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谷胱甘肽S-转移酶O2基因rs157077多态性预测肝细胞癌经动脉化疗栓塞术的疗效。

Glutathione S-transferase O2 gene rs157077 polymorphism predicts response to transarterial chemoembolization in hepatocellular carcinoma.

作者信息

Wang Zhixin, Qu Kai, Huang Zhichao, Xu Xinsen, Zhang Jingyao, Zhang Li, Liu Sinan, Chang Hulin, Lin Ting, Liu Yamin, Niu Wenquan, Liu Chang

机构信息

Department of Hepatobiliary Surgery, The First Affiliated Hospital of Medical College, Xi'an Jiaotong University, Yanta West Road 277, Xi'an, 710061, Shaanxi Province, China.

出版信息

Tumour Biol. 2015 Aug;36(8):6463-9. doi: 10.1007/s13277-015-3336-z. Epub 2015 Apr 3.

Abstract

Some genetic alterations of glutathione S-transferase omega 2 (GSTO2) have been reported to increase the risk of many malignancies, including hepatocellular carcinoma (HCC); however, their prognostic capability remained unresolved in HCC patients treated with transarterial chemoembolization (TACE). To fill this gap, we genotyped three well-defined polymorphisms in GSTO2 to assess whether they can predict overall survival among 228 HCC patients under TACE treatment. The median follow-up time and survival time were 22.0 months (range 3.0-60.0) and 19.2 months, respectively. Only one of three polymorphisms examined, rs157077, was significantly associated with overall survival of TACE-treated HCC (P = 0.003), and its mutant allele conferred a higher risk of death than its wild homozygotes (hazard ratio 1.58, 95 % confidence interval 1.17-2.14). Moreover, carriers of this mutant allele had higher tissue GSTO2 expression, reinforcing the prognostic capability of GSTO2 rs157077 for HCC, especially in combination with age and tumor-node-metastasis (TNM) stage. Taken together, we for the first time provided evidence supporting the prognostic role of GSTO2 in the progression of TACE-treated HCC.

摘要

据报道,谷胱甘肽S-转移酶ω2(GSTO2)的一些基因改变会增加包括肝细胞癌(HCC)在内的多种恶性肿瘤的风险;然而,在接受经动脉化疗栓塞(TACE)治疗的HCC患者中,其预后能力仍未明确。为填补这一空白,我们对GSTO2中三个明确的多态性进行基因分型,以评估它们是否能预测228例接受TACE治疗的HCC患者的总生存期。中位随访时间和生存时间分别为22.0个月(范围3.0 - 60.0)和19.2个月。在所检测的三个多态性中,只有rs157077与TACE治疗的HCC的总生存期显著相关(P = 0.003),其突变等位基因比野生纯合子具有更高的死亡风险(风险比1.58,95%置信区间1.17 - 2.14)。此外,该突变等位基因的携带者具有更高的组织GSTO2表达,这增强了GSTO2 rs157077对HCC的预后能力,特别是与年龄和肿瘤-淋巴结-转移(TNM)分期相结合时。综上所述,我们首次提供了支持GSTO2在TACE治疗的HCC进展中具有预后作用的证据。

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