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CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers

Betel quid (BQ) has been classified as a Group I human carcinogen in light of evidence demonstrating an association with an elevated risk of oral and pharyngeal cancers. To date, the incidence rate of oral and pharynx cancers among Taiwanese men ranks the highest worldwide. However, no study has yet...

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Autores principales: Chen, Ping-Ho, Chung, Chia-Min, Wang, Yen-Yun, Huang, Hurng-Wern, Huang, Bin, Lee, Ka-Wo, Yuan, Shyng-Shiou, Wu, Che-Wei, Lin, Lee-Shuan, Chan, Leong-Perng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700252/
https://www.ncbi.nlm.nih.gov/pubmed/33233443
http://dx.doi.org/10.3390/diagnostics10110982
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author Chen, Ping-Ho
Chung, Chia-Min
Wang, Yen-Yun
Huang, Hurng-Wern
Huang, Bin
Lee, Ka-Wo
Yuan, Shyng-Shiou
Wu, Che-Wei
Lin, Lee-Shuan
Chan, Leong-Perng
author_facet Chen, Ping-Ho
Chung, Chia-Min
Wang, Yen-Yun
Huang, Hurng-Wern
Huang, Bin
Lee, Ka-Wo
Yuan, Shyng-Shiou
Wu, Che-Wei
Lin, Lee-Shuan
Chan, Leong-Perng
author_sort Chen, Ping-Ho
collection PubMed
description Betel quid (BQ) has been classified as a Group I human carcinogen in light of evidence demonstrating an association with an elevated risk of oral and pharyngeal cancers. To date, the incidence rate of oral and pharynx cancers among Taiwanese men ranks the highest worldwide. However, no study has yet confirmed variants of CYP26A1 was associated with the risks of oral and pharyngeal cancers. A case-control study was conducted (n = 339). CYP26A1 polymorphism was performed using SNP assay. Real-time qRT-PCR and Western blotting were used to determine the levels of CYP26A1 expression. The cancer cell model involved treatment with arecoline. Our findings showed that the downregulation of CYP26A1 mRNA and protein expression are more frequently observed in cancerous tissues than adjacent normal tissues in patients with oral and pharynx cancers (p < 0.01). We found that CYP26A1 was downregulated as the arecoline dose increased. We hypothesized that lower levels of CYP26A1 mRNA expression can be utilized a clinically biomarker causes oral and pharynx cancers. Arecoline appears to modulate CYP26A1 expression through specific pathways. Carriers of CYP26A1 SNP, rs2068888 (G/G)/rs4418728 (G/G) and who have lower levels of CYP26A1 expression are associated with an increased risk of oral and pharyngeal cancers.
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spelling pubmed-77002522020-11-30 CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers Chen, Ping-Ho Chung, Chia-Min Wang, Yen-Yun Huang, Hurng-Wern Huang, Bin Lee, Ka-Wo Yuan, Shyng-Shiou Wu, Che-Wei Lin, Lee-Shuan Chan, Leong-Perng Diagnostics (Basel) Article Betel quid (BQ) has been classified as a Group I human carcinogen in light of evidence demonstrating an association with an elevated risk of oral and pharyngeal cancers. To date, the incidence rate of oral and pharynx cancers among Taiwanese men ranks the highest worldwide. However, no study has yet confirmed variants of CYP26A1 was associated with the risks of oral and pharyngeal cancers. A case-control study was conducted (n = 339). CYP26A1 polymorphism was performed using SNP assay. Real-time qRT-PCR and Western blotting were used to determine the levels of CYP26A1 expression. The cancer cell model involved treatment with arecoline. Our findings showed that the downregulation of CYP26A1 mRNA and protein expression are more frequently observed in cancerous tissues than adjacent normal tissues in patients with oral and pharynx cancers (p < 0.01). We found that CYP26A1 was downregulated as the arecoline dose increased. We hypothesized that lower levels of CYP26A1 mRNA expression can be utilized a clinically biomarker causes oral and pharynx cancers. Arecoline appears to modulate CYP26A1 expression through specific pathways. Carriers of CYP26A1 SNP, rs2068888 (G/G)/rs4418728 (G/G) and who have lower levels of CYP26A1 expression are associated with an increased risk of oral and pharyngeal cancers. MDPI 2020-11-21 /pmc/articles/PMC7700252/ /pubmed/33233443 http://dx.doi.org/10.3390/diagnostics10110982 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Ping-Ho
Chung, Chia-Min
Wang, Yen-Yun
Huang, Hurng-Wern
Huang, Bin
Lee, Ka-Wo
Yuan, Shyng-Shiou
Wu, Che-Wei
Lin, Lee-Shuan
Chan, Leong-Perng
CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers
title CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers
title_full CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers
title_fullStr CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers
title_full_unstemmed CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers
title_short CYP26A1 Is a Novel Biomarker for Betel Quid-Related Oral and Pharyngeal Cancers
title_sort cyp26a1 is a novel biomarker for betel quid-related oral and pharyngeal cancers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7700252/
https://www.ncbi.nlm.nih.gov/pubmed/33233443
http://dx.doi.org/10.3390/diagnostics10110982
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