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Updated: May 4, 2026

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
Integrated CTC Enrichment and Dual-Responsive Nanoprobe Identification Enable Intelligent Liquid Biopsy-Based Cancer
Sitian He1, Lihua Ding2, Clement Yaw Effah2
1The Medical Laboratory Center, Hainan General Hospital, Hainan Medical University Hainan Hospital, Haikou, Hainan 570311, China.
None:
This work addresses the challenge of accurately identifying living circulating tumor cell (CTC) from contaminating leukocytes by developing a novel, fixation-free dual-marker sensing strategy that preserves cell viability and biomolecular integrity for downstream analysis. Our strategy utilizes telomerase-responsive gold nanoparticles (polyA-TSP-AuNPs) to increase intracellular negative charge, which in turn enhances the electrostatic accumulation of a custom-synthesized, mitochondria-targeting aggregation-induced emission probe (DSA-PPh3). This dual-marker identification system was then integrated with our rVAR2-FETCH enrichment method, and the resulting CTC counts were combined with hematological parameters in a supervised machine learning model for diagnosis. The dual-marker system amplified the tumor-to-leukocyte signal ratio to 10.03 and showed excellent concordance with the CellSearch reagent (R = 0.97) while preserving RNA integrity. When integrated with rVAR2-FETCH enrichment, our platform detected CTC in 83.67% (41/49) of non-small cell lung cancer patients, outperforming the complete CellSearch kit. Furthermore, machine learning models integrating CTC counts with hematological biomarkers achieved excellent diagnostic performance for lung cancer, with support vector machine demonstrating the best results (AUC = 0.977).

