Júlia Costa de Sousa

Mrs. Júlia Costa de Sousa

orcid

Research Focus & Metrics

Academic Career Length

3Years (2024-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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Journal Article
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AGAndré Luiz Gouvêa Gouvêa
André Luiz Gouvêa Gouvêa
AAAnna Luisa Rosa Alves
Anna Luisa Rosa Alves
CMCamila Martinez
Camila Martinez
JSJúlia Costa de Sousa
Júlia Costa de Sousa
EKEleonora Kurtenbach
Eleonora Kurtenbach
Muscle atrophy leads to decreased muscle mass, weakness, inactivity, and increased mortality. E3 ubiquitin ligases, key regulators of protein degradation via the ubiquitin–proteasome system, play a critical role in atrophic mechanisms. This meta-analysis followed Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines, and its objective was to evaluate the association between E3 ligases Muscle Atrophy F-box (MAFbx)/Atrogin-1 (Fbxo32) and Muscle RING-finger protein 1 (MuRF-1) (TRIM63) E3 ligase mRNA levels, reductions in skeletal muscle CSA measures, and atrophy conditions. We examined papers published on PubMed®, Scopus, and Web of Science that studied E3 ligase gene expression signatures for Fbxo32 (MAFbx/Atrogin-1) and Trim63 (MuRF1) in different types of muscle atrophy and hypertrophy murine models. Twenty-nine studies selected by two independent raters were analyzed. Standardized mean differences (SMDs)/effect sizes (ESs) and 95% confidence intervals (CIs) were calculated for the outcomes using fixed-effects models. We found that 6- and 4.8-fold upregulation, respectively, of Fbxo32 and Trim63 was sufficient to reduce the ES to −3.89 (95% CI: −4.45 to −3.32) for the muscle fiber cross-sectional area and the development of skeletal muscle atrophy. I² and Q test statistics did not indicate heterogeneous data. There was a low probability of bias after both the funnel plot and Egger’s test analyses. These results were sustained independently of the atrophic model and muscle type. Therefore, the magnitude of the increase in muscle Fbxo32 and Trim63 mRNA is a feasible, reliable molecular marker for skeletal muscle atrophy in mice. The next step for the Ubiquitin-proteasome system (UPS) field involves elucidating the targets of E3 ligases, paving the way for diagnostic and treatment applications in humans.

19 February 2025
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Closed access
AGAndré Luiz Gouvêa Gouvêa
André Luiz Gouvêa Gouvêa
AAAnna Luisa Rosa Alves
Anna Luisa Rosa Alves
CMCamila Martinez
Camila Martinez
JSJúlia Costa de Sousa
Júlia Costa de Sousa
EKEleonora Kurtenbach
Eleonora Kurtenbach
INPLASY202520089 Biomarkers of Skeletal Muscle Atrophy Based on Atrogenes Evaluation: A Systematic Review and Meta-Analysis Study Keywords: musculoskeletal; atrophy; E3 ligases; molecular research;…

5 August 2024 in Journal of Immunological Methods
Verified
Journal Article
Closed access
JSJúlia Costa de Sousa
Júlia Costa de Sousa
SSStephanie Alexia Cristina Silva Santos
Stephanie Alexia Cristina Silva Santos
EKEleonora Kurtenbach
Eleonora Kurtenbach