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Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis

BACKGROUND: Evodiamine (EVO), an alkaloid extracted from the traditional Chinese medicine Euodia rutaecarpa, plays an important role in the treatment of cancer. This study was performed to clarify the effects of evodiamine in mice tumor model studies. METHODS: Electronic databases and search engines...

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Autores principales: Yin, Cong, Cheng, Jing, Peng, Hongbing, Yuan, Shijun, Chen, Keli, Li, Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8660089/
https://www.ncbi.nlm.nih.gov/pubmed/34900724
http://dx.doi.org/10.3389/fonc.2021.774201
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author Yin, Cong
Cheng, Jing
Peng, Hongbing
Yuan, Shijun
Chen, Keli
Li, Juan
author_facet Yin, Cong
Cheng, Jing
Peng, Hongbing
Yuan, Shijun
Chen, Keli
Li, Juan
author_sort Yin, Cong
collection PubMed
description BACKGROUND: Evodiamine (EVO), an alkaloid extracted from the traditional Chinese medicine Euodia rutaecarpa, plays an important role in the treatment of cancer. This study was performed to clarify the effects of evodiamine in mice tumor model studies. METHODS: Electronic databases and search engines involved China Knowledge Resource Integrated Database (CNKI), Wanfang Database, Chinese Scientific Journal Database (CSJD-VIP), China Biomedical Literature Database (CBM), PubMed, Embase, Web of Science, and ClinicalTrials.gov databases, which were searched for literature related to the antitumor effects of evodiamine in animal tumor models (all until 1 October 2021). The evodiamine effects on the tumor volume and tumor weight were compared between the treatment and control groups using the standardized mean difference (SMD). RESULTS: Evodiamine significantly inhibited tumor growth in mice, as was assessed with tumor volume [13 studies, n=267; 138 for EVO and 129 for control; standard mean difference (SMD)= -5.99; 95% (CI): -8.89 to -3.10; I(2) = 97.69%, p ≤ 0.00], tumor weight [6 studies, n=89; 49 for EVO and 40 for control; standard mean difference (SMD)= -3.51; 95% (CI): -5.13 to -3.90; I(2) = 83.02%, p ≤ 0.00]. CONCLUSION: EVO significantly suppresses tumor growth in mice models, which would be beneficial for clinical transformation. However, due to the small number of studies included in this meta-analysis, the experimental design and experimental method limitations should be considered when interpreting the results. Significant clinical and animal studies are still required to evaluate whether EVO can be used in the adjuvant treatment of clinical tumor patients.
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spelling pubmed-86600892021-12-10 Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis Yin, Cong Cheng, Jing Peng, Hongbing Yuan, Shijun Chen, Keli Li, Juan Front Oncol Oncology BACKGROUND: Evodiamine (EVO), an alkaloid extracted from the traditional Chinese medicine Euodia rutaecarpa, plays an important role in the treatment of cancer. This study was performed to clarify the effects of evodiamine in mice tumor model studies. METHODS: Electronic databases and search engines involved China Knowledge Resource Integrated Database (CNKI), Wanfang Database, Chinese Scientific Journal Database (CSJD-VIP), China Biomedical Literature Database (CBM), PubMed, Embase, Web of Science, and ClinicalTrials.gov databases, which were searched for literature related to the antitumor effects of evodiamine in animal tumor models (all until 1 October 2021). The evodiamine effects on the tumor volume and tumor weight were compared between the treatment and control groups using the standardized mean difference (SMD). RESULTS: Evodiamine significantly inhibited tumor growth in mice, as was assessed with tumor volume [13 studies, n=267; 138 for EVO and 129 for control; standard mean difference (SMD)= -5.99; 95% (CI): -8.89 to -3.10; I(2) = 97.69%, p ≤ 0.00], tumor weight [6 studies, n=89; 49 for EVO and 40 for control; standard mean difference (SMD)= -3.51; 95% (CI): -5.13 to -3.90; I(2) = 83.02%, p ≤ 0.00]. CONCLUSION: EVO significantly suppresses tumor growth in mice models, which would be beneficial for clinical transformation. However, due to the small number of studies included in this meta-analysis, the experimental design and experimental method limitations should be considered when interpreting the results. Significant clinical and animal studies are still required to evaluate whether EVO can be used in the adjuvant treatment of clinical tumor patients. Frontiers Media S.A. 2021-11-09 /pmc/articles/PMC8660089/ /pubmed/34900724 http://dx.doi.org/10.3389/fonc.2021.774201 Text en Copyright © 2021 Yin, Cheng, Peng, Yuan, Chen and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Yin, Cong
Cheng, Jing
Peng, Hongbing
Yuan, Shijun
Chen, Keli
Li, Juan
Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis
title Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis
title_full Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis
title_fullStr Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis
title_full_unstemmed Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis
title_short Antitumor Effects of Evodiamine in Mice Model Experiments: A Systematic Review and Meta-Analysis
title_sort antitumor effects of evodiamine in mice model experiments: a systematic review and meta-analysis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8660089/
https://www.ncbi.nlm.nih.gov/pubmed/34900724
http://dx.doi.org/10.3389/fonc.2021.774201
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