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从头脂肪生成途径基因中的遗传变异可预测手术治疗的肝细胞癌的预后。

Genetic variants in de novo lipogenic pathway genes predict the prognosis of surgically-treated hepatocellular carcinoma.

作者信息

Jiang Hequn, Dai Jingyao, Huang Xiaojun, Chen Yibing, Qu Ping, Li Jibin, Yi Cheng, Yang Yefa, Zhang Kejing, Huang Qichao

机构信息

Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, China.

Department of Hepatobiliary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, 710032, China.

出版信息

Sci Rep. 2015 Mar 26;5:9536. doi: 10.1038/srep09536.

Abstract

Over-expression of de novo lipogenesis (DNL) pathway genes is associated with the prognosis of various types of cancers. However, effects of single nucleotide polymorphisms (SNPs) in these genes on recurrence and death of hepatocellular carcinoma (HCC) patients after surgery are still unknown. A total of 492 primary HCC patients treated with surgery were included in this study. Nine SNPs in 3 genes (ACACA, FASN and ACLY) of DNL pathway were genotyped. Multivariate Cox proportional hazard regression model and Kaplan-Meier curve were used to analyze the association of SNPs with clinical outcomes. Two SNPs in ACACA gene were significantly associated with overall survival of HCC patients. Patients carrying homozygous variant genotype (VV) in rs7211875 had significantly increased risk of death, while patients carrying VV genotype in rs11871275 had significant decreased risk of death, when compared with those carrying homozygous wild-type or heterozygous genotypes. Moreover, patients carrying VV genotype in rs11871275 had decreased recurrence risk, while patients carrying variant genotype in rs4485435 of FASN gene had increased recurrence risk. Further cumulative effect analysis showed significant dose-dependent effects of unfavorable SNPs on both death and recurrence. SNPs in DNL genes may serve as independent prognostic markers for HCC patients after surgery.

摘要

从头脂肪生成(DNL)途径基因的过表达与多种癌症的预后相关。然而,这些基因中的单核苷酸多态性(SNP)对肝细胞癌(HCC)患者术后复发和死亡的影响仍不清楚。本研究共纳入492例接受手术治疗的原发性HCC患者。对DNL途径的3个基因(ACACA、FASN和ACLY)中的9个SNP进行基因分型。采用多变量Cox比例风险回归模型和Kaplan-Meier曲线分析SNP与临床结局的相关性。ACACA基因中的两个SNP与HCC患者的总生存期显著相关。与携带纯合野生型或杂合基因型的患者相比,rs7211875中携带纯合变异基因型(VV)的患者死亡风险显著增加,而rs11871275中携带VV基因型的患者死亡风险显著降低。此外,rs11871275中携带VV基因型的患者复发风险降低,而FASN基因rs4485435中携带变异基因型的患者复发风险增加。进一步的累积效应分析表明,不利SNP对死亡和复发均有显著的剂量依赖性效应。DNL基因中的SNP可能作为HCC患者术后独立的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4997/4379911/c29ee51a65e8/srep09536-f1.jpg

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