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Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma

A disintegrin and metalloproteinase domain‐containing protein 10 (ADAM‐10) involves in the tumour progression, but the impacts of single‐nucleotide polymorphism (SNP) of ADAM‐10 on oral squamous cell carcinoma (OSCC) remain unclear. The aim of this study was to investigate the influence of SNP of AD...

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Autores principales: Chen, Yi‐Tzu, Lin, Chiao‐Wen, Chou, Ying‐Erh, Su, Shih‐Chi, Chang, Lun‐Ching, Lee, Chia‐Yi, Hsieh, Ming‐Ju, Yang, Shun‐Fa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098292/
https://www.ncbi.nlm.nih.gov/pubmed/36946281
http://dx.doi.org/10.1111/jcmm.17728
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author Chen, Yi‐Tzu
Lin, Chiao‐Wen
Chou, Ying‐Erh
Su, Shih‐Chi
Chang, Lun‐Ching
Lee, Chia‐Yi
Hsieh, Ming‐Ju
Yang, Shun‐Fa
author_facet Chen, Yi‐Tzu
Lin, Chiao‐Wen
Chou, Ying‐Erh
Su, Shih‐Chi
Chang, Lun‐Ching
Lee, Chia‐Yi
Hsieh, Ming‐Ju
Yang, Shun‐Fa
author_sort Chen, Yi‐Tzu
collection PubMed
description A disintegrin and metalloproteinase domain‐containing protein 10 (ADAM‐10) involves in the tumour progression, but the impacts of single‐nucleotide polymorphism (SNP) of ADAM‐10 on oral squamous cell carcinoma (OSCC) remain unclear. The aim of this study was to investigate the influence of SNP of ADAM‐10 on the clinical features of OSCC in male Taiwanese. Five loci of ADAM‐10 SNPs including rs653765 (C/T), rs2305421 (A/G), rs514049 (A/C), rs383902 (T/C) and rs2054096 (A/T) were genotyped by TaqMan allelic discrimination in 1138 OSCC patients and 1199 non‐OSCC individuals. The ADAM‐10 SNP rs2305421 GG (AOR: 1.399, 95% CI: 1.045–1.874, p = 0.024) and G allele (AOR: 1.170, 95% CI: 1.012–1.351, p = 0.034) illustrated a significantly higher genotypic frequencies in the OSCC group compared to the distribution of the ADAM‐10 SNP rs2305421 AA wild type. In the subgroup analysis, the ADAM‐10 SNP rs383902 TC+CC was significantly correlated to tumour size larger than T2 in betel quid chewer (AOR: 1.375, 95% CI: 1.010–1.872, p = 0.043), while the ADAM‐10 SNP rs653765 CT+TT was significantly associated with tumour size larger than T2 in cigarette smoker (AOR: 1.346, 95% CI: 1.023–1.772, p = 0.034). The results from The Cancer Genome Atlas revealed highest ADAM‐10 mRNA level in T2 stage of current smokers with head and neck squamous cell carcinoma (HNSCC). In conclusions, the ADAM‐10 SNP rs2305421 G allele is associated with the presence of OSCC, and the ADAM‐10 SNP rs383902 TC+CC and ADAM‐10 SNP rs653765 CT+TT correlates to large tumour size in specific conditions.
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spelling pubmed-100982922023-04-14 Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma Chen, Yi‐Tzu Lin, Chiao‐Wen Chou, Ying‐Erh Su, Shih‐Chi Chang, Lun‐Ching Lee, Chia‐Yi Hsieh, Ming‐Ju Yang, Shun‐Fa J Cell Mol Med Original Articles A disintegrin and metalloproteinase domain‐containing protein 10 (ADAM‐10) involves in the tumour progression, but the impacts of single‐nucleotide polymorphism (SNP) of ADAM‐10 on oral squamous cell carcinoma (OSCC) remain unclear. The aim of this study was to investigate the influence of SNP of ADAM‐10 on the clinical features of OSCC in male Taiwanese. Five loci of ADAM‐10 SNPs including rs653765 (C/T), rs2305421 (A/G), rs514049 (A/C), rs383902 (T/C) and rs2054096 (A/T) were genotyped by TaqMan allelic discrimination in 1138 OSCC patients and 1199 non‐OSCC individuals. The ADAM‐10 SNP rs2305421 GG (AOR: 1.399, 95% CI: 1.045–1.874, p = 0.024) and G allele (AOR: 1.170, 95% CI: 1.012–1.351, p = 0.034) illustrated a significantly higher genotypic frequencies in the OSCC group compared to the distribution of the ADAM‐10 SNP rs2305421 AA wild type. In the subgroup analysis, the ADAM‐10 SNP rs383902 TC+CC was significantly correlated to tumour size larger than T2 in betel quid chewer (AOR: 1.375, 95% CI: 1.010–1.872, p = 0.043), while the ADAM‐10 SNP rs653765 CT+TT was significantly associated with tumour size larger than T2 in cigarette smoker (AOR: 1.346, 95% CI: 1.023–1.772, p = 0.034). The results from The Cancer Genome Atlas revealed highest ADAM‐10 mRNA level in T2 stage of current smokers with head and neck squamous cell carcinoma (HNSCC). In conclusions, the ADAM‐10 SNP rs2305421 G allele is associated with the presence of OSCC, and the ADAM‐10 SNP rs383902 TC+CC and ADAM‐10 SNP rs653765 CT+TT correlates to large tumour size in specific conditions. John Wiley and Sons Inc. 2023-03-22 /pmc/articles/PMC10098292/ /pubmed/36946281 http://dx.doi.org/10.1111/jcmm.17728 Text en © 2023 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Chen, Yi‐Tzu
Lin, Chiao‐Wen
Chou, Ying‐Erh
Su, Shih‐Chi
Chang, Lun‐Ching
Lee, Chia‐Yi
Hsieh, Ming‐Ju
Yang, Shun‐Fa
Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma
title Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma
title_full Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma
title_fullStr Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma
title_full_unstemmed Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma
title_short Potential impact of ADAM‐10 genetic variants with the clinical features of oral squamous cell carcinoma
title_sort potential impact of adam‐10 genetic variants with the clinical features of oral squamous cell carcinoma
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10098292/
https://www.ncbi.nlm.nih.gov/pubmed/36946281
http://dx.doi.org/10.1111/jcmm.17728
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