Abstract | BACKGROUND/AIM: MATERIALS AND METHODS: The MMP-1 promoter -1607 genotypes were examined for 352 age- and gender-matched controls and 176 NPC patients by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methodology. RESULTS: We found that the MMP-1 promoter -1607 heterozygous 1G/2G and homozygous 1G/1G genotypes, were more and more prone to be associated with NPC risk (odds ratio (OR)=0.64 and 0.63, 95% confidence interval (CI)=0.43-1.03 and 0.36-0.96, p=0.0659 and 0.0932, respectively). In the dominant models, there was a significant association between the genotype of MMP-1 promoter -1607 and NPC risk (OR=0.64, 95% CI=0.43-0.91, p=0.0359). In addition, individuals carrying the 1G allele at MMP-1 promoter -1607 were less susceptible to NPC (OR=0.73; 95%CI=0.59 to 0.96, p=0.0418) after adjustment for age, gender, cigarette, alcohol and areca consumption. CONCLUSION: The 1G/1G genotype of MMP-1 promoter -1607 may independently have a protective effect on NPC risk, without interaction with behavioral factors, including cigarette, alcohol and areca consumption.
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Authors | Chia-Wen Tsai, Wen-Shin Chang, Chi-Li Gong, Liang-Chun Shih, Liang-Yu Chen, En-Yuan Lin, Hsin-Ting Li, Shiou-Ting Yen, Cheng-Nan Wu, DA-Tian Bau |
Journal | Anticancer research
(Anticancer Res)
Vol. 36
Issue 7
Pg. 3335-40
(Jul 2016)
ISSN: 1791-7530 [Electronic] Greece |
PMID | 27354591
(Publication Type: Journal Article)
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Copyright | Copyright© 2016 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved. |
Chemical References |
- MMP1 protein, human
- Matrix Metalloproteinase 1
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Topics |
- Alcohol Drinking
(genetics, metabolism)
- Areca
- Case-Control Studies
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Genotype
- Humans
- Male
- Matrix Metalloproteinase 1
(genetics, metabolism)
- Middle Aged
- Nasopharyngeal Neoplasms
(enzymology, etiology, genetics)
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Promoter Regions, Genetic
- Smoking
(genetics, metabolism)
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