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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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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. |
format | Online Article Text |
id | pubmed-7700252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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