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Association of TNFAIP8 gene polymorphisms with endometrial cancer in northern Chinese women

机译:TNFAIP8基因多态性与中国北方女性子宫内膜癌的关系

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Tumor necrosis factor-a-induced protein 8 (TNFAIP8) presented a elevated expression in endometrial cancer (EC). However, the relationship of TNFAIP8 gene polymorphisms with EC risk remains unclear. This case–control study aimed to investigate the effect of single nucleotide polymorphisms (SNPs) in TNFAIP8 on northern Chinese women with EC. SNP rs11064, rs1045241, and rs1045242 in TNFAIP8 were successfully genotyped in 248 cancer-free controls and 226 ECs by SNaPshot method, respectively. Logistic regression was performed to assess relationship of SNPs with EC risk. The relationships of SNPs with clinicopathological variables were evaluated by Chi-square test or Student’s t-test or Fisher’s text. The minor alleles of rs11064 in TNFAIP8 were strongly associated with EC risk, with adjust odds ratio (OR) of 1.719 (95% CI 1.180–2.506, P?=?0.005). The minor allele of rs1045242 in the TNFAIP8 gene was strongly associated with with EC risk (adjust OR: 1.636, 95% CI 1.107–2.417, P?=?0.014). rs11064 SNPs correlated with TNFAIP8 protein expression in EC (P?=?0.015). For rs1045242, patients with AG?+?GG presented higher TNFAIP8 protein expression than that with AA (P?=?0.020). It also showed that SNP rs11064 was associated with advanced FIGO stage (P?=?0.001), deep myometrial invasion (P?=?0.047), and lymph node metastasis (P?=?0.048) under the codominant model in ECs. SNP rs11064 in TNFAIP8 increased EC risk and significantly related with its protein expression in northern Chinese women.
机译:肿瘤坏死因子-α诱导蛋白8(TNFAIP8)在子宫内膜癌(EC)中表达升高。然而,TNFAIP8基因多态性与EC风险的关系仍不清楚。这项病例对照研究旨在研究TNFAIP8中单核苷酸多态性(SNP)对中国北方女性EC的影响。通过SNaPshot方法分别在248个无癌对照和226个EC中成功分型了TNFAIP8中的SNP rs11064,rs1045241和rs1045242。进行逻辑回归以评估SNP与EC风险的关系。通过卡方检验或学生t检验或Fisher文本评估SNP与临床病理变量之间的关系。 TNFAIP8中rs11064的次要等位基因与EC风险密切相关,调整比值比(OR)为1.719(95%CI 1.180-2.506,P <= 0.005)。 TNFAIP8基因中rs1045242的次要等位基因与EC风险密切相关(调整OR:1.636,95%CI 1.107-2.417,P <= 0.014)。 rs11064 SNPs与EC中的TNFAIP8蛋白表达相关(P = 0.015)。对于rs1045242,AGα+ΔGG患者的TNFAIP8蛋白表达高于AA患者(Pα=α0.020)。这也表明在ECs的显性模型下,SNP rs11064与FIGO的晚期阶段(P <= 0.001),深肌层浸润(P = 0.047)和淋巴结转移(P = 0.048)有关。在中国北方女性中,TNFAIP8中的SNP rs11064增加EC风险,并与其蛋白表达显着相关。

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