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The function of BCL9 in Wnt/beta-catenin signaling and colorectal cancer cells.

BMC cancer | 2008

Most cases of colorectal cancer are initiated by hyperactivation of the Wnt/beta-catenin pathway due to mutations in the APC tumour suppressor, or in beta-catenin itself. A recently discovered component of this pathway is Legless, which is essential for Wnt-induced transcription during Drosophila development. Limited functional information is available for its two mammalian relatives, BCL9 and B9L/BCL9-2: like Legless, these proteins bind to beta-catenin, and RNAi-mediated depletion of B9L/BCL9-2 has revealed that this protein is required for efficient beta-catenin-mediated transcription in mammalian cell lines. No loss-of-function data are available for BCL9.

Pubmed ID: 18627596 RIS Download

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Associated grants

  • Agency: Medical Research Council, United Kingdom
    Id: MC_U105184273
  • Agency: Medical Research Council, United Kingdom
    Id: MC_U105192713
  • Agency: Cancer Research UK, United Kingdom
    Id: C7379/A8709

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SW480 (tool)

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