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Entopic overexpression of Ascl2 does not accelerate tumourigenesis in ApcMin mice
  1. Karen R Reed,
  2. Simon J Tunster,
  3. Madeleine Young,
  4. Adam Carrico,
  5. Rosalind M John,
  6. Alan R Clarke
  1. Cardiff School of Biosciences, Cardiff University, Cardiff, UK
  1. Correspondence to Dr Karen R Reed, Cardiff School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK; reedkr{at}


Objective Expression of the Wnt target gene ASCL2 is elevated in 78% of intestinal neoplasia datasets (Oncomine), suggesting a role for deregulated ASCL2 in the aetiology of intestinal tumourigenesis. Furthermore, ectopic expression of Ascl2 has previously been shown to lead to hyperplasia in the mouse. However, elevated levels of ASCL2 does not have an impact on the overall survival or recurrence-free survival rates in colorectal cancer patients. Here the authors use a novel mouse model to analyse the role of Ascl2 in intestinal tumourigenesis and address the controversy surrounding the relevance of this gene to the aetiology of colorectal cancer.

Design The authors have generated a mouse possessing a transgene carrying the Ascl2 gene together with its endogenous promoter and regulatory regions, thereby elevating Ascl2 expression in an authentic manner. The authors have further intercrossed these Ascl2 overexpressers to the classic ApcMin model, to study the consequence of elevated Ascl2 expression in intestinal tumourigenesis.

Results Here the authors genetically demonstrate that elevated expression of Ascl2 in a Wnt signalling dependent manner specifically in the stem cell compartment of the intestine neither increases tumour formation nor diminishes survival in a well established intestinal tumour model, the Apcmin mouse.

Conclusion The authors conclude that ectopic expression of Ascl2 is more important in the aetiology of neoplasia than overexpression of Ascl2.

  • Ascl2
  • colorectal cancer
  • intestine
  • ApcMin
  • BAC transgenic
  • cancer genetics
  • cell biology
  • colorectal cancer genes
  • gene expression
  • gene regulation

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  • Funding This study was funded by Cancer Research UK programme grant (C1295/A9590 awarded to ARC). KRR was funded by a Wellcome Trust Value in People award.

  • Competing interests None.

  • Provenance and peer review Not commissioned; externally peer reviewed.

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