4.7 Article

Label-free detection and enumeration of rare circulating tumor cells by bright-field image cytometry and multi-frame image correlation analysis

期刊

LAB ON A CHIP
卷 22, 期 18, 页码 3390-3401

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2lc00190j

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资金

  1. National Natural Science Foundation of China [61874099, 81802325, 62104248]
  2. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB44000000]
  3. Beijing Municipal Natural Science Foundation [4214083]
  4. Natural Science Foundation of Henan Province [202300410398]
  5. Opening Project of Key Laboratory of Microelectronic Devices & Integrated Technology, Institute of Microelectronics, Chinese Academy of Sciences
  6. Science and Technology Research Program of Henan Province [202102310209]
  7. Key Project of Scientific Research Foundation for Colleges and Universities in Henan Province [20B320025]

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This study introduces a bright-field image cytometry technique and a multi-frame image correlation algorithm for tumor cell detection. The results show that this method can detect tumor cells in real time, with high throughput and accuracy, and is of great significance for detecting rare cells.
Identification and enumeration of circulating tumor cells (CTCs) in peripheral blood are proved to correlate with the progress of metastatic cancer and can provide valuable information for diagnosis and monitoring of cancer. Here, we introduce a bright-field image cytometry (BFIC) technique, assisted by a multi-frame image correlation (MFIC) algorithm, as a label-free approach for tumor cell detection in peripheral blood. For this method, images of flowing cells in a wide channel were continuously recorded and cell types were determined simultaneously using a deep neural network of YOLO-V4 with an average precision (AP) of 98.63%, 99.04%, and 98.95% for cancer cell lines HT29, A549, and KYSE30, respectively. The use of the wide microfluidic channel (400 mu m width) allowed for a high throughput of 50 000 cells per min without clogging. Then erroneous or missed cell classifications caused by imaging angle differences or accidental misinterpretations in single frames were corrected by the multi-frame correlation analysis. This further improved the AP to 99.40%, 99.52%, and 99.47% for HT29, A549, and KYSE30, respectively. Meanwhile, cell counting was also accomplished in this dynamic process. Moreover, our imaging cytometry method can readily detect as few as 10 tumor cells from 100 000 white blood cells and was unaffected by the EMT process. Furthermore, CTCs from 8 advanced-stage cancer clinical samples were also successfully detected, while none for 6 healthy control subjects. Although this method is implemented for CTCs, it can also be used for the detection of other rare cells.

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