Chen R H, McCormick F
Cancer Research Institute, University of California San Francisco, 2340 Sutter Street, San Francisco, CA 94115, USA.
Cancer Res. 2001 Jun 1;61(11):4445-9.
Many colon cancers suffer mutations in either the adenomatous polyposis coli or beta-catenin genes that lead to stabilization of beta-catenin and activation of downstream T-cell factor (Tcf) target genes. We have developed a novel approach targeting colon cancer cells based on their aberrant beta-catenin/Tcf signaling pathway. A recombinant adenovirus, in which an apoptosis gene fadd is under the control of the promoter containing Tcf-responsive elements, selectively and efficiently kills colon cancer cells in which the beta-catenin/Tcf pathway is hyperactivated. Our data therefore provide a conceptual proof that aberrantly activated Wnt/beta-catenin/Tcf pathways can be used to selectively target colon cancers.
许多结肠癌在腺瘤性息肉病基因或β-连环蛋白基因中发生突变,这些突变导致β-连环蛋白的稳定以及下游T细胞因子(Tcf)靶基因的激活。我们基于其异常的β-连环蛋白/Tcf信号通路,开发了一种靶向结肠癌细胞的新方法。一种重组腺病毒,其中凋亡基因fadd受含Tcf反应元件的启动子控制,可选择性且高效地杀死β-连环蛋白/Tcf通路过度激活的结肠癌细胞。因此,我们的数据提供了一个概念证明,即异常激活的Wnt/β-连环蛋白/Tcf通路可用于选择性靶向结肠癌。