Evaluating the utility of brightfield image data for mechanism of action prediction.


Journal

PLoS computational biology
ISSN: 1553-7358
Titre abrégé: PLoS Comput Biol
Pays: United States
ID NLM: 101238922

Informations de publication

Date de publication:
07 2023
Historique:
received: 27 12 2022
accepted: 02 07 2023
revised: 04 08 2023
medline: 7 8 2023
pubmed: 25 7 2023
entrez: 25 7 2023
Statut: epublish

Résumé

Fluorescence staining techniques, such as Cell Painting, together with fluorescence microscopy have proven invaluable for visualizing and quantifying the effects that drugs and other perturbations have on cultured cells. However, fluorescence microscopy is expensive, time-consuming, labor-intensive, and the stains applied can be cytotoxic, interfering with the activity under study. The simplest form of microscopy, brightfield microscopy, lacks these downsides, but the images produced have low contrast and the cellular compartments are difficult to discern. Nevertheless, by harnessing deep learning, these brightfield images may still be sufficient for various predictive purposes. In this study, we compared the predictive performance of models trained on fluorescence images to those trained on brightfield images for predicting the mechanism of action (MoA) of different drugs. We also extracted CellProfiler features from the fluorescence images and used them to benchmark the performance. Overall, we found comparable and largely correlated predictive performance for the two imaging modalities. This is promising for future studies of MoAs in time-lapse experiments for which using fluorescence images is problematic. Explorations based on explainable AI techniques also provided valuable insights regarding compounds that were better predicted by one modality over the other.

Identifiants

pubmed: 37490493
doi: 10.1371/journal.pcbi.1011323
pii: PCOMPBIOL-D-22-01901
pmc: PMC10403126
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1011323

Informations de copyright

Copyright: © 2023 Harrison et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Philip John Harrison (PJ)

Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Science for Life Laboratory, Uppsala, Sweden.

Ankit Gupta (A)

Department of Information Technology, Uppsala University, Uppsala, Sweden.

Jonne Rietdijk (J)

Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Science for Life Laboratory, Uppsala, Sweden.

Håkan Wieslander (H)

Department of Information Technology, Uppsala University, Uppsala, Sweden.

Jordi Carreras-Puigvert (J)

Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Science for Life Laboratory, Uppsala, Sweden.

Polina Georgiev (P)

Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Science for Life Laboratory, Uppsala, Sweden.

Carolina Wählby (C)

Science for Life Laboratory, Uppsala, Sweden.
Department of Information Technology, Uppsala University, Uppsala, Sweden.

Ola Spjuth (O)

Department of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Science for Life Laboratory, Uppsala, Sweden.

Ida-Maria Sintorn (IM)

Department of Information Technology, Uppsala University, Uppsala, Sweden.

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