Specific features of ß-catenin-mutated hepatocellular carcinomas.
Camille DantzerLydia DifJustine VachéSara BasbousClotilde BillottetViolaine MoreauPublished in: British journal of cancer (2024)
CTNNB1, encoding the ß-catenin protein, is a key oncogene contributing to liver carcinogenesis. Hepatocellular carcinoma (HCC) is the most common form of primary liver cancer in adult, representing the third leading cause of cancer-related death. Aberrant activation of the Wnt/ß-catenin pathway, mainly due to mutations of the CTNNB1 gene, is observed in a significant subset of HCC. In this review, we first resume the major recent advances in HCC classification with a focus on CTNNB1-mutated HCC subclass. We present the regulatory mechanisms involved in β-catenin stabilisation, transcriptional activity and binding to partner proteins. We then describe specific phenotypic characteristics of CTNNB1-mutated HCC thanks to their unique gene expression patterns. CTNNB1-mutated HCC constitute a full-fledged subclass of HCC with distinct pathological features such as well-differentiated cells with low proliferation rate, association to cholestasis, metabolic alterations, immune exclusion and invasion. Finally, we discuss therapeutic approaches to target ß-catenin-mutated liver tumours and innovative perspectives for future drug developments.
Keyphrases
- gene expression
- cell proliferation
- epithelial mesenchymal transition
- wild type
- machine learning
- signaling pathway
- transcription factor
- stem cells
- induced apoptosis
- deep learning
- small molecule
- cell death
- genome wide
- copy number
- endoplasmic reticulum stress
- current status
- hiv infected
- men who have sex with men
- heat shock protein
- genome wide analysis
- heat shock