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The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids

SIMPLE SUMMARY: Patients diagnosed with pancreatic cancer have very few treatment options. In order to identify new treatment opportunities, and develop new drugs for clinical use, appropriate model systems that take into account the complexities of a tumor are required. In this review, we summarize...

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Autores principales: Low, Ronnie Ren Jie, Lim, Wei Wen, Nguyen, Paul M., Lee, Belinda, Christie, Michael, Burgess, Antony W., Gibbs, Peter, Grimmond, Sean M., Hollande, Frédéric, Putoczki, Tracy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508245/
https://www.ncbi.nlm.nih.gov/pubmed/34638463
http://dx.doi.org/10.3390/cancers13194979
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author Low, Ronnie Ren Jie
Lim, Wei Wen
Nguyen, Paul M.
Lee, Belinda
Christie, Michael
Burgess, Antony W.
Gibbs, Peter
Grimmond, Sean M.
Hollande, Frédéric
Putoczki, Tracy L.
author_facet Low, Ronnie Ren Jie
Lim, Wei Wen
Nguyen, Paul M.
Lee, Belinda
Christie, Michael
Burgess, Antony W.
Gibbs, Peter
Grimmond, Sean M.
Hollande, Frédéric
Putoczki, Tracy L.
author_sort Low, Ronnie Ren Jie
collection PubMed
description SIMPLE SUMMARY: Patients diagnosed with pancreatic cancer have very few treatment options. In order to identify new treatment opportunities, and develop new drugs for clinical use, appropriate model systems that take into account the complexities of a tumor are required. In this review, we summarize the current and emerging opportunities to accurately model pancreatic cancer using organoid technologies. We highlight the need for continued development of these complex model systems in order to inform personalized treatment. ABSTRACT: Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal solid malignancies. While immortalized cancer cell lines and genetically engineered murine models have increased our understanding of PDAC tumorigenesis, they do not recapitulate inter- and intra-patient heterogeneity. PDAC patient derived organoid (PDO) biobanks have overcome this hurdle, and provide an opportunity for the high throughput screening of potential new therapies. This review provides a summary of the PDAC PDO biobanks established to date, and discusses how they have advanced our understanding of PDAC biology. Looking forward, the development of coculturing techniques for specific immune or stromal cell populations will enable a better understanding of the crosstalk that occurs within the tumor microenvironment, and the impact of this crosstalk on treatment response.
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spelling pubmed-85082452021-10-13 The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids Low, Ronnie Ren Jie Lim, Wei Wen Nguyen, Paul M. Lee, Belinda Christie, Michael Burgess, Antony W. Gibbs, Peter Grimmond, Sean M. Hollande, Frédéric Putoczki, Tracy L. Cancers (Basel) Review SIMPLE SUMMARY: Patients diagnosed with pancreatic cancer have very few treatment options. In order to identify new treatment opportunities, and develop new drugs for clinical use, appropriate model systems that take into account the complexities of a tumor are required. In this review, we summarize the current and emerging opportunities to accurately model pancreatic cancer using organoid technologies. We highlight the need for continued development of these complex model systems in order to inform personalized treatment. ABSTRACT: Pancreatic ductal adenocarcinoma (PDAC) is one of the most lethal solid malignancies. While immortalized cancer cell lines and genetically engineered murine models have increased our understanding of PDAC tumorigenesis, they do not recapitulate inter- and intra-patient heterogeneity. PDAC patient derived organoid (PDO) biobanks have overcome this hurdle, and provide an opportunity for the high throughput screening of potential new therapies. This review provides a summary of the PDAC PDO biobanks established to date, and discusses how they have advanced our understanding of PDAC biology. Looking forward, the development of coculturing techniques for specific immune or stromal cell populations will enable a better understanding of the crosstalk that occurs within the tumor microenvironment, and the impact of this crosstalk on treatment response. MDPI 2021-10-04 /pmc/articles/PMC8508245/ /pubmed/34638463 http://dx.doi.org/10.3390/cancers13194979 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Low, Ronnie Ren Jie
Lim, Wei Wen
Nguyen, Paul M.
Lee, Belinda
Christie, Michael
Burgess, Antony W.
Gibbs, Peter
Grimmond, Sean M.
Hollande, Frédéric
Putoczki, Tracy L.
The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids
title The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids
title_full The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids
title_fullStr The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids
title_full_unstemmed The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids
title_short The Diverse Applications of Pancreatic Ductal Adenocarcinoma Organoids
title_sort diverse applications of pancreatic ductal adenocarcinoma organoids
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8508245/
https://www.ncbi.nlm.nih.gov/pubmed/34638463
http://dx.doi.org/10.3390/cancers13194979
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