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Paulina Rampetsreiter1, Emilio Casanova, Robert Eferl
1Ludwig Boltzmann Institute for Cancer Research (LBI-CR) , Währinger Strasse 13a, A-1090 Vienna, Austria.
Abstract:
Tumor invasion and metastasis is a multi-step process that requires adaptation of cancer cells to conditions that they encounter during their journey to distant body sites. Understanding the molecular processes that underlie this adaptation is of exceeding importance because most cancer patients die because of metastases rather than primary tumors. In this review we assess genetically engineered mouse models (GEMMs) that have been established to investigate mechanisms of cancer invasion and metastasis.
Insights
Cancer cells must adapt to survive and spread to distant sites. This review examines genetically engineered mouse models (GEMMs) to understand the molecular mechanisms of tumor invasion and metastasis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Tumor invasion and metastasis are critical determinants of cancer patient mortality.
- Understanding cancer cell adaptation during metastasis is crucial for developing effective treatments.
Purpose of the Study:
- To review genetically engineered mouse models (GEMMs) used for studying cancer invasion and metastasis.
- To highlight the utility of GEMMs in elucidating molecular mechanisms of metastasis.
Main Methods:
- Assessment of existing literature on genetically engineered mouse models (GEMMs).
- Analysis of how GEMMs facilitate the study of cancer cell adaptation and spread.
Main Results:
- GEMMs provide powerful tools to investigate the complex molecular processes of cancer metastasis.
- These models allow for in vivo studies of cancer cell adaptation to microenvironments encountered during metastasis.
Conclusions:
- Genetically engineered mouse models are invaluable for dissecting the mechanisms of tumor invasion and metastasis.
- Further research using GEMMs will advance our understanding of metastatic disease and inform therapeutic strategies.