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Wnt Signaling in Liver Cancer

Overview
Specialty Pharmacology
Date 2008 Nov 11
PMID 18991612
Citations 69
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Abstract

Hepatocellular carcinoma (HCC) is a major cause of cancer death worldwide. As in many other types of cancer, aberrant activation of the canonical Wnt/beta-catenin signaling pathway is an important contributor to tumorigenesis. In HCC this frequently occurs through mutations in the N-terminal region of beta-catenin that stabilize the protein and permit an elevated level of constitutive transcriptional activation by beta-catenin/TCF complexes. In this article we review the abundant evidence that Wnt/beta-catenin signaling contributes to liver carcinogenesis. We also discuss what is known about the roles of Wnt signaling in liver development, regeneration, and stem cell behavior, in an effort to understand the mechanisms by which activation of the canonical Wnt pathway promotes tumor formation in this organ. The Wnt/beta-catenin pathway presents itself as an attractive target for developing novel rational therapies for HCC, a disease for which few successful treatment strategies are currently available.

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References
1.
Wirths O, Waha A, Weggen S, Schirmacher P, Kuhne T, Goodyer C . Overexpression of human Dickkopf-1, an antagonist of wingless/WNT signaling, in human hepatoblastomas and Wilms' tumors. Lab Invest. 2003; 83(3):429-34. DOI: 10.1097/01.lab.0000059926.66359.bd. View

2.
Xu Q, Wang Y, Dabdoub A, Smallwood P, Williams J, Woods C . Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair. Cell. 2004; 116(6):883-95. DOI: 10.1016/s0092-8674(04)00216-8. View

3.
Cadoret A, Ovejero C, Terris B, Souil E, Levy L, Lamers W . New targets of beta-catenin signaling in the liver are involved in the glutamine metabolism. Oncogene. 2002; 21(54):8293-301. DOI: 10.1038/sj.onc.1206118. View

4.
Benhamouche S, Decaens T, Godard C, Chambrey R, Rickman D, Moinard C . Apc tumor suppressor gene is the "zonation-keeper" of mouse liver. Dev Cell. 2006; 10(6):759-70. DOI: 10.1016/j.devcel.2006.03.015. View

5.
Satoh S, Daigo Y, Furukawa Y, Kato T, Miwa N, Nishiwaki T . AXIN1 mutations in hepatocellular carcinomas, and growth suppression in cancer cells by virus-mediated transfer of AXIN1. Nat Genet. 2000; 24(3):245-50. DOI: 10.1038/73448. View