Oral potentially malignant disorders are associated with the development of oral squamous cell carcinoma (OSCC). Most OSCCs are diagnosed via histopathology as oral epithelial dysplasia (OED), but the histologic diagnostic criteria remain non-uniform. Accordingly, the establishment of a diagnostic marker to assist in diagnosis could contribute towards cancer prevention. Melanoma inhibitory activity (MIA) and MIA2 are involved in tumor growth, invasion, and lymph node metastasis in various malignancies. The purpose of this study was to clarify the usefulness of MIA and MIA2 as diagnostic markers of oral mucosal lesions. The expression of MIA and MIA2 was analyzed immunohistochemically in 100 specimens (10 specimens with normal oral mucosa (NOM) and 30 specimens each with low-grade epithelial dysplasia (LED), high-grade epithelial dysplasia (HED), and OSCC). Immunohistochemical results were evaluated based on the Allred scoring system. Cytoplasmic expression of MIA and MIA2 increased in the order of LED, HED, and OSCC. All NOM specimens were negative for cytoplasmic expression. Significant differences were observed between the groups (NOM vs. HED, p < 0.05, NOM vs. OSCC, p < 0.001). These results demonstrate that MIA and MIA2 are expressed in the oral mucosa within early neoplastic lesions and suggest that MIA and MIA2 are useful novel immunohistochemical markers for discriminating between normal tissue and OED.

Objective: This study aimed to evaluate the photobiomodulatory (PBM) effects of low-power light-emitting diode (LED) irradiation on cultured human umbilical vein endothelial cells (HUVECs), focusing on changes in cellular metabolic activity and morphology. Materials and Methods: HUVECs were cultured and divided into three groups: control (no irradiation), red LED (655 nm), and blue LED (455 nm). Cells were irradiated once with a total energy dose of 4 J over 60 s. Cellular metabolic activity was assessed at 0, 1, 3, and 6 h post-irradiation using the WST-8 assay. Morphological changes were examined 3 h post-irradiation using rhodamine–phalloidin staining and confocal laser scanning microscopy. Results: Red LED irradiation significantly enhanced metabolic activity immediately and at 3 h post-irradiation compared to the control group. Blue LED irradiation showed a non-significant trend toward increased metabolic activity at 1 and 3 h. Morphometric analysis revealed increases in cell area, perimeter, and Feret diameter in both LED-irradiated groups, with more pronounced changes observed in the red LED group. Conclusions: Low-power red LED light (655 nm) effectively promotes metabolic activation and induces morphological changes in vascular endothelial cells, suggesting its potential application in angiogenesis and wound healing. Due to its safety and accessibility, LED-based PBM may serve as a promising therapeutic modality for soft tissue regeneration in both clinical and home-care settings.