Title : Simvastatin Inhibits Wnt/β-Catenin Pathway in Uterine Leiomyoma.

Pub. Date : 2021 Dec 1

PMID : 34614511






7 Functional Relationships(s)
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1 Simvastatin inhibits Wnt/beta-catenin pathway in uterine leiomyoma. Simvastatin Wnt family member 4 Homo sapiens
2 The objective of this study is to examine the effects of simvastatin on the Wnt/beta-catenin signaling pathway in leiomyoma. Simvastatin Wnt family member 4 Homo sapiens
3 The results of this study reveal that simvastatin significantly reduced the expression of Wnt4 and its co-receptor LRP5. Simvastatin Wnt family member 4 Homo sapiens
4 Additionally, simvastatin reduced the expression of Wnt4 and total beta-catenin, as well as non-phosphorylated beta-catenin protein expression in response to estrogen and progesterone. Simvastatin Wnt family member 4 Homo sapiens
5 Simvastatin also inhibited the expression of c-Myc, a downstream target of the Wnt/beta-catenin pathway. Simvastatin Wnt family member 4 Homo sapiens
6 The effect of simvastatin on non-phosphorylated-beta-catenin, the key regulator of the Wnt/beta-catenin pathway, was recapitulated in human leiomyoma tissue. Simvastatin Wnt family member 4 Homo sapiens
7 These results suggest that simvastatin may have a beneficial effect on uterine leiomyoma through suppressing the overactive Wnt/beta-catenin pathway. Simvastatin Wnt family member 4 Homo sapiens