Li Hongbin, Ye Xiaoqin, Mahanivong Chitladda, Bian Dafang, Chun Jerold, Huang Shuang
Department of Immunology and Molecular Biology, The Scripps Research Institute, 10550 N. Torrey Pines Rd., La Jolla, California 92037, USA.
J Biol Chem. 2005 Mar 18;280(11):10564-71. doi: 10.1074/jbc.M412152200. Epub 2005 Jan 14.
Lysophosphatidic acid (LPA) enhances urokinase plasminogen activator (uPA) expression in ovarian cancer cells; however, the molecular mechanisms responsible for this event have not been investigated. In this study, we used the invasive ovarian cancer SK-OV-3 cell line to explore the signaling molecules and pathways essential for LPA-induced uPA up-regulation. With the aid of specific inhibitors and dominant negative forms of signaling molecules, we determined that the G(i)-associated pathway mediates this LPA-induced event. Moreover, constitutively active H-Ras and Raf-1-activating H-Ras mutant enhance uPA expression, whereas dominant negative H-Ras and Raf-1 block LPA-induced uPA up-regulation, suggesting that the Ras-Raf pathway works downstream of G(i) to mediate this LPA-induced process. Surprisingly, dominant negative MEK1 or Erk2 displays only marginal inhibitory effect on LPA-induced uPA up-regulation, suggesting that a signaling pathway distinct from Raf-MEK1/2-Erk is the prominent pathway responsible for this process. In this report, we demonstrate that LPA activates NF-kappaB in a Ras-Raf-dependent manner and that blocking NF-kappaB activation with either non-phosphorylable IkappaB or dominant negative IkappaB kinase abolished LPA-induced uPA up-regulation and uPA promoter activation. Furthermore, introducing mutations to knock out the NF-kappaB binding site of the uPA promoter results in over 80% reduction in LPA-induced uPA promoter activation, whereas this activity is largely intact with the promoter containing mutations in the AP1 binding sites. Thus these results suggest that the G(i)-Ras-Raf-NF-kappaB signaling cascade is responsible for LPA-induced uPA up-regulation in ovarian cancer cells.
溶血磷脂酸(LPA)可增强卵巢癌细胞中尿激酶型纤溶酶原激活剂(uPA)的表达;然而,导致这一现象的分子机制尚未得到研究。在本研究中,我们使用侵袭性卵巢癌SK-OV-3细胞系来探索LPA诱导uPA上调所必需的信号分子和信号通路。借助特异性抑制剂和信号分子的显性负性形式,我们确定G(i)相关信号通路介导了这一LPA诱导的事件。此外,组成型激活的H-Ras和激活Raf-1的H-Ras突变体可增强uPA表达,而显性负性H-Ras和Raf-1则可阻断LPA诱导的uPA上调,这表明Ras-Raf信号通路在G(i)下游发挥作用,介导了这一LPA诱导的过程。令人惊讶的是,显性负性MEK1或Erk2对LPA诱导的uPA上调仅表现出微弱的抑制作用,这表明一条不同于Raf-MEK1/2-Erk的信号通路是介导这一过程的主要信号通路。在本报告中,我们证明LPA以Ras-Raf依赖的方式激活NF-κB,并且用不可磷酸化的IκB或显性负性IκB激酶阻断NF-κB激活可消除LPA诱导的uPA上调和uPA启动子激活。此外,引入突变以敲除uPA启动子的NF-κB结合位点可导致LPA诱导的uPA启动子激活降低80%以上,而含有AP1结合位点突变的启动子的这种活性基本保持完整。因此,这些结果表明G(i)-Ras-Raf-NF-κB信号级联反应负责卵巢癌细胞中LPA诱导的uPA上调。