Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
Share this content! On (X network) By
Identification of Candidate Microrna Markers of Endometriosis With the Use of Next-Generation Sequencing and Quantitative Real-Time Polymerase Chain Reaction Publisher Pubmed



Papari E1 ; Noruzinia M1 ; Kashani L2 ; Foster WG3
Authors
Show Affiliations
Authors Affiliations
  1. 1. Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
  2. 2. Arash Women's Hospital, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. McMaster University, Department of Obstetrics and Gynecology, Hamilton, Ontario, Canada

Source: Fertility and Sterility Published:2020


Abstract

Objective: To identify novel candidate diagnostic microRNA (miRNA) markers of endometriosis by means of an unbiased search with confirmation by means of targeted polymerase chain reaction (PCR). Design: Retrospective cohort. Setting: University teaching hospitals. Patient(s): Women with endometriosis and control women, confirmed with the use of laparoscopy. Interventions(s): Diagnostic laparoscopy and blood sample. Main Outcome Measure(s): Next-generation sequencing (NGS) and quantitative real-time PCR (qRT-PCR). Result(s): Candidate miRNAs differentially expressed in women with endometriosis compared with control women were identified by means of NGS and selected for qRT-PCR. Plasma samples from another cohort of women with surgically confirmed endometriosis (n = 53) and disease-free control women (n = 53) were checked for hemolysis using spectrophotometry and the ratio of miR-23a and miR-451 by means of qRT-PCR. MicroRNA signatures were quantified by means of qRT-PCR in hemolysis-free plasma samples of case subjects (n = 25) and control subjects (n = 28) with the use of miRcury LNA miRNA. Circulating levels of eight miRNAs (miR-199a-3p, miR-143-3p, miR-340-5p, let-7b-5p, miR-21-5p, miR-17-5p, miR-20a-5p, and miR-103a-3p) were significantly lower in case subjects compared to control subjects. The sensitivity and specificity for individual miRNAs ranged from 0.36 to 1.00 and from 0.43 to 1.00, respectively, but when combined produced sensitivity and specificity of 0.92 and 0.86 with positive (PPV) and (NPV) predictive values of 0.85 and 0.92, respectively. However, combination of five miRNAs (miR-17-5p, miR-20a-5p, miR-199a-3p, miR-143-3p, and let-7b-5p) produced sensitivity and specificity of 0.96 and 0.79 with PPV and NPV of 0.80 and 0.96, respectively. Conclusion(s): We conclude that a panel of candidate miRNAs was comparable to laparoscopy in distinguishing between women with endometriosis and control women. © 2020 The Authors
Other Related Docs
16. Autophagy in Cancers Including Brain Tumors: Role of Micrornas, Cell Communication and Signaling (2020)
19. Micrornas and Long Non-Coding Rnas As Biomarkers for Polycystic Ovary Syndrome, Journal of Cellular and Molecular Medicine (2022)
23. Exosomal Micrornas in Regulation of Tumor Cells Resistance to Apoptosis, Biochemistry and Biophysics Reports (2024)
26. Tumor Suppressive Function of Microrna-192 in Acute Lymphoblastic Leukemia, Bosnian Journal of Basic Medical Sciences (2017)
29. Impact of Endometriosis on Reproductive Health: An Integrative Review, Journal of Obstetrics and Gynaecology (2021)