Inappropriate activation of the Wnt signaling pathway is observed
in many human cancers and is sufficient to drive tumor initiation
and progression in numerous contexts. Multiple mechanisms, such as
overexpression of Wnt ligands, inactivation of the APC and Axin
tumor suppressors, and mutation of -catenin, are responsible for
pathway activation in tumor cells. The development of potent Wnt
pathway antagonists for therapeutic use has been a major effort for
investigators in both academia and industry in recent years. This
book will provide an overview of the Wnt pathway as a therapeutic
target for cancer, and discuss the preclinical development of
inhibitors specifically directed to upstream and downstream
components of the pathway.
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