Table 1.
Biological Process | Count | p-value |
---|---|---|
G1/S Transition of Mitotic Cell Cycle | 5 | 3.10E-05 |
Negative Regulation of Protein Kinase Activity | 4 | 7.20E-04 |
Cell Cycle Arrest | 4 | 2.00E-03 |
Negative Regulation of Cell Proliferation | 5 | 5.10E-03 |
DNA Damage Response, Signal Transduction by P53 Class Mediator Resulting in Cell Cycle Arrest | 3 | 5.50E-03 |
Negative Regulation of Monocyte Differentiation | 2 | 1.20E-02 |
Regulation of Cell Cycle | 3 | 2.10E-02 |
Replicative Senescence | 2 | 2.10E-02 |
T-Cell Receptor Signaling Pathway | 3 | 2.90E-02 |
Cellular Response to Extracellular Stimulus | 2 | 3.20E-02 |
Response to Corticosterone | 2 | 3.20E-02 |
Negative Regulation of Phosphorylation | 2 | 3.50E-02 |
Negative Regulation of Cyclin-Dependent Protein Serine/Threonine Kinase Activity | 2 | 3.90E-02 |
Cellular Senescence | 2 | 4.00E-02 |
To analyze the involvement of DEGs in different biological functional groups, all 35 common genes between HL-60 and BV173 were annotated for their role in biological processes. Differentially expressed genes IDs were uploaded into online DAVID bioinformatics software, and functional annotation clustering analysis was performed on GOTERM_BP_FAT gene ontology (GO). Categories with a p<0.05 were considered as statistically significant. The software mapped 31 of 35 genes and highlighted 14 different biological processes in leukemic cells cultured in the presence of UC-MSCs.