The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective

Background. This study utilized network pharmacology and bioinformatics analysis to identify the hub genes influenced by scopolamine in lung cancer. Methods. The effect of scopolamine on lung cancer was investigated by cell invasion assay and cell scratch assay. The analysis involved protein-protein...

Full description

Saved in:
Bibliographic Details
Main Authors: Yang Xiao, Mengcong Ma, Qing Gu, Yunfeng Xiao
Format: Article
Language:English
Published: Wiley 2024-01-01
Series:International Journal of Clinical Practice
Online Access:http://dx.doi.org/10.1155/2024/5081383
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832546238696783872
author Yang Xiao
Mengcong Ma
Qing Gu
Yunfeng Xiao
author_facet Yang Xiao
Mengcong Ma
Qing Gu
Yunfeng Xiao
author_sort Yang Xiao
collection DOAJ
description Background. This study utilized network pharmacology and bioinformatics analysis to identify the hub genes influenced by scopolamine in lung cancer. Methods. The effect of scopolamine on lung cancer was investigated by cell invasion assay and cell scratch assay. The analysis involved protein-protein interaction (PPI) networks topology analysis to identify these genes, and subsequent differential analysis and survival analysis were conducted using gene expression profile interaction analysis (GEPIA). Furthermore, the findings were supported by molecular docking experiments for verification. Results. Results from cell invasion and scratch assays suggest that scopolamine inhibits the migration of lung cancer cells. JAK2, JAK3, CCR5, and ACE were identified as the top four hub genes that have an impact on lung cancer. KEGG enrichment analysis revealed that the scopolamine response in lung cancer is significantly associated with ten pathways, including “neuroactive ligand-receptor interaction in cancer,” “PD-1 checkpoint pathway in cancer,” “chemokine signaling pathway,” “PD-L1 expression,” and others. Additionally, the expression levels of JAK2, JAK3, CCR5, and ACE were found to be correlated with survival in patients with lung cancer. Furthermore, molecular docking experiments demonstrated that scopolamine binds and forms stable complexes with the protein products of all four aforementioned genes. The main targets of scopolamine in the treatment of lung cancer are JAK2, JAK3, CCR5, and ACE. Conclusion. Scopolamine has a significant effect on various cellular functions in lung cancer cells, potentially reducing the likelihood of metastasis. Based on these findings, it is recommended to consider administering scopolamine as part of the preoperative phase for patients with lung cancer.
format Article
id doaj-art-f5d4e347984d4caca06506914aab63fa
institution Kabale University
issn 1742-1241
language English
publishDate 2024-01-01
publisher Wiley
record_format Article
series International Journal of Clinical Practice
spelling doaj-art-f5d4e347984d4caca06506914aab63fa2025-02-03T07:23:37ZengWileyInternational Journal of Clinical Practice1742-12412024-01-01202410.1155/2024/5081383The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics PerspectiveYang Xiao0Mengcong Ma1Qing Gu2Yunfeng Xiao3Xuzhou Medical UniversityXuzhou Medical UniversityXuzhou Medical UniversityXuzhou Medical UniversityBackground. This study utilized network pharmacology and bioinformatics analysis to identify the hub genes influenced by scopolamine in lung cancer. Methods. The effect of scopolamine on lung cancer was investigated by cell invasion assay and cell scratch assay. The analysis involved protein-protein interaction (PPI) networks topology analysis to identify these genes, and subsequent differential analysis and survival analysis were conducted using gene expression profile interaction analysis (GEPIA). Furthermore, the findings were supported by molecular docking experiments for verification. Results. Results from cell invasion and scratch assays suggest that scopolamine inhibits the migration of lung cancer cells. JAK2, JAK3, CCR5, and ACE were identified as the top four hub genes that have an impact on lung cancer. KEGG enrichment analysis revealed that the scopolamine response in lung cancer is significantly associated with ten pathways, including “neuroactive ligand-receptor interaction in cancer,” “PD-1 checkpoint pathway in cancer,” “chemokine signaling pathway,” “PD-L1 expression,” and others. Additionally, the expression levels of JAK2, JAK3, CCR5, and ACE were found to be correlated with survival in patients with lung cancer. Furthermore, molecular docking experiments demonstrated that scopolamine binds and forms stable complexes with the protein products of all four aforementioned genes. The main targets of scopolamine in the treatment of lung cancer are JAK2, JAK3, CCR5, and ACE. Conclusion. Scopolamine has a significant effect on various cellular functions in lung cancer cells, potentially reducing the likelihood of metastasis. Based on these findings, it is recommended to consider administering scopolamine as part of the preoperative phase for patients with lung cancer.http://dx.doi.org/10.1155/2024/5081383
spellingShingle Yang Xiao
Mengcong Ma
Qing Gu
Yunfeng Xiao
The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective
International Journal of Clinical Practice
title The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective
title_full The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective
title_fullStr The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective
title_full_unstemmed The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective
title_short The Mechanism of Scopolamine’s Effect on Migration Function of Lung Cancer Cells: A Network Pharmacology and Bioinformatics Perspective
title_sort mechanism of scopolamine s effect on migration function of lung cancer cells a network pharmacology and bioinformatics perspective
url http://dx.doi.org/10.1155/2024/5081383
work_keys_str_mv AT yangxiao themechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT mengcongma themechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT qinggu themechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT yunfengxiao themechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT yangxiao mechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT mengcongma mechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT qinggu mechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective
AT yunfengxiao mechanismofscopolamineseffectonmigrationfunctionoflungcancercellsanetworkpharmacologyandbioinformaticsperspective