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EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways

Background: Breast cancer (BC) ranks among the most common cancers in Sudan and worldwide with hefty toll on female health and human resources. Recent studies have uncovered a common BC signature characterized by low frequency of oncogenic mutations and high frequency of epigenetic silencing of majo...

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Autores principales: Abdallah, Mohammad O. E., Algizouli, Ubai K., Suliman, Maram A., Abdulrahman, Rawya A., Koko, Mahmoud, Fessahaye, Ghimja, Shakir, Jamal H., Fahal, Ahmed H., Elhassan, Ahmed M., Ibrahim, Muntaser E., Mohamed, Hiba S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099083/
https://www.ncbi.nlm.nih.gov/pubmed/30151354
http://dx.doi.org/10.3389/fonc.2018.00316
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author Abdallah, Mohammad O. E.
Algizouli, Ubai K.
Suliman, Maram A.
Abdulrahman, Rawya A.
Koko, Mahmoud
Fessahaye, Ghimja
Shakir, Jamal H.
Fahal, Ahmed H.
Elhassan, Ahmed M.
Ibrahim, Muntaser E.
Mohamed, Hiba S.
author_facet Abdallah, Mohammad O. E.
Algizouli, Ubai K.
Suliman, Maram A.
Abdulrahman, Rawya A.
Koko, Mahmoud
Fessahaye, Ghimja
Shakir, Jamal H.
Fahal, Ahmed H.
Elhassan, Ahmed M.
Ibrahim, Muntaser E.
Mohamed, Hiba S.
author_sort Abdallah, Mohammad O. E.
collection PubMed
description Background: Breast cancer (BC) ranks among the most common cancers in Sudan and worldwide with hefty toll on female health and human resources. Recent studies have uncovered a common BC signature characterized by low frequency of oncogenic mutations and high frequency of epigenetic silencing of major BC tumor suppressor genes. Therefore, we conducted a pilot genome-wide methylome study to characterize aberrant DNA methylation in breast cancer. Results: Differential methylation analysis between primary tumor samples and normal samples from healthy adjacent tissues yielded 20,188 differentially methylated positions (DMPs), which is further divided into 13,633 hypermethylated sites corresponding to 5339 genes and 6,555 hypomethylated sites corresponding to 2811 genes. Moreover, bioinformatics analysis revealed epigenetic dysregulation of major developmental pathways including hippo signaling pathway. We also uncovered many clues to a possible role for EBV infection in BC. Conclusion: Our results clearly show the utility of epigenetic assays in interrogating breast cancer tumorigenesis, and pinpointing specific developmental and viral pathways dysregulation that might serve as potential biomarkers or targets for therapeutic interventions.
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spelling pubmed-60990832018-08-27 EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways Abdallah, Mohammad O. E. Algizouli, Ubai K. Suliman, Maram A. Abdulrahman, Rawya A. Koko, Mahmoud Fessahaye, Ghimja Shakir, Jamal H. Fahal, Ahmed H. Elhassan, Ahmed M. Ibrahim, Muntaser E. Mohamed, Hiba S. Front Oncol Oncology Background: Breast cancer (BC) ranks among the most common cancers in Sudan and worldwide with hefty toll on female health and human resources. Recent studies have uncovered a common BC signature characterized by low frequency of oncogenic mutations and high frequency of epigenetic silencing of major BC tumor suppressor genes. Therefore, we conducted a pilot genome-wide methylome study to characterize aberrant DNA methylation in breast cancer. Results: Differential methylation analysis between primary tumor samples and normal samples from healthy adjacent tissues yielded 20,188 differentially methylated positions (DMPs), which is further divided into 13,633 hypermethylated sites corresponding to 5339 genes and 6,555 hypomethylated sites corresponding to 2811 genes. Moreover, bioinformatics analysis revealed epigenetic dysregulation of major developmental pathways including hippo signaling pathway. We also uncovered many clues to a possible role for EBV infection in BC. Conclusion: Our results clearly show the utility of epigenetic assays in interrogating breast cancer tumorigenesis, and pinpointing specific developmental and viral pathways dysregulation that might serve as potential biomarkers or targets for therapeutic interventions. Frontiers Media S.A. 2018-08-13 /pmc/articles/PMC6099083/ /pubmed/30151354 http://dx.doi.org/10.3389/fonc.2018.00316 Text en Copyright © 2018 Abdallah, Algizouli, Suliman, Abdulrahman, Koko, Fessahaye, Shakir, Fahal, Elhassan, Ibrahim and Mohamed. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Abdallah, Mohammad O. E.
Algizouli, Ubai K.
Suliman, Maram A.
Abdulrahman, Rawya A.
Koko, Mahmoud
Fessahaye, Ghimja
Shakir, Jamal H.
Fahal, Ahmed H.
Elhassan, Ahmed M.
Ibrahim, Muntaser E.
Mohamed, Hiba S.
EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways
title EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways
title_full EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways
title_fullStr EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways
title_full_unstemmed EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways
title_short EBV Associated Breast Cancer Whole Methylome Analysis Reveals Viral and Developmental Enriched Pathways
title_sort ebv associated breast cancer whole methylome analysis reveals viral and developmental enriched pathways
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099083/
https://www.ncbi.nlm.nih.gov/pubmed/30151354
http://dx.doi.org/10.3389/fonc.2018.00316
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