Evidence map›Paper›PMID 42143015›Full record

ArticleCell reports methods2026

Data modeling the interplay between single-cell shape, single-cell protein expression, and tissue state.

Yuval Tamir, Yuval Bussi, Claudia Owczarek, Luciana Luque, Giuseppe Torrisi, Leor Ariel Rose, Orit Kliper-Gross, Linus Schumacher, Maddy Parsons, Leeat Keren and 1 more

Abstract read
In one paragraph

Article in Cell reports methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Yuval TamirInstitute for Interdisciplinary Computational Science, Stein Faculty of Computer and Information Science, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Yuval BussiDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 761001, Israel; Department of Mathematics and Computer Science, Weizmann Institute of Science, Rehovot 761001, Israel.
Claudia OwczarekRandall Centre for Cell and Molecular Biophysics, King's College London, Guy's Campus, London SE1 1UL, UK.
Luciana LuqueCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Giuseppe TorrisiCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Leor Ariel RoseInstitute for Interdisciplinary Computational Science, Stein Faculty of Computer and Information Science, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Orit Kliper-GrossInstitute for Interdisciplinary Computational Science, Stein Faculty of Computer and Information Science, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel.
Linus SchumacherCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, UK.
Maddy ParsonsRandall Centre for Cell and Molecular Biophysics, King's College London, Guy's Campus, London SE1 1UL, UK.
Leeat KerenDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 761001, Israel.
Assaf ZaritskyInstitute for Interdisciplinary Computational Science, Stein Faculty of Computer and Information Science, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel. Electronic address: assafzar@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While cell shape fundamentally governs tissue function, the underlying links between single-cell shape and protein expression have been difficult to resolve due to limitations in imaging multiplexing and population averaging. Here, we use multiplexed imaging and machine learning to investigate the coupling of cell shape and protein expression in heterogeneous human tissues. Our analysis establishes a universal, bi-directional link between a cell's shape and its protein expression across cell types, diseases, and disease states, amplified for cell state markers. Machine learning interpretability shows that shape features can potentially generate hypotheses of protein functions. Screening all protein-cell type pairs identified a subpopulation of large, p53-positive tumor cells across two cancers. Shape properties further enhanced graph neural network disease state prediction. Our results open the door to unraveling the intricate connections between protein expression, cell shape, tissue organization, and tissue state in a physiological context.

Indexed as

Cell ShapeSingle-Cell AnalysisGraph Neural NetworksHumansMachine Learningcell shapeCP: systems biologygraph neural networkmachine learningmultiplexed imagingspatial proteomics

Identifiers

PMID42143015
PMCPMC13390080

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Registered trials

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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.