Domon-Dell C, Wang Q, Kim S, Kedinger M, Evers B M, Freund J-N
Institut National de la Santé et de la Recherche Médicale, Unité 381, Strasbourg, France.
Gut. 2002 Apr;50(4):525-9. doi: 10.1136/gut.50.4.525.
The transcription factor encoded by the intestinal Cdx2 homeobox gene and treatment with sodium butyrate (NaB), a byproduct of fibre fermentation by colonic bacteria, exert similar effects on colon cancer cell lines as they both inhibit cell growth and stimulate cell differentiation and apoptosis.
To investigate whether NaB regulates expression of the Cdx2 gene in colon cancer cell lines.
Human adenocarcinoma cell lines Caco2 and HT29 were grown in the presence or absence of NaB. Cells were analysed for Cdx2 mRNA expression by reverse transcription-polymerase chain reaction, for protein expression by western blotting and electromobility shift assays, and for transcriptional activity of the Cdx2 promoter by transfection with luciferase reporter plasmids.
In HT29 and Caco2 cells, NaB stimulated Cdx2 mRNA and protein expression as well as transcriptional activity of the Cdx2 promoter. Stimulation of the activity of the Cdx2 promoter by NaB was dose and time dependent. The Cdx2 promoter contains discrete regions that participate in or inversely that blunt the stimulatory effect exerted by NaB. In addition, NaB stimulated the transcriptional activity of the Cdx2 promoter downregulated by oncogenic ras.
This study is the first report of an intestine specific transcription factor, Cdx2, stimulated by butyrate. Thus it provides a new mechanism whereby butyrate controls proliferation and differentiation of colon cancer cells.
肠道Cdx2同源框基因编码的转录因子以及丁酸钠(NaB,结肠细菌纤维发酵的副产物)对结肠癌细胞系具有相似的作用,因为它们都能抑制细胞生长并刺激细胞分化和凋亡。
研究丁酸钠是否调节结肠癌细胞系中Cdx2基因的表达。
人腺癌细胞系Caco2和HT29在有或无丁酸钠的情况下培养。通过逆转录-聚合酶链反应分析细胞中Cdx2 mRNA的表达,通过蛋白质印迹法和电泳迁移率变动分析检测蛋白质表达,并通过转染荧光素酶报告质粒分析Cdx2启动子的转录活性。
在HT29和Caco2细胞中,丁酸钠刺激Cdx2 mRNA和蛋白质表达以及Cdx2启动子的转录活性。丁酸钠对Cdx2启动子活性的刺激呈剂量和时间依赖性。Cdx2启动子包含参与或相反地减弱丁酸钠刺激作用的离散区域。此外,丁酸钠刺激了由致癌性ras下调的Cdx2启动子的转录活性。
本研究首次报道了丁酸盐刺激肠道特异性转录因子Cdx2。因此,它提供了一种新的机制,通过该机制丁酸盐可控制结肠癌细胞的增殖和分化。