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Meta-gene markers predict meningioma recurrence with high accuracy

Meningiomas, the most common adult brain tumors, recur in up to half of cases. This requires timely intervention and therefore accurate risk assessment of recurrence is essential. Our current practice relies heavily on histological grade and extent of surgical excision to predict meningioma recurren...

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Autores principales: Zador, Zsolt, Landry, Alexander P., Haibe-Kains, Benjamin, Cusimano, Michael D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582964/
https://www.ncbi.nlm.nih.gov/pubmed/33093491
http://dx.doi.org/10.1038/s41598-020-74482-2
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author Zador, Zsolt
Landry, Alexander P.
Haibe-Kains, Benjamin
Cusimano, Michael D.
author_facet Zador, Zsolt
Landry, Alexander P.
Haibe-Kains, Benjamin
Cusimano, Michael D.
author_sort Zador, Zsolt
collection PubMed
description Meningiomas, the most common adult brain tumors, recur in up to half of cases. This requires timely intervention and therefore accurate risk assessment of recurrence is essential. Our current practice relies heavily on histological grade and extent of surgical excision to predict meningioma recurrence. However, prediction accuracy can be as poor as 50% for low or intermediate grade tumors which constitute the majority of cases. Moreover, attempts to find molecular markers to predict their recurrence have been impeded by low or heterogenous genetic signal. We therefore sought to apply systems-biology approaches to transcriptomic data to better predict meningioma recurrence. We apply gene co-expression networks to a cohort of 252 adult patients from the publicly available genetic repository Gene Expression Omnibus. Resultant gene clusters (“modules”) were represented by the first principle component of their expression, and their ability to predict recurrence assessed with a logistic regression model. External validation was done using two independent samples: one merged microarray-based cohort with a total of 108 patients and one RNA-seq-based cohort with 145 patients, using the same modules. We used the bioinformatics database Enrichr to examine the gene ontology associations and driver transcription factors of each module. Using gene co-expression analysis, we were able predict tumor recurrence with high accuracy using a single module which mapped to cell cycle-related processes (AUC of 0.81 ± 0.09 and 0.77 ± 0.10 in external validation using microarray and RNA-seq data, respectively). This module remained predictive when controlling for WHO grade in all cohorts, and was associated with several cancer-associated transcription factors which may serve as novel therapeutic targets for patients with this disease. With the easy accessibility of gene panels in healthcare diagnostics, our results offer a basis for routine molecular testing in meningioma management and propose potential therapeutic targets for future research.
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spelling pubmed-75829642020-10-23 Meta-gene markers predict meningioma recurrence with high accuracy Zador, Zsolt Landry, Alexander P. Haibe-Kains, Benjamin Cusimano, Michael D. Sci Rep Article Meningiomas, the most common adult brain tumors, recur in up to half of cases. This requires timely intervention and therefore accurate risk assessment of recurrence is essential. Our current practice relies heavily on histological grade and extent of surgical excision to predict meningioma recurrence. However, prediction accuracy can be as poor as 50% for low or intermediate grade tumors which constitute the majority of cases. Moreover, attempts to find molecular markers to predict their recurrence have been impeded by low or heterogenous genetic signal. We therefore sought to apply systems-biology approaches to transcriptomic data to better predict meningioma recurrence. We apply gene co-expression networks to a cohort of 252 adult patients from the publicly available genetic repository Gene Expression Omnibus. Resultant gene clusters (“modules”) were represented by the first principle component of their expression, and their ability to predict recurrence assessed with a logistic regression model. External validation was done using two independent samples: one merged microarray-based cohort with a total of 108 patients and one RNA-seq-based cohort with 145 patients, using the same modules. We used the bioinformatics database Enrichr to examine the gene ontology associations and driver transcription factors of each module. Using gene co-expression analysis, we were able predict tumor recurrence with high accuracy using a single module which mapped to cell cycle-related processes (AUC of 0.81 ± 0.09 and 0.77 ± 0.10 in external validation using microarray and RNA-seq data, respectively). This module remained predictive when controlling for WHO grade in all cohorts, and was associated with several cancer-associated transcription factors which may serve as novel therapeutic targets for patients with this disease. With the easy accessibility of gene panels in healthcare diagnostics, our results offer a basis for routine molecular testing in meningioma management and propose potential therapeutic targets for future research. Nature Publishing Group UK 2020-10-22 /pmc/articles/PMC7582964/ /pubmed/33093491 http://dx.doi.org/10.1038/s41598-020-74482-2 Text en © The Author(s) 2020 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zador, Zsolt
Landry, Alexander P.
Haibe-Kains, Benjamin
Cusimano, Michael D.
Meta-gene markers predict meningioma recurrence with high accuracy
title Meta-gene markers predict meningioma recurrence with high accuracy
title_full Meta-gene markers predict meningioma recurrence with high accuracy
title_fullStr Meta-gene markers predict meningioma recurrence with high accuracy
title_full_unstemmed Meta-gene markers predict meningioma recurrence with high accuracy
title_short Meta-gene markers predict meningioma recurrence with high accuracy
title_sort meta-gene markers predict meningioma recurrence with high accuracy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582964/
https://www.ncbi.nlm.nih.gov/pubmed/33093491
http://dx.doi.org/10.1038/s41598-020-74482-2
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