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Please use this identifier to cite or link to this item:
https://ir.csmu.edu.tw:8080/ir/handle/310902500/23806
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Title: | TRIM21 Polymorphisms are associated with Susceptibility and Clinical Status of Oral Squamous Cell Carcinoma patients |
Authors: | Chuang, CY;Chien, YC;Lin, CW;Chou, CH;Chen, SC;Liu, CL;Bai, LY;Yang, SF;Yu, YL |
Keywords: | tripartite motif 21 (TRIM21);oral squamous cell carcinoma (OSCC);single-nucleotide polymorphism (SNP) |
Date: | 2021 |
Issue Date: | 2022-08-05T09:43:10Z (UTC)
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Publisher: | IVYSPRING INT PUBL |
ISSN: | 1449-1907 |
Abstract: | Squamous cell cancer of head and neck (HNSCC) is the sixth most common malignancy worldwide. One of the most common HNSCC types is oral squamous cell carcinoma (OSCC), which is the fifth leading cause of cancer death in Taiwan. Tripartite motif 21 (TRIM21) has been reported to play an important role in different cancer types. We found a correlation between TRIM21 and survival of HNSCC patients, but little information exists about how altered TRIM21 expression contributes to tumorigenesis. Thus, we investigated the combined effect of TRIM21 polymorphisms and exposure to environmental carcinogens on the susceptibility and clinicopathological characteristics of OSCC. Two single-nucleotide polymorphisms (SNPs) of TRIM21 (rs4144331, rs915956) from 1194 healthy controls and 1192 OSCC patients were analyzed by real-time PCR. Among 1632 smokers, TRIM21 polymorphism carriers with the betel-nut chewing habit had a similar to 4.8-fold greater risk of OSCC than TRIM21 wild-type carriers without the betel-nut chewing habit. After adjusting for other covariants, OSCC patients with G/T at TRIM21 rs4144331 had a high risk for distant metastasis compared with G/G homozygotes. This study is the first to examine the risk factors associated with TRIM21 SNPs in OSCC progression and development. Thus, our findings suggest that this study is the first to examine the risk factors associated with TRIM21 SNPs in OSCC progression and development and suggest that interactions between mutant genes may alter the susceptibility to OSCC. |
URI: | http://dx.doi.org/10.7150/ijms.56614 https://www.webofscience.com/wos/woscc/full-record/WOS:000669029400026 https://ir.csmu.edu.tw:8080/handle/310902500/23806 |
Relation: | INTERNATIONAL JOURNAL OF MEDICAL SCIENCES ,2021,v18,issue 13, P2997-3003 |
Appears in Collections: | [中山醫學大學研究成果] 期刊論文
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