A functional polymorphism in PER3 gene is associated with prognosis in hepatocellular carcinoma

Abstract Background Previous studies have revealed that circadian genes play important roles in cell proliferation, apoptosis, cell cycle control, DNA damage response and treatment response of chemotherapy agents in cancers. Aims We hypothesized that the polymorphisms in circadian genes may be associated with prognosis of hepatocellular carcinoma ( HCC ) patients treated with transcatheter arterial chemoembolization ( TACE ). Methods Twelve functional single nucleotide polymorphisms ( SNP s) in circadian negative feedback regulation genes (including CRY 1, CRY 2, PER 1, PER 2 and PER 3 ) were genotyped using S equenom iPLEX genotyping method in 337 HCC patients treated with TACE and analysed for associations with overall survival. Results Our data showed that one SNP rs2640908 in PER 3 gene was significantly associated with overall survival of HCC patients ( P = 0.027). Patients carrying at least one variant allele of rs2640908 ( WV + VV ) had a significantly decreased risk of death (hazard ratio, 0.71; 95% confidence interval, 0.53–0.90), when compared with those carrying homozygous wild‐type alleles ( WW ). K aplan– M eier analyses showed a significantly longer median survival time in patients with WV + VV genotypes of SNP rs2640908 than those with WW genotype (11.6 months vs. 8.1 months; log rank P = 0.030). In addition, we also observed a significant difference on the genotype distribution of SNP rs2640908 in patients with and without portal vein thrombus ( P = 0.041). Conclusions Our study provides the first evidence that a single functional polymorphism of PER 3 gene is significantly associated with overall survival in HCC patients treated with TACE .