Evidence map›Paper›PMID 41644582›Full record

ArticleScientific reports2026

Integrative analyses of metastatic cancer transcriptome reveal clinically distinct cellular States and ecosystems.

Can Zhang, Si Li, Yun Yu, Meng Chi, Ziming Yuan, Kun Wang

Abstract read
In one paragraph

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

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Can ZhangDepartment of Anesthesiology, The First Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.
Si LiDepartment of Anesthesiology, The First Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China.
Yun YuSchool of Interdisciplinary Medicine and Engineering, Harbin Medical University, Harbin, 150081, Heilongjiang, People's Republic of China.
Meng ChiDepartment of Anesthesiology, Harbin Medical University Cancer Hospital, Harbin, 150081, China. chimeng1876@hrbmu.edu.cn.
Ziming YuanDepartment of Colorectal Cancer Surgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, 150000, Heilongjiang, People's Republic of China. yuanziming@hrbmu.edu.cn.
Kun WangDepartment of Anesthesiology, The First Affiliated Hospital of Harbin Medical University, Harbin, People's Republic of China. hydwangkun@126.com.

Funding

Science and Technology Innovation Program of Xiongan New Area 2023XAGG0070Scientific Research Fund Project of Heilongjiang Provincial Health Commission 20220404110978
6 · The paper itself

Abstract

Determining the diverse cellular states and their organization into cellular ecosystems that make up metastatic tumor is vital for elucidating the biological and prognostic diversity of cancer. However, large-scale studies profiling the clinical relevance of these cellular states and ecotypes are still lacking in metastatic cancers. In this study, we used EcoTyper, a machine learning framework, to comprehensively analyze transcriptomes from 2822 metastatic cancer patient samples covering 25 cancer types, enabling characterization of the fundamental cellular states and tumor ecosystems integral to metastatic cancer. We identified 45 distinct cellular states across 12 cell types and validated their robustness in validation cohorts. We observed that they differed in functional and prognostic associations. Survival analysis revealed that the clinically relevant cellular states, highlighting their promise as predictors of clinical outcomes. Functional enrichment analysis exhibited that the marker genes of cellular states were significantly enriched in cancer hallmark and immune-related pathways. In addition, our analysis identified five ecotypes associated with different clinical outcomes. Transcription factor enrichment analysis revealed key transcription factors (i.e. SPIB, SRF, and NR1D1) that were significantly associated with patient clinical outcomes. In conclusion, this study provided a high-resolution landscape of cellular states and ecosystems in metastatic tumors, offering new potential targets for the development of cancer treatment strategies and prognostic assessment.

Indexed as

NeoplasmsTranscriptomeBiomarkers, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansNeoplasm MetastasisPrognosisTumor MicroenvironmentBiomarkers, TumorCellular statesClinical prognosisMachine learningMetastatic cancerTranscriptional regulationTumor microenvironment

Identifiers

PMID41644582
PMCPMC12923827

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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.