Loss of Expressions of Dusp6, Sprouty4, and Sef, Negative Regulators of FGF2/ERK1/2 Signaling, in the Endometrium of Women With Adenomyosis

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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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Abstract

Dual-specificity phosphatase 6 (Dusp6), Sprouty4, and similar expression to FGF (Sef) are negative modulators of FGF2/ERK1/2 signaling. The objective of the study was to evaluate the expressions of Dusp6, Sprouty4, and Sef in eutopic endometria of patients with adenomyosis. Endometria from 30 women with adenomyosis and 29 women without adenomyosis were used in this study. The expressions of Dusp6, Sprouty4, and Sef were investigated by immunohistochemical analysis. We found that Dusp6, Sprouty4, and Sef expressions were present in endometrial epithelial cells of normal endometria and eutopic endometria of adenomyosis. Weak immunostainings were noted in stromal cells in both endometria. No cyclical change was noted either in normal endometria or in eutopic endometria of adenomyosis during menstrual cycle. By immunohistochemical analysis, we found that eutopic endometria of adenomyosis showed significantly decreased Dusp6, Sprouty4, and Sef expressions compared with normal endometria. By in situ hybridization analysis, we found that the mRNA expressions of Dusp6, Sprouty4, and Sef were downregulated in eutopic endometria of adenomyosis compared with normal endometria. We conclude that downregulation of Dusp6, Sprouty4, and Sef--negative modulators of FGF2/ERK1/2 signaling--was present in eutopic endometria of adenomyosis, which may play critical roles in the development of adenomyosis.
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Loss of Expressions of Dusp6, Sprouty4, and Sef, Negative Regulators of FGF2/ERK1/2 Signaling, in the Endometrium of Women With Adenomyosis - Qiufen Guo - Hui Zhang - Xingbo Zhao - Yibing Fu - Jie Zhang - Mingjiang Li Dual-specificity phosphatase 6 (Dusp6), Sprouty4, and similar expression to FGF (Sef) are negative modulators of FGF2/ERK1/2 signaling. The objective of the study was to evaluate the expressions of Dusp6, Sprouty4, and Sef in eutopic endometria of patients with adenomyosis. Endometria from 30 women with adenomyosis and 29 women without adenomyosis were used in this study. The expressions of Dusp6, Sprouty4, and Sef were investigated by immunohistochemical analysis. We found that Dusp6, Sprouty4, and Sef expressions were present in endometrial epithelial cells of normal endometria and eutopic endometria of adenomyosis. Weak immunostainings were noted in stromal cells in both endometria. No cyclical change was noted either in normal endometria or in eutopic endometria of adenomyosis during menstrual cycle. By immunohistochemical analysis, we found that eutopic endometria of adenomyosis showed significantly decreased Dusp6, Sprouty4, and Sef expressions compared with normal endometria. By in situ hybridization analysis, we found that the mRNA expressions of Dusp6, Sprouty4, and Sef were downregulated in eutopic endometria of adenomyosis compared with normal endometria. We conclude that downregulation of Dusp6, Sprouty4, and Sef—negative modulators of FGF2/ERK1/2 signaling—was present in eutopic endometria of adenomyosis, which may play critical roles in the development of adenomyosis.

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Condition tags

adenomyosis

MeSH descriptors

Adenomyosis Dual Specificity Phosphatase 6 Intracellular Signaling Peptides and Proteins Nerve Tissue Proteins Receptors, Interleukin Signal Transduction Adenomyosis Adenomyosis Adult Down-Regulation Dual Specificity Phosphatase 6 Dual Specificity Phosphatase 6 Endometrium Endometrium Endometrium Female Gene Expression Regulation Humans Immunohistochemistry In Situ Hybridization

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