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Multiplex screening of 275 plasma protein biomarkers to identify a signature for early detection of colorectal cancer

机译:多重筛选275血浆蛋白生物标志物,以确定早期检测结直肠癌的签名

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Blood‐based protein biomarkers may be an attractive option for early detection of colorectal cancer (CRC). Here, we used a two‐stage design to measure 275 protein markers by proximity extension assay (PEA), first in plasma samples of a discovery set consisting of 98 newly diagnosed CRC cases and 100 age‐ and gender‐matched controls free of neoplasm at screening colonoscopy. An algorithm predicting the presence of early‐ or late‐stage CRC was derived by least absolute shrinkage and selection operator regression with .632+ bootstrap method, and the algorithms were then validated using PEA again in an independent validation set consisting of participants of screening colonoscopy with and without CRC ( n =?56 and 102, respectively). Three different signatures for all‐, early‐, and late‐stage CRC consisting of 9, 12, and 11 protein markers were obtained in the discovery set with areas under the curves (AUCs) after .632?+?bootstrap adjustment of 0.92, 0.91, and 0.96, respectively. External validation among participants of screening colonoscopy yielded AUCs of 0.76 [95% confidence interval (95% CI), 0.67–0.84], 0.75 (95% CI, 0.62–0.87), and 0.80 (95% CI, 0.68–0.89) for all‐, early‐, and late‐stage CRC, respectively. Although the identified protein markers are not competitive with the best available stool tests, these proteins may contribute to the development of powerful blood‐based tests for CRC early detection in the future.
机译:血基蛋白质生物标志物可能是早期检测结直肠癌(CRC)的有吸引力的选择。在这里,我们使用了两阶段设计来测量275蛋白标记物通过邻近延伸测定(豌豆),首先是由98例新诊断的CRC病例和100岁和性别匹配的对照组成的血浆样本,其在筛选结肠镜检查。预测早期或后期CRC的存在的算法是通过与.632+引导方法的最小绝对收缩和选择操作员回归来源的,然后在由筛选结肠镜检查的参与者组成的独立验证集中使用豌豆验证算法没有CRC(分别为n =?56和102)。由9,12和11个蛋白质标记组成的全部,早期和晚期CRC的三种不同签名,在曲线(AUC)之下的区域,如0.632?+ +?左右左右的区域, 0.91和0.96分别。筛选结肠镜检查的参与者之间的外部验证产生0.76的AUC,0.76 [95%置信区间(95%CI),0.67-0.84],0.75(95%CI,0.62-0.87),0.80(95%CI,0.68-0.89)分别为期,早期和晚期CRC。虽然所鉴定的蛋白质标记与最佳可用粪便测试不具有竞争力,但这些蛋白质可能有助于在未来的CRC早期检测的强大血基测试的发展。

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