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Immunological Investigations
A Journal of Molecular and Cellular Immunology
Volume 46, 2017 - Issue 5
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Original Articles

Association of PD-1.5 C/T, but Not PD-1.3 G/A, with Malignant and Benign Brain Tumors in Iranian Patients

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Pages 469-480 | Published online: 23 May 2017
 

ABSTRACT

Programmed death-1 (PD-1) negatively regulates the immune response. The aims of this study were to assess the association of two single nucleotide polymorphisms in the PD-1 gene, PD-1.5 (+7785 C/T–rs2227981) and PD-1.3 (+7146 G/A- rs11568821), with benign and malignant brain tumors. Patients with brain tumors (96 patients with benign and 56 with malignant brain tumors) and 150 healthy control individuals were included. PCR-RFLP was performed for genotyping. It was revealed that the genotype and allele frequencies of PD-1.5 C/T polymorphism were significantly different between all brain tumor patients and the control group. The frequencies of the CT genotype and T allele were higher in brain tumor patients. In contrast, the frequency of PD-1.3 G/A genotypes and alleles showed no significant difference between all brain tumor patients and controls. Patients were then divided into malignant and benign groups. The results revealed a significant difference in both patients groups compared with the controls only at PD-1.5 C/T position. Arlequin analysis showed the GC haplotype was the most frequent haplotype in the whole group of patients and controls, and the GT haplotype was significantly different between patient and control groups. In conclusion, we demonstrate that PD-1.5 C/T polymorphism, but not PD-1.3 G/A, is associated with brain tumors in Iranian patients.

Acknowledgment

The present study was a part of the M.Sc. thesis by F. Namavar Jahromi, Department of Immunology, International Campus, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Declaration of interest

The authors state that there are no conflicts of interest.

Funding

This work was supported by grants from Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran.

Additional information

Funding

This work was supported by grants from Shiraz Institute for Cancer Research, Shiraz University of Medical Sciences, Shiraz, Iran.

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