1. Detection of circulating tumor cells by means of machine learning using Smart-Seq2 sequencing.
- Author
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Pastuszak K, Sieczczyński M, Dzięgielewska M, Wolniak R, Drewnowska A, Korpal M, Zembrzuska L, Supernat A, and Żaczek AJ
- Subjects
- Humans, Female, Single-Cell Analysis methods, Leukocytes, Mononuclear metabolism, Triple Negative Breast Neoplasms genetics, Triple Negative Breast Neoplasms pathology, Triple Negative Breast Neoplasms diagnosis, Sequence Analysis, RNA methods, Algorithms, Biomarkers, Tumor genetics, Neoplastic Cells, Circulating metabolism, Neoplastic Cells, Circulating pathology, Machine Learning, Breast Neoplasms genetics, Breast Neoplasms pathology, Breast Neoplasms diagnosis, Breast Neoplasms blood
- Abstract
Circulating tumor cells (CTCs) are tumor cells that separate from the solid tumor and enter the bloodstream, which can cause metastasis. Detection and enumeration of CTCs show promising potential as a predictor for prognosis in cancer patients. Furthermore, single-cells sequencing is a technique that provides genetic information from individual cells and allows to classify them precisely and reliably. Sequencing data typically comprises thousands of gene expression reads per cell, which artificial intelligence algorithms can accurately analyze. This work presents machine-learning-based classifiers that differentiate CTCs from peripheral blood mononuclear cells (PBMCs) based on single cell RNA sequencing data. We developed four tree-based models and we trained and tested them on a dataset consisting of Smart-Seq2 sequenced data from primary tumor sections of breast cancer patients and PBMCs and on a public dataset with manually annotated CTC expression profiles from 34 metastatic breast patients, including triple-negative breast cancer. Our best models achieved about 95% balanced accuracy on the CTC test set on per cell basis, correctly detecting 133 out of 138 CTCs and CTC-PBMC clusters. Considering the non-invasive character of the liquid biopsy examination and our accurate results, we can conclude that our work has potential application value., (© 2024. The Author(s).)
- Published
- 2024
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