Ye Ting, Ge Yang, Zhang Jing, Gao Hang, Zhang Peng-Cheng, Shen Rui, Peng Can, Liu Bin, Song Hang
School of Integrated Chinese and Western Medicine, Anhui University of Chinese Medicine, Hefei, China.
School of Pharmacy, Anhui University of Chinese Medicine, Hefei, China.
Phytother Res. 2025 Apr 6. doi: 10.1002/ptr.8493.
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.
肝母细胞瘤(HB)是儿童最常见的原发性恶性肝肿瘤,具有高转移潜能和预后不良的特点。灵芝多糖(GLP)是灵芝的主要生物活性化合物,其对HB的治疗作用尚未得到充分研究。本研究旨在评估GLP对HB细胞的抗肿瘤作用,并探讨其潜在的生物学机制。通过紫外可见光谱、单糖组成分析、傅里叶变换红外(FTIR)光谱和扫描电子显微镜对GLP进行化学表征。使用CCK-8、EdU、Transwell实验和其他标准体外技术评估GLP对HB细胞恶性表型的影响。机制研究包括蛋白质组学、蛋白质印迹、染色质免疫沉淀(ChIP)和双荧光素酶报告基因实验。通过动物模型评估GLP的体内抗HB作用。通过水提取、醇沉淀和柱色谱法制备具有抗肿瘤活性的粗GLP。在体外,GLP抑制HuH6和HepG2细胞的增殖、侵袭并诱导其凋亡。在体内,GLP以剂量依赖性方式抑制肿瘤生长。机制上,GLP通过下调组蛋白去乙酰化酶4(HDAC4)表达并增强p16组蛋白乙酰化来诱导细胞衰老,从而激活p16-视网膜母细胞瘤(p16-RB)通路并抑制HB细胞的恶性表型。此外,HDAC4过表达逆转了GLP的衰老诱导作用。GLP通过HDAC4-p16-RB轴促进细胞衰老来抑制HB进展。这些发现建立了GLP抗肿瘤活性与细胞衰老之间的机制联系,为其潜在的临床应用提供了新的见解。