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首页> 外文期刊>Annals of Coloproctology >Effects of Delay in the Snap Freezing of Colorectal Cancer Tissues on the Quality of DNA and RNA
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Effects of Delay in the Snap Freezing of Colorectal Cancer Tissues on the Quality of DNA and RNA

机译:结直肠癌组织速冻延迟对DNA和RNA质量的影响

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Purpose The success of basic molecular research using biospecimens strongly depends on the quality of the specimen. In this study, we evaluated the effects of delayed freezing time on the stability of DNA and RNA in fresh frozen tissue from patients with colorectal cancer. Methods Tissues were frozen at 10, 30, 60, and 90 minutes after extirpation of colorectal cancer in 20 cases. Absorbance ratio of 260 to 280 nm (A260/A280) and agarose gel electrophoresis were evaluated. In addition, the RNA integrity number (RIN) was assayed for the analysis of the RNA integrity. Results Regardless of delayed freezing time, all DNA and RNA samples revealed A260/A280 ratios of more than 1.9, and all DNA samples showed a discrete, high-molecular-weight band on agarose gel electrophoresis. The RINs were 7.53 ± 2.04, 6.70 ± 1.88, 6.47 ± 2.58, and 4.22 ± 2.34 at 10, 30, 60, and 90 minutes, respectively. Though the concentration of RNA was not affected by delayed freezing, the RNA integrity was decreased with increasing delayed freezing time. Conclusion According to the RIN results, we recommend that the collection of colorectal cancer tissue should be done within 10 minutes for studies requiring RNA of high quality and within 30 minutes for usual RNA studies.
机译:目的使用生物标本进行基本分子研究的成功很大程度上取决于标本的质量。在这项研究中,我们评估了延迟冷冻时间对结直肠癌患者新鲜冷冻组织中DNA和RNA稳定性的影响。方法20例结直肠癌根治术后10、30、60和90分钟冷冻组织。评价了260至280 nm的吸光度比(A 260 / A 280 )和琼脂糖凝胶电泳。另外,测定RNA完整性数(RIN)以分析RNA完整性。结果无论延迟冷冻时间如何,所有DNA和RNA样品的A 260 / A 280 比率均大于1.9,并且所有DNA样品均显示出离散的,琼脂糖凝胶电泳上的重带。在10、30、60和90分钟时的RIN分别为7.53±2.04、6.70±1.88、6.47±2.58和4.22±2.34。尽管RNA的浓度不受延迟冷冻的影响,但RNA完整性随延迟冷冻时间的增加而降低。结论根据RIN结果,我们建议对于需要高质量RNA的研究,应在10分钟内收集大肠癌组织,对于常规RNA研究,应在30分钟内进行。

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