电化学端粒酶检测用于口腔癌筛查

K. Tominaga, Mana Hayakawa, Shinobu Sato, M. Kodama, M. Habu, S. Takenaka
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引用次数: 0

摘要

端粒酶一直被认为是一种癌症标志物。作为一种易于操作的口腔癌筛查系统,我们建立了一种新的电化学端粒酶测定(ECTA)方法,该方法优于端粒酶重复扩增法(一种常用的检测端粒酶活性的方法)。在本研究中,我们采用3种临床样本来检验ECTA的敏感性和特异性。从44例口腔鳞状细胞癌患者和16例健康志愿者中获得3种类型的样本;整个口腔的脱落细胞,局部病变的脱落细胞,病变组织样本。用ECTA法测定端粒酶活性。口腔癌组各样本类型电流的增加均显著高于健康志愿者组,而口腔癌组3种样本类型之间无显著差异。ECTA的敏感性为94.6%,特异性为88.6%。该方法具有较好的端粒酶活性检测效果,可作为口腔癌筛查系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical telomerase assay for oral cancer screening
Telomerase has long been known as a cancer marker. As an easy-to-perform oral cancer screening system, we established a new electrochemical telomerase assay (ECTA) method that is superior to a telomerase repeat amplification protocol assay, a popular method for detection of telomerase activity. In the present study, we employed 3 types of clinical samples to examine the sensitivity and specificity of ECTA. Three types of samples were obtained from 44 oral squamous cell carcinoma patients and 16 healthy volunteers; exfoliated cells from the whole oral cavity, exfoliated cells from local lesions, and tissue samples from lesions. Telomerase activity was determined in the samples using ECTA. The increase in current in the oral cancer group was significantly higher than that in the healthy volunteer group for each sample type, while there were no significant differences among the 3 sample types in the oral cancer group. The sensitivity and specificity of ECTA was 94.6% and 88.6%, respectively. Our novel ECTA method showed excellent detection of telomerase activity and is consider applicable as an oral cancer screening system.
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