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基质金属蛋白酶-1(-1607 1G/2G)基因多态性与口腔鳞状细胞癌风险增加的关联。

Association of matrix metalloproteinase-1 (-1607 1G/2G) polymorphism with increased risk for oral squamous cell carcinoma.

作者信息

Vairaktaris Eleftherios, Yapijakis Christos, Derka Spyridoula, Serefoglou Zoe, Vassiliou Stavros, Nkenke Emeka, Ragos Vassilis, Vylliotis Antonis, Spyridonidou Sofia, Tsigris Christos, Yannopoulos Athanasios, Tesseromatis Christina, Neukam Friedrich W, Patsouris Efstratios

机构信息

Department of Oral and Maxillofacial Surgery, University of Athens Medical School, Vas. Sofias 93 and Dim. Soutsou 1, Athens 11521, Greece.

出版信息

Anticancer Res. 2007 Jan-Feb;27(1A):459-64.

Abstract

BACKGROUND

The purpose of this study was to investigate the possible relation of matrix metalloproteinase-1 (MMP-1) to increased risk for oral cancer, in light of recently found contribution of angiogenesis and thrombosis-related factors to the development of malignancies.

MATERIALS AND METHODS

The 1G/2G polymorphism in the MMP-1 gene, which influences its expression, was examined in 156 patients with oral squamous cell carcinoma and 141 healthy controls of comparable ethnicity (Greeks and Germans), gender and age.

RESULTS

In comparison to controls, the detected 2G allele frequency was significantly lower in the patient group and in subgroups with early cancer stages, with positive family history of thrombophilia, with tobacco abuse and without alcohol abuse (p < 0.05). These findings were mainly due to a significant decrease in 2G/2G homozygotes despite a small increase in 1G/2G heterozygotes in the above groups.

CONCLUSION

These findings suggest a significant involvement of the MMP-1 -1607 1G/2G polymorphism in the increasing risk for oral cancer in the 1G allele European carriers.

摘要

背景

鉴于最近发现血管生成和血栓形成相关因素对恶性肿瘤发展的作用,本研究旨在探讨基质金属蛋白酶-1(MMP-1)与口腔癌风险增加之间的可能关系。

材料与方法

在156例口腔鳞状细胞癌患者和141名种族(希腊人和德国人)、性别及年龄匹配的健康对照者中,检测了影响MMP-1基因表达的1G/2G多态性。

结果

与对照组相比,患者组以及癌症早期、有血栓形成倾向阳性家族史、有烟草滥用且无酒精滥用的亚组中,检测到的2G等位基因频率显著降低(p < 0.05)。这些发现主要是由于上述组中2G/2G纯合子显著减少,尽管1G/2G杂合子略有增加。

结论

这些发现表明,MMP-1 -1607 1G/2G多态性在欧洲1G等位基因携带者口腔癌风险增加中起重要作用。

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