Chen Qin, Hu Yiqiu, Fang Zhihao, Ye Minfeng, Li Jingqing, Zhang Suzhan, Yuan Ying, Guo Cheng
Cancer Institute (Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education), The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Department of Gastrointestinal Surgery, Shaoxing People's Hospital, Shaoxing Hospital of Zhejiang University, Shaoxing, China.
Front Chem. 2020 Dec 17;8:606495. doi: 10.3389/fchem.2020.606495. eCollection 2020.
Oxidative nucleic acid modifications have attracted increasing attention in recent years since they have been found to be related to a number of diseases including cancer. 8-Hydroxy-2'-deoxyguanosine (8-OHdG) and 8-hydroxyguanosine (8-OHG) are the typical markers of oxidative modification of DNA and RNA, respectively, and they are emerging biomarkers for the early detection of diseases. Urine is a favored biofluid for biomarker discovery due to its noninvasiveness to patients. Accurate quantification of these oxidative nucleic acid modifications still has challenges because their amounts in urine are very low and the interferences in urine samples are complicated. Herein, we developed and validated an accurate and robust solid-phase extraction (SPE) coupled with ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the simultaneous quantification of these oxidative nucleic acid modifications in human urine. Stable isotope dilution strategy was utilized and the method shows good precision on intraday and interday measurements. Meanwhile, recovery was satisfactory by utilizing the Oasis hydrophilic-lipophilic balance (HLB) cartridge for sample pretreatment at three spiked levels. We successfully quantified urinary 8-OHdG and 8-OHG from 60 gastric cancer patients and 70 healthy controls by using this method. The measured contents of 8-OHdG and 8-OHG in urine from gastric cancer patients are both increased, compared with those in urine from healthy controls, indicating these oxidative nucleic acid modifications could act as potential non-invasive markers for early diagnosis of gastric cancer. Moreover, the present study will stimulate investigations of the effects of oxidative stress and nucleic acid modifications on the initiation and progression of gastric cancer.
近年来,氧化核酸修饰因其与包括癌症在内的多种疾病相关而受到越来越多的关注。8-羟基-2'-脱氧鸟苷(8-OHdG)和8-羟基鸟苷(8-OHG)分别是DNA和RNA氧化修饰的典型标志物,并且它们正成为疾病早期检测的新兴生物标志物。尿液因其对患者无创,是发现生物标志物的理想生物流体。准确定量这些氧化核酸修饰仍然具有挑战性,因为它们在尿液中的含量非常低,并且尿液样品中的干扰因素复杂。在此,我们开发并验证了一种准确且稳健的固相萃取(SPE)结合超高效液相色谱-串联质谱(UPLC-MS/MS)方法,用于同时定量人尿液中的这些氧化核酸修饰。采用了稳定同位素稀释策略,该方法在日内和日间测量中显示出良好的精密度。同时,通过使用Oasis亲水亲脂平衡(HLB)柱在三个加标水平下进行样品预处理,回收率令人满意。我们使用该方法成功定量了60例胃癌患者和70例健康对照者尿液中的8-OHdG和8-OHG。与健康对照者尿液中的含量相比,胃癌患者尿液中8-OHdG和8-OHG的测量含量均升高,表明这些氧化核酸修饰可能作为胃癌早期诊断的潜在非侵入性标志物。此外,本研究将激发对氧化应激和核酸修饰对胃癌发生和发展影响的研究。