ArticleDiscover oncology2025
Single-cell transcriptomic insights into ccRCC: a stemness gene signature for prognosis and treatment response prediction.
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.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
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
Identifiers
What OpenQuestion holds
Registered trials
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.