Association between Programmed Cell Death 6 Interacting Protein Insertion/Deletion Polymorphism and the Risk of Breast Cancer in a Sample of Iranian Population

Author:

Hashemi Mohammad12,Yousefi Javad3,Hashemi Seyed Mehdi3,Amininia Shadi2,Ebrahimi Mahboubeh2,Taheri Mohsen4,Ghavami Saeid567

Affiliation:

1. Cellular and Molecular Research Center, Zahedan University of Medical Sciences, Zahedan, Iran

2. Department of Clinical Biochemistry, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran

3. Department of Internal Medicine, School of Medicine, Zahedan University of Medical Sciences, Zahedan, Iran

4. Genetic of Non-Communicable Disease Research Center, Zahedan University of Medical Sciences, Zahedan, Iran

5. Department of Human Anatomy and Cell Science, College of Medicine, Faculty of Health Sciences, University of Manitoba, Winnipeg, MB, Canada R3E 0J9

6. Manitoba Institute of Child Health, University of Manitoba, Winnipeg, MB, Canada R3E 0J9

7. Health Policy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

Abstract

It has been suggested that genetic factors contribute to patients’ vulnerability to breast cancer (BC). The programmed cell death 6 interacting protein (PDCD6IP) encodes for a protein that is known to bind to the products of the PDCD6 gene, which is involved in the apoptosis pathway. The aim of this case-control study is to investigate the relationship between thePDCD6IP15 bp insertion/deletion (I/D) polymorphism (rs28381975) and BC risk in an Iranian population. A total of 491 females, including 266 BC patients and 225 control subjects without cancer, were enrolled into the study. Our findings revealed that thePDCD6IP15 bp I/D polymorphism decreased the risk of BC in codominant (OR=0.44, 95%CI=0.31–0.65,p<0.0001, I/D versus DD;OR=0.39, 95%CI=0.17–0.88,p=0.030, I/I versus DD) and dominant (OR=0.44, 95%CI=0.30–0.63,p<0.0001, D/I + I/I versus D/D) tested inheritance models. Also, thePDCD6IPI allele significantly decreased the risk of BC (OR=0.59, 95%CI=0.45–0.78,p<0.001) compared to the D allele.

Funder

Zahedan University of Medical Sciences

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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