Loss of Expressions of Dusp6, Sprouty4, and Sef, Negative Regulators of FGF2/ERK1/2 Signaling, in the Endometrium of Women With Adenomyosis
Adenomyosis endometria showed significantly decreased DUSP6, SPRY4, and SEF expression, negative regulators of FGF2/ERK1/2 signaling, compared to normal endometria.
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This study investigated the expression levels of Dusp6, Sprouty4, and Sef, which are negative regulators of FGF2/ERK1/2 signaling, in the eutopic endometria of women with adenomyosis. Researchers compared tissue samples from 30 patients with adenomyosis against 29 controls without the condition using immunohistochemical analysis and in situ hybridization. The results demonstrated significantly decreased protein and mRNA expressions of these three genes in the adenomyosis group compared to normal endometria, indicating a potential role for their downregulation in disease development. This paper is centrally about adenomyosis — specifically examining molecular mechanisms involving FGF2/ERK1/2 signaling pathway regulators in the eutopic endometrium.
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Cited by (3)
- Aberrant expression of Notch1/numb/snail signaling, an epithelial mesenchymal transition related pathway, in adenomyosis 2015
- Iron overload–modulated nuclear factor kappa-B activation in human endometrial stromal cells as a mechanism postulated in endometriosis pathogenesis 2014
- Bioinformatics strategy for the screening of key genes to differentiate adenomyosis from endometriosis (Review) 2019
References (6)
- Adenomyosis: A Challenge in Clinical Gynecology via openalex
- W1972850991 via openalex
- W1983523339 via openalex
- W2081554709 via openalex
- W2082512712 via openalex
- W2128251228 via openalex
Cited by (3)
- Bioinformatics strategy for the screening of key genes to differentiate adenomyosis from endometriosis (Review) 2019
- Aberrant expression of Notch1/numb/snail signaling, an epithelial mesenchymal transition related pathway, in adenomyosis 2015
- Iron overload–modulated nuclear factor kappa-B activation in human endometrial stromal cells as a mechanism postulated in endometriosis pathogenesis 2014
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