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脱落结肠细胞的 DNA 定量分析作为结直肠癌的一种新型筛查工具。

DNA quantification of exfoliated colonocytes as a novel screening tool for colorectal cancer.

机构信息

University College London Hospital, 235 Euston Road, London NW1 2BU, United Kingdom.

出版信息

Eur J Surg Oncol. 2013 Dec;39(12):1423-7. doi: 10.1016/j.ejso.2013.08.029. Epub 2013 Sep 7.

DOI:10.1016/j.ejso.2013.08.029
PMID:24094980
Abstract

AIMS

Colorectal cancer (CRC) sheds viable cells in the mucocelluar layer overlaying the colonic mucosa which travels distally alongside the faecal stream. These cells can be retrieved from the surface of the rectal mucosa. DNA quantification of these cells may be a marker of CRC, assessment of which was aim of this study.

METHODS

A prospective double-blinded study of 467 consecutive patients referred with symptoms suggestive of CRC. Cells were collected from the surface of the rectal mucosa and total DNA quantified. DNA scores were compared with outcome after subjects had completed bowel investigations. Analysis of receiver operating characteristic (ROC) curves was performed to determine the optimum cut-off point for a positive result.

RESULTS

107 of the 467 patients were excluded due to; excessive faecal contamination of samples (n = 84); declined investigations (n = 17); inappropriate referral (n = 5); unfit (n = 1). 263 patients had lower GI endoscopy; 89 CT colonography and 8 barium enema. The diagnosis were; CRC (n = 23), inflammatory bowel disease (IBD) (n = 7), adenomatous polyps (AP) (n = 20) and no significant abnormality detected (n = 310). ROC analysis revealed that sensitivities at a specificity of 60% for detecting CRC were 91.3%; for CRC and IBD 86.7%; and for CRC, IBD and AP 72.0%.

CONCLUSION

In symptomatic patients DNA quantification of cells retrieved from the surface of the rectal mucosa is sensitive for the detection of CRC. Although faecal contamination is a limitation of this technique, refinement and application of other molecular tests hold promise for a better non invasive method for the detection of CRC.

摘要

目的

结直肠癌(CRC)在覆盖结肠黏膜的黏膜细胞层中脱落有活力的细胞,这些细胞沿着粪便流的方向向远端移动。这些细胞可以从直肠黏膜表面提取。这些细胞的 DNA 定量可能是 CRC 的标志物,本研究旨在评估这一标志物。

方法

对 467 例因疑似 CRC 症状而就诊的连续患者进行前瞻性双盲研究。从直肠黏膜表面采集细胞并定量总 DNA。在受试者完成肠道检查后,比较 DNA 评分与结果。进行接收者操作特征(ROC)曲线分析,以确定阳性结果的最佳截断点。

结果

467 例患者中有 107 例因以下原因被排除在外;样本中粪便过多污染(n=84);拒绝检查(n=17);不当转诊(n=5);不适合(n=1)。263 例患者进行了下胃肠道内镜检查;89 例 CT 结肠成像和 8 例钡灌肠。诊断结果为;CRC(n=23)、炎症性肠病(IBD)(n=7)、腺瘤性息肉(AP)(n=20)和无明显异常(n=310)。ROC 分析显示,在特异性为 60%时,检测 CRC 的敏感性为 91.3%;检测 CRC 和 IBD 的敏感性为 86.7%;检测 CRC、IBD 和 AP 的敏感性为 72.0%。

结论

在有症状的患者中,从直肠黏膜表面提取的细胞 DNA 定量对 CRC 的检测具有较高的敏感性。尽管粪便污染是该技术的一个限制,但对其他分子检测的改进和应用有望为非侵入性检测 CRC 提供更好的方法。

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