Inhibition of Hepatoblastoma by Ganoderma Lucidum Polysaccharide via the Induction of HDAC4-p16-RB Axis-Mediated Cellular Senescence.

Abstract

Hepatoblastoma (HB), the most common primary malignant liver tumor in children, is characterized by high metastatic potential and poor prognosis. Ganoderma lucidum polysaccharide (GLP), the main bioactive compound of Ganoderma lucidum, has not been fully investigated for its therapeutic effects on HB. This study aimed to evaluate the anti-tumor effects of GLP on HB cells and explore the underlying biological mechanisms. GLP was chemically characterized using ultraviolet-visible spectroscopy, monosaccharide composition analysis, Fourier transform infrared (FTIR) spectroscopy, and scanning electron microscopy. The effects of GLP on the malignant phenotype of HB cells were assessed using CCK-8, EdU, Transwell assays, and other standard in vitro techniques. Mechanistic investigations included proteomics, western blotting, chromatin immunoprecipitation (ChIP), and dual-luciferase reporter assays. In vivo anti-HB effects of GLP were evaluated through animal models. Crude GLP, exhibiting anti-tumor activity, was prepared through water extraction, alcohol precipitation, and column chromatography. In vitro, GLP inhibited proliferation, invasion, and induced apoptosis in HuH6 and HepG2 cells. In vivo, GLP suppressed tumor growth in a dose-dependent manner. Mechanistically, GLP induced cellular senescence by downregulating histone deacetylase 4 (HDAC4) expression and enhancing p16 histone acetylation, which activated the p16-retinoblastoma (p16-RB) pathway and suppressed the malignant phenotype of HB cells. Furthermore, overexpression of HDAC4 reversed the senescence-inducing effects of GLP. GLP inhibits HB progression by promoting cellular senescence via the HDAC4-p16-RB axis. These findings establish a mechanistic link between GLP's anti-tumor activity and cellular senescence, providing new insights for its potential clinical application.