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Epigenomics and immunotherapeutic advances in pediatric brain tumors
Brain tumors are the leading cause of childhood cancer-related deaths. Similar to adult brain tumors, pediatric brain tumors are classified based on histopathological evaluations. However, pediatric brain tumors are often histologically inconsistent with adult brain tumors. Recent research findings...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087701/ https://www.ncbi.nlm.nih.gov/pubmed/33931704 http://dx.doi.org/10.1038/s41698-021-00173-4 |
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author | Abedalthagafi, Malak Mobark, Nahla Al-Rashed, May AlHarbi, Musa |
author_facet | Abedalthagafi, Malak Mobark, Nahla Al-Rashed, May AlHarbi, Musa |
author_sort | Abedalthagafi, Malak |
collection | PubMed |
description | Brain tumors are the leading cause of childhood cancer-related deaths. Similar to adult brain tumors, pediatric brain tumors are classified based on histopathological evaluations. However, pediatric brain tumors are often histologically inconsistent with adult brain tumors. Recent research findings from molecular genetic analyses have revealed molecular and genetic changes in pediatric tumors that are necessary for appropriate classification to avoid misdiagnosis, the development of treatment modalities, and the clinical management of tumors. As many of the molecular-based therapies developed from clinical trials on adults are not always effective against pediatric brain tumors, recent advances have improved our understanding of the molecular profiles of pediatric brain tumors and have led to novel epigenetic and immunotherapeutic treatment approaches currently being evaluated in clinical trials. In this review, we focus on primary malignant brain tumors in children and genetic, epigenetic, and molecular characteristics that differentiate them from brain tumors in adults. The comparison of pediatric and adult brain tumors highlights the need for treatments designed specifically for pediatric brain tumors. We also discuss the advancements in novel molecularly targeted drugs and how they are being integrated with standard therapy to improve the classification and outcomes of pediatric brain tumors in the future. |
format | Online Article Text |
id | pubmed-8087701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80877012021-05-05 Epigenomics and immunotherapeutic advances in pediatric brain tumors Abedalthagafi, Malak Mobark, Nahla Al-Rashed, May AlHarbi, Musa NPJ Precis Oncol Review Article Brain tumors are the leading cause of childhood cancer-related deaths. Similar to adult brain tumors, pediatric brain tumors are classified based on histopathological evaluations. However, pediatric brain tumors are often histologically inconsistent with adult brain tumors. Recent research findings from molecular genetic analyses have revealed molecular and genetic changes in pediatric tumors that are necessary for appropriate classification to avoid misdiagnosis, the development of treatment modalities, and the clinical management of tumors. As many of the molecular-based therapies developed from clinical trials on adults are not always effective against pediatric brain tumors, recent advances have improved our understanding of the molecular profiles of pediatric brain tumors and have led to novel epigenetic and immunotherapeutic treatment approaches currently being evaluated in clinical trials. In this review, we focus on primary malignant brain tumors in children and genetic, epigenetic, and molecular characteristics that differentiate them from brain tumors in adults. The comparison of pediatric and adult brain tumors highlights the need for treatments designed specifically for pediatric brain tumors. We also discuss the advancements in novel molecularly targeted drugs and how they are being integrated with standard therapy to improve the classification and outcomes of pediatric brain tumors in the future. Nature Publishing Group UK 2021-04-30 /pmc/articles/PMC8087701/ /pubmed/33931704 http://dx.doi.org/10.1038/s41698-021-00173-4 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Abedalthagafi, Malak Mobark, Nahla Al-Rashed, May AlHarbi, Musa Epigenomics and immunotherapeutic advances in pediatric brain tumors |
title | Epigenomics and immunotherapeutic advances in pediatric brain tumors |
title_full | Epigenomics and immunotherapeutic advances in pediatric brain tumors |
title_fullStr | Epigenomics and immunotherapeutic advances in pediatric brain tumors |
title_full_unstemmed | Epigenomics and immunotherapeutic advances in pediatric brain tumors |
title_short | Epigenomics and immunotherapeutic advances in pediatric brain tumors |
title_sort | epigenomics and immunotherapeutic advances in pediatric brain tumors |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087701/ https://www.ncbi.nlm.nih.gov/pubmed/33931704 http://dx.doi.org/10.1038/s41698-021-00173-4 |
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