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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/111623


    Title: The Contribution of MMP-7 Promoter Polymorphisms to Taiwan Lung Cancer Susceptibility
    Authors: GUAN-LIANG, C;CHEN, GUAN-LIANG;SHEN, TE-CHUN;SHEN, TE-CHUN;CHA, WEN-SHIN;CHANG, WEN-SHIN;TSA, CHIA-WEN;TSAI, CHIA-WEN;LI, HSIN-TING;LI, HSIN-TING;CHIH-LIANG, CHIH-LIANG C;CHUANG, CHIH-LIANG;LAI, YI-LIANG;LAI, YI-LIANG;YUE, TE-CHENG;YUEH, TE-CHENG;HSIA, TE-CHUN;HSIA, TE-CHUN;SHOU-CHENG, W;WANG, SHOU-CHENG;包大?;Bau, Da-Tian
    Contributors: 生物資訊與醫學工程學系
    Date: 2018-10
    Issue Date: 2018-12-24 16:08:08 (UTC+8)
    Abstract: Background/aim: Matrix metalloproteinase-7 (MMP-7) plays an important role in metastasis behavior of cancer cells, and overexpression of MMP-7 has been associated with poor prognosis in non-small cell lung cancer. However, the contribution of various genotypes of MMP-7 has not yet been investigated in lung cancer in Taiwan. Therefore, this study aimed to investigate the association of MMP-7 genotypes with lung cancer risk among the Taiwanese. Materials and methods: In this hospital-based case-control study, genotypes and distributions at two promoter sites of MMP-7, A-181G and C-153T, were determined, and their association with lung cancer risk in Taiwan was evaluated among 358 lung cancer patients and 716 age- and gender-matched healthy control individuals. In addition, the interaction of MMP-7 genotypes and smoking status were also examined. Results: The percentages of variant AG and GG at MMP-7 A-181G in the lung cancer group were similar to the control group (12.8% and 2.3% vs. 11.3% and 1.5%, respectively; ptrend=0.5294). The allelic frequency distribution analysis showed that the variant G allele at MMP-7 A-181G conferred non-significant elevated lung cancer risk compared to the wild-type A allele [odds ratio (OR)=1.18, 95% confidence interval (CI)=0.85-1.66, p=0.2289]. As for the genotypes of MMP-7 C-153T, all the studied Taiwanese population was of CC genotype. Furthermore, there was no obvious joint effect of MMP-7 A-181G genotype and smoking status on the lung cancer risk. No statistically significant correlation was observed between MMP-7 A-181G genotype distributions and gender. Conclusion: There was no evidence that the genotypes of MMP-7 A-181G may act as a biomarker in determining personal susceptibility to lung cancer in Taiwan.
    Relation: ANTICANCER RESEARCH
    Appears in Collections:[生物資訊與醫學工程學系 ] 期刊論文

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