3 research outputs found
Possibilities in the application of solid lipid nanoparticles in combination with 5-fluorouracil to overcome the drugresistance of non-small cell lung cancer cell line A549
Introduction: Multidrug resistance of non-small cell lung cancer cells is associated with a high percentageof therapeutic failures. The aim of this study was to assess the ability of solid lipid nanoparticles as atransporter of the conventionally used cytostatic (5-fluorouracil) to overcome the resistance of A549 cells.Material and methods: MTT assay was used to assess the differences in viability of cells treated with5-fluorouracil alone or in combination with different types of solid lipid nanoparticles. Type of cell deathand distribution of cell cycle phases were evaluated using flow cytometry.Results: The use of nanoparticles as a 5-fluorouracil transporter reduced the viability of A549 cells to agreater extent than the cytostatic alone. This was mainly due to the increase in apoptosis, but also necrosisand cell cycle arrest.Conclusion: Our results indicate the great potential of nanotechnology in the treatment of non-small celllung cancer. By using nanoparticles, it is possible to sensitise tumour cells to cytostatics to which theyare normally resistant. In addition, literature data confirm the safety of solid lipid nanoparticle application
The influence of house dust extract on normal lung cell Mrc5 and non-small lung carcinoma A549
Introduction. Desensitisation is a therapeutic method of allergic disease treatment, but its impact on the cellular level remains to be elucidated. The purpose of this study was to identify the influence of house dust extract on two cell lines types: non-small lung cancer A549 and non-cancerous lung fibroblast Mrc5. Furthermore, we analysed cell viability, type of cell death, and reorganisation of mainly cytoskeletal proteins such as vimentin, F-actin, and b-tubulin. Material and methods. To determine the cell viability, the MTT test was used. The type of cell death was analysed using double staining of annexin V and iodide propidium. The reorganisation of cytoskeletal proteins was evaluated by fluorescent staining and microscopy observation. Results. Our data presented non-statistical differences in a population of live, apoptotic, and necrotic cells. We did not observe significant abnormalities in cytoskeletal reorganisation. Moreover, Mrc5 cell line exhibited a lower sensitivity for house dust extract in comparison to A549 cell line. Conclusions. Our study suggests that desensitisation has no significant influence on survival and cytoskeleton in both cell lines, which correlate with potential use of this method in cancer patients. Obviously, the choice of these kinds of treatment should be used carefully in consultation with a specialist. Additionally, to our knowledge, it was the first presentation of the influence of house dust extract on cells in the context of the main cytoskeletal reorganisations.