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基质金属蛋白酶-2和基质金属蛋白酶-9启动子多态性与涎腺癌易感性

The MMP-2 and MMP-9 promoter polymorphisms and susceptibility to salivary gland cancer.

作者信息

Radunovic Milena, Nikolic Nadja, Milenkovic Sanja, Tomanovic Nada, Boricic Ivan, Dimitrijevic Milovan, Novakovic Ivana, Basta-Jovanovic Gordana

机构信息

Department of Microbiology and Immunology, School of Dental Medicine, University of Belgrade, Belgrade, Serbia.

出版信息

J BUON. 2016 May-Jun;21(3):597-602.

Abstract

PURPOSE

Matrix metalloproteinases (MMPs) are a family of endopeptidases that may play an important role in the development of salivary gland cancer (SGC). MMP-2 and MMP-9, members of the gelatinase protein family, are capable of degrading type IV collagen of basement membranes, and their overexpression is often associated with tumor aggressiveness and poor prognosis. The aim of this study was to establish the role of single nucleotide polymorphisms (SNPs) in MMP-2 and MMP-9 genes as putative susceptibility factors for the development of SGC.

METHODS

The MMP-2 -1306 C>T, MMP-2 -1575 G>A and MMP-9 -1562 C>T polymorphisms were analyzed in 93 SGC cases and 100 controls using PCR-RFLP.

RESULTS

The T allele for the MMP-2-1306 C>T polymorphism exhibited its effect in heterozygous carriers, increasing the risk for SGC (odds ratio/OR 1.98, 95% CI 1.07-3.65, p=0.03). According to the dominant model, CT+TT genotypes had a 2-fold increased risk of developing SGCs (p=0.02).When the dominant model was applied for the MMP2 -1575 G>A, individuals with GA+AA genotypes exhibited a 1.77-fold increase in cancer risk, but with borderline significance (p=0.049). Heterozygous carriers of the variant T allele for the MMP-9 -1562 C>T polymorphism had roughly a 2-fold increase in susceptibility for SGC compared to wild type homozygotes (CC) (p=0.02).

CONCLUSION

Our findings suggest MMP-2-1306 C>T and MMP-9-1562 C>T polymorphisms genotypes seem to influence the development of SGCs, whereas MMP-2 -1575 G>A seems to be of a minor importance.

摘要

目的

基质金属蛋白酶(MMPs)是一类内肽酶,可能在涎腺癌(SGC)的发生发展中起重要作用。明胶酶蛋白家族成员MMP-2和MMP-9能够降解基底膜的IV型胶原,它们的过度表达常与肿瘤侵袭性和不良预后相关。本研究旨在确定MMP-2和MMP-9基因中的单核苷酸多态性(SNP)作为SGC发生的假定易感因素的作用。

方法

采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术分析93例SGC患者和100例对照者的MMP-2 -1306 C>T、MMP-2 -1575 G>A和MMP-9 -1562 C>T多态性。

结果

MMP-2 -1306 C>T多态性的T等位基因在杂合子携带者中显示出其作用,增加了SGC的发病风险(优势比/OR 1.98,95%可信区间1.07-3.65,p=0.03)。根据显性模型,CT+TT基因型发生SGC的风险增加2倍(p=0.02)。当对MMP2 -1575 G>A应用显性模型时,GA+AA基因型个体的癌症风险增加1.77倍,但具有临界显著性(p=0.049)。与野生型纯合子(CC)相比,MMP-9 -1562 C>T多态性变异T等位基因的杂合子携带者患SGC的易感性大约增加2倍(p=0.02)。

结论

我们的研究结果表明,MMP-2-1306 C>T和MMP-9-1562 C>T多态性基因型似乎影响SGC的发生发展,而MMP-2 -1575 G>A似乎不太重要。

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