Hsu Jinn-Yuan, Chang Jang-Yang, Chang Kwang-Yu, Chang Wen-Chang, Chen Ben-Kuen
Center of Infectious Disease and Signaling Research, National Cheng Kung University, Tainan, Taiwan.
National Institute of Cancer Research, National Health Research Institutes, Tainan, Taiwan.
FASEB J. 2017 Oct;31(10):4265-4276. doi: 10.1096/fj.201700156R. Epub 2017 Jun 8.
Epidermal growth factor receptor (EGFR) activation is a major cause of metastasis in such cancers as head and neck squamous cell carcinoma (HNSCC); however, whether the metabolic enzyme, pyruvate dehydrogenase kinase 1 (PDK1), mediates EGF-enhanced HNSCC metastasis remains unclear. Of interest, we found that EGF induced PDK1 expression in HNSCC. Tumor cell transformation induced by EGF was repressed by PDK1 knockdown, and the down-regulation of PDK1 expression or inhibition of its activity significantly blocked EGF-enhanced cell migration and invasion. In addition, depletion of PDK1 impeded EGF-enhanced binding of HNSCC cells to endothelial cells as well as the metastatic seeding of tumor cells in lungs. PDK1 depletion inhibited EGF-induced matrix metalloproteinase-1 (MMP-1), MMP-2, MMP-3, MMP-9, and fibronectin expression and Rac1/cdc42 activation. Furthermore, PDK1 overexpression induced MMP-1, MMP-2, MMP-3, MMP-9, and fibronectin expression and Rac1/cdc42 activation. Of interest, depletion of fibronectin inhibited PDK1-enhanced MMP-1-3 and MMP-9 expression as well as Rac1/cdc42 activation and tumor invasion. These results demonstrate that EGF-induced PDK1 expression enhances HNSCC metastasis activation of the fibronectin signaling pathway. Inhibition of PDK1 may be a potential strategy for the treatment of EGFR-mediated HNSCC metastasis.-Hsu, J.-Y., Chang, J.-Y., Chang, K.-Y., Chang, W.-C., Chen B.-K. Epidermal growth factor-induced pyruvate dehydrogenase kinase 1 expression enhances head and neck squamous cell carcinoma metastasis up-regulation of fibronectin.
表皮生长因子受体(EGFR)激活是头颈部鳞状细胞癌(HNSCC)等癌症转移的主要原因;然而,代谢酶丙酮酸脱氢酶激酶1(PDK1)是否介导表皮生长因子(EGF)增强的HNSCC转移尚不清楚。有趣的是,我们发现EGF可诱导HNSCC中PDK1的表达。PDK1基因敲低可抑制EGF诱导的肿瘤细胞转化,PDK1表达下调或其活性受到抑制可显著阻断EGF增强的细胞迁移和侵袭。此外,PDK1缺失会阻碍EGF增强的HNSCC细胞与内皮细胞的结合以及肿瘤细胞在肺部的转移定植。PDK1缺失可抑制EGF诱导的基质金属蛋白酶-1(MMP-1)、MMP-2、MMP-3、MMP-9和纤连蛋白的表达以及Rac1/cdc42的激活。此外,PDK1过表达可诱导MMP-1、MMP-2、MMP-3、MMP-9和纤连蛋白的表达以及Rac1/cdc42的激活。有趣的是,纤连蛋白缺失可抑制PDK1增强的MMP-1-3和MMP-9表达以及Rac1/cdc42激活和肿瘤侵袭。这些结果表明,EGF诱导的PDK1表达通过激活纤连蛋白信号通路增强了HNSCC转移。抑制PDK1可能是治疗EGFR介导的HNSCC转移的潜在策略。-许,J.-Y.,张,J.-Y.,张,K.-Y.,张,W.-C.,陈,B.-K. 表皮生长因子诱导丙酮酸脱氢酶激酶1表达增强头颈部鳞状细胞癌转移 纤连蛋白上调。