Matrix stiffness mechanically conditions EMT and migratory behavior of oral squamous cell carcinoma

• Autor(a) principal: Matte, Bibiana Franzen
• Data de Publicação: 2019
• Outros Autores: Kumar, Aditya, Placone, Jesse K., Zanella, Virgilio Gonzales, Martins, Manoela Domingues, Engler, Adam J., Lamers, Marcelo Lazzaron
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UFRGS
• Texto Completo: http://hdl.handle.net/10183/200746
• topic: Carcinoma de células escamosas; Transição epitelial-mesenquimal; Neoplasias; Matriz extracelular; Elasticidade; Colágeno; Hidrogel de polietilenoglicol-dimetacrilato; Cancer; Extracellular matrix; Elasticity; Hydrogel; Neoplasms; Collagen; Hydrogel, Polyethylene Glycol Dimethacrylate

Tumors are composed of heterogeneous phenotypes, each having different sensitivities to the microenvironment. One microenvironment characteristic – matrix stiffness – helps to regulate malignant transformation and invasion in mammary tumors, but its influence on oral squamous cell carcinoma (OSCC) is unclear. We observed that, on stiff matrices, a highly invasive OSCC cell line (SCC25) comprising a low E-cad toN-cad ratio (InvH/E:NL; SCC25) had increasedmigration velocity and decreased adhesion strength compared to a less invasive OSCC cell line (Cal27) with high E-cad to N-cad ratio (InvL/E:NH; Cal27). However, InvL/E:NH cells acquire a mesenchymal signature and begin to migrate faster when exposed to prolonged time on a stiff niche, suggesting that cells can be mechanically conditioned.Owing to increased focal adhesion assembly, InvL/E:NH cells migrated faster, which could be reduced when increasing integrin affinity with high divalent cation concentrations.Mirroring these data in human patients, we observed that collagen organization, an indicator of matrix stiffness, was increased with advanced disease and correlated with early recurrence. Consistent with epithelial tumors, our data suggest that OSCC cells are mechanically sensitive and that their contribution to tumor progression is mediated in part by this sensitivity.