Liao Cheng-Hsi, Chang Wen-Shin, Liao Jiuan-Miaw, Wu Hsi-Chin, Shen Te-Chun, Yang Jai-Sing, Tsai Fuu-Jen, Tsai Chia-Wen, Yu Chien-Chih, Bau Da-Tian
Graduate Institute of Biomedical Sciences, China Medical University; Taichung Armed Forces General Hospital, Taichung; National Defense Medical Center, Taipei, Taiwan.
Graduate Institute of Biomedical Sciences, China Medical University; Terry Fox Cancer Research Laboratory, Translational Medicine Research Center, China Medical University Hospital, Taichung, Taiwan.
Chin J Physiol. 2020 Jan-Feb;63(1):43-49. doi: 10.4103/CJP.CJP_72_19.
The DNA repair capacity plays a critical role in maintaining the genomic stability and gatekeeping for individual cancer risk. In this study, we aim at evaluation the role of the AspGlu (rs1130409) variant at apurinic/apyrimidinic endonuclease (APE) gene in renal cell carcinoma (RCC) risk and the contribution of different genotypes to its transcriptional mRNA levels. In the case-control study, 92 RCC patients and 580 cancer-free patients matched by age and gender were recruited. The apurinic/APE genotyping work was conducted with typical restriction fragment length polymorphism methodology after polymerase chain reaction. At the meanwhile, thirty renal tissue samples with variant genotypes were examined for their apurinic/APE mRNA and protein expressions by real-time quantitative reverse transcription method and Western blotting. The results showed that compared with the wild-type TT genotype, the people with TG and GG genotypes of apurinic/APE AspGlu had 0.88- and 1.09-fold risk of RCC, respectively. We have also examined the in vivo transcriptional (RNA) and translational (protein) levels with renal tissues of various apurinic/APE AspGlu genotypes, revealing that the apurinic/APE mRNA and protein were of similar levels among people of TT, TG, or GG genotypes. There was no joint gene-environment effect of apurinic/APE AspGlu genotype and smoking habit on RCC risk. The evidence indicated that apurinic/APE AspGlu genotypic variants did not alter its mRNA and protein expression among RCC patients. The genotype of apurinic/APE AspGlu may not serve as a proper predictive marker for RCC risk in Taiwan.
DNA修复能力在维持基因组稳定性以及把控个体患癌风险方面发挥着关键作用。在本研究中,我们旨在评估脱嘌呤/脱嘧啶内切酶(APE)基因上的天冬氨酸-谷氨酸(rs1130409)变异在肾细胞癌(RCC)风险中的作用,以及不同基因型对其转录mRNA水平的影响。在这项病例对照研究中,招募了92例RCC患者以及580例年龄和性别相匹配的无癌患者。在聚合酶链反应后,采用典型的限制性片段长度多态性方法进行脱嘌呤/APE基因分型工作。与此同时,通过实时定量逆转录法和蛋白质印迹法检测了30个具有变异基因型的肾组织样本的脱嘌呤/APE mRNA和蛋白表达。结果显示,与野生型TT基因型相比,脱嘌呤/APE天冬氨酸-谷氨酸的TG和GG基因型人群患RCC的风险分别为0.88倍和1.09倍。我们还检测了不同脱嘌呤/APE天冬氨酸-谷氨酸基因型肾组织的体内转录(RNA)和翻译(蛋白质)水平,发现TT、TG或GG基因型人群中脱嘌呤/APE mRNA和蛋白水平相似。脱嘌呤/APE天冬氨酸-谷氨酸基因型与吸烟习惯对RCC风险不存在联合基因-环境效应。证据表明,脱嘌呤/APE天冬氨酸-谷氨酸基因型变异在RCC患者中并未改变其mRNA和蛋白表达。在台湾,脱嘌呤/APE天冬氨酸-谷氨酸基因型可能无法作为RCC风险的合适预测标志物。