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Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment

Malignant gliomas are heterogeneous diseases in genetic basis. The development of sequencing techniques has identified many gene rearrangements encoding novel oncogenic fusions in malignant glioma to date. Understanding the gene fusions and how they regulate cellular processes in different subtypes...

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Detalles Bibliográficos
Autores principales: Xu, Tao, Wang, Hongxiang, Huang, Xiaoquan, Li, Weiqing, Huang, Qilin, Yan, Yong, Chen, Juxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071515/
https://www.ncbi.nlm.nih.gov/pubmed/29571074
http://dx.doi.org/10.1016/j.tranon.2018.02.020
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author Xu, Tao
Wang, Hongxiang
Huang, Xiaoquan
Li, Weiqing
Huang, Qilin
Yan, Yong
Chen, Juxiang
author_facet Xu, Tao
Wang, Hongxiang
Huang, Xiaoquan
Li, Weiqing
Huang, Qilin
Yan, Yong
Chen, Juxiang
author_sort Xu, Tao
collection PubMed
description Malignant gliomas are heterogeneous diseases in genetic basis. The development of sequencing techniques has identified many gene rearrangements encoding novel oncogenic fusions in malignant glioma to date. Understanding the gene fusions and how they regulate cellular processes in different subtypes of glioma will shed light on genomic diagnostic approaches for personalized treatment. By now, studies of gene fusions in glioma remain limited, and no medication has been approved for treating the malignancy harboring gene fusions. This review will discuss the current characterization of gene fusions occurring in both adult and pediatric malignant gliomas, their roles in oncogenesis, and the potential clinical implication as therapeutic targets.
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spelling pubmed-60715152018-08-09 Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment Xu, Tao Wang, Hongxiang Huang, Xiaoquan Li, Weiqing Huang, Qilin Yan, Yong Chen, Juxiang Transl Oncol Review article Malignant gliomas are heterogeneous diseases in genetic basis. The development of sequencing techniques has identified many gene rearrangements encoding novel oncogenic fusions in malignant glioma to date. Understanding the gene fusions and how they regulate cellular processes in different subtypes of glioma will shed light on genomic diagnostic approaches for personalized treatment. By now, studies of gene fusions in glioma remain limited, and no medication has been approved for treating the malignancy harboring gene fusions. This review will discuss the current characterization of gene fusions occurring in both adult and pediatric malignant gliomas, their roles in oncogenesis, and the potential clinical implication as therapeutic targets. Neoplasia Press 2018-03-20 /pmc/articles/PMC6071515/ /pubmed/29571074 http://dx.doi.org/10.1016/j.tranon.2018.02.020 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review article
Xu, Tao
Wang, Hongxiang
Huang, Xiaoquan
Li, Weiqing
Huang, Qilin
Yan, Yong
Chen, Juxiang
Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment
title Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment
title_full Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment
title_fullStr Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment
title_full_unstemmed Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment
title_short Gene Fusion in Malignant Glioma: An Emerging Target for Next-Generation Personalized Treatment
title_sort gene fusion in malignant glioma: an emerging target for next-generation personalized treatment
topic Review article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6071515/
https://www.ncbi.nlm.nih.gov/pubmed/29571074
http://dx.doi.org/10.1016/j.tranon.2018.02.020
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