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Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas
PURPOSE: Gene-targeting therapy provides a novel therapeutic approach for tumor treatment using genetically modified endothelial progenitor cells (EPCs) as cellular carriers. This study applied EPCs armed with cytosine deaminase (CD) and endostatin (ES) fusion gene in liver cancer to explore its the...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198450/ https://www.ncbi.nlm.nih.gov/pubmed/32431545 http://dx.doi.org/10.2147/CMAR.S245998 |
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author | Zhang, Yue-Lin Zhou, Tan-Yang Ai, Jing Chen, Sheng-Qun Chen, Feng Nie, Chun-Hui Chen, Xin-Hua Zhou, Guan-Hui Wang, Hong-Liang Zhu, Tong-Yin Wang, Bao-Quan Yu, Zi-Niu Jing, Li Wu, Li-Ming Zheng, Shu-Sen Sun, Jun-Hui |
author_facet | Zhang, Yue-Lin Zhou, Tan-Yang Ai, Jing Chen, Sheng-Qun Chen, Feng Nie, Chun-Hui Chen, Xin-Hua Zhou, Guan-Hui Wang, Hong-Liang Zhu, Tong-Yin Wang, Bao-Quan Yu, Zi-Niu Jing, Li Wu, Li-Ming Zheng, Shu-Sen Sun, Jun-Hui |
author_sort | Zhang, Yue-Lin |
collection | PubMed |
description | PURPOSE: Gene-targeting therapy provides a novel therapeutic approach for tumor treatment using genetically modified endothelial progenitor cells (EPCs) as cellular carriers. This study applied EPCs armed with cytosine deaminase (CD) and endostatin (ES) fusion gene in liver cancer to explore its therapeutic effect. MATERIALS AND METHODS: EPCs from heart blood of male BALB/c nude mice were cultured and transfected with CD and ES fusion gene. Subsequently, these genetically modified cells were injected into mice bearing hepatoma through their tail veins. The tumor volumes and cell apoptosis were followed up. RESULTS: Tumor volume in the group injected CD/ES-EPCs greatly decreased. The positive rate of VEGF and CD31 in the tumor tissue was lowest in the CD/ES-EPC group. Furthermore, the number of apoptotic cells was highest in the CD/ES-EPC group. CONCLUSION: The EPCs transfected with CD/ES inhibited tumor growth and preferentially induced tumor cell apoptosis, providing a novel methodology for cancer-targeting therapy. |
format | Online Article Text |
id | pubmed-7198450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-71984502020-05-19 Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas Zhang, Yue-Lin Zhou, Tan-Yang Ai, Jing Chen, Sheng-Qun Chen, Feng Nie, Chun-Hui Chen, Xin-Hua Zhou, Guan-Hui Wang, Hong-Liang Zhu, Tong-Yin Wang, Bao-Quan Yu, Zi-Niu Jing, Li Wu, Li-Ming Zheng, Shu-Sen Sun, Jun-Hui Cancer Manag Res Original Research PURPOSE: Gene-targeting therapy provides a novel therapeutic approach for tumor treatment using genetically modified endothelial progenitor cells (EPCs) as cellular carriers. This study applied EPCs armed with cytosine deaminase (CD) and endostatin (ES) fusion gene in liver cancer to explore its therapeutic effect. MATERIALS AND METHODS: EPCs from heart blood of male BALB/c nude mice were cultured and transfected with CD and ES fusion gene. Subsequently, these genetically modified cells were injected into mice bearing hepatoma through their tail veins. The tumor volumes and cell apoptosis were followed up. RESULTS: Tumor volume in the group injected CD/ES-EPCs greatly decreased. The positive rate of VEGF and CD31 in the tumor tissue was lowest in the CD/ES-EPC group. Furthermore, the number of apoptotic cells was highest in the CD/ES-EPC group. CONCLUSION: The EPCs transfected with CD/ES inhibited tumor growth and preferentially induced tumor cell apoptosis, providing a novel methodology for cancer-targeting therapy. Dove 2020-04-30 /pmc/articles/PMC7198450/ /pubmed/32431545 http://dx.doi.org/10.2147/CMAR.S245998 Text en © 2020 Zhang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Zhang, Yue-Lin Zhou, Tan-Yang Ai, Jing Chen, Sheng-Qun Chen, Feng Nie, Chun-Hui Chen, Xin-Hua Zhou, Guan-Hui Wang, Hong-Liang Zhu, Tong-Yin Wang, Bao-Quan Yu, Zi-Niu Jing, Li Wu, Li-Ming Zheng, Shu-Sen Sun, Jun-Hui Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas |
title | Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas |
title_full | Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas |
title_fullStr | Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas |
title_full_unstemmed | Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas |
title_short | Gene Therapy with Cytosine Deaminase and Endostatin Fusion Gene Mediated by Endothelial Progenitor Cells in Hepatomas |
title_sort | gene therapy with cytosine deaminase and endostatin fusion gene mediated by endothelial progenitor cells in hepatomas |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7198450/ https://www.ncbi.nlm.nih.gov/pubmed/32431545 http://dx.doi.org/10.2147/CMAR.S245998 |
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