Evidence map›Paper›PMID 37490493›Full record

ArticlePLoS computational biology2023

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

Philip John Harrison, Ankit Gupta, Jonne Rietdijk, Håkan Wieslander, Jordi Carreras-Puigvert, Polina Georgiev, Carolina Wählby, Ola Spjuth, Ida-Maria Sintorn

Abstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Review
  3. Deep Learning-Powered Scalable Cancer Organ Chip for Cancer Precision Medicine.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Alternate dyes for image-based profiling assays.SLAS discovery : advancing life sciences R & D · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Integrating Biological Knowledge for Robust Microscopy Image Profiling onProceedings. IEEE International Conference on Computer Vision · 2025
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Philip John HarrisonDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.ORCID 0000-0003-4046-9017
Ankit GuptaDepartment of Information Technology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-9961-1041
Jonne RietdijkDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Håkan WieslanderDepartment of Information Technology, Uppsala University, Uppsala, Sweden.
Jordi Carreras-PuigvertDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Polina GeorgievDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.
Carolina WählbyScience for Life Laboratory, Uppsala, Sweden.
Ola SpjuthDepartment of Pharmaceutical Biosciences, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-8083-2864
Ida-Maria SintornDepartment of Information Technology, Uppsala University, Uppsala, Sweden.ORCID 0000-0002-8307-7411

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Image Processing, Computer-AssistedCells, CulturedMicroscopy, Fluorescence

Identifiers

PMID37490493
PMCPMC10403126

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.