Cell Competition Drives the Growth of Intestinal Adenomas in Drosophila

Saskia J E Suijkerbuijk1, Golnar Kolahgar1, Iwo Kucinski1

  • 1The Wellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Tennis Court Road, Cambridge CB2 1QN, UK.

Current Biology : CB
|February 9, 2016
PubMed

Insights

Tumor cells kill surrounding host tissue to grow, a process essential for adenoma expansion. Inhibiting this cell competition halts tumor growth, revealing a potential therapeutic strategy.

Area of Science:

  • Developmental Biology
  • Cancer Biology
  • Cellular Interactions

Background:

  • Tumor-host interactions significantly influence cancer progression.
  • The role of competitive tumor-host interactions in tumor expansion remains experimentally unverified.

Purpose of the Study:

  • To investigate and characterize competitive tumor-host interactions in a fly intestine model.
  • To determine the necessity of cell competition for tumor growth and identify underlying molecular mechanisms.

Main Methods:

  • Utilized APC(-/-)-driven intestinal adenomas in adult flies.
  • Manipulated apoptosis pathways and analyzed JNK signaling and Yorkie (YAP) activity.
  • Assessed Hippo pathway activity in relation to adenoma growth.

Main Results:

  • APC(-/-) adenomas were shown to compete with and kill surrounding host cells, causing tissue attrition.
  • Inhibiting cell competition via apoptosis inhibitors restored host tissue growth and contained adenoma expansion.
  • JNK signaling activation within and near tumors was required for tumor growth and cell competition.
  • Higher Yorkie (YAP) activity in APC(-/-) cells promoted tumor growth partly through cell competition.
  • Relative Hippo pathway activity, not absolute levels, determined adenoma growth.

Conclusions:

  • Cell competition is a critical driver of tumor growth, essential for adenoma expansion.
  • Inhibiting cell competition offers a potential therapeutic strategy to constrain tumor growth.
  • JNK and YAP signaling pathways are key mediators of tumor-host competitive interactions.