Cargando…
Identification of five important genes to predict glioblastoma subtypes
BACKGROUND: Glioblastoma (GBM), the most common and aggressive primary brain tumour in adults, has been classified into three subtypes: classical, mesenchymal, and proneural. While the original classification relied on an 840 gene-set, further clarification on true GBM subtypes uses a 150-gene signa...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577514/ https://www.ncbi.nlm.nih.gov/pubmed/34765972 http://dx.doi.org/10.1093/noajnl/vdab144 |
_version_ | 1784596075434213376 |
---|---|
author | Tang, Yang Qazi, Maleeha A Brown, Kevin R Mikolajewicz, Nicholas Moffat, Jason Singh, Sheila K McNicholas, Paul D |
author_facet | Tang, Yang Qazi, Maleeha A Brown, Kevin R Mikolajewicz, Nicholas Moffat, Jason Singh, Sheila K McNicholas, Paul D |
author_sort | Tang, Yang |
collection | PubMed |
description | BACKGROUND: Glioblastoma (GBM), the most common and aggressive primary brain tumour in adults, has been classified into three subtypes: classical, mesenchymal, and proneural. While the original classification relied on an 840 gene-set, further clarification on true GBM subtypes uses a 150-gene signature to accurately classify GBM into the three subtypes. We hypothesized whether a machine learning approach could be used to identify a smaller gene-set to accurately predict GBM subtype. METHODS: Using a supervised machine learning approach, extreme gradient boosting (XGBoost), we developed a classifier to predict the three subtypes of glioblastoma (GBM): classical, mesenchymal, and proneural. We tested the classifier on in-house GBM tissue, cell lines, and xenograft samples to predict their subtype. RESULTS: We identified the five most important genes for characterizing the three subtypes based on genes that often exhibited high Importance Scores in our XGBoost analyses. On average, this approach achieved 80.12% accuracy in predicting these three subtypes of GBM. Furthermore, we applied our five-gene classifier to successfully predict the subtype of GBM samples at our centre. CONCLUSION: Our 5-gene set classifier is the smallest classifier to date that can predict GBM subtypes with high accuracy, which could facilitate the future development of a five-gene subtype diagnostic biomarker for routine assays in GBM samples. |
format | Online Article Text |
id | pubmed-8577514 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-85775142021-11-10 Identification of five important genes to predict glioblastoma subtypes Tang, Yang Qazi, Maleeha A Brown, Kevin R Mikolajewicz, Nicholas Moffat, Jason Singh, Sheila K McNicholas, Paul D Neurooncol Adv Basic and Translational Investigations BACKGROUND: Glioblastoma (GBM), the most common and aggressive primary brain tumour in adults, has been classified into three subtypes: classical, mesenchymal, and proneural. While the original classification relied on an 840 gene-set, further clarification on true GBM subtypes uses a 150-gene signature to accurately classify GBM into the three subtypes. We hypothesized whether a machine learning approach could be used to identify a smaller gene-set to accurately predict GBM subtype. METHODS: Using a supervised machine learning approach, extreme gradient boosting (XGBoost), we developed a classifier to predict the three subtypes of glioblastoma (GBM): classical, mesenchymal, and proneural. We tested the classifier on in-house GBM tissue, cell lines, and xenograft samples to predict their subtype. RESULTS: We identified the five most important genes for characterizing the three subtypes based on genes that often exhibited high Importance Scores in our XGBoost analyses. On average, this approach achieved 80.12% accuracy in predicting these three subtypes of GBM. Furthermore, we applied our five-gene classifier to successfully predict the subtype of GBM samples at our centre. CONCLUSION: Our 5-gene set classifier is the smallest classifier to date that can predict GBM subtypes with high accuracy, which could facilitate the future development of a five-gene subtype diagnostic biomarker for routine assays in GBM samples. Oxford University Press 2021-10-10 /pmc/articles/PMC8577514/ /pubmed/34765972 http://dx.doi.org/10.1093/noajnl/vdab144 Text en © The Author(s) 2021. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic and Translational Investigations Tang, Yang Qazi, Maleeha A Brown, Kevin R Mikolajewicz, Nicholas Moffat, Jason Singh, Sheila K McNicholas, Paul D Identification of five important genes to predict glioblastoma subtypes |
title | Identification of five important genes to predict glioblastoma subtypes |
title_full | Identification of five important genes to predict glioblastoma subtypes |
title_fullStr | Identification of five important genes to predict glioblastoma subtypes |
title_full_unstemmed | Identification of five important genes to predict glioblastoma subtypes |
title_short | Identification of five important genes to predict glioblastoma subtypes |
title_sort | identification of five important genes to predict glioblastoma subtypes |
topic | Basic and Translational Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8577514/ https://www.ncbi.nlm.nih.gov/pubmed/34765972 http://dx.doi.org/10.1093/noajnl/vdab144 |
work_keys_str_mv | AT tangyang identificationoffiveimportantgenestopredictglioblastomasubtypes AT qazimaleehaa identificationoffiveimportantgenestopredictglioblastomasubtypes AT brownkevinr identificationoffiveimportantgenestopredictglioblastomasubtypes AT mikolajewicznicholas identificationoffiveimportantgenestopredictglioblastomasubtypes AT moffatjason identificationoffiveimportantgenestopredictglioblastomasubtypes AT singhsheilak identificationoffiveimportantgenestopredictglioblastomasubtypes AT mcnicholaspauld identificationoffiveimportantgenestopredictglioblastomasubtypes |