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Non-stem cell lineages as an alternative origin of intestinal tumorigenesis in the context of inflammation

  • Mathijs P. Verhagen,
  • Rosalie Joosten,
  • Mark Schmitt,
  • Niko Välimäki,
  • Andrea Sacchetti,
  • Kristiina Rajamäki,
  • Jiahn Choi,
  • Paola Procopio,
  • Sara Silva,
  • Berdine van der Steen,
  • Thierry P. P. van den Bosch,
  • Danielle Seinstra,
  • Annemarie C. de Vries,
  • Michail Doukas,
  • Leonard H. Augenlicht,
  • Lauri A. Aaltonen,
  • Riccardo Fodde

摘要

According to conventional views, colon cancer originates from stem cells. However, inflammation, a key risk factor for colon cancer, has been shown to suppress intestinal stemness. Here, we used Paneth cells as a model to assess the capacity of differentiated lineages to trigger tumorigenesis in the context of inflammation in mice. Upon inflammation, Paneth cell-specific Apc mutations led to intestinal tumors reminiscent not only of those arising in patients with inflammatory bowel disease, but also of a larger fraction of human sporadic colon cancers. The latter is possibly because of the inflammatory consequences of western-style dietary habits, a major colon cancer risk factor. Machine learning methods designed to predict the cell-of-origin of cancer from patient-derived tumor samples confirmed that, in a substantial fraction of sporadic cases, the origins of colon cancer reside in secretory lineages and not in stem cells.