The development of tumor is closely related to extracellular matrix, which changes the biomechanical behavior of cells.Research have prepared polyacrylamide hydrogel substrates of differing stiffness according to the hardness values of breast tissue under normal and tumor physiological conditions. Then AFM was used to measure the mechanical properties of breast cells with different degrees of malignancy grown on different stiffness substrates. To explore the reasons for the changes in the young’s modulus of three breast cells, the distribution of cellular actin filaments were observed with a confocal microscope. These results showed that when the substrate hardened, the viscoelasticity of benign breast cells increased significantly, and the other two cancer cells also changed to some extent. We also found that the harder the substrate, the more conducive to the spreading behavior of cells, and the weaker response of malignant cells to substrates.
The phosphatase and tensin homolog on chromosome 10 (PTEN) is one of important tumor suppressor proteins in ovarian cancer via negatively regulating the phosphatidylinositol 3-kinase–AKT signaling pathway and controlling genomic stability. Recent studies showed the physiological function of PTEN was closely related with its subcellular compartments. But only a few technologies could quantitatively measure the concentration of PTEN at different subcellular compartments in living cells. In this study, we used fluorescence correlation spectroscopy to measure the concentrations and dynamics of EGFP-PTEN in ovarian cancer cells HO-8910. Our results showed the increasing concentration of PTEN in the cytoplasm had an opposite trends with the nucleus after the oxidative stress stimulation which was induced by H2O2. Furthermore, the altered diffusion of PTEN at different subcellular compartments also illustrated the PTEN was trafficked from the cytoplasm to nucleus.
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