
PP50. INVESTIGATION THE ASSOCIATION BETWEEN HUMAN HERPESVIRUS (HSV) 1, 2, 6 , 7 POSITIVE AND TLR9 GENE POLYMORPHISM IN THE PROSTATE CANCER EBRU ETEM1, Yasemin Bulut2, Nusret Akpolat3, Ebru Korkmaz2, Hüseyin Yüce1, Mehmet Yapar4.
1. Firat University, Medical Faculty, Department of Medical Biology and Genetic, ELAZIG. 2. Firat University, Medical Faculty, Department of Microbiology and Clinical Microbiology, ELAZIG. 3. Firat University, Medical Faculty, Department of Pathology, ELAZIG. 4. Gulhane Military Medical Academy, Deparment of Virology, ANKARA.
e-mail: ebruetem@gmail.com
*Corresponding Author: page: 70
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Abstract
Objective: The secretion of type 1 IFN in response to herpes simplex virus type 1 (HSV-1) and 2 in vitro is mediated by TLR9. In this study, we purpose whether the any association between TLR9 1635G/A poymorphisms and HSV1,2,6,7 positivity and the incidence of HSV1,2,6,7 are positively linked to infection in the prostate tissue samples.
Material and methods: The DNA was extracted from the parraffin embedded tissues. Four different HSV DNA detection were done by polymerase chain reaction (PCR). Genotyping of TLR9 1635 G/A polymorphism was performed by PCR-Restriction Fragment Lenght Polymorphism (PCR-RFLP). Fischer's test was used for statistical analysis.
Results: HSV DNA positive was detected in 12 of 21 (57.1%) prostate cancer (PCa), in 15 of 24 (62.5%) prostatic intraepithelial neoplasia (PIN) and in 14 of 21 (66.7%) benign prostatic hyperplasia (BPH), all of total 66 samples. Differences in TLR9 1635A/G allelic frequencies were not statistically observed, neither between PCa, PIN and BPH nor between HSV-positive and HSV-negative all samples.
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HSV1 |
HSV2 |
HSV6 |
HSV7 |
Pca (21) |
7 (33.3%) |
7 (33.3%) |
3 (14.3%) |
2 (9.5%) |
PIN (24) |
4 (16.7%) |
7 (29.2%) |
4 (16.7%) |
6 (25%) |
BPH (21) |
2 (9.5%) |
7 (33.3%) |
6 (28.6%) |
2 (9.5%) |
Total |
13 |
21 |
13 |
10 |
Discussion: Our findings indicate that it was not found statiscially significant association between HSV1,2,6,7 and TLR9 1635 G/A polymorphism. As result, we consider that future investigations are needed to provided conclusive evidence on the role of these pathogen and gene in the prostate cancer.
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