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全反式维甲酸通过抑制编码Kruppel样因子5的基因表达来抑制肠上皮细胞的增殖。

All-trans retinoic acid inhibits proliferation of intestinal epithelial cells by inhibiting expression of the gene encoding Kruppel-like factor 5.

作者信息

Chanchevalap Sengthong, Nandan Mandayam O, Merlin Didier, Yang Vincent W

机构信息

Division of Digestive Diseases, Department of Medicine, Emory University School of Medicine, 201 Whitehead Research Building, 615 Michael Street, Atlanta, GA, USA.

出版信息

FEBS Lett. 2004 Dec 3;578(1-2):99-105. doi: 10.1016/j.febslet.2004.10.079.

Abstract

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.

摘要

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。

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本文引用的文献

1
Growth and EGFR regulation in breast cancer cells by vitamin D and retinoid compounds.
Breast Cancer Res Treat. 2004 Jul;86(1):55-73. doi: 10.1023/B:BREA.0000032923.66250.92.
2
Retinoic acid regulates cell cycle progression and cell differentiation in human monocytic THP-1 cells.
Exp Cell Res. 2004 Jul 1;297(1):68-81. doi: 10.1016/j.yexcr.2004.02.017.
3
Krüppel-like factor 5 mediates the transforming activity of oncogenic H-Ras.
Oncogene. 2004 Apr 22;23(19):3404-13. doi: 10.1038/sj.onc.1207397.
4
Staf50 is a novel p53 target gene conferring reduced clonogenic growth of leukemic U-937 cells.
Oncogene. 2004 May 20;23(23):4050-9. doi: 10.1038/sj.onc.1207524.
5
Nuclear retinoid receptors and the transcription of retinoid-target genes.
Gene. 2004 Mar 17;328:1-16. doi: 10.1016/j.gene.2003.12.005.
6
Intestinal tumor progression is associated with altered function of KLF5.
J Biol Chem. 2004 Mar 26;279(13):12093-101. doi: 10.1074/jbc.M311532200. Epub 2004 Jan 15.
7
Retinoic acid-induced cell cycle arrest of human myeloid cell lines.
Leuk Lymphoma. 2003 Oct;44(10):1641-50. doi: 10.1080/1042819031000083316.
8
Requirement of Krüppel-like factor 4 in preventing entry into mitosis following DNA damage.
J Biol Chem. 2004 Feb 6;279(6):5035-41. doi: 10.1074/jbc.M307631200. Epub 2003 Nov 19.

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