Evidence map›Paper›PMID 40000764›Full record

ArticleCommunications biology2025

Evaluating feature extraction in ovarian cancer cell line co-cultures using deep neural networks.

Osheen Sharma, Greta Gudoityte, Rezan Minozada, Olli P Kallioniemi, Riku Turkki, Lassi Paavolainen, Brinton Seashore-Ludlow

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

7 authors.

Osheen SharmaDepartment of Oncology-Pathology, Karolinska Institutet, Science for Life Laboratory, Stockholm, Sweden. osheen.sharma@ki.se.ORCID http://orcid.org/0009-0007-6079-0189
Greta GudoityteDepartment of Oncology-Pathology, Karolinska Institutet, Science for Life Laboratory, Stockholm, Sweden.
Rezan MinozadaDepartment of Oncology-Pathology, Karolinska Institutet, Science for Life Laboratory, Stockholm, Sweden.
Olli P KallioniemiDepartment of Oncology-Pathology, Karolinska Institutet, Science for Life Laboratory, Stockholm, Sweden.
Riku TurkkiInstitute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.
Lassi PaavolainenInstitute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0003-1508-2718
Brinton Seashore-LudlowDepartment of Oncology-Pathology, Karolinska Institutet, Science for Life Laboratory, Stockholm, Sweden. brinton.seashore-ludlow@ki.se.ORCID http://orcid.org/0000-0001-8658-5967

Funding

Knut och Alice Wallenbergs Stiftelse (Knut and Alice Wallenberg Foundation) 2015.0291Vetenskapsrådet (Swedish Research Council) 2017-06095Vetenskapsrådet (Swedish Research Council) 2021-03420
6 · The paper itself

Abstract

Single-cell image analysis is crucial for studying drug effects on cellular morphology and phenotypic changes. Most studies focus on single cell types, overlooking the complexity of cellular interactions. Here, we establish an analysis pipeline to extract phenotypic features of cancer cells cultured with fibroblasts. Using high-content imaging, we analyze an oncology drug library across five cancer and fibroblast cell line co-culture combinations, generating 61,440 images and ∼170 million single-cell objects. Traditional phenotyping with CellProfiler achieves an average enrichment score of 62.6% for mechanisms of action, while pre-trained neural networks (EfficientNetB0 and MobileNetV2) reach 61.0% and 62.0%, respectively. Variability in enrichment scores may reflect the use of multiple drug concentrations since not all induce significant morphological changes, as well as the cellular and genetic context of the treatment. Our study highlights nuanced drug-induced phenotypic variations and underscores the morphological heterogeneity of ovarian cancer cell lines and their response to complex co-culture environments.

Indexed as

Neural Networks, ComputerOvarian NeoplasmsAntineoplastic AgentsCell Line, TumorCoculture TechniquesFemaleFibroblastsHumansPhenotypeSingle-Cell AnalysisAntineoplastic Agents

Identifiers

PMID40000764
PMCPMC11862010

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.