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Expression Analysis of Microrna-222 in Breast Cancer Publisher Pubmed



Amini S1, 2 ; Abak A1, 2 ; Estiar MA3 ; Montazeri V4 ; Abhari A5 ; Sakhinia E1, 2
Authors
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Authors Affiliations
  1. 1. Biotechnology Research Center, Tabriz University of Medical Sciences, Division of Medical Genetics, Faculty of Medicine, Tabriz Genetic Analysis Centre (TGAC), Tabriz, Iran
  2. 2. Department of Biochemistry and Clinical Laboratory, Division of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
  3. 3. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Thorax Surgery, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
  5. 5. Department of Biochemistry and Clinical Laboratory, Division of Clinical Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

Source: Clinical Laboratory Published:2018


Abstract

Background: miR-221 and miR-222 are homologous miRNAs located in tandem, within 1 kb from each other, on human x chromosome. Recent studies declared that microRNA-222 is aberrantly expressed in various malignancies. The goal of this research was to measure the expression level of has-miR-222-3P and reveal its diagnostic and prognostic importance in breast malignancy. Methods: In this study, 40 pairs of cancerous and matched adjacent non-cancerous breast tissue were collected from patients, and real-time PCR was used to measure the relative expression of miR-222. Results: Our study clarified that microRNA-222 is enhanced in tumor tissues in comparison with normal tissue margins (p ≤ 0.05) and overexpression of miR-222 was not associated with clinicopathological factors such as age, BMI, menopausal status, histological type, grade, stage, tumor size, lymph node metastasis (p > 0.05). The receiver operating characteristic (ROC) curve analysis displayed an optimum cutoff point of < 4.17 to prove that miR-222 is a useful biomarker in breast cancer diagnosis. Conclusions: Our findings on miR-222 suggest that it could be a potentially useful target for control and management of breast malignancy. © 2018 Verlag Klinisches Labor GmbH. All rights reserved.