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A Novel Stromal Fibroblast-Modulated 3D Tumor Spheroid Model for Studying Tumor-Stroma Interaction and Drug Discovery
Published on: February 28, 2020
Anti-angiogenesis and metastasis: a tumour and stromal cell alliance
1Tumor Angiogenesis Group, Catalan Institute of Oncology - IDIBELL, Spain.
Abstract:
Tumour progression requires the activation of a tumour and stromal cell-driven angiogenic programme, and the targeting of this process demonstrates an impact on tumour growth and progression. The results of preclinical studies have demonstrated a proinvasive/metastatic effect of antiangiogenic treatments with recent evidence supporting a contribution of the stroma to tumour aggressiveness and the short-term effects of antivascular endothelial growth factor therapy. Furthermore, hypoxia-dependent and -independent factors are considered as driving forces for tumour cell escape by altering both the tumour cells themselves and the stroma. This tumour-stromal cell alliance should be taken into consideration for the development of innovative therapeutic options targeting both tumour components to improve clinical benefits for cancer patients.
Insights
Tumour progression relies on angiogenesis, driven by tumour and stromal cells. Targeting this process, along with the tumour-stromal alliance, is crucial for effective cancer therapies.
Area of Science:
- Oncology
- Cancer Biology
- Tumour Microenvironment
Background:
- Tumour progression necessitates an angiogenic program orchestrated by both tumour and stromal cells.
- Antiangiogenic therapies, while impacting tumour growth, may promote invasion and metastasis.
- The tumour microenvironment, particularly stromal cells, significantly influences tumour aggressiveness and treatment response.
Purpose of the Study:
- To investigate the role of the tumour-stromal cell alliance in tumour progression.
- To highlight the impact of antiangiogenic therapies on tumour invasiveness.
- To emphasize the need for therapeutic strategies targeting both tumour and stromal components.
Main Methods:
- Review of preclinical studies on antiangiogenic treatments.
- Analysis of factors contributing to tumour cell escape.
- Examination of the tumour-stromal interaction in cancer aggressiveness.
Main Results:
- Preclinical data indicate a proinvasive/metastatic effect of antiangiogenic treatments.
- Stromal cells contribute to tumour aggressiveness and mediate short-term effects of antivascular endothelial growth factor therapy.
- Hypoxia-dependent and -independent factors drive tumour cell escape by altering tumour and stromal cells.
Conclusions:
- The tumour-stromal cell alliance is a critical factor in tumour progression and metastasis.
- Targeting angiogenesis alone may have limited long-term efficacy and could promote invasiveness.
- Innovative therapeutic strategies must consider the dual targeting of tumour and stromal cells to improve clinical outcomes in cancer patients.
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