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

Lab on a Chip · 2015 · Vol. 16(3) · pp. 489–496
Zheng ZhaoYang YangYong ZengMei He

Abstract

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 μL 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.

Extracellular vesicles in diseaseAnodic Oxide Films and NanostructuresMicroRNA in disease regulationExosomeMicrovesiclesOvarian cancerCirculating tumor cellBiomarkerWhole bloodCancer biomarkersCancerNanoparticle tracking analysisMedicine

MeSH terms

FemaleHumansOvarian NeoplasmsSensitivity and SpecificityBiomarkers, TumorMicrofluidic Analytical TechniquesExosomes

Funding

  • University of Kansas
  • Kansas IDeA Network of Biomedical Research Excellence
  • National Institutes of Health
  • Johnson Cancer Research Center, Kansas State University
  • Cancer Center, University of Kansas
  • National Cancer Institute
  • National Institute of General Medical Sciences
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