Evidence map›Paper›PMID 41326702›Full record

ArticleCommunications biology2025

Hypergraph-driven spatial multimodal fusion for precise domain delineation and tumor microenvironment decoding.

Chengyang Zhang, Xulong Li, Bo Li, Chenxun Deng, Mengran Li, Shiqi Zhang, Weijiang Yu, Hongyu Zhang, Zheng Wang, Yuedong Yang and 1 more

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Decoding the breast cancer microenvironment by spatial multi-omics: from architecture to clinical translation.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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.

Chengyang Zhang *School of Big Data and Software Engineering, Chongqing University, Chongqing, China.ORCID http://orcid.org/0000-0003-3658-5779
Xulong Li *Faculty of Mechanical Engineering, Southwest Jiaotong University, Chengdu, China.
Bo LiDepartment of Computer and Information Science, University of Macau, Taipa, China.ORCID http://orcid.org/0000-0003-0608-1502
Chenxun DengInstitute of Automation, Chinese Academy of Sciences, Beijing, China.
Mengran LiSchool of Intelligent Systems Engineering, Sun Yat-sen University, Shenzhen, China.
Shiqi ZhangSchool of Big Data and Software Engineering, Chongqing University, Chongqing, China.ORCID http://orcid.org/0009-0006-4224-9607
Weijiang YuSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.
Hongyu ZhangSchool of Big Data and Software Engineering, Chongqing University, Chongqing, China.ORCID http://orcid.org/0000-0002-3063-9425
Zheng WangJinfeng Laboratory, Chongqing, China.
Yuedong YangSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou, China.ORCID http://orcid.org/0000-0002-6782-2813
Yuansong ZengSchool of Big Data and Software Engineering, Chongqing University, Chongqing, China. zengys@cqu.edu.cn.ORCID http://orcid.org/0009-0003-6470-0671

Funding

China Postdoctoral Science Foundation 2025T180408National Natural Science Foundation of China (National Science Foundation of China) 62402071
6 · The paper itself

Abstract

Recent advancements in spatial transcriptomics have transformed tumor microenvironment research by providing insights into cellular interactions and spatial heterogeneity. A fundamental challenge is the precise delineation of spatial domains. However, existing methods remain limited in accurately identifying spatial domains, partially due to their reliance on single-view features. Moreover, these methods often struggle with many-to-many spot relationships, such as shared biological functions. To this end, we propose HAST, a hypergraph-driven spatial multimodal fusion tool for precise domain delineation and tumor microenvironment decoding. HAST integrates gene expression, spatial coordinates, and histological features to construct local hypergraphs that effectively model many-to-many spatial relationships. These local hypergraphs are dynamically aggregated into a global hypergraph, capturing higher-order interactions. To learn discriminative and biologically meaningful representations, we employ a hypergraph convolutional network, coupled with self-supervised contrastive learning, to fuse multi-view information. Extensive benchmarking across multiple datasets demonstrates that HAST outperforms state-of-the-art methods, accurately delineating spatial domains and uncovering domain-associated genes. Functional enrichment analyses further reveal biologically relevant pathways and provide novel insights into tumor microenvironment. In summary, HAST is a robust framework for decoding the spatial complexity of tumors, paving the way for precise spatial omics analyses in cancer research.

Indexed as

Computational BiologyNeoplasmsTumor MicroenvironmentGene Expression ProfilingHumansTranscriptome

Identifiers

PMID41326702
PMCPMC12789518

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.