D-MAINS: A Deep-Learning Model for the Label-Free Detection of Mitosis, Apoptosis, Interphase, Necrosis, and Senescence in Cancer Cells

Author:

He Sarah12,Sillah Muhammed23,Cole Aidan R.24,Uboveja Apoorva24,Aird Katherine M.24,Chen Yu-Chih2567ORCID,Gong Yi-Nan23ORCID

Affiliation:

1. Department of Biological Sciences, Carnegie Mellon University, 5000 Forbes Avenue, Pittsburgh, PA 15213, USA

2. Hillman Cancer Center, UPMC, 5115 Center Avenue, Pittsburgh, PA 15232, USA

3. Department of Immunology, University of Pittsburgh School of Medicine, 3420 Forbes Avenue, Pittsburgh, PA 15260, USA

4. Department of Pharmacology & Chemical Biology, University of Pittsburgh School of Medicine, 3420 Forbes Avenue, Pittsburgh, PA 15260, USA

5. Department of Computational and Systems Biology, University of Pittsburgh School of Medicine, 3420 Forbes Avenue, Pittsburgh, PA 15260, USA

6. Department of Bioengineering, Swanson School of Engineering, University of Pittsburgh, 3700 O’Hara Street, Pittsburgh, PA 15260, USA

7. CMU-Pitt Ph.D. Program in Computational Biology, University of Pittsburgh, 3420 Forbes Avenue, Pittsburgh, PA 15260, USA

Abstract

Background: Identifying cells engaged in fundamental cellular processes, such as proliferation or living/death statuses, is pivotal across numerous research fields. However, prevailing methods relying on molecular biomarkers are constrained by high costs, limited specificity, protracted sample preparation, and reliance on fluorescence imaging. Methods: Based on cellular morphology in phase contrast images, we developed a deep-learning model named Detector of Mitosis, Apoptosis, Interphase, Necrosis, and Senescence (D-MAINS). Results: D-MAINS utilizes machine learning and image processing techniques, enabling swift and label-free categorization of cell death, division, and senescence at a single-cell resolution. Impressively, D-MAINS achieved an accuracy of 96.4 ± 0.5% and was validated with established molecular biomarkers. D-MAINS underwent rigorous testing under varied conditions not initially present in the training dataset. It demonstrated proficiency across diverse scenarios, encompassing additional cell lines, drug treatments, and distinct microscopes with different objective lenses and magnifications, affirming the robustness and adaptability of D-MAINS across multiple experimental setups. Conclusions: D-MAINS is an example showcasing the feasibility of a low-cost, rapid, and label-free methodology for distinguishing various cellular states. Its versatility makes it a promising tool applicable across a broad spectrum of biomedical research contexts, particularly in cell death and oncology studies.

Funder

National Institutes of Health

Ovarian Cancer Research Alliance

Publisher

MDPI AG

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