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Updated: Jan 17, 2026

Defining Gene Functions in Tumorigenesis by Ex vivo Ablation of Floxed Alleles in Malignant Peripheral Nerve Sheath Tumor Cells
Published on: August 25, 2021
Leveraging selection for function in tumor evolution: System-level cancer therapies
Frédéric Thomas1, Jean-Pascal Capp2, Antoine M Dujon1,3
1CREEC/CANECEV, MIVEGEC (CREES) Department, University of Montpellier, CNRS, IRD, Montpellier, France.
Abstract:
Current cancer therapies often fail due to tumor heterogeneity and rapid resistance evolution. A new evolutionary framework, 'selection for function,' proposes that tumor progression is driven by group phenotypic composition (GPC) and its interaction with the microenvironment, not by individual cell traits. This perspective opens new therapeutic avenues: targeting the tumor's functional networks rather than individual cells. Real-time tracking of GPC changes could inform adaptive treatments, delaying progression and resistance. By integrating evolutionary and ecological principles with conventional therapies, this strategy aims to transform cancer from a fatal to a manageable chronic disease. Crucially, it does not necessarily require new drugs but offers a way to repurpose existing therapies to impair a tumor's evolutionary potential. By steering tumor evolution toward less aggressive states, this approach could improve prognosis and long-term patient survival compared to current methods. We argue that leveraging GPC dynamics represents a critical, yet underexplored, opportunity in oncology.
Insights
Cancer progression is driven by group traits, not individual cells. Targeting tumor networks with existing therapies can manage cancer as a chronic disease by impairing evolutionary potential.
Area of Science:
- Evolutionary biology
- Cancer research
- Tumor microenvironment
Background:
- Cancer therapies face challenges from tumor heterogeneity and resistance.
- Tumor progression is often viewed through the lens of individual cell mutations.
Purpose of the Study:
- Introduce a new evolutionary framework, 'selection for function,' for understanding tumor progression.
- Propose targeting tumor functional networks and group phenotypic composition (GPC) for novel therapeutic strategies.
Main Methods:
- Conceptual framework integrating evolutionary and ecological principles.
- Focus on group phenotypic composition (GPC) dynamics within the tumor microenvironment.
- Proposes real-time tracking of GPC changes to guide adaptive therapy.
Main Results:
- Tumor progression is driven by GPC interacting with the microenvironment, not solely by individual cell traits.
- Targeting tumor functional networks offers new therapeutic avenues.
- Repurposing existing therapies can impair tumor evolutionary potential.
Conclusions:
- Leveraging GPC dynamics represents a critical, underexplored opportunity in oncology.
- This approach aims to transform cancer into a manageable chronic disease.
- Steering tumor evolution can improve prognosis and long-term patient survival.
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