Cargando…
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...
Autores principales: | , , |
---|---|
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 |
_version_ | 1783379325709451264 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6284383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT chengalexandrepellan biopsyfreescreeningforglioma AT burnhamphilip biopsyfreescreeningforglioma AT devlaminckiwijn biopsyfreescreeningforglioma |