Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy , Xuzhou Medical University , 209 Tongshan Road , Xuzhou 221004 , Jiangsu P.R.China.
Department of Pharmaceutical Analysis, School of Pharmacy , Xuzhou Medical University , 209 Tongshan Road , Xuzhou 221004 , Jiangsu P.R.China.
Anal Chem. 2018 Nov 20;90(22):13290-13298. doi: 10.1021/acs.analchem.8b02625. Epub 2018 Oct 30.
Circulating tumor cells (CTCs) served as an important biomarker for tumor recurrence and prediction of prognosis. However, selective capture and quantification of CTCs from whole blood was still full of challenge due to the extremely scare number of CTCs. Moreover, how to keep a high cell viability after capture remained to be solved. Here, we described a ratiometric fluorescent probe for the efficient capture and accurate determination of CTCs by conjugating graphitic carbon nitride quantum dots (g-CNQDs) with gold nanoclusters (AuNCs) and further linking with anti-EpCAM antibody to acquire the CTC-specific immune probe. In this probe, AuNCs protected by albumin V bovine played the role as the fluorophore reference and anti-EpCAM-attached g-CNQDs acted as both the response signal and specific recognition element for sensing CTCs. In the presence of CTCs, the quenched fluorescence of the immune probe at 500 nm was recovered due to the detachment of anti-EpCAM from the probe, whereas the intensity at 650 nm was essentially unchanged. This strategy realized the highly sensitive detection of CTCs in whole blood down to one CTC. Furthermore, it was demonstrated that the designed probe allowed capturing living CTCs with minimal cell damage. The subsequent reculture of captured cells for proliferation revealed that after a 7 day proliferation, almost 28 MCF-7 cells were obtained from one target cell. The immune probe was successfully applied into capture and detection of CTCs from clinical cancer patients. Our data suggested the good potential of fluorescent probe for the clinical diagnosis of cancers.
循环肿瘤细胞(CTCs)作为肿瘤复发和预后预测的重要生物标志物。然而,由于 CTCs 的数量极其稀少,从全血中选择性捕获和定量 CTCs 仍然充满挑战。此外,如何在捕获后保持高细胞活力仍然是一个待解决的问题。在这里,我们描述了一种比率荧光探针,通过将石墨相氮化碳量子点(g-CNQDs)与金纳米簇(AuNCs)偶联,并进一步与抗 EpCAM 抗体连接,获得用于捕获 CTC 的免疫探针,从而实现了对 CTC 的高效捕获和准确测定。在该探针中,牛血清白蛋白 V 保护的 AuNCs 起到荧光团参考的作用,而附着在抗 EpCAM 上的 g-CNQDs 则作为响应信号和用于检测 CTC 的特异性识别元件。在存在 CTC 的情况下,由于抗 EpCAM 从探针上脱离,探针在 500nm 处的荧光被猝灭得以恢复,而 650nm 处的强度基本不变。该策略实现了对全血中低至一个 CTC 的高度敏感的 CTC 检测。此外,结果表明,设计的探针允许以最小的细胞损伤捕获活的 CTC。随后对捕获细胞的增殖进行再培养,结果显示,从一个靶细胞中可以获得几乎 28 个 MCF-7 细胞。该免疫探针成功应用于从临床癌症患者中捕获和检测 CTCs。我们的数据表明,荧光探针在癌症的临床诊断中有很好的应用潜力。