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Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis

Advances in three-dimensional (3D) cell culture technology have led to the development of more biologically and physiologically relevant models to study organ development, disease, toxicology and drug screening. Organoids have been derived from many mammalian tissues, both normal and tumour, from ad...

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Detalles Bibliográficos
Autores principales: Caipa Garcia, Angela L, Arlt, Volker M, Phillips, David H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071088/
https://www.ncbi.nlm.nih.gov/pubmed/34147034
http://dx.doi.org/10.1093/mutage/geab023
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author Caipa Garcia, Angela L
Arlt, Volker M
Phillips, David H
author_facet Caipa Garcia, Angela L
Arlt, Volker M
Phillips, David H
author_sort Caipa Garcia, Angela L
collection PubMed
description Advances in three-dimensional (3D) cell culture technology have led to the development of more biologically and physiologically relevant models to study organ development, disease, toxicology and drug screening. Organoids have been derived from many mammalian tissues, both normal and tumour, from adult stem cells and from pluripotent stem cells. Tissue organoids can retain many of the cell types and much of the structure and function of the organ of origin. Organoids derived from pluripotent stem cells display increased complexity compared with organoids derived from adult stem cells. It has been shown that organoids express many functional xenobiotic-metabolising enzymes including cytochrome P450s (CYPs). This has benefitted the drug development field in facilitating pre-clinical testing of more personalised treatments and in developing large toxicity and efficacy screens for a range of compounds. In the field of environmental and genetic toxicology, treatment of organoids with various compounds has generated responses that are close to those obtained in primary tissues and in vivo models, demonstrating the biological relevance of these in vitro multicellular 3D systems. Toxicological investigations of compounds in different tissue organoids have produced promising results indicating that organoids will refine future studies on the effects of environmental exposures and carcinogenic risk to humans. With further development and standardised procedures, advancing our understanding on the metabolic capabilities of organoids will help to validate their use to investigate the modes of action of environmental carcinogens.
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spelling pubmed-90710882022-05-06 Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis Caipa Garcia, Angela L Arlt, Volker M Phillips, David H Mutagenesis Review Advances in three-dimensional (3D) cell culture technology have led to the development of more biologically and physiologically relevant models to study organ development, disease, toxicology and drug screening. Organoids have been derived from many mammalian tissues, both normal and tumour, from adult stem cells and from pluripotent stem cells. Tissue organoids can retain many of the cell types and much of the structure and function of the organ of origin. Organoids derived from pluripotent stem cells display increased complexity compared with organoids derived from adult stem cells. It has been shown that organoids express many functional xenobiotic-metabolising enzymes including cytochrome P450s (CYPs). This has benefitted the drug development field in facilitating pre-clinical testing of more personalised treatments and in developing large toxicity and efficacy screens for a range of compounds. In the field of environmental and genetic toxicology, treatment of organoids with various compounds has generated responses that are close to those obtained in primary tissues and in vivo models, demonstrating the biological relevance of these in vitro multicellular 3D systems. Toxicological investigations of compounds in different tissue organoids have produced promising results indicating that organoids will refine future studies on the effects of environmental exposures and carcinogenic risk to humans. With further development and standardised procedures, advancing our understanding on the metabolic capabilities of organoids will help to validate their use to investigate the modes of action of environmental carcinogens. Oxford University Press 2021-06-19 /pmc/articles/PMC9071088/ /pubmed/34147034 http://dx.doi.org/10.1093/mutage/geab023 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the UK Environmental Mutagen Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Caipa Garcia, Angela L
Arlt, Volker M
Phillips, David H
Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
title Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
title_full Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
title_fullStr Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
title_full_unstemmed Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
title_short Organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
title_sort organoids for toxicology and genetic toxicology: applications with drugs and prospects for environmental carcinogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9071088/
https://www.ncbi.nlm.nih.gov/pubmed/34147034
http://dx.doi.org/10.1093/mutage/geab023
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