Active elimination of intestinal cells drives oncogenic growth in organoids

Cell Rep. 2021 Jul 6;36(1):109307. doi: 10.1016/j.celrep.2021.109307.

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.

Keywords: JNK; cancer; cell competition; fetal-like; organoids; small intestine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Carcinogenesis / metabolism
  • Carcinogenesis / pathology*
  • Cell Competition
  • Cell Line, Tumor
  • Fetus / pathology
  • Intestines / pathology*
  • MAP Kinase Signaling System
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Organoids / metabolism
  • Organoids / pathology*
  • Receptors, G-Protein-Coupled / metabolism
  • Stem Cells / metabolism

Substances

  • Lgr5 protein, mouse
  • Receptors, G-Protein-Coupled