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Objectives: Proliferative hepatocellular carcinoma (HCC) is an aggressive tumor with varying prognosis depending on the different disease stages and subsequent treatment. This study aims to develop and validate a deep learning radiomics (DLR) model based on contrast-enhanced CT to predict proliferative HCC and to implement risk prediction in patients treated with transarterial chemoembolization (TACE) and radiofrequency ablation (RFA).
Materials And Methods: 312 patients (mean age, 58 years ± 10 [SD]; 261 men and 51 women) with HCC undergoing surgery at two medical centers were included, who were divided into a training set ( = 182), an internal test set ( = 46) and an external test set ( = 84). DLR features were extracted from preoperative contrast-enhanced CT images. Multiple machine learning algorithms were used to develop and validate proliferative HCC prediction models in training and test sets. Subsequently, patients from two independent new sets (RFA and TACE sets) were divided into high- and low-risk groups using the DLR score generated by the optimal model. The risk prediction value of DLR scores in recurrence-free survival (RFS) and time to progression (TTP) was examined separately in RFA and TACE sets.
Results: The DLR proliferative HCC prediction model demonstrated excellent predictive performance with an AUC of 0.906 (95% CI 0.861–0.952) in the training set, 0.901 (95% CI 0.779–1.000) in the internal test set and 0.837 (95% CI 0.746–0.928) in the external test set. The DLR score effectively enables risk prediction for patients in RFA and TACE sets. For the RFA set, the low-risk group had significantly longer RFS compared to the high-risk group ( = 0.037). Similarly, the low-risk group showed a longer TTP than the high-risk group for the TACE set ( = 0.034).
Conclusions: The DLR-based contrast-enhanced CT model enables non-invasive prediction of proliferative HCC. Furthermore, the DLR risk prediction helps identify high-risk patients undergoing RFA or TACE, providing prognostic insights for personalized management.
Supplementary Information: The online version contains supplementary material available at 10.1186/s12880-025-01913-9.
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http://dx.doi.org/10.1186/s12880-025-01913-9 | DOI Listing |
Front Biosci (Landmark Ed)
August 2025
Department of Hepatobiliary Surgery, General Hospital of Ningxia Medical University, 750004 Yinchuan, Ningxia Hui Autonomous Region, China.
Background: Mediator complex subunit 10 (MED10) serves as a critical regulator of eukaryotic gene expression by facilitating RNA polymerase II activity. Our investigation aims to characterize MED10's functional contributions and underlying molecular pathways in hepatocellular carcinoma (HCC) development.
Methods: MED10 expression patterns in HCC and their correlation with clinicopathological parameters and patient outcomes were examined using bioinformatics databases and immunohistochemistry.
Bioorg Chem
August 2025
Wenzhou Medical University, Wenzhou 325035, PR China; Zhejiang Cancer Hospital, Hangzhou 310022, PR China. Electronic address:
Transcriptional enhanced associate domain (TEAD), overexpressed in hepatocellular carcinoma (HCC) and inversely correlated to prognosis, has emerged as a promising target for HCC therapy. To date, no small-molecule inhibitors targeting TEAD have been reported for HCC treatment. In this study, a bioinformatic analysis has been performed and has demonstrated that TEAD is a promising target for therapeutic intervention in HCC.
View Article and Find Full Text PDFEur J Pharmacol
September 2025
Department of Emergency Medicine, Shuang-Ho Hospital, Taipei Medical University, New Taipei City, Taiwan; Department of Emergency Medicine, School of Medicine, Taipei Medical University, Taipei, Taiwan. Electronic address:
Background: This study seeks to provide preclinical evidence demonstrating the potential of Antrocinol, a derivative of antrocin derived from the active compound of Antrodia cinnamomea, as a promising small-molecule drug candidate for overcoming drug-resistant hepatocellular carcinoma (HCC).
Methods: We developed Lenvatinib-resistant Huh-7 and HepG cell lines (Huh-7/LR, HepG2/LR) to evaluate their viability and apoptotic response to Antrocinol. Autophagy-dependent cell death was assessed in Huh-7/LR cells using Z-VAD-FMK and shATG5 transfection.
Front Immunol
September 2025
Medical Integration and Practice Center, Shandong University, Jinan, China.
Background: Malignant tumors remain a major threat to global human health. This study aimed to systematically integrate multi-omics data to identify a candidate gene with biomarker potential across diverse cancer types and to evaluate its possible clinical applications in oncology.
Methods: We first performed Mendelian randomization based on summary statistics to integrate blood expression quantitative trait loci data with genome-wide association study results from esophageal adenocarcinoma, stomach cancer, and clear cell renal cell carcinoma.
BMC Med Imaging
September 2025
Department of Radiology, Tianjin First Central Hospital, Tianjin Institute of Imaging Medicine, School of Medicine, Nankai University, 24 Fukang Road, Nankai District, Tianjin, 300192, China.
Objectives: Proliferative hepatocellular carcinoma (HCC) is an aggressive tumor with varying prognosis depending on the different disease stages and subsequent treatment. This study aims to develop and validate a deep learning radiomics (DLR) model based on contrast-enhanced CT to predict proliferative HCC and to implement risk prediction in patients treated with transarterial chemoembolization (TACE) and radiofrequency ablation (RFA).
Materials And Methods: 312 patients (mean age, 58 years ± 10 [SD]; 261 men and 51 women) with HCC undergoing surgery at two medical centers were included, who were divided into a training set ( = 182), an internal test set ( = 46) and an external test set ( = 84).