Association of Matrix Metalloproteinase-9 Genotypes With Nasopharyngeal Carcinoma Risk

被引:6
作者
Chen, Chao-Hsuan [2 ,3 ]
Shih, Liang-Chun [1 ,3 ,4 ]
Hsu, Shih-Wei [2 ,6 ]
Tien, Hui-Chi [7 ]
Liu, Yen-Fang [3 ]
Wang, Yun-Chi [2 ,3 ]
Tsai, Chia-Wen [2 ,3 ]
Bau, Da-Tian [2 ,3 ,5 ,8 ]
Chang, Wen-Shin [2 ,3 ]
机构
[1] China Med Univ Hosp, Dept Neurosurg, Taichung, Taiwan
[2] China Med Univ, Grad Inst Biomed Sci, Taichung, Taiwan
[3] China Med Univ Hosp, Dept Med Res, Terry Fox Canc Res Lab, Taichung, Taiwan
[4] China Med Univ Hosp, Dept Otorhinolaryngol Head & Neck Surg, Taichung, Taiwan
[5] Taichung Armed Forces Gen Hosp, Dept Surg, Div Neurosurg, Taichung, Taiwan
[6] Natl Def Med Ctr, Taipei, Taiwan
[7] Asia Univ, Dept Audiol & Speech Language Pathol, Taichung, Taiwan
[8] Asia Univ, Dept Bioinformat & Med Engn, Taichung, Taiwan
来源
IN VIVO | 2024年 / 38卷 / 04期
关键词
Genotype; matrix metalloproteinase-9; nasopharyngeal carcinoma; polymorphism; Taiwan; PROMOTER POLYMORPHISMS; ANDROGEN RECEPTOR; PROGNOSTIC MARKER; MMP-9; SUSCEPTIBILITY; EXPRESSION; GENE;
D O I
10.21873/invivo.13623
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background/Aim: The up -regulation of matrix metalloproteinase-9 (MMP-9) expression is a characteristic feature observed across various malignancies, including nasopharyngeal carcinoma (NPC). Nevertheless, the influence of MMP-9 genotype in the context of NPC remains underexplored. This study examined the implications of MMP-9 promoter rs3918242 genotypes on the susceptibility to NPC in Taiwan. Materials and Methods: In a cohort comprising 208 NPC cases and 416 healthy controls, genotyping of MMP-9 rs3918242 was conducted utilizing polymerase chain reaction -restriction fragment length polymorphism methodology. Results: Individuals harbouring the variant CT or TT genotype of MMP-9 rs3918242 did not demonstrate a discernible alteration in NPC risk when compared to wild -type CC carriers [odds ratio (OR)=0.83 and 0.79, with 95% confidence intervals (95%CI)=0.56-1.24 and 0.27-2.29; p=0.4205 and 0.8675, respectively]. Moreover, the presence of the variant T allele did not confer a modified risk of NPC (OR=0.84, 95%CI=0.60-1.19, p=0.3761). Intriguingly, a protective effect associated with the MMP-9 rs3918242 CT genotype against NPC risk was discerned among individuals abstaining from betel quid chewing behaviour (OR=0.51, 95%CI=0.30-0.87, p=0.0166). Notably, no significant association was established between the MMP-9 rs3918242 CT or TT genotype and NPC risk among individuals with or without smoking or alcohol consumption habits. Conclusion: Presence of the variant CT or TT genotype at MMP-9 rs3918242 did not appear to substantially contribute to an elevated risk of NPC. Notably, a protective effect against NPC risk was observed in individuals carrying the CT genotype, particularly in those abstaining from betel quid chewing.
引用
收藏
页码:1731 / 1739
页数:9
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