Evidence map›Paper›PMID 42869978›Full record

ArticleNature biomedical engineering2026

Interpretable AI model reveals spatial codes of cell recruitment in tissues.

Jia Yao, Ji Seon Shim, Kelly Wong, James Zhu, Yunhe Liu, Sung Wook Kang, Kelli McCord, Bryan M Burt, Jong Min Choi, Claire Lee and 19 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature biomedical engineering, 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

29 authors.

Jia Yao *Peter O'Donnell Jr. School of Public Health, UT Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0009-0005-5489-9853
Ji Seon Shim *David J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
Kelly WongChildren's Medical Center Research Institute, UT Southwestern Medical Center, Dallas, TX, USA.
James ZhuDepartment of Bioinformatics and Computational Biology, UT MD Anderson Cancer Center, Houston, TX, USA.
Yunhe LiuDepartment of Genomic Medicine, UT MD Anderson Cancer Center, Houston, TX, USA.
Sung Wook KangDavid J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
Kelli McCordDan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
Bryan M BurtDivision of Thoracic Surgery, Department of Surgery, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA.
Jong Min ChoiDavid J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
Claire LeeDavid J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
Idania Carolina Lubo JulioDepartment of Translational Molecular Pathology, UT MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0009-0002-0545-1444
Luisa Maren Solis SotoDepartment of Translational Molecular Pathology, UT MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-1253-630X
Sharia HernandezDepartment of Translational Molecular Pathology, UT MD Anderson Cancer Center, Houston, TX, USA.
Karen Colbert MaressoDepartment of Clinical Cancer Prevention, UT MD Anderson Cancer Center, Houston, TX, USA.
Yang LiuDepartment of Genomic Medicine, UT MD Anderson Cancer Center, Houston, TX, USA.
Yibo DaiDepartment of Genomic Medicine, UT MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0009-0007-8023-4665
Tian ChuDepartment of Genomic Medicine, UT MD Anderson Cancer Center, Houston, TX, USA.ORCID http://orcid.org/0000-0002-6840-0452
Wei LuDepartment of Translational Molecular Pathology, UT MD Anderson Cancer Center, Houston, TX, USA.
Khaja KhanDepartment of Translational Molecular Pathology, UT MD Anderson Cancer Center, Houston, TX, USA.
Paul F MansfieldDepartment of Surgical Oncology, UT MD Anderson Cancer Center, Houston, TX, USA.
Hee-Jin JangDavid J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA.
William H HudsonDan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0002-2513-1213
Tao YueCenter for the Genetics of Host Defense, UT Southwestern Medical Center, Dallas, TX, USA.
Bing ZhangLester and Sue Smith Breast Center, Baylor College of Medicine, Houston, TX, USA.ORCID http://orcid.org/0000-0001-8676-2425
Changwei LiPeter O'Donnell Jr. School of Public Health, UT Southwestern Medical Center, Dallas, TX, USA.
Linghua WangDepartment of Genomic Medicine, UT MD Anderson Cancer Center, Houston, TX, USA. LWang22@mdanderson.org.ORCID http://orcid.org/0000-0001-9380-0266
Hao ZhuChildren's Medical Center Research Institute, UT Southwestern Medical Center, Dallas, TX, USA. Hao.Zhu@UTSouthwestern.edu.ORCID http://orcid.org/0000-0002-8417-9698
Hyun-Sung LeeDavid J. Sugarbaker Division of Thoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, TX, USA. Hyun-Sung.Lee@bcm.edu.ORCID http://orcid.org/0000-0001-8259-046X
Tao WangDepartment of Bioinformatics and Computational Biology, UT MD Anderson Cancer Center, Houston, TX, USA. TWang10@mdanderson.org.ORCID http://orcid.org/0000-0002-4355-149X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Understanding which molecular signals recruit specific cells to precise tissue locations is fundamental to tissue biology, immunity and disease. Existing computational tools for spatially resolved transcriptomics (SRT) describe where cells reside but cannot explain why. Here we introduce SPACER, a fully interpretable multi-instance learning framework that decodes gene-level recruitment rules directly from SRT data. Applied to 37 SRT datasets spanning multiple human tumour types and mouse heart, SPACER achieved 4-21-fold improvement over existing methods in various tasks of recovering biologically meaningful recruitment signals. SPACER revealed (1) that tumour-expressed mucins are associated with physical barriers to T cell engagement, which predicts resistance to immune checkpoint inhibitors and patient prognosis, (2) that local antigen presentation is the dominant correlate of T cell engagement across cancer types and (3) that Cd4

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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.