Evidence map›Paper›PMID 37524741›Full record

ArticleCell death discovery2023

CellDeathPred: a deep learning framework for ferroptosis and apoptosis prediction based on cell painting.

Kenji Schorpp, Alaa Bessadok, Aidin Biibosunov, Ina Rothenaigner, Stefanie Strasser, Tingying Peng, Kamyar Hadian

Abstract read
In one paragraph

Article in Cell death discovery, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

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  11. A morphology and secretome map of pyroptosis.Molecular biology of the cell · 2025
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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.

Kenji Schorpp *Research Unit Signaling and Translation, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.
Alaa Bessadok *Helmholtz AI, Helmholtz Zentrum München, Neuherberg, Germany.
Aidin Biibosunov *Helmholtz AI, Helmholtz Zentrum München, Neuherberg, Germany.
Ina RothenaignerResearch Unit Signaling and Translation, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.
Stefanie StrasserResearch Unit Signaling and Translation, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0003-3968-1192
Tingying PengHelmholtz AI, Helmholtz Zentrum München, Neuherberg, Germany. tingying.peng@helmholtz-munich.de.ORCID http://orcid.org/0000-0002-7881-1749
Kamyar HadianResearch Unit Signaling and Translation, Molecular Targets and Therapeutics Center, Helmholtz Zentrum München, Neuherberg, Germany. kamyar.hadian@helmholtz-munich.de.ORCID http://orcid.org/0000-0001-8727-2575

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cell death, such as apoptosis and ferroptosis, play essential roles in the process of development, homeostasis, and pathogenesis of acute and chronic diseases. The increasing number of studies investigating cell death types in various diseases, particularly cancer and degenerative diseases, has raised hopes for their modulation in disease therapies. However, identifying the presence of a particular cell death type is not an obvious task, as it requires computationally intensive work and costly experimental assays. To address this challenge, we present CellDeathPred, a novel deep-learning framework that uses high-content imaging based on cell painting to distinguish cells undergoing ferroptosis or apoptosis from healthy cells. In particular, we incorporate a deep neural network that effectively embeds microscopic images into a representative and discriminative latent space, classifies the learned embedding into cell death modalities, and optimizes the whole learning using the supervised contrastive loss function. We assessed the efficacy of the proposed framework using cell painting microscopy data sets from human HT-1080 cells, where multiple inducers of ferroptosis and apoptosis were used to trigger cell death. Our model confidently separates ferroptotic and apoptotic cells from healthy controls, with an average accuracy of 95% on non-confocal data sets, supporting the capacity of the CellDeathPred framework for cell death discovery.

Identifiers

PMID37524741
PMCPMC10390533

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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 OpenQuestion graph.