Promoter methylation and loss of p16INK4a gene expression in head and neck cancer

Background Silencing of tumor suppressor genes plays a vital role in head and neck carcinogenesis. In this study we aimed to evaluate aberrant p16INK4a gene promoter methylation in patients with head and neck cancer. Methods Methylation of the gene was investigated by bisulfite modification/methylat...

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Veröffentlicht in:Head & neck 2012-10, Vol.34 (10), p.1470-1475
Hauptverfasser: Demokan, Semra, Chuang, Alice, Suoğlu, Yusufhan, Ulusan, Murat, Yalnız, Zubeyde, Califano, Joseph A., Dalay, Nejat
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container_end_page 1475
container_issue 10
container_start_page 1470
container_title Head & neck
container_volume 34
creator Demokan, Semra
Chuang, Alice
Suoğlu, Yusufhan
Ulusan, Murat
Yalnız, Zubeyde
Califano, Joseph A.
Dalay, Nejat
description Background Silencing of tumor suppressor genes plays a vital role in head and neck carcinogenesis. In this study we aimed to evaluate aberrant p16INK4a gene promoter methylation in patients with head and neck cancer. Methods Methylation of the gene was investigated by bisulfite modification/methylation‐specific polymerase chain reaction and gene expression levels were analyzed by quantitative reverse transcription–polymerase chain reaction in tumors and matched normal tissue samples from Turkish patients with head and neck cancer. Results The promoter region of the p16INK4a gene was methylated in 67.5% and 28.6% of the primary tumors and the corresponding normal tissue, respectively. This difference was highly significant. In concordance, p16INK4a gene expression was downregulated in 67.5% of the tumor samples. Methylation and the absence of expression in the tumors were observed in 48% of the patients. Conclusions Our data indicate that methylation of the p16INK4a gene is a frequent event in primary head and neck cancer and that it plays a major role in the silencing of p16INK4a gene expression during tumor development. © 2011 Wiley Periodicals, Inc. Head Neck, 2011
doi_str_mv 10.1002/hed.21949
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In this study we aimed to evaluate aberrant p16INK4a gene promoter methylation in patients with head and neck cancer. Methods Methylation of the gene was investigated by bisulfite modification/methylation‐specific polymerase chain reaction and gene expression levels were analyzed by quantitative reverse transcription–polymerase chain reaction in tumors and matched normal tissue samples from Turkish patients with head and neck cancer. Results The promoter region of the p16INK4a gene was methylated in 67.5% and 28.6% of the primary tumors and the corresponding normal tissue, respectively. This difference was highly significant. In concordance, p16INK4a gene expression was downregulated in 67.5% of the tumor samples. Methylation and the absence of expression in the tumors were observed in 48% of the patients. 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In this study we aimed to evaluate aberrant p16INK4a gene promoter methylation in patients with head and neck cancer. Methods Methylation of the gene was investigated by bisulfite modification/methylation‐specific polymerase chain reaction and gene expression levels were analyzed by quantitative reverse transcription–polymerase chain reaction in tumors and matched normal tissue samples from Turkish patients with head and neck cancer. Results The promoter region of the p16INK4a gene was methylated in 67.5% and 28.6% of the primary tumors and the corresponding normal tissue, respectively. This difference was highly significant. In concordance, p16INK4a gene expression was downregulated in 67.5% of the tumor samples. Methylation and the absence of expression in the tumors were observed in 48% of the patients. 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source Wiley Online Library Journals Frontfile Complete
subjects Biological and medical sciences
expression
head and neck cancer
Medical sciences
methylation
Otorhinolaryngology (head neck, general aspects and miscellaneous)
Otorhinolaryngology. Stomatology
p16INK4a
Tumors
title Promoter methylation and loss of p16INK4a gene expression in head and neck cancer
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