YAP1 gene and application of inhibitor in enhancing chemosensitivity of stem cell of bladder cancer
A bladder cancer and stem cell technology, applied in the field of biochemistry, can solve the problem of YAP1 gene and its inhibitor enhancing the chemosensitivity of bladder cancer stem cells
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Embodiment 1
[0025] Example 1: Sorting of Bladder Cancer Stem Cells
[0026] 1. Experimental materials
[0027] Human bladder cancer T24 cell line was cultured in RPMI-1640 medium containing 10% fetal bovine serum (containing 100 U / mL penicillin and 100 μg / mL streptomycin), incubator temperature 37°C, CO2 concentration 5%, every 2 Change the solution once a day.
[0028] The cell inhibition rate experiment used CCK-8 cell proliferation and cytotoxicity detection kit: according to the instructions, the more and faster the cell proliferation, the darker the color; the greater the cytotoxicity, the lighter the color, the depth of the color and the number of cells linear relationship.
[0029] Cell cycle detection was detected using a cell cycle point-of-care detection kit, followed by flow cytometry analysis.
[0030] 2. Experimental method
[0031] 1. Chemotherapy drug intervention culture sorting drug-resistant bladder cancer cells
[0032] Inoculate 5×10 T24 cells in T75 culture flask...
Embodiment 2
[0047] Example 2: Expression of YAP1 gene in bladder cancer stem cells and its relationship with chemotherapy sensitivity
[0048] 1. Experimental materials
[0049] Human bladder cancer T24 cell line was cultured in RPMI-1640 medium containing 10% fetal bovine serum (containing 100 U / mL penicillin and 100 μg / mL streptomycin), incubator temperature 37°C, CO2 concentration 5%, every 2 Change the solution once a day.
[0050] Bladder cancer stem cells were sorted by the method in Example 1 to obtain drug-resistant cells.
[0051] The siRNA targeting YAP1 and the siRNA negative control were provided by Shanghai Gemma.
[0052] 2. Experimental method
[0053] 1. Cell culture and transfection
[0054] Drug-resistant cells were collected and inoculated on culture plates, and randomly divided into blank control group, siRNA interference group and siRNA negative control group. The blank control group was not transfected; the siRNA interference group was transfected with siRNA tha...
Embodiment 3
[0066] Example 3: Effects of Small Molecular Compounds on Chemosensitivity of Bladder Cancer Stem Cells
[0067] 1. Experimental materials
[0068] Relevant experimental material is the same as embodiment 1 and embodiment 2.
[0069] 2. Experimental method
[0070] 1. Cell culture and grouping
[0071] Drug-resistant cells were collected, and after being cultured with RPMI-1640 medium containing 5% fetal bovine serum for 4 hours, they were randomly divided into blank control group and experimental group 1-3. The sensitizer continued to intervene and cultivate for 12 hours.
[0072] The chemical structure and concentration in the culture medium of each group of sensitizers in table 1
[0073]
[0074] 2. RT-PCR determination of YAP1 expression in bladder cancer stem cells
[0075] After 12 hours of intervening culture, collect the drug-resistant cells of the blank control group and the experimental group 1-3, wash with PBS, centrifuge and discard the supernatant, use th...
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