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TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma

BACKGROUND: The incidence of oral squamous cell carcinoma (OSCC) continues to increase each year. Clinical examination and biopsy usually detect OSCC at an advanced stage that is difficult to treat, leading to poor prognosis. DNA methylation pattern is tissue specific and has emerged as a biomarker...

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Autores principales: Puttipanyalears, C., Arayataweegool, A., Chalertpet, K., Rattanachayoto, P., Mahattanasakul, P., Tangjaturonsasme, N., Kerekhanjanarong, V., Mutirangura, A., Kitkumthorn, N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080527/
https://www.ncbi.nlm.nih.gov/pubmed/30081853
http://dx.doi.org/10.1186/s12885-018-4706-x
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author Puttipanyalears, C.
Arayataweegool, A.
Chalertpet, K.
Rattanachayoto, P.
Mahattanasakul, P.
Tangjaturonsasme, N.
Kerekhanjanarong, V.
Mutirangura, A.
Kitkumthorn, N.
author_facet Puttipanyalears, C.
Arayataweegool, A.
Chalertpet, K.
Rattanachayoto, P.
Mahattanasakul, P.
Tangjaturonsasme, N.
Kerekhanjanarong, V.
Mutirangura, A.
Kitkumthorn, N.
author_sort Puttipanyalears, C.
collection PubMed
description BACKGROUND: The incidence of oral squamous cell carcinoma (OSCC) continues to increase each year. Clinical examination and biopsy usually detect OSCC at an advanced stage that is difficult to treat, leading to poor prognosis. DNA methylation pattern is tissue specific and has emerged as a biomarker for the detection of cancers of tissue origin. Herein, we aimed to discover a novel site-specific methylation marker for OSCC. METHODS: We selected OSCC datasets analyzed using the IlluminaHumanMethylation27 BeadChip from the Gene Expression Omnibus repository of the National Center for Biotechnology Information using a bioinformatics approach. From 27,578 CG dinucleotide (CpG) sites, the CpG site with the highest difference in methylation level between healthy and cancerous cells was selected for further validation. A total of 18 mucosal tissue samples were collected from nine healthy controls and nine from OSCC subjects and subjected to microdissection for cell purification, followed by DNA extraction, bisulfite conversion, and pyrosequencing. Additionally, epithelial cells were collected from 2 cohorts including oral rinse from healthy controls, oral rinse and oral swab from OSCC subjects and oral rinse from oropharyngeal squamous cell carcinoma (SCC) were examined for their methylation status using real-time polymerase chain reaction (PCR). RESULTS: Among the 27,578 differentially methylated CpG sites, cg01009664 of the thyrotropin-releasing hormone (TRH) gene showed the greatest difference in methylation level between healthy and cancerous cells. Validation of the TRH gene using pyrosequencing revealed a methylation percentage of 7% ± 3.43% in healthy cells in contrast to 63% ± 19.81% in cancerous cells. Screening of epithelial cells using real-time PCR showed that the DNA methylation level was significantly higher in oral swab and rinse samples collected from OSCC and oropharyngeal SCC subjects than those from healthy controls (p < 0.001). In addition, when using a cutoff at 3.31 ng/μL, the TRH methylation biomarker was able to distinguish OSCC and oropharyngeal SCC subjects from healthy controls with high level of area under the curve, sensitivity and specificity. CONCLUSION: We demonstrated cg01009664 of TRH as a potential biomarker for OSCC and oropharyngeal SCC screening using oral rinse and swab techniques. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4706-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-60805272018-08-09 TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma Puttipanyalears, C. Arayataweegool, A. Chalertpet, K. Rattanachayoto, P. Mahattanasakul, P. Tangjaturonsasme, N. Kerekhanjanarong, V. Mutirangura, A. Kitkumthorn, N. BMC Cancer Research Article BACKGROUND: The incidence of oral squamous cell carcinoma (OSCC) continues to increase each year. Clinical examination and biopsy usually detect OSCC at an advanced stage that is difficult to treat, leading to poor prognosis. DNA methylation pattern is tissue specific and has emerged as a biomarker for the detection of cancers of tissue origin. Herein, we aimed to discover a novel site-specific methylation marker for OSCC. METHODS: We selected OSCC datasets analyzed using the IlluminaHumanMethylation27 BeadChip from the Gene Expression Omnibus repository of the National Center for Biotechnology Information using a bioinformatics approach. From 27,578 CG dinucleotide (CpG) sites, the CpG site with the highest difference in methylation level between healthy and cancerous cells was selected for further validation. A total of 18 mucosal tissue samples were collected from nine healthy controls and nine from OSCC subjects and subjected to microdissection for cell purification, followed by DNA extraction, bisulfite conversion, and pyrosequencing. Additionally, epithelial cells were collected from 2 cohorts including oral rinse from healthy controls, oral rinse and oral swab from OSCC subjects and oral rinse from oropharyngeal squamous cell carcinoma (SCC) were examined for their methylation status using real-time polymerase chain reaction (PCR). RESULTS: Among the 27,578 differentially methylated CpG sites, cg01009664 of the thyrotropin-releasing hormone (TRH) gene showed the greatest difference in methylation level between healthy and cancerous cells. Validation of the TRH gene using pyrosequencing revealed a methylation percentage of 7% ± 3.43% in healthy cells in contrast to 63% ± 19.81% in cancerous cells. Screening of epithelial cells using real-time PCR showed that the DNA methylation level was significantly higher in oral swab and rinse samples collected from OSCC and oropharyngeal SCC subjects than those from healthy controls (p < 0.001). In addition, when using a cutoff at 3.31 ng/μL, the TRH methylation biomarker was able to distinguish OSCC and oropharyngeal SCC subjects from healthy controls with high level of area under the curve, sensitivity and specificity. CONCLUSION: We demonstrated cg01009664 of TRH as a potential biomarker for OSCC and oropharyngeal SCC screening using oral rinse and swab techniques. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4706-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-06 /pmc/articles/PMC6080527/ /pubmed/30081853 http://dx.doi.org/10.1186/s12885-018-4706-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Puttipanyalears, C.
Arayataweegool, A.
Chalertpet, K.
Rattanachayoto, P.
Mahattanasakul, P.
Tangjaturonsasme, N.
Kerekhanjanarong, V.
Mutirangura, A.
Kitkumthorn, N.
TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma
title TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma
title_full TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma
title_fullStr TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma
title_full_unstemmed TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma
title_short TRH site-specific methylation in oral and oropharyngeal squamous cell carcinoma
title_sort trh site-specific methylation in oral and oropharyngeal squamous cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6080527/
https://www.ncbi.nlm.nih.gov/pubmed/30081853
http://dx.doi.org/10.1186/s12885-018-4706-x
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