Abstract
Circulating tumour nucleic acids (ctNAs) are released from tumours cells and can be detected in blood samples, providing a way to track tumors without requiring a tissue sample. This “liquid biopsy” approach has the potential to replace invasive, painful, and costly tissue biopsies in cancer diagnosis and management. However, a very sensitive and specific approach is required to detect relatively low amounts of mutant sequences linked to cancer because they are masked by the high levels of wild-type sequences. This review discusses high-performance nucleic acid biosensors for ctNA analysis in patient samples. We compare sequencing- and amplification-based methods to next-generation sensors for ctDNA and ctRNA (including microRNA) profiling, such as electrochemical methods, surface plasmon resonance, Raman spectroscopy, and microfluidics and dielectrophoresis-based assays. We present an overview of the analytical sensitivity and accuracy of these methods as well as the biological and technical challenges they present.
Original language | English (US) |
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Pages (from-to) | 2554-2564 |
Number of pages | 11 |
Journal | Angewandte Chemie - International Edition |
Volume | 59 |
Issue number | 7 |
DOIs | |
State | Published - Feb 10 2020 |
Keywords
- DNA sequencing
- circulating nucleic acids
- electrochemical methods
- liquid biopsy
- microfluidics
ASJC Scopus subject areas
- General Chemistry
- Catalysis