Active elimination of intestinal cells drives oncogenic growth in organoids

  • Ana Krotenberg Garcia
  • , Arianna Fumagalli
  • , Huy Quang Le
  • , Rene Jackstadt
  • , Tamsin Rosemary Margaret Lannagan
  • , Owen James Sansom
  • , Jacco van Rheenen
  • , Saskia Jacoba Elisabeth Suijkerbuijk

Research output: Contribution to journalArticlepeer-review

25 Citations (Scopus)

Abstract

Competitive cell interactions play a crucial role in quality control during development and homeostasis. Here, we show that cancer cells use such interactions to actively eliminate wild-type intestine cells in enteroid monolayers and organoids. This apoptosis-dependent process boosts proliferation of intestinal cancer cells. The remaining wild-type population activates markers of primitive epithelia and transits to a fetal-like state. Prevention of this cell-state transition avoids elimination of wild-type cells and, importantly, limits the proliferation of cancer cells. Jun N-terminal kinase (JNK) signaling is activated in competing cells and is required for cell-state change and elimination of wild-type cells. Thus, cell competition drives growth of cancer cells by active out-competition of wild-type cells through forced cell death and cell-state change in a JNK-dependent manner.

Original languageEnglish
Article number109307
JournalCell reports
Volume36
Issue number1
DOIs
Publication statusPublished - 6 Jul 2021
Externally publishedYes

Keywords

  • JNK
  • cancer
  • cell competition
  • fetal-like
  • organoids
  • small intestine

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