Selective targeting to the hyperactive beta-catenin/T-cell factor pathway in colon cancer cells |
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Authors: | Chen R H McCormick F |
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Affiliation: | Cancer Research Institute, University of California San Francisco, 2340 Sutter Street, San Francisco, CA 94115, USA. |
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Abstract: | 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. |
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