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Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent
Development of treatment resistance is a major concern during treatment of cancer, and there is an unmet need for therapeutic strategies with novel modes of action. Polyvinyl alcohol carbazate (PVAC) is a polymer compound with unique biological properties. Herein, we describe the antitumoral effects...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831155/ https://www.ncbi.nlm.nih.gov/pubmed/33505913 http://dx.doi.org/10.3389/fonc.2020.598394 |
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author | Sellberg, Felix Fröbom, Robin Binder, Christian Berglund, Erik Berglund, David |
author_facet | Sellberg, Felix Fröbom, Robin Binder, Christian Berglund, Erik Berglund, David |
author_sort | Sellberg, Felix |
collection | PubMed |
description | Development of treatment resistance is a major concern during treatment of cancer, and there is an unmet need for therapeutic strategies with novel modes of action. Polyvinyl alcohol carbazate (PVAC) is a polymer compound with unique biological properties. Herein, we describe the antitumoral effects of PVAC. Three well-established cell lines GIST-T1, B16.F10, and A375 were used to determine the in vitro antitumoral effects of PVAC. Assessments included light microscopy, cell viability, cell cycle, and apoptosis assays. In vivo treatment safety and efficacy were characterized in one immunocompetent (B16.F10) mouse model and one athymic nude (MDA-MB-231) mouse model. Excised tumors were measured, weighed, stained for Ki-67, CD3, and histopathologically evaluated. Intact PVAC expressed a non-linear dose-response antitumoral effect in vitro, whereas its separate components, PVA and carbazate, did not display antitumoral effects alone. In vivo, PVAC induced a significant intratumoral CD3(+) T-cell recruitment in immunocompetent mice (B16.F10), which was associated with tumor growth inhibition. Although growth inhibition was not significant in athymic mice (MDA-MB-231), histopathological evaluation detected an increase in stromal tissue and leukocyte infiltration. In conclusion, we present evidence for PVAC antitumoral effects both in vitro and in vivo. The mode of action was not elucidated in vitro, but a potential mechanism of in vivo activity was observed, characterized by an increase of immune cells into both immunocompetent and athymic mice. This finding warrants further study to validate its possible role as an immunomodulatory polymeric agent. |
format | Online Article Text |
id | pubmed-7831155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78311552021-01-26 Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent Sellberg, Felix Fröbom, Robin Binder, Christian Berglund, Erik Berglund, David Front Oncol Oncology Development of treatment resistance is a major concern during treatment of cancer, and there is an unmet need for therapeutic strategies with novel modes of action. Polyvinyl alcohol carbazate (PVAC) is a polymer compound with unique biological properties. Herein, we describe the antitumoral effects of PVAC. Three well-established cell lines GIST-T1, B16.F10, and A375 were used to determine the in vitro antitumoral effects of PVAC. Assessments included light microscopy, cell viability, cell cycle, and apoptosis assays. In vivo treatment safety and efficacy were characterized in one immunocompetent (B16.F10) mouse model and one athymic nude (MDA-MB-231) mouse model. Excised tumors were measured, weighed, stained for Ki-67, CD3, and histopathologically evaluated. Intact PVAC expressed a non-linear dose-response antitumoral effect in vitro, whereas its separate components, PVA and carbazate, did not display antitumoral effects alone. In vivo, PVAC induced a significant intratumoral CD3(+) T-cell recruitment in immunocompetent mice (B16.F10), which was associated with tumor growth inhibition. Although growth inhibition was not significant in athymic mice (MDA-MB-231), histopathological evaluation detected an increase in stromal tissue and leukocyte infiltration. In conclusion, we present evidence for PVAC antitumoral effects both in vitro and in vivo. The mode of action was not elucidated in vitro, but a potential mechanism of in vivo activity was observed, characterized by an increase of immune cells into both immunocompetent and athymic mice. This finding warrants further study to validate its possible role as an immunomodulatory polymeric agent. Frontiers Media S.A. 2021-01-11 /pmc/articles/PMC7831155/ /pubmed/33505913 http://dx.doi.org/10.3389/fonc.2020.598394 Text en Copyright © 2021 Sellberg, Fröbom, Binder, Berglund and Berglund http://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 Sellberg, Felix Fröbom, Robin Binder, Christian Berglund, Erik Berglund, David Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent |
title | Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent |
title_full | Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent |
title_fullStr | Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent |
title_full_unstemmed | Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent |
title_short | Polyvinyl Alcohol Carbazate as a Polymer-Based Antitumoral Agent |
title_sort | polyvinyl alcohol carbazate as a polymer-based antitumoral agent |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7831155/ https://www.ncbi.nlm.nih.gov/pubmed/33505913 http://dx.doi.org/10.3389/fonc.2020.598394 |
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