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Updated: May 4, 2026

Tissue Engineering of Tumor Stromal Microenvironment with Application to Cancer Cell Invasion
Published on: March 18, 2014
Collagen as a double-edged sword in tumor progression
Min Fang1, Jingping Yuan, Chunwei Peng
1Department of Oncology, Zhongnan Hospital of Wuhan University, Hubei Key Laboratory of Tumor Biological Behaviors and Hubei Cancer Clinical Study Center, No. 169 Donghu Road, Wuchang District, Wuhan, 430071, China.
Collagen in the tumor microenvironment acts as a double-edged sword, influencing cancer progression. Its degradation and re-deposition impact tumor cell behavior, promoting or inhibiting cancer development.
Area of Science:
- Oncology
- Biomedical Engineering
- Cancer Biology
Background:
- Cancer involves complex interactions between tumor cells, stromal cells, and the tumor microenvironment (TME).
- The extracellular matrix (ECM), primarily composed of collagen, is a critical component of the TME.
- ECM remodeling by collagen influences tissue tension and tumor cell behavior.
Purpose of the Study:
- To explore the dual role of collagen in cancer progression.
- To understand how collagen degradation and re-deposition impact the TME.
- To elucidate the biomechanical signaling of collagen in cancer development.
Main Methods:
- Review of existing literature on collagen's role in the TME.
- Analysis of collagen's involvement in ECM remodeling.
- Discussion of biomechanical signals generated by collagen changes.
Main Results:
- Collagen acts as a scaffold in the TME, regulating ECM remodeling.
- Collagen degradation and re-deposition promote tumor infiltration, angiogenesis, invasion, and migration.
- Altered collagen in the TME releases biomechanical signals affecting tumor and stromal cells.
Conclusions:
- Collagen is actively involved in promoting tumor progression, not just a passive barrier.
- Collagen's role is context-dependent, potentially inhibiting or promoting tumor progression at different cancer stages.
- Understanding collagen's dual role is crucial for developing targeted cancer therapies.
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