Breast cancer dormancy: need for clinically relevant models to address current gaps in knowledge
Grace G Bushnell1, Abhijeet P Deshmukh2, Petra den Hollander2
1Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA.
NPJ Breast Cancer
|May 29, 2021
Summary
Understanding breast cancer dormancy is crucial for preventing late-stage metastasis. This review examines current models and proposes criteria for developing better tools to study dormant tumor cells and improve patient outcomes.
Area of Science:
- Oncology
- Cancer Biology
- Metastasis Research
Background:
- Estrogen receptor-positive breast cancer survivors face lifelong risk of metastatic relapse.
- Disseminated tumor cells (DTCs) are believed to cause late relapses after prolonged dormancy.
- The biology and natural history of dormant DTCs remain poorly understood.
Purpose of the Study:
- To review existing models of tumor dormancy in breast cancer.
- To identify gaps in the biological understanding of dormant tumor cells.
- To propose criteria for developing clinically relevant dormancy models.
Main Methods:
- Literature review of existing tumor dormancy models.
- Analysis of current knowledge gaps in dormant cell biology.
- Formulation of criteria for future model development.
Main Results:
- Current dormancy models have limitations in clinical relevance.
- Significant gaps exist in understanding the mechanisms driving dormancy and reactivation.
- There is a need for models that accurately recapitulate the patient experience of dormancy.
Conclusions:
- Improved preclinical models are essential for advancing breast cancer metastasis research.
- Future models should focus on recapitulating the long-term dormancy and reactivation of DTCs.
- Developing better models will facilitate the discovery of therapeutic strategies to prevent late relapse.
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