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The natural compound GL22 isolated from Ganoderma mushrooms suppresses tumor growth by altering lipid metabolism and triggering cell death

机译:从灵芝蘑菇中分离出的天然化合物GL22通过改变脂质代谢和触发细胞死亡来抑制肿瘤生长

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摘要

Cancer cells rewire their metabolism to satisfy the demands of uncontrolled proliferation and survival. The reprogramming of lipid metabolism supports tumor growth, metastasis, and therapy-resistance. Therefore, targeting lipid metabolic reprogramming is a potential cancer treatment strategy. We recently isolated the novel natural triterpene GL22 from Ganoderma leucocontextum, a traditional Chinese medicine. Here, we show that GL22 significantly inhibits the growth of the liver cancer cell line Huh7.5 in vitro and of Huh7.5-derived tumor xenografts in vivo. We further find that GL22 induces mitochondrial dysfunction and cell death in Huh7.5 cells, in part due to fatty acid immobilization and loss of the mitochondrial lipid cardiolipin, which has vital structural and metabolic functions. Importantly, we demonstrate that GL22 treatment decreases the expression of fatty acid-binding proteins (FABPs), which likely underlies the loss of cardiolipin, mitochondrial dysfunction, and cell death. The over-expressions of FABPs prevented the GL22-induced cell death, loss of cardiolipin, decrease of ATP production, and reduction of oxygen consumption rate in Huh7.5 cells. Our results support targeting lipid metabolism via manipulating FABPs as a cancer treatment strategy, and promote Chinese medicine as an important source of novel anticancer drugs.
机译:癌细胞重新调整其新陈代谢,以满足不受控制的增殖和存活的需求。脂质代谢的重新编程支持肿瘤的生长,转移和治疗耐药性。因此,靶向脂质代谢重编程是一种潜在的癌症治疗策略。我们最近从灵芝中药中分离出了新型天然三萜GL22。在这里,我们显示GL22在体外显着抑制肝癌细胞系Huh7.5的生长,在体内抑制Huh7.5衍生的肿瘤异种移植物的生长。我们进一步发现,GL22在Huh7.5细胞中诱导线粒体功能障碍和细胞死亡,部分原因是脂肪酸固定化和线粒体脂质心磷脂的丧失,后者具有重要的结构和代谢功能。重要的是,我们证明GL22处理可降低脂肪酸结合蛋白(FABPs)的表达,这可能是心磷脂,线粒体功能障碍和细胞死亡的基础。 FABPs的过表达防止了Huh7.5细胞中GL22诱导的细胞死亡,心磷脂的丢失,ATP生成的减少以及氧消耗率的降低。我们的研究结果支持通过操纵FABP作为一种癌症治疗策略来靶向脂质代谢,并促进中药成为新型抗癌药物的重要来源。

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