Title:Research of Active Compounds from Allii Macrostemonis Bulbus and
Potential Targets against Non-Hodgkin’s Lymphoma Based on Network
Pharmacology
Volume: 20
Issue: 3
Author(s): Xiuliang Qiu, QiuLing Zhao, Hongqiang Qiu, Yu Cheng, WenBin Liu and Lin Yang*
Affiliation:
- Department of Pharmacy, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, Fujian, China
Keywords:
Allii Macrostemonis Bulbus, non-hodgkin’s lymphoma, network pharmacology, targets, mechanism, molecular docking.
Abstract:
Background: Non-Hodgkin’s Lymphoma (NHL) is a series of lymphoid malignancies
in some aggressive subtypes with unsatisfactory treatment effects. Allii Macrostemonis Bulbus
(Xie Bai) is a traditional Chinese medicine with anti-cancer activities, which may potentially suppress
aggressive NHL.
Objective: This study tries to discover active components and targets of Xie Bai in treating NHL
by network pharmacology-based approaches.
Methods: Compounds and related targets of Xie Bai were collected from the Traditional Chinese
Medicine Database and Analysis Platform. Target genes associated with NHL were searched by
GeneCards and DisGeNET, then the overlapped targets were further analyzed by STRING tool,
GO, and KEGG pathway enrichment analysis. Molecular docking was employed to verify the interaction
between compounds and targets.
Results: 11 bioactive compounds were successfully identified, with 30 targets that were screened
out for the treatment of NHL. Functional enrichment analysis suggested that Xie Bai exerted its
potential effects against NHL via pathways in cancer, such as PI3K/ AKT, p53, and MAPK signaling
pathways. Molecular docking results showed that 3 active compounds (quercetin, betasitosterol,
and naringenin) had good affinity with selected 6 targets (TP53, AKT1, CASP3,
CCND1, HPK1, and NLRP3).
Conclusion: Identifying six potential genes could accurately be docked with Xie Bai and had
close interactions with NHL, which may provide insight into further research and new treatment
strategy.