ZEB1 expression is a potential indicator of invasive endometriosis
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This study found ZEB1 expression in epithelial cells of endometriotic lesions, but not normal endometria, suggesting it may indicate invasiveness and mesenchymal features.
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Abstract
INTRODUCTION: Although endometriosis is a benign disease, it shares some features with cancers, such as invasiveness and the potential to metastasize. This study sought to investigate the epithelial-mesenchymal transition status in human endometriotic lesions. MATERIAL AND METHODS: Thirteen endometriosis patients and 10 control women without endometriosis undergoing surgery for benign indications were recruited. We examined the expression of E-cadherin, vimentin, and epithelial-mesenchymal transition-induced transcriptional factors, such as Snail and ZEB1, by immunohistochemistry. We evaluated the expression of each marker in epithelial cells of both endometriotic lesions (ovarian endometrioma, deep infiltrating endometriosis, adenomyosis) and normal endometria. The correlation between ZEB1 expression and serum level of CA125 was also investigated. RESULTS: Immunohistochemical analysis revealed that although E-cadherin, vimentin, and Snail were expressed in epithelia of normal endometria and endometriotic lesions, ZEB1 expression was only expressed in epithelia of endometriotic lesions. Additionally, ZEB1 was most frequently observed in epithelial cells of invasive endometriosis. The endometriosis patients with high serum CA125 level were more likely to have ZEB1-positive lesions. CONCLUSIONS: This is the first observation of ZEB1 expression in epithelial cells of benign disease. The preferential expression of ZEB1 in epithelial cells of endometriotic lesions suggests that these cells may have, at least in part, a higher level of mesenchymal features possibly via ZEB1-driven epithelial-mesenchymal transition than normal endometria and that ZEB1 can be a potential indicator of invasiveness or severity of endometriosis.
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Cited by (36)
- Shared Biology Underlying Benign Endometrial Diseases and Endometrial Cancer: Current Knowledge and Future Prospectives 2026
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- Wnt/β-catenin signaling pathway role in the endometriosis pathogenesis 2025
- Expression profiles of E-cadherin and N-cadherin in endometriosis and other gynecological diseases towards targeted treatment: a systematic review 2025
- Epithelial-mesenchymal transition links inflammation and fibrosis in the pathogenesis of endometriosis: a narrative review 2025
- Иммуногистохимическая оценка маркеров эпителиально-мезенхимального перехода ZEB1, SNAIL, SLUGпри различных формах эндометриоза 2025
- Endometriosis and Endometriosis-Associated Tumors 2025
- The influence of menstrual cycle and endometriosis on endometrial expression of epithelial-to-mesenchymal transition (EMT)-related genes 2025
- Endometriosis and Endometriosis-Associated Tumors 2024
- Endometriosis: Pathogenesis, Diagnosis and Treatment, volume II 2024
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- Expression of ZEB1 in different forms of endometriosis: A pilot study 2023
- Inflammatory Cytokine-Induced HIF-1 Activation Promotes Epithelial–Mesenchymal Transition in Endometrial Epithelial Cells 2023
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- circPLOD2 knockdown suppresses endometriosis progression via the miR-216a-5p/ZEB1 axis 2023
- T-Cadherin, E-Cadherin, PR-A, and ER-α Levels in Deep Infiltrating Endometriosis 2022
- Oestrogen-induced epithelial-mesenchymal transition (EMT) in endometriosis: Aetiology of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome 2022
- Immune micro-environment and drug analysis of peritoneal endometriosis based on epithelial-mesenchymal transition classification 2022
- Exploring Epithelial–Mesenchymal Transition Signals in Endometriosis Diagnosis and In Vitro Fertilization Outcomes 2021
- Pathogenesis of Endometriosis: New Insights into Prospective Therapies 2021
- Disturbed progesterone signalling in an advanced preclinical model of endometriosis 2021
- Epithelial-to-mesenchymal transition contributes to the downregulation of progesterone receptor expression in endometriosis lesions 2021
- The deep infiltrating endometriosis tissue has lower T-cadherin, E-cadherin, progesterone receptor and oestrogen receptor than endometrioma tissue 2021
- Circular RNA circZFPM2 promotes epithelial-mesenchymal transition in endometriosis by regulating miR-205-5p/ZEB1 signalling pathway 2021
- Role of molecular signaling pathways in the pathogenesis of adenomyosis 2021
- MiR‐370‐3p inhibits the development of human endometriosis by downregulating EDN1 expression in endometrial stromal cells 2021
- Epithelial–Mesenchymal Transition in Endometriosis—When Does It Happen? 2020
- Mucin gene polymorphisms are associated with endometriosis in Korean women 2019
- Endometriosis and Endometriosis-Associated Tumors 2019
- Upregulation of miR‑33b promotes endometriosis via inhibition of Wnt/β‑catenin signaling and ZEB1 expression 2019
- Invasion of human deep nodular endometriotic lesions is associated with collective cell migration and nerve development 2018
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- Anti-endometriosis Mechanism of Jiawei Foshou San Based on Network Pharmacology 2018
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