Apoptosis pathways and osteoporosis: An approach to genomic analysis

• Published in: The journal of gene medicine Vol. 25; no. 11; p. e3555
• Main Authors: Huang, Hsiao‐Ling, Wu, Chung‐Ken, Wu, Dai‐Jia, Liu, Wen‐Hsiu, Lee, Ying‐Shiung, Wu, Chi‐Ling
• Format: Journal Article
• Language: English
• Published: England Wiley Periodicals Inc 01.11.2023
• Subjects: Apoptosis; Biotechnology; Bone mass; C2 gene; Caspase; DNA microarrays; Fractures; Gene expression; Gene set enrichment analysis; Gene therapy; Genes; Genomic analysis; Life span; Osteoporosis; p53 Protein; Public health; Signal transduction; GSEA; bone; osteoporosis; apoptosis pathway
• ISSN: 1099-498X; 1521-2254; 1521-2254
• DOI: 10.1002/jgm.3555

Osteoporosis is a disease of the bone system that causes a decrease in skeletal density and degrades skeletal tissue. Decreased bone quality, so that bones are easily broken, damaged and fractured, is an important public health problem. Previous studies have shown that the maintenance of adult bone mass is not only due to changes in bone marrow and bone cells. By regulating apoptosis, they change the lifespan of each individual. This study influences understanding of the function of apoptosis in the pathogenesis of osteoporosis and the importance of controlling the mechanisms of osteoporosis. On the National Institute of Biotechnology Information website, Gene Expression Omnibus (GEO) microarray data and GSE551495 GEO profiles were collected. The gene set enrichment analysis tool was used to confirm the enrichment of genetic sets in relation to the gene set. The collection of C2 gene sets is compiled from the KEGG (https://www.gsea-msigdb.org/gsea/msigdb/human/search.jsp and https://www.kegg.jp/kegg/) online database and REACTOME (https://www.gsea-msigdb.org/gsea/msigdb/human/search.jsp and https://reactome.org/) pathway analysis. The Search Tool for the Retrieval of Interaction Genes (STRING) website was used to construct and select proteins and genes. The comparative toxicological genomic database (CTD) tools can be used to predict the relationship between apoptosis, osteoporosis-related genes and interactions between central genes and osteoporosis. These results generally expand our understanding of the path of apoptosis in osteoporosis. We have discovered genes CASP9, CASP8, CASP3, BAX and TP53 associated with osteoporosis. In activation of KEGG apoptosis and REACTOME, caspase activation through the extrinsic apoptotic signaling pathway is characterized by the identification of a subcollection of C2. Other STRINGs show the formation of protein networks and central gene selection, and CTD can accurately predict the relationship between these apoptosis pathways and central genes. Our research has highlighted the importance of the osteoporosis pathway associated with osteoporosis apoptosis with several analytical approaches. These results have broadened our understanding of the pathways of osteoporosis apoptosis. It is particularly possible to predict the sensitivity and vulnerability to osteoporosis.