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MODL-07. DNA methylation-based biobank of murine models for pediatric tumors

Recent advances in molecular profiling methods led to the identification of multiple new molecularly defined tumor types and subtypes, distinguished by distinct molecular markers and characteristic DNA methylation signatures. While the analysis of human methylome using microarrays has become an affo...

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Autores principales: Zheng, Tuyu, Sill, Martin, Imle, Roland, Shiraishi, Ryo, Wang, Wanchen, Morcavallo, Alaide, Chesler, Louis, Kawauchi, Daisuke, Ayrault, Olivier, Pavlo, Lutsik, Pfister, Stefan M, Kutscher, Lena M, Banito, Ana, Jones, David W, Pajtler, Kristian W, Zuckermann, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164985/
http://dx.doi.org/10.1093/neuonc/noac079.630
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author Zheng, Tuyu
Sill, Martin
Imle, Roland
Shiraishi, Ryo
Wang, Wanchen
Morcavallo, Alaide
Chesler, Louis
Kawauchi, Daisuke
Ayrault, Olivier
Pavlo, Lutsik
Pfister, Stefan M
Kutscher, Lena M
Banito, Ana
Jones, David W
Pajtler, Kristian W
Zuckermann, Marc
author_facet Zheng, Tuyu
Sill, Martin
Imle, Roland
Shiraishi, Ryo
Wang, Wanchen
Morcavallo, Alaide
Chesler, Louis
Kawauchi, Daisuke
Ayrault, Olivier
Pavlo, Lutsik
Pfister, Stefan M
Kutscher, Lena M
Banito, Ana
Jones, David W
Pajtler, Kristian W
Zuckermann, Marc
author_sort Zheng, Tuyu
collection PubMed
description Recent advances in molecular profiling methods led to the identification of multiple new molecularly defined tumor types and subtypes, distinguished by distinct molecular markers and characteristic DNA methylation signatures. While the analysis of human methylome using microarrays has become an affordable and a routine in many labs, this technology until recently was not available for murine samples. In the past years, we have successfully generated a variety of mouse models for childhood tumors (e.g brain tumors and sarcomas) using different techniques, most of which faithfully reflect the human tumor counterparts at the histological level. With the recently released Infinium Mouse Methylation BeadChip, we now set out to use our models to generate the first DNA methylation database for murine pediatric tumors. We profiled more than 70 mouse models of pediatric tumors including gliomas, medulloblastomas, ependymomas and sarcomas, as well as 40 normal brain and muscle control tissues. We are currently performing a cross-species comparative analysis of established mouse models and the human counterparts. This will assess, how faithfully each models reflect the human situation and examine the effects of multiple passages of allografting. We will also analyze purified immune cell populations and use the derived methylation signatures to assess the model-specific immune microenvironment. Furthermore, we will investigate the methylomes of multiple putative cells-of-origin, which is hardly possible in the human context due to the lack of purified material. We will correlate these to murine tumor samples and thereby provide novel insights into tumor origins. In summary, our study will generate a validated biobank of murine models for pediatric cancers and provide a valuable resource for future developmental studies and preclinical trials.
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spelling pubmed-91649852022-06-05 MODL-07. DNA methylation-based biobank of murine models for pediatric tumors Zheng, Tuyu Sill, Martin Imle, Roland Shiraishi, Ryo Wang, Wanchen Morcavallo, Alaide Chesler, Louis Kawauchi, Daisuke Ayrault, Olivier Pavlo, Lutsik Pfister, Stefan M Kutscher, Lena M Banito, Ana Jones, David W Pajtler, Kristian W Zuckermann, Marc Neuro Oncol Preclinical Models/Experimental Therapy/Drug Discovery Recent advances in molecular profiling methods led to the identification of multiple new molecularly defined tumor types and subtypes, distinguished by distinct molecular markers and characteristic DNA methylation signatures. While the analysis of human methylome using microarrays has become an affordable and a routine in many labs, this technology until recently was not available for murine samples. In the past years, we have successfully generated a variety of mouse models for childhood tumors (e.g brain tumors and sarcomas) using different techniques, most of which faithfully reflect the human tumor counterparts at the histological level. With the recently released Infinium Mouse Methylation BeadChip, we now set out to use our models to generate the first DNA methylation database for murine pediatric tumors. We profiled more than 70 mouse models of pediatric tumors including gliomas, medulloblastomas, ependymomas and sarcomas, as well as 40 normal brain and muscle control tissues. We are currently performing a cross-species comparative analysis of established mouse models and the human counterparts. This will assess, how faithfully each models reflect the human situation and examine the effects of multiple passages of allografting. We will also analyze purified immune cell populations and use the derived methylation signatures to assess the model-specific immune microenvironment. Furthermore, we will investigate the methylomes of multiple putative cells-of-origin, which is hardly possible in the human context due to the lack of purified material. We will correlate these to murine tumor samples and thereby provide novel insights into tumor origins. In summary, our study will generate a validated biobank of murine models for pediatric cancers and provide a valuable resource for future developmental studies and preclinical trials. Oxford University Press 2022-06-03 /pmc/articles/PMC9164985/ http://dx.doi.org/10.1093/neuonc/noac079.630 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
Zheng, Tuyu
Sill, Martin
Imle, Roland
Shiraishi, Ryo
Wang, Wanchen
Morcavallo, Alaide
Chesler, Louis
Kawauchi, Daisuke
Ayrault, Olivier
Pavlo, Lutsik
Pfister, Stefan M
Kutscher, Lena M
Banito, Ana
Jones, David W
Pajtler, Kristian W
Zuckermann, Marc
MODL-07. DNA methylation-based biobank of murine models for pediatric tumors
title MODL-07. DNA methylation-based biobank of murine models for pediatric tumors
title_full MODL-07. DNA methylation-based biobank of murine models for pediatric tumors
title_fullStr MODL-07. DNA methylation-based biobank of murine models for pediatric tumors
title_full_unstemmed MODL-07. DNA methylation-based biobank of murine models for pediatric tumors
title_short MODL-07. DNA methylation-based biobank of murine models for pediatric tumors
title_sort modl-07. dna methylation-based biobank of murine models for pediatric tumors
topic Preclinical Models/Experimental Therapy/Drug Discovery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164985/
http://dx.doi.org/10.1093/neuonc/noac079.630
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