[Common cause and mechanism for all pathologies of aging?]

Cause commune et mécanisme commun aux maladies du vieillissement ?

Journal

Medecine sciences : M/S
ISSN: 1958-5381
Titre abrégé: Med Sci (Paris)
Pays: France
ID NLM: 8710980

Informations de publication

Date de publication:
Dec 2020
Historique:
entrez: 9 12 2020
pubmed: 10 12 2020
medline: 26 1 2021
Statut: ppublish

Résumé

Health is harmony, aging and its diseases (are) functional disharmony at the molecular, cellular and tissue levels. Our observations lead us to think that there seems to be a common cause and a common mechanism for aging and its many and diverse diseases. This common cause is the oxidative damage to particular proteins emerging from a combination of imperfect folding and oxidative stress. This common cause jointly goes with the biological clock common to various age-related diseases, whose the incidence increases exponentially over time and causes 90% of human mortality. Pharmacological interventions on the common cause could avoid and simultaneously attenuate all degenerative and malignant diseases, as it is the natural case of super-centenarians. Cause commune et mécanisme commun aux maladies du vieillissement ? La santé est l’harmonie, le vieillissement et ses maladies la dysharmonie fonctionnelle aux niveaux moléculaire, cellulaire et tissulaire. Nos observations semblent suggérer une cause commune et un mécanisme commun du vieillissement et de ses nombreuses et diverses maladies. Cette cause commune est le dommage oxydatif de protéines particulières, résultant à la fois de leur mauvais repliement et du stress oxydatif. La cause commune va de pair avec l’horloge biologique des diverses maladies du vieillissement, dont l’incidence augmente exponentiellement avec l’âge, responsables de 90 % de la mortalité humaine. Des interventions pharmacologiques sur la cause commune pourraient éviter et atténuer simultanément toutes les maladies dégénératives et malignes, comme c’est le cas naturellement chez les super-centenaires.

Autres résumés

Type: Publisher (fre)
Cause commune et mécanisme commun aux maladies du vieillissement ?

Identifiants

pubmed: 33296629
doi: 10.1051/medsci/2020221
pii: msc200068
doi:

Types de publication

Journal Article Review

Langues

fre

Sous-ensembles de citation

IM

Pagination

1129-1134

Informations de copyright

© 2020 médecine/sciences – Inserm.

Références

Krisko A, Radman M. Protein damage, ageing and age-related diseases. Open Biol 2019; 9 : 180249.
Radman M. Cellular parabiosis and the latency of age-related diseases. Open Biol 2019; 9.
Krisko A, Radman M. Phenotypic and genetic consequences of protein damage. PLoS Genet 2013 ; 9.
Kirkwood TB. Understanding the odd science of aging. Cell 2005 ; 120 : 437–447.
Krisko A, Radman M. Protein damage and death by radiation in Escherichia coli and Deinococcus radiodurans. Proc Natl Acad Sci USA 2010 ; 107 : 14373–14377.
Krisko A, Leroy M, Radman M, et al. Extreme anti-oxidant protection against ionizing radiation in bdelloid rotifers. Proc Natl Acad Sci USA 2012 ; 109 : 2354–2357.
Sulston JE, Brenner S. The DNA of Caenorhabditis elegans. Genetics 1974; 77 : 95-LP-104.
Hengartner MO. Robert Horvitz H. Programmed cell death in Caenorhabditis elegans. Curr Opin Genet Dev 1994 ; 4 : 581–586.
Metzstein MM, Stanfield GM, Horvitz HR. Genetics of programmed cell death in C. elegans: past, present and future. Trends Genet 1998 ; 14 : 410–416.
Krisko A, Radman M. Biology of extreme radiation resistance: the way of Deinococcus radiodurans. Cold Spring Harb Perspect Biol 2013 ; 5 : a012765–a012765.
López-otín C, Blasco MA, Partridge L, et al. The Hallmarks of aging longevity. Cell 2013 ; 153 : 1194–1217.
Speakman JR. Body size, energy metabolism and lifespan. J Exp Biol 2005; 208 : 1717-LP-30.
Karras GI, Yi S, Sahni N, et al. HSP90 shapes the consequences of human genetic variation. Cell 2017 ; 168 : 856–66 e12.
Bert P.. Expériences et considérations sur la greffe animale. J Anat Physiol 1864 ; 1 : 69–87.
Nawaz M, Fatima F. Extracellular vesicles, tunneling nanotubes, and cellular interplay: synergies and missing links. Front Mol Biosci 2017 ; 4 : 1–12.
Gerdes HH, Bukoreshtliev N V, Barroso JFV. Tunneling nanotubes: a new route for the exchange of components between animal cells. FEBS Lett 2007 ; 581 : 2194–2201.
Vignais ML, Caicedo A, Brondello JM, et al. Cell connections by tunneling nanotubes: effects of mitochondrial trafficking on target cell metabolism, homeostasis, and response to therapy. Stem Cells Int 2017; 2017.
Spees JL, Olson SD, Whitney MJ, et al. Mitochondrial transfer between cells can rescue aerobic respiration. Proc Natl Acad Sci USA 2006 ; 103 : 1283–1288.
Orgel LE. The maintenance of the accuracy of protein synthesis and its relevance to ageing. Proc Natl Acad Sci USA 1963 ; 49 : 517–521.
Orgel LE. The maintenance of the accuracy of protein synthesis and its relevance to ageing: a correction. Proc Natl Acad Sci USA 1970 ; 67 : 1476.
Oliver CN, Ahn BW, Moerman EJ, et al. Age-related changes in oxidized proteins. J Biol Chem 1987 ; 262 : 5488–5491.
Stadtman ER. Protein oxidation and aging. Free Radic Res 2006 ; 40 : 1250–1258.
De Graff AMR, Hazoglou MJ, Dill KA.. Highly charged proteins: the Achilles’ heel of aging proteomes. Structure 2016 ; 24 : 329–336.
Castro JP, Ott C, Jung T, et al. Carbonylation of the cytoskeletal protein actin leads to aggregate formation. Free Radic Biol Med 2012 ; 53 : 91625.
Tanase M, Urbanska AM, Zolla V, et al. Role of carbonyl modifications on aging-associated protein aggregation. Sci Rep 2016 ; 6 : 1–14.
Rahim A, Saha P, Jha KK, et al. Reciprocal carbonyl-carbonyl interactions in small molecules and proteins. Nat Commun 2017 ; 8 : 1–12.
Karri S, Singh S, Paripati AK, et al. Adaptation of Mge1 to oxidative stress by local unfolding and altered Interaction with mitochondrial Hsp70 and Mxr2. Mitochondrion 2019 ; 46 : 140–148.
Korovila I, Hugo M, Castro JP, et al. Proteostasis, oxidative stress and aging. Redox Biol 2017 ; 13 : 550–567.
Xu J, Reumers J, Couceiro JR, et al. Gain of function of mutant p53 by coaggregation with multiple tumor suppressors. Nat Chem Biol 2011 ; 7 : 285–295.
Sengupta U, Nilson AN, Kayed R. The role of amyloid-beta oligomers in toxicity, propagation, and immunotherapy. EBioMedicine 2016 ; 6 : 42–49.
Ludtmann MHR, Angelova PR, Horrocks MH, et al. α-synuclein oligomers interact with ATP synthase and open the permeability transition pore in Parkinson’s disease. Nat Commun 2018; 9.

Auteurs

Guillaume F Combes (GF)

Mediterranean Institute for Life Sciences (MedILS), Meštrovic΄evo šetalište 45, 21000 Split, Croatie - Naos Institute for Life Sciences, 355 rue Pierre-Simon Laplace, 13593 Aix-en-Provence, France - Inserm U1001, Université Paris-Descartes, Faculté de médecine Paris-Descartes, 24 rue du faubourg Saint-Jacques, 75014 Paris, France - Center of Excellence for Science and Technology-Integration of Mediterranean Region (STIM-REI), Interdisciplinary Center for Advanced Sciences and Technology (ICAST), Université de Split, Poljička cesta 35, 21000 Split, Croatie.

François-Xavier Pellay (FX)

Mediterranean Institute for Life Sciences (MedILS), Meštrovic΄evo šetalište 45, 21000 Split, Croatie - Naos Institute for Life Sciences, 355 rue Pierre-Simon Laplace, 13593 Aix-en-Provence, France.

Miroslav Radman (M)

Mediterranean Institute for Life Sciences (MedILS), Meštrovic΄evo šetalište 45, 21000 Split, Croatie - Naos Institute for Life Sciences, 355 rue Pierre-Simon Laplace, 13593 Aix-en-Provence, France - Inserm U1001, Université Paris-Descartes, Faculté de médecine Paris-Descartes, 24 rue du faubourg Saint-Jacques, 75014 Paris, France - Center of Excellence for Science and Technology-Integration of Mediterranean Region (STIM-REI), Interdisciplinary Center for Advanced Sciences and Technology (ICAST), Université de Split, Poljička cesta 35, 21000 Split, Croatie.

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