Gu Cheng-Yuan, Qin Xiao-Jian, Qu Yuan-Yuan, Zhu Yu, Wan Fang-Ning, Zhang Gui-Ming, Sun Li-Jiang, Zhu Yao, Ye Ding-Wei
Department of Urology, Fudan University Shanghai Cancer Center Department of Oncology, Shanghai Medical College, Fudan University, Shanghai Department of Urology, the Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Medicine (Baltimore). 2016 Jul;95(27):e4066. doi: 10.1097/MD.0000000000004066.
Clinically localized prostate cancer is curative. Nevertheless many patients suffered from biochemical recurrence (BCR) after radical prostatectomy (RP). Mounting evidence suggest that estrogen and xenobiotic carcinogens play an essential role in progression of prostate cancervia oxidative estrogen metabolism. CYP1B1 is an enzyme involved in the hydroxylation of estrogens, a reaction of key relevance in estrogen metabolism. Given the role of CYP1B1 in the oxidative metabolism of endogenous/exogenous estrogen and compounds, CYP1B1 polymorphisms have the potential to modify its expression and subsequently lead to progression. We hypothesize that genetic variants of the CYP1B1 gene may influence clinical outcome in clinically localized prostate cancer patients. In this cohort study, we genotyped 9 tagging single nucleotide polymorphisms (SNPs) from the CYP1B1 gene in 312 patients treated with RP. For replication, these SNPs were genotyped in an independent cohort of 426 patients. The expression level of CYP1B1 in the adjacent normal prostate tissues was quantified by reverse transcription and real-time polymerase chain reaction. Kaplan-Meier analysis and Cox proportional hazard models were utilized to identify SNPs that correlated with BCR. CYP1B1 rs1056836 was significantly associated with BCR (hazard ratio [HR]: 0.69; 95% confidence interval [CI]: 0.40-0.89, P = 0.002) and relative CYP1B1 mRNA expression. Our findings suggest inherited genetic variation in the CYP1B1 gene may contribute to variable clinical outcomes for patients with clinically localized prostate cancer.
临床局限性前列腺癌是可治愈的。然而,许多患者在根治性前列腺切除术(RP)后出现生化复发(BCR)。越来越多的证据表明,雌激素和外源性致癌物通过氧化雌激素代谢在前列腺癌进展中起重要作用。CYP1B1是一种参与雌激素羟基化的酶,这是雌激素代谢中的一个关键反应。鉴于CYP1B1在内源性/外源性雌激素及化合物的氧化代谢中的作用,CYP1B1基因多态性有可能改变其表达,进而导致疾病进展。我们假设CYP1B1基因的遗传变异可能影响临床局限性前列腺癌患者的临床结局。在这项队列研究中,我们对312例接受RP治疗的患者的CYP1B1基因中的9个标签单核苷酸多态性(SNP)进行了基因分型。为了进行验证,在一个由426例患者组成的独立队列中对这些SNP进行了基因分型。通过逆转录和实时聚合酶链反应对相邻正常前列腺组织中CYP1B1的表达水平进行定量。采用Kaplan-Meier分析和Cox比例风险模型来确定与BCR相关的SNP。CYP1B1 rs1056836与BCR(风险比[HR]:0.69;95%置信区间[CI]:0.40-0.89,P = 0.002)及相对CYP1B1 mRNA表达显著相关。我们的研究结果表明,CYP1B1基因中的遗传变异可能导致临床局限性前列腺癌患者出现不同的临床结局。