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Altered Glycan Expression on Breast Cancer Cells Facilitates Infection by T3 Seroptype Oncolytic Reovirus
[Image: see text] Breast cancer is the most common cancer in women. Although current therapies have increased survival rates for some breast cancer types, other aggressive invasive breast cancers remain difficult to treat. As the onset of breast cancer is often associated with the appearance of extr...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631336/ https://www.ncbi.nlm.nih.gov/pubmed/34762801 http://dx.doi.org/10.1021/acs.nanolett.1c03608 |
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author | Mohammed, Danahe Koehler, Melanie Dumitru, Andra C. Aravamudhan, Pavithra Sutherland, Danica M. Dermody, Terence S. Alsteens, David |
author_facet | Mohammed, Danahe Koehler, Melanie Dumitru, Andra C. Aravamudhan, Pavithra Sutherland, Danica M. Dermody, Terence S. Alsteens, David |
author_sort | Mohammed, Danahe |
collection | PubMed |
description | [Image: see text] Breast cancer is the most common cancer in women. Although current therapies have increased survival rates for some breast cancer types, other aggressive invasive breast cancers remain difficult to treat. As the onset of breast cancer is often associated with the appearance of extracellular markers, these could be used to better target therapeutic agents. Here, we demonstrated by nanobiophysical approaches that overexpression of α-sialylated glycans in breast cancer provides an opportunity to combat cancer cells with oncolytic reoviruses. Notably, a correlation between cellular glycan expression and the mechanical properties of reovirus attachment and infection is observed in a serotype-dependent manner. Furthermore, we enhance the infectivity of reoviruses in malignant cells by the coinjection of α-sialylated glycans. In conclusion, this study supports both the use of reoviruses as an oncolytic agent in nanomedicine and the role of α-sialylated glycans as adjuvants in oncolysis, offering new perspective in oncolytic cancer therapy. |
format | Online Article Text |
id | pubmed-8631336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-86313362022-11-15 Altered Glycan Expression on Breast Cancer Cells Facilitates Infection by T3 Seroptype Oncolytic Reovirus Mohammed, Danahe Koehler, Melanie Dumitru, Andra C. Aravamudhan, Pavithra Sutherland, Danica M. Dermody, Terence S. Alsteens, David Nano Lett [Image: see text] Breast cancer is the most common cancer in women. Although current therapies have increased survival rates for some breast cancer types, other aggressive invasive breast cancers remain difficult to treat. As the onset of breast cancer is often associated with the appearance of extracellular markers, these could be used to better target therapeutic agents. Here, we demonstrated by nanobiophysical approaches that overexpression of α-sialylated glycans in breast cancer provides an opportunity to combat cancer cells with oncolytic reoviruses. Notably, a correlation between cellular glycan expression and the mechanical properties of reovirus attachment and infection is observed in a serotype-dependent manner. Furthermore, we enhance the infectivity of reoviruses in malignant cells by the coinjection of α-sialylated glycans. In conclusion, this study supports both the use of reoviruses as an oncolytic agent in nanomedicine and the role of α-sialylated glycans as adjuvants in oncolysis, offering new perspective in oncolytic cancer therapy. American Chemical Society 2021-11-11 2021-11-24 /pmc/articles/PMC8631336/ /pubmed/34762801 http://dx.doi.org/10.1021/acs.nanolett.1c03608 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Mohammed, Danahe Koehler, Melanie Dumitru, Andra C. Aravamudhan, Pavithra Sutherland, Danica M. Dermody, Terence S. Alsteens, David Altered Glycan Expression on Breast Cancer Cells Facilitates Infection by T3 Seroptype Oncolytic Reovirus |
title | Altered Glycan Expression on Breast Cancer Cells Facilitates
Infection by T3 Seroptype Oncolytic Reovirus |
title_full | Altered Glycan Expression on Breast Cancer Cells Facilitates
Infection by T3 Seroptype Oncolytic Reovirus |
title_fullStr | Altered Glycan Expression on Breast Cancer Cells Facilitates
Infection by T3 Seroptype Oncolytic Reovirus |
title_full_unstemmed | Altered Glycan Expression on Breast Cancer Cells Facilitates
Infection by T3 Seroptype Oncolytic Reovirus |
title_short | Altered Glycan Expression on Breast Cancer Cells Facilitates
Infection by T3 Seroptype Oncolytic Reovirus |
title_sort | altered glycan expression on breast cancer cells facilitates
infection by t3 seroptype oncolytic reovirus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631336/ https://www.ncbi.nlm.nih.gov/pubmed/34762801 http://dx.doi.org/10.1021/acs.nanolett.1c03608 |
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