Single-nucleotide variant profiling in liquid biopsy with RECO-Cas

Mutation detection of cell-free DNA (cfDNA) through liquid biopsy is essential for precision oncology, resistance profiling, and informed clinical decision-making. However, its clinical application has remained limited by the lack of simple, rapid, accurate, and cost-effective detection approaches. Here, we report a recombined DNA construct–activated Cas12a (RECO-Cas) assay for profiling cfDNA mutations. The RECO-Cas assay uses a recombined DNA construct generated from Argonaute-nicked mutant DNA and an artificial DNA activator to selectively trigger CRISPR-Cas12a, enabling 0.01% variant allele frequency sensitivity and single-nucleotide resolution. Using the assay, we detect KRAS , EGFR , and PIK3CA point mutations in cfDNA from clinical plasma samples, demonstrating high sensitivity (90.48%) and excellent specificity (100%). We also apply it to successfully classify and identify KRAS missense variants. RECO-Cas provides a simple, rapid, and affordable solution that is compatible with a compact, wirelessly powered point-of-care diagnostic platform incorporating smartphone-based fluorescence detection. This assay enables highly sensitive and specific detection of low-frequency mutations, facilitating early cancer diagnosis and supporting the development of personalized treatment strategies.

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Publication Details

Journal
Science Advances
Published
2026-05-22
DOI
https://doi.org/10.1126/sciadv.aed1757
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
0.00

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article

Single-nucleotide variant profiling in liquid biopsy with RECO-Cas

Lorrie Perpetua, Jiongyu Zhang, Minjie Pei, Wenqi Gan et al.
Science Advances
Cancer Genomics and Diagnostics
article

Single-nucleotide variant profiling in liquid biopsy with RECO-Cas

Lorrie Perpetua, Jiongyu Zhang, Minjie Pei, Wenqi Gan, Chengyu Hou, Omar M. Ibrahim, Xingye Liu, Ziyue Li, Kurt T. Schalper, Rui Yang, Rachael A. Clark, Ramachandra Yerramsetti, Xin Guan, Shuo Zhang, Changchun Liu, Chong Guo
article en

Abstract

Mutation detection of cell-free DNA (cfDNA) through liquid biopsy is essential for precision oncology, resistance profiling, and informed clinical decision-making. However, its clinical application has remained limited by the lack of simple, rapid, accurate, and cost-effective detection approaches. Here, we report a recombined DNA construct–activated Cas12a (RECO-Cas) assay for profiling cfDNA mutations. The RECO-Cas assay uses a recombined DNA construct generated from Argonaute-nicked mutant DNA and an artificial DNA activator to selectively trigger CRISPR-Cas12a, enabling 0.01% variant allele frequency sensitivity and single-nucleotide resolution. Using the assay, we detect KRAS , EGFR , and PIK3CA point mutations in cfDNA from clinical plasma samples, demonstrating high sensitivity (90.48%) and excellent specificity (100%). We also apply it to successfully classify and identify KRAS missense variants. RECO-Cas provides a simple, rapid, and affordable solution that is compatible with a compact, wirelessly powered point-of-care diagnostic platform incorporating smartphone-based fluorescence detection. This assay enables highly sensitive and specific detection of low-frequency mutations, facilitating early cancer diagnosis and supporting the development of personalized treatment strategies.

Science AdvancesVol. 12(21)
Brigham and Women's Hospital (US), Harvard University (US), University of Connecticut (US), UConn Health (US)
National Institutes of Health
Peace, Justice and strong institutions
Openalex Percentile: Top 6%
Cancer Genomics and Diagnostics
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