Im Eunok, Martinez Jesse D
Arizona Cancer Center, Department of Radiation Oncology, University of Arizona, Tucson, AZ 85724, USA.
J Nutr. 2004 Feb;134(2):483-6. doi: 10.1093/jn/134.2.483.
Ursodeoxycholic acid (UDCA), a hydrophilic bile acid, is known as a cytoprotective agent. UDCA prevents apoptosis induced by a variety of stress stimuli including cytotoxic bile acids such as deoxycholic acid (DCA). Here we examined the molecular mechanism by which UDCA can antagonize DCA-induced apoptosis in human colon cancer cells. UDCA pretreatment decreases the number of apoptotic cells caused by exposure to DCA and UDCA. Further studies of the signaling pathway showed that UDCA pretreatment suppressed DNA binding activity of activator protein-1 and this was accompanied by downregulation of both extracellular signal-regulated kinase (ERK) and Raf-1 kinase activities stimulated by exposure to DCA. DCA was also found to activate epidermal growth factor receptor (EGFR) activity and UDCA inhibited this. Collectively, these findings suggest that the inhibitory effect of UDCA in DCA-induced apoptosis is partly mediated by modulation of EGFR/Raf-1/ERK signaling.
熊去氧胆酸(UDCA)是一种亲水性胆汁酸,作为一种细胞保护剂而为人所知。UDCA可预防由多种应激刺激诱导的细胞凋亡,这些应激刺激包括细胞毒性胆汁酸,如脱氧胆酸(DCA)。在此,我们研究了UDCA拮抗DCA诱导人结肠癌细胞凋亡的分子机制。UDCA预处理可减少因暴露于DCA和UDCA而导致的凋亡细胞数量。对信号通路的进一步研究表明,UDCA预处理可抑制激活蛋白-1的DNA结合活性,同时伴随着细胞外信号调节激酶(ERK)和Raf-1激酶活性的下调,这两种激酶活性是由暴露于DCA所刺激的。还发现DCA可激活表皮生长因子受体(EGFR)活性,而UDCA可抑制这一活性。总体而言,这些发现表明,UDCA对DCA诱导的细胞凋亡的抑制作用部分是通过调节EGFR/Raf-1/ERK信号传导介导的。