Investigation on the Therapeutic Mechanism of Danbie Capsules for Endometriosis: A Network Pharmacology Approach
This network pharmacology study identified quercetin, β-sitosterol, and luteolin as active substances in Danbie Capsules that target TP53 and AKT1 for endometriosis treatment.
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This paper used a network pharmacology approach to identify active substances and molecular targets of Danbie Capsules for endometriosis by screening 183 compounds from TCMSP and published literature and intersecting their predicted targets with endometriosis-related gene targets derived from the GEO database, yielding 24 target genes. Network mapping with Cytoscape and protein–protein interaction analysis using STRING highlighted three critical active substances (quercetin, β-sitosterol, and luteolin) and seven critical targets, with TP53 and AKT1 emphasized and additionally supported by molecular docking and immunohistochemical verification. A major caveat is that the study relies on in silico network analyses and curated database-derived targets before focusing on limited experimentally supported genes. This paper is centrally about endometriosis — it investigates Danbie Capsules’ therapeutic mechanisms via active compound–target network analysis centered on TP53 and AKT1.
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