Application of ganoderic acid G as immune synergist and super-antigen dependent therapeutic medicine in tumour treatments
A technology of ganoderma acid and superantigen, which is applied in the direction of antitumor drugs, medical preparations containing active ingredients, drug combinations, etc., can solve problems such as tumor drug resistance, achieve low cytotoxicity, good application prospects, and reduce side effects effect of possibility
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Embodiment 1
[0037] use 3 H method was used to determine the inhibitory effect of U-937, Ramos, K562, Raji, THP-1 tumor cells. logarithmic phase cells by 10 4 Inoculate each well in a 96-well round-bottom culture plate, 200 μl per well, parallel 3 wells, add the same amount of culture medium to the control group, add ganoderma acid G with concentrations of 0, 30, 100, and 300 μg / ml respectively, and place at 37 °C 5%CO 2 Incubate for 72 hours in the incubator, add 6 hours before counting 3 H, and then count the growth of tumor cells and make a graph.
Embodiment 2
[0039] KB-A-1 cells in logarithmic phase 10 6 / ml concentration, 0.2ml / inoculate underarms of nude mice, grow in nude mice SPF environment for 15 days, separate solid tumors, inoculate left and right armpits of experimental nude mice under sterile conditions, and treat with intraperitoneal injection of drugs after 5 days, according to cisplatin (Cisplatin DDP) group and cisplatin plus ganoderma acid G group were treated. 5 days as a course of treatment, a total of 2 courses of treatment. The nude mice were sacrificed 6 days after drug withdrawal, and the solid tumors were weighed to calculate the tumor inhibition rate.
[0040] Tumor inhibition rate (%)=[(average weight of solid tumors in the control group-average weight of solid tumors in the administration group) / average weight of solid tumors in the control group]×100
Embodiment 3
[0042] use 3 Determination of KB-A-1, U-937, Ramos, K562, Raji, THP-1, A20, Hela and CD4 by H method + Toxic effect of normal human T cells, logarithmic phase cells by 10 4Inoculate each well in a 96-well round-bottom culture plate, 200 μl per well, parallel 3 wells, add the same amount of culture medium to the control wells, stimulate with 100 μg / ml ganoderma acid G, and place at 37°C in 5% CO 2 Incubate for 72 hours in the incubator, add 6 hours before counting 3 H, and then calculate the inhibitory rate of the drug on the cells, and plot it with the half inhibitory concentration of the cells.
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