Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells

<p>Abstract</p> <p>Background</p> <p>Nasopharyngeal carcinoma (NPC) is a head and neck malignancy with high occurrence in South-East Asia and Southern China. Recent findings suggest that epigenetic inactivation of multiple tumor suppressor genes plays an important role...

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Main Authors: Shi Lei, Deng Tan, Li Xiayu, Peng Cong, Zhou Ming, Niu Zhaoxia, Zhang Liming, Liu Huaying, Tan Yixin, Li Guiyuan
Format: Article
Language:English
Published: BMC 2008-09-01
Series:BMC Cancer
Online Access:http://www.biomedcentral.com/1471-2407/8/253
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spelling doaj-68ac51cc56f1490cb721e8ee978a410c2020-11-24T20:47:26ZengBMCBMC Cancer1471-24072008-09-018125310.1186/1471-2407-8-253Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cellsShi LeiDeng TanLi XiayuPeng CongZhou MingNiu ZhaoxiaZhang LimingLiu HuayingTan YixinLi Guiyuan<p>Abstract</p> <p>Background</p> <p>Nasopharyngeal carcinoma (NPC) is a head and neck malignancy with high occurrence in South-East Asia and Southern China. Recent findings suggest that epigenetic inactivation of multiple tumor suppressor genes plays an important role in the tumourigenesis of NPC. BRD7 is a NPC-associated bromodomain gene that exhibits a much higher-level of mRNA expression in normal than in NPC biopsies and cell lines. In this study, we explored the role of DNA methylation in regulation of BRD7 transcription.</p> <p>Methods</p> <p>The presence of CpG islands within BRD7 promoter was predicted by EMBOSS CpGplot and Softberry CpGFinder, respectively. Nested methylation-specific PCR and RT-PCR were employed to detect the methylation status of BRD7 promoter and the mRNA expression of BRD7 gene in tumor cell lines as well as clinical samples. Electrophoretic mobility shift assays (EMSA) and luciferase assay were used to detect the effects of cytosine methylation on the nuclear protein binding to BRD7 promoter.</p> <p>Results</p> <p>We found that DNA methylation suppresses BRD7 expression in NPC cells. In vitro DNA methylation in NPC cells silenced BRD7 promoter activity and inhibited the binding of the nuclear protein (possibly Sp1) to Sp1 binding sites in the BRD7 promoter. In contrast, inhibition of DNA methylation augments induction of endogenous BRD7 mRNA in NPC cells. We also found that methylation frequency of BRD7 promoter is much higher in the tumor and matched blood samples from NPC patients than in the blood samples from normal individuals.</p> <p>Conclusion</p> <p>BRD7 promoter demethylation is a prerequisite for high level induction of BRD7 gene expression. DNA methylation of BRD7 promoter might serve as a diagnostic marker in NPC.</p> http://www.biomedcentral.com/1471-2407/8/253
collection DOAJ
language English
format Article
sources DOAJ
author Shi Lei
Deng Tan
Li Xiayu
Peng Cong
Zhou Ming
Niu Zhaoxia
Zhang Liming
Liu Huaying
Tan Yixin
Li Guiyuan
spellingShingle Shi Lei
Deng Tan
Li Xiayu
Peng Cong
Zhou Ming
Niu Zhaoxia
Zhang Liming
Liu Huaying
Tan Yixin
Li Guiyuan
Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells
BMC Cancer
author_facet Shi Lei
Deng Tan
Li Xiayu
Peng Cong
Zhou Ming
Niu Zhaoxia
Zhang Liming
Liu Huaying
Tan Yixin
Li Guiyuan
author_sort Shi Lei
title Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells
title_short Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells
title_full Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells
title_fullStr Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells
title_full_unstemmed Promoter methylation inhibits BRD7 expression in human nasopharyngeal carcinoma cells
title_sort promoter methylation inhibits brd7 expression in human nasopharyngeal carcinoma cells
publisher BMC
series BMC Cancer
issn 1471-2407
publishDate 2008-09-01
description <p>Abstract</p> <p>Background</p> <p>Nasopharyngeal carcinoma (NPC) is a head and neck malignancy with high occurrence in South-East Asia and Southern China. Recent findings suggest that epigenetic inactivation of multiple tumor suppressor genes plays an important role in the tumourigenesis of NPC. BRD7 is a NPC-associated bromodomain gene that exhibits a much higher-level of mRNA expression in normal than in NPC biopsies and cell lines. In this study, we explored the role of DNA methylation in regulation of BRD7 transcription.</p> <p>Methods</p> <p>The presence of CpG islands within BRD7 promoter was predicted by EMBOSS CpGplot and Softberry CpGFinder, respectively. Nested methylation-specific PCR and RT-PCR were employed to detect the methylation status of BRD7 promoter and the mRNA expression of BRD7 gene in tumor cell lines as well as clinical samples. Electrophoretic mobility shift assays (EMSA) and luciferase assay were used to detect the effects of cytosine methylation on the nuclear protein binding to BRD7 promoter.</p> <p>Results</p> <p>We found that DNA methylation suppresses BRD7 expression in NPC cells. In vitro DNA methylation in NPC cells silenced BRD7 promoter activity and inhibited the binding of the nuclear protein (possibly Sp1) to Sp1 binding sites in the BRD7 promoter. In contrast, inhibition of DNA methylation augments induction of endogenous BRD7 mRNA in NPC cells. We also found that methylation frequency of BRD7 promoter is much higher in the tumor and matched blood samples from NPC patients than in the blood samples from normal individuals.</p> <p>Conclusion</p> <p>BRD7 promoter demethylation is a prerequisite for high level induction of BRD7 gene expression. DNA methylation of BRD7 promoter might serve as a diagnostic marker in NPC.</p>
url http://www.biomedcentral.com/1471-2407/8/253
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