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Spatially gradated segregation and recovery of circulating tumor cells from peripheral blood of cancer patients

机译:癌症患者外周血中循环肿瘤细胞的空间分级分离和恢复

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摘要

For cancer patients, the enumeration of rare circulating tumor cells (CTCs) in peripheral blood is a strong prognostic indicator of the severity of the cancer; for the general population, the capture of CTCs is needed for use as a clinical tool for cancer screening, early detection, and treatment assessment. Here, we present a fast, high-purity (∼90%) and high-efficiency (>90%) method for the segregation and undamaged recovery of CTCs using a spatially gradated microfluidic chip. Further, by lysing the red blood cells we achieved not only a significant reduction in the overall processing time but also mitigated the blood clogging problem commonly encountered in microfluidic-based CTC isolation systems. To clinically validate the chip, we employed it to detect and capture CTCs from 10 liver cancer patients. Positive CTC enumeration was observed in all the blood samples, and the readings ranged from a low of 1–2 CTCs (1 patient) to a high of >20 CTCs (2 patients) with the balance having 3–20 CTCs per 3-ml blood sample. The work here indicates that our system can be developed for use in cancer screening, metastatic assessment, and chemotherapeutic response and for pharmacological and genetic evaluation of single CTCs.
机译:对于癌症患者,外周血中稀有循环肿瘤细胞(CTC)的计数是癌症严重程度的有力预后指标。对于一般人群,需要捕获CTC才能将其用作癌症筛查,早期发现和治疗评估的临床工具。在这里,我们提出了一种使用空间渐变的微流控芯片分离四氯化碳的快速,高纯度(〜90%)和高效(> 90%)的方法。此外,通过裂解红细胞,我们不仅实现了整体处理时间的显着减少,而且还缓解了基于微流体的CTC分离系统中常见的血液堵塞问题。为了临床验证该芯片,我们将其用于检测和捕获10位肝癌患者的CTC。在所有血样中均观察到CTC计数为阳性,读数范围从低至1-2个CTC(1名患者)到高至大于20个CTC(2名患者),其余每3毫升中有3至20个CTC。血液样本。此处的工作表明我们的系统可以开发用于癌症筛查,转移评估和化学治疗反应以及单个CTC的药理和遗传评估。

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