首页> 美国卫生研究院文献>The Journal of Biological Chemistry >4-Methylene-2-octyl-5-oxotetrahydrofuran-3-carboxylic Acid (C75) an Inhibitor of Fatty-acid Synthase Suppresses the Mitochondrial Fatty Acid Synthesis Pathway and Impairs Mitochondrial Function
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4-Methylene-2-octyl-5-oxotetrahydrofuran-3-carboxylic Acid (C75) an Inhibitor of Fatty-acid Synthase Suppresses the Mitochondrial Fatty Acid Synthesis Pathway and Impairs Mitochondrial Function

机译:脂肪酸合酶抑制剂4-亚甲基-2-辛基-5-氧代四氢呋喃-3-羧酸(C75)抑制线粒体脂肪酸合成途径并损害线粒体功能

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摘要

4-Methylene-2-octyl-5-oxotetrahydrofuran-3-carboxylic acid (C75) is a synthetic fatty-acid synthase (FASN) inhibitor with potential therapeutic effects in several cancer models. Human mitochondrial β-ketoacyl-acyl carrier protein synthase (HsmtKAS) is a key enzyme in the newly discovered mitochondrial fatty acid synthesis pathway that can produce the substrate for lipoic acid (LA) synthesis. HsmtKAS shares conserved catalytic domains with FASN, which are responsible for binding to C75. In our study, we explored the possible effect of C75 on HsmtKAS and mitochondrial function. C75 treatment decreased LA content, impaired mitochondrial function, increased reactive oxygen species content, and reduced cell viability. HsmtKAS but not FASN knockdown had an effect that was similar to C75 treatment. In addition, an LA supplement efficiently inhibited C75-induced mitochondrial dysfunction and oxidative stress. Overexpression of HsmtKAS showed cellular protection against low dose C75 addition, whereas there was no protective effect upon high dose C75 addition. In summary, the mitochondrial fatty acid synthesis pathway has a vital role in mitochondrial function. Besides FASN, C75 might also inhibit HsmtKAS, thereby reducing LA production, impairing mitochondrial function, and potentially having toxic effects. LA supplements sufficiently ameliorated the toxicity of C75, showing that a combination of C75 and LA may be a reliable cancer treatment.
机译:4-亚甲基-2-辛基-5-氧代四氢呋喃-3-羧酸(C75)是一种合成的脂肪酸合酶(FASN)抑制剂,在几种癌症模型中均具有潜在的治疗作用。人线粒体β-酮酰基-酰基载体蛋白合酶(HsmtKAS)是新发现的线粒体脂肪酸合成途径中的关键酶,可产生硫辛酸(LA)合成的底物。 HsmtKAS与FASN共享保守的催化结构域,负责与C75结合。在我们的研究中,我们探讨了C75对HsmtKAS和线粒体功能的可能作用。 C75处理可降低LA含量,损害线粒体功能,增加活性氧含量并降低细胞活力。 HsmtKAS而不是FASN敲低具有类似于C75处理的效果。此外,LA补充剂可有效抑制C75诱导的线粒体功能障碍和氧化应激。 HsmtKAS的过表达显示出针对低剂量C75添加的细胞保护作用,而对高剂量C75添加没有保护作用。总之,线粒体脂肪酸合成途径在线粒体功能中起着至关重要的作用。除FASN外,C75还可能抑制HsmtKAS,从而减少LA的产生,损害线粒体功能,并可能具有毒性作用。 LA补充剂充分改善了C75的毒性,表明C75和LA的组合可能是可靠的癌症治疗方法。

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