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多态性对肝细胞癌发生发展及临床特征的影响。

Effects of polymorphisms on hepatocellular carcinoma development and clinical characteristics.

作者信息

Lin Chien-Hua, Hsieh Ming-Ju, Lee Hsiang-Lin, Yang Shun-Fa, Su Shih-Chi, Lee Wei-Jiunn, Chou Ying-Erh

机构信息

Department of Surgery, Chang Bing Show Chwan Memorial Hospital, Changhua, Taiwan.

Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan.

出版信息

J Cancer. 2020 Jan 14;11(6):1641-1647. doi: 10.7150/jca.38856. eCollection 2020.

Abstract

Hepatocellular carcinoma (HCC) is a major malignancy of cancer-related mortality worldwide. Metastasis-associated in colon cancer-1 (MACC1) was suggested as a marker for vascular invasive HCC. This study investigated the single-nucleotide polymorphisms (SNPs) to evaluate HCC susceptibility and clinicopathological characteristics. In this study, real-time polymerase chain reaction was applied to analyze five SNPs of rs1990172, rs975263, rs3095007, rs4721888, and rs3735615 in 378 patients with HCC and 1199 cancer-free controls. The results showed that in 151 HCC patients among smokers who carried rs1990172 "CA + AA" variants had a lower risk of developing a large tumor (odds ratio [OR] = 0.375, = 0.026), more advanced clinical stage ([OR] = 0.390, =0.032), and vascular invasion ([OR] = 0.198, = 0.034). In 137 HCC patients among drinkers who carried rs4721888 "GC + CC" variants had a higher risk to develop vascular invasion ([OR] = 3.780, = 0.009). Further analyses revealed a statistical significance of aberrant AST/ALT ratio in HCC patients with rs975263 "AG+GG" variants before adjustment of age and alcohol drinking. In conclusion, our results suggested that the SNPs rs1990172, rs4721888, and rs975263 are involved in HCC progression and clinical characteristics. polymorphisms may serve as a marker or a predictor to evaluate HCC progression and prognosis.

摘要

肝细胞癌(HCC)是全球癌症相关死亡的主要恶性肿瘤。结肠癌转移相关蛋白1(MACC1)被认为是血管侵袭性HCC的标志物。本研究调查了单核苷酸多态性(SNP)以评估HCC易感性和临床病理特征。在本研究中,应用实时聚合酶链反应分析了378例HCC患者和1199例无癌对照者中rs1990172、rs975263、rs3095007、rs4721888和rs3735615的五个SNP。结果显示,在151例携带rs1990172“CA + AA”变体的吸烟HCC患者中,发生大肿瘤的风险较低(优势比[OR]=0.375,P = 0.026),临床分期更晚([OR]=0.390,P = 0.032),且血管侵袭发生率更低([OR]=0.198,P = 0.034)。在137例携带rs4721888“GC + CC”变体的饮酒HCC患者中,发生血管侵袭的风险较高([OR]=3.780,P = 0.009)。进一步分析显示,在调整年龄和饮酒因素之前,携带rs975263“AG+GG”变体的HCC患者中异常AST/ALT比值具有统计学意义。总之,我们的结果表明,SNP rs1990172、rs4721888和rs975263参与了HCC的进展和临床特征。这些多态性可能作为评估HCC进展和预后的标志物或预测指标。

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