From the Institute of Medicine, Chung Shan Medical University, Taichung 402, Taiwan.
J Biol Chem. 2010 Sep 24;285(39):29808-16. doi: 10.1074/jbc.M110.108183. Epub 2010 Jul 20.
Oral squamous cell carcinoma has a striking tendency to migrate and metastasize. Cyclooxygenase (COX)-2, the inducible isoform of prostaglandin (PG) synthase, has been implicated in tumor metastasis. However, the effects of COX-2 on human oral cancer cells are largely unknown. We found that overexpression of COX-2 or exogenous PGE(2) increased migration and intercellular adhesion molecule 1 (ICAM)-1 expression in human oral cancer cells. Using pharmacological inhibitors, activators, and genetic inhibition of EP receptors, we discovered that the EP1 receptor, but not other PGE receptors, is involved in PGE(2)-mediated cell migration and ICAM-1 expression. PGE(2)-mediated migration and ICAM-1 up-regulation were attenuated by inhibitors of protein kinase C (PKC)δ, and c-Src. Activation of the PKCδ, c-Src, and AP-1 signaling pathway occurred after PGE(2) treatment. PGE(2)-induced expression of ICAM-1 and migration activity were inhibited by a specific inhibitor, siRNA, and mutants of PKCδ, c-Src, and AP-1. In addition, migration-prone sublines demonstrated that cells with increased migration ability had higher expression of COX-2 and ICAM-1. Taken together, these results indicate that the PGE(2) and EP1 interaction enhanced migration of oral cancer cells through an increase in ICAM-1 production.
口腔鳞状细胞癌具有显著的迁移和转移倾向。环氧化酶(COX)-2 是前列腺素(PG)合酶的诱导同工酶,与肿瘤转移有关。然而,COX-2 对人口腔癌细胞的影响在很大程度上尚不清楚。我们发现 COX-2 的过表达或外源性 PGE(2)增加了人口腔癌细胞的迁移和细胞间黏附分子 1(ICAM-1)的表达。通过使用药理学抑制剂、激动剂和 EP 受体的基因抑制,我们发现 EP1 受体,而不是其他 PGE 受体,参与了 PGE(2)介导的细胞迁移和 ICAM-1 表达。PKCδ 和 c-Src 的抑制剂可减弱 PGE(2)介导的迁移和 ICAM-1 的上调。PKCδ、c-Src 和 AP-1 信号通路在 PGE(2)处理后被激活。PKCδ、c-Src 和 AP-1 的特异性抑制剂、siRNA 和突变体可抑制 PGE(2)诱导的 ICAM-1 表达和迁移活性。此外,迁移倾向的亚系表明,迁移能力增强的细胞具有更高的 COX-2 和 ICAM-1 表达。综上所述,这些结果表明,PGE(2)和 EP1 相互作用通过增加 ICAM-1 的产生来增强口腔癌细胞的迁移。