乳酸氧化酶破坏乳酸激活的RAS和PI3K瘤信号传输
Chandler R Keller1, Steve R Martinez2,3,4, Alexys Keltz1,5
1Department of Translational Medicine and Physiology, Elson S. Floyd College of Medicine, Washington State University, Spokane, WA 99202, USA.
Cancers
|August 29, 2024
概括
烯酸氧化酶 (LOX) 通过破坏氧化碳酸受体1 (HCAR1) 信号复合体来抑制乳腺癌. 这种机制与以前的理解不同,它针对潜在治疗策略的关键瘤性途径.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 在瘤学瘤学.
背景情况:
- lysyl氧化酶 (LOX) 抑制癌细胞的增殖和瘤的生长.
- 以前的机制集中在LOX耗尽瘤微环境 (TME) 乳酸并产生H2O2.
研究的目的:
- 阐明LOX抑制乳腺癌 (BCa) 进展的新机制.
- 研究氧碳酸受体1 (HCAR1) 在乳酸介导的瘤原体信号传递中的作用.
主要方法:
- 研究了BCa细胞中HCAR1关联蛋白质复合物的组装.
- 评估了LOX治疗对蛋白质复合体水平和乳酸转运体 (MCT1,MCT4) 的影响.
- 分析了RAS和PI3K信号通路的激活.
主要成果:
- TME乳酸会触发HCAR1复合组合 (GRB2,SOS1,KRAS,GAB1,PI3K),从而激活RAS和PI3K通路.
- 通过蛋白质体降解,LOX治疗降低了蛋白质复合物的水平.
- LOX抑制了乳酸刺激的MCT1和MCT4表达.
结论:
- 乳酸酸激活HCAR1对于RAS/PI3K信号连接组合和BCa中的功能至关重要.
- 通过抑制HCAR1来破坏这种乳酸信号连接,对癌细胞是有害的.
- HCAR1是控制BCa进展的潜在治疗点.
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