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Organoid in colorectal cancer: progress and challenges

Patient-derived tumor organoids (PDOs) currently represent important modeling tools in pre-clinical investigation of malignancies. Organoid cultures conserve the genetic and phenotypic characteristics of the original tumor and maintain its heterogeneity, allowing their application in many research f...

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Detalles Bibliográficos
Autores principales: Ji, Deng-Bo, Wu, Ai-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462208/
https://www.ncbi.nlm.nih.gov/pubmed/32826461
http://dx.doi.org/10.1097/CM9.0000000000000882
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author Ji, Deng-Bo
Wu, Ai-Wen
author_facet Ji, Deng-Bo
Wu, Ai-Wen
author_sort Ji, Deng-Bo
collection PubMed
description Patient-derived tumor organoids (PDOs) currently represent important modeling tools in pre-clinical investigation of malignancies. Organoid cultures conserve the genetic and phenotypic characteristics of the original tumor and maintain its heterogeneity, allowing their application in many research fields. PDOs derived from colorectal cancer (CRC) have been used for genetic modeling to investigate the function of driver genes. Some researchers have been exploring the value of CRC PDOs in chemotherapy, targeted therapy, and radiotherapy response prediction. The successful generation of PDOs derived from CRC could deepen our understanding of CRC biology and provide novel tools for cancer modeling, for realizing precision medicine by assessing specimens from individual patients ex vivo. The present review discusses recently reported advances in CRC PDOs and the challenges they face as pre-clinical models in CRC research.
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spelling pubmed-74622082020-09-16 Organoid in colorectal cancer: progress and challenges Ji, Deng-Bo Wu, Ai-Wen Chin Med J (Engl) Review Articles Patient-derived tumor organoids (PDOs) currently represent important modeling tools in pre-clinical investigation of malignancies. Organoid cultures conserve the genetic and phenotypic characteristics of the original tumor and maintain its heterogeneity, allowing their application in many research fields. PDOs derived from colorectal cancer (CRC) have been used for genetic modeling to investigate the function of driver genes. Some researchers have been exploring the value of CRC PDOs in chemotherapy, targeted therapy, and radiotherapy response prediction. The successful generation of PDOs derived from CRC could deepen our understanding of CRC biology and provide novel tools for cancer modeling, for realizing precision medicine by assessing specimens from individual patients ex vivo. The present review discusses recently reported advances in CRC PDOs and the challenges they face as pre-clinical models in CRC research. Lippincott Williams & Wilkins 2020-08-20 2020-07-01 /pmc/articles/PMC7462208/ /pubmed/32826461 http://dx.doi.org/10.1097/CM9.0000000000000882 Text en Copyright © 2020 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Review Articles
Ji, Deng-Bo
Wu, Ai-Wen
Organoid in colorectal cancer: progress and challenges
title Organoid in colorectal cancer: progress and challenges
title_full Organoid in colorectal cancer: progress and challenges
title_fullStr Organoid in colorectal cancer: progress and challenges
title_full_unstemmed Organoid in colorectal cancer: progress and challenges
title_short Organoid in colorectal cancer: progress and challenges
title_sort organoid in colorectal cancer: progress and challenges
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7462208/
https://www.ncbi.nlm.nih.gov/pubmed/32826461
http://dx.doi.org/10.1097/CM9.0000000000000882
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