Chanchevalap Sengthong, Nandan Mandayam O, Merlin Didier, Yang Vincent W
Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, 201 Whitehead Research Building, 615 Michael Street, Atlanta, GA, USA.
FEBS Lett. 2004 Dec 3;578(1-2):99-105. doi: 10.1016/j.febslet.2004.10.079.
Retinoids are known inhibitors of epithelial cell proliferation. Previous studies indicate that Kruppel-like factor 5 (KLF5) is a pro-proliferative transcription factor. Here, we examined the effect of all-trans retinoid acid (ATRA) on proliferation of the intestinal epithelial cell line, IEC6. Treatment of IEC6 cells with ATRA inhibited their proliferation due to G1 cell cycle arrest. This inhibition was correlated with a decrease in the levels of KLF5 mRNA and promoter activity. In contrast, constitutive expression of KLF5 in stably transfected IEC6 cells with a KLF5-expressing plasmid driven by a viral promoter abrogated the growth inhibitory effect of ATRA. Moreover, ATRA inhibited proliferation of several human colon cancer cell lines with high levels of KLF5 expression but not those with low levels of KLF5 expression. Our results indicate that KLF5 is a potential mediator for the inhibitory effect of ATRA on intestinal epithelial cell proliferation.
维甲酸是已知的上皮细胞增殖抑制剂。先前的研究表明, Kruppel样因子5(KLF5)是一种促进增殖的转录因子。在此,我们研究了全反式维甲酸(ATRA)对肠上皮细胞系IEC6增殖的影响。用ATRA处理IEC6细胞会抑制其增殖,这是由于G1期细胞周期阻滞所致。这种抑制作用与KLF5 mRNA水平和启动子活性的降低相关。相反,在由病毒启动子驱动的稳定转染了KLF5表达质粒的IEC6细胞中,KLF5的组成型表达消除了ATRA的生长抑制作用。此外,ATRA抑制了几种KLF5表达水平高的人结肠癌细胞系的增殖,但不抑制KLF5表达水平低的细胞系。我们的结果表明,KLF5是ATRA对肠上皮细胞增殖抑制作用的潜在介导因子。