Differences in cellular death between melanoma (Me45) cells and fibroblasts (CCL-110) were investigated after irradiation with UV-C (1.5-15 J/m²) and incubation for up to 48 h. The role of DNA double strand breaks in this process was assessed. Decrease of the Me45 cells viability began about 6 h after irradiation. The fibroblasts viability negatively correlated with the dose applied, since necrosis within this cell population began immediately after irradiation. The enhanced apoptosis of fibroblasts was observed between 6 and 24 h, while for melanoma cells, high level of apoptotic cells was still detected after 48 h. Statistically significant correlation between the percentage of apoptotic cells and DSBs was estimated for both cell lines. The melanoma cells responded differently to the UV-C radiation than did the fibroblasts. These differences were explained by deficiency of the necrotic processes as well as the delay of apoptotic melanoma response to UV-C damage.
Speckle technique is based on the light intensity distribution randomly formed when a laser light is reflected on a rough surface, creating a pattern of illuminated grains (constructively) and dark (destructive) on scales of 1 μm. When the samples are displaced or deformed, the speckle pattern is altered. In this paper we present speckle patterns obtained from samples of gastric mucosa that is physically altered for the carcinogenesis process. Biopsies were studied with different diagnoses and were grouped according to the characteristics of speckle patterns. Speckle patterns were obtained by illuminating the samples with green laser. Morphological parameters of the speckle patterns reveal existence of 3 descriptors: the average grain size, hydraulic radius and the radio of the Weddel disc, which showed a high, intermediate and low value. The comparison shows agreement between the histopathological diagnosis and the values obtained by the speckle technique, making this technique emerge as a new classification system for quantitative diagnosis of precancerous lesions.
The aim of this study was to investigate the effect of the red light (630 nm) upon reactive oxygen species production by neutrophils in vitro. Blood samples were used for the study. The flow cytometry method was used for estimation of hydrogen peroxide production. A statistically significant decrease of reactive oxygen species production by neutrophils was observed. The level of the decrease varied and it was dependent on the kind of spectrum of applied signals and different levels of energy light.
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