Polymorphism and CDC25A Gene Expression in Pancreatic Cancer
Abstract
Background and Aim: The aim of this study is to determine the relationship between CDC25A gene polymorphism and pancreatic cancer via determining
CDC25A gene expression and polymorphisms of tumor tissues of pancreatic cancer cases. Additionally, it is aimed to prove the
possible relationship between cancer development and the gene expression level with determining CDC25A gene expression
levels in tumor tissue and normal tissue.
Materials and Methods: 118 patients (patients with pancreatic cancer who received surgery (n=28) and patients with pancreatic cancer who are in followup (n=90) and 83 healthy volunteers not having any known chronic disease and first degree relatives having cancer were included
in this study as a control group.
Results: Ser88Phee polymorphisms in CDC25A gene of pancreatic cancer and control groups were compared according to C/C, C/T, T/T
genotype frequencies and allele frequencies of C and T and no statistically significant difference was detected between two
groups (p>0.05). RS3731485 polymorphisms in CDC25A gene of pancreatic cancer and control groups were compared with
respect to C/C, C/G, G/G genotype frequencies and allele frequencies of C and G and there was no significant difference between
them statistically (p>0.05). There were no differences in CDC25A gene expression between control group and pancreatic cancer
group (p>0.05).
Conclusion: In the light of the data obtained, any significant relationship at the CDC25A gene polymorphism and expression in pancreatic
cancer was not detected. All in all, pancreatic cancer is a disease with high mortality and the place of genetics in the etiology of
cancer is indisputable. Therefore, we think the polymorphism and expression studies should be continued..
Keywords
References
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Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Research Article
Authors
Başar Aksoy
This is me
Sacit Çoban
This is me
Serdar Öztuzcu
This is me
Erdal Uysal
This is me
Publication Date
March 14, 2016
Submission Date
March 14, 2016
Acceptance Date
-
Published in Issue
Year 2016 Volume: 6 Number: 1