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CCR5-Delta32 polymorphism and susceptibility to cervical cancer: association with early stage of cervical cancer.

机译:CCR5-Delta32基因多态性和对子宫颈癌的易感性:与子宫颈癌的早期阶段相关。

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摘要

Inflammation plays a major role in the pathogenesis of cervical cancer. Chemokines are involved in inflammation, cancer, and infectious diseases. Therefore, we evaluated the association of the chemokine receptor gene polymorphism CCR5 Delta32 with risk of cervical cancer. A total of 150 histopathologically confirmed patients with cervical cancer and 162 age and ethnically matched cervical cytology negative healthy controls were genotyped for CCR5 Delta32 polymorphisms using PCR. Association of CCR5 Delta32 genotypes with risk of cervical cancer, clinical stages, and tobacco exposure was analyzed using chi-square statistical tests. The frequency of the mutant allele CCR5 Delta32 was higher in patients with cervical carcinoma (2.3%) but there was no statistically significant difference (OR = 1.51; p = 0.685;). Association of CCR5 genotypes with clinical phenotypes showed significant risk with stage IB patients due to CCR5+/Delta32 genotype (OR = 4.43; p = 0.021). Furthermore, patients with CCR5+/Delta32 genotype and tobacco usage were at risk of cervical cancer (OR = 1.73, 95% CI = 0.27-1.28). In summary, CCR5 heterozygous genotype (+/Delta32) may significantly influence the early stage of cervical cancer development. However, the cervical cancer risk due to tobacco usage was not significantly modulated after interaction with CCR5+/Delta32 genotype.
机译:炎症在子宫颈癌的发病机理中起主要作用。趋化因子与炎症,癌症和传染病有关。因此,我们评估了趋化因子受体基因多态性CCR5 Delta32与宫颈癌风险的关联。使用PCR对150例经组织病理学证实的宫颈癌和162例年龄与种族相匹配的宫颈细胞学阴性健康对照患者进行了CCR5 Delta32多态性基因分型。使用卡方统计检验分析了CCR5 Delta32基因型与子宫颈癌风险,临床分期和烟草暴露的关系。宫颈癌患者中突变等位基因CCR5 Delta32的频率较高(2.3%),但无统计学差异(OR = 1.51; p = 0.685;)。 CCR5基因型与临床表型的关联显示,由于CCR5 + / Delta32基因型,IB期患者存在显着风险(OR = 4.43; p = 0.021)。此外,具有CCR5 + / Delta32基因型和吸烟习惯的患者有患宫颈癌的风险(OR = 1.73,95%CI = 0.27-1.28)。总之,CCR5杂合基因型(+ / Delta32)可能会显着影响子宫颈癌发展的早期阶段。然而,与CCR5 + / Delta32基因型相互作用后,由于吸烟引起的宫颈癌风险并未得到明显调节。

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