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Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip

In this study, we used three-dimensional (3D) printing to prepare a template of a microfluidic chip from which a polydimethylsiloxane (PDMS)lung chip was successfully constructed. The upper and lower channels of the chip are separated by a microporous membrane. The upper channel is seeded with lung...

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Detalles Bibliográficos
Autores principales: Tan, Jianfeng, Sun, Xindi, Zhang, Jianhua, Li, Huili, Kuang, Jun, Xu, Lulu, Gao, Xinghua, Zhou, Chengbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405841/
https://www.ncbi.nlm.nih.gov/pubmed/36005014
http://dx.doi.org/10.3390/bios12080618
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author Tan, Jianfeng
Sun, Xindi
Zhang, Jianhua
Li, Huili
Kuang, Jun
Xu, Lulu
Gao, Xinghua
Zhou, Chengbin
author_facet Tan, Jianfeng
Sun, Xindi
Zhang, Jianhua
Li, Huili
Kuang, Jun
Xu, Lulu
Gao, Xinghua
Zhou, Chengbin
author_sort Tan, Jianfeng
collection PubMed
description In this study, we used three-dimensional (3D) printing to prepare a template of a microfluidic chip from which a polydimethylsiloxane (PDMS)lung chip was successfully constructed. The upper and lower channels of the chip are separated by a microporous membrane. The upper channel is seeded with lung cancer cells, and the lower channel is seeded with vascular endothelial cells and continuously perfused with cell culture medium. This lung chip can simulate the microenvironment of lung tissue and realize the coculture of two kinds of cells at different levels. We used a two-dimensional (2D) well plate and a 3D lung chip to evaluate the effects of different EGFR-targeting drugs (gefitinib, afatinib, and osimertinib) on tumor cells. The 3D lung chip was superior to the 2D well plate at evaluating the effect of drugs on the NCI-H650, and the results were more consistent with existing clinical data. For primary tumor cells, 3D lung chips have more advantages because they simulate conditions that are more similar to the physiological cell microenvironment. The evaluation of EGFR-targeted drugs on lung chips is of great significance for personalized diagnosis and treatment and pharmacodynamic evaluation.
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spelling pubmed-94058412022-08-26 Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip Tan, Jianfeng Sun, Xindi Zhang, Jianhua Li, Huili Kuang, Jun Xu, Lulu Gao, Xinghua Zhou, Chengbin Biosensors (Basel) Article In this study, we used three-dimensional (3D) printing to prepare a template of a microfluidic chip from which a polydimethylsiloxane (PDMS)lung chip was successfully constructed. The upper and lower channels of the chip are separated by a microporous membrane. The upper channel is seeded with lung cancer cells, and the lower channel is seeded with vascular endothelial cells and continuously perfused with cell culture medium. This lung chip can simulate the microenvironment of lung tissue and realize the coculture of two kinds of cells at different levels. We used a two-dimensional (2D) well plate and a 3D lung chip to evaluate the effects of different EGFR-targeting drugs (gefitinib, afatinib, and osimertinib) on tumor cells. The 3D lung chip was superior to the 2D well plate at evaluating the effect of drugs on the NCI-H650, and the results were more consistent with existing clinical data. For primary tumor cells, 3D lung chips have more advantages because they simulate conditions that are more similar to the physiological cell microenvironment. The evaluation of EGFR-targeted drugs on lung chips is of great significance for personalized diagnosis and treatment and pharmacodynamic evaluation. MDPI 2022-08-09 /pmc/articles/PMC9405841/ /pubmed/36005014 http://dx.doi.org/10.3390/bios12080618 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tan, Jianfeng
Sun, Xindi
Zhang, Jianhua
Li, Huili
Kuang, Jun
Xu, Lulu
Gao, Xinghua
Zhou, Chengbin
Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip
title Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip
title_full Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip
title_fullStr Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip
title_full_unstemmed Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip
title_short Exploratory Evaluation of EGFR-Targeted Anti-Tumor Drugs for Lung Cancer Based on Lung-on-a-Chip
title_sort exploratory evaluation of egfr-targeted anti-tumor drugs for lung cancer based on lung-on-a-chip
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9405841/
https://www.ncbi.nlm.nih.gov/pubmed/36005014
http://dx.doi.org/10.3390/bios12080618
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