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Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements

BACKGROUND: Traditional in vitro cell invasion assays focus on measuring one cell parameter at a time and are often less than ideal in terms of reproducibility and quantification. Further, many techniques are not suitable for quantifying the advancing margin of collectively migrating cells, arguably...

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Autores principales: Kam, Yoonseok, Karperien, Audrey, Weidow, Brandy, Estrada, Lourdes, Anderson, Alexander R, Quaranta, Vito
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716356/
https://www.ncbi.nlm.nih.gov/pubmed/19594934
http://dx.doi.org/10.1186/1756-0500-2-130
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author Kam, Yoonseok
Karperien, Audrey
Weidow, Brandy
Estrada, Lourdes
Anderson, Alexander R
Quaranta, Vito
author_facet Kam, Yoonseok
Karperien, Audrey
Weidow, Brandy
Estrada, Lourdes
Anderson, Alexander R
Quaranta, Vito
author_sort Kam, Yoonseok
collection PubMed
description BACKGROUND: Traditional in vitro cell invasion assays focus on measuring one cell parameter at a time and are often less than ideal in terms of reproducibility and quantification. Further, many techniques are not suitable for quantifying the advancing margin of collectively migrating cells, arguably the most important area of activity during tumor invasion. We have developed and applied a highly quantitative, standardized, reproducible Nest Expansion Assay (NEA) to measure cancer cell invasion in vitro, which builds upon established wound-healing techniques. This assay involves creating uniform circular "nests" of cells within a monolayer of cells using a stabilized, silicone-tipped drill press, and quantifying the margin expansion into an overlaid extracellular matrix (ECM)-like component using computer-assisted applications. FINDINGS: The NEA was applied to two human-derived breast cell lines, MCF10A and MCF10A-CA1d, which exhibit opposite degrees of tumorigenicity and invasion in vivo. Assays were performed to incorporate various microenvironmental conditions, in order to test their influence on cell behavior and measures. Two types of computer-driven image analysis were performed using Java's freely available ImageJ software and its FracLac plugin to capture nest expansion and fractal dimension, respectively – which are both taken as indicators of invasiveness. Both analyses confirmed that the NEA is highly reproducible, and that the ECM component is key in defining invasive cell behavior. Interestingly, both analyses also detected significant differences between non-invasive and invasive cell lines, across various microenvironments, and over time. CONCLUSION: The spatial nature of the NEA makes its outcome susceptible to the global influence of many cellular parameters at once (e.g., motility, protease secretion, cell-cell adhesion). We propose the NEA as a mid-throughput technique for screening and simultaneous examination of factors contributing to cancer cell invasion, particularly suitable for parameterizing and validating Cancer Systems Biology approaches such as mathematical modeling.
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spelling pubmed-27163562009-07-28 Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements Kam, Yoonseok Karperien, Audrey Weidow, Brandy Estrada, Lourdes Anderson, Alexander R Quaranta, Vito BMC Res Notes Technical Note BACKGROUND: Traditional in vitro cell invasion assays focus on measuring one cell parameter at a time and are often less than ideal in terms of reproducibility and quantification. Further, many techniques are not suitable for quantifying the advancing margin of collectively migrating cells, arguably the most important area of activity during tumor invasion. We have developed and applied a highly quantitative, standardized, reproducible Nest Expansion Assay (NEA) to measure cancer cell invasion in vitro, which builds upon established wound-healing techniques. This assay involves creating uniform circular "nests" of cells within a monolayer of cells using a stabilized, silicone-tipped drill press, and quantifying the margin expansion into an overlaid extracellular matrix (ECM)-like component using computer-assisted applications. FINDINGS: The NEA was applied to two human-derived breast cell lines, MCF10A and MCF10A-CA1d, which exhibit opposite degrees of tumorigenicity and invasion in vivo. Assays were performed to incorporate various microenvironmental conditions, in order to test their influence on cell behavior and measures. Two types of computer-driven image analysis were performed using Java's freely available ImageJ software and its FracLac plugin to capture nest expansion and fractal dimension, respectively – which are both taken as indicators of invasiveness. Both analyses confirmed that the NEA is highly reproducible, and that the ECM component is key in defining invasive cell behavior. Interestingly, both analyses also detected significant differences between non-invasive and invasive cell lines, across various microenvironments, and over time. CONCLUSION: The spatial nature of the NEA makes its outcome susceptible to the global influence of many cellular parameters at once (e.g., motility, protease secretion, cell-cell adhesion). We propose the NEA as a mid-throughput technique for screening and simultaneous examination of factors contributing to cancer cell invasion, particularly suitable for parameterizing and validating Cancer Systems Biology approaches such as mathematical modeling. BioMed Central 2009-07-13 /pmc/articles/PMC2716356/ /pubmed/19594934 http://dx.doi.org/10.1186/1756-0500-2-130 Text en Copyright © 2009 Quaranta et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Note
Kam, Yoonseok
Karperien, Audrey
Weidow, Brandy
Estrada, Lourdes
Anderson, Alexander R
Quaranta, Vito
Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
title Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
title_full Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
title_fullStr Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
title_full_unstemmed Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
title_short Nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
title_sort nest expansion assay: a cancer systems biology approach to in vitro invasion measurements
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716356/
https://www.ncbi.nlm.nih.gov/pubmed/19594934
http://dx.doi.org/10.1186/1756-0500-2-130
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