Circulating tumor cells (CTCs) serve as critical biomarkers for early diagnosis, prognosis monitoring, and treatment response evaluation in lung cancer. Herein, we report a novel "off-on" fluorescent aptasensor based on fluorescence resonance energy transfer (FRET) and streptavidin-modified magnetic beads (MBs) for the sensitive and specific detection of A549 CTCs in lung cancer. The sensing strategy employs a biotinylated EGFR-targeting aptamer (Apt) labeled with FAM (donor) and a complementary S1 strand modified with BHQ-1 (acceptor). In the absence of target cells, the aptamer hybridizes with S1, bringing FAM and BHQ into close proximity, resulting in efficient fluorescence quenching ("off" state). Upon recognition of EGFR-overexpressing A549 cells, the aptamer undergoes a conformational change or strand displacement, releasing S1-BHQ and restoring FAM fluorescence ("on" state). Under optimized conditions, the aptasensor exhibited a linear response to A549 cell concentrations ranging from 50 to 5 × 105 cells per mL, with a detection limit as low as 34 cells per mL. The assay also demonstrated excellent selectivity against non-target cancer cells (SW620, HGC-27, MCF-7) and performed well in human serum samples, achieving a limit of detection of 105 (1.05 × 102) cells per mL. This FRET-based magnetic platform offers a simple and sensitive approach for CTC detection and shows potential as a tool for lung cancer liquid biopsy pending further validation with clinical patient samples.
Qiongdan Zhang, Jianfeng Tang, Bin Li et al.· Analytical Methods· 0 citations
A ratiometric fluorescence nanosensor using dual-emission CdTe quantum dots (R-QDs) for sensitive detection of APE1, a DNA repair enzyme and cancer biomarker, successfully detected APE1 in breast cancer cell lysates with good linearity and recovery rates.