:: Volume 27, Issue 5 (12-2019) ::
Journal of Ilam University of Medical Sciences 2019, 27(5): 65-72 Back to browse issues page
Evaluation of the Association between the Risk of Breast Cancer and rs17065417 Polymorphism in the LIN28B Gene
Seyed saleh Sajadi1 , Mohammad mehdi Moghani bashi mansooryeh * 2, Sirus Naeimi1
1- Dept of Genetics, Faculty of Basic Sciences, Kazerun Branch, Islamic Azad University, Kazerun, Iran
2- Dept of Genetics, Faculty of Medicine, Kazerun Branch, Islamic Azad University, Kazerun, Iran , amir.sinaei2017@gmail.com
Abstract:   (2899 Views)
Introduction: LIN28B is one of the genes that have been shown to be involved in various cancers and diseases, such as cervical, neuroblastoma, and breast cancers. This gene is a key inhibitor of the let-7 miRNA and can inhibit let-7 expression. This study aimed to investigate the association between the risk of breast cancer and rs17065417 polymorphism in the LIN28B gene.
 
Materials & Methods: In this case-control study, genomic DNA was extracted from whole blood samples of 100 patients with breast cancer and 100 healthy individuals. The polymerase chain reaction (PCR) technique was used to amplify the region containing the polymorphic site. Finally, PCR products were sequenced and genotypes were determined using Chromas software.
Findings: Based on the results of the statistical test, regarding the AA genotype, the control (80%) and patient (73%) groups obtained the highest frequency. Moreover, the lowest frequencies in the AC and CC genotypes were reported in the control (8%) and patient groups (5%). In addition, the genotype AC associated with a 6-fold increased risk of breast cancer (P=0.005; OR=6.600; CI=1.763-24.714).
 
Discussion & Conclusions:  It seems that there is a relationship between rs17065417 polymorphism and an increased risk of breast cancer in the LIN28B gene.
 
Keywords: Breast cancer, LIN28B gene, rs17065417 polymorphism
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Type of Study: Research | Subject: Molecular Genetics
Received: 2019/02/4 | Accepted: 2019/11/2 | Published: 2019/12/31



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Volume 27, Issue 5 (12-2019) Back to browse issues page