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Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer

PURPOSE: The human EGFR2 (HER2) signaling pathway is one of the most actively studied targets in cancer transformation research. Ttriplex-forming oligonucleotides (TFOs) activate DNA damage and induce apoptosis. We aim to encapsulate TFO-HER2 with nano-particle ZW-128 to suppress breast cell growth...

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Detalles Bibliográficos
Autores principales: Yang, Xiaojing, Xu, Yi, Fu, Jie, Shen, Zan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357592/
https://www.ncbi.nlm.nih.gov/pubmed/37468837
http://dx.doi.org/10.1186/s12885-023-11176-8
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author Yang, Xiaojing
Xu, Yi
Fu, Jie
Shen, Zan
author_facet Yang, Xiaojing
Xu, Yi
Fu, Jie
Shen, Zan
author_sort Yang, Xiaojing
collection PubMed
description PURPOSE: The human EGFR2 (HER2) signaling pathway is one of the most actively studied targets in cancer transformation research. Ttriplex-forming oligonucleotides (TFOs) activate DNA damage and induce apoptosis. We aim to encapsulate TFO-HER2 with nano-particle ZW-128 to suppress breast cell growth in vitro and in vivo. EXPERIMENTAL DESIGN: We designed a set of TFO fragments targeting HER2 and verified their effectiveness. We encapsulated TFO-HER2 in ZW-128 to form nano-drug TFO@ZW-128. Cell counting kit 8, flow cytometry, and western blotting were used to evaluate the effect of TFO@ZW-128 on cell proliferation and the expressions of related proteins. The ant-itumor effect of TFO@ZW-128 was evaluated in vivo using nude mice breast cancer model. RESULTS: TFO@ZW-128 had efficient cellular uptake in amplified HER2 breast cancer cells. TFO@ZW-128 showed an 80-fold increase in TFO utilization compared with TFO-HER2 in the nude mouse breast cancer model. Meanwhile, TFO@ZW-128 dramatically inhibited the growth of HER2-overexpressing tumors compared with TFO-HER2 (P < 0.05). Furthermore, TFO@ZW-128-induced cell apoptosis was in a p53-independent manner. CONCLUSIONS: In this study, we designed nano-drug TFO@ZW-128, which has proven effective and non-toxic in targeted therapy for ectopic HER2-expressing tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11176-8.
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spelling pubmed-103575922023-07-21 Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer Yang, Xiaojing Xu, Yi Fu, Jie Shen, Zan BMC Cancer Research PURPOSE: The human EGFR2 (HER2) signaling pathway is one of the most actively studied targets in cancer transformation research. Ttriplex-forming oligonucleotides (TFOs) activate DNA damage and induce apoptosis. We aim to encapsulate TFO-HER2 with nano-particle ZW-128 to suppress breast cell growth in vitro and in vivo. EXPERIMENTAL DESIGN: We designed a set of TFO fragments targeting HER2 and verified their effectiveness. We encapsulated TFO-HER2 in ZW-128 to form nano-drug TFO@ZW-128. Cell counting kit 8, flow cytometry, and western blotting were used to evaluate the effect of TFO@ZW-128 on cell proliferation and the expressions of related proteins. The ant-itumor effect of TFO@ZW-128 was evaluated in vivo using nude mice breast cancer model. RESULTS: TFO@ZW-128 had efficient cellular uptake in amplified HER2 breast cancer cells. TFO@ZW-128 showed an 80-fold increase in TFO utilization compared with TFO-HER2 in the nude mouse breast cancer model. Meanwhile, TFO@ZW-128 dramatically inhibited the growth of HER2-overexpressing tumors compared with TFO-HER2 (P < 0.05). Furthermore, TFO@ZW-128-induced cell apoptosis was in a p53-independent manner. CONCLUSIONS: In this study, we designed nano-drug TFO@ZW-128, which has proven effective and non-toxic in targeted therapy for ectopic HER2-expressing tumors. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-023-11176-8. BioMed Central 2023-07-20 /pmc/articles/PMC10357592/ /pubmed/37468837 http://dx.doi.org/10.1186/s12885-023-11176-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yang, Xiaojing
Xu, Yi
Fu, Jie
Shen, Zan
Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer
title Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer
title_full Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer
title_fullStr Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer
title_full_unstemmed Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer
title_short Nanoparticle delivery of TFOs is a novel targeted therapy for HER2 amplified breast cancer
title_sort nanoparticle delivery of tfos is a novel targeted therapy for her2 amplified breast cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357592/
https://www.ncbi.nlm.nih.gov/pubmed/37468837
http://dx.doi.org/10.1186/s12885-023-11176-8
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