Expression of miR-21 & IL-4 in endometriosis

(2024) Expression of miR-21 & IL-4 in endometriosis. Human Immunology. p. 5. ISSN 0198-8859

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Abstract

Background: Endometriosis characterized with existence of endometrial-like tissue outside the uterus. Fibrosis of ectopic lesions is an important feature of endometriosis. IL-4 induces fibrosis via fibroblast proliferation, collagen production and myofibroblast differentiation. Increasing of miR-21 expression promotes fibroblast activation and fibrosis expansion. The aim of study was to evaluate the expression of miR-21 and its relationship with IL-4 gene expression in endometrial ectopic and eutopic tissues of endometriosis patients. Methods and Results: Ectopic and eutopic tissue samples were taken from 20 women with endometriosis, and control samples were taken from the endometrium of 20 endometriosis-free women. The relative expression of IL-4 and miR-21 evaluated by Real Time PCR. IL-4 relative gene expression was significantly increased in ectopic tissue compared to eutopic (p = 0.025) and control tissue (p = 0.021). The relative expression of miR-21 gene in ectopic tissue was increased compared to eutopic (p = 0.850) and control tissue (p = 0.978) but these differences were not significant. Also, the correlation between IL-4 and miR-21 relative gene expression was not significant (p = 0.083). Conclusion: The increased expression of miR-21 in endometrium of women with endometriosis may upregulate the IL-4 gene expression and lead to fibrosis. Further studies may suggest miR-21 and IL-4 as candidates for diagnosis of endometriosis.

Item Type: Article
Keywords: Endometriosis miR-21 Fibrosis Q-PCR IL-4 interleukin-4 fibrosis pathogenesis fibroblasts activation apoptosis cytokines severity pathway level Immunology
Page Range: p. 5
Journal or Publication Title: Human Immunology
Journal Index: ISI
Volume: 85
Number: 1
Identification Number: https://doi.org/10.1016/j.humimm.2023.110746
ISSN: 0198-8859
Depositing User: خانم ناهید ضیائی
URI: http://eprints.mui.ac.ir/id/eprint/28867

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