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Urothelial cancer organoids: a tool for bladder cancer research

BACKGROUND: Bladder cancer ranks among the top ten most common tumor types worldwide and represents a growing healthcare problem, accounting for a large part of total healthcare costs. Chemotherapy is effective in a subset of patients, while causing severe side effects. Tumor pathogenesis and drug r...

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Autor principal: Meijer, R. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695536/
https://www.ncbi.nlm.nih.gov/pubmed/34623463
http://dx.doi.org/10.1007/s00292-021-00988-9
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author Meijer, R. P.
author_facet Meijer, R. P.
author_sort Meijer, R. P.
collection PubMed
description BACKGROUND: Bladder cancer ranks among the top ten most common tumor types worldwide and represents a growing healthcare problem, accounting for a large part of total healthcare costs. Chemotherapy is effective in a subset of patients, while causing severe side effects. Tumor pathogenesis and drug resistance mechanisms are largely unknown. Precision medicine is failing in bladder cancer, as bladder tumors are genetically and molecularly very heterogeneous. Currently, therapeutic decision-making depends on assessing a single fragment of surgically acquired tumor tissue. OBJECTIVE: New preclinical model systems for bladder cancer are indispensable for developing therapeutic strategies tailored to individual patient and tumor characteristics. Organoids are small 3D tissue cultures that simulate small-size organs “in a dish” and tumoroids are a special type of cancer organoid (i.e., malignant tissue). MATERIALS AND METHODS: Since 2016, we have collaborated with the renowned Hubrecht Institute to provide proof of concept of tissue-based bladder tumoroids mimicking parental tumors. We have developed a living biobank containing bladder organoids and tumoroids grown from over 50 patient samples, which reflect crucial aspects of bladder cancer pathogenesis. RESULTS: Histological and immunofluorescence analysis indicated that the heterogeneity and subclassification of tumoroids mimicked those of corresponding parental tumor samples. Thus, urothelial tumoroids mimic crucial aspects of bladder cancer pathogenesis. CONCLUSION: Research with urothelial tumoroids will open up new avenues for bladder cancer pathogenesis and drug-resistance research as well as for precision medicine approaches.
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spelling pubmed-86955362022-01-07 Urothelial cancer organoids: a tool for bladder cancer research Meijer, R. P. Pathologe Hauptreferate - Hauptprogramm BACKGROUND: Bladder cancer ranks among the top ten most common tumor types worldwide and represents a growing healthcare problem, accounting for a large part of total healthcare costs. Chemotherapy is effective in a subset of patients, while causing severe side effects. Tumor pathogenesis and drug resistance mechanisms are largely unknown. Precision medicine is failing in bladder cancer, as bladder tumors are genetically and molecularly very heterogeneous. Currently, therapeutic decision-making depends on assessing a single fragment of surgically acquired tumor tissue. OBJECTIVE: New preclinical model systems for bladder cancer are indispensable for developing therapeutic strategies tailored to individual patient and tumor characteristics. Organoids are small 3D tissue cultures that simulate small-size organs “in a dish” and tumoroids are a special type of cancer organoid (i.e., malignant tissue). MATERIALS AND METHODS: Since 2016, we have collaborated with the renowned Hubrecht Institute to provide proof of concept of tissue-based bladder tumoroids mimicking parental tumors. We have developed a living biobank containing bladder organoids and tumoroids grown from over 50 patient samples, which reflect crucial aspects of bladder cancer pathogenesis. RESULTS: Histological and immunofluorescence analysis indicated that the heterogeneity and subclassification of tumoroids mimicked those of corresponding parental tumor samples. Thus, urothelial tumoroids mimic crucial aspects of bladder cancer pathogenesis. CONCLUSION: Research with urothelial tumoroids will open up new avenues for bladder cancer pathogenesis and drug-resistance research as well as for precision medicine approaches. Springer Medizin 2021-10-08 2021 /pmc/articles/PMC8695536/ /pubmed/34623463 http://dx.doi.org/10.1007/s00292-021-00988-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Hauptreferate - Hauptprogramm
Meijer, R. P.
Urothelial cancer organoids: a tool for bladder cancer research
title Urothelial cancer organoids: a tool for bladder cancer research
title_full Urothelial cancer organoids: a tool for bladder cancer research
title_fullStr Urothelial cancer organoids: a tool for bladder cancer research
title_full_unstemmed Urothelial cancer organoids: a tool for bladder cancer research
title_short Urothelial cancer organoids: a tool for bladder cancer research
title_sort urothelial cancer organoids: a tool for bladder cancer research
topic Hauptreferate - Hauptprogramm
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695536/
https://www.ncbi.nlm.nih.gov/pubmed/34623463
http://dx.doi.org/10.1007/s00292-021-00988-9
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