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OPN gene polymorphisms are associated with susceptibility and clinicopatholigical characteristics of cervical cancer in a Chinese cohort

机译:OPN基因多态性与中国人群子宫颈癌的易感性和临床病理特征相关

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摘要

Aim: To explore the possible association between Osteopontin (OPN) genetic polymorphisms and cervical cancer risk,nwhich remains undocumented yet.nMethod: We enrolled 300 patients with histologically confirmed cervical squamous cell carcinoma and 774 age-matched healthy,nunrelated, cancer-free female healthy subjects as control subjects. Three OPN gene polymorphisms were determined.nReulsts: The genotype distributions and allele frequencies of −156 GG/G and −443 T/C polymorphisms were significantlyndiffered between cervical cancer patients and controls. The cervical cancer cases had markedly higher percentage of −156 GGncarriage and significantly lower TT and TC of −443 genotypes than controls. The Logistic regression analysis showed that then−156 GG carriage was associated with significantly elevated OR of 2.492 for cervical cancer while the TT and TC of −443nrepresented lower risks. This trend was not seen in subjects without human papillomavirus infections. In addition, the −156 GGncarriages was significantly associated with poorer clinical conditions, including higher clinical stage, poorer tumor differentiation,nhigher positive lymph node status and higher chance of parametrical invasion. The −443 T/C and −66 T/G polymorphisms didnnot show any association with the clinicopathological feature.nConclusion: These results suggest that the −156 GG/G and −443T/C polymorphisms might be used as a genetic marker forncervical cancer susceptibility.
机译:目的:探讨骨桥蛋白(OPN)基因多态性与宫颈癌风险之间的可能关联,目前尚未有文献报道。n方法:我们招募了300例经组织学证实为宫颈鳞状细胞癌的患者和774例年龄相匹配的健康,无相关性,无癌的女性健康受试者作为对照受试者。确定了三个OPN基因多态性。n结果:子宫颈癌患者和对照组的基因型分布和-156 GG / G和-443 T / C基因型的等位基因差异显着。与对照组相比,宫颈癌病例的-156 G导流百分比显着较高,而-443基因型的TT和TC明显较低。 Logistic回归分析显示,当时-156 GG携带子宫颈癌的OR显着升高,为2.492,而TT和TC为-443n则代表较低的风险。在没有人乳头瘤病毒感染的受试者中未观察到这种趋势。此外,−156 GGncarriages与较差的临床状况显着相关,包括较高的临床分期,较差的肿瘤分化,较高的阳性淋巴结状态和较高的参数侵入机率。 −443 T / C和-66 T / G多态性与临床病理特征没有任何关联。n结论:这些结果表明,−156 GG / G和−443T / C多态性可作为宫颈癌易感性的遗传标记。 。

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