白介素-10基因与易感性和宫颈癌发展相关的遗传变异:一项病例对照研究

IF 1.2 Q4 GENETICS & HEREDITY Global Medical Genetics Pub Date : 2022-02-01 DOI:10.1055/s-0042-1743262
Pushpendra D. Pratap, Syed Tasleem Raza, Ghazala Zaidi, Shipra Kunwar, Sharique Ahmad, M. Charles, A. Eba, Muneshwar Rajput
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引用次数: 2

摘要

目标 癌症(CC)是由持续性HPV感染引起的最具破坏性的疾病之一,影响着世界各地的妇女,尤其是发展中国家的妇女。宿主免疫反应,特别是细胞因子功能的遗传基础已被证明会影响CC易感性。研究表明,IL-10基因多态性与许多恶性肿瘤有关,但与CC相关的结果尚不确定。尽管如此,本研究的目的是研究IL-10-1082A/G和-819C/T启动子多态性与CC易感性之间的关系。材料和方法 这项研究包括192名患有CC的女性和200名对照者。HPV检测采用RT-PCR法,基因分型采用PCR-RFLP法。ELISA法测定血清IL-10浓度。后果 与对照组相比,具有IL-10-1082A/G AG和AG+GG基因型的女性患CC的风险增加了两倍[OR,2.35(95%CI,1.54–3.58),p=0.005],[OR,2.03(95%CI),1.36–3.04),p=0.0005]。与对照组相比,具有-1082A/G多态性的G等位基因的女性与CC易感性相关[OR,1.39(95%CI,1.02-1.88),p=0.036]。IL-10-819C/T多态性的基因型或等位基因频率在患者和对照组之间没有发现显著差异[or,1.00(95%CI,0.63-1.58),p=0.99]。与对照组相比,病例的血清IL-10浓度水平显著升高。结论 这些发现有助于理解IL-10-1082A/G基因多态性与CC发生风险增加有关,并可作为CC遗传易感性的标志。
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Genetic Variants in Interleukin-10 Gene Association with Susceptibility and Cervical Cancer Development: A Case Control Study
Objectives  Cervical cancer (CC) is one of the most destructive disease caused by persistent HPV infection which affects women worldwide, especially in developing countries. The genetic basis of host immune response especially cytokine function has been shown to influence CC susceptibility. Studies have demonstrated that IL-10 gene polymorphism have been associated with numerous malignancies, but in context to CC results were inconclusive. Though, aim of our study to investigate the association between IL-10 -1082A/G and -819C/T promoter polymorphism and CC susceptibility. Material and Methods  This study comprised 192 women with CC and 200 controls. HPV detection was done by RT-PCR and genotyping was assessed through PCR-RFLP method. Serum concentration of IL-10 measured by ELISA. Results  Women with AG and AG+GG genotypes of IL-10 -1082A/G had two-fold increased risk of CC [OR, 2.35 (95% CI, 1.54–3.58), p = 0.005], [OR, 2.03 (95% CI, 1.36–3.04), p = 0.0005] compared to controls. Women with G allele of -1082A/G polymorphism had linked with CC susceptibility [OR, 1.39 (95% CI, 1.02–1.88), p = 0.036] compared to controls. No significant difference was found between patients and controls in the genotype or allele frequencies of IL–10 -819C/T polymorphism [OR, 1.00 (95% CI, 0.63–1.58), p = 0.99]. The level of serum concentration of IL-10 was significantly higher in cases compared to controls. Conclusion  These findings help to understand that polymorphism of IL-10 -1082A/G gene is associated with increased risk of CC development and can serve as a marker of genetic susceptibility to CC.
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来源期刊
Global Medical Genetics
Global Medical Genetics GENETICS & HEREDITY-
自引率
11.80%
发文量
30
审稿时长
14 weeks
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