Evidence map›Paper›PMID 40263498›Full record

ArticleScientific reports2025

Multi-omics analysis constructs a novel neuroendocrine prostate cancer classifier and classification system.

Junxiao Shen, Luyuan Lu, Zujie Chen, Wei Guo, Shuwen Wang, Ziqiao Liu, Xuke Gong, Yiming Qi, Ruyi Jin, Cheng Zhang

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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  5. Review
  6. Genomic insights for neuroendocrine prostate cancer.Journal of the Chinese Medical Association : JCMA · 2025
    Article
  7. 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

10 authors.

Junxiao ShenDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Luyuan LuDepartment of General Surgery, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Zujie ChenDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Wei GuoDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Shuwen WangDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Ziqiao LiuDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Xuke GongDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Yiming QiDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China.
Ruyi JinDepartment of Dermatology, NHC Key Laboratory of Immunodermatology, The First Hospital of China Medical University, China Medical University, Shenyang, 110001, People's Republic of China.
Cheng ZhangDepartment of Urology, The Fourth Affiliated Hospital of the School of Medicine, International School of Medicine, International Institutes of Medicine, Zhejiang University, Yiwu, 322000, China. 8021006@zju.edu.c.

Funding

Natural Science Foundation of Zhejiang Province LZ22H160008
6 · The paper itself

Abstract

Neuroendocrine prostate cancer (NEPC), a subtype of prostate cancer (PCa) with poor prognosis and high heterogeneity, currently lacks accurate markers. This study aims to identify a robust NEPC classifier and provide new perspectives for resolving intra- tumoral heterogeneity. Multi-omics analysis included 19 bulk transcriptomics, 14 single-cell transcriptomics, 1 spatial transcriptomics, 16 published NE signatures and 10 cellular experiments combined with multiple machine learning algorithms to construct a novel NEPC classifier and classification. A comprehensive single-cell atlas of prostate cancer was created from 70 samples, comprising 196,309 cells, among which 9% were identified as NE cells. Within this framework and in combination with bulk transcriptomics, a total of 100 high-quality NE-specific feature genes were identified and differentiated into NEPup sig and NEPdown sig. The random forest (RF) algorithm proved to be the most effective classifier for NEPC, leading to the establishment of the NEP100 model, which demonstrated robust validation across various datasets. In clinical settings, the use of the NEP100 model can greatly improve the diagnostic and prognostic prediction of NEPC. Hierarchical clustering based on NEP100 revealed four distinct NEPC subtypes, designated VR_O, Prol_N, Prol_P, and EMT_Y, each of which presented unique biological characteristics. This allows us to select different targeted therapeutic strategies for different subtypes of phenotypic pathways. Notably, NEP100 expression correlated positively with neuroendocrine differentiation and disease progression, while the VR-NE phenotype dominated by VR_O cells indicated a propensity for treatment resistance. Furthermore, AMIGO2, a component of the NEP100 signature, was associated with chemotherapy resistance and a poor prognosis, indicating that it is a pivotal target for future therapeutic strategies. This study used multi-omics analysis combined with machine learning to construct a novel NEPC classifier and classification system. NEP100 provides a clinically actionable framework for NEPC diagnosis and subtyping.

Indexed as

Carcinoma, NeuroendocrineNeuroendocrine TumorsProstatic NeoplasmsAlgorithmsBiomarkers, TumorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMachine LearningMaleMultiomicsPrognosisSingle-Cell AnalysisTranscriptomeBiomarkers, TumorComputational biology and bioinformaticsMulti-omicsNeuroendocrine prostate cancer (NEPC)Tumor biomarkersTumor heterogeneity

Identifiers

PMID40263498
PMCPMC12015331

What OpenQuestion holds

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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.