Label-Free Single-Cell Cancer Classification from the Spatial Distribution of Adhesion Contact Kinetics

被引:0
|
作者
Beres, Balint [1 ,2 ]
Kovacs, Kinga Dora [1 ,3 ]
Kanyo, Nicolett [1 ]
Peter, Beatrix [1 ]
Szekacs, Inna [1 ]
Horvath, Robert [1 ]
机构
[1] HUN REN Ctr Energy Res, Inst Tech Phys & Mat Sci, Nanobiosensor Lab, H-1121 Budapest, Hungary
[2] Budapest Univ Technol & Econ, Fac Elect Engn & Informat, Dept Automat & Appl Informat, H-1111 Budapest, Hungary
[3] Eotvos Lorand Univ, Dept Biol Phys, H-1117 Budapest, Hungary
来源
ACS SENSORS | 2024年 / 9卷 / 11期
关键词
resonant waveguide grating biosensor; celltype classification; phase-contrast microscope; deep learning; convolutionalneural network; cell activity-based classification; single-cell selection; BIOSENSOR;
D O I
10.1021/acssensors.4c01139
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There is an increasing need for simple-to-use, noninvasive, and rapid tools to identify and separate various cell types or subtypes at the single-cell level with sufficient throughput. Often, the selection of cells based on their direct biological activity would be advantageous. These steps are critical in immune therapy, regenerative medicine, cancer diagnostics, and effective treatment. Today, live cell selection procedures incorporate some kind of biomolecular labeling or other invasive measures, which may impact cellular functionality or cause damage to the cells. In this study, we first introduce a highly accurate single-cell segmentation methodology by combining the high spatial resolution of a phase-contrast microscope with the adhesion kinetic recording capability of a resonant waveguide grating (RWG) biosensor. We present a classification workflow that incorporates the semiautomatic separation and classification of single cells from the measurement data captured by an RWG-based biosensor for adhesion kinetics data and a phase-contrast microscope for highly accurate spatial resolution. The methodology was tested with one healthy and six cancer cell types recorded with two functionalized coatings. The data set contains over 5000 single-cell samples for each surface and over 12,000 samples in total. We compare and evaluate the classification using these two types of surfaces (fibronectin and noncoated) with different segmentation strategies and measurement timespans applied to our classifiers. The overall classification performance reached nearly 95% with the best models showing that our proof-of-concept methodology could be adapted for real-life automatic diagnostics use cases. The label-free measurement technique has no impact on cellular functionality, directly measures cellular activity, and can be easily tuned to a specific application by varying the sensor coating. These features make it suitable for applications requiring further processing of selected cells.
引用
收藏
页码:5815 / 5827
页数:13
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