肝细胞癌
脂蛋白脂酶
脂质代谢
雷公藤甲素
癌症研究
下调和上调
脂肪酶
癌症
医学
化学
内科学
细胞凋亡
酶
生物化学
脂肪组织
基因
作者
Wei‐Chiao Chang,Jingjing Wang,Yuanqi You,Hongqian Wang,Shendong Xu,Stephen Vulcano,Changlu Xu,Chenlin Shen,Zhi Li,Jie Wang
出处
期刊:Cancers
[MDPI AG]
日期:2024-01-27
卷期号:16 (3): 550-550
标识
DOI:10.3390/cancers16030550
摘要
Hepatocellular carcinoma (HCC), which is the third leading cause of cancer-related mortality in the world, presents a significant medical challenge. Triptolide (TP) has been identified as an effective therapeutic drug for HCC. However, its precise therapeutic mechanism is still unknown. Understanding the mechanism of action of TP against HCC is crucial for its implementation in the field of HCC treatment. We hypothesize that the anti-HCC actions of TP might be related to its modulation of HCC lipid metabolism given the crucial role that lipid metabolism plays in promoting the progression of HCC. In this work, we first demonstrate that, both in vitro and in vivo, TP significantly reduces lipid accumulation in HCC cells. Additionally, we notice that lipoprotein lipase (LPL) expression is markedly upregulated in HCC, and that its levels are positively connected with the disease’s progression. It is interesting to note that TP dramatically reduces LPL activity, which in turn prevents HCC growth and reduces lipid accumulation. Additionally, the effect of TP on LPL is a direct correlation. These results definitely demonstrate that TP protects hepatocytes against abnormal accumulation of lipids by transcriptionally suppressing LPL, which reduces the development of HCC. This newly identified pathway provides insight into the process through which TP exerts its anti-HCC actions.
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