Evidence map›Paper›PMID 41787910›Full record

ArticleJournal of Yeungnam medical science2026

Gene expression-based machine learning model for diagnosis, prognosis, and treatment response prediction in hepatocellular carcinoma: a retrospective study.

Tan Thinh Nguyen, Thanh Dat Nguyen, Phu Qui Le Nguyen, Phuong Thi Bui, Minh Nam Nguyen

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Article in Journal of Yeungnam medical science, 2026. 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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5 · Who and what money

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5 authors.

Tan Thinh NguyenFaculty of Medicine, University of Health Sciences, Thu Duc District, Ho Chi Minh City, Vietnam.
Thanh Dat NguyenResearch Center for Genetics and Reproductive Health (CGRH), University of Health Sciences, Thu Duc District, Ho Chi Minh City, Vietnam.
Phu Qui Le NguyenFaculty of Medicine, University of Health Sciences, Thu Duc District, Ho Chi Minh City, Vietnam.
Phuong Thi BuiFaculty of Pharmacy, University of Health Sciences, Thu Duc District, Ho Chi Minh City, Vietnam.
Minh Nam NguyenFaculty of Medicine, University of Health Sciences, Thu Duc District, Ho Chi Minh City, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) remains a leading cause of cancer-related mortality worldwide, largely because of challenges in early diagnosis and the limited sensitivity of conventional biomarkers. Therefore, reliable molecular tools for early detection, prognostic stratification, and individualized treatment predictions are urgently required.

methodsThis retrospective study analyzed publicly available gene expression datasets. Candidate biomarkers were identified from the GSE14520 cohort using a multistep screening workflow that integrated differential expression analysis, diagnostic performance, and prognostic relevance. A 10-gene diagnostic model was constructed using least absolute shrinkage and selection operator logistic regression and subsequently validated across multiple independent cohorts. Survival outcomes were evaluated using the Kaplan-Meier analysis and treatment responses to sorafenib and transarterial chemoembolization (TACE) were assessed using receiver operating characteristic analysis.

resultsA 10-gene signature (TOP2A, CDK1, CYP3A4, MASP2, EPHX2, HAO1, RACGAP1, GLYAT, ADH1B, and CYP4A11) was established. The model demonstrated robust internal performance and consistent accuracy across external validation cohorts (area under the curve [AUC], >0.9). This signature effectively identified early-stage HCC and distinguished malignancy from cirrhosis. High-risk scores were significantly associated with poor overall survival and recurrence-free survival (p<0.05). Furthermore, the model could predict treatment sensitivity, with higher risk scores associated with better outcomes for sorafenib (AUC, 0.791), whereas lower risk scores correlated with an improved response to TACE (AUC, 0.768).

conclusionOur gene expression-based machine learning model provides a robust tool for HCC diagnosis, prognosis, and treatment response prediction, with potential as a supportive system for personalized clinical decision-making.

Indexed as

Early diagnosisGene expression profilingHepatocellular carcinomaMachine learningPrognosisTreatment response

Identifiers

PMID41787910
PMCPMC13107085

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