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Modular bioinformatics analysis demonstrates that a Toll‑like receptor signaling pathway is involved in the regulation of macrophage polarization
- Source :
- Molecular Medicine Reports
- Publication Year :
- 2018
-
Abstract
- In recent years, an increasing number of studies on the roles of macrophages in tumors, immune responses and metabolism have been published, in which macrophage polarization has been an extensively discussed topic. In the present study, differentially expressed genes in various types of macrophages were analyzed using the Gene Expression Omnibus database. Cluster analysis of differentially expressed genes was conducted, and a protein‑protein interaction (PPI) network was constructed. Finally, modular analysis and functional enrichment analysis revealed that a Toll‑like receptor (TLR) signaling pathway is involved in the regulation of macrophage polarization. Furthermore, the high‑degree proteins in the PPI network that are involved in the molecular regulation of macrophage polarization are closely associated with proteins of the TLR signaling pathway. These results suggested that the TLR signaling pathways may be a principal direction of future research on the regulation of macrophage polarization.
- Subjects :
- 0301 basic medicine
Cancer Research
macrophage polarization
Macrophage polarization
Gene regulatory network
Biology
Biochemistry
Transcriptome
03 medical and health sciences
Toll-like receptor signaling pathway
Databases, Genetic
Genetics
Humans
Gene Regulatory Networks
Receptor
Molecular Biology
Regulation of gene expression
Gene Expression Profiling
Macrophages
Toll-Like Receptors
Computational Biology
Articles
Macrophage Activation
modular bioinformatics analysis
Cell biology
Gene expression profiling
030104 developmental biology
Oncology
Gene Expression Regulation
Molecular Medicine
Signal transduction
Signal Transduction
Subjects
Details
- ISSN :
- 17913004
- Volume :
- 18
- Issue :
- 5
- Database :
- OpenAIRE
- Journal :
- Molecular medicine reports
- Accession number :
- edsair.doi.dedup.....75ff3c9422a05f45a0669b95a2cf580d