Evidence map›Paper›PMID 41759628›Full record

ArticleMolecular & cellular proteomics : MCP2026

mosna Reveals Different Types of Cellular Interactions Predictive of Response to Immunotherapies and Survival in Cancer.

Alexis Coullomb, Colas Foulon, Bram van Haastrecht, Paul Monsarrat, Vera Pancaldi

Abstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
4 · The record

Corrections and comments

  • Update of
    2024
5 · Who and what money

Authors and funding

5 authors.

Alexis CoullombCRCT Cancer Research Center of Toulouse, Université de Toulouse, Inserm, Toulouse, France; University of Toulouse, CNRS UMR 5070, INSERM U1301, EFS, ENVT, Institut RESTORE, Toulouse, France. Electronic address: alexis.coullomb@inserm.fr.
Colas FoulonUniversity of Toulouse, CNRS UMR 5070, INSERM U1301, EFS, ENVT, Institut RESTORE, Toulouse, France.
Bram van HaastrechtCRCT Cancer Research Center of Toulouse, Université de Toulouse, Inserm, Toulouse, France.
Paul MonsarratUniversity of Toulouse, CNRS UMR 5070, INSERM U1301, EFS, ENVT, Institut RESTORE, Toulouse, France; Oral Medicine Department and Hospital of Toulouse - Toulouse Institute of Oral Medicine and Science, Toulouse, France.
Vera PancaldiCRCT Cancer Research Center of Toulouse, Université de Toulouse, Inserm, Toulouse, France. Electronic address: vera.pancaldi@inserm.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spatially resolved omics enable the discovery of tissue organization of biological or clinical importance. Despite the existence of several methods, performing a rational analysis, including multiple algorithms while integrating different conditions such as clinical data, is still not trivial. To make such investigations more accessible, we developed mosna, a Python package to analyze spatial omics data in integration with clinical or biological data, providing insight into cell interaction patterns or tissue architecture. mosna is compatible with all spatial omics techniques, leverages tysserand to build accurate spatial networks, and is compatible with Squidpy. It proposes an analysis pipeline in which increasingly complex features computed at each step with either the mosna-algorithms or others can be explored in integration with clinical data. The approach produces easy-to-use descriptive statistics and data visualization while seamlessly training machine learning models and identifying variables with the most predictive power. mosna can take as input any dataset produced by spatial omics methods, including sub-cellular resolved transcriptomics (MERFISH, seqFISH, and Xenium) and proteomics (CODEX, MIBI-TOF, and low-plex immuno-fluorescence) as well as spot-based spatial transcriptomics (10x Visium, Slide-seq, and Stereo-seq). Integration with experimental metadata or clinical data is adapted to binary conditions, such as biological treatments or response status of patients, and to survival data. We demonstrate the proposed analysis pipeline on two spatially resolved proteomic datasets and a spatial transcriptomics dataset containing either binary response to immunotherapy or survival data, and we assess the performance of the proposed niche discovering method in a manually annotated spatial transcriptomic dataset. mosna identifies features describing cellular composition and spatial patterns that can provide biological insight regarding factors that affect response to immunotherapies or survival. mosna is made publicly available to the community, together with relevant documentation at https://mosna-documentation.readthedocs.io/en/latest/index.html and tutorials implemented as Jupyter notebooks to reproduce the result at https://github.com/AlexCoul/mosna.

Indexed as

Cell CommunicationImmunotherapyNeoplasmsSoftwareAlgorithmsHumansMultiomicsProteomicsSpatial Transcriptomicsbiomarkerscancercellular interactionsmulti-omicsspatial-omics

Identifiers

PMID41759628
PMCPMC13137193

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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.