尿
DNA
泌尿系统
聚合酶链反应
实时聚合酶链反应
化学
胎儿游离DNA
分子生物学
男科
基因
生物
医学
生物化学
内科学
遗传学
胎儿
产前诊断
怀孕
作者
Pei Li,Jun Ning,Xipeng Luo,Hongli Du,Qing Zhang,Ganlin Zhou,Qiu Lei Du,Zhenyu Ou,Long Wang,Yu Wang
摘要
Background Due to high nuclease activity and complex contents in urine, urinary cell‐free DNA (ucf DNA ) was prone to degrade. So, we developed standardized urine collection tube ( UCT ) to prevent ucf DNA degradation and simultaneously maintain urinary cells in their original form during the sample collection process, ensuring stabilization of the original proportion and integrity of ucf DNA . Methods Urine samples were collected from bladder cancer patients and divided into 10‐mL normal tubes and 10‐mL UCT s, respectively, and kept at ambient temperature. Urine supernatant was separated by centrifuging, and ucfDNA was extracted. Then ucfDNA was quantified by quantitative real‐time polymerase chain reaction. UcfDNA fragments distribution was analyzed by Agilent 2200, and the frequency of specific mutations of urinary system disease was detected by next‐generation sequencing method. Results Urine collected into UCT s showed no statistically significant changes in their original proportion and integrity of ucf DNA up to 7 days at ambient temperature and also ucf DNA fragments were maintained well. Conversely, urine collected into normal tubes was observed an obviously decline in their original proportion of ucf DNA and ucf DNA fragments changed greatly. The △% of allele fraction ( AF ) for specific genes of ucf DNA from UCTs was lower than from normal tubes by 3.7‐fold. Conclusion Using UCTs, they can maximally keep the original proportion and integrity of ucfDNA and stabilize urinary cells and minimize the background noise caused by urinary cellular DNA releasing, it will be help to open the door of next‐generation noninvasive liquid biopsy applications utilizing urine.
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