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首页> 外文期刊>Clinical and experimental obstetrics and gynecology >Effect of Wnt/beta-catenin signal pathway on of matrix metalloproteinase-7 and vascular endothelial growth factor gene expressions in endometriosis
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Effect of Wnt/beta-catenin signal pathway on of matrix metalloproteinase-7 and vascular endothelial growth factor gene expressions in endometriosis

机译:Wnt /β-catenin信号通路对子宫内膜异位症患者基质金属蛋白酶7和血管内皮生长因子基因表达的影响

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Purpose: To explore the function of Wnt/beta-catenin signal pathway on promoting the adhesion, invasion, and metastasis of endometriosis tissues by analyzing its effects on the expressions of matrix metalloproteinase-7 (MMP-7) and vascular endothelial growth factor in endometriosis. Materials and Methods: Endometriosis nude mice models were included. Small RNA interference technology was used to block Wnt/beta-catenin signal pathway. HE staining technique was adopted to observe the difference of pathological morphology among groups. The immunohistochemistry and real-time quantitative PCR were performed to analyze the expressions of beta-catenin. NIMP-7 and VEGF from protein and mRNA levels. Results: Whether the Wnt/beta-catenin signal pathway was blocked or not had little effect on the pathological morphology of lesions. The expressions of P-catenin, MMP-7 and VEGF in siRNA group were much lower than those in negative control group and control group (p < 0.05), while there was no statistical significance in the difference of expressions between negative control group and control group > 0.05). Conclusion: Blocking of Wnt/beta-catenin signal pathway caused the decrease of MMP-7 and VEGF expressions, indicating that Wnt/beta-catenin signal pathway plays an important role in the adhesion, invasion, and metastasis of endometriosis tissues.
机译:目的:通过分析Wnt /β-catenin信号通路对子宫内膜异位症中基质金属蛋白酶7(MMP-7)和血管内皮生长因子表达的影响,探讨Wnt /β-catenin信号通路在促进子宫内膜异位症组织黏附,侵袭和转移中的作用。 。材料与方法:包括子宫内膜异位症裸鼠模型。小RNA干扰技术被用来阻断Wnt /β-catenin信号通路。采用HE染色技术观察各组之间的病理形态学差异。进行了免疫组织化学和实时定量PCR分析β-catenin的表达。 NIMP-7和VEGF来自蛋白质和mRNA水平。结果:Wnt /β-catenin信号通路是否受阻对病变的病理形态影响不大。 siRNA组中P-catenin,MMP-7和VEGF的表达明显低于阴性对照组和对照组(p <0.05),而阴性对照组和对照组之间的表达差异无统计学意义。组> 0.05)。结论:阻断Wnt /β-catenin信号通路可降低MMP-7和VEGF的表达,提示Wnt /β-catenin信号通路在子宫内膜异位症组织的黏附,侵袭和转移中起重要作用。

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