Park Chi Hoon, Chang Joon Young, Hahm Eun Ryeong, Park Seyeon, Kim Hyun-Kyung, Yang Chul Hak
Division of Chemistry and Molecular Engineering, Seoul National University, Seoul 151-742, Republic of Korea.
Biochem Biophys Res Commun. 2005 Mar 4;328(1):227-34. doi: 10.1016/j.bbrc.2004.12.151.
Dysregulation of Wnt/beta-catenin pathway plays a central role in early events in colorectal carcinogenesis. We examined the effect of quercetin, a famous anti-tumor agent, against beta-catenin/Tcf signaling in SW480 cells. Quercetin inhibited the transcriptional activity of beta-catenin/Tcf in SW480 and also in HEK293 cells transiently transfected with constitutively active mutant beta-catenin gene, whose product is not induced to be degraded by APC-Axin-GSK3beta complex, so we concluded that its inhibitory mechanism was related to beta-catenin itself or downstream components. To investigate the precise inhibitory mechanism, we performed EMSA showing that binding of the Tcf complexes to its specific DNA-binding sites was strongly suppressed by quercetin. Immunoprecipitation analysis also showed that the binding of beta-catenin to Tcf-4 was also disrupted by quercetin. Western blot analysis proved these decreased bindings resulted from decreased level of beta-catenin and Tcf-4 product in nucleus caused by quercetin. Together, we suggest that quercetin is an excellent inhibitor of beta-catenin/Tcf signaling in SW480 cell lines, and the reduced beta-catenin/Tcf transcriptional activity is due to the decreased nuclear beta-catenin and Tcf-4 proteins.
Wnt/β-连环蛋白信号通路失调在结直肠癌发生的早期事件中起核心作用。我们研究了著名的抗肿瘤药物槲皮素对SW480细胞中β-连环蛋白/Tcf信号传导的影响。槲皮素抑制了SW480细胞以及瞬时转染组成型活性突变β-连环蛋白基因的HEK293细胞中β-连环蛋白/Tcf的转录活性,该基因的产物不会被APC-Axin-GSK3β复合物诱导降解,因此我们得出结论,其抑制机制与β-连环蛋白本身或下游成分有关。为了研究确切的抑制机制,我们进行了电泳迁移率变动分析(EMSA),结果表明槲皮素强烈抑制了Tcf复合物与其特异性DNA结合位点的结合。免疫沉淀分析还表明,槲皮素也破坏了β-连环蛋白与Tcf-4的结合。蛋白质免疫印迹分析证明,这些结合减少是由于槲皮素导致细胞核中β-连环蛋白和Tcf-4产物水平降低所致。总之,我们认为槲皮素是SW480细胞系中β-连环蛋白/Tcf信号传导的优秀抑制剂,β-连环蛋白/Tcf转录活性降低是由于细胞核中β-连环蛋白和Tcf-4蛋白减少所致。