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A microfluidic ExoSearch chip for multiplexed exosome detection towards blood-based ovarian cancer diagnosis

机译:一种微流ExoSearch芯片,用于多重外泌体检测,用于基于血的卵巢癌诊断

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摘要

Tumor-derived circulating exosomes, enriched with a group of tumor antigens, have been recognized as a promising biomarker source for cancer diagnosis via a less invasive procedure. Quantitatively pinpointing exosome tumor markers is appealing, yet challenging. In this study, we developed a simple microfluidic approach (ExoSearch) which provides enriched preparation of blood plasma exosomes for in situ, multiplexed detection using immunomagnetic beads. The ExoSearch chip offers a robust, continuous-flow design for quantitative isolation and release of blood plasma exosomes in a wide range of preparation volumes (10 mu L to 10 mL). We employed the ExoSearch chip for blood-based diagnosis of ovarian cancer by multiplexed measurement of three exosomal tumor markers (CA-125, EpCAM, CD24) using a training set of ovarian cancer patient plasma, which showed significant diagnostic power (a. u. c. = 1.0, p = 0.001) and was comparable with the standard Bradford assay. This work provides an essentially needed platform for utilization of exosomes in clinical cancer diagnosis, as well as fundamental exosome research.
机译:肿瘤来源的循环外泌体,富含一组肿瘤抗原,已被认为是通过微创程序进行癌症诊断的有前途的生物标志物来源。精确定位外泌体肿瘤标志物很有吸引力,但具有挑战性。在这项研究中,我们开发了一种简单的微流控方法(ExoSearch),该方法可提供丰富的血浆外泌体制备方法,以便使用免疫磁珠进行原位多重检测。 ExoSearch芯片提供了强大的连续流设计,可在各种制备体积(10μL至10 mL)中定量分离和释放血浆外泌体。我们使用一套训练性的卵巢癌患者血浆,通过对三种外泌体肿瘤标志物(CA-125,EpCAM,CD24)进行多重测量,将ExoSearch芯片用于基于血液的卵巢癌诊断中,这显示出了强大的诊断能力(auc = 1.0, p = 0.001),与标准的Bradford分析法相当。这项工作提供了在临床癌症诊断以及基础外泌体研究中利用外泌体的基本必要平台。

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