Radiotherapy tolerance lung cancer cell line, construction method thereof and application of cell line
A radiotherapy-resistant, lung cancer cell technology, applied in the direction of tumor/cancer cells, animal cells, vertebrate cells, etc., can solve the problem of lack of radiotherapy-resistant lung cancer cell lines, etc., achieve good application prospects, strong radiotherapy tolerance, Radiotherapy tolerance and stable effect
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Embodiment 1
[0024] 1. Cell culture: use RPMI-1640 medium (which contains 10% fetal bovine serum, 100U / ml penicillin, 100 μg / ml streptomycin and 2mM glutamine), and placed in 5% CO 2 , Cultured in a constant temperature incubator at 37°C.
[0025] 2. Cell irradiation: Cells in the exponential growth phase are irradiated by 6MV X-rays from the Swedish Elekta Precise linear accelerator, the source-to-skin distance is 100cm, the irradiation field is 30cm×30cm, and the dose rate is 500Gy / min. compensation block.
[0026] 3. Establishment of radiotherapy-resistant cell line PC9-RR: Human lung adenocarcinoma cell line PC9 (purchased from the Cell Resource Center, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences) cells (about 35×10 4 1) were inoculated in T25 culture flasks, and were irradiated by X-Ray 4Gy when the cells grew to 60% density; fresh culture medium was replaced immediately after irradiation, and the medium was changed every 2 days. Continue to culture unti...
Embodiment 2
[0028] Observation of cell morphology: Take monolayer cells in the exponential growth phase and observe their morphological differences under an inverted phase-contrast microscope.
[0029] refer to figure 1 As shown, under the phase-contrast microscope, the normal growth of PC9 and PC9-RR cells were similar in shape, and they both showed monolayer adherent growth. Among them, PC9 cells were relatively uniform in size, and PC9-RR elongated spindle cells increased.
Embodiment 3
[0031] Cell proliferation kinetics: Take 1×10 PC9 and PC9-RR cells each 4 Inoculated in 24-well plates (21 wells each), digested and counted the cells after inoculation and culture for 24h, 48h, 72h, 96h, 120h, 144h, and 168h respectively, counted the cells in 3 wells at each time node, and calculated the average value to draw the cell growth curve, and calculate the population doubling time PDT=t×lg2 / (1gN t -lgN 0 ), where N0 is the initial cell number, Nt is the final cell number, and t is N t -N 0 time.
[0032] refer to figure 2 As shown, the cell doubling time was calculated according to the growth curve, and the PC9 and PC9-RR cells were 34h and 37h respectively, and the PC9-RR cell doubling time was longer than that of the parental cell PC9.
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