Department of Life Sciences, Division of Life and Pharmaceutical Sciences and the Center for Cell Signaling & Drug Discovery Research, Ewha Womans University, Seoul 120-750, Republic of Korea.
Biochem Biophys Res Commun. 2010 Jan 1;391(1):921-5. doi: 10.1016/j.bbrc.2009.11.165. Epub 2009 Dec 4.
Expression of the cell surface adhesion receptor syndecan-2 is known to be involved in the regulation of cancer cell migration. However, the molecular mechanism of syndecan-2-mediated cell migration remains unknown. Here we report that Rac contributes to the regulation of syndecan-2-mediated cancer cell migration. Overexpression of syndecan-2 enhanced migration and invasion of human colon adenocarcinoma cells Caco-2 and HCT116 cells. In parallel with the increased cell migration/invasion, syndecan-2 overexpression enhanced Rac activity, while dominant negative Rac (RacN17) diminished syndecan-2-mediated increased cancer cell migration. In addition syndecan-2 expression increased membrane localization of Tiam1 and syndecan-2-mediated cell migration/invasion of Caco-2 cells was diminished when Tiam1 levels were knocked-down with small inhibitory RNAs. Furthermore, oligomerization-defective syndecan-2 mutants failed to increase membrane localization of Tiam1, activation of Rac and subsequent cell migration of both Caco-2 and HCT116 cells. Taken together, these results suggest that syndecan-2 regulates cell migration of colon carcinoma cells through Tiam1-dependent Rac activation in colon cancer cells.
细胞表面黏附受体 syndecan-2 的表达被认为参与了癌细胞迁移的调控。然而,syndecan-2 介导的细胞迁移的分子机制仍不清楚。在这里,我们报告 Rac 有助于调控 syndecan-2 介导的癌细胞迁移。syndecan-2 的过表达增强了人结肠腺癌 Caco-2 和 HCT116 细胞的迁移和侵袭能力。随着细胞迁移/侵袭的增加,syndecan-2 的过表达增强了 Rac 的活性,而显性失活 Rac(RacN17)则减弱了 syndecan-2 介导的癌细胞迁移增加。此外,syndecan-2 的表达增加了 Tiam1 的膜定位,并且当用小干扰 RNA 敲低 Tiam1 水平时,syndecan-2 介导的 Caco-2 细胞迁移/侵袭减少。此外,寡聚缺陷 syndecan-2 突变体不能增加 Tiam1 的膜定位、Rac 的激活以及随后的 Caco-2 和 HCT116 细胞的迁移。总之,这些结果表明 syndecan-2 通过 Tiam1 依赖性 Rac 激活调节结肠癌细胞的迁移。