Integrating single-cell RNA sequencing and artificial intelligence for multitargeted drug design for combating resistance in liver cancer

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.

Authors

Institutions

Publication Details

Journal
npj Precision Oncology
Published
2025-09-02
DOI
https://doi.org/10.1038/s41698-025-00952-3
Citations
3
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
2.81

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Integrating single-cell RNA sequencing and artificial intelligence for multitargeted drug design for combating resistance in liver cancer

Youyuan Yang, Wenli Chen, Changquan Li, Jingyou Dai et al.
3 citations
npj Precision Oncology
Cancer Genomics and Diagnostics
2.81
article

Integrating single-cell RNA sequencing and artificial intelligence for multitargeted drug design for combating resistance in liver cancer

Youyuan Yang, Wenli Chen, Changquan Li, Jingyou Dai, Houhong Wang, Jun Zhang, Qing Li
article en
3 citations

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.

npj Precision OncologyVol. 9(1)
Fuyang Normal University (CN), Daping Hospital (CN), Chengdu Military General Hospital (CN), Bozhou People's Hospital (CN)
Anhui Medical University, Anhui Provincial Department of Education
Openalex Percentile: Top 9%
Cancer Genomics and Diagnostics
2.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.