Yu Guo-Peng, Xiao Qian-Yi, Shi Zhu-Qing, Tang Li-Sha, Ma Xiao-Pin, Zhang Lu-Yao, Chen Hai-Tao, Wang Wen-Jia, Zhang Peng-Yin, Ding Dong-Lin, Huang Hui-Xing, Saiyin Hexige, Chen Tao-Yang, Lu Pei-Xin, Wang Neng-Jin, Yu Hong-Jie, Sun Jie-Lin, Zheng S Lilly, Xu Jian-Feng, Yu Long, Jiang De-Ke
State Key Laboratory of Genetic Engineering, Collaborative Innovation Center for Genetics and Development, School of Life Sciences, Fudan University Shanghai, China ; Ministry of Education Key Laboratory of Contemporary Anthropology, School of Life Sciences, Fudan University Shanghai, China ; Center for genetic Epidemiology, School of Life Sciences, Fudan University Shanghai, China ; Center for Genetic Translational Medicine and Prevention, School of Public Health, Fudan University Shanghai, China ; Fudan Institute of Urology, Huashan Hospital, Fudan University Shanghai, China ; Department of Urology, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University Shanghai, China ; Center for Cancer Genomics, Wake Forest University School of Medicine Winston-Salem, North Carolina, USA.
Center for Genetic Translational Medicine and Prevention, School of Public Health, Fudan University Shanghai, China.
Am J Cancer Res. 2015 Sep 15;5(10):3249-59. eCollection 2015.
The apoptotic pathway is important in the control of vital processes of hepatocellular carcinoma (HCC). In the current study, we aimed to determine whether apoptotic gene-related polymorphisms modified HCC prognosis. We genotyped 16 single nucleotide polymorphisms (SNPs) in 10 core genes (TP53, TP53INP1, TP53BP1, CDKN2A, CDKN1A, CDKN1B, MDM2, BAX, CCDN1 and BCL2) in the apoptotic pathway by using DNA from blood samples of 362 HCC patients receiving surgical resection of HCC tumor. The associations between genotypes/haplotypes of the 10 genes and overall survival (OS) of HCC patients were assessed using the Cox proportional hazards model. We found one CDKN1B haplotype CCT/ACT (constructed by rs36228499 C>A, rs34330 C>T and rs2066827 T>G) significantly associated with decreased OS of HCC patients, compared to the common haplotype ACT/CTT both in univariate analysis (P=0.013, HR=1.198, 95% CI: 1.039-1.381) and multivariate analysis (P=0.006, HR=1.224, 95% CI: 1.059-1.413). We also find two SNPs (rs560191 G>C and rs2602141 T>G) in TP53BP1 shown to be marginally significantly associated with decreased OS of HCC patients. However, none of the other SNPs or haplotypes were significantly associated with HCC OS. Our results illustrated the potential use of CDKN1B haplotype as a prognostic marker for HCC patients with surgical resection of tumor.
凋亡途径在肝细胞癌(HCC)重要生命过程的控制中发挥着重要作用。在本研究中,我们旨在确定凋亡基因相关多态性是否会改变HCC的预后。我们利用362例接受HCC肿瘤手术切除的患者血样中的DNA,对凋亡途径中10个核心基因(TP53、TP53INP1、TP53BP1、CDKN2A、CDKN1A、CDKN1B、MDM2、BAX、CCDN1和BCL2)中的16个单核苷酸多态性(SNP)进行了基因分型。使用Cox比例风险模型评估这10个基因的基因型/单倍型与HCC患者总生存期(OS)之间的关联。我们发现,与常见单倍型ACT/CTT相比,一个CDKN1B单倍型CCT/ACT(由rs36228499 C>A、rs34330 C>T和rs2066827 T>G构建)在单因素分析(P=0.013,HR=1.198,95%CI:1.039-1.381)和多因素分析(P=0.006,HR=1.224,95%CI:1.059-1.413)中均与HCC患者OS降低显著相关。我们还发现TP53BP1中的两个SNP(rs560191 G>C和rs2602141 T>G)与HCC患者OS降低存在边缘显著关联。然而,其他SNP或单倍型均与HCC的OS无显著关联。我们的结果表明,CDKN1B单倍型有可能作为接受肿瘤手术切除的HCC患者的预后标志物。