A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions

Bioluminescent tumor cell lines are used extensively in vivo to monitor tumor growth and metastasis but rarely used in vitro to follow tumor cell behavior. Tumor cell migration is frequently studied in vitro using transwell assays, however, current methods do not permit the co-incubation of tumor ce...

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Main Authors: Jinsoo Yoon, Christopher R. Parish, Lucy A. Coupland
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Methods and Protocols
Subjects:
Online Access:https://www.mdpi.com/2409-9279/3/1/10
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author Jinsoo Yoon
Christopher R. Parish
Lucy A. Coupland
author_facet Jinsoo Yoon
Christopher R. Parish
Lucy A. Coupland
author_sort Jinsoo Yoon
collection DOAJ
description Bioluminescent tumor cell lines are used extensively in vivo to monitor tumor growth and metastasis but rarely used in vitro to follow tumor cell behavior. Tumor cell migration is frequently studied in vitro using transwell assays, however, current methods do not permit the co-incubation of tumor cells with different stromal cell types for analysis of the effects of intercellular cross-talk on tumor cell migration. We describe a novel migration assay using bioluminescent tumor cell lines that is rapid, accurate, and permits the study of the effects of tumor cell-stromal cell interactions on tumor cell migratory behavior.
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spelling doaj.art-e68dcbe5d17d46eaadf537793d41cc3c2022-12-21T20:04:24ZengMDPI AGMethods and Protocols2409-92792020-01-01311010.3390/mps3010010mps3010010A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell InteractionsJinsoo Yoon0Christopher R. Parish1Lucy A. Coupland2The ACRF Department of Cancer Biology & Therapeutics, John Curtin School of Medical Research, The Australian National University, Canberra 2601, AustraliaThe ACRF Department of Cancer Biology & Therapeutics, John Curtin School of Medical Research, The Australian National University, Canberra 2601, AustraliaThe ACRF Department of Cancer Biology & Therapeutics, John Curtin School of Medical Research, The Australian National University, Canberra 2601, AustraliaBioluminescent tumor cell lines are used extensively in vivo to monitor tumor growth and metastasis but rarely used in vitro to follow tumor cell behavior. Tumor cell migration is frequently studied in vitro using transwell assays, however, current methods do not permit the co-incubation of tumor cells with different stromal cell types for analysis of the effects of intercellular cross-talk on tumor cell migration. We describe a novel migration assay using bioluminescent tumor cell lines that is rapid, accurate, and permits the study of the effects of tumor cell-stromal cell interactions on tumor cell migratory behavior.https://www.mdpi.com/2409-9279/3/1/10transwell migration assaytumor/stromal interactionsbioluminescence
spellingShingle Jinsoo Yoon
Christopher R. Parish
Lucy A. Coupland
A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
Methods and Protocols
transwell migration assay
tumor/stromal interactions
bioluminescence
title A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
title_full A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
title_fullStr A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
title_full_unstemmed A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
title_short A Rapid and Accurate Bioluminescence-Based Migration Assay Permitting Analysis of Tumor Cell/Stromal Cell Interactions
title_sort rapid and accurate bioluminescence based migration assay permitting analysis of tumor cell stromal cell interactions
topic transwell migration assay
tumor/stromal interactions
bioluminescence
url https://www.mdpi.com/2409-9279/3/1/10
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