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MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling
Brain tumors have become the leading cause of cancer-related death in children. An important hurdle to scientific and clinical progress in the field has been the limited availability of preclinical tumor models. Historically, few pediatric brain tumor cell lines have been established and these often...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164649/ http://dx.doi.org/10.1093/neuonc/noac079.651 |
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author | Baubet, Valerie Beale, David Mariarita, Santi Viaene, Angela Madsen, Peter Jacob, Fadi Ming, Guo-li Hongjun, Song Phillip, Storm Koptyra, Mateusz Adam, Resnick |
author_facet | Baubet, Valerie Beale, David Mariarita, Santi Viaene, Angela Madsen, Peter Jacob, Fadi Ming, Guo-li Hongjun, Song Phillip, Storm Koptyra, Mateusz Adam, Resnick |
author_sort | Baubet, Valerie |
collection | PubMed |
description | Brain tumors have become the leading cause of cancer-related death in children. An important hurdle to scientific and clinical progress in the field has been the limited availability of preclinical tumor models. Historically, few pediatric brain tumor cell lines have been established and these often poorly recapitulate the phenotypes of the original tumors. In recent years, the Children’s Brain Tumor Network (CBTN) has accelerated the development of patient-derived cell lines and xenografts, offering these resources to the community through open-source access. While these models are extremely valuable, their development process can be lengthy and result in clonally selected lines which presents a challenge for studying complex tumor biology. To address the need for three-dimensional tissue culture, our group in conjunction with CBTN, utilized organoid culture from fresh tissue specimens obtained directly from surgical resection of various pediatric brain tumor histologies. This resulted in the development and banking of over 30 organoid models, which included ependymoma, high-grade glioma, medulloblastoma, atypical teratoid-rhabdoid tumor, diffuse midline glioma, and low-grade glioma diagnoses. Tissue was processed within an hour post extraction and cultured with universal media composition for each diagnosis. Organoid growth was observed within 2-3 weeks of initiation and continued for up to three months before banking. Banked organoids established growth upon return to culture. Phenotypic analysis revealed organoid cell composition that represented clinical histology. Importantly, organoids returned to culture post-banking demonstrated similar cell composition to those in the original culture, indicating their utility for subsequent preclinical testing. Here we provide a simple and efficient workflow for the generation and characterization of three-dimensional tumor organoids generated from fresh surgical pediatric brain tumor tissue. The platform has the potential to accelerate investigations into tumor biology and empower a diverse array of translational studies for the pediatric brain tumor field. |
format | Online Article Text |
id | pubmed-9164649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91646492022-06-05 MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling Baubet, Valerie Beale, David Mariarita, Santi Viaene, Angela Madsen, Peter Jacob, Fadi Ming, Guo-li Hongjun, Song Phillip, Storm Koptyra, Mateusz Adam, Resnick Neuro Oncol Preclinical Models/Experimental Therapy/Drug Discovery Brain tumors have become the leading cause of cancer-related death in children. An important hurdle to scientific and clinical progress in the field has been the limited availability of preclinical tumor models. Historically, few pediatric brain tumor cell lines have been established and these often poorly recapitulate the phenotypes of the original tumors. In recent years, the Children’s Brain Tumor Network (CBTN) has accelerated the development of patient-derived cell lines and xenografts, offering these resources to the community through open-source access. While these models are extremely valuable, their development process can be lengthy and result in clonally selected lines which presents a challenge for studying complex tumor biology. To address the need for three-dimensional tissue culture, our group in conjunction with CBTN, utilized organoid culture from fresh tissue specimens obtained directly from surgical resection of various pediatric brain tumor histologies. This resulted in the development and banking of over 30 organoid models, which included ependymoma, high-grade glioma, medulloblastoma, atypical teratoid-rhabdoid tumor, diffuse midline glioma, and low-grade glioma diagnoses. Tissue was processed within an hour post extraction and cultured with universal media composition for each diagnosis. Organoid growth was observed within 2-3 weeks of initiation and continued for up to three months before banking. Banked organoids established growth upon return to culture. Phenotypic analysis revealed organoid cell composition that represented clinical histology. Importantly, organoids returned to culture post-banking demonstrated similar cell composition to those in the original culture, indicating their utility for subsequent preclinical testing. Here we provide a simple and efficient workflow for the generation and characterization of three-dimensional tumor organoids generated from fresh surgical pediatric brain tumor tissue. The platform has the potential to accelerate investigations into tumor biology and empower a diverse array of translational studies for the pediatric brain tumor field. Oxford University Press 2022-06-03 /pmc/articles/PMC9164649/ http://dx.doi.org/10.1093/neuonc/noac079.651 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Preclinical Models/Experimental Therapy/Drug Discovery Baubet, Valerie Beale, David Mariarita, Santi Viaene, Angela Madsen, Peter Jacob, Fadi Ming, Guo-li Hongjun, Song Phillip, Storm Koptyra, Mateusz Adam, Resnick MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
title | MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
title_full | MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
title_fullStr | MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
title_full_unstemmed | MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
title_short | MODL-28. Patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
title_sort | modl-28. patient-derived, three-dimensional organoid platform for pediatric brain tumor modeling |
topic | Preclinical Models/Experimental Therapy/Drug Discovery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164649/ http://dx.doi.org/10.1093/neuonc/noac079.651 |
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