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Engineering prostate cancer in vitro: what does it take?

A key challenge in the clinical management and cause of treatment failure of prostate cancer (PCa) is its molecular, cellular and clinical heterogeneity. Modelling systems that fully recapitulate clinical diversity and resistant phenotypes are urgently required for the development of successful pers...

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Autores principales: Buskin, Adriana, Scott, Emma, Nelson, Ryan, Gaughan, Luke, Robson, Craig N., Heer, Rakesh, Hepburn, Anastasia C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403358/
https://www.ncbi.nlm.nih.gov/pubmed/37438470
http://dx.doi.org/10.1038/s41388-023-02776-6
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author Buskin, Adriana
Scott, Emma
Nelson, Ryan
Gaughan, Luke
Robson, Craig N.
Heer, Rakesh
Hepburn, Anastasia C.
author_facet Buskin, Adriana
Scott, Emma
Nelson, Ryan
Gaughan, Luke
Robson, Craig N.
Heer, Rakesh
Hepburn, Anastasia C.
author_sort Buskin, Adriana
collection PubMed
description A key challenge in the clinical management and cause of treatment failure of prostate cancer (PCa) is its molecular, cellular and clinical heterogeneity. Modelling systems that fully recapitulate clinical diversity and resistant phenotypes are urgently required for the development of successful personalised PCa therapies. The advent of the three-dimensional (3D) organoid model has revolutionised preclinical cancer research through reflecting heterogeneity and offering genomic and environmental manipulation that has opened up unparalleled opportunities for applications in disease modelling, high-throughput drug screening and precision medicine. Despite these remarkable achievements of organoid technology, several shortcomings in emulating the complex tumor microenvironment and dynamic process of metastasis as well as the epigenome profile limit organoids achieving true in vivo functionality. Technological advances in tissue engineering have enabled the development of innovative tools to facilitate the design of improved 3D cancer models. In this review, we highlight the current in vitro 3D PCa models with a special focus on organoids and discuss engineering approaches to create more physiologically relevant PCa organoid models and maximise their translational relevance that ultimately will help to realise the transformational power of precision medicine.
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spelling pubmed-104033582023-08-06 Engineering prostate cancer in vitro: what does it take? Buskin, Adriana Scott, Emma Nelson, Ryan Gaughan, Luke Robson, Craig N. Heer, Rakesh Hepburn, Anastasia C. Oncogene Review Article A key challenge in the clinical management and cause of treatment failure of prostate cancer (PCa) is its molecular, cellular and clinical heterogeneity. Modelling systems that fully recapitulate clinical diversity and resistant phenotypes are urgently required for the development of successful personalised PCa therapies. The advent of the three-dimensional (3D) organoid model has revolutionised preclinical cancer research through reflecting heterogeneity and offering genomic and environmental manipulation that has opened up unparalleled opportunities for applications in disease modelling, high-throughput drug screening and precision medicine. Despite these remarkable achievements of organoid technology, several shortcomings in emulating the complex tumor microenvironment and dynamic process of metastasis as well as the epigenome profile limit organoids achieving true in vivo functionality. Technological advances in tissue engineering have enabled the development of innovative tools to facilitate the design of improved 3D cancer models. In this review, we highlight the current in vitro 3D PCa models with a special focus on organoids and discuss engineering approaches to create more physiologically relevant PCa organoid models and maximise their translational relevance that ultimately will help to realise the transformational power of precision medicine. Nature Publishing Group UK 2023-07-12 2023 /pmc/articles/PMC10403358/ /pubmed/37438470 http://dx.doi.org/10.1038/s41388-023-02776-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Article
Buskin, Adriana
Scott, Emma
Nelson, Ryan
Gaughan, Luke
Robson, Craig N.
Heer, Rakesh
Hepburn, Anastasia C.
Engineering prostate cancer in vitro: what does it take?
title Engineering prostate cancer in vitro: what does it take?
title_full Engineering prostate cancer in vitro: what does it take?
title_fullStr Engineering prostate cancer in vitro: what does it take?
title_full_unstemmed Engineering prostate cancer in vitro: what does it take?
title_short Engineering prostate cancer in vitro: what does it take?
title_sort engineering prostate cancer in vitro: what does it take?
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10403358/
https://www.ncbi.nlm.nih.gov/pubmed/37438470
http://dx.doi.org/10.1038/s41388-023-02776-6
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