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A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples

Drug-based treatments are the most widely used interventions for cancer management. Personalized drug response profiling remains inherently challenging with low cell count harvested from tumour sample. We present a 96well-formatted microfluidic plate with built-in micro-gap that preserves up to 99.2...

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Autores principales: Ma, Wei-Yuan, Hsiung, Lo-Chang, Wang, Chen-Ho, Chiang, Chi-Ling, Lin, Ching-Hung, Huang, Chiun-Sheng, Wo, Andrew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394194/
https://www.ncbi.nlm.nih.gov/pubmed/25866290
http://dx.doi.org/10.1038/srep09656
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author Ma, Wei-Yuan
Hsiung, Lo-Chang
Wang, Chen-Ho
Chiang, Chi-Ling
Lin, Ching-Hung
Huang, Chiun-Sheng
Wo, Andrew M.
author_facet Ma, Wei-Yuan
Hsiung, Lo-Chang
Wang, Chen-Ho
Chiang, Chi-Ling
Lin, Ching-Hung
Huang, Chiun-Sheng
Wo, Andrew M.
author_sort Ma, Wei-Yuan
collection PubMed
description Drug-based treatments are the most widely used interventions for cancer management. Personalized drug response profiling remains inherently challenging with low cell count harvested from tumour sample. We present a 96well-formatted microfluidic plate with built-in micro-gap that preserves up to 99.2% of cells during multiple assay/wash operation and only 9,000 cells needed for a single reagent test (i.e. 1,000 cells per test spot x 3 selected concentration x triplication), enabling drug screening and compatibility with conventional automated workstations. Results with MCF7 and MDA-MB-231 cell lines showed that no statistical significance was found in dose-response between the device and conventional 96-well plate control. Primary tumour samples from breast cancer patients tested in the device also showed good IC(50) prediction. With drug screening of primary cancer cells must consider a wide range of scenarios, e.g. suspended/attached cell types and rare/abundant cell availability, the device enables high throughput screening even for suspended cells with low cell count since the signature microfluidic cell-trapping feature ensures cell preservation in a multiple solution exchange protocol.
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spelling pubmed-43941942015-04-21 A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples Ma, Wei-Yuan Hsiung, Lo-Chang Wang, Chen-Ho Chiang, Chi-Ling Lin, Ching-Hung Huang, Chiun-Sheng Wo, Andrew M. Sci Rep Article Drug-based treatments are the most widely used interventions for cancer management. Personalized drug response profiling remains inherently challenging with low cell count harvested from tumour sample. We present a 96well-formatted microfluidic plate with built-in micro-gap that preserves up to 99.2% of cells during multiple assay/wash operation and only 9,000 cells needed for a single reagent test (i.e. 1,000 cells per test spot x 3 selected concentration x triplication), enabling drug screening and compatibility with conventional automated workstations. Results with MCF7 and MDA-MB-231 cell lines showed that no statistical significance was found in dose-response between the device and conventional 96-well plate control. Primary tumour samples from breast cancer patients tested in the device also showed good IC(50) prediction. With drug screening of primary cancer cells must consider a wide range of scenarios, e.g. suspended/attached cell types and rare/abundant cell availability, the device enables high throughput screening even for suspended cells with low cell count since the signature microfluidic cell-trapping feature ensures cell preservation in a multiple solution exchange protocol. Nature Publishing Group 2015-04-13 /pmc/articles/PMC4394194/ /pubmed/25866290 http://dx.doi.org/10.1038/srep09656 Text en Copyright © 2015, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ma, Wei-Yuan
Hsiung, Lo-Chang
Wang, Chen-Ho
Chiang, Chi-Ling
Lin, Ching-Hung
Huang, Chiun-Sheng
Wo, Andrew M.
A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples
title A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples
title_full A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples
title_fullStr A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples
title_full_unstemmed A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples
title_short A Novel 96well-formatted Micro-gap Plate Enabling Drug Response Profiling on Primary Tumour Samples
title_sort novel 96well-formatted micro-gap plate enabling drug response profiling on primary tumour samples
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394194/
https://www.ncbi.nlm.nih.gov/pubmed/25866290
http://dx.doi.org/10.1038/srep09656
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