+44-7360-538437The extracellular matrix molecule tenascin-C promotes metastasis by multiple mechanisms
Joint Event on International Conference on Molecular Biology, Tissue Science and Regenerative Medicine & 4th World Heart Congress
November 19-20, 2018 | Paris, France
Gertraud Orend
Universite de Strasbourg, France
Posters & Accepted Abstracts : Biomed Res
DOI: 10.4066/biomedicalresearch-C8-023
Abstract:
Today, an orchestrating role of the tumor microenvironment is widely accepted where especially stromal cells and soluble factors are recognized as active players. Yet, the extracellular matrix, although highly abundant, is often considered as passive bystander. A better understanding of the functions of the extracellular matrix in cancer is largely hampered by the lack of relevant models. This applies also to the extracellular matrix molecule tenascin-C, which is a marker of the cancer specific tumor microenvironment. We used a comprehensive approach comprising novel immune competent mouse models (with engineered tenascin-C levels) and demonstrated that tenascin-C plays multiple roles in cancer. Tenascin-C is dangerous as soon as it is expressed out of control. Through assembly into âTumor Matrix Tracksâ, tenascin-C impacts tumor and stromal cells including immune cells thereby regulating tumor immunity. Tenascin-C also enhances formation of new but leaky blood vessels. Direct interactions with tenascin-C causes endothelial cell rounding and death or survival upon induction of an insulating pericellular fibronectin coat. Tenascin-C enhances the angiogenic switch and upregulates a proangiogenic secretome. Finally, tenascin-C is an important component of metastatic vascular invasions by promoting endothelialization and cellular plasticity thereby increasing lung metastasis.
Biography:
E-mail:
PDF HTML