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Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging

机译:捕获和鉴定使用透明纳米材料和基于量子点的多路复用成像异质循环肿瘤细胞。

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>Background: Capture and identification of circulating tumor cells (CTCs) in the blood system can help guide therapy and predict the prognosis of cancer patients. However, simultaneous capture and identification of CTCs with both epithelial and mesenchymal phenotypes remains a formidable technical challenge for cancer research. This study aimed at developing a system to efficiently capture and identify these CTCs with heterogeneous phenotypes using transparent nanomaterials and quantum dots (QDs)-based multiplexed imaging.>Methods: Hydroxyapatite-chitosan (HA-CTS) nanofilm-coated substrates were modified based on our previous work to increase the capture efficiency of cancer cell lines by extending baking and incubating time. QDs-based imaging was applied to detect cytokeratin, epithelial cell adhesion molecule (EpCAM), and vimentin of cancer cells to demonstrate the feasibility of multiplexed imaging. And QDs-based multiplexed imaging of CD45, cytokeratin and vimentin was applied to detect CTCs from different cancer patients that were captured using HA-CTS nanofilm substrates.>Results: Comparisons of the capture efficiencies of cancer cells at different baking time of film formation and incubating time of cell capture revealed the optimal baking and incubating time. Optimal time was chosen to develop a modified CTCs capture system that could capture EpCAM-positive cancer cells at an efficiency > 80%, and EpCAM-negative cancer cells at an efficiency > 50%. QDs-based imaging exhibited comparable detection ability but higher photostability compared to organic dyes imaging in staining cells. In addition, QDs-based multiplexed imaging also showed the molecular profiles of cancer cell lines with different phenotypes well. The integrated CTCs capture and identification system successfully captured and imaged CTCs with different sub-phenotypes in blood samples from cancer patients.>Conclusion: This study demonstrated a reliable capture and detection system for heterogeneous CTCs that combined enrichment equipment based on HA-CTS nanofilm substrates with QDs-based multiplexed imaging.
机译:>背景:捕获和识别血液系统中的循环肿瘤细胞(CTC)可帮助指导治疗并预测癌症患者的预后。然而,同时捕获和鉴定具有上皮和间质表型的CTC仍然是癌症研究的巨大技术挑战。这项研究旨在开发一种系统,以使用透明的纳米材料和基于量子点(QD)的多重成像技术有效捕获和识别具有异型表型的CTC。>方法:羟基磷灰石-壳聚糖(HA-CTS)纳米膜-基于我们以前的工作对涂层底物进行了改良,以通过延长烘烤和孵育时间来提高癌细胞系的捕获效率。基于QDs的成像技术被用于检测癌细胞的细胞角蛋白,上皮细胞粘附分子(EpCAM)和波形蛋白,以证明多重成像的可行性。并使用基于QDs的CD45,细胞角蛋白和波形蛋白的多重成像技术检测了使用HA-CTS纳米膜底物捕获的不同癌症患者的CTC。>结果:比较不同情况下癌细胞的捕获效率成膜的烘烤时间和细胞捕获的孵育时间揭示了最佳的烘烤和孵育时间。选择最佳时间来开发改良的CTC捕获系统,该系统可捕获效率> 80%的EpCAM阳性癌细胞和捕获效率> 50%的EpCAM阴性癌细胞。与染色细胞中的有机染料成像相比,基于QDs的成像具有可比的检测能力,但具有更高的光稳定性。此外,基于量子点的多重成像也很好地显示了具有不同表型的癌细胞系的分子概况。集成的CTC捕获和识别系统成功捕获和成像了癌症患者血液样本中具有不同亚表型的CTC。>结论:该研究证明了一种可靠的异种CTC捕获和检测系统,该系统结合了基于浓缩设备的基于QDs的多重成像技术在HA-CTS纳米膜基质上的应用。

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