中山醫學大學機構典藏 CSMUIR:Item 310902500/15776
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    题名: Effect of CC chemokine ligand 5 and CC chemokine receptor 5 genes polymorphisms on the risk and clinicopathological development of oral cancer.
    作者: CJ, Weng
    MH, Chien
    CW, Lin
    TT, Chung
    AI, Zavras
    CM, Tsai
    MK, Chen
    SF, Yang
    贡献者: 中山醫大口腔科學研究所
    关键词: CC chemokine ligand 5;CC chemokine receptor 5;Oral cancer;Single nucleotide polymorphism
    日期: 2010-08-21
    上传时间: 2016-08-11T07:35:08Z (UTC)
    ISSN: 1368-8375
    摘要: Inflammation can be induced by cytokines, chemokines, and their receptors, and it is believed to be a risk factor on tumor initiation and progression. The contribution of CC chemokine ligand 5 (CCL5) and CC chemokine receptor 5 (CCR5) on the risk and prognosis of oral cancer is still poorly investigated. The aims of this study were to investigate the impacts of single nucleotide polymorphisms (SNPs) in CCL5 and CCR5 genes and the synergistic effects of these SNPs on the risk and clinicopathological characteristics of oral cancer. In this case-control study, a total of 253 oral cancer patients and 347 controls were recruited. The genetic polymorphisms of CCL5-28, -403 and CCR5-59029 were analyzed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) genotyping analysis. The results of statistical analysis showed that the subjects with CCL5-28 CG, CCL5-28 CG or GG, and CCL5-403 TT polymorphic genotype as well as the subjects with the combinations of CCL5-28 CG/-403 CT and CCL5-28 CG/-403 TT genotypes having a significant higher risk to oral cancer than those with wild-type genotypes. Moreover, the oral cancer patients with the combination of CCL5-28 CG/-403 TT genotype presented a lower risk for developing a moderately or poorly differentiated status as compared to those with the combination of CCL5-28 CC/-403 CC genotype. These results suggest that the SNPs in CCL5-28 and -403 genes could increase the risk to have oral cancer, and the combinative effect of CCL5-28 CG and -403 TT genes might also increase the oral cancer risk but reduce the clinicopathological development of oral cancer patients.
    URI: http://dx.doi.org/10.1016/j.oraloncology.2010.07.011
    https://ir.csmu.edu.tw:8080/ir/handle/310902500/15776
    關聯: Oral Oncol. 2010 Oct;46(10):767-72
    显示于类别:[牙醫學系暨碩士班] 期刊論文

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