Evidence map›Paper›PMID 40275021›Full record

ArticleScientific reports2025

Leveraging TME features and multi-omics data with an advanced deep learning framework for improved Cancer survival prediction.

Xuan Fan, Zihao He, Jing Guo, Dechao Bu, Dongchen Han, Xinchi Qu, Qihang Li, Sen Cheng, Aiqing Han, Jincheng Guo

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Integrating multi-omics data for next-generation cancer research and precision medicine.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  3. Article
  4. Review
  5. Review
  6. Artificial Intelligence-Driven Multi-Omics Approaches in Glioblastoma.International journal of molecular sciences · 2025
    Review
  7. Article
  8. Microbial signatures in metastatic cancer.Frontiers in medicine · 2025
    Review
  9. Article
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

10 authors.

Xuan Fan *School of Management, Beijing University of Chinese Medicine, Ningbo, China.
Zihao He *Ningbo No. 2 Hospital, Ningbo, 315010, China.
Jing Guo *Department of Neurosurgery, Peking University Third Hospital, Peking University, Beijing, China.
Dechao BuResearch Center for Ubiquitous Computing Systems, Institute of Computing Technology, Chinese Academy of Sciences, Beijing, China.
Dongchen HanSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Ningbo, China.
Xinchi QuSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Ningbo, China.
Qihang LiHenan University, Kaifeng, 475004, China.
Sen ChengDepartment of Neurosurgery, Beijing Tiantan Hospital Affiliated to Capital Medical University, Beijing, 100070, China. dr.sencheng@hotmail.com.
Aiqing HanSchool of Management, Beijing University of Chinese Medicine, Ningbo, China. aqhan@hotmail.com.
Jincheng GuoSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Ningbo, China. guojincheng@bucm.edu.cn.

Funding

National Key Research and Development Program of China 2022YFF1203303Ningbo Science and Technology Innovation Yongjiang 2035 Project 2024Z229
6 · The paper itself

Abstract

Glioma, a malignant intracranial tumor with high invasiveness and heterogeneity, significantly impacts patient survival. This study integrates multi-omics data to improve prognostic prediction and identify therapeutic targets. Using single-cell data from glioblastoma (GBM) and low-grade glioma (LGG) samples, we identified 55 distinct cell states via the EcoTyper framework, validated for stability and prognostic impact in an independent cohort. We constructed multi-omics datasets of 620 samples, integrating transcriptomic, copy number variation (CNV), somatic mutation (MUT), Microbe (MIC), EcoTyper result data. A scRNA-seq enhanced Self-Normalizing Network-based glioma prognosis model achieved a C-index of 0.822 (training) and 0.817 (test), with AUC values of 0.867, 0.876, and 0.844 at 1, 3, and 5 years in the training set, and 0.820, 0.947, and 0.936 in the test set. Gradient attribution analysis enhanced the interpretability of the model and identified key molecular markers. The classification into high- and low-risk groups was validated as an independent prognostic factor. HDAC inhibitors are proposed as potential treatments. This study demonstrates the potential of integrating scRNA-seq and multi-omics data for robust glioma prognosis and clinical decision-making support.

Indexed as

Brain NeoplasmsDeep LearningGlioblastomaGliomaTumor MicroenvironmentBiomarkers, TumorDNA Copy Number VariationsFemaleHumansMaleMultiomicsMutationPrognosisSingle-Cell AnalysisTranscriptomeBiomarkers, Tumor

Identifiers

PMID40275021
PMCPMC12022115

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.