Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, 710038, China.
Department of Pharmacology, School of Pharmacy, Fourth Military Medical University, Xi'an, 710038, China.
Front Med. 2024 Oct;18(5):878-895. doi: 10.1007/s11684-024-1057-7. Epub 2024 Sep 13.
Aerobic glycolysis is critical for tumor growth and metastasis. Previously, we have found that the overexpression of the inhibitor of growth 5 (ING5) inhibits lung cancer aggressiveness and epithelial-mesenchymal transition (EMT). However, whether ING5 regulates lung cancer metabolism reprogramming remains unknown. Here, by quantitative proteomics, we showed that ING5 differentially regulates protein phosphorylation and identified a new site (Y163) of the key glycolytic enzyme PDK1 whose phosphorylation was upregulated 13.847-fold. By clinical study, decreased p-PDK1Y163 was observed in lung cancer tissues and correlated with poor survival. p-PDK1Y163 represents the negative regulatory mechanism of PDK1 by causing PDHA1 dephosphorylation and activation, leading to switching from glycolysis to oxidative phosphorylation, with increasing oxygen consumption and decreasing lactate production. These effects could be impaired by PDK1Y163F mutation, which also impaired the inhibitory effects of ING5 on cancer cell EMT and invasiveness. Mouse xenograft models confirmed the indispensable role of p-PDK1Y163 in ING5-inhibited tumor growth and metastasis. By siRNA screening, ING5-upregulated TIE1 was identified as the upstream tyrosine protein kinase targeting PDK1Y163. TIE1 knockdown induced the dephosphorylation of PDK1Y163 and increased the migration and invasion of lung cancer cells. Collectively, ING5 overexpression-upregulated TIE1 phosphorylates PDK1Y163, which is critical for the inhibition of aerobic glycolysis and invasiveness of lung cancer cells.
有氧糖酵解对肿瘤的生长和转移至关重要。此前,我们发现生长抑制剂 5(ING5)的过表达可抑制肺癌的侵袭性和上皮-间充质转化(EMT)。然而,ING5 是否调节肺癌代谢重编程尚不清楚。在这里,通过定量蛋白质组学,我们表明 ING5 差异调节蛋白磷酸化,并鉴定了关键糖酵解酶 PDK1 的新磷酸化位点(Y163),其磷酸化水平上调了 13.847 倍。通过临床研究,我们观察到肺癌组织中 p-PDK1Y163 减少,且与不良预后相关。p-PDK1Y163 通过引起 PDHA1 去磷酸化和激活来代表 PDK1 的负调控机制,导致从糖酵解向氧化磷酸化转变,增加耗氧量和减少乳酸生成。这种作用可被 PDK1Y163F 突变所损害,该突变也损害了 ING5 对癌细胞 EMT 和侵袭性的抑制作用。小鼠异种移植模型证实了 p-PDK1Y163 在 ING5 抑制肿瘤生长和转移中的不可或缺作用。通过 siRNA 筛选,我们鉴定出 ING5 上调的 TIE1 是靶向 PDK1Y163 的上游酪氨酸蛋白激酶。TIE1 敲低诱导 PDK1Y163 的去磷酸化,并增加肺癌细胞的迁移和侵袭。总之,ING5 过表达上调 TIE1 磷酸化 PDK1Y163,这对于抑制肺癌细胞的有氧糖酵解和侵袭性至关重要。