Biopsy‐free screening for glioma

Abstract 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 av...

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Main Authors: Alexandre Pellan Cheng, Philip Burnham, Iwijn De Vlaminck
Format: Article
Language:English
Published: Springer Nature 2018-11-01
Series:EMBO Molecular Medicine
Online Access:https://doi.org/10.15252/emmm.201809484
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author Alexandre Pellan Cheng
Philip Burnham
Iwijn De Vlaminck
author_facet Alexandre Pellan Cheng
Philip Burnham
Iwijn De Vlaminck
author_sort Alexandre Pellan Cheng
collection DOAJ
description Abstract 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 doaj.art-2219ca548b834b2e8489be76740f0d182024-10-28T08:56:59ZengSpringer NatureEMBO Molecular Medicine1757-46761757-46842018-11-0110121310.15252/emmm.201809484Biopsy‐free screening for gliomaAlexandre Pellan Cheng0Philip Burnham1Iwijn De Vlaminck2Meinig School of Biomedical Engineering, Cornell UniversityMeinig School of Biomedical Engineering, Cornell UniversityMeinig School of Biomedical Engineering, Cornell UniversityAbstract 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.https://doi.org/10.15252/emmm.201809484
spellingShingle Alexandre Pellan Cheng
Philip Burnham
Iwijn De Vlaminck
Biopsy‐free screening for glioma
EMBO Molecular Medicine
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
url https://doi.org/10.15252/emmm.201809484
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