Evidence map›Paper›PMID 41085922›Full record

ArticleDiscover oncology2025

Single-cell transcriptomic insights into ccRCC: a stemness gene signature for prognosis and treatment response prediction.

Jianhui Chen, Xinyi Wu, Guo Han, Chao Xu

Abstract read
In one paragraph

Article in Discover oncology, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

4 authors.

Jianhui Chen *School of Nursing, Jiangsu Food and Pharmaceutical Science College, Huai'an, Jiangsu, China.
Xinyi Wu *Department of Lung Cancer, Tianjin Lung Cancer Center, Key Laboratory of Cancer Prevention and Therapy, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Guo Han *Medical School of Southeast University, Nanjing, China.
Chao XuDepartment of Oncology, Shuyang Hospital of Traditional Chinese Medicine, Suqian, China. xu_chao1238@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC), the most prevalent renal malignancy, exhibits remarkable intratumoral heterogeneity that challenges precise prognostication and treatment stratification. Leveraging single-cell RNA sequencing (scRNA-seq) and an advanced artificial intelligence (AI)-driven analytical framework, we comprehensively dissected the cellular complexity of ccRCC and developed a robust prognostic model. Analyzing scRNA-seq data from 44 ccRCC samples, we identified a distinct proliferative epithelial cell subtype strongly correlated with adverse clinical outcomes. Through a sophisticated LASSO-XGBoost machine learning approach, we constructed a novel stemness-related gene signature (SGS) that demonstrated exceptional predictive capabilities across multiple independent cohorts. The SGS effectively stratified patients into high-risk and low-risk groups, with high-risk individuals experiencing significantly reduced overall survival. Notably, our model outperformed conventional clinicopathological parameters and existing prognostic signatures. Critically, patients with elevated SGS scores exhibited diminished responsiveness to targeted therapies and immune checkpoint inhibitors, suggesting its potential as a predictive biomarker for treatment efficacy. Our findings not only illuminate the pivotal role of proliferative epithelial cells in ccRCC progression but also underscore the transformative potential of AI-driven approaches in precision oncology. This study provides a foundational framework for enhanced patient stratification and personalized therapeutic interventions in ccRCC.

Indexed as

CcRCCClear cell renal cell carcinomaMachine learningStemness genes signature

Identifiers

PMID41085922
PMCPMC12521704

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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.