| Literature DB >> 27436104 |
Vasudha Murlidhar1,2,3, Lianette Rivera-Báez1,2,3, Sunitha Nagrath1,2,3.
Abstract
The study of circulating tumor cells (CTCs) has been made possible by many technological advances in their isolation. Their isolation has seen many fronts, but each technology brings forth a new set of challenges to overcome. Microfluidics has been a key player in the capture of CTCs and their downstream analysis, with the aim of shedding light into their clinical application in cancer and metastasis. Researchers have taken diverging paths to isolate such cells from blood, ranging from affinity-based isolation targeting surface antigens expressed on CTCs, to label-free isolation taking advantage of the size differences between CTCs and other blood cells. For both major groups, many microfluidic technologies have reported high sensitivity and specificity for capturing CTCs. However, the question remains as to the superiority among these two isolation techniques, specifically to identify different CTC populations. This review highlights the key aspects of affinity and label-free microfluidic CTC technologies, and discusses which of these two would be the highest benefactor for the study of CTCs.Entities:
Keywords: affinity isolation; circulating tumor cells (CTCs); label-free isolation; microfluidics
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Year: 2016 PMID: 27436104 DOI: 10.1002/smll.201601394
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281