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Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods
BACKGROUND: The human body has more than 600 kinds of skeletal muscles, which accounts for about 40% of the whole weight. Most skeletal muscles can make bones move, and their strength and endurance directly affect their performance during exercise. METHODS: To determine the effects of exercise and t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420641/ https://www.ncbi.nlm.nih.gov/pubmed/36072011 http://dx.doi.org/10.1155/2022/9582363 |
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author | Feng, Mufang Ji, Jie Li, Xiaoliu Ye, Xinming |
author_facet | Feng, Mufang Ji, Jie Li, Xiaoliu Ye, Xinming |
author_sort | Feng, Mufang |
collection | PubMed |
description | BACKGROUND: The human body has more than 600 kinds of skeletal muscles, which accounts for about 40% of the whole weight. Most skeletal muscles can make bones move, and their strength and endurance directly affect their performance during exercise. METHODS: To determine the effects of exercise and time on human skeletal muscle, we downloaded the microarray expression profile of GSE1832 and analyzed it to select differentially expressed genes (DEGs). Then, a protein-protein interaction (PPI) network was established, and the hub genes were identified. Afterwards, DEGs were applied to perform Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Finally, with the help of Gene Set Enrichment Analysis (GSEA), the gene sets in the 7 samples were enriched in the KEGG pathway. RESULTS: Through a series of bioinformatics analyses, we obtained a total of 271 DEGs. After that, four hub genes were determined through the PPI network, namely, EP300, STAT1, CDKN1A, and RAC2. In addition, we got that these DEGs were enriched in GO, such as regulation of cell population proliferation, cellular water homeostasis, and so on, and in KEGG, namely, hepatitis B, Epstein–Barr virus infection, small cell lung cancer, pathways in cancer, and others. Finally, the gene set in the samples obtained by GSEA was enriched in the cell cycle, chemokine signaling pathway, DNA replication, cytokine receptor interaction, ECM receptor interaction, and focal adhesion in KEGG. CONCLUSION: The findings obtained in this study will provide new clues for elucidating the mechanism of exercise and time on human skeletal muscles. |
format | Online Article Text |
id | pubmed-9420641 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-94206412022-09-06 Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods Feng, Mufang Ji, Jie Li, Xiaoliu Ye, Xinming Genet Res (Camb) Research Article BACKGROUND: The human body has more than 600 kinds of skeletal muscles, which accounts for about 40% of the whole weight. Most skeletal muscles can make bones move, and their strength and endurance directly affect their performance during exercise. METHODS: To determine the effects of exercise and time on human skeletal muscle, we downloaded the microarray expression profile of GSE1832 and analyzed it to select differentially expressed genes (DEGs). Then, a protein-protein interaction (PPI) network was established, and the hub genes were identified. Afterwards, DEGs were applied to perform Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis. Finally, with the help of Gene Set Enrichment Analysis (GSEA), the gene sets in the 7 samples were enriched in the KEGG pathway. RESULTS: Through a series of bioinformatics analyses, we obtained a total of 271 DEGs. After that, four hub genes were determined through the PPI network, namely, EP300, STAT1, CDKN1A, and RAC2. In addition, we got that these DEGs were enriched in GO, such as regulation of cell population proliferation, cellular water homeostasis, and so on, and in KEGG, namely, hepatitis B, Epstein–Barr virus infection, small cell lung cancer, pathways in cancer, and others. Finally, the gene set in the samples obtained by GSEA was enriched in the cell cycle, chemokine signaling pathway, DNA replication, cytokine receptor interaction, ECM receptor interaction, and focal adhesion in KEGG. CONCLUSION: The findings obtained in this study will provide new clues for elucidating the mechanism of exercise and time on human skeletal muscles. Hindawi 2022-08-21 /pmc/articles/PMC9420641/ /pubmed/36072011 http://dx.doi.org/10.1155/2022/9582363 Text en Copyright © 2022 Mufang Feng et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Feng, Mufang Ji, Jie Li, Xiaoliu Ye, Xinming Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods |
title | Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods |
title_full | Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods |
title_fullStr | Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods |
title_full_unstemmed | Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods |
title_short | Identification of the Exercise and Time Effects on Human Skeletal Muscle through Bioinformatics Methods |
title_sort | identification of the exercise and time effects on human skeletal muscle through bioinformatics methods |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9420641/ https://www.ncbi.nlm.nih.gov/pubmed/36072011 http://dx.doi.org/10.1155/2022/9582363 |
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