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Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study
BACKGROUND: The Mono-amine oxidase-A (MAO-A) enzyme is involved in the degradation and regulation of catecholamines such as serotonin, dopamine, epinephrine and nor-epinephrine. Preclinical studies suggest that this enzyme may contribute to an environment favorable for growth of malignant glioma. Th...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856259/ https://www.ncbi.nlm.nih.gov/pubmed/31556016 http://dx.doi.org/10.1007/s11060-019-03294-w |
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author | Sjöberg, Rickard L. Wu, Wendy Yi-Ying Dahlin, Anna M. Tsavachidis, Spiridon Bondy, Melissa L. Melin, Beatrice |
author_facet | Sjöberg, Rickard L. Wu, Wendy Yi-Ying Dahlin, Anna M. Tsavachidis, Spiridon Bondy, Melissa L. Melin, Beatrice |
author_sort | Sjöberg, Rickard L. |
collection | PubMed |
description | BACKGROUND: The Mono-amine oxidase-A (MAO-A) enzyme is involved in the degradation and regulation of catecholamines such as serotonin, dopamine, epinephrine and nor-epinephrine. Preclinical studies suggest that this enzyme may contribute to an environment favorable for growth of malignant glioma. The MAO-A gene is located on the X-chromosome and has at least one functional genetic polymorphism. The aim of the present study was to explore possible effects of MAO-A genotype on development of glioblastoma in males. METHODS: Genotypes for 437 glioma cases and 876 population-based controls from the Swedish Glioma International Case–Control study (GICC) were compared. We analyzed the germline DNA using the Illumina Oncoarray. We selected seven single nucleotide polymorphisms (SNPs) located in the MAO-A gene, and imputed genotypes based on data from the 1000 genomes project. We used 1579 male glioblastoma cases and 1875 controls comprising the whole GICC cohort for subsequent validation of findings. RESULTS: The rs144551722 SNP was a significant predictor of development of glioblastoma in males (p-value = 0.0056) but not in females even after correction for multiple testing. We conducted haplotype analysis to confirm an association between MAO-A gene and risk of glioblastoma (p-value = 0.016). We found similar results in the validation sample. CONCLUSIONS: These results suggest the possibility of a role for the MAO-A enzyme and the MAO-A gene in the development of glioblastoma in males. |
format | Online Article Text |
id | pubmed-6856259 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-68562592019-12-03 Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study Sjöberg, Rickard L. Wu, Wendy Yi-Ying Dahlin, Anna M. Tsavachidis, Spiridon Bondy, Melissa L. Melin, Beatrice J Neurooncol Clinical Study BACKGROUND: The Mono-amine oxidase-A (MAO-A) enzyme is involved in the degradation and regulation of catecholamines such as serotonin, dopamine, epinephrine and nor-epinephrine. Preclinical studies suggest that this enzyme may contribute to an environment favorable for growth of malignant glioma. The MAO-A gene is located on the X-chromosome and has at least one functional genetic polymorphism. The aim of the present study was to explore possible effects of MAO-A genotype on development of glioblastoma in males. METHODS: Genotypes for 437 glioma cases and 876 population-based controls from the Swedish Glioma International Case–Control study (GICC) were compared. We analyzed the germline DNA using the Illumina Oncoarray. We selected seven single nucleotide polymorphisms (SNPs) located in the MAO-A gene, and imputed genotypes based on data from the 1000 genomes project. We used 1579 male glioblastoma cases and 1875 controls comprising the whole GICC cohort for subsequent validation of findings. RESULTS: The rs144551722 SNP was a significant predictor of development of glioblastoma in males (p-value = 0.0056) but not in females even after correction for multiple testing. We conducted haplotype analysis to confirm an association between MAO-A gene and risk of glioblastoma (p-value = 0.016). We found similar results in the validation sample. CONCLUSIONS: These results suggest the possibility of a role for the MAO-A enzyme and the MAO-A gene in the development of glioblastoma in males. Springer US 2019-09-25 2019 /pmc/articles/PMC6856259/ /pubmed/31556016 http://dx.doi.org/10.1007/s11060-019-03294-w Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Clinical Study Sjöberg, Rickard L. Wu, Wendy Yi-Ying Dahlin, Anna M. Tsavachidis, Spiridon Bondy, Melissa L. Melin, Beatrice Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study |
title | Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study |
title_full | Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study |
title_fullStr | Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study |
title_full_unstemmed | Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study |
title_short | Role of monoamine-oxidase-A-gene variation in the development of glioblastoma in males: a case control study |
title_sort | role of monoamine-oxidase-a-gene variation in the development of glioblastoma in males: a case control study |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6856259/ https://www.ncbi.nlm.nih.gov/pubmed/31556016 http://dx.doi.org/10.1007/s11060-019-03294-w |
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