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Generation of stable PDX derived cell lines using conditional reprogramming
Efforts to develop effective cancer therapeutics have been hindered by a lack of clinically predictive preclinical models which recapitulate this complex disease. Patient derived xenograft (PDX) models have emerged as valuable tools for translational research but have several practical limitations i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719579/ https://www.ncbi.nlm.nih.gov/pubmed/29212548 http://dx.doi.org/10.1186/s12943-017-0745-1 |
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author | Borodovsky, Alexandra McQuiston, Travis J. Stetson, Daniel Ahmed, Ambar Whitston, David Zhang, Jingwen Grondine, Michael Lawson, Deborah Challberg, Sharon S. Zinda, Michael Pollok, Brian A. Dougherty, Brian A. D’Cruz, Celina M. |
author_facet | Borodovsky, Alexandra McQuiston, Travis J. Stetson, Daniel Ahmed, Ambar Whitston, David Zhang, Jingwen Grondine, Michael Lawson, Deborah Challberg, Sharon S. Zinda, Michael Pollok, Brian A. Dougherty, Brian A. D’Cruz, Celina M. |
author_sort | Borodovsky, Alexandra |
collection | PubMed |
description | Efforts to develop effective cancer therapeutics have been hindered by a lack of clinically predictive preclinical models which recapitulate this complex disease. Patient derived xenograft (PDX) models have emerged as valuable tools for translational research but have several practical limitations including lack of sustained growth in vitro. In this study, we utilized Conditional Reprogramming (CR) cell technology- a novel cell culture system facilitating the generation of stable cultures from patient biopsies- to establish PDX-derived cell lines which maintain the characteristics of the parental PDX tumor. Human lung and ovarian PDX tumors were successfully propagated using CR technology to create stable explant cell lines (CR-PDX). These CR-PDX cell lines maintained parental driver mutations and allele frequency without clonal drift. Purified CR-PDX cell lines were amenable to high throughput chemosensitivity screening and in vitro genetic knockdown studies. Additionally, re-implanted CR-PDX cells proliferated to form tumors that retained the growth kinetics, histology, and drug responses of the parental PDX tumor. CR technology can be used to generate and expand stable cell lines from PDX tumors without compromising fundamental biological properties of the model. It offers the ability to expand PDX cells in vitro for subsequent 2D screening assays as well as for use in vivo to reduce variability, animal usage and study costs. The methods and data detailed here provide a platform to generate physiologically relevant and predictive preclinical models to enhance drug discovery efforts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12943-017-0745-1) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5719579 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57195792017-12-08 Generation of stable PDX derived cell lines using conditional reprogramming Borodovsky, Alexandra McQuiston, Travis J. Stetson, Daniel Ahmed, Ambar Whitston, David Zhang, Jingwen Grondine, Michael Lawson, Deborah Challberg, Sharon S. Zinda, Michael Pollok, Brian A. Dougherty, Brian A. D’Cruz, Celina M. Mol Cancer Letter to the Editor Efforts to develop effective cancer therapeutics have been hindered by a lack of clinically predictive preclinical models which recapitulate this complex disease. Patient derived xenograft (PDX) models have emerged as valuable tools for translational research but have several practical limitations including lack of sustained growth in vitro. In this study, we utilized Conditional Reprogramming (CR) cell technology- a novel cell culture system facilitating the generation of stable cultures from patient biopsies- to establish PDX-derived cell lines which maintain the characteristics of the parental PDX tumor. Human lung and ovarian PDX tumors were successfully propagated using CR technology to create stable explant cell lines (CR-PDX). These CR-PDX cell lines maintained parental driver mutations and allele frequency without clonal drift. Purified CR-PDX cell lines were amenable to high throughput chemosensitivity screening and in vitro genetic knockdown studies. Additionally, re-implanted CR-PDX cells proliferated to form tumors that retained the growth kinetics, histology, and drug responses of the parental PDX tumor. CR technology can be used to generate and expand stable cell lines from PDX tumors without compromising fundamental biological properties of the model. It offers the ability to expand PDX cells in vitro for subsequent 2D screening assays as well as for use in vivo to reduce variability, animal usage and study costs. The methods and data detailed here provide a platform to generate physiologically relevant and predictive preclinical models to enhance drug discovery efforts. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12943-017-0745-1) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-06 /pmc/articles/PMC5719579/ /pubmed/29212548 http://dx.doi.org/10.1186/s12943-017-0745-1 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Letter to the Editor Borodovsky, Alexandra McQuiston, Travis J. Stetson, Daniel Ahmed, Ambar Whitston, David Zhang, Jingwen Grondine, Michael Lawson, Deborah Challberg, Sharon S. Zinda, Michael Pollok, Brian A. Dougherty, Brian A. D’Cruz, Celina M. Generation of stable PDX derived cell lines using conditional reprogramming |
title | Generation of stable PDX derived cell lines using conditional reprogramming |
title_full | Generation of stable PDX derived cell lines using conditional reprogramming |
title_fullStr | Generation of stable PDX derived cell lines using conditional reprogramming |
title_full_unstemmed | Generation of stable PDX derived cell lines using conditional reprogramming |
title_short | Generation of stable PDX derived cell lines using conditional reprogramming |
title_sort | generation of stable pdx derived cell lines using conditional reprogramming |
topic | Letter to the Editor |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5719579/ https://www.ncbi.nlm.nih.gov/pubmed/29212548 http://dx.doi.org/10.1186/s12943-017-0745-1 |
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