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Paper-Based MicroRNA Expression Profiling from Plasma and Circulating Tumor Cells.

Authors :
Leong SM
Tan KM
Chua HW
Huang MC
Cheong WC
Li MH
Tucker S
Koay ES
Source :
Clinical chemistry [Clin Chem] 2017 Mar; Vol. 63 (3), pp. 731-741. Date of Electronic Publication: 2017 Jan 10.
Publication Year :
2017

Abstract

Background: Molecular characterization of circulating tumor cells (CTCs) holds great promise for monitoring metastatic progression and characterizing metastatic disease. However, leukocyte and red blood cell contamination of routinely isolated CTCs makes CTC-specific molecular characterization extremely challenging.<br />Methods: Here we report the use of a paper-based medium for efficient extraction of microRNAs (miRNAs) from limited amounts of biological samples such as rare CTCs harvested from cancer patient blood. Specifically, we devised a workflow involving the use of Flinders Technology Associates (FTA) <superscript>®</superscript> Elute Card with a digital PCR-inspired "partitioning" method to extract and purify miRNAs from plasma and CTCs.<br />Results: We demonstrated the sensitivity of this method to detect miRNA expression from as few as 3 cancer cells spiked into human blood. Using this method, background miRNA expression was excluded from contaminating blood cells, and CTC-specific miRNA expression profiles were derived from breast and colorectal cancer patients. Plasma separated out during purification of CTCs could likewise be processed using the same paper-based method for miRNA detection, thereby maximizing the amount of patient-specific information that can be derived from a single blood draw.<br />Conclusions: Overall, this paper-based extraction method enables an efficient, cost-effective workflow for maximized recovery of small RNAs from limited biological samples for downstream molecular analyses.<br /> (© 2016 American Association for Clinical Chemistry.)

Details

Language :
English
ISSN :
1530-8561
Volume :
63
Issue :
3
Database :
MEDLINE
Journal :
Clinical chemistry
Publication Type :
Academic Journal
Accession number :
28073899
Full Text :
https://doi.org/10.1373/clinchem.2016.264432