Cellular and Molecular Mechanisms of MT1-MMP-Dependent Cancer Cell Invasion

• Published in: Annual review of cell and developmental biology Vol. 32; no. 1; pp. 555 - 576
• Main Authors: Castro-Castro, Antonio, Marchesin, Valentina, Monteiro, Pedro, Lodillinsky, Catalina, Rossé, Carine, Chavrier, Philippe
• Format: Journal Article
• Language: English
• Published: United States Annual Reviews 06.10.2016
• Subjects: actin; Animals; cancer; Cell Polarity; exocytosis; Humans; invadopodia; Matrix Metalloproteinase 14 - metabolism; metastasis; Models, Biological; MT1-MMP; Neoplasm Invasiveness; Neoplasms - enzymology; Neoplasms - pathology; Podosomes - metabolism; MT1-MMP; actin; invadopodia; cancer; exocytosis; metastasis
• ISSN: 1081-0706; 1530-8995
• DOI: 10.1146/annurev-cellbio-111315-125227

Metastasis is responsible for most cancer-associated deaths. Accumulating evidence based on 3D migration models has revealed a diversity of invasive migratory schemes reflecting the plasticity of tumor cells to switch between proteolytic and nonproteolytic modes of invasion. Yet, initial stages of localized regional tumor dissemination require proteolytic remodeling of the extracellular matrix to overcome tissue barriers. Recent data indicate that surface-exposed membrane type 1-matrix metalloproteinase (MT1-MMP), belonging to a group of membrane-anchored MMPs, plays a central role in pericellular matrix degradation during basement membrane and interstitial tissue transmigration programs. In addition, a large body of work indicates that MT1-MMP is targeted to specialized actin-rich cell protrusions termed invadopodia, which are responsible for matrix degradation. This review describes the multistep assembly of actin-based invadopodia in molecular details. Mechanisms underlying MT1-MMP traffic to invadopodia through endocytosis recycling cycles, which are key to the invasive program of carcinoma cells, are discussed.