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Lipoxygenase‐mediated generation of lipid peroxides enhances ferroptosis induced by erastin and RSL3

机译:脂氧合酶介导的脂质过氧化物的产生增强了由蛋白蛋白和RSL3引起的肥大症

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摘要

In cancer cells the small compounds erastin and RSL3 promote a novel type of cell death called ferroptosis, which requires iron‐dependent accumulation of lipid reactive oxygen species. Here we assessed the contribution of lipid peroxidation activity of lipoxygenases (LOX) to ferroptosis in oncogenic Ras‐expressing cancer cells. Several 12/15‐LOX inhibitors prevented cell death induced by erastin and RSL3. Furthermore, siRNA‐mediated silencing of ALOX15 significantly decreased both erastin‐induced and RSL3‐induced ferroptotic cell death, whereas exogenous overexpression of ALOX15 enhanced the effect of these compounds. Immunofluorescence analyses revealed that the ALOX15 protein consistently localizes to cell membrane during the course of ferroptosis. Importantly, treatments of cells with ALOX15‐activating compounds accelerated cell death at low, but not high doses of erastin and RSL3. These observations suggest that tumor ferroptosis is promoted by LOX‐catalyzed lipid hydroperoxide generation in cellular membranes.
机译:在癌细胞中,小的化合物erastin和RSL3促进了一种新型的细胞死亡,称为铁锈病,这需要铁依赖脂质活性氧的积累。在这里,我们评估了脂加氧酶(LOX)的脂质过氧化活性对致癌性表达Ras的癌细胞的肥大作用的贡献。几种12 / 15-LOX抑制剂可防止由Estin和RSL3诱导的细胞死亡。此外,siRNA介导的ALOX15沉默显着降低了蛋白的诱导和RSL3诱导的肥大细胞死亡,而外源性ALOX15的过表达增强了这些化合物的作用。免疫荧光分析表明,在肥大症的过程中,ALOX15蛋白始终位于细胞膜上。重要的是,用ALOX15活化化合物处理细胞可在低剂量(但不是高剂量)的Estin和RSL3加速细胞死亡。这些观察结果表明,LOX催化细胞膜中脂质过氧化氢的生成促进了肿瘤的肥大症。

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