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Induction and Diagnosis of Tumors in Drosophila Imaginal Disc Epithelia
Published on: July 25, 2017
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.
Abstract:
Tumor-host interactions play an increasingly recognized role in modulating tumor growth. Thus, understanding the nature and impact of this complex bidirectional communication is key to identifying successful anti-cancer strategies. It has been proposed that tumor cells compete with and kill neighboring host tissue to clear space that they can expand into; however, this has not been demonstrated experimentally. Here we use the adult fly intestine to investigate the existence and characterize the role of competitive tumor-host interactions. We show that APC(-/-)-driven intestinal adenomas compete with and kill surrounding cells, causing host tissue attrition. Importantly, we demonstrate that preventing cell competition, by expressing apoptosis inhibitors, restores host tissue growth and contains adenoma expansion, indicating that cell competition is essential for tumor growth. We further show that JNK signaling is activated inside the tumor and in nearby tissue and is required for both tumor growth and cell competition. Lastly, we find that APC(-/-) cells display higher Yorkie (YAP) activity than host cells and that this promotes tumor growth, in part via cell competition. Crucially, we find that relative, rather than absolute, Hippo activity determines adenoma growth. Overall, our data indicate that the intrinsic over-proliferative capacity of APC(-/-) cells is not uncontrolled and can be constrained by host tissues if cell competition is inhibited, suggesting novel possible therapeutic approaches.
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.
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