ArticleNPJ precision oncology2025
Integrating single-cell RNA sequencing and artificial intelligence for multitargeted drug design for combating resistance in liver cancer.
Article in NPJ precision oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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.
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.
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Who cites it
4 citing papers in PubMed.
- BRAF inhibitor resistance in melanoma: from resistance mechanisms to therapeutic innovations.Molecular biomedicine · 2026Review
- Biomimetic Polymer-Based Nanomaterials for Immune-Responsive Hepatocellular Carcinoma Therapy.International journal of nanomedicine · 2026Review
- The translational paradox of AI in hepatocellular carcinoma: from algorithmic over-engineering to real-world clinical utility.Frontiers in oncology · 2026Review
- Artificial Intelligence for the Diagnosis and Management of Cancers: Potentials and Challenges.MedComm · 2025Review
Corrections and comments
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Authors and funding
7 authors.
Funding
Abstract
Hepatocellular carcinoma (HCC) is an aggressive and heterogeneous liver cancer with restricted therapy selections and poor diagnosis. Although there have been great advances in genomics, the molecular mechanisms essential to HCC progression are not yet fully implicit, particularly at the single-cell stage. This research utilized single-cell RNA sequencing technology to evaluate transcriptional heterogeneity, immune cell infiltration, and potential therapeutic targets in HCC. A detailed bioinformatics pipeline used in the experiment included quality control, feature selection, dimensionality reduction using Principal Component Analysis (PCA), Uniform Manifold Approximation and Projection (UMAP), and t-distributed stochastic neighbor embedding (t-SNE), clustering, differential gene expression, pseudotime trajectory inference, and immune cell profiling with GSEA and survival analysis examining potential biomarkers of survival. Key findings include the identification of 1178 differentially expressed genes (DEGs), with macrophage infiltration contributing to immune evasion. Notably, APOE and ALB are linked to a better prognosis, while XIST and FTL are associated with poor survival. The potential drug candidates include IGMESINE in the case of SERPINA1 and PKR-A/MITZ for APOA2 in the gene-drug interaction analysis. Graph Neural Network (GNN) is used to predict drug-gene interactions and rank potential therapeutic candidates. The model shows robust predictive performance (R²: 0.9867, MSE: 0.0581) and identifies important drug candidates, such as Gadobenate Dimeglumine and Fluvastatin, and describes repurposing opportunities in network analysis, enhancing computational drug discovery for novel treatments. This research sheds new light on HCC tumor evolution, immune suppression, and the potential drug target based on the viewpoint of the importance of single-cell approaches in liver cancer research.
Identifiers
What Socratic 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 Socratic graph.