IL17A and IL17F Genetic Variations in Iranian Patients with Urothelial Bladder Cancer: A Case-Control Study

IF 0.4 Q4 ONCOLOGY
Arsalan Aslani, M. Haghshenas, N. Erfani, A. Khezri
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引用次数: 1

Abstract

Background: Interleukin 17 (IL17) is a pro-inflammatory cytokine with pivotal modulatory effects on antitumor immune responses and has been reported to play a particularly important role in the occurrence and development of bladder cancer. We aimed to investigate the possible influence of IL17 genetic variations on loci rs22775913 and rs763780 with genetic susceptibility to bladder cancer in southern Iran. Method: In this case-control study, we enrolled 180 patients with urothelial bladder cancer (mean age 64 years) and 180 age/gender matched healthy controls without any family history of cancer and autoimmune disorders. Genomic DNA was extracted from peripheral whole blood, and genotyping was performed using PCR-RFLP method. Results: Genotype distributions in both the patients and controls were in agreement with Hardy-Weinberg equilibrium. The frequency of GG, GA, and AA genotypes for IL17A were 87 (48.3%), 72 (40%), and 21 (11.7%) among patients, and 92 (51.1%), 75 (41.6%), and 13 (7.3%) in the controls. The frequency of AA, AG, and GG genotypes for IL17F in both the patients/controls were 160 (88.9%)/ 158 (87.8%), 16 (8.9%)/ 21 (11.7%), and 4 (2.2%)/ 1 (0.5%), respectively. Statistical analysis revealed no significant differences between the two groups regarding the frequency of genotypes and alleles (P>0.05). Conclusion: Our data collectively suggested that genetic variations on loci rs22775913 and rs763780 of IL17 genes were not associated with bladder cancer susceptibility in the Iranian population. Our finding has to be confirmed in different ethnic groups.
伊朗尿路上皮性膀胱癌患者IL17A和IL17F基因变异:一项病例对照研究
背景:白细胞介素17(IL17)是一种促炎细胞因子,对抗肿瘤免疫反应具有关键的调节作用,已被报道在膀胱癌症的发生和发展中起着特别重要的作用。我们的目的是研究IL17基因在rs22775913和rs763780位点的遗传变异对伊朗南部癌症遗传易感性的可能影响。方法:在这项病例对照研究中,我们招募了180名癌症尿路上皮患者(平均年龄64岁)和180名年龄/性别匹配的健康对照者,他们没有任何癌症和自身免疫性疾病的家族史。从外周血中提取基因组DNA,用PCR-RFLP方法进行基因分型。结果:患者和对照组的基因型分布符合Hardy-Weinberg平衡。患者中IL17A的GG、GA和AA基因型频率分别为87(48.3%)、72(40%)和21(11.7%),对照组为92(51.1%)、75(41.6%)和13(7.3%)。患者/对照组IL17F的AA、AG和GG基因型频率分别为160(88.9%)/158(87.8%)、16(8.9%)/21(11.7%)和4(2.2%)/1(0.5%)。统计分析显示,两组基因型和等位基因频率无显著差异(P>0.05)。结论:我们的数据共同表明,伊朗人群IL17基因rs22775913和rs763780位点的遗传变异与膀胱癌症易感性无关。我们的发现必须在不同的种族群体中得到证实。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
0
审稿时长
12 weeks
期刊介绍: Middle East Journal of Cancer (MEJC) is an international peer-reviewed journal which aims to publish high-quality basic science and clinical research in the field of cancer. This journal will also reflect the current status of research as well as diagnostic and treatment practices in the field of cancer in the Middle East, where cancer is becoming a growing health problem. Lastly, MEJC would like to become a model for regional journals with an international outlook. Accordingly, manuscripts from authors anywhere in the world will be considered for publication. MEJC will be published on a quarterly basis.
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