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从人类粪便样本中增强DNA提取可提高结直肠癌筛查测试的性能。

Enhanced retrieval of DNA from human fecal samples results in improved performance of colorectal cancer screening test.

作者信息

Whitney Duncan, Skoletsky Joel, Moore Kent, Boynton Kevin, Kann Lisa, Brand Randall, Syngal Sapna, Lawson Michael, Shuber Anthony

机构信息

Applied Research Group, EXACT Sciences Corporation, 100 Campus Drive, Marlborough, MA, USA.

出版信息

J Mol Diagn. 2004 Nov;6(4):386-95. doi: 10.1016/S1525-1578(10)60536-3.

Abstract

Colorectal cancer accounts for more than 10% of all cancer deaths but is curable, if detected early. We reported previously on a stool-based screening test in which DNA from stool samples is subjected to genome analysis; sensitivity of the test has been limited in part by inefficiency of retrieving DNA from stool. Our aim was to test the impact of a new purification method that would increase the yield of human DNA from stool. DNA from 86 cancer and 100 non-cancer subjects (diagnosed by colonoscopy) were purified from stool with a new method for DNA recovery based on sequence-specific capture with acrylamide gel immobilized capture probes as well as with a previously developed magnetic bead-capture procedure. The new purification method gives an average 5.4-fold increase in the quantity of human DNA that can routinely be retrieved from fecal samples. The increased recovery of DNA corresponds with an increase in assay sensitivity from 53% (CI: 42 to 64%) to 70% (CI: 59 to 79%); P = 0.0005 (by McNemar's test), with no change in specificity. The newly developed sample preparation method mitigates a major problem in detecting rare cancer-associated genetic changes in heterogeneous clinical samples such as stool.

摘要

结直肠癌占所有癌症死亡病例的10%以上,但如果早期发现是可治愈的。我们之前报道了一种基于粪便的筛查测试,其中粪便样本的DNA会进行基因组分析;该测试的敏感性部分受到从粪便中提取DNA效率低下的限制。我们的目的是测试一种新的纯化方法的效果,该方法可提高从粪便中获取人类DNA的产量。采用一种基于丙烯酰胺凝胶固定捕获探针的序列特异性捕获以及先前开发的磁珠捕获程序的新型DNA回收方法,从86名癌症患者和100名非癌症患者(通过结肠镜检查诊断)的粪便中纯化DNA。这种新的纯化方法使从粪便样本中常规获取的人类DNA数量平均增加了5.4倍。DNA回收率的提高相应地使检测灵敏度从53%(置信区间:42%至64%)提高到70%(置信区间:59%至79%);P = 0.0005(通过McNemar检验),特异性无变化。新开发的样本制备方法缓解了在检测粪便等异质性临床样本中罕见的癌症相关基因变化时的一个主要问题。

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