Abstract
β-catenin and Tcf4 are the downstream effectors of the Wnt signaling cascade. In colorectal cancer, mutations in Wnt cascade genes such as APC lead to the inappropriate formation of β-catenin/Tcf4 complexes. Earlier work has predicted that disruption of the β-catenin/Tcf4 protein-protein interaction could revert the proliferative phenotype of colorectal cancer cells. In this issue of Cancer Cell, Shivdasani and colleagues (Lepourcelet et al., 2004) have explored high-throughput screening of compound libraries in a search for small molecule inhibitors of the Wnt cascade. Ultimately, such inhibitors could become a novel class of smart anticancer drugs.
| Original language | English |
|---|---|
| Pages (from-to) | 5-6 |
| Number of pages | 2 |
| Journal | Cancer Cell |
| Volume | 5 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - Jan 2004 |
| Externally published | Yes |