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Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing
BACKGROUND: Osteoporosis (OP) is a systemic disease with bone loss and microstructural deterioration. Numerous noncoding RNAs (ncRNAs) have been proved to participate in various diseases, especially circular RNAs (circRNAs). However, the expression profile and mechanisms underlying circRNAs in male...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164409/ https://www.ncbi.nlm.nih.gov/pubmed/34123587 http://dx.doi.org/10.7717/peerj.11420 |
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author | Zhang, Haijin Song, Xue Teng, Zongyan Cheng, Sujun Yu, Weigang Yao, Xiaoyi Song, Zhiqiang Zhang, Yina |
author_facet | Zhang, Haijin Song, Xue Teng, Zongyan Cheng, Sujun Yu, Weigang Yao, Xiaoyi Song, Zhiqiang Zhang, Yina |
author_sort | Zhang, Haijin |
collection | PubMed |
description | BACKGROUND: Osteoporosis (OP) is a systemic disease with bone loss and microstructural deterioration. Numerous noncoding RNAs (ncRNAs) have been proved to participate in various diseases, especially circular RNAs (circRNAs). However, the expression profile and mechanisms underlying circRNAs in male osteoporosis have not yet been explored. METHODS: The whole transcriptome expression profile and differences in mRNAs, circRNAs, and microRNAs (miRNAs) were investigated in peripheral blood samples of patients with osteoporosis and healthy controls consisting of males ≥ 60-years-old. RESULTS: A total of 398 circRNAs, 51 miRNAs, and 642 mRNAs were significantly and differentially expressed in osteoporosis compared to healthy controls. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that the host genes of significantly differentially expressed circRNAs were mainly enriched in the regulation of cell cycle process: biological process (BP), organelle part cellular components (CC), protein binding molecular function (MF), Toll-like receptor signaling pathway, tumor necrosis factor (TNF) signaling pathway, and thyroid hormone signaling pathway. circRNA-miRNA-mRNA regulatory network was constructed using the differentially expressed RNAs. Moreover, key circRNAs (hsa_circ_0042409) in osteoporosis were discovered and validated by qPCR. CONCLUSIONS: The key cicrRNAs plays a major role in the pathogenesis of osteoporosis and could be used as potential biomarkers or targets in the diagnosis and treatment of osteoporosis. |
format | Online Article Text |
id | pubmed-8164409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-81644092021-06-10 Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing Zhang, Haijin Song, Xue Teng, Zongyan Cheng, Sujun Yu, Weigang Yao, Xiaoyi Song, Zhiqiang Zhang, Yina PeerJ Molecular Biology BACKGROUND: Osteoporosis (OP) is a systemic disease with bone loss and microstructural deterioration. Numerous noncoding RNAs (ncRNAs) have been proved to participate in various diseases, especially circular RNAs (circRNAs). However, the expression profile and mechanisms underlying circRNAs in male osteoporosis have not yet been explored. METHODS: The whole transcriptome expression profile and differences in mRNAs, circRNAs, and microRNAs (miRNAs) were investigated in peripheral blood samples of patients with osteoporosis and healthy controls consisting of males ≥ 60-years-old. RESULTS: A total of 398 circRNAs, 51 miRNAs, and 642 mRNAs were significantly and differentially expressed in osteoporosis compared to healthy controls. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis showed that the host genes of significantly differentially expressed circRNAs were mainly enriched in the regulation of cell cycle process: biological process (BP), organelle part cellular components (CC), protein binding molecular function (MF), Toll-like receptor signaling pathway, tumor necrosis factor (TNF) signaling pathway, and thyroid hormone signaling pathway. circRNA-miRNA-mRNA regulatory network was constructed using the differentially expressed RNAs. Moreover, key circRNAs (hsa_circ_0042409) in osteoporosis were discovered and validated by qPCR. CONCLUSIONS: The key cicrRNAs plays a major role in the pathogenesis of osteoporosis and could be used as potential biomarkers or targets in the diagnosis and treatment of osteoporosis. PeerJ Inc. 2021-05-26 /pmc/articles/PMC8164409/ /pubmed/34123587 http://dx.doi.org/10.7717/peerj.11420 Text en ©2021 Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Molecular Biology Zhang, Haijin Song, Xue Teng, Zongyan Cheng, Sujun Yu, Weigang Yao, Xiaoyi Song, Zhiqiang Zhang, Yina Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing |
title | Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing |
title_full | Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing |
title_fullStr | Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing |
title_full_unstemmed | Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing |
title_short | Key circular RNAs identified in male osteoporosis patients by whole transcriptome sequencing |
title_sort | key circular rnas identified in male osteoporosis patients by whole transcriptome sequencing |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8164409/ https://www.ncbi.nlm.nih.gov/pubmed/34123587 http://dx.doi.org/10.7717/peerj.11420 |
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