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TNF-α、白细胞介素-18 多态性与埃及患者肝细胞癌风险的相关性。

Association between TNF-α, Interleukin-18 Polymorphisms and Risk of Hepatocellular Carcinoma in Egyptian patients.

机构信息

Clinical and Chemical Pathology, Cairo University, Cairo, Egypt.

Clinical and Chemical Pathology, Theodor Bilharz Research Institute, Cairo, Egypt.

出版信息

Asian Pac J Cancer Prev. 2021 Mar 1;22(3):887-891. doi: 10.31557/APJCP.2021.22.3.887.

Abstract

OBJECTIVE

To evaluate the association of gene polymorphisms of the SNP of TNF-α gene -238G>A and IL-18 gene-607C>A with the development of hepatocellular carcinoma among Egyptian patients.

METHODS

One hundred and fifty patients were allocated to this study; eighty patients with hepatocellular carcinoma (Group A), seventy cancer-free HCV age, and sex-matched patients (Group B). We analyzed two Single nucleotide polymorphisms (SNPs) (TNF-α-238G>A and IL-18-607C>A) by real-time polymerase chain reaction using sequence-specific primers (PCR-SSP).

RESULTS

Significant higher risk of HCC was associated with genotype IL-18-607AA (p <0.001), OR: 5(2.188-11.47), allele IL-18 -607⁄A (P=0.001), OR: 2.1(1.32-3.3). A significant association was found between the size of HFL in the HCC group and different genotypes of IL18 genes (P=0.013) where 62.5% of patients with tumor size >5 cm carried the risky (AA) genotype on the other hand the SNP of TNF-α gene -238G>A showed no statistically significant association between the two groups.

CONCLUSION

The SNP -607C>A in the IL18 gene was associated with increased HCC risk in Egyptian patients suggesting its use as a potential diagnostic non-invasive tool that allows to identify a new group of HCC patients at an earlier stage.
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摘要

目的

评估 TNF-α 基因 -238G>A 和 IL-18 基因-607C>A 单核苷酸多态性与埃及患者肝细胞癌发展的相关性。

方法

将 150 例患者纳入本研究;80 例肝细胞癌患者(A 组),70 例无癌症 HCV 年龄和性别匹配患者(B 组)。我们使用序列特异性引物(PCR-SSP)通过实时聚合酶链反应分析了两个单核苷酸多态性(SNP)(TNF-α-238G>A 和 IL-18-607C>A)。

结果

IL-18-607AA 基因型与 HCC 显著相关(p <0.001),OR:5(2.188-11.47),IL-18-607/A 等位基因(P=0.001),OR:2.1(1.32-3.3)。在 HCC 组中,HFL 大小与不同的 IL18 基因基因型之间存在显著相关性(P=0.013),其中 62.5%肿瘤大小>5cm 的患者携带风险(AA)基因型,另一方面 TNF-α基因-238G>A 显示两组之间无统计学显著相关性。

结论

IL18 基因中的 SNP-607C>A 与埃及患者 HCC 风险增加相关,表明其可作为一种潜在的诊断非侵入性工具,可更早识别新的 HCC 患者群体。

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