Departments of Endoscopic Diagnostics and Therapeutics, Kochi University, Nankoku, Kochi 783-8505, Japan.
Departments of Pathology, Kochi University, Nankoku, Kochi 783-8505, Japan.
Int J Oncol. 2018 Nov;53(5):2224-2240. doi: 10.3892/ijo.2018.4549. Epub 2018 Aug 31.
Rho guanine nucleotide exchange factor 4 (ARHGEF4) is a guanine nucleotide exchange factor that is specific for Rac1 and Cdc42. The aim of the present study was to investigate the role of ARHGEF4 in the motility and invasiveness of pancreatic cancer cells. Evaluation of an immunohistochemical staining of 102 resected pancreatic cancer samples demonstrated that high ARHGEF4 expression was correlated with an independent predictor of worse overall survival in univariate and multivariate analyses. Immunofluorescence analyses and Matrigel invasion assays demonstrated that suppression of ARHGEF4 inhibited the formation of membrane protrusions, and in turn inhibited cell motility and invasion. A phosphoprotein array analysis demonstrated that knockdown of ARHGEF4 decreased phosphorylated extracellular signal-regulated kinase (ERK)1/2 and glycogen synthase kinase-3 (GSK-3)α/β in pancreatic cancer cells, and ERK1/2 and GSK-3α/β were associated with ARHGEF4-related motility and invasiveness through an increase in cell protrusions. These results suggested that ARHGEF4 stimulates ERK1/2 and GSK-3α/β, and provided evidence that ARHGEF4 promotes cell motility and invasiveness. Inhibition of ARHGEF4 may be a novel approach to a targeted molecular therapy, as any such therapy would limit the motility and invasiveness of pancreatic cancer cells.
Rho 鸟嘌呤核苷酸交换因子 4(ARHGEF4)是一种鸟嘌呤核苷酸交换因子,特异性针对 Rac1 和 Cdc42。本研究旨在探讨 ARHGEF4 在胰腺癌细胞运动和侵袭中的作用。对 102 例切除的胰腺癌样本进行免疫组织化学染色评估表明,高 ARHGEF4 表达与单因素和多因素分析中独立预测总生存率差相关。免疫荧光分析和 Matrigel 侵袭试验表明,抑制 ARHGEF4 抑制了膜突起的形成,进而抑制了细胞的运动和侵袭。磷酸化蛋白芯片分析表明,敲低 ARHGEF4 降低了胰腺癌细胞中磷酸化细胞外信号调节激酶 1/2(ERK1/2)和糖原合成酶激酶 3α/β(GSK-3α/β),ERK1/2 和 GSK-3α/β 通过增加细胞突起与 ARHGEF4 相关的运动和侵袭相关。这些结果表明,ARHGEF4 刺激 ERK1/2 和 GSK-3α/β,并提供了证据表明 ARHGEF4 促进了细胞的运动和侵袭。抑制 ARHGEF4 可能是一种针对胰腺癌的新型靶向分子治疗方法,因为任何此类治疗方法都将限制胰腺癌细胞的运动和侵袭能力。