在日本人群中,基质金属蛋白酶-1和-9启动子多态性与子宫平滑肌瘤风险增加无关。

Naoya Takemura, Shigeki Yoshida, Stephen Kennedy, Masashi Deguchi, Noriyuki Ohara, Takeshi Maruo
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引用次数: 6

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中发挥重要作用。因此,我们研究了平滑肌瘤与日本人群中MMP-1和MMP-9基因启动子多态性之间是否存在关联。方法:采用聚合酶链反应-片段长度多态性(PCR-RFLP)方法比较267例平滑肌瘤患者和184例对照患者MMP-1 (-1607 1G/2G)和MMP-9 (-1562 C/T)启动子区域多态性的分布。结果:MMP-1 -1607 2G和MMP-9 -1562 T多态性的等位基因频率在平滑肌瘤患者中分别为74.6%和18.6%,在对照组中分别为71.3%和18.6%。在平滑肌瘤患者和对照组之间,等位基因频率和基因型分布无显著差异。此外,没有发现MMP-1和MMP-9基因型与平滑肌瘤大小或家族史之间的关联。结论:这些发现提示MMP-1和MMP-9启动子多态性不太可能与日本女性子宫平滑肌瘤风险增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Matrix metalloproteinase-1 and -9 promoter polymorphisms are not associated with an increased risk of uterine leiomyomas in a Japanese population.

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.

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