线粒体YBX1通过抑制丙酮酸摄取促进癌细胞转移

Huan Chen, Ting Ling, Di Chen, Wenjuan Liu, Huan Qi, Tian Xia, Xiaolong Liu, Wen Wang, Xin Guo, Wuxiyar Otkur, Fangjun Wang, Zhaochao Xu, Jean-Claude Martinou, Hai-long Piao
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引用次数: 0

摘要

丙酮酸是维持线粒体中三羧酸(TCA)循环的必需燃料。然而,线粒体丙酮酸载体(MPC)摄取丙酮酸的确切分子机制在很大程度上是未知的。在这里,我们报道了DNA/ rna结合蛋白Y-box结合蛋白1 (YBX1)在癌细胞中通过其c -末端结构域(CTD)定位于线粒体膜间隙(IMS)。在线粒体中,YBX1通过与MPC1/2结合抑制丙酮酸摄取,从而抑制丙酮酸依赖的TCA循环通量。这种关联反过来促进mpc介导的谷氨酰胺水解和组蛋白乳酸化。我们的研究结果表明,YBX1-MPC轴与转移潜能呈正相关,而不影响培养细胞和肿瘤移植细胞的增殖。因此,限制丙酮酸进入线粒体可能代表了转移能力的标志,这表明YBX1-MPC轴是对抗癌症转移的治疗靶点。
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Mitochondrial YBX1 promotes cancer cell metastasis by inhibiting pyruvate uptake
Abstract Pyruvate is an essential fuel for maintaining the tricarboxylic acid (TCA) cycle in the mitochondria. However, the precise molecular mechanism of pyruvate uptake by mitochondrial pyruvate carrier (MPC) is largely unknown. Here, we report that the DNA/RNA-binding protein Y-box binding protein 1 (YBX1) is localized to the mitochondrial inter-membrane space (IMS) by its C-terminal domain (CTD) in cancer cells. In mitochondria, YBX1 inhibits pyruvate uptake by associating with MPC1/2, thereby suppressing pyruvate-dependent TCA cycle flux. This association, in turn, promotes MPC-mediated glutaminolysis and histone lactylation. Our findings reveal that the YBX1-MPC axis exhibits a positive correlation with metastatic potential, while does not affect cell proliferation in both cultured cells and tumor xenografts. Therefore, the restricted pyruvate uptake into mitochondria potentially represents a hallmark of metastatic capacity, suggesting that the YBX1-MPC axis is a therapeutic target for combating cancer metastasis.
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