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Eurasian Journal of
            Medicine and Oncology                                          QGJSF multi-target mechanisms in osteoporosis

















































                                  Figure 3. Core target network diagram involved in the treatment of OP using QGJSF
                                      Abbreviations: OP: Osteoporosis; QGJSF: Qiang-gu-jian-shen formula.

            RNA polymerase II transcription, positive regulation of   activities and identifies key protein targets and their
            DNA-templated transcription, response  to exogenous   respective pathways. A total of 133 primary pathways were
            stimulus, positive regulation of cell population proliferation,   collected in the KEGG enrichment analysis. After excluding
            negative regulation of apoptotic processes, response to   disease-named and cancer-related signaling pathways,
            lipopolysaccharide,  inflammatory  response,  response  the top 20 pathways were visualized using MicroSignal
            to hypoxia, and negative regulation of cell population   (Figure 5B). The enriched pathways are mainly involved
            proliferation. The CC is primarily associated with extracellular   in  the PI3K/AKT  signaling  pathway, FoxO  signaling
            space, extracellular region, extracellular vesicle (exosome), cell   pathway,  HIF-1  signaling  pathway,  cellular  senescence,
            surface, protein complex-containing structures, endoplasmic   osteoclast differentiation, TNF signaling pathway, Th17
            reticulum lumen, collagen-containing extracellular matrix,   cell differentiation, IL-17 signaling pathway, prolactin
            receptor complexes, plasma membrane side, and plasma   signaling pathway, and apoptosis signaling pathway.
            membrane (cell membrane). The MF mainly concerns
            binding to identical proteins, enzyme binding, protein   3.7. Molecular docking
            binding, nuclear receptor activity, signal receptor binding,   To investigate the interactions between the main active
            DNA-binding transcription factor activity, cytokine activity,   components of the potent bone-strengthening and
            protein homodimerization activity, and RNA polymerase   kidney-nourishing formula and their corresponding core
            II-specific DNA-binding transcriptional activator activity.  targets, molecular docking analysis was conducted using
              KEGG pathway enrichment analysis predicts the role   the AutoDock platform. The molecular structures of the
            of protein target interaction networks in various cellular   compounds were downloaded from the PubChem database,


            Volume 9 Issue 2 (2025)                        274                         doi: 10.36922/EJMO025150103
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