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Original Research Article | OPEN ACCESS

A network pharmacology-based investigation of the mechanism involved in the anti-gastric cancer effect of Oldenlandia diffusan, a traditional Chinese medicine

Zhenchi Ma, Peng Zhao

Tianjin Cancer Hospital Airport Hospital, No. 99 East 5th Road, Tianjin Airport Economic Zone 300304, Tianjin, China;

For correspondence:-  Peng Zhao   Email: pengtuopa415285192@163.com

Accepted: 31 October 2022        Published: 30 November 2022

Citation: Ma Z, Zhao P. A network pharmacology-based investigation of the mechanism involved in the anti-gastric cancer effect of Oldenlandia diffusan, a traditional Chinese medicine. Trop J Pharm Res 2022; 21(11):2403-2410 doi: 10.4314/tjpr.v21i11.20

© 2022 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the potential mechanism underlying the anti-gastric cancer (GC) effect of Oldenlandia diffusa using network pharmacology, and to provide scientific guidance for subsequent pharmacological and clinical translational studies.
Methods: The potential bioactive compounds in Oldenlandia diffusa and their related targets were obtained through TCMSP online platform. The GeneCards and MalaCards databases were used to search for GC-related disease targets. The targets shared by the two databases were entered into STRING protein interactions online database to obtain the interaction network of potential therapeutic targets. These were further screened for potential core targets through MCODE plugin. Cytoscape 3.2.1 software was used to construct the "component-target-disease" and PPI network, while GO and KEGG enrichment analyses were performed using DAVID v6.8 online software.
Results: Seven bioactive components and 180 drug targets were screened in Oldenlandia diffusa, out of which 167 targets were co-activated with GC, and 28 potential core targets were identified. The results of GO function enrichment analysis of the hub targets showed that they were related to gene transcription and expression, cytokine-mediated signaling pathway and inflammation response. The results of KEGG signaling pathway enrichment analysis showed that they were mainly associated with cancer signaling, IL-17-related signaling and TNF signaling pathways.
Conclusion: Oldenlandia diffusa exerts its therapeutic effect on GC through multi-component, multi-target and multi-signaling pathways. This finding provides novel evidence for the application of Oldenlandia diffusa in GC treatment.

Keywords: Oldenlandia diffusa, Gastric cancer, Network pharmacology, Bioinformatics, Mechanism of drug action

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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