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基质金属蛋白酶-1和-9启动子多态性与日本人群子宫肌瘤风险增加无关。

Matrix metalloproteinase-1 and -9 promoter polymorphisms are not associated with an increased risk of uterine leiomyomas in a Japanese population.

作者信息

Takemura Naoya, Yoshida Shigeki, Kennedy Stephen, Deguchi Masashi, Ohara Noriyuki, Maruo Takeshi

机构信息

Department of Obstetrics and Gynecology, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

J Soc Gynecol Investig. 2006 Apr;13(3):232-6. doi: 10.1016/j.jsgi.2006.02.004.

Abstract

OBJECTIVE

Matrix metalloproteinases (MMPs) play an important role in modeling and remodeling the extracellular matrix in leiomyomas. Hence, we investigated whether associations exist between leiomyomas and promoter polymorphisms in the MMP-1 and MMP-9 genes in a Japanese population.

METHODS

We compared the distribution of polymorphisms in the promoter regions of MMP-1 (-1607 1G/2G) and MMP-9 (-1562 C/T) in 267 leiomyoma patients and 184 control patients using polymerase chain reaction-fragment-length polymorphism (PCR-RFLP) analysis.

RESULTS

The allele frequencies of the MMP-1 -1607 2G and MMP-9 -1562 T polymorphisms were 74.6% and 18.6% in leiomyoma patients, and 71.3% and 18.6% in control patients, respectively. No significant differences in allele frequencies or genotype distributions were found between leiomyoma and control patients. Moreover, no associations were found between MMP-1 and MMP-9 genotypes and leiomyoma size or a family history of the condition.

CONCLUSION

These findings suggest that MMP-1 and MMP-9 promoter polymorphisms are unlikely to be associated with an increased risk of uterine leiomyomas in Japanese women.

摘要

目的

基质金属蛋白酶(MMPs)在平滑肌瘤细胞外基质的塑造和重塑过程中发挥重要作用。因此,我们研究了日本人群中平滑肌瘤与MMP - 1和MMP - 9基因启动子多态性之间是否存在关联。

方法

我们采用聚合酶链反应 - 片段长度多态性(PCR - RFLP)分析方法,比较了267例平滑肌瘤患者和184例对照患者中MMP - 1(-1607 1G/2G)和MMP - 9(-1562 C/T)启动子区域多态性的分布情况。

结果

平滑肌瘤患者中MMP - 1 -1607 2G和MMP - 9 -1562 T多态性的等位基因频率分别为74.6%和18.6%,对照患者中分别为71.3%和18.6%。平滑肌瘤患者与对照患者之间在等位基因频率或基因型分布上未发现显著差异。此外,未发现MMP - 1和MMP - 9基因型与平滑肌瘤大小或该病家族史之间存在关联。

结论

这些发现表明,在日本女性中,MMP - 1和MMP - 9启动子多态性不太可能与子宫平滑肌瘤风险增加相关。

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