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Detection of circulating tumour cell clusters in human glioblastoma
Human glioblastoma (GBM) is a highly aggressive, invasive and hypervascularised malignant brain cancer. Individual circulating tumour cells (CTCs) are sporadically found in GBM patients, yet it is unclear whether multicellular CTC clusters are generated in this disease and whether they can bypass th...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134152/ https://www.ncbi.nlm.nih.gov/pubmed/30065256 http://dx.doi.org/10.1038/s41416-018-0186-7 |
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author | Krol, Ilona Castro-Giner, Francesc Maurer, Martina Gkountela, Sofia Szczerba, Barbara Maria Scherrer, Ramona Coleman, Niamh Carreira, Suzanne Bachmann, Felix Anderson, Stephanie Engelhardt, Marc Lane, Heidi Evans, Thomas Ronald Jeffry Plummer, Ruth Kristeleit, Rebecca Lopez, Juanita Aceto, Nicola |
author_facet | Krol, Ilona Castro-Giner, Francesc Maurer, Martina Gkountela, Sofia Szczerba, Barbara Maria Scherrer, Ramona Coleman, Niamh Carreira, Suzanne Bachmann, Felix Anderson, Stephanie Engelhardt, Marc Lane, Heidi Evans, Thomas Ronald Jeffry Plummer, Ruth Kristeleit, Rebecca Lopez, Juanita Aceto, Nicola |
author_sort | Krol, Ilona |
collection | PubMed |
description | Human glioblastoma (GBM) is a highly aggressive, invasive and hypervascularised malignant brain cancer. Individual circulating tumour cells (CTCs) are sporadically found in GBM patients, yet it is unclear whether multicellular CTC clusters are generated in this disease and whether they can bypass the physical hurdle of the blood–brain barrier. Here, we assessed CTC presence and composition at multiple time points in 13 patients with progressing GBM during an open-label phase 1/2a study with the microtubule inhibitor BAL101553. We observe CTC clusters ranging from 2 to 23 cells and present at multiple sampling time points in a GBM patient with pleomorphism and extensive necrosis, throughout disease progression. Exome sequencing of GBM CTC clusters highlights variants in 58 cancer-associated genes including ATM, PMS2, POLE, APC, XPO1, TFRC, JAK2, ERBB4 and ALK. Together, our findings represent the first evidence of the presence of CTC clusters in GBM. |
format | Online Article Text |
id | pubmed-6134152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-61341522019-09-04 Detection of circulating tumour cell clusters in human glioblastoma Krol, Ilona Castro-Giner, Francesc Maurer, Martina Gkountela, Sofia Szczerba, Barbara Maria Scherrer, Ramona Coleman, Niamh Carreira, Suzanne Bachmann, Felix Anderson, Stephanie Engelhardt, Marc Lane, Heidi Evans, Thomas Ronald Jeffry Plummer, Ruth Kristeleit, Rebecca Lopez, Juanita Aceto, Nicola Br J Cancer Brief Communication Human glioblastoma (GBM) is a highly aggressive, invasive and hypervascularised malignant brain cancer. Individual circulating tumour cells (CTCs) are sporadically found in GBM patients, yet it is unclear whether multicellular CTC clusters are generated in this disease and whether they can bypass the physical hurdle of the blood–brain barrier. Here, we assessed CTC presence and composition at multiple time points in 13 patients with progressing GBM during an open-label phase 1/2a study with the microtubule inhibitor BAL101553. We observe CTC clusters ranging from 2 to 23 cells and present at multiple sampling time points in a GBM patient with pleomorphism and extensive necrosis, throughout disease progression. Exome sequencing of GBM CTC clusters highlights variants in 58 cancer-associated genes including ATM, PMS2, POLE, APC, XPO1, TFRC, JAK2, ERBB4 and ALK. Together, our findings represent the first evidence of the presence of CTC clusters in GBM. Nature Publishing Group UK 2018-08-01 2018-08-14 /pmc/articles/PMC6134152/ /pubmed/30065256 http://dx.doi.org/10.1038/s41416-018-0186-7 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Brief Communication Krol, Ilona Castro-Giner, Francesc Maurer, Martina Gkountela, Sofia Szczerba, Barbara Maria Scherrer, Ramona Coleman, Niamh Carreira, Suzanne Bachmann, Felix Anderson, Stephanie Engelhardt, Marc Lane, Heidi Evans, Thomas Ronald Jeffry Plummer, Ruth Kristeleit, Rebecca Lopez, Juanita Aceto, Nicola Detection of circulating tumour cell clusters in human glioblastoma |
title | Detection of circulating tumour cell clusters in human glioblastoma |
title_full | Detection of circulating tumour cell clusters in human glioblastoma |
title_fullStr | Detection of circulating tumour cell clusters in human glioblastoma |
title_full_unstemmed | Detection of circulating tumour cell clusters in human glioblastoma |
title_short | Detection of circulating tumour cell clusters in human glioblastoma |
title_sort | detection of circulating tumour cell clusters in human glioblastoma |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6134152/ https://www.ncbi.nlm.nih.gov/pubmed/30065256 http://dx.doi.org/10.1038/s41416-018-0186-7 |
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