细胞病理学
病理
形态学(生物学)
细针穿刺
免疫染色
生物
体细胞
单元格排序
细胞
细胞学
流式细胞术
计算生物学
医学
活检
免疫组织化学
分子生物学
基因
生物化学
遗传学
作者
Anastasia Mavropoulos,Chassidy Johnson,Vivian Lu,Jordan Nieto,Emilie C. Schneider,Kiran Saini,Michael L. Phelan,Linda Hsie,Maggie J. Wang,Janifer Cruz,Jeanette Mei,Julie Kim,Zhouyang Lian,Nianzhen Li,Stéphane C. Boutet,Amy Wong-Thai,Weibo Yu,Qing‐Yi Lu,Teresa Kim,Yipeng Geng
出处
期刊:Modern Pathology
[Elsevier BV]
日期:2023-04-24
卷期号:36 (8): 100195-100195
被引量:30
标识
DOI:10.1016/j.modpat.2023.100195
摘要
Cell morphology is a fundamental feature used to evaluate patient specimens in pathologic analysis. However, traditional cytopathology analysis of patient effusion samples is limited by low tumor cell abundance coupled with the high background of nonmalignant cells, restricting the ability of downstream molecular and functional analyses to identify actionable therapeutic targets. We applied the Deepcell platform that combines microfluidic sorting, brightfield imaging, and real-time deep learning interpretations based on multidimensional morphology to enrich carcinoma cells from malignant effusions without cell staining or labels. Carcinoma cell enrichment was validated with whole genome sequencing and targeted mutation analysis, which showed a higher sensitivity for detection of tumor fractions and critical somatic variant mutations that were initially at low levels or undetectable in presort patient samples. Our study demonstrates the feasibility and added value of supplementing traditional morphology-based cytology with deep learning, multidimensional morphology analysis, and microfluidic sorting.
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