Open AccessMonolithic Chip for High-throughput Blood Cell Depletion to Sort Rare Circulating Tumor Cells
Author(s) -
Fabio Fachin,
Philipp S. Spuhler,
Joseph M. Martel-Foley,
Jon F.,
Thomas A. Barber,
John R. Walsh,
Murat Karabacak,
Vincent Pai,
Melissa Yu,
Kyle C. Smith,
Henry H. Hwang,
Jennifer Yang,
Sahil Shah,
Ruby Yarmush,
Lecia V. Sequist,
Shan L. Stott,
Shyamala Maheswaran,
Daniel A. Haber,
Ravi Kapur,
Mehmet Toner
Publication year - 2017
Publication title -
scientific reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.24
H-Index - 213
ISSN - 2045-2322
DOI - 10.1038/s41598-017-11119-x
Subject(s) - circulating tumor cell , epithelial cell adhesion molecule , metastasis , cancer research , melanoma , cancer , biology , medicine
Circulating tumor cells (CTCs) are a treasure trove of information regarding the location, type and stage of cancer and are being pursued as both a diagnostic target and a means of guiding personalized treatment. Most isolation technologies utilize properties of the CTCs themselves such as surface antigens (e.g., epithelial cell adhesion molecule or EpCAM) or size to separate them from blood cell populations. We present an automated monolithic chip with 128 multiplexed deterministic lateral displacement devices containing ~1.5 million microfabricated features (12 µm–50 µm) used to first deplete red blood cells and platelets. The outputs from these devices are serially integrated with an inertial focusing system to line up all nucleated cells for multi-stage magnetophoresis to remove magnetically-labeled white blood cells. The monolithic CTC-iChip enables debulking of blood samples at 15–20 million cells per second while yielding an output of highly purified CTCs. We quantified the size and EpCAM expression of over 2,500 CTCs from 38 patient samples obtained from breast, prostate, lung cancers, and melanoma. The results show significant heterogeneity between and within single patients. Unbiased, rapid, and automated isolation of CTCs using monolithic CTC-iChip will enable the detailed measurement of their physicochemical and biological properties and their role in metastasis.