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Updated: Apr 2, 2026

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Published on: January 22, 2021
A Physical Framework to Control Cancer Cell Heterogeneity and Plasticity
Hadrien De Blander1,2, Jean-Christophe Marine1,2
1Laboratory for Molecular Cancer Biology, Center for Cancer Biology, VIB, Leuven, Belgium.
This study introduces a physics-based cancer model using cell surface area and volume to track cell plasticity. This framework allows designing drug combinations to guide cancer cells toward nonviable states.
Area of Science:
- Quantitative Biology
- Biophysics
- Cancer Research
Background:
- Cancer cell plasticity allows adaptation to therapies, leading to treatment resistance.
- Current cancer therapies often target specific mutations or cell types, which can be circumvented by cell plasticity.
- A predictive framework is needed to understand and control cancer cell state transitions.
Purpose of the Study:
- To propose a physics-based framework defining cancer cell state by physical variables.
- To utilize cell surface area (S) and volume (V) as measurable proxies for cell plasticity.
- To enable the design of targeted therapies based on physical principles.
Main Methods:
- Defining cancer cell state by position and velocity in a continuous S-V space.
- Modeling therapy as generating S-V vector fields that dictate cell trajectories.
- Using S-V space dynamics to predict and steer cell populations toward nonviable states.
Main Results:
- Cancer cell state and plasticity can be represented by movement in a continuous S-V space.
- Therapeutic interventions can be modeled as vector fields influencing S-V trajectories.
- This approach offers a physically interpretable method for designing drug combinations.
Conclusions:
- A physics-based framework using S-V space provides a novel way to understand cancer cell plasticity.
- This model enables the design of therapies that steer cancer cells toward nonviable states.
- It offers a predictive and interpretable alternative to mutation-targeted therapies.
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