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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...

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Autores principales: Tang, Yang, Qazi, Maleeha A, Brown, Kevin R, Mikolajewicz, Nicholas, Moffat, Jason, Singh, Sheila K, McNicholas, Paul D
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
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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.
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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
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