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Lack of Associations between XPC Gene Polymorphisms and Neuroblastoma Susceptibility in a Chinese Population

机译:中国人口中XPC基因多态性与神经母细胞瘤易感性之间缺乏关联。

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摘要

Neuroblastoma is one of the most malignant solid tumors in infants and young children. No more than 40% of neuroblastoma patients can survive for longer than five years after it has been diagnosed. XPC protein is a pivotal factor that recognizes DNA damage and starts up the nucleotide excision repair (NER) in mammalian cells. This makes up the first group to defend against the cancer. Previous studies have identified that XPC gene polymorphisms were associated with various types of cancer. However, the associations between XPC gene polymorphisms and neuroblastoma risk have not yet been studied. We investigated the associations between three XPC gene polymorphisms (rs2228001 A>C, rs2228000 C>T, and rs2229090 G>C) and neuroblastoma risk with 256 neuroblastoma patients and 531 healthy controls in a Chinese Han population. Odds ratios and 95% confidence intervals were used to access the association between these three polymorphisms and neuroblastoma risk. No significant association was detected between these three polymorphisms and neuroblastoma risk in the overall analysis as well as in the stratification analysis. These results suggest that none of these three polymorphisms may be associated with the risk of neuroblastoma in the Chinese Han population.
机译:神经母细胞瘤是婴幼儿中最恶性的实体瘤之一。诊断后,不超过40%的神经母细胞瘤患者可以存活超过五年。 XPC蛋白是识别DNA损伤并启动哺乳动物细胞中核苷酸切除修复(NER)的关键因素。这是第一个防御癌症的人群。先前的研究已经确定XPC基因多态性与各种类型的癌症有关。但是,尚未研究XPC基因多态性与神经母细胞瘤风险之间的关联。我们调查了中国汉族人群中256名成神经细胞瘤患者和531名健康对照者的3种XPC基因多态性(rs2228001 A> C,rs2228000 C> T和rs2229090 G> C)与神经母细胞瘤风险之间的关联。使用赔率和95%置信区间来了解这三个多态性与成神经细胞瘤风险之间的关联。在整体分析和分层分析中,这三种多态性与神经母细胞瘤风险之间未发现显着关联。这些结果表明,这三种多态性可能与中国汉族人群神经母细胞瘤的风险无关。

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