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Automatic detection of circulating tumor cells and cancer associated fibroblasts using deep learning.
Shen, Cheng; Rawal, Siddarth; Brown, Rebecca; Zhou, Haowen; Agarwal, Ashutosh; Watson, Mark A; Cote, Richard J; Yang, Changhuei.
Affiliation
  • Shen C; Department of Electrical Engineering, California Institute of Technology, Pasadena, CA, 91125, USA.
  • Rawal S; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
  • Brown R; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
  • Zhou H; Department of Electrical Engineering, California Institute of Technology, Pasadena, CA, 91125, USA.
  • Agarwal A; Department of Biomedical Engineering, DJTMF Biomedical Nanotechnology Institute, University of Miami, Coral Gables, FL, 33146, USA.
  • Watson MA; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA.
  • Cote RJ; Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 63110, USA. rcote@wustl.edu.
  • Yang C; Department of Electrical Engineering, California Institute of Technology, Pasadena, CA, 91125, USA. chyang@caltech.edu.
Sci Rep ; 13(1): 5708, 2023 04 07.
Article in En | MEDLINE | ID: mdl-37029224
ABSTRACT
Circulating tumor cells (CTCs) and cancer-associated fibroblasts (CAFs) from whole blood are emerging as important biomarkers that potentially aid in cancer diagnosis and prognosis. The microfilter technology provides an efficient capture platform for them but is confounded by two challenges. First, uneven microfilter surfaces makes it hard for commercial scanners to obtain images with all cells in-focus. Second, current analysis is labor-intensive with long turnaround time and user-to-user variability. Here we addressed the first challenge through developing a customized imaging system and data pre-processing algorithms. Utilizing cultured cancer and CAF cells captured by microfilters, we showed that images from our custom system are 99.3% in-focus compared to 89.9% from a top-of-the-line commercial scanner. Then we developed a deep-learning-based method to automatically identify tumor cells serving to mimic CTC (mCTC) and CAFs. Our deep learning method achieved precision and recall of 94% (± 0.2%) and 96% (± 0.2%) for mCTC detection, and 93% (± 1.7%) and 84% (± 3.1%) for CAF detection, significantly better than a conventional computer vision method, whose numbers are 92% (± 0.2%) and 78% (± 0.3%) for mCTC and 58% (± 3.9%) and 56% (± 3.5%) for CAF. Our custom imaging system combined with deep learning cell identification method represents an important advance on CTC and CAF analysis.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cancer-Associated Fibroblasts / Deep Learning / Neoplastic Cells, Circulating Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Sci Rep Year: 2023 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cancer-Associated Fibroblasts / Deep Learning / Neoplastic Cells, Circulating Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Sci Rep Year: 2023 Type: Article Affiliation country: United States