Quadriceps Muscle Weakness and Atrophy Are Associated with a Differential Epigenetic Profile in Advanced COPD
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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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].”
From Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting (2023) · cites this paper as [157]
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Seigneurin-Berny, D., Verdel, A., Curtet, S., Lemercier, C., Garin, J., Rousseaux, S., & Khochbin, S. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.23.8035-8044.2001 · Cited by 335 · see citing works
Barreiro, E., Peinado, V. I., Galdiz, J. B., Ferrer, E., Marin-Corral, J., Sánchez, F., Gea, J., & Barberà, J. A. (2010) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200908-1220oc · Cited by 272 · see citing works
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Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting
Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076454 · Cited by 85 · see citing works
“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].”
ResultBin, Y., Xiao, Y., Huang, D., Ma, Z., Liang, Y., Bai, J., Zhang, W., Liang, Q., Zhang, J., Zhong, X., et al. (2019) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00005.2018 · Cited by 35 · see citing works
Byrne, C. A., McNeil, A. T., Koh, T. J., Brunskill, A. F., & Fantuzzi, G. (2019) · PLOS ONE · doi:10.1371/journal.pone.0222345 · Cited by 15 · see citing works
- 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
- Publisher
- Portland Press Ltd.
- 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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