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Active elimination of intestinal cells drives oncogenic growth in organoids
Author(s) -
Ana Krotenberg García,
Arianna Fumagalli,
Huy Quang Le,
René Jackstadt,
Tamsin Rosemary Margaret Lannagan,
Owen J. Sansom,
Jacco van Rheenen,
Saskia J.E. Suijkerbuijk
Publication year - 2021
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2021.109307
Subject(s) - microbiology and biotechnology , cell growth , biology , organoid , cancer cell , cell , population , cell type , cancer , biochemistry , genetics , demography , sociology
Summary 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.

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