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Targeting Wnt signaling in colorectal cancer. A Review in the Theme: Cell Signaling: Proteins, Pathways and Mechanisms

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY
Volume 309, Issue 8, Pages C511-C521

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpcell.00117.2015

Keywords

Wnt signaling pathway; colorectal cancer; adenomatous polyposis coli; beta-catenin; drug targeting; small molecules

Funding

  1. UK Medical Research Council [MC_UP_1202/7]
  2. Francis Crick Institute
  3. Medical Research Council [MC_UP_1202/7, 1363171] Funding Source: researchfish
  4. The Francis Crick Institute [10105] Funding Source: researchfish
  5. MRC [MC_UP_1202/7] Funding Source: UKRI

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The evolutionarily conserved Wnt signaling pathway plays essential roles during embryonic development and tissue homeostasis. Notably, comprehensive genetic studies in Drosophila and mice in the past decades have demonstrated the crucial role of Wnt signaling in intestinal stem cell maintenance by regulating proliferation, differentiation, and cell-fate decisions. Wnt signaling has also been implicated in a variety of cancers and other diseases. Loss of the Wnt pathway negative regulator adenomatous polyposis coli (APC) is the hallmark of human colorectal cancers (CRC). Recent advances in high-throughput sequencing further reveal many novel recurrent Wnt pathway mutations in addition to the well-characterized APC and beta-catenin mutations in CRC. Despite attractive strategies to develop drugs for Wnt signaling, major hurdles in therapeutic intervention of the pathway persist. Here we discuss the Wnt-activating mechanisms in CRC and review the current advances and challenges in drug discovery.

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