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DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma

BACKGROUND: It remains important to understand the biology and identify biomarkers for less studied cancers like testicular cancer. The purpose of this study was to determine the methylation frequency of several cancer-related genes in different histological types of testicular cancer and normal tes...

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Autores principales: Brait, M, Maldonado, L, Begum, S, Loyo, M, Wehle, D, Tavora, F F, Looijenga, L H J, Kowalski, J, Zhang, Z, Rosenbaum, E, Halachmi, S, Netto, G J, Hoque, M O
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261686/
https://www.ncbi.nlm.nih.gov/pubmed/22068818
http://dx.doi.org/10.1038/bjc.2011.468
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author Brait, M
Maldonado, L
Begum, S
Loyo, M
Wehle, D
Tavora, F F
Looijenga, L H J
Kowalski, J
Zhang, Z
Rosenbaum, E
Halachmi, S
Netto, G J
Hoque, M O
author_facet Brait, M
Maldonado, L
Begum, S
Loyo, M
Wehle, D
Tavora, F F
Looijenga, L H J
Kowalski, J
Zhang, Z
Rosenbaum, E
Halachmi, S
Netto, G J
Hoque, M O
author_sort Brait, M
collection PubMed
description BACKGROUND: It remains important to understand the biology and identify biomarkers for less studied cancers like testicular cancer. The purpose of this study was to determine the methylation frequency of several cancer-related genes in different histological types of testicular cancer and normal testis tissues (NT). METHODS: DNA was isolated from 43 seminomas (SEs), 14 non-SEs (NSEs) and 23 NT, and was assayed for promoter methylation status of 15 genes by quantitative methylation-specific PCR. The methylation status was evaluated for an association with cancer, and between SEs and NSEs. RESULTS: We found differential methylation pattern in SEs and NSEs. MGMT, VGF, ER-β and FKBP4 were predominately methylated in NSEs compared with SEs. APC and hMLH1 are shown to be significantly more methylated in both subtypes in comparison with NT. When combining APC, hMLH1, ER-β and FKBP4, it is possible to identify 86% of the NSEs, whereas only 7% of the SEs. CONCLUSIONS: Our results indicate that the methylation profile of cancer-associated genes in testicular cancer correlates with histological types and show cancer-specific pattern for certain genes. Further methylation analysis, in a larger cohort is needed to elucidate their role in testicular cancer development and potential for therapy, early detection and disease monitoring.
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spelling pubmed-32616862013-01-17 DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma Brait, M Maldonado, L Begum, S Loyo, M Wehle, D Tavora, F F Looijenga, L H J Kowalski, J Zhang, Z Rosenbaum, E Halachmi, S Netto, G J Hoque, M O Br J Cancer Genetics and Genomics BACKGROUND: It remains important to understand the biology and identify biomarkers for less studied cancers like testicular cancer. The purpose of this study was to determine the methylation frequency of several cancer-related genes in different histological types of testicular cancer and normal testis tissues (NT). METHODS: DNA was isolated from 43 seminomas (SEs), 14 non-SEs (NSEs) and 23 NT, and was assayed for promoter methylation status of 15 genes by quantitative methylation-specific PCR. The methylation status was evaluated for an association with cancer, and between SEs and NSEs. RESULTS: We found differential methylation pattern in SEs and NSEs. MGMT, VGF, ER-β and FKBP4 were predominately methylated in NSEs compared with SEs. APC and hMLH1 are shown to be significantly more methylated in both subtypes in comparison with NT. When combining APC, hMLH1, ER-β and FKBP4, it is possible to identify 86% of the NSEs, whereas only 7% of the SEs. CONCLUSIONS: Our results indicate that the methylation profile of cancer-associated genes in testicular cancer correlates with histological types and show cancer-specific pattern for certain genes. Further methylation analysis, in a larger cohort is needed to elucidate their role in testicular cancer development and potential for therapy, early detection and disease monitoring. Nature Publishing Group 2012-01-17 2011-11-08 /pmc/articles/PMC3261686/ /pubmed/22068818 http://dx.doi.org/10.1038/bjc.2011.468 Text en Copyright © 2012 Cancer Research UK https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/.
spellingShingle Genetics and Genomics
Brait, M
Maldonado, L
Begum, S
Loyo, M
Wehle, D
Tavora, F F
Looijenga, L H J
Kowalski, J
Zhang, Z
Rosenbaum, E
Halachmi, S
Netto, G J
Hoque, M O
DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
title DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
title_full DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
title_fullStr DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
title_full_unstemmed DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
title_short DNA methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
title_sort dna methylation profiles delineate epigenetic heterogeneity in seminoma and non-seminoma
topic Genetics and Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3261686/
https://www.ncbi.nlm.nih.gov/pubmed/22068818
http://dx.doi.org/10.1038/bjc.2011.468
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