Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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
_version_ 1783284521116893184
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
work_keys_str_mv AT borodovskyalexandra generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT mcquistontravisj generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT stetsondaniel generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT ahmedambar generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT whitstondavid generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT zhangjingwen generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT grondinemichael generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT lawsondeborah generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT challbergsharons generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT zindamichael generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT pollokbriana generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT doughertybriana generationofstablepdxderivedcelllinesusingconditionalreprogramming
AT dcruzcelinam generationofstablepdxderivedcelllinesusingconditionalreprogramming