# Kinic index: an artificial intelligence-driven predictive model and multitarget drug discovery framework for hepatocellular carcinoma patients

**Authors:** Jinglin Zhou, Yuhan Jiang, Miao Yu, Mengyuan Wang, Yixiao Li, Dengbo Ji, Jun Zhan, Hongquan Zhang

PMC · DOI: 10.1038/s41698-026-01324-1 · 2026-02-14

## TL;DR

This paper introduces KinicI, an AI model that classifies liver cancer patients and identifies potential drug targets to improve treatment outcomes.

## Contribution

The novel Kinic Index integrates multi-omics data and AI to classify HCC patients and prioritize multitarget drug candidates.

## Key findings

- High-Kinic subgroup patients have significantly worse survival outcomes.
- CYP2C9 and G6PD are key prognostic markers linked to HCC progression.
- Candidate compounds targeting CYP2C9 and G6PD show strong binding affinities.

## Abstract

Hepatocellular carcinoma (HCC) remains a major global health challenge due to its molecular heterogeneity, late diagnosis, and limited therapeutic options. Recent studies have identified isonicotinylation (Kinic), a novel lysine acylation, as a regulatory modification influencing carcinogenic protein activity and liver cancer progression. In this study, we established the Kinic Index (KinicI), an artificial intelligence (AI)-driven predictive model that integrates multi-omics data and consensus clustering to classify HCC patients into two distinct Kinic subgroups. Patients in the high-Kinic subgroup exhibited significantly worse overall survival, demonstrating the value of KinicI for risk stratification and outcome prediction. Machine learning approaches (LASSO, RSF) coupled with Shapley additive explanation (SHAP) analysis identified CYP2C9 and G6PD as the most influential prognostic variables associated with HCC progression. Single-cell and spatial transcriptomic analyses confirmed that CYP2C9 and G6PD are primarily localized in malignant hepatocytes with high metastatic potential, underscoring their clinical relevance. Importantly, using the GraphBAN deep learning framework and ADMET-AI screening, we prioritized candidate compounds targeting CYP2C9 and G6PD, followed by molecular docking that validated strong binding affinities, suggesting their potential as novel therapeutics. Together, our study demonstrates that KinicI is a powerful AI-enabled platform for prognostic modeling, molecular stratification, and multitarget drug discovery, providing a foundation for precision oncology and resistance-aware treatment strategies in HCC patients.

## Linked entities

- **Genes:** CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559], G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539]
- **Diseases:** hepatocellular carcinoma (MONDO:0007256), HCC (MONDO:0007256)

## Full-text entities

- **Genes:** CYP2C9 (cytochrome P450 family 2 subfamily C member 9) [NCBI Gene 1559] {aka CPC9, CYP2C, CYP2C10, CYPIIC9, P450-2C9, P450IIC9}, G6PD (glucose-6-phosphate dehydrogenase) [NCBI Gene 2539] {aka CNSHA1, G6PD1}
- **Diseases:** HCC (MESH:D006528)
- **Chemicals:** lysine (MESH:D008239)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13018533/full.md

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Source: https://tomesphere.com/paper/PMC13018533