Chou An-Kuo, Shen Ming-Yi, Chen Fang-Yu, Hsiao Chieh-Lun, Shih Liang-Chun, Chang Wen-Shin, Tsai Chia-Wen, Ying Tsung-Ho, Wu Ming-Hsien, Huang Chung-Yu, Bau DA-Tian
Department of Anesthesiology, China Medical University Hospital, Taichung, Taiwan, R.O.C.
Department of Medical Research, China Medical University Hospital, Taichung, Taiwan Hospital, Taichung, Taiwan, R.O.C.
Cancer Genomics Proteomics. 2017 Nov-Dec;14(6):455-460. doi: 10.21873/cgp.20055.
BACKGROUND/AIM: Flap endonuclease 1 (FEN1), a protein with multiple functions in genome stability maintenance, is important in cancer prevention. The two functional germline variants of FEN1, rs174538 and rs4246215, regarding cancer susceptibility have been reported in lung, breast, liver, esophageal, gastric, colorectal cancer, glioma and leukemia, but not endometriosis. In this study, we firstly aimed at evaluating the contribution of FEN1 genotypes to endometriosis risk in a representative Taiwan population.
In total, 153 patients with endometriosis and 636 non-cancer healthy controls were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) methodology.
The genotypes of FEN1 rs174538, but not those of rs4246215, were differently distributed between the endometriosis and control groups. In detail, the AA of FEN1 rs174538 genotypes were significantly less frequently found among endometriosis patients than among controls (odds ratio [OR]=0.43, 95% confidence interval [CI]=0.24-0.78, p=0.0125). The A allele at FEN1 rs174538 was also significantly less frequent among cases than controls (OR=0.65, 95%CI=0.50-0.86, p=0.0021). As for age of first menarche, those with first menarche at the age >12.8 carrying the FEN1 rs174538 AA genotype conferred lower OR of 0.29 (95%CI=0.11-0.78, p=0.0381) for endometriosis. Regarding the full pregnancy status, those without having had a full-term pregnancy carrying the FEN1 rs174538 AA genotype were of lower risk (ORs=0.12, 95%CI=0.03-0.53, p=0.0050).
The FEN1 rs174538 A allele is a novel protective biomarker for endometriosis and this genotype may have interactions with age- and hormone-related factors on the development of endometriosis.
背景/目的:瓣内切核酸酶1(FEN1)是一种在维持基因组稳定性方面具有多种功能的蛋白质,在癌症预防中具有重要作用。FEN1的两个功能性种系变体rs174538和rs4246215与癌症易感性有关,已在肺癌、乳腺癌、肝癌、食管癌、胃癌、结直肠癌、神经胶质瘤和白血病中报道,但尚未在内异症中报道。在本研究中,我们首先旨在评估FEN1基因分型对台湾代表性人群内异症风险的影响。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对153例内异症患者和636例非癌健康对照进行基因分型。
FEN1 rs174538的基因型在内异症组和对照组之间分布不同,而rs4246215的基因型则无差异。具体而言,FEN1 rs174538基因型的AA型在内异症患者中的出现频率显著低于对照组(优势比[OR]=0.43,95%置信区间[CI]=0.24-0.78,p=0.0125)。FEN1 rs174538的A等位基因在病例组中的频率也显著低于对照组(OR=0.65,95%CI=0.50-0.86,p=0.0021)。至于初潮年龄,初潮年龄>12.8岁且携带FEN1 rs174538 AA基因型的个体患内异症的OR较低,为0.29(95%CI=0.11-0.78,p=0.0381)。关于足月妊娠情况,未足月妊娠且携带FEN1 rs174538 AA基因型的个体风险较低(OR=0.12,95%CI=0.03-0.53,p=0.0050)。
FEN1 rs174538的A等位基因是内异症的一种新型保护生物标志物,该基因型可能在内异症的发生发展中与年龄和激素相关因素存在相互作用。