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Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection

Oncolytic viruses are being heavily investigated as novel methods to treat cancers; however, predicting their therapeutic efficacy remains challenging. The most commonly used predictive tests involve determining the in vitro susceptibility of a tumor’s malignant cells to infection with an oncolytic...

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Autores principales: Thomas, Raquela J., Bartee, Mee Y., Valenzuela-Cardenas, Miriam, Bartee, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507476/
https://www.ncbi.nlm.nih.gov/pubmed/37732297
http://dx.doi.org/10.1016/j.omto.2023.08.014
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author Thomas, Raquela J.
Bartee, Mee Y.
Valenzuela-Cardenas, Miriam
Bartee, Eric
author_facet Thomas, Raquela J.
Bartee, Mee Y.
Valenzuela-Cardenas, Miriam
Bartee, Eric
author_sort Thomas, Raquela J.
collection PubMed
description Oncolytic viruses are being heavily investigated as novel methods to treat cancers; however, predicting their therapeutic efficacy remains challenging. The most commonly used predictive tests involve determining the in vitro susceptibility of a tumor’s malignant cells to infection with an oncolytic agent. Whether these tests are truly predictive of in vivo efficacy, however, remains unclear. Here we demonstrate that a recombinant, oncolytic myxoma virus shows efficacy in two murine models of triple negative breast cancer despite extremely low permissivity of these models to viral infection. These data demonstrate that in vitro infectivity studies are not an accurate surrogate for therapeutic efficacy and suggest that other tests need to be developed.
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spelling pubmed-105074762023-09-20 Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection Thomas, Raquela J. Bartee, Mee Y. Valenzuela-Cardenas, Miriam Bartee, Eric Mol Ther Oncolytics Brief Report Oncolytic viruses are being heavily investigated as novel methods to treat cancers; however, predicting their therapeutic efficacy remains challenging. The most commonly used predictive tests involve determining the in vitro susceptibility of a tumor’s malignant cells to infection with an oncolytic agent. Whether these tests are truly predictive of in vivo efficacy, however, remains unclear. Here we demonstrate that a recombinant, oncolytic myxoma virus shows efficacy in two murine models of triple negative breast cancer despite extremely low permissivity of these models to viral infection. These data demonstrate that in vitro infectivity studies are not an accurate surrogate for therapeutic efficacy and suggest that other tests need to be developed. American Society of Gene & Cell Therapy 2023-09-01 /pmc/articles/PMC10507476/ /pubmed/37732297 http://dx.doi.org/10.1016/j.omto.2023.08.014 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Brief Report
Thomas, Raquela J.
Bartee, Mee Y.
Valenzuela-Cardenas, Miriam
Bartee, Eric
Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
title Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
title_full Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
title_fullStr Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
title_full_unstemmed Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
title_short Oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
title_sort oncolytic myxoma virus is effective in murine models of triple negative breast cancer despite poor rates of infection
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10507476/
https://www.ncbi.nlm.nih.gov/pubmed/37732297
http://dx.doi.org/10.1016/j.omto.2023.08.014
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