Metabonomic-Transcriptome Integration Analysis on Osteoarthritis and Rheumatoid Arthritis.


Journal

International journal of genomics
ISSN: 2314-4378
Titre abrégé: Int J Genomics
Pays: United States
ID NLM: 101605206

Informations de publication

Date de publication:
2020
Historique:
received: 26 05 2019
accepted: 20 11 2019
entrez: 25 1 2020
pubmed: 25 1 2020
medline: 25 1 2020
Statut: epublish

Résumé

This study is aimed at exploring the potential metabolite/gene biomarkers, as well as the differences between the molecular mechanisms, of osteoarthritis (OA) and rheumatoid arthritis (RA). Transcriptome dataset GSE100786 was downloaded to explore the differentially expressed genes (DEGs) between OA samples and RA samples. Meanwhile, metabolomic dataset MTBLS564 was downloaded and preprocessed to obtain metabolites. Then, the principal component analysis (PCA) and linear models were used to reveal DEG-metabolite relations. Finally, metabolic pathway enrichment analysis was performed to investigate the differences between the molecular mechanisms of OA and RA. A total of 976 DEGs and 171 metabolites were explored between OA samples and RA samples. The PCA and linear module analysis investigated 186 DEG-metabolite interactions including Glycogenin 1- (GYG1-) asparagine_54, hedgehog acyltransferase- (HHAT-) glucose_70, and TNF receptor-associated factor 3- (TRAF3-) acetoacetate_35. Finally, the KEGG pathway analysis showed that these metabolites were mainly enriched in pathways like gap junction, phagosome, NF-kappa B, and IL-17 pathway. Genes such as HHAT, GYG1, and TRAF3, as well as metabolites including glucose, asparagine, and acetoacetate, might be implicated in the pathogenesis of OA and RA. Metabolites like ethanol and tyrosine might participate differentially in OA and RA progression via the gap junction pathway and phagosome pathway, respectively. TRAF3-acetoacetate interaction may be involved in regulating inflammation in OA and RA by the NF-kappa B and IL-17 pathway.

Identifiants

pubmed: 31976312
doi: 10.1155/2020/5925126
pmc: PMC6961787
doi:

Types de publication

Journal Article

Langues

eng

Pagination

5925126

Informations de copyright

Copyright © 2020 Ningyang Gao et al.

Déclaration de conflit d'intérêts

The authors declare that there is no conflict of interest.

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Auteurs

Ningyang Gao (N)

Shi's Center of Orthopedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Li Ding (L)

Institute of Traumatology & Orthopedics, Shanghai Academy of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Jian Pang (J)

Institute of Traumatology & Orthopedics, Shanghai Academy of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Yuxin Zheng (Y)

Shi's Center of Orthopedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Yuelong Cao (Y)

Institute of Traumatology & Orthopedics, Shanghai Academy of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Hongsheng Zhan (H)

Shi's Center of Orthopedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Yinyu Shi (Y)

Shi's Center of Orthopedics and Traumatology, Shuguang Hospital Affiliated to Shanghai University of TCM, No. 528 Zhangheng Road, Shanghai 201203, China.

Classifications MeSH