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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.
Afiliação
  • Chen PH; School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
  • Chung CM; Institute of Biomedical Sciences, National Sun Yat-sen University, No. 70 Lienhai Road, Kaohsiung 80424, Taiwan.
  • Wang YY; Center for Cancer Research, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
  • Huang HW; Cancer Center, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
  • Huang B; Cohort Research Center, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
  • Lee KW; Center for Drug Abuse and Addiction, China Medical University Hospital, China Medical University, Taichung 406040, Taiwan.
  • Yuan SS; Graduate Institute of Biomedical Sciences, China Medical University, Taichung 406040, Taiwan.
  • Wu CW; School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
  • Lin LS; Center for Cancer Research, Kaohsiung Medical University, Kaohsiung 80708, Taiwan.
  • Chan LP; Institute of Biomedical Sciences, National Sun Yat-sen University, No. 70 Lienhai Road, Kaohsiung 80424, Taiwan.
Diagnostics (Basel) ; 10(11)2020 Nov 21.
Article em En | MEDLINE | ID: mdl-33233443
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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article