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dc.contributor.authorAbbasabad, GD
dc.contributor.authorKhojasteh, SMB
dc.contributor.authorNaji, HE
dc.contributor.authorZamani, MR
dc.contributor.authorHajipour, H
dc.contributor.authorSerati-Nouri, H
dc.date.accessioned2018-08-26T08:34:01Z
dc.date.available2018-08-26T08:34:01Z
dc.date.issued2018
dc.identifier10.22034/APJCP.2018.19.6.1717
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52500
dc.description.abstractObjective: Interleukin-6 (IL-6) is an inflammatory cytokine shown to be a strong factor for growth, proliferation and metastasis with many malignancies. The promoter single nucleotide polymorphism (SNPs) -174G > C (rs1800795) can alter the transcriptional pattern of this gene. The present study was aimed at assessing effects of the IL-6 (rs1800795) SNP on risk of benign prostate hyperplasia (BPH) and prostatic adenocarcinoma (PCa). Methods: The project was performed on 112 men with PCa, 118 with BPH and 250 healthy controls. After DNA extraction, genotyping of IL-6 (rs1800795) was performed using PCR TaqMan Allelic Discrimination (ABI MGB). Results: The G allele frequency for rs1800795 of the IL-6 gene was 74.1%, 68.6% and 67% in PCa patients, BPH patients and healthy men, respectively. PCa and control groups showed significant differences (P =0.030, OR = 1.73, 95% CI: 1.05-2.21). The GG genotype was more frequent in the PCa group, whereas the GC genotype was more common in the BPH in comparison to other groups. Conclusion: The current study identified IL-6 -174G > C (rs1800795) as a significant predictor of susceptibility for prostate cancer and bone metastasis in a northwest Iranian population. é 2018, Asian Pacific Organization for Cancer Prevention.
dc.language.isoEnglish
dc.relation.ispartofAsian Pacific Journal of Cancer Prevention
dc.titleAn interleukin-6 single nucleotide polymorphism and susceptibility to prostate adenocarcinoma and bone metastasis in an Iranian population
dc.typeArticle
dc.citation.volume19
dc.citation.issue6
dc.citation.spage1717
dc.citation.epage1720
dc.citation.indexScopus
dc.identifier.DOI10.22034/APJCP.2018.19.6.1717


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