Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer

This study aims to identify the mechanism of geniposide regulating oxidative stress in colorectal cancer (CRC) through network pharmacology and bioinformatics analysis. Targets of geniposide, oxidative stress-related targets and targets related to CRC were applied from databases. The hub genes for g...

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Main Authors: Yingzi Wu, Jinhai Luo, Baojun Xu
Format: Article
Language:English
Published: MDPI AG 2023-10-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/24/20/15222
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author Yingzi Wu
Jinhai Luo
Baojun Xu
author_facet Yingzi Wu
Jinhai Luo
Baojun Xu
author_sort Yingzi Wu
collection DOAJ
description This study aims to identify the mechanism of geniposide regulating oxidative stress in colorectal cancer (CRC) through network pharmacology and bioinformatics analysis. Targets of geniposide, oxidative stress-related targets and targets related to CRC were applied from databases. The hub genes for geniposide regulating oxidative stress in CRC were identified with the protein–protein interaction (PPI) network. Furthermore, we applied Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment to analyze the hub genes from a macro perspective. We verified the hub genes by molecular docking, GEPIA, HPA and starBase database. We identified five hub genes: <i>IL1B, GSK3B, NOS3, RELA and CDK4</i>. GO analysis results suggested that the anti-colorectal cancer effect of geniposide by regulating oxidative stress is possibly related to the influence of multiple biological processes, including response to temperature stimulus, response to alkaloid, nitric oxide biosynthetic process, nitric oxide metabolic process, reactive nitrogen species metabolic process, cellular response to peptide, etc. KEGG enrichment analysis results indicated that the PI3K–Akt signaling pathway, IL-17 signaling pathway, p53 signaling pathway, NF-κB signaling pathway and NOD-like receptor signaling pathway are likely to be the significant pathways. Molecular docking results showed that the geniposide had a good binding activity with the hub genes. This study demonstrates that geniposide can regulate oxidative stress in CRC, and induction of oxidative stress is one of the possible mechanisms of anti-recurrence and metastasis effects of geniposide against CRC.
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spelling doaj.art-496b26edf95c497c9635197a193f8b4c2023-11-19T16:43:33ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672023-10-0124201522210.3390/ijms242015222Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal CancerYingzi Wu0Jinhai Luo1Baojun Xu2Guangdong Provincial Key Laboratory IRADS, Department of Life Sciences, BNU-HKBU United International College, Zhuhai 519087, ChinaGuangdong Provincial Key Laboratory IRADS, Department of Life Sciences, BNU-HKBU United International College, Zhuhai 519087, ChinaGuangdong Provincial Key Laboratory IRADS, Department of Life Sciences, BNU-HKBU United International College, Zhuhai 519087, ChinaThis study aims to identify the mechanism of geniposide regulating oxidative stress in colorectal cancer (CRC) through network pharmacology and bioinformatics analysis. Targets of geniposide, oxidative stress-related targets and targets related to CRC were applied from databases. The hub genes for geniposide regulating oxidative stress in CRC were identified with the protein–protein interaction (PPI) network. Furthermore, we applied Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment to analyze the hub genes from a macro perspective. We verified the hub genes by molecular docking, GEPIA, HPA and starBase database. We identified five hub genes: <i>IL1B, GSK3B, NOS3, RELA and CDK4</i>. GO analysis results suggested that the anti-colorectal cancer effect of geniposide by regulating oxidative stress is possibly related to the influence of multiple biological processes, including response to temperature stimulus, response to alkaloid, nitric oxide biosynthetic process, nitric oxide metabolic process, reactive nitrogen species metabolic process, cellular response to peptide, etc. KEGG enrichment analysis results indicated that the PI3K–Akt signaling pathway, IL-17 signaling pathway, p53 signaling pathway, NF-κB signaling pathway and NOD-like receptor signaling pathway are likely to be the significant pathways. Molecular docking results showed that the geniposide had a good binding activity with the hub genes. This study demonstrates that geniposide can regulate oxidative stress in CRC, and induction of oxidative stress is one of the possible mechanisms of anti-recurrence and metastasis effects of geniposide against CRC.https://www.mdpi.com/1422-0067/24/20/15222oxidative stressCRCnetwork pharmacologymolecular dockingbioinformaticsgeniposide
spellingShingle Yingzi Wu
Jinhai Luo
Baojun Xu
Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer
International Journal of Molecular Sciences
oxidative stress
CRC
network pharmacology
molecular docking
bioinformatics
geniposide
title Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer
title_full Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer
title_fullStr Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer
title_full_unstemmed Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer
title_short Network Pharmacology and Bioinformatics Study of Geniposide Regulating Oxidative Stress in Colorectal Cancer
title_sort network pharmacology and bioinformatics study of geniposide regulating oxidative stress in colorectal cancer
topic oxidative stress
CRC
network pharmacology
molecular docking
bioinformatics
geniposide
url https://www.mdpi.com/1422-0067/24/20/15222
work_keys_str_mv AT yingziwu networkpharmacologyandbioinformaticsstudyofgeniposideregulatingoxidativestressincolorectalcancer
AT jinhailuo networkpharmacologyandbioinformaticsstudyofgeniposideregulatingoxidativestressincolorectalcancer
AT baojunxu networkpharmacologyandbioinformaticsstudyofgeniposideregulatingoxidativestressincolorectalcancer