Adenogenesis Factors FGF7, FGF10, FGF23, IFN-τ and HGF in Endometriosis Tissue Respect to Eutopic Endometrium: An Immunohistochemical Study
This study found altered expression of adenogenesis factors FGF7, FGF10, HGF, FGF23, and IFN-τ in ectopic endometrial tissue compared to eutopic endometrium, supporting a link between adenogenesis dysregulation and endometriosis.
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This immunohistochemical study compared expression of adenogenesis- and survival-related factors (FGF7, FGF10, FGF23, IFN-τ, and HGF) in deep endometriotic lesions versus normal eutopic endometrium, assessing both epithelial and stromal compartments. The authors reported significantly higher epithelial and stromal expression of FGF7, FGF10, and HGF in controls than in endometriosis samples, while FGF23 and IFN-τ showed significantly higher expression in ectopic endometrial stroma compared with eutopic endometrium, without a significant epithelial difference. A major caveat stated in the paper’s framing is that its interpretation relies on tissue-phenotype differences inferred from immunohistochemical expression patterns rather than functional causality. This paper is centrally about endometriosis — it measures adenogenesis/survival factor expression in deep endometriotic lesions relative to eutopic endometrium to support a shifted uterine gland developmental phenotype.
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Cited by (4)
- The Role of Adenogenesis Factors in the Pathogenesis of Endometriosis 2025
- Screening and identification of key biomarkers associated with endometriosis using bioinformatics and next generation sequencing data analysis 2024
- Screening and identification of key biomarkers associated with endometriosis using bioinformatics and next-generation sequencing data analysis 2024
- Pathogenesis of Endometriosis: Focus on Adenogenesis-related Factors 2023
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- pubmed
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