Evidence map›Paper›PMID 40998830›Full record

ArticleNature communications2025

Graph neural networks learn emergent tissue properties from spatial molecular profiles.

Mayar Ali, Sabrina Richter, Ali Ertürk, David S Fischer, Fabian J Theis

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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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

5 authors.

Mayar Ali *Institute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany.
Sabrina Richter *Institute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany.
Ali ErtürkInstitute for Tissue Engineering and Regenerative Medicine, Helmholtz Zentrum München, Neuherberg, Germany.ORCID http://orcid.org/0000-0001-5163-5100
David S FischerInstitute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany. david.fischer@meduniwien.ac.at.
Fabian J TheisInstitute of Computational Biology, Helmholtz Zentrum München, Neuherberg, Germany. fabian.theis@helmholtz-munich.de.ORCID http://orcid.org/0000-0002-2419-1943

Funding

Wellcome Trust
6 · The paper itself

Abstract

Tissue phenotypes, such as metabolic states, inflammation, and tumor properties, emerge from both molecular states and spatial cell organization. Spatial molecular assays provide an unbiased view of tissue architecture, enabling phenotype prediction. Graph neural networks (GNNs) offer a natural framework for analyzing spatial proteomics by integrating expression profiles with structure. We apply GNNs to classify tissue phenotypes using spatial cell patterns. We show that for relatively simple classification tasks, such as tumor grading in breast cancer, incorporating spatial context does not significantly improve predictive performance over models trained on single-cell or pseudobulk representations. However, GNNs capture meaningful spatial features, retaining prognostic signals beyond tumor labels, highlighting tumor-grade-specific cell type interactions, and uncovering complex immune infiltration patterns in colorectal cancer not detectable with traditional approaches. These findings suggest that while spatial dependencies may not always enhance classification performance in small datasets, GNNs remain valuable tools for characterizing tissue organization and interactions.

Indexed as

Breast NeoplasmsNeural Networks, ComputerColorectal NeoplasmsFemaleGraph Neural NetworksHumansPhenotypeProteomics

Identifiers

PMID40998830
PMCPMC12462520

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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.