Brauer Philip R, Kim Jee Hun, Ochoa Humberto J, Stratton Elizabeth R, Black Kathryn M, Rosencrans William, Stacey Eliza, Hagos Engda G
a Department of Biology , Colgate University , Hamilton , NY , USA.
b Center for Cancer Research, Lab of Cancer Biology and Genetics , National Cancer Institute , Bethesda , MD , USA.
Cell Commun Adhes. 2018 Dec;24(1):1-10. doi: 10.1080/15419061.2018.1444034.
Kru¨ppel like factor 4 (KLF4) is a transcription factor that regulates genes related to differentiation and proliferation. KLF4 also plays a role in metastasis via epithelial to mesenchymal transition. Here, we investigate the function of Klf4 in migration and invasion using mouse embryonic fibroblasts and the RKO human colon cancer cell line. Compared to wild-type, cells lacking Klf4 exhibited increased migration-associated phenotypes. In addition, overexpression of Klf4 in Klf4 MEFs attenuated the presence of stress fibers to wild-type levels. An invasion assay suggested that lack of Klf4 resulted in increased invasive capacity. Finally, analysis of RhoA showed elevated RhoA activity in both RKO and MEF cells. Taken together, our results strongly support the novel role of KLF4 in a post-translational regulatory mechanism where KLF4 indirectly modulates the actin cytoskeleton morphology via activity of RhoA in order to inhibit cellular migration and invasion.
Kruppel样因子4(KLF4)是一种转录因子,可调节与分化和增殖相关的基因。KLF4还通过上皮-间质转化在转移过程中发挥作用。在此,我们使用小鼠胚胎成纤维细胞和RKO人结肠癌细胞系研究Klf4在迁移和侵袭中的功能。与野生型相比,缺乏Klf4的细胞表现出与迁移相关的表型增加。此外,在Klf4基因敲除的小鼠胚胎成纤维细胞中过表达Klf4可使应力纤维的存在减弱至野生型水平。侵袭实验表明,缺乏Klf4会导致侵袭能力增强。最后,对RhoA的分析显示,RKO和小鼠胚胎成纤维细胞中的RhoA活性均升高。综上所述,我们的结果有力地支持了KLF4在翻译后调控机制中的新作用,即KLF4通过RhoA的活性间接调节肌动蛋白细胞骨架形态,从而抑制细胞迁移和侵袭。