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膳食促氧化剂治疗通过维生素 K 前体靶向 PI 3-激酶 VPS34 功能。

Dietary pro-oxidant therapy by a vitamin K precursor targets PI 3-kinase VPS34 function.

机构信息

Cold Spring Harbor Laboratory, Cold Spring Harbor, NY 11771, USA.

Graduate Program in Molecular and Cellular Biology, Stony Brook University, Stony Brook, NY 11794, USA.

出版信息

Science. 2024 Oct 25;386(6720):eadk9167. doi: 10.1126/science.adk9167.

Abstract

Men taking antioxidant vitamin E supplements have increased prostate cancer (PC) risk. However, whether pro-oxidants protect from PC remained unclear. In this work, we show that a pro-oxidant vitamin K precursor [menadione sodium bisulfite (MSB)] suppresses PC progression in mice, killing cells through an oxidative cell death: MSB antagonizes the essential class III phosphatidylinositol (PI) 3-kinase VPS34-the regulator of endosome identity and sorting-through oxidation of key cysteines, pointing to a redox checkpoint in sorting. Testing MSB in a myotubular myopathy model that is driven by loss of -the phosphatase antagonist of VPS34-we show that dietary MSB improved muscle histology and function and extended life span. These findings enhance our understanding of pro-oxidant selectivity and show how definition of the pathways they impinge on can give rise to unexpected therapeutic opportunities.

摘要

服用抗氧化维生素 E 补充剂的男性患前列腺癌(PC)的风险增加。然而,促氧化剂是否能预防 PC 仍不清楚。在这项工作中,我们表明一种促氧化剂维生素 K 前体[亚硫酸氢钠甲萘醌(MSB)]可抑制小鼠的 PC 进展,通过氧化细胞死亡杀死细胞:MSB 通过氧化关键半胱氨酸拮抗必需的 III 类磷脂酰肌醇(PI)3-激酶 VPS34-内体身份和分选的调节剂,指向分选中的氧化还原检查点。在由 VPS34 的磷酸酶拮抗剂丧失驱动的肌小管肌病模型中测试 MSB,我们表明饮食 MSB 改善了肌肉组织学和功能,并延长了寿命。这些发现增进了我们对促氧化剂选择性的理解,并表明它们影响的途径的定义如何产生意想不到的治疗机会。

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