RESUMEN
Approximately 15% of cancers are attributable to the inflammatory process, and growing evidence supports an association between oral squamous cell carcinoma (OSCC) and chronic inflammation. Different oral inflammatory conditions, such as oral lichen planus (OLP), submucous fibrosis, and oral discoid lupus, are all predisposing for the development of OSCC. The microenvironment of these conditions contains various transcription factors and inflammatory mediators with the ability to induce proliferation, epithelial-to-mesenchymal transition (EMT), and invasion of genetically predisposed lesions, thereby promoting tumor development. In this review, we will focus on the main inflammatory molecules and transcription factors activated in OSCC, with emphasis on their translational potential.
RESUMEN
Current management of oral potentially malignant disorders is careful monitoring. Unfortunately, the 'watch and wait' approach only generates anxiety and a feeling of powerlessness, especially to those caring for patients. Photobiomodulation (PBM) has emerged as a potential strategy to inhibit possible transforming cells. The aim of this study was to investigate the effect of LED-based PBM on the progression of malignant invasion into a fibroblast-based stroma. An in vitro model of carcinoma in situ (CIS) containing stromal fibroblasts and carcinoma cells in co-culture was used to study the effect of PBM on the expansion of CIS colonies. A second model of co-culture (cells separated by membrane), was used to study cell counts, viability and apoptosis following PBM at high doses (36â¯J/cm2). The data was analyzed using Kruskal-Wallis, Dunn's test and non-linear regression, wherever appropriate. PBM was able to inhibit the expansion of CIS colonies as well as the total number of colonies after 72â¯h of treatment (pâ¯<â¯0.05). Cell viability, apoptosis and death assays revealed an overall advantage of stromal fibroblasts over carcinoma cells after high-dose PBM. In conclusion, LED-based PBM at high doses inhibited the progression and number of oral squamous cell carcinoma colonies without affecting the surrounding stromal fibroblasts in vitro.