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Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma

Lymph node metastasis (LNM) of esophageal squamous cell carcinoma (ESCC) is well-known to be an early event associated with poor prognosis in patients with ESCC. Recently, tumor-specific aberrant DNA methylation of CpG islands around the promoter regions of tumor-related genes has been investigated...

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Autores principales: Nagata, Hiroaki, Kozaki, Ken-Ichi, Muramatsu, Tomoki, Hiramoto, Hidekazu, Tanimoto, Kousuke, Fujiwara, Naoto, Imoto, Seiya, Ichikawa, Daisuke, Otsuji, Eigo, Miyano, Satoru, Kawano, Tatsuyuki, Inazawa, Johji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514945/
https://www.ncbi.nlm.nih.gov/pubmed/28465481
http://dx.doi.org/10.18632/oncotarget.17147
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author Nagata, Hiroaki
Kozaki, Ken-Ichi
Muramatsu, Tomoki
Hiramoto, Hidekazu
Tanimoto, Kousuke
Fujiwara, Naoto
Imoto, Seiya
Ichikawa, Daisuke
Otsuji, Eigo
Miyano, Satoru
Kawano, Tatsuyuki
Inazawa, Johji
author_facet Nagata, Hiroaki
Kozaki, Ken-Ichi
Muramatsu, Tomoki
Hiramoto, Hidekazu
Tanimoto, Kousuke
Fujiwara, Naoto
Imoto, Seiya
Ichikawa, Daisuke
Otsuji, Eigo
Miyano, Satoru
Kawano, Tatsuyuki
Inazawa, Johji
author_sort Nagata, Hiroaki
collection PubMed
description Lymph node metastasis (LNM) of esophageal squamous cell carcinoma (ESCC) is well-known to be an early event associated with poor prognosis in patients with ESCC. Recently, tumor-specific aberrant DNA methylation of CpG islands around the promoter regions of tumor-related genes has been investigated as a possible biomarker for use in early diagnosis and prediction of prognosis. However, there are few DNA methylation markers able to predict the presence of LNM in ESCC. To identify DNA methylation markers associated with LNM of ESCC, we performed a genome-wide screening of DNA methylation status in a discovery cohort of 67 primary ESCC tissues and their paired normal esophageal tissues using the Illumina Infinium HumanMethylation450 BeadChip. In this screening, we focused on differentially methylated regions (DMRs) that were associated with LNM of ESCC, as prime candidates for DNA methylation markers. We extracted three genes, HOXB2, SLC15A3, and SEPT9, as candidates predicting LNM of ESCC, using pyrosequencing and several statistical analyses in the discovery cohort. We confirmed that HOXB2 and SEPT9 were highly methylated in LNM-positive tumors in 59 ESCC validation samples. These results suggested that HOXB2 and SEPT9 may be useful epigenetic biomarkers for the prediction of the presence of LNM in ESCC.
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spelling pubmed-55149452017-07-24 Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma Nagata, Hiroaki Kozaki, Ken-Ichi Muramatsu, Tomoki Hiramoto, Hidekazu Tanimoto, Kousuke Fujiwara, Naoto Imoto, Seiya Ichikawa, Daisuke Otsuji, Eigo Miyano, Satoru Kawano, Tatsuyuki Inazawa, Johji Oncotarget Research Paper Lymph node metastasis (LNM) of esophageal squamous cell carcinoma (ESCC) is well-known to be an early event associated with poor prognosis in patients with ESCC. Recently, tumor-specific aberrant DNA methylation of CpG islands around the promoter regions of tumor-related genes has been investigated as a possible biomarker for use in early diagnosis and prediction of prognosis. However, there are few DNA methylation markers able to predict the presence of LNM in ESCC. To identify DNA methylation markers associated with LNM of ESCC, we performed a genome-wide screening of DNA methylation status in a discovery cohort of 67 primary ESCC tissues and their paired normal esophageal tissues using the Illumina Infinium HumanMethylation450 BeadChip. In this screening, we focused on differentially methylated regions (DMRs) that were associated with LNM of ESCC, as prime candidates for DNA methylation markers. We extracted three genes, HOXB2, SLC15A3, and SEPT9, as candidates predicting LNM of ESCC, using pyrosequencing and several statistical analyses in the discovery cohort. We confirmed that HOXB2 and SEPT9 were highly methylated in LNM-positive tumors in 59 ESCC validation samples. These results suggested that HOXB2 and SEPT9 may be useful epigenetic biomarkers for the prediction of the presence of LNM in ESCC. Impact Journals LLC 2017-04-17 /pmc/articles/PMC5514945/ /pubmed/28465481 http://dx.doi.org/10.18632/oncotarget.17147 Text en Copyright: © 2017 Nagata et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Nagata, Hiroaki
Kozaki, Ken-Ichi
Muramatsu, Tomoki
Hiramoto, Hidekazu
Tanimoto, Kousuke
Fujiwara, Naoto
Imoto, Seiya
Ichikawa, Daisuke
Otsuji, Eigo
Miyano, Satoru
Kawano, Tatsuyuki
Inazawa, Johji
Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
title Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
title_full Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
title_fullStr Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
title_full_unstemmed Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
title_short Genome-wide screening of DNA methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
title_sort genome-wide screening of dna methylation associated with lymph node metastasis in esophageal squamous cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514945/
https://www.ncbi.nlm.nih.gov/pubmed/28465481
http://dx.doi.org/10.18632/oncotarget.17147
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