Panka D J, Mano T, Suhara T, Walsh K, Mier J W
Department of Hematology and Oncology, Beth Israel Deaconess Medical Center, Boston, Massachusetts 02215, USA.
J Biol Chem. 2001 Mar 9;276(10):6893-6. doi: 10.1074/jbc.C000569200. Epub 2001 Jan 5.
The caspase-8 homologue FLICE-inhibitory protein (FLIP) functions as a caspase-8 dominant negative, blocking apoptosis induced by the oligomerization of the adapter protein FADD/MORT-1. FLIP expression correlates with resistance to apoptosis induced by various members of the tumor necrosis factor family such as TRAIL. Furthermore, forced expression of FLIP renders cells resistant to Fas-mediated apoptosis. Although FLIP expression is regulated primarily by MEK1 activity in activated T cells, the oncogenic signaling pathways that regulate FLIP expression in tumor cells are largely unknown. In this report, we examined the roles of the MAP kinase and phosphatidylinositol (PI) 3-kinase signaling pathways in the regulation of FLIP expression in tumor cells. We observed that the MEK1 inhibitor PD98059 reduced FLIP levels in only 2 of 11 tumor cell lines tested. In contrast, disruption of the PI 3-kinase pathway with the specific inhibitor LY294002 reduced Akt (protein kinase B) phosphorylation and the levels of FLIP protein and mRNA in all cell lines evaluated. The introduction of a dominant negative Akt adenoviral construct also consistently reduced FLIP expression as well as the phosphorylation of the Akt target glycogen synthase kinase-3. In addition, infection of the same cell lines with a constitutively active Akt adenovirus increased FLIP expression and the phosphorylation of GSK-3. These data add FLIP to the growing list of apoptosis inhibitors in which expression or function is regulated by the PI 3-kinase-Akt pathway.
半胱天冬酶 -8 同源物FLICE抑制蛋白(FLIP)作为半胱天冬酶 -8 的显性负性蛋白发挥作用,可阻断衔接蛋白FADD/MORT-1寡聚化诱导的细胞凋亡。FLIP的表达与对肿瘤坏死因子家族各种成员(如TRAIL)诱导的细胞凋亡的抗性相关。此外,强制表达FLIP可使细胞对Fas介导的细胞凋亡产生抗性。虽然在活化的T细胞中,FLIP的表达主要受MEK1活性调节,但调节肿瘤细胞中FLIP表达的致癌信号通路在很大程度上尚不清楚。在本报告中,我们研究了丝裂原活化蛋白激酶(MAP激酶)和磷脂酰肌醇(PI)3-激酶信号通路在调节肿瘤细胞中FLIP表达中的作用。我们观察到,MEK1抑制剂PD98059仅在11个测试的肿瘤细胞系中的2个中降低了FLIP水平。相比之下,用特异性抑制剂LY294002破坏PI 3-激酶途径可降低Akt(蛋白激酶B)的磷酸化以及所有评估细胞系中FLIP蛋白和mRNA的水平。引入显性负性Akt腺病毒构建体也持续降低了FLIP表达以及Akt靶标糖原合酶激酶 -3的磷酸化。此外,用组成型活性Akt腺病毒感染相同的细胞系可增加FLIP表达和GSK-3的磷酸化。这些数据将FLIP添加到越来越多的凋亡抑制剂列表中,其表达或功能受PI 3-激酶 -Akt途径调节。