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Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula
BACKGROUND: Tao-He-Cheng-Qi Formula (THCQF) is a traditional Chinese medicine that has been proven to have antitumor effects. The aim of this study was to elucidate the molecular targets and mechanisms of THCQF against colon cancer and construct a prognostic model based on network pharmacology, bioi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038428/ https://www.ncbi.nlm.nih.gov/pubmed/35479514 http://dx.doi.org/10.1155/2022/7998664 |
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author | Zhang, Zexin Lin, Siqi Liu, Zifeng Han, Jun Li, Jing Yu, Yi |
author_facet | Zhang, Zexin Lin, Siqi Liu, Zifeng Han, Jun Li, Jing Yu, Yi |
author_sort | Zhang, Zexin |
collection | PubMed |
description | BACKGROUND: Tao-He-Cheng-Qi Formula (THCQF) is a traditional Chinese medicine that has been proven to have antitumor effects. The aim of this study was to elucidate the molecular targets and mechanisms of THCQF against colon cancer and construct a prognostic model based on network pharmacology, bioinformatics analysis, and in vitro experiments. METHODS: Potential THCQF compounds and targets were retrieved from the Traditional Chinese Medicine Systems Pharmacology and Bioinformatics Analysis Tool for Molecular Mechanism of Traditional Chinese Medicine databases. Differentially expressed genes for colon cancer were screened in The Cancer Genome Atlas and Gene Expression Omnibus databases. The anticolon cancer mechanisms of THCQF were explored using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. Molecular docking simulations and molecular dynamics analysis were used to evaluate the binding between target proteins and active compounds. Finally, the identified compounds were used to treat colon cancer cells from the HCT116 cell line, and expression of mRNA and protein after relevant posttreatment were tested using real-time polymerase chain reaction and western blotting. RESULTS: A total of 27 anticolon cancer targets of THCQF were selected, among which four genes (CCNB1, CCNA2, IL1A, and MMP3) were shown to effectively predict patient outcomes in a prognostic colon cancer model. GO and KEGG enrichment analyses indicated that the activity against colon cancer of THCQF was associated with the interleukin (IL)-4 and IL-3 signaling pathways. Two compounds in THCQF, aloe emodin (AE) and quercetin (QR), were shown to efficiently bind to cyclin B1, the protein encoded by CCNB1. Finally, incubation of HCT116 cells with AE and QR significantly decreased CCNB1 mRNA expression and cyclin B1 levels. CONCLUSIONS: Taken together, the results indicate that AE and QR are the pivotal active compounds of THCQF, and CCNB1 is the main molecular target through which THCQF exerts its anticolon cancer effects. The study findings provide insight for studies investigating the anticancer effects of other traditional Chinese medicines. |
format | Online Article Text |
id | pubmed-9038428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-90384282022-04-26 Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula Zhang, Zexin Lin, Siqi Liu, Zifeng Han, Jun Li, Jing Yu, Yi Evid Based Complement Alternat Med Research Article BACKGROUND: Tao-He-Cheng-Qi Formula (THCQF) is a traditional Chinese medicine that has been proven to have antitumor effects. The aim of this study was to elucidate the molecular targets and mechanisms of THCQF against colon cancer and construct a prognostic model based on network pharmacology, bioinformatics analysis, and in vitro experiments. METHODS: Potential THCQF compounds and targets were retrieved from the Traditional Chinese Medicine Systems Pharmacology and Bioinformatics Analysis Tool for Molecular Mechanism of Traditional Chinese Medicine databases. Differentially expressed genes for colon cancer were screened in The Cancer Genome Atlas and Gene Expression Omnibus databases. The anticolon cancer mechanisms of THCQF were explored using Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analyses. Molecular docking simulations and molecular dynamics analysis were used to evaluate the binding between target proteins and active compounds. Finally, the identified compounds were used to treat colon cancer cells from the HCT116 cell line, and expression of mRNA and protein after relevant posttreatment were tested using real-time polymerase chain reaction and western blotting. RESULTS: A total of 27 anticolon cancer targets of THCQF were selected, among which four genes (CCNB1, CCNA2, IL1A, and MMP3) were shown to effectively predict patient outcomes in a prognostic colon cancer model. GO and KEGG enrichment analyses indicated that the activity against colon cancer of THCQF was associated with the interleukin (IL)-4 and IL-3 signaling pathways. Two compounds in THCQF, aloe emodin (AE) and quercetin (QR), were shown to efficiently bind to cyclin B1, the protein encoded by CCNB1. Finally, incubation of HCT116 cells with AE and QR significantly decreased CCNB1 mRNA expression and cyclin B1 levels. CONCLUSIONS: Taken together, the results indicate that AE and QR are the pivotal active compounds of THCQF, and CCNB1 is the main molecular target through which THCQF exerts its anticolon cancer effects. The study findings provide insight for studies investigating the anticancer effects of other traditional Chinese medicines. Hindawi 2022-04-18 /pmc/articles/PMC9038428/ /pubmed/35479514 http://dx.doi.org/10.1155/2022/7998664 Text en Copyright © 2022 Zexin Zhang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhang, Zexin Lin, Siqi Liu, Zifeng Han, Jun Li, Jing Yu, Yi Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula |
title | Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula |
title_full | Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula |
title_fullStr | Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula |
title_full_unstemmed | Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula |
title_short | Anticolon Cancer Targets and Molecular Mechanisms of Tao-He-Cheng-Qi Formula |
title_sort | anticolon cancer targets and molecular mechanisms of tao-he-cheng-qi formula |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9038428/ https://www.ncbi.nlm.nih.gov/pubmed/35479514 http://dx.doi.org/10.1155/2022/7998664 |
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