A Novel In Vitro Pathological Model for Studying Neural Invasion in Non-Melanoma Skin Cancer

Author:

Ávila-Fernández Paula123ORCID,Etayo-Escanilla Miguel12ORCID,Sánchez-Porras David12ORCID,Blanco-Elices Cristina12ORCID,Campos Fernando12ORCID,Carriel Víctor12ORCID,García-García Óscar Darío12ORCID,Chato-Astrain Jesús12ORCID

Affiliation:

1. Tissue Engineering Group, Department of Histology, Faculty of Medicine, University of Granada, 18016 Granada, Spain

2. Instituto de Investigación Biosanitaria (ibs.GRANADA), 18012 Granada, Spain

3. Doctoral Program in Biomedicine, University of Granada, 18071 Granada, Spain

Abstract

Neural Invasion (NI) is a key pathological feature of cancer in the colonization of distant tissues, and its underlying biological mechanisms are still scarcely known. The complex interactions between nerve and tumor cells, along with the stroma, make it difficult to reproduce this pathology in effective study models, which in turn has limited the understanding of NI pathogenesis. In this study, we have designed a three-dimensional model of NI squamous cell carcinoma combining human epidermoid carcinoma cells (hECCs) with a complete peripheral nerve segment encapsulated in a fibrine-agarose hydrogel. We recreated two vital processes of NI: a pre-invasive NI model in which hECCs were seeded on the top of the nerve-enriched stroma, and an invasive NI model in which cancer cells were immersed with the nerve in the hydrogel. Histological, histochemical and immunohistochemical analyses were performed to validate the model. Results showed that the integration of fibrin-agarose advanced hydrogel with a complete nerve structure and hECCs successfully generated an environment in which tumor cells and nerve components coexisted. Moreover, this model correctly preserved components of the neural extracellular matrix as well as allowing the proliferation and migration of cells embedded in hydrogel. All these results suggest the suitability of the model for the study of the mechanisms underlaying NI.

Publisher

MDPI AG

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