Association of PON1-L55M Genetic Variation and Breast Cancer Risk: A Case-Control Trial
(ندگان)پدیدآور
Farmohammadi, AmirMomeni, AliBahmani, BanafsheGhorbani, HosseinRamzanpour, Raminنوع مدرک
TextResearch Articles
زبان مدرک
Englishچکیده
Background: Paraoxonase 1 (PON1), a multifactorial antioxidant enzyme, has a defensive role against oxidative stress, which is believed to contribute to cancer development. This study aimed to investigate the association of PON1-L55M functional polymorphism with breast cancer risk. Material and methods: In the experimental study, blood samples were collected from 150 healthy women controls and 150 breast cancer subjects. The L55M genotyping was performed by polymerase chain reaction-restriction fragment length polymorphism. Results: Our analysis showed that the genotypes distribution is in Hardy-Weinberg equilibrium for both case and control groups. Our data revealed that there are significant associations between PON1-L55M polymorphism and breast cancer risk in homozygote (OR= 2.13, 95%CI= 1.14-4.00, p= 0.018), dominant (OR= 1.72, 95%CI= 1.07-2.76, p= 0.024), and allelic (OR= 1.55, 95%CI= 1.12-2.15, p= 0.008) models. Conclusions: Our results suggest that the PON1-L55M genetic variation could be a genetic risk factor for breast cancer risk and it could be considered as a molecular biomarker for screening of susceptible women.
کلید واژگان
breast cancerParaoxonase 1
Genetic polymorphism
PCR-RFLP
Biology
شماره نشریه
1تاریخ نشر
2020-01-011398-10-11
ناشر
West Asia Organization for Cancer Prevention (WAOCP)سازمان پدید آورنده
Student Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran.School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Pathology, Faculty of Medicine, Kashan University of Medical Sciences, Kashan, Iran.
Pathology Department, Babol University of Medical Sciences, Babol, Iran.
Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.
شاپا
1513-73682476-762X




