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Cell of origin of glioma: biological and clinical implications

The cellular origin of gliomas remains a topic of controversy in cancer research. Advances in neurobiology, molecular genetics, and functional genomics have ushered new insights through exploiting the development of more sophisticated tools to address this question. Diverse distinct cell populations...

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Detalles Bibliográficos
Autores principales: Alcantara Llaguno, Sheila R, Parada, Luis F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155355/
https://www.ncbi.nlm.nih.gov/pubmed/27832665
http://dx.doi.org/10.1038/bjc.2016.354
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author Alcantara Llaguno, Sheila R
Parada, Luis F
author_facet Alcantara Llaguno, Sheila R
Parada, Luis F
author_sort Alcantara Llaguno, Sheila R
collection PubMed
description The cellular origin of gliomas remains a topic of controversy in cancer research. Advances in neurobiology, molecular genetics, and functional genomics have ushered new insights through exploiting the development of more sophisticated tools to address this question. Diverse distinct cell populations in the adult brain have been reported to give rise to gliomas, although how these studies relate physiologically to mechanisms of spontaneous tumour formation via accumulation of tumour-initiating mutations within a single cell are less well developed. Recent studies in animal models indicate that the lineage of the tumour-initiating cell may contribute to the biological and genomic phenotype of glioblastoma. These results suggest that the cell of origin may not only serve as a source of diversity for these tumours, but may also provide new avenues for improved diagnostics and therapeutic targeting that may prolong the lives of patients.
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spelling pubmed-51553552016-12-29 Cell of origin of glioma: biological and clinical implications Alcantara Llaguno, Sheila R Parada, Luis F Br J Cancer Minireviews The cellular origin of gliomas remains a topic of controversy in cancer research. Advances in neurobiology, molecular genetics, and functional genomics have ushered new insights through exploiting the development of more sophisticated tools to address this question. Diverse distinct cell populations in the adult brain have been reported to give rise to gliomas, although how these studies relate physiologically to mechanisms of spontaneous tumour formation via accumulation of tumour-initiating mutations within a single cell are less well developed. Recent studies in animal models indicate that the lineage of the tumour-initiating cell may contribute to the biological and genomic phenotype of glioblastoma. These results suggest that the cell of origin may not only serve as a source of diversity for these tumours, but may also provide new avenues for improved diagnostics and therapeutic targeting that may prolong the lives of patients. Nature Publishing Group 2016-12-06 2016-11-10 /pmc/articles/PMC5155355/ /pubmed/27832665 http://dx.doi.org/10.1038/bjc.2016.354 Text en Copyright © 2016 The Author(s) http://creativecommons.org/licenses/by-nc-sa/4.0/ This work is licensed under the Creative Commons Attribution-Non-Commercial-Share Alike 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/
spellingShingle Minireviews
Alcantara Llaguno, Sheila R
Parada, Luis F
Cell of origin of glioma: biological and clinical implications
title Cell of origin of glioma: biological and clinical implications
title_full Cell of origin of glioma: biological and clinical implications
title_fullStr Cell of origin of glioma: biological and clinical implications
title_full_unstemmed Cell of origin of glioma: biological and clinical implications
title_short Cell of origin of glioma: biological and clinical implications
title_sort cell of origin of glioma: biological and clinical implications
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5155355/
https://www.ncbi.nlm.nih.gov/pubmed/27832665
http://dx.doi.org/10.1038/bjc.2016.354
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