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Quantitative analysis of tumour spheroid structure
Tumour spheroids are common in vitro experimental models of avascular tumour growth. Compared with traditional two-dimensional culture, tumour spheroids more closely mimic the avascular tumour microenvironment where spatial differences in nutrient availability strongly influence growth. We show that...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741212/ https://www.ncbi.nlm.nih.gov/pubmed/34842141 http://dx.doi.org/10.7554/eLife.73020 |
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author | Browning, Alexander P Sharp, Jesse A Murphy, Ryan J Gunasingh, Gency Lawson, Brodie Burrage, Kevin Haass, Nikolas K Simpson, Matthew |
author_facet | Browning, Alexander P Sharp, Jesse A Murphy, Ryan J Gunasingh, Gency Lawson, Brodie Burrage, Kevin Haass, Nikolas K Simpson, Matthew |
author_sort | Browning, Alexander P |
collection | PubMed |
description | Tumour spheroids are common in vitro experimental models of avascular tumour growth. Compared with traditional two-dimensional culture, tumour spheroids more closely mimic the avascular tumour microenvironment where spatial differences in nutrient availability strongly influence growth. We show that spheroids initiated using significantly different numbers of cells grow to similar limiting sizes, suggesting that avascular tumours have a limiting structure; in agreement with untested predictions of classical mathematical models of tumour spheroids. We develop a novel mathematical and statistical framework to study the structure of tumour spheroids seeded from cells transduced with fluorescent cell cycle indicators, enabling us to discriminate between arrested and cycling cells and identify an arrested region. Our analysis shows that transient spheroid structure is independent of initial spheroid size, and the limiting structure can be independent of seeding density. Standard experimental protocols compare spheroid size as a function of time; however, our analysis suggests that comparing spheroid structure as a function of overall size produces results that are relatively insensitive to variability in spheroid size. Our experimental observations are made using two melanoma cell lines, but our modelling framework applies across a wide range of spheroid culture conditions and cell lines. |
format | Online Article Text |
id | pubmed-8741212 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-87412122022-01-11 Quantitative analysis of tumour spheroid structure Browning, Alexander P Sharp, Jesse A Murphy, Ryan J Gunasingh, Gency Lawson, Brodie Burrage, Kevin Haass, Nikolas K Simpson, Matthew eLife Cancer Biology Tumour spheroids are common in vitro experimental models of avascular tumour growth. Compared with traditional two-dimensional culture, tumour spheroids more closely mimic the avascular tumour microenvironment where spatial differences in nutrient availability strongly influence growth. We show that spheroids initiated using significantly different numbers of cells grow to similar limiting sizes, suggesting that avascular tumours have a limiting structure; in agreement with untested predictions of classical mathematical models of tumour spheroids. We develop a novel mathematical and statistical framework to study the structure of tumour spheroids seeded from cells transduced with fluorescent cell cycle indicators, enabling us to discriminate between arrested and cycling cells and identify an arrested region. Our analysis shows that transient spheroid structure is independent of initial spheroid size, and the limiting structure can be independent of seeding density. Standard experimental protocols compare spheroid size as a function of time; however, our analysis suggests that comparing spheroid structure as a function of overall size produces results that are relatively insensitive to variability in spheroid size. Our experimental observations are made using two melanoma cell lines, but our modelling framework applies across a wide range of spheroid culture conditions and cell lines. eLife Sciences Publications, Ltd 2021-11-29 /pmc/articles/PMC8741212/ /pubmed/34842141 http://dx.doi.org/10.7554/eLife.73020 Text en © 2021, Browning et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cancer Biology Browning, Alexander P Sharp, Jesse A Murphy, Ryan J Gunasingh, Gency Lawson, Brodie Burrage, Kevin Haass, Nikolas K Simpson, Matthew Quantitative analysis of tumour spheroid structure |
title | Quantitative analysis of tumour spheroid structure |
title_full | Quantitative analysis of tumour spheroid structure |
title_fullStr | Quantitative analysis of tumour spheroid structure |
title_full_unstemmed | Quantitative analysis of tumour spheroid structure |
title_short | Quantitative analysis of tumour spheroid structure |
title_sort | quantitative analysis of tumour spheroid structure |
topic | Cancer Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8741212/ https://www.ncbi.nlm.nih.gov/pubmed/34842141 http://dx.doi.org/10.7554/eLife.73020 |
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