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Integrated analysis of radiomics and RNA reveals the biological basis and therapeutic implications of aggressive hepatocellular carcinoma subtypes.

January 3, 2026pubmed logopapers

Authors

Chen Y,Cai Z,Luo C,Zhang R,Guo B,Chen H,Ouyang F,Chen X,Li X,Liu W,Zhou C,Guan X,Zeng X,Liu Z,Hu Q

Affiliations (5)

  • Department of Radiology, The Eighth Affiliated Hospital, Southern Medical University (The First People's Hospital of Shunde, Foshan), Foshan, Guangdong, China.
  • Department of Radiology, The First People's Hospital of Foshan, Foshan, Guangdong, China.
  • Department of Pathology, The Eighth Affiliated Hospital, Southern Medical University (The First People's Hospital of Shunde, Foshan), Foshan, Guangdong, China.
  • Department of Radiology, The Eighth Affiliated Hospital, Southern Medical University (The First People's Hospital of Shunde, Foshan), Foshan, Guangdong, China. [email protected].
  • Department of Radiology, The Eighth Affiliated Hospital, Southern Medical University (The First People's Hospital of Shunde, Foshan), Foshan, Guangdong, China. [email protected].

Abstract

The aggressive subtype of hepatocellular carcinoma (HCC) is associated with a poor prognosis, and histopathological biopsy is the current method used for its diagnosis and tumour microenvironment analysis. Hence, we constructed a radiomics-based artificial intelligence model with robust predictive performance and explored the underlying biological characteristics by analysing mRNA data. The predictive performance was validated in two external centres, yielding areas under the curve ranging from 0.79 to 0.84, and their ability to predict progression-free survival (PFS) was evaluated. Radiogenomics analysis revealed that the high-risk group exhibited increased cell proliferation and tumour immune suppression. KIT inhibitors may serve as potential therapeutic drugs, whereas ADAM9 and PTK2B are key genes influencing patient prognosis. The artificial intelligence model developed from MRI has emerged as a dependable method for predicting aggressive HCC, with further biological exploration offering the potential to augment its clinical utility.

Topics

Journal Article

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