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论文摘要

基质金属蛋白酶1、3和9基因多态性与云南汉族人群口腔鳞状细胞癌发病风险的相关性研究

Matrix metalloproteinase 1, 3 and 9 gene polymorphism and the risk of oral squamous cell carcinomas among Han Chinese in Yunnan

作者:李蓝江1 许冰莹1 杨春艳2 赵川3 田心2

Author:Li Lanjiang1, Xu Bingying1, Yang Chunyan2, Zhao Chuan3, Tian Xin2.

收稿日期:2015-01-02          年卷(期)页码:2015,42(6):631-634

期刊名称:国际口腔医学杂志

Journal Name:International Journal of Stomatology

关键字:口腔鳞状细胞癌,基质金属蛋白酶,单核苷酸多态性,

Key words:oral squamous cell carcinomas,matrix metalloproteinase,single nucleotide polymorphism,

基金项目:

2011年云南省应用基础研究计划项目(2011FZ103)

中文摘要

目的 探讨基质金属蛋白酶(MMP)1、3和9基因多态性与云南汉族人群口腔鳞状细胞癌(OSCC)发病风险的相关性。方法 检测选择55例OSCC患者为OSCC组,54例健康人为健康对照组,采用聚合酶链反应-限制性片段长度多态性法检测分析其MMP1启动子(1607 1G/2G)、MMP3启动子(1171 5A/6A)、MMP9启动子(1562 C/T)3个位点的单核苷酸多态性(SNP)。结果 健康对照组和OSCC组在MMP1启动子(1607 1G/2G)中1G/1G、2G/2G、1G/2G的基因型频率分别为11.11%、37.04%、51.85%和5.66%、43.40%、50.94%,在MMP3启动子(1171 5A/6A)中5A/5A、6A/6A、5A/6A的基因型频率分别为0、75.93%、24.07%和8.33%、72.92%、18.75%,在MMP9启动子(1562 C/T)中CC、TT、CT的基因型频率分别为100%、0、0和100%、0、0。MMP1、MMP3、MMP9的SNP与OSCC发病风险无相关性(P>0.05),这3个位点分别与高、中、低分化OSCC发病风险亦无相关性(P>0.05)。结论 MMP1启动子1607 1G/2G、MMP3启动子1171 5A/6A、MMP9启动子1562 C/T这3个位点的SNP可能与云南汉族OSCC发病风险无相关性。

英文摘要

Objective To explore matrix metalloproteinase(MMP)1, MMP3, and MMP9 gene polymorphisms are studied to determine the risk of developing oral squamous cell carcinoma(OSCC) among Han Chinesein Yunnan. Methods The polymerase chain reaction-restriction fragment length polymorphism method is used to detect 3 loci single nucleotide polymorphisms(SNPs) of the MMP1 promoter(1607 1G/2G), MMP3 promoter(1171 5A/6A), and MMP9 promoter(1562C/T) among 54 patients diagnosed with OSCC(OSCC group) and 55 healthy subjects(control group). Results The distribution of the 3 loci of the MMP1 promoter(1607 1G/2G, 2G/2G, 1G/2G) genotype frequencies among the control group were 11.11%, 37.04%, and 51.85%, respectively, and 5.66%, 43.40%, and 50.94%, respectively, among the OSCC group. The distributions of 5A/5A, 6A/6A, and 5A/6A of the MMP3 promoter(1171 5A/6A) were 0, 75.93%, and 24.07% among the control group, respectively, and 8.33%, 72.92%, and 18.75% among the OSCC group, respectively. The distributions of CC, TT, and CT of the MMP9 promoter(1562C/T) were 100%, 0, and 0 among the control group, respectively, and 100%, 0, and 0 among the OSCC group, respectively. The SNPs of MMP1, MMP3, MMP9, and the risk of OSCC have no significant correlation(P>0.05). The 3 sites with high-, medium-, and low-risk differentiation of OSCC have no significant correlation(P>0.05). Conclusion The existence of 3 loci SNPs of the MMP1 promoter(1607 1G/2G), MMP3 promoter(1171 5A/6A), and MMP9 promoter(1562C/T) among Han Chinese in Yunnan has an insignificant correlation to the risk of developing OSCC.

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