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      Pretreatment dietary intake is associated with tumor suppressor DNA methylation in head and neck squamous cell carcinomas

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          Abstract

          Diet is associated with cancer prognosis, including head and neck cancer (HNC), and has been hypothesized to influence epigenetic state by determining the availability of functional groups involved in the modification of DNA and histone proteins. The goal of this study was to describe the association between pretreatment diet and HNC tumor DNA methylation. Information on usual pretreatment food and nutrient intake was estimated via food frequency questionnaire (FFQ) on 49 HNC cases. Tumor DNA methylation patterns were assessed using the Illumina Goldengate Methylation Cancer Panel. First, a methylation score, the sum of individual hypermethylated tumor suppressor associated CpG sites, was calculated and associated with dietary intake of micronutrients involved in one-carbon metabolism and antioxidant activity, and food groups abundant in these nutrients. Second, gene specific analyses using linear modeling with empirical Bayesian variance estimation were conducted to identify if methylation at individual CpG sites was associated with diet. All models were controlled for age, sex, smoking, alcohol and HPV status. Individuals reporting in the highest quartile of folate, vitamin B12 and vitamin A intake, compared with those in the lowest quartile, showed significantly less tumor suppressor gene methylation, as did patients reporting the highest cruciferous vegetable intake. Gene specific analyses identified differential associations between DNA methylation and vitamin B12 and vitamin A intake when stratifying by HPV status. These preliminary results suggest that intake of folate, vitamin A and vitamin B12 may be associated with the tumor DNA methylation profile in HNC and enhance tumor suppression.

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          Most cited references36

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          Head and neck cancer.

          Most head and neck cancers are squamous cell carcinomas that develop in the upper aerodigestive epithelium after exposure to carcinogens such as tobacco and alcohol. Human papillomavirus has also been strongly implicated as a causative agent in a subset of these cancers. The complex anatomy and vital physiological role of the tumour-involved structures dictate that the goals of treatment are not only to improve survival outcomes but also to preserve organ function. Major improvements have been accomplished in surgical techniques and radiotherapy delivery. Moreover, systemic therapy including chemotherapy and molecularly targeted agents--namely, the epidermal growth factor receptor inhibitors--has been successfully integrated into potentially curative treatment of locally advanced squamous-cell carcinoma of the head and neck. In deciding which treatment strategy would be suitable for an individual patient, important considerations include expected functional outcomes, ability to tolerate treatment, and comorbid illnesses. The collaboration of many specialties is the key for optimum assessment and decision making. We review the epidemiology, molecular pathogenesis, diagnosis and staging, and the latest multimodal management of squamous cell carcinoma of the head and neck.
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            The role of histone deacetylases (HDACs) in human cancer.

            The balance of histone acetylation and deacetylation is an epigenetic layer with a critical role in the regulation of gene expression. Histone acetylation induced by histone acetyl transferases (HATs) is associated with gene transcription, while histone hypoacetylation induced by histone deacetylase (HDAC) activity is associated with gene silencing. Altered expression and mutations of genes that encode HDACs have been linked to tumor development since they both induce the aberrant transcription of key genes regulating important cellular functions such as cell proliferation, cell-cycle regulation and apoptosis. Thus, HDACs are among the most promising therapeutic targets for cancer treatment, and they have inspired researchers to study and develop HDAC inhibitors.
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              High-throughput DNA methylation profiling using universal bead arrays.

              We have developed a high-throughput method for analyzing the methylation status of hundreds of preselected genes simultaneously and have applied it to the discovery of methylation signatures that distinguish normal from cancer tissue samples. Through an adaptation of the GoldenGate genotyping assay implemented on a BeadArray platform, the methylation state of 1536 specific CpG sites in 371 genes (one to nine CpG sites per gene) was measured in a single reaction by multiplexed genotyping of 200 ng of bisulfite-treated genomic DNA. The assay was used to obtain a quantitative measure of the methylation level at each CpG site. After validating the assay in cell lines and normal tissues, we analyzed a panel of lung cancer biopsy samples (N = 22) and identified a panel of methylation markers that distinguished lung adenocarcinomas from normal lung tissues with high specificity. These markers were validated in a second sample set (N = 24). These results demonstrate the effectiveness of the method for reliably profiling many CpG sites in parallel for the discovery of informative methylation markers. The technology should prove useful for DNA methylation analyses in large populations, with potential application to the classification and diagnosis of a broad range of cancers and other diseases.
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                Author and article information

                Journal
                Epigenetics
                Epigenetics
                EPI
                Epigenetics
                Landes Bioscience
                1559-2294
                1559-2308
                01 August 2012
                01 August 2012
                : 7
                : 8
                : 883-891
                Affiliations
                [1 ]Department of Environmental Health Sciences, University of Michigan School of Public Health; Ann Arbor, MI USA
                [2 ]Department of Computational Medicine and Bioinformatics, University of Michigan; Ann Arbor, MI USA
                [3 ]The University of Michigan School of Nursing; Ann Arbor, MI USA
                [4 ]Department of Otolaryngology, University of Michigan; Ann Arbor, MI USA
                [5 ]Department of Pathology, University of Michigan; Ann Arbor, MI USA
                [6 ]University of Michigan School of Dentistry; Ann Arbor, MI USA
                [7 ]Department of Biostatistics; University of Michigan School of Public Health; Ann Arbor, MI USA
                [8 ]Human Nutrition Program, Department of Environmental Health Sciences, University of Michigan School of Public Health; Ann Arbor, MI USA
                [9 ]Department of Nutrition; Harvard School of Public Health; Cambridge, MA USA
                Author notes
                [†]

                These authors contributed equally to this work.

                [* ]Correspondence to: Laura S. Rozek, Email: rozekl@ 123456umich.edu
                Article
                2012EPI0138R 21038
                10.4161/epi.21038
                3427284
                22722388
                6f641c1e-4d89-4213-9dc2-c7d87df779ea
                Copyright © 2012 Landes Bioscience

                This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.

                History
                Categories
                Research Paper

                Genetics
                diet,dna methylation,folate,tumor suppressor,vitamin b12
                Genetics
                diet, dna methylation, folate, tumor suppressor, vitamin b12

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