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Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells
Significance: Decreasing the oxygen consumption rate (OCR) of tumor cells is a powerful method for ameliorating tumor hypoxia. However, quantifying the change in OCR is challenging in complex experimental systems. Aim: We present a method for quantifying the OCR of two tumor cell lines using oxygen-...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society of Photo-Optical Instrumentation Engineers
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682476/ https://www.ncbi.nlm.nih.gov/pubmed/33231018 http://dx.doi.org/10.1117/1.JBO.25.11.116504 |
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author | Rickard, Ashlyn G. Zhuang, Meng DeRosa, Christopher A. Zhang, Xiaojie Dewhirst, Mark W. Fraser, Cassandra L. Palmer, Gregory M. |
author_facet | Rickard, Ashlyn G. Zhuang, Meng DeRosa, Christopher A. Zhang, Xiaojie Dewhirst, Mark W. Fraser, Cassandra L. Palmer, Gregory M. |
author_sort | Rickard, Ashlyn G. |
collection | PubMed |
description | Significance: Decreasing the oxygen consumption rate (OCR) of tumor cells is a powerful method for ameliorating tumor hypoxia. However, quantifying the change in OCR is challenging in complex experimental systems. Aim: We present a method for quantifying the OCR of two tumor cell lines using oxygen-sensitive dual-emissive boron nanoparticles (BNPs). We hypothesize that our BNP results are equivalent to the standard Seahorse assay. Approach: We quantified the spectral emissions of the BNP and accounted for external oxygen diffusion to quantify OCR over 24 h. The BNP-computed OCR of two breast cancer cell lines, E0771 and 4T07, were compared with their respective Seahorse assays. Both cell lines were also irradiated to quantify radiation-induced changes in the OCR. Results: Using a Bland–Altman analysis, our BNPs OCR was equivalent to the standard Seahorse assay. Moreover, in an additional experiment in which we irradiated the cells at their 50% survival fraction, the BNPs were sensitive enough to quantify 24% reduction in OCR after irradiation. Conclusions: Our results conclude that the BNPs are a viable alternative to the Seahorse assay for quantifying the OCR in cells. The Bland–Altman analysis showed that these two methods result in equivalent OCR measurements. Future studies will extend the OCR measurements to complex systems including 3D cultures and in vivo models, in which OCR measurements cannot currently be made. |
format | Online Article Text |
id | pubmed-7682476 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Society of Photo-Optical Instrumentation Engineers |
record_format | MEDLINE/PubMed |
spelling | pubmed-76824762020-11-27 Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells Rickard, Ashlyn G. Zhuang, Meng DeRosa, Christopher A. Zhang, Xiaojie Dewhirst, Mark W. Fraser, Cassandra L. Palmer, Gregory M. J Biomed Opt Microscopy Significance: Decreasing the oxygen consumption rate (OCR) of tumor cells is a powerful method for ameliorating tumor hypoxia. However, quantifying the change in OCR is challenging in complex experimental systems. Aim: We present a method for quantifying the OCR of two tumor cell lines using oxygen-sensitive dual-emissive boron nanoparticles (BNPs). We hypothesize that our BNP results are equivalent to the standard Seahorse assay. Approach: We quantified the spectral emissions of the BNP and accounted for external oxygen diffusion to quantify OCR over 24 h. The BNP-computed OCR of two breast cancer cell lines, E0771 and 4T07, were compared with their respective Seahorse assays. Both cell lines were also irradiated to quantify radiation-induced changes in the OCR. Results: Using a Bland–Altman analysis, our BNPs OCR was equivalent to the standard Seahorse assay. Moreover, in an additional experiment in which we irradiated the cells at their 50% survival fraction, the BNPs were sensitive enough to quantify 24% reduction in OCR after irradiation. Conclusions: Our results conclude that the BNPs are a viable alternative to the Seahorse assay for quantifying the OCR in cells. The Bland–Altman analysis showed that these two methods result in equivalent OCR measurements. Future studies will extend the OCR measurements to complex systems including 3D cultures and in vivo models, in which OCR measurements cannot currently be made. Society of Photo-Optical Instrumentation Engineers 2020-11-23 2020-11 /pmc/articles/PMC7682476/ /pubmed/33231018 http://dx.doi.org/10.1117/1.JBO.25.11.116504 Text en © 2020 The Authors https://creativecommons.org/licenses/by/4.0/ Published by SPIE under a Creative Commons Attribution 4.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI. |
spellingShingle | Microscopy Rickard, Ashlyn G. Zhuang, Meng DeRosa, Christopher A. Zhang, Xiaojie Dewhirst, Mark W. Fraser, Cassandra L. Palmer, Gregory M. Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
title | Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
title_full | Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
title_fullStr | Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
title_full_unstemmed | Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
title_short | Dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
title_sort | dual-emissive, oxygen-sensing boron nanoparticles quantify oxygen consumption rate in breast cancer cells |
topic | Microscopy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682476/ https://www.ncbi.nlm.nih.gov/pubmed/33231018 http://dx.doi.org/10.1117/1.JBO.25.11.116504 |
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