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The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology
In the era of precision medicine, cancer researchers and oncologists are eagerly searching for more realistic, cost effective, and timely tumor models to aid drug development and precision oncology. Tumor models that can faithfully recapitulate the histological and molecular characteristics of vario...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6762043/ https://www.ncbi.nlm.nih.gov/pubmed/31773090 http://dx.doi.org/10.1002/ame2.12077 |
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author | Granat, Lauren M. Kambhampati, Ooha Klosek, Stephanie Niedzwecki, Brian Parsa, Kian Zhang, Dong |
author_facet | Granat, Lauren M. Kambhampati, Ooha Klosek, Stephanie Niedzwecki, Brian Parsa, Kian Zhang, Dong |
author_sort | Granat, Lauren M. |
collection | PubMed |
description | In the era of precision medicine, cancer researchers and oncologists are eagerly searching for more realistic, cost effective, and timely tumor models to aid drug development and precision oncology. Tumor models that can faithfully recapitulate the histological and molecular characteristics of various human tumors will be extremely valuable in increasing the successful rate of oncology drug development and discovering the most efficacious treatment regimen for cancer patients. Two‐dimensional (2D) cultured cancer cell lines, genetically engineered mouse tumor (GEMT) models, and patient‐derived tumor xenograft (PDTX) models have been widely used to investigate the biology of various types of cancers and test the efficacy of oncology drug candidates. However, due to either the failure to faithfully recapitulate the complexity of patient tumors in the case of 2D cultured cancer cells, or high cost and untimely for drug screening and testing in the case of GEMT and PDTX, new tumor models are urgently needed. The recently developed patient‐derived tumor organoids (PDTO) offer great potentials in uncovering novel biology of cancer development, accelerating the discovery of oncology drugs, and individualizing the treatment of cancers. In this review, we will summarize the recent progress in utilizing PDTO for oncology drug discovery. In addition, we will discuss the potentials and limitations of the current PDTO tumor models. |
format | Online Article Text |
id | pubmed-6762043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67620432019-11-26 The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology Granat, Lauren M. Kambhampati, Ooha Klosek, Stephanie Niedzwecki, Brian Parsa, Kian Zhang, Dong Animal Model Exp Med Review Articles In the era of precision medicine, cancer researchers and oncologists are eagerly searching for more realistic, cost effective, and timely tumor models to aid drug development and precision oncology. Tumor models that can faithfully recapitulate the histological and molecular characteristics of various human tumors will be extremely valuable in increasing the successful rate of oncology drug development and discovering the most efficacious treatment regimen for cancer patients. Two‐dimensional (2D) cultured cancer cell lines, genetically engineered mouse tumor (GEMT) models, and patient‐derived tumor xenograft (PDTX) models have been widely used to investigate the biology of various types of cancers and test the efficacy of oncology drug candidates. However, due to either the failure to faithfully recapitulate the complexity of patient tumors in the case of 2D cultured cancer cells, or high cost and untimely for drug screening and testing in the case of GEMT and PDTX, new tumor models are urgently needed. The recently developed patient‐derived tumor organoids (PDTO) offer great potentials in uncovering novel biology of cancer development, accelerating the discovery of oncology drugs, and individualizing the treatment of cancers. In this review, we will summarize the recent progress in utilizing PDTO for oncology drug discovery. In addition, we will discuss the potentials and limitations of the current PDTO tumor models. John Wiley and Sons Inc. 2019-08-13 /pmc/articles/PMC6762043/ /pubmed/31773090 http://dx.doi.org/10.1002/ame2.12077 Text en © 2019 The Authors. Animal Models and Experimental Medicine published by John Wiley & Sons Australia, Ltd on behalf of The Chinese Association for Laboratory Animal Sciences This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Granat, Lauren M. Kambhampati, Ooha Klosek, Stephanie Niedzwecki, Brian Parsa, Kian Zhang, Dong The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
title | The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
title_full | The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
title_fullStr | The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
title_full_unstemmed | The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
title_short | The promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
title_sort | promises and challenges of patient‐derived tumor organoids in drug development and precision oncology |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6762043/ https://www.ncbi.nlm.nih.gov/pubmed/31773090 http://dx.doi.org/10.1002/ame2.12077 |
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