Wang Tiancai, Li Xiabing, Liao Guangqin, Wang Zishuang, Han Xiaoxu, Gu Jingyi, Mu Xiyan, Qiu Jing, Qian Yongzhong
Key Laboratory of Agro-Product Quality and Safety, Institute of Quality Standards and Testing Technology for Agro-Products, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Key Laboratory of Agri-Food Quality and Safety, Ministry of Agriculture and Rural Affairs, Beijing 100081, China.
Foods. 2024 Jan 3;13(1):163. doi: 10.3390/foods13010163.
As the most prevalent mycotoxin in agricultural products, aflatoxin B1 not only causes significant economic losses but also poses a substantial threat to human and animal health. AFB1 has been shown to increase the risk of hepatocellular carcinoma (HCC) but the underlying mechanism is not thoroughly researched. Here, we explored the toxicity mechanism of AFB1 on human hepatocytes following low-dose exposure based on transcriptomics and lipidomics. Apoptosis-related pathways were significantly upregulated after AFB1 exposure in all three hES-Hep, HepaRG, and HepG2 hepatogenic cell lines. By conducting a comparative analysis with the TCGA-LIHC database, four biomarkers (MTCH1, PPM1D, TP53I3, and UBC) shared by AFB1 and HCC were identified (hazard ratio > 1), which can be used to monitor the degree of AFB1-induced hepatotoxicity. Simultaneously, AFB1 induced abnormal metabolism of glycerolipids, sphingolipids, and glycerophospholipids in HepG2 cells (FDR < 0.05, impact > 0.1). Furthermore, combined analysis revealed strong regulatory effects between PIK3R1 and sphingolipids (correlation coefficient > 0.9), suggesting potential mediation by the phosphatidylinositol 3 kinase (PI3K) /protein kinase B (AKT) signaling pathway within mitochondria. This study revealed the dysregulation of lipid metabolism induced by AFB1 and found novel target genes associated with AFB-induced HCC development, providing reliable evidence for elucidating the hepatotoxicity of AFB as well as assessing food safety risks.
作为农产品中最普遍存在的霉菌毒素,黄曲霉毒素B1不仅会造成重大经济损失,还对人类和动物健康构成重大威胁。黄曲霉毒素B1已被证明会增加肝细胞癌(HCC)的风险,但其潜在机制尚未得到充分研究。在此,我们基于转录组学和脂质组学,探讨了低剂量暴露后黄曲霉毒素B1对人肝细胞的毒性机制。在所有三种人胚胎干细胞来源的肝细胞系(hES-Hep)、HepaRG细胞系和HepG2细胞系中,黄曲霉毒素B1暴露后凋亡相关通路均显著上调。通过与TCGA-LIHC数据库进行比较分析,鉴定出黄曲霉毒素B1和肝细胞癌共有的四个生物标志物(MTCH1、PPM1D、TP53I3和UBC)(风险比>1),可用于监测黄曲霉毒素B1诱导的肝毒性程度。同时,黄曲霉毒素B1诱导HepG2细胞中甘油脂、鞘脂和甘油磷脂的代谢异常(FDR<0.05,影响>0.1)。此外,联合分析显示PIK3R1与鞘脂之间存在强烈的调控作用(相关系数>0.9),提示线粒体中的磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(AKT)信号通路可能起介导作用。本研究揭示了黄曲霉毒素B1诱导的脂质代谢失调,并发现了与黄曲霉毒素诱导的肝细胞癌发展相关的新靶基因,为阐明黄曲霉毒素的肝毒性以及评估食品安全风险提供了可靠证据。