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Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy
PURPOSE: Cancer treatment still faces big challenges in the clinic, which is raising concerns over the world. In this study, we report the novel strategy of combing bacteriotherapy with high-intensity focused ultrasound (HIFU) therapy for more efficient breast cancer treatment. METHODS: The acoustic...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802776/ https://www.ncbi.nlm.nih.gov/pubmed/33447030 http://dx.doi.org/10.2147/IJN.S292432 |
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author | Yang, Haiyan Jiang, Fujie Ji, Xiaojuan Wang, Lu Wang, Yaotai Zhang, Liang Tang, Yu Wang, Disen Luo, Yong Li, Ningshan Wang, Qi Zou, Jianzhong |
author_facet | Yang, Haiyan Jiang, Fujie Ji, Xiaojuan Wang, Lu Wang, Yaotai Zhang, Liang Tang, Yu Wang, Disen Luo, Yong Li, Ningshan Wang, Qi Zou, Jianzhong |
author_sort | Yang, Haiyan |
collection | PubMed |
description | PURPOSE: Cancer treatment still faces big challenges in the clinic, which is raising concerns over the world. In this study, we report the novel strategy of combing bacteriotherapy with high-intensity focused ultrasound (HIFU) therapy for more efficient breast cancer treatment. METHODS: The acoustic reporter gene (ARG) was genetically engineered to be expressed successfully in Escherichia coli (E. coli) to produce the protein nanoparticles-gas vesicles (GVs). Ultrasound was utilized to visualize the GVs in E. coli. In addition, it was injected intravenously for targeted breast cancer therapy by combing the bacteriotherapy with HIFU therapy. RESULTS: ARG expressed in E. coli can be visualized in vitro and in vivo by ultrasound. After intravenous injection, E. coli containing GVs could specifically target the tumor site, colonize consecutively in the tumor microenvironment, and it could obviously inhibit tumor growth. Meanwhile, E. coli which contained GVs could synergize HIFU therapy efficiently both in vitro and in vivo as the cavitation nuclei. Furthermore, the tumor inhibition rate in the combination therapy group could be high up to 87% compared with that in the control group. CONCLUSION: Our novel strategy of combing bacteriotherapy with HIFU therapy can treat breast cancers more effectively than the monotherapies, so it can be seen as a promising strategy. |
format | Online Article Text |
id | pubmed-7802776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-78027762021-01-13 Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy Yang, Haiyan Jiang, Fujie Ji, Xiaojuan Wang, Lu Wang, Yaotai Zhang, Liang Tang, Yu Wang, Disen Luo, Yong Li, Ningshan Wang, Qi Zou, Jianzhong Int J Nanomedicine Original Research PURPOSE: Cancer treatment still faces big challenges in the clinic, which is raising concerns over the world. In this study, we report the novel strategy of combing bacteriotherapy with high-intensity focused ultrasound (HIFU) therapy for more efficient breast cancer treatment. METHODS: The acoustic reporter gene (ARG) was genetically engineered to be expressed successfully in Escherichia coli (E. coli) to produce the protein nanoparticles-gas vesicles (GVs). Ultrasound was utilized to visualize the GVs in E. coli. In addition, it was injected intravenously for targeted breast cancer therapy by combing the bacteriotherapy with HIFU therapy. RESULTS: ARG expressed in E. coli can be visualized in vitro and in vivo by ultrasound. After intravenous injection, E. coli containing GVs could specifically target the tumor site, colonize consecutively in the tumor microenvironment, and it could obviously inhibit tumor growth. Meanwhile, E. coli which contained GVs could synergize HIFU therapy efficiently both in vitro and in vivo as the cavitation nuclei. Furthermore, the tumor inhibition rate in the combination therapy group could be high up to 87% compared with that in the control group. CONCLUSION: Our novel strategy of combing bacteriotherapy with HIFU therapy can treat breast cancers more effectively than the monotherapies, so it can be seen as a promising strategy. Dove 2021-01-08 /pmc/articles/PMC7802776/ /pubmed/33447030 http://dx.doi.org/10.2147/IJN.S292432 Text en © 2021 Yang 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 Yang, Haiyan Jiang, Fujie Ji, Xiaojuan Wang, Lu Wang, Yaotai Zhang, Liang Tang, Yu Wang, Disen Luo, Yong Li, Ningshan Wang, Qi Zou, Jianzhong Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy |
title | Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy |
title_full | Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy |
title_fullStr | Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy |
title_full_unstemmed | Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy |
title_short | Genetically Engineered Bacterial Protein Nanoparticles for Targeted Cancer Therapy |
title_sort | genetically engineered bacterial protein nanoparticles for targeted cancer therapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7802776/ https://www.ncbi.nlm.nih.gov/pubmed/33447030 http://dx.doi.org/10.2147/IJN.S292432 |
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