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Updated: May 19, 2026

A Mouse Model to Investigate the Role of Cancer-Associated Fibroblasts in Tumor Growth
Published on: December 22, 2020
A mouse model to identify cooperating signaling pathways in cancer
Monica Musteanu1, Leander Blaas, Rainer Zenz
1Ludwig Boltzmann Institute for Cancer Research, Vienna, Austria.
Abstract:
We here establish a mouse cancer model called Multi-Hit that allows for the evaluation of oncogene cooperativities in tumor development. The model is based on the stochastic expression of oncogene combinations ('hits') that are mediated by Cre in a given tissue. Cells with cooperating hits are positively selected and give rise to tumors. We used this approach to evaluate the requirement of Ras downstream effector pathways in tumorigenesis.
Insights
A new Multi-Hit mouse cancer model evaluates oncogene cooperation in tumor growth. This model uses stochastic oncogene expression to identify cooperating pathways essential for cancer development and progression.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Understanding oncogene cooperation is crucial for cancer research.
- Existing models have limitations in evaluating complex oncogenic interactions.
Purpose of the Study:
- To establish a novel mouse cancer model, termed Multi-Hit, for studying oncogene cooperativities.
- To assess the role of Ras downstream effector pathways in tumorigenesis using this model.
Main Methods:
- The Multi-Hit model utilizes Cre-mediated stochastic expression of oncogene combinations within specific tissues.
- Cells exhibiting cooperating oncogenic hits are positively selected, leading to tumor formation.
Main Results:
- The Multi-Hit model successfully allows for the evaluation of oncogene cooperativities.
- The study initiated the evaluation of Ras downstream effector pathways' requirement in tumorigenesis.
Conclusions:
- The Multi-Hit mouse model provides a powerful platform for dissecting oncogene cooperation in cancer.
- Further studies using this model can elucidate the specific roles of various signaling pathways in tumor development.
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