Cited by 84Muscle Physiology and DisordersChronic Obstructive Pulmonary Disease (COPD) ResearchNutrition and Health in Aging

Quadriceps Muscle Weakness and Atrophy Are Associated with a Differential Epigenetic Profile in Advanced COPD

Puig-Vilanova, Ester, Martínez-Llorens, Juana, Ausin, Pilar, Roca, Josep, Gea, Joaquim, Barreiro, Esther·2015·Clinical Science

Abstract

Epigenetic mechanisms regulate muscle mass and function in models of muscle dysfunction and atrophy. We assessed whether quadriceps muscle weakness and atrophy are associated with a differential expression profile of epigenetic events in patients with advanced COPD (chronic obstructive pulmonary disease). In vastus lateralis (VL) of sedentary severe COPD patients (n=41), who were further subdivided into those with (n=25) and without (n=16) muscle weakness and healthy controls (n=19), expression of muscle-enriched miRNAs, histone acetyltransferases (HATs) and deacetylases (HDACs), growth and atrophy signalling markers, total protein and histone acetylation, transcription factors, small ubiquitin-related modifier (SUMO) ligases and muscle structure were explored. All subjects were clinically evaluated. Compared with controls, in VL of all COPD together and in muscle-weakness patients, expression of miR-1, miR-206 and miR-27a, levels of lysine-acetylated proteins and histones and acetylated histone 3 were increased, whereas expression of HDAC3, HDAC4, sirtuin-1 (SIRT-1), IGF-1 (insulin-like growth factor-1) were decreased, Akt (v-akt murine thymoma viral oncogene homologue 1) expression did not differ, follistatin expression was greater, whereas myostatin expression was lower, serum reponse factor (SRF) expression was increased and fibre size of fast-twitch fibres was significantly reduced. In VL of severe COPD patients with muscle weakness and atrophy, epigenetic events regulat…

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Crossref · 10.1042/cs20140428

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  • Puig-Vilanova and colleagues found inverse results with a local decrease of miR-1 and miR-206 and an increase in HDAC4 in COPD quadriceps, including sarcopenic and nonsarcopenic patients.

    “Then, Puig-Vilanova and colleagues found inverse results with a local decrease of miR-1 and miR-206 and an increase in HDAC4 in COPD quadriceps (including sarcopenic and nonsarcopenic patients) [157].”

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Authors
Puig-Vilanova, E., Martínez-Llorens, J., Ausin, P., Roca, J., Gea, J., & Barreiro, E.
Affiliations
  • Pulmonology Department-Muscle and Respiratory System Research Unit (URMAR), IMIM-Hospital del Mar, Parc de Salut Mar, Health and Experimental Sciences Department (CEXS), Universitat Pompeu Fabra (UPF), Barcelona Biomedical Research Park (PRBB), C/ Dr. Aiguader, 88, Barcelona, Catalonia, E-08003 Spain
  • Instituto de Salud Carlos III (ES)
  • Universitat Pompeu Fabra (ES)
Corresponding author
Barreiro, Esther
Venue
Clinical Science
Published
2015-03-27
Volume
128
Issue
12
Pages
905-921
ISSN
  • 0143-5221 (ISSN-L)
  • 1470-8736
OpenAlex
W2039652066
Cited by
84
References
2
Citations by year
2026: 9 · 2024: 5 · 2023: 6 · 2022: 8 · 2021: 5 · 2020: 4 · 2019: 6 · 2018: 14 · 2017: 10 · 2016: 10 · 2015: 6 · 2014: 1
FWCI
5.78
Type
journal article
Language
en
Open access
closed
Locations
  • Clinical Science (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
  • Health Sciences › Medicine › Physiology › Nutrition and Health in Aging
Keywords
chronic obstructive pulmonary disease, muscle weakness, muscle atrophy, quadriceps, vastus lateralis, epigenetics, histone acetylation, microRNA, miR-1, miR-206, miR-27a, histone deacetylase, HDAC3, SIRT1, insulin-like growth factor I, myostatin, follistatin, SRF, protein degradation, myogenesis
MeSH terms
Anthropometry, Humans, Male, Muscular Atrophy, Biomarkers, Case-Control Studies, Muscle Weakness, Pulmonary Disease, Chronic Obstructive, MicroRNAs, Epigenesis, Genetic, Quadriceps Muscle

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