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Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?

SIMPLE SUMMARY: Malignant pleural mesothelioma (MPM) is an extremely lethal cancer, notoriously known for its limited treatment options, lack of targeted therapies, and catastrophic survival rates. MPM tumors are highly heterogeneous and exhibit substantial variance in the genome landscape among ind...

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Autores principales: Gao, Yanyun, Kruithof-de Julio, Marianna, Peng, Ren-Wang, Dorn, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367391/
https://www.ncbi.nlm.nih.gov/pubmed/35954422
http://dx.doi.org/10.3390/cancers14153758
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author Gao, Yanyun
Kruithof-de Julio, Marianna
Peng, Ren-Wang
Dorn, Patrick
author_facet Gao, Yanyun
Kruithof-de Julio, Marianna
Peng, Ren-Wang
Dorn, Patrick
author_sort Gao, Yanyun
collection PubMed
description SIMPLE SUMMARY: Malignant pleural mesothelioma (MPM) is an extremely lethal cancer, notoriously known for its limited treatment options, lack of targeted therapies, and catastrophic survival rates. MPM tumors are highly heterogeneous and exhibit substantial variance in the genome landscape among individual patients, characterized by widespread loss-of-function mutations of tumor suppressor genes (TSGs) that are difficult to target. Therefore, there is an urgent and unmet need for novel therapeutic targets and strategies for personalized treatment. Patient-derived organoids (PDOs), the next generation tumor models that have significantly influenced the discovery of anticancer drugs and biomarkers of response to therapies in many other cancers, are emerging and promise to play a critical role in understanding the biology of MPM and, importantly, in identifying and developing precision oncology approaches tailored to specific subsets of MPM patients. ABSTRACT: MPM is an aggressive tumor originating from pleural mesothelial cells. A characteristic feature of the disease is the dominant prevalence of therapeutically intractable inactivating alterations in TSGs, making MPM one of the most difficult cancers to treat and the epitome of a cancer characterized by a significant lack of therapy options and an extremely poor prognosis (5-year survival rate of only 5% to 10%). Extensive interpatient heterogeneity poses another major challenge for targeted therapy of MPM, warranting stratified therapy for specific subgroups of MPM patients. Accurate preclinical models are critical for the discovery of new therapies and the development of personalized medicine. Organoids, an in vitro ‘organ-like’ 3D structure derived from patient tumor tissue that faithfully mimics the biology and complex architecture of cancer and largely overcomes the limitations of other existing models, are the next-generation tumor model. Although organoids have been successfully produced and used in many cancers, the development of MPM organoids is still in its infancy. Here, we provide an overview of recent advances in cancer organoids, focusing on the progress and challenges in MPM organoid development. We also elaborate the potential of MPM organoids for understanding MPM pathobiology, discovering new therapeutic targets, and developing personalized treatments for MPM patients.
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spelling pubmed-93673912022-08-12 Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today? Gao, Yanyun Kruithof-de Julio, Marianna Peng, Ren-Wang Dorn, Patrick Cancers (Basel) Review SIMPLE SUMMARY: Malignant pleural mesothelioma (MPM) is an extremely lethal cancer, notoriously known for its limited treatment options, lack of targeted therapies, and catastrophic survival rates. MPM tumors are highly heterogeneous and exhibit substantial variance in the genome landscape among individual patients, characterized by widespread loss-of-function mutations of tumor suppressor genes (TSGs) that are difficult to target. Therefore, there is an urgent and unmet need for novel therapeutic targets and strategies for personalized treatment. Patient-derived organoids (PDOs), the next generation tumor models that have significantly influenced the discovery of anticancer drugs and biomarkers of response to therapies in many other cancers, are emerging and promise to play a critical role in understanding the biology of MPM and, importantly, in identifying and developing precision oncology approaches tailored to specific subsets of MPM patients. ABSTRACT: MPM is an aggressive tumor originating from pleural mesothelial cells. A characteristic feature of the disease is the dominant prevalence of therapeutically intractable inactivating alterations in TSGs, making MPM one of the most difficult cancers to treat and the epitome of a cancer characterized by a significant lack of therapy options and an extremely poor prognosis (5-year survival rate of only 5% to 10%). Extensive interpatient heterogeneity poses another major challenge for targeted therapy of MPM, warranting stratified therapy for specific subgroups of MPM patients. Accurate preclinical models are critical for the discovery of new therapies and the development of personalized medicine. Organoids, an in vitro ‘organ-like’ 3D structure derived from patient tumor tissue that faithfully mimics the biology and complex architecture of cancer and largely overcomes the limitations of other existing models, are the next-generation tumor model. Although organoids have been successfully produced and used in many cancers, the development of MPM organoids is still in its infancy. Here, we provide an overview of recent advances in cancer organoids, focusing on the progress and challenges in MPM organoid development. We also elaborate the potential of MPM organoids for understanding MPM pathobiology, discovering new therapeutic targets, and developing personalized treatments for MPM patients. MDPI 2022-08-02 /pmc/articles/PMC9367391/ /pubmed/35954422 http://dx.doi.org/10.3390/cancers14153758 Text en © 2022 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
Gao, Yanyun
Kruithof-de Julio, Marianna
Peng, Ren-Wang
Dorn, Patrick
Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?
title Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?
title_full Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?
title_fullStr Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?
title_full_unstemmed Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?
title_short Organoids as a Model for Precision Medicine in Malignant Pleural Mesothelioma: Where Are We Today?
title_sort organoids as a model for precision medicine in malignant pleural mesothelioma: where are we today?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9367391/
https://www.ncbi.nlm.nih.gov/pubmed/35954422
http://dx.doi.org/10.3390/cancers14153758
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