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Biopsy‐free screening for glioma

Circulating tumor DNA (ctDNA) is a promising diagnostic marker for many cancers and can be noninvasively assayed from blood. For diagnosing glioma, this approach has unfortunately proven to be of limited use since glioma contribute minimal ctDNA to the blood circulation. A more promising avenue may...

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Detalles Bibliográficos
Autores principales: Cheng, Alexandre Pellan, Burnham, Philip, De Vlaminck, Iwijn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284383/
https://www.ncbi.nlm.nih.gov/pubmed/30401728
http://dx.doi.org/10.15252/emmm.201809484
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author Cheng, Alexandre Pellan
Burnham, Philip
De Vlaminck, Iwijn
author_facet Cheng, Alexandre Pellan
Burnham, Philip
De Vlaminck, Iwijn
author_sort Cheng, Alexandre Pellan
collection PubMed
description Circulating tumor DNA (ctDNA) is a promising diagnostic marker for many cancers and can be noninvasively assayed from blood. For diagnosing glioma, this approach has unfortunately proven to be of limited use since glioma contribute minimal ctDNA to the blood circulation. A more promising avenue may therefore be to hunt for ctDNA in cerebrospinal fluid (CSF). The study by Mouliere et al in this issue of EMBO Molecular Medicine demonstrates that shallow whole‐genome sequencing of CSF‐cfDNA can be used to detect copy number alterations in glioma‐derived ctDNA, providing a low cost strategy to screen for glioma.
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spelling pubmed-62843832018-12-14 Biopsy‐free screening for glioma Cheng, Alexandre Pellan Burnham, Philip De Vlaminck, Iwijn EMBO Mol Med News & Views Circulating tumor DNA (ctDNA) is a promising diagnostic marker for many cancers and can be noninvasively assayed from blood. For diagnosing glioma, this approach has unfortunately proven to be of limited use since glioma contribute minimal ctDNA to the blood circulation. A more promising avenue may therefore be to hunt for ctDNA in cerebrospinal fluid (CSF). The study by Mouliere et al in this issue of EMBO Molecular Medicine demonstrates that shallow whole‐genome sequencing of CSF‐cfDNA can be used to detect copy number alterations in glioma‐derived ctDNA, providing a low cost strategy to screen for glioma. John Wiley and Sons Inc. 2018-11-06 2018-12 /pmc/articles/PMC6284383/ /pubmed/30401728 http://dx.doi.org/10.15252/emmm.201809484 Text en © 2018 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle News & Views
Cheng, Alexandre Pellan
Burnham, Philip
De Vlaminck, Iwijn
Biopsy‐free screening for glioma
title Biopsy‐free screening for glioma
title_full Biopsy‐free screening for glioma
title_fullStr Biopsy‐free screening for glioma
title_full_unstemmed Biopsy‐free screening for glioma
title_short Biopsy‐free screening for glioma
title_sort biopsy‐free screening for glioma
topic News & Views
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6284383/
https://www.ncbi.nlm.nih.gov/pubmed/30401728
http://dx.doi.org/10.15252/emmm.201809484
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