016/s1262-3636(03)72786-4 · Cited by 71 · see citing works
Centenarian lamins: rapamycin targets in longevity
Lattanzi, G., Ortolani, M., Columbaro, M., Prencipe, S., Mattioli, E., Lanzarini, C., Maraldi, N. M., Cenni, V., Garagnani, P., Salvioli, S., et al. (2013) · Journal of Cell Science · doi:10.1242/jcs.133983 · Cited by 69 · see citing works
Self-citationDual mTORC1/C2 inhibitors suppress cellular geroconversion (a senescence program)
Leontieva, O. V., Demidenko, Z. N., & Blagosklonny, M. V. (2015) · Oncotarget · doi:10.18632/oncotarget.4836 · Cited by 65 · see citing works
Talaei, F., van Praag, V. M., & Henning, R. H. (2013) · Pharmacological Research · doi:10.1016/j.phrs.2013.04.011 · Cited by 62 · see citing works
Cenni, V., Sabatelli, P., Mattioli, E., Marmiroli, S., Capanni, C., Ognibene, A., Squarzoni, S., Maraldi, N. M., Bonne, G., Columbaro, M., et al. (2005) · Journal of Medical Genetics · doi:10.1136/jmg.2004.026112 · Cited by 60 · see citing works
Self-citationPelosini, C., Martinelli, S., Ceccarini, G., Magno, S., Barone, I., Basolo, A., Fierabracci, P., Vitti, P., Maffei, M., & Santini, F. (2014) · Metabolism · doi:10.1016/j.metabol.2014.07.010 · Cited by 59 · see citing works
Dynamics of the nuclear envelope at mitosis and during apoptosis
Buendia, B., Courvalin, J., & Collas, P. (2001) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000818 · Cited by 57 · see citing works
Nuclear Lamins and Neurobiology
Young, S. G., Jung, H.-J., Lee, J. M., & Fong, L. G. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00486-14 · Cited by 52 · see citing works
Immortalization of Werner syndrome and progeria fibroblasts
Saitō, H., & Moses, R. E. (1991) · Experimental Cell Research · doi:10.1016/0014-4827(91)90054-x · Cited by 48 · see citing works
Lamin A precursor induces barrier-to-autointegration factor nuclear localization
Capanni, C., Cenni, V., Haraguchi, T., Squarzoni, S., Schüchner, S., Ogris, E., Novelli, G., Maraldi, N. M., & Lattanzi, G. (2010) · Cell Cycle · doi:10.4161/cc.9.13.12080 · Cited by 47 · see citing works
Self-citationA‐type lamins and signaling: The PI 3‐kinase/Akt pathway moves forward
Marmiroli, S., Bertacchini, J., Beretti, F., Cenni, V., Guida, M., Pol, A. D., Maraldi, N. M., & Lattanzi, G. (2009) · Journal of Cellular Physiology · doi:10.1002/jcp.21807 · Cited by 46 · see citing works
Self-citationHuman POLD1 modulates cell cycle progression and DNA damage repair
Song, J., Hong, P., Liu, C., Zhang, Y., Wang, J., & Wang, P. (2015) · BMC Biochemistry · doi:10.1186/s12858-015-0044-7 · Cited by 43 · see citing works
Kamenisch, Y., Fousteri, M. I., Knoch, J., von Thaler, A., Fehrenbacher, B., Kato, H., Becker, T., Dollé, M. E. T., Kuiper, R., Majora, M., et al. (2010) · F1000Research · doi:10.7490/f1000research.515.1 · Cited by 42 · see citing works
Systems medicine of inflammaging
Castellani, G., Menichetti, G., Garagnani, P., Bacalini, M. G., Pirazzini, C., Franceschi, C., Collino, S., Sala, C., Remondini, D., Giampieri, E., et al. (2015) · Briefings in Bioinformatics · doi:10.1093/bib/bbv062 · Cited by 42 · see citing works
Insights into melanoma: targeting the mTOR pathway for therapeutics
Pópulo, H., Soares, P., & Lopes, J. M. (2012) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2012.691472 · Cited by 42 · see citing works
High frequency of PTEN mutations in nevi and melanomas from xeroderma pigmentosum patients
Masaki, T., Wang, Y., DiGiovanna, J. J., Khan, S. G., Raffeld, M. A., Beltaifa, S., Hornyak, T. J., Darling, T. N., Lee, C. R., & Kraemer, K. H. (2014) · Pigment Cell & Melanoma Research · doi:10.1111/pcmr.12226 · Cited by 41 · see citing works
Martelli, A. M., Chiarini, F., Evangelisti, C., Ognibene, A., Bressanin, D., Billi, A. M., Manzoli, L., Cappellini, A., & McCubrey, J. A. (2012) · Expert Opinion on Therapeutic Targets · doi:10.1517/14728222.2012.694869 · Cited by 39 · see citing works
Self-citationCapanni, C., Squarzoni, S., Cenni, V., D’Apice, M. R., Gambineri, A., Novelli, G., Wehnert, M. S., Pasquali, R., Maraldi, N. M., & Lattanzi, G. (2012) · Cell Cycle · doi:10.4161/cc.21869 · Cited by 35 · see citing works
Self-citationAvnet, S., Pallotta, R., Perut, F., Baldini, N., Pittis, M. G., Saponari, A., Lucarelli, E., Dozza, B., Greggi, T., Maraldi, N. M., et al. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.03.006 · Cited by 34 · see citing works
Self-citationCenni, V., Capanni, C., Mattioli, E., Columbaro, M., Wehnert, M. S., Ortolani, M., Fini, M., Novelli, G., Bertacchini, J., Maraldi, N. M., et al. (2014) · Aging · doi:10.18632/aging.100680 · Cited by 34 · see citing works
Self-citationRapamycin, anti-aging, and avoiding the fate of Tithonus
Richardson, A. (2013) · Journal of Clinical Investigation · doi:10.1172/jci70800 · Cited by 33 · see citing works
Camozzi, D., D’Apice, M. R., Schena, E., Cenni, V., Columbaro, M., Capanni, C., Maraldi, N. M., Squarzoni, S., Ortolani, M., Novelli, G., et al. (2012) · Histochemistry and Cell Biology · doi:10.1007/s00418-012-0977-5 · Cited by 31 · see citing works
Self-citationEvangelisti, C., Bernasconi, P., Cavalcante, P., Cappelletti, C., D’Apice, M. R., Sbraccia, P., Novelli, G., Prencipe, S., Lemma, S., Baldini, N., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3232 · Cited by 30 · see citing works
Self-citationStrandgren, C., Nasser, H. A., McKenna, T., Koskela, A., Tuukkanen, J., Ohlsson, C., Rozell, B., & Eriksson, M. (2015) · The FASEB Journal · doi:10.1096/fj.14-269217 · Cited by 28 · see citing works
Prelamin A-mediated nuclear envelope dynamics in normal and laminopathic cells
Lattanzi, G. (2011) · Biochemical Society Transactions · doi:10.1042/bst20110657 · Cited by 27 · see citing works
Self-citationHow Does the Huntington's Disease Mutation Damage Cells?
Rubinsztein, D. C. (2003) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2003.37.pe26 · Cited by 24 · see citing works
Prelamin A processing and functional effects in restrictive dermopathy
Columbaro, M., Mattioli, E., Schena, E., Capanni, C., Cenni, V., Lévy, N., Navarro, C. L., Coco, R. D., Squarzoni, S., Camozzi, D., et al. (2010) · Cell Cycle · doi:10.4161/cc.9.23.14210 · Cited by 23 · see citing works
Self-citationThe InflammTORy Powers of Senescence
Serrano, M. (2015) · Trends in Cell Biology · doi:10.1016/j.tcb.2015.09.011 · Cited by 13 · see citing works
WRNIP1 functions upstream of DNA polymerase η in the UV-induced DNA damage response
Yoshimura, A., Kobayashi, Y., Tada, S., Seki, M., & Enomoto, T. (2014) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2014.08.043 · Cited by 13 · see citing works
The Bud Scar‐Based Screening System for Hunting Human Genes Extending Life Span
Chen, C., & Contreras, R. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1297.061 · Cited by 11 · see citing works
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Targeting the PI3K/AKT/mTOR and RAF/MEK/ERK pathways for cancer therapy
Li, Q., Li, Z., Luo, T. L., & Shi, H. (2022) · Molecular Biomedicine · doi:10.1186/s43556-022-00110-2 · Cited by 274 · see citing works
Senescence-induced inflammation: an important player and key therapeutic target in atherosclerosis
Stojanović, S. D., Fiedler, J., Bauersachs, J., Thum, T., & Sedding, D. G. (2020) · European Heart Journal · doi:10.1093/eurheartj/ehz919 · Cited by 188 · see citing works
The multifaceted role of the SASP in atherosclerosis: from mechanisms to therapeutic opportunities
Sun, Y., Wang, X., Liu, T., Zhu, X., & Pan, X. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00815-5 · Cited by 151 · see citing works
Sanches-Silva, A. T., Testai, L., Nabavi, S. F., Battino, M. A., Devi, K. P., Tejada, S., Sureda, A., Xu, S., Yousefi, B., Majidinia, M., et al. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2019.104626 · Cited by 135 · see citing works
Cellular senescence and cardiovascular diseases: moving to the “heart” of the problem
Evangelou, K., Vasileiou, P. V. S., Papaspyropoulos, A., Hazapis, O. G., Petty, R., Demaria, M., & Gorgoulis, V. G. (2022) · Physiological Reviews · doi:10.1152/physrev.00007.2022 · Cited by 124 · see citing works
Mandibuloacral dysplasia: A premature ageing disease with aspects of physiological ageing
Cenni, V., D’Apice, M. R., Garagnani, P., Columbaro, M., Novelli, G., Franceschi, C., & Lattanzi, G. (2017) · Ageing Research Reviews · doi:10.1016/j.arr.2017.12.001 · Cited by 90 · see citing works
Self-citationLamin A involvement in ageing processes
Cenni, V., Capanni, C., Mattioli, E., Schena, E., Squarzoni, S., Bacalini, M. G., Garagnani, P., Salvioli, S., Franceschi, C., & Lattanzi, G. (2020) · Ageing Research Reviews · doi:10.1016/j.arr.2020.101073 · Cited by 85 · see citing works
Self-citationDrug discovery targeting the mTOR pathway
Martelli, A. M., Buontempo, F., & McCubrey, J. A. (2018) · Clinical Science · doi:10.1042/cs20171158 · Cited by 76 · see citing works
A targeted antisense therapeutic approach for Hutchinson–Gilford progeria syndrome
Erdos, M. R., Cabral, W. A., Tavarez, U. L., Cao, K., Gvozdenovic‐Jeremic, J., Narisu, N., Zerfas, P. M., Crumley, S. L., Boku, Y. D., Hanson, G. J., et al. (2021) · Nature Medicine · doi:10.1038/s41591-021-01274-0 · Cited by 75 · see citing works
Cell Senescence, Multiple Organelle Dysfunction and Atherosclerosis
Machado-Oliveira, G., Ramos, C., Marques, A. R. A., & Vieira, O. V. (2020) · Cells · doi:10.3390/cells9102146 · Cited by 66 · see citing works
Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
Piekarowicz, K., Machowska, M., Dzianisava, V., & Rzepecki, R. (2019) · Cells · doi:10.3390/cells8020088 · Cited by 60 · see citing works
Mattioli, E., Andrenacci, D., Garofalo, C., Prencipe, S., Scotlandi, K., Remondini, D., Gentilini, D., Blasio, A. M. D., Valente, S., Scarano, E., et al. (2018) · Aging Cell · doi:10.1111/acel.12824 · Cited by 56 · see citing works
Self-citationRapamycin Rescues Age-Related Changes in Muscle-Derived Stem/Progenitor Cells from Progeroid Mice
Kawakami, Y., Hambright, W. S., Takayama, K., Mu, X., Lu, A., Cummins, J. H., Matsumoto, T., Yurube, T., Kuroda, R., Kurosaka, M., et al. (2019) · Molecular Therapy — Methods & Clinical Development · doi:10.1016/j.omtm.2019.05.011 · Cited by 48 · see citing works
Molecular mechanisms and cardiovascular implications of cancer therapy-induced senescence
Abdelgawad, I. Y., Sadak, K. T., Lone, D. W., Dabour, M. S., Niedernhofer, L. J., & Zordoky, B. N. M. (2020) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2020.107751 · Cited by 47 · see citing works
Genetic reduction of mTOR extends lifespan in a mouse model of Hutchinson‐Gilford Progeria syndrome
Cabral, W. A., Tavarez, U. L., Beeram, I. R., Yeritsyan, D., Boku, Y. D., Eckhaus, M., Nazarian, A., Erdos, M. R., & Collins, F. S. (2021) · Aging Cell · doi:10.1111/acel.13457 · Cited by 47 · see citing works
Metabolic Dysfunction in Hutchinson–Gilford Progeria Syndrome
Kreienkamp, R., & Gonzalo, S. (2020) · Cells · doi:10.3390/cells9020395 · Cited by 45 · see citing works
Reprogramming towards anabolism impedes degeneration in a preclinical model of retinitis pigmentosa
Zhang, L., Justus, S., Xu, Y. H., Pluchenik, T., Hsu, C., Yang, J., Duong, J., Lin, C., Jia, Y., Bassuk, A. G., et al. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw256 · Cited by 40 · see citing works
Bernasconi, P., Carboni, N., Ricci, G., Siciliano, G., Politano, L., Maggi, L., Mongini, T., Vercelli, L., Rodolico, C., Biagini, E., et al. (2018) · Nucleus · doi:10.1080/19491034.2018.1467722 · Cited by 38 · see citing works
Self-citationBikkul, M. U., Clements, C. S., Godwin, L. S., Goldberg, M. W., Kill, I. R., & Bridger, J. M. (2018) · Biogerontology · doi:10.1007/s10522-018-9758-4 · Cited by 38 · see citing works
Aged induced pluripotent stem cell (iPSCs) as a new cellular model for studying premature aging
Petrini, S., Borghi, R., Doria, V., Restaldi, F., Moreno, S., Novelli, A., Bertini, E., & Compagnucci, C. (2017) · Aging · doi:10.18632/aging.101248 · Cited by 36 · see citing works
Hwang, D., Lee, H., Lee, J., Lee, M., Cho, S., Kim, T., & Kim, H. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094361 · Cited by 37 · see citing works
The Cutting Edge: The Role of mTOR Signaling in Laminopathies
Chiarini, F., Evangelisti, C., Cenni, V., Fazio, A., Paganelli, F., Martelli, A. M., & Lattanzi, G. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040847 · Cited by 35 · see citing works
Self-citationThyroid Hormones Enhance Mitochondrial Function in Human Epidermis
Vidali, S., Chéret, J., Giesen, M., Haeger, S., Alam, M. A., Watson, R. E. B., Langton, A. K., Klinger, M. H. F., Knuever, J., Funk, W., et al. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.05.118 · Cited by 35 · see citing works
Linking skeletal muscle aging with osteoporosis by lamin A/C deficiency
Xiong, L., Zhao, K., Cao, Y. W., Guo, H.-H., Pan, J., Yang, X., Ren, X., Mei, L., & Xiong, W. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000731 · Cited by 31 · see citing works
Mattioli, E., Andrenacci, D., Mai, A., Valente, S., Robijns, J., Vos, W. H. D., Capanni, C., & Lattanzi, G. (2019) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2019.00006 · Cited by 28 · see citing works
Self-citationFlorwick, A., Dharmaraj, T., Jurgens, J. A., Valle, D. L., & Wilson, K. L. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00079 · Cited by 26 · see citing works
OGT (O-GlcNAc Transferase) Selectively Modifies Multiple Residues Unique to Lamin A
Simon, D. N., Wriston, A., Fan, Q., Shabanowitz, J., Florwick, A., Dharmaraj, T., Peterson, S. B., Gruenbaum, Y., Carlson, C. R., Grønning-Wang, L. M., et al. (2018) · Cells · doi:10.3390/cells7050044 · Cited by 25 · see citing works
Lamins and bone disorders: current understanding and perspectives
Gargiuli, C., Schena, E., Mattioli, E., Columbaro, M., D’Apice, M. R., Novelli, G., Greggi, T., & Lattanzi, G. (2018) · Oncotarget · doi:10.18632/oncotarget.25071 · Cited by 23 · see citing works
Self-citationBiological Activities of Cyclic and Acyclic B-Type Laxaphycins in SH-SY5Y Human Neuroblastoma Cells
Alvariño, R., Alonso, E., Bornancin, L., Bonnard, I., Inguimbert, N., Banaigs, B., & Botana, L. M. (2020) · Marine Drugs · doi:10.3390/md18070364 · Cited by 23 · see citing works
Charar, C., & Gruenbaum, Y. (2016) · Clinical Science · doi:10.1042/cs20160488 · Cited by 23 · see citing works
Saxena, S., & Kumar, S. (2020) · GeroScience · doi:10.1007/s11357-020-00167-3 · Cited by 22 · see citing works
Hitzert, M. M., van der Crabben, S. N., Baldewsingh, G., van Amstel, H. K. P., van den Wijngaard, A., van Ravenswaaij‐Arts, C. M. A., & Zijlmans, W. C. W. R. (2019) · Orphanet Journal of Rare Diseases · doi:10.1186/s13023-019-1269-0 · Cited by 20 · see citing works
The Nuclear Lamina: Protein Accumulation and Disease
Almendáriz-Palacios, C., Gillespie, Z. E., Janzen, M., Martinez, V., Bridger, J. M., Harkness, T. A. A., Mousseau, D. D., & Eskiw, C. H. (2020) · Biomedicines · doi:10.3390/biomedicines8070188 · Cited by 18 · see citing works
Mechanistic target of rapamycin signaling in mouse models of accelerated aging
Lee, J. Y., Kennedy, B. K., & Liao, C. (2019) · The Journals of Gerontology Series A · doi:10.1093/gerona/glz059 · Cited by 13 · see citing works
Balistreri, C. R., Madonna, R., & Ferdinandy, P. (2021) · Current Research in Pharmacology and Drug Discovery · doi:10.1016/j.crphar.2021.100027 · Cited by 12 · see citing works
STAT1 Drives the Interferon-Like Response and Aging Hallmarks in Progeria
Gonzalo, S., de Faria, R. C., Shashkova, E. V., Flaveny, C. A., Baldán, Á., & McCommis, K. S. (2023) · doi:10.59368/agingbio.20230009 · Cited by 10 · see citing works
Rejeki, P. S., Pranoto, A., Widiatmaja, D. M., Utami, D. M., Izzatunnisa, N., Sugiharto, S., Lesmana, R., & Halim, S. (2024) · Sports · doi:10.3390/sports12050116 · Cited by 9 · see citing works
Monterrubio-Ledezma, F., Salcido-Gómez, A., Zavaleta-Vásquez, T. I., Navarro‐García, F., Cisneros, B., & Massieu, L. (2025) · GeroScience · doi:10.1007/s11357-024-01501-9 · Cited by 7 · see citing works
Rajeev, M., Ratan, C., Krishnan, K., & Vijayan, M. (2021) · Recent Patents on Biotechnology · doi:10.2174/1872208315666210928114720 · Cited by 7 · see citing works
Lehky, T., Sackstein, P. E., Tamura, D., Quezado, M., Wu, T., Khan, S. G., Patronas, N. J., Wiggs, E. A., Brewer, C. C., DiGiovanna, J. J., et al. (2021) · BMC Neurology · doi:10.1186/s12883-021-02414-2 · Cited by 6 · see citing works
Ferro, A. (2016) · British Journal of Clinical Pharmacology · doi:10.1111/bcp.13117 · Cited by 5 · see citing works
Saito, A., NAGAYAMA, K., Okada, H., Onodera, S., Aida, N., Nakamura, T., Sawada, T., Hojo, H., Kato, S., & Azuma, T. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2320138122 · Cited by 4 · see citing works
Lin, C.-M., Yang, J.-H., Lee, H., Lin, Y.-P., Tsai, L., Hsu, C., Luxton, G. W. G., & Hu, C.-F. (2021) · Life · doi:10.3390/life11111230 · Cited by 4 · see citing works
The Hutchinson-Gilford Progeria Syndrome and Treatment: Updated Review of the Literature
Rahman, M. M., Jahan, F. I., Bashira, J., Akter, M., Islam, F., & Jubayer, A. M. (2020) · Scholars Academic Journal of Pharmacy · doi:10.36347/sajp.2020.v09i02.003 · Cited by 3 · see citing works
Cardiac phenotypes in LMNA mutations
Rouhi, L. (2025) · Current Opinion in Cardiology · doi:10.1097/hco.0000000000001209 · Cited by 2 · see citing works
Evangelisti, C., & Martelli, A. M. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-821618-7.00081-x · Cited by 2 · see citing works
Self-citationAmmar, R. M. (2015) · INFM-OAR (INFN Catania) · doi:10.5281/zenodo.32654
Genetics of Human Laminopathies
Novelli, G., & D’Apice, M. R. (2017) · Encyclopedia of Life Sciences · doi:10.1002/9780470015902.a0024693
Differences in Peripheral Neuropathy in Xeroderma Pigmentosum Complementation Groups A and DPreprint
Lehky, T., Sackstein, P. E., Tamura, D., Quezado, M., Wu, T., Khan, S. G., Patronas, N. J., Wiggs, E. A., Brewer, C. C., DiGiovanna, J. J., et al. (2021) · Research Square · doi:10.21203/rs.3.rs-351476/v1
Chen, H. (2017) · Springer eBooks · doi:10.1007/978-1-4939-2401-1_197
Chen, H. (2016) · Springer eBooks · doi:10.1007/978-1-4614-6430-3_197-2
- Authors
- Evangelisti, C., Cenni, V., & Lattanzi, G.
- Affiliations
- Istituto Ortopedico Rizzoli (IT)
- Corresponding author
- Lattanzi, Giovanna
- Venue
- British Journal of Clinical Pharmacology
- Publisher
- Wiley
- Published
- 2016-05-18
- Volume
- 82
- Issue
- 5
- Pages
- 1229-1244
- ISSN
- 0306-5251 (ISSN-L)
- 1365-2125
- PMC
- PMC5061804
- OpenAlex
- W2296384686
- Cited by
- 53
- References
- 150
- Citations by year
- 2025: 3 · 2024: 1 · 2023: 1 · 2022: 4 · 2021: 8 · 2020: 10 · 2019: 8 · 2018: 7 · 2017: 5 · 2016: 5 · 2015: 1
- FWCI
- 0.83
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- British Journal of Clinical Pharmacology (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- mTOR signaling, rapamycin, mTOR inhibitors, aging, Hutchinson-Gilford progeria syndrome, lifespan extension, longevity, autophagy, signal transduction
- MeSH terms
- Aging, Animals, Humans, Models, Biological, Progeria, Protein Kinase Inhibitors, TOR Serine-Threonine Kinases
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