Volume 22, Issue 12 (December 2024)                   IJRM 2024, 22(12): 1003-1014 | Back to browse issues page

Ethics code: IR.MUBABOL.REC.1401.050


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Nazari Hagh Y, Ahmadifard M, Esmaelzadeh S, abbaszadeh S, Shokrzadeh N. Decreased expression of miRNA-200a and miRNA-223-3p in endometriosis cases during the secretory phase of the menstrual cycle: insights from a comprehensive case-control study with analysis of molecular biomarkers and their potential role in disease-induced infertility.. IJRM 2024; 22 (12) :1003-1014
URL: http://ijrm.ir/article-1-3306-en.html
1- School of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.
2- Department of Medical Genetics, School of Medicine, Babol University of Medical Sciences, Babol, Iran.
3- Infertility and Reproductive Health Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
4- Reproductive Health Research Center, Clinical Research Institute, Urmia University of Medical Sciences, Urmia, Iran. , shokrzadeh.n@umsu.ac.ir
Abstract:   (101 Views)
Background: Endometriosis (EM) is a condition that causes infertility with decreasing uterine receptivity. It is reported that it affects about 20-25% of all infertile women. Some genetic markers play a crucial role in pathogenesis and infertility.
Objective: This study investigates the role of miR-200a and miR-223-3p in embryo implantation and their association with EM-related infertility.
Materials and Methods: In this case-control study, 36 women who referred to the Center for Research on Reproductive Health and Infertility of Babol University of Medical Sciences and Fatemeh Al-Zahra Infertility Specialized Treatment Center in Babol, Iran between June 2022 and July 2023 were evaluated. Participants were divided into 2 EM and control groups (n = 18/each). Endometrial samples were collected from participants between 17th and 24th days of their menstrual cycle. Histopathological examination (hematoxylin and eosin and periodic acid schiff) was performed to confirm the secretory stage, and miR-200a and miR-223-3p expressions were analyzed by quantitative reverse transcriptase-polymerase chain reaction.
Results: Histological analysis confirmed that both groups were in the secretory stage. Additionally, miRNA expression results showed a significant decrease in the miR-200a and miR-223-3p expression levels in EM group compared to control group. The expression level of miR-223-3p and miR-200a in the eutopic endometrial tissue of women with EM was notably lower than those in the control group.
Conclusion: Our results suggest that miR-200a and miR-223-3p are involved in the EM pathogenesis, while other genes and signaling pathways are probably involved in the implantation failure.

 
This article has been extracted from M.Sc. Thesis. (Yasaman Nazari Hagh)
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