The deep infiltrating endometriosis tissue has lower T-cadherin, E-cadherin, progesterone receptor and oestrogen receptor than endometrioma tissue
Deep infiltrating endometriosis tissue showed significantly lower T-cadherin, E-cadherin, progesterone receptor, and estrogen receptor expression compared to ovarian endometrioma and normal endometrial tissues.
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Cited by (13)
- Thyroid autoimmunity, thyroid function, and endometriosis: reproductive immune-endocrine crosstalk and causal uncertainty 2026
- Hormonal Dysregulation and Neuroinflammation in Endometriosis: Convergent Druggable Pathways 2026
- Analysis of clinical characteristics, diagnosis, treatment, and postoperative outcomes in deep infiltrating endometriosis: a retrospective study 2025
- Pathophysiology of Endometriosis: Insights from Immunohistochemical Analysis of Ectopic and Eutopic Tissues 2025
- Expression profiles of E-cadherin and N-cadherin in endometriosis and other gynecological diseases towards targeted treatment: a systematic review 2025
- Combined targeting of TCF7L1/2, PTEN, CDK6, and BCCIP by microRNA miR-29c-3p is associated with reduced invasion and proliferation of endometriotic cells 2025
- Leveraging epigenetic aberrations in the pathogenesis of endometriosis: from DNA methylation to non-coding RNAs 2025
- Overview of crosstalk between stromal and epithelial cells in the pathogenesis of adenomyosis and shared features with deep endometriotic nodules 2024
- The significance of immune microenvironment in patients with endometriosis 2023
- High Expression of PR-A and Low Expression of PR-B is Correlated with Inflammation in Endometrioma Cases 2023
- Identification and validation of risk score model based on gene set activity as a diagnostic biomarker for endometriosis 2023
- T-Cadherin, E-Cadherin, PR-A, and ER-α Levels in Deep Infiltrating Endometriosis 2022
- Revisit pure laparoscopic surgery for patients with complicated benign diseases 2022
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