Dual-patterned immunofiltration (DIF) device for the rapid efficient negative selection of heterogeneous circulating tumor cells.
نویسندگان
چکیده
The analysis of circulating tumor cells (CTCs) is an emerging field for estimating the metastatic relapse and tumor burden of cancer patients. However, the isolation of CTCs is still challenging due to their ambiguity, rarity, and heterogeneity. Here, we present an anti-CD45 antibody based dual-patterned immunofiltration (DIF) device for the enrichment of heterogeneous CTC subtypes by effective elimination of leukocytes. Our uniquely designed dual-patterned layers significantly enhance the binding chance between immuno-patterns and leukocytes due to the fluidic whirling and the increased binding sites, thus achieving superior negative selection in terms of high-throughput and high purity. From the experiments using lung cancer cells, 97.07 ± 2.79% of leukocytes were eliminated with less than 10% loss of cancerous cells at the flow rate of 1 mL h-1. To verify the device as a potential diagnostic tool, CTCs were collected from 11 cancer patients' blood and an average of 283.3 CTC-like cells were identified while less than 1 CTC-like cells were found from healthy donors. The samples were also analyzed by immunohistochemistry and the reverse transcription polymerase chain reaction to identify their heterogeneous characteristics. These remarkable results demonstrate that the present device could help to understand the unknown properties or undiscovered roles of CTCs with a non-biased view.
منابع مشابه
High-purity capture and release of circulating exosomes using an exosome-specific dual-patterned immunofiltration (ExoDIF) device.
We present a microfluidic device for the capture and release of circulating exosomes from human blood. The exosome-specific dual-patterned immunofiltration (ExoDIF) device is composed of two distinct immuno-patterned layers, and is capable of enhancing the chance of binding between the antibody and exosomes by generating mechanical whirling, thus achieving high-throughput exosome isolation with...
متن کاملAn Integrated Microfluidic Platform for Negative Selection and Enrichment of Circulating Tumor Cells
Circulating tumor cells (CTCs) are indicators for cancer diagnosis and prognosis. In this work, a new integrated microfluidic system capable of un-biased and sensitive “negative” enrichment of CTCs was developed. By using anti-human CD45 coated magnetic beads, leukocytes were removed by external magnetic force, leaving behind an enriched target cell population. The results demonstrated that the...
متن کاملPlasmacytoid Myoepithelioma of the Palate with Rapid Growth: A Case Report
Myoepitheliomas are benign tumors which account for less than 1% of all salivary gland tumors. In this article, we report the clinical, pathologic, and immunohistochemical features of plasmacytoid myoepithelioma of the hard palate in a 73-year-old man having a painless hard palate mass with progressiv...
متن کاملA cross-sectional study of clinical, histopathological and direct immmunofluorescence diagnosis in autoimmune bullous diseases
Background: Immunobullous diseases are morphologically heterogeneous and the differentiation between various subtypes is essential for proper treatment and prognosis. The aim of our study was to analyze and correlate clinical, histopathological, and immunofluorescence findings in autoimmune bullous diseases.Method: A c...
متن کاملComprehensive isolation, identification, and nucleic acid analysis of single breast cancer cells: CTC-isoTECH
The ability to isolate, phenotypically characterize, and profile the gene signature of single circulating tumor cells (CTCs) will provide deeper insight into cancer metastasis and will lead to improved diagnosis and treatment of cancer patients. Using current methods based on positive selection of epithelial markers, up to 40% of patients with highly aggressive metastatic breast cancer have no ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Lab on a chip
دوره 16 24 شماره
صفحات -
تاریخ انتشار 2016