| Autor: |
Hashemi M; Zahedan University of Medical Sciences Cellular and Molecular Research Center Zahedan Iran mhd.hashemi@gmail.com., Shahkar G; Zahedan University of Medical Sciences Department of Clinical Biochemistry, School of Medicine Zahedan Iran., Simforoosh N; Shahid Beheshti University of Medical Sciences Urology and Nephrology Research Center; Department of Urology, Shahid Labbafinejad Medical Center Tehran Iran., Basiri A; Shahid Beheshti University of Medical Sciences Urology and Nephrology Research Center; Department of Urology, Shahid Labbafinejad Medical Center Tehran Iran., Ziaee SA; Shahid Beheshti University of Medical Sciences Urology and Nephrology Research Center; Department of Urology, Shahid Labbafinejad Medical Center Tehran Iran., Narouie B; Shahid Beheshti University of Medical Sciences Urology and Nephrology Research Center; Department of Urology, Shahid Labbafinejad Medical Center Tehran Iran., Taheri M; Zahedan University of Medical Sciences Genetics of Non Communicable Disease Research Center Zahedan Iran. |
| Jazyk: |
angličtina |
| Zdroj: |
Cellular and molecular biology (Noisy-le-Grand, France) [Cell Mol Biol (Noisy-le-grand)] 2015 Oct 16; Vol. 61 (5), pp. 16-21. Date of Electronic Publication: 2015 Oct 16. |
| Abstrakt: |
The atypical protein kinase C iota (aPKCι) is an oncoprotein encoded by the PRKCI gene. It has been reported to play multifunctional roles in cellular maintenance, cell proliferation, survival, differentiation and apoptosis. In the present study we aimed to assess the impact of PRKCI rs546950 C>T and rs4955720 C>A polymorphisms on prostate cancer (PCa) risk in a sample of Iranian population. This case-control study was done on 169 patients with pathologically confirmed PCa and 182 benign prostatic hyperplasia (BPH). The PCR-RFLP method was used for detection rs546950 C>T and rs4955720 C>A polymorphisms. Our findings showed that rs546950 polymorphism of PRKCI decreased the risk of PCa in codominant (OR=0.35, 95%CI=0.19-0.64, P<0.001, CT vs CC) and dominant (OR=0.39, 95%CI=0.22-0.69, P=0.001, CT+TT vs CC) inheritance model tested. No significant association was found between rs4955720 C>A polymorphism and PCa. In the combined analysis of these two variants subjects carrying CT/CC, CT/CA, TT/AA and CT/AA significantly decreased the risk of PCa in comparison with rs546950 CC/rs4955720 CC genotype. Haplotype analysis indicated that rs546950T/rs4955720A decreased the risk of PCa compared to CC. In conclusion, the results revealed that PRKCI rs546950 variant decreased the risk of PCa in an Iranian population. Further studies with larger sample sizes and different ethnicities are required to confirm our findings. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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