Application of FICZ in inhibition of tumor cell migration
A glioma cell, cell technology, applied in the application of FICZ in inhibiting the migration of glioblastoma cells, in the field of cancer treatment, can solve the problems of poor prognosis and low long-term survival rate
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Embodiment 1FI
[0053] Example 1 Exploration of the Toxic Effect of FICZ on Glioblastoma
[0054] U87 cells were treated with 1×10 5 Cells / mL were inoculated into 96-well plates with 100 mL of cell suspension per well. Incubate overnight to allow cells to attach. Take out the 96-well plate, aspirate the original medium, and wash once with phosphate buffered saline (PBS). The experiment set up background control group, solvent control group and drug treatment group. Correspondingly, low-serum medium (1% serum concentration, no cells in the background control well), low-serum medium containing solvent dimethyl sulfoxide (DMSO) or different concentrations of FICZ was added to each well, and the volume of the solvent was maintained at 0.1%. Put the 96-well plate after adding the drug into the incubator to continue culturing for 24h or 48h. After reaching the end point of the culture, add 10 μL of CCK8 reagent to each well according to the instructions of the kit, put the well plate into the ...
Embodiment 2FI
[0056] Example 2FICZ inhibits the migration of glioblastoma cells
[0057] Cell migration ability was evaluated by scratch test. Use a marker pen to draw 3 straight lines horizontally on the bottom of the 6-well plate to locate the scratches. cells in 4 x 10 5 Inoculate 2 mL of cells / mL in a 6-well plate, culture overnight and wait for the cells to adhere to the wall. After the cells have completely covered the bottom of the well plate, scratch the cell monolayer with the tip of a 1 mL pipette to form a scratch. Choose the junction of the scratch and the marker line as the photo location. Floating cells were removed by washing with phosphate-buffered saline, and then low-serum medium containing the solvent DMSO or FICZ was added. Images were collected under an inverted microscope with a digital camera at 0-24 hours after scratching. A total of three independent repeated experiments were carried out, each concentration group in each independent experiment had 3 replicate w...
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