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Pancreatic Organoids for Regenerative Medicine and Cancer Research

In recent years, the development of ex vivo organoid cultures has gained substantial attention as a model to study regenerative medicine and diseases in several tissues. Diabetes and pancreatic ductal adenocarcinoma (PDAC) are the two major devastating diseases affecting the pancreas. Suitable model...

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Detalles Bibliográficos
Autores principales: Casamitjana, Joan, Espinet, Elisa, Rovira, Meritxell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110799/
https://www.ncbi.nlm.nih.gov/pubmed/35592251
http://dx.doi.org/10.3389/fcell.2022.886153
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author Casamitjana, Joan
Espinet, Elisa
Rovira, Meritxell
author_facet Casamitjana, Joan
Espinet, Elisa
Rovira, Meritxell
author_sort Casamitjana, Joan
collection PubMed
description In recent years, the development of ex vivo organoid cultures has gained substantial attention as a model to study regenerative medicine and diseases in several tissues. Diabetes and pancreatic ductal adenocarcinoma (PDAC) are the two major devastating diseases affecting the pancreas. Suitable models for regenerative medicine in diabetes and to accurately study PDAC biology and treatment response are essential in the pancreatic field. Pancreatic organoids can be generated from healthy pancreas or pancreatic tumors and constitute an important translational bridge between in vitro and in vivo models. Here, we review the rapidly emerging field of pancreatic organoids and summarize the current applications of the technology to tissue regeneration, disease modelling, and drug screening.
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spelling pubmed-91107992022-05-18 Pancreatic Organoids for Regenerative Medicine and Cancer Research Casamitjana, Joan Espinet, Elisa Rovira, Meritxell Front Cell Dev Biol Cell and Developmental Biology In recent years, the development of ex vivo organoid cultures has gained substantial attention as a model to study regenerative medicine and diseases in several tissues. Diabetes and pancreatic ductal adenocarcinoma (PDAC) are the two major devastating diseases affecting the pancreas. Suitable models for regenerative medicine in diabetes and to accurately study PDAC biology and treatment response are essential in the pancreatic field. Pancreatic organoids can be generated from healthy pancreas or pancreatic tumors and constitute an important translational bridge between in vitro and in vivo models. Here, we review the rapidly emerging field of pancreatic organoids and summarize the current applications of the technology to tissue regeneration, disease modelling, and drug screening. Frontiers Media S.A. 2022-05-03 /pmc/articles/PMC9110799/ /pubmed/35592251 http://dx.doi.org/10.3389/fcell.2022.886153 Text en Copyright © 2022 Casamitjana, Espinet and Rovira. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Casamitjana, Joan
Espinet, Elisa
Rovira, Meritxell
Pancreatic Organoids for Regenerative Medicine and Cancer Research
title Pancreatic Organoids for Regenerative Medicine and Cancer Research
title_full Pancreatic Organoids for Regenerative Medicine and Cancer Research
title_fullStr Pancreatic Organoids for Regenerative Medicine and Cancer Research
title_full_unstemmed Pancreatic Organoids for Regenerative Medicine and Cancer Research
title_short Pancreatic Organoids for Regenerative Medicine and Cancer Research
title_sort pancreatic organoids for regenerative medicine and cancer research
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9110799/
https://www.ncbi.nlm.nih.gov/pubmed/35592251
http://dx.doi.org/10.3389/fcell.2022.886153
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