Whole blood stabilization for the microfluidic isolation and molecular characterization of circulating tumor cells

用于循环肿瘤细胞微流控分离和分子表征的全血稳定化

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作者:Keith H K Wong ,Shannon N Tessier ,David T Miyamoto ,Kathleen L Miller ,Lauren D Bookstaver ,Thomas R Carey ,Cleo J Stannard ,Vishal Thapar ,Eric C Tai ,Kevin D Vo ,Erin S Emmons ,Haley M Pleskow ,Rebecca D Sandlin ,Lecia V Sequist ,David T Ting ,Daniel A Haber ,Shyamala Maheswaran ,Shannon L Stott ,Mehmet Toner

Abstract

Precise rare-cell technologies require the blood to be processed immediately or be stabilized with fixatives. Such restrictions limit the translation of circulating tumor cell (CTC)-based liquid biopsy assays that provide accurate molecular data in guiding clinical decisions. Here we describe a method to preserve whole blood in its minimally altered state by combining hypothermic preservation with targeted strategies that counter cooling-induced platelet activation. Using this method, whole blood preserved for up to 72 h can be readily processed for microfluidic sorting without compromising CTC yield and viability. The tumor cells retain high-quality intact RNA suitable for single-cell RT-qPCR as well as RNA-Seq, enabling the reliable detection of cancer-specific transcripts including the androgen-receptor splice variant 7 in a cohort of prostate cancer patients with an overall concordance of 92% between fresh and preserved blood. This work will serve as a springboard for the dissemination of diverse blood-based diagnostics.

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