Comparative Analysis of Vascular Mimicry in Head and Neck Squamous Cell Carcinoma: In Vitro and In Vivo Approaches

• Published in: Cancers Vol. 13; no. 19; p. 4747
• Main Authors: Hujanen, Roosa, Almahmoudi, Rabeia, Salo, Tuula, Salem, Abdelhakim
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 23.09.2021; MDPI
• Subjects: Antibodies; Antigens; Blood vessels; Cancer; Comparative analysis; Cytology; Endothelial cells; Extracellular matrix; Head and neck carcinoma; head and neck squamous cell carcinoma; Heat; Matrigel; Medical prognosis; Metastases; Metastasis; Mimicry; Myogel; Neoplasia; Otolaryngology; Patients; Phenotypes; Solid tumors; Squamous cell carcinoma; Tumors; vascular mimicry; Vascularization; zebrafish; Denmark; St Louis Missouri; United Kingdom > UK; United States > US; Japan; Germany; Myogel; zebrafish; metastasis; vascular mimicry; Matrigel; head and neck squamous cell carcinoma
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers13194747

Tissue vasculature provides the main conduit for metastasis in solid tumours including head and neck squamous cell carcinoma (HNSCC). Vascular mimicry (VM) is an endothelial cell (EC)-independent neovascularization pattern, whereby tumour cells generate a perfusable vessel-like meshwork. Yet, despite its promising clinical utility, there are limited approaches to better identify VM in HNSCC and what factors may influence such a phenomenon in vitro. Therefore, we employed different staining procedures to assess their utility in identifying VM in tumour sections, wherein mosaic vessels may also be adopted to further assess the VM-competent cell phenotype. Using 13 primary and metastatic HNSCC cell lines in addition to murine- and human-derived matrices, we elucidated the impact of the extracellular matrix, tumour cell type, and density on the formation and morphology of cell-derived tubulogenesis in HNSCC. We then delineated the optimal cell numbers needed to obtain a VM meshwork in vitro, which revealed cell-specific variations and yet consistent expression of the EC marker CD31. Finally, we proposed the zebrafish larvae as a simple and cost-effective model to evaluate VM development in vivo. Taken together, our findings offer a valuable resource for designing future studies that may facilitate the therapeutic exploitation of VM in HNSCC and other tumours.