Application of S-propargyl-cysteine to preparation of medicament for treating digestive system tumors
A cysteine and digestive system technology, which is used in the field of propargyl cysteine in the preparation of drugs for treating digestive system tumors
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Embodiment 1
[0024] Example 1 Cell Lines and Culture Mode
[0025] Human gastric cancer cell line (SGC-7901) and human liver cancer cell line (HepG2) (purchased from Cell Bank of Shanghai Institute of Biological Sciences, China). Culture conditions: culture SGC-7901 and HepG2 cells in RPMI 1640 and DMEM medium containing 10% fetal bovine serum and 1-2% penicillin and streptomycin (100U / ml), respectively, and place the cells at 37°C, 5% CO 2 cultured in an incubator.
Embodiment 2
[0026] Embodiment 2SPRC reduces cell viability experiment
[0027] 10 per hole 3 -10 4 SGC and HepG2 cells were seeded in a 96-well plate with a volume of 200ul per well. Add SPRC to final concentration respectively to 10 -5 、10 -6 、10 -7 、10 -8 and 10 -9 mol / L. After 24 hours of treatment, the cell viability was detected by MTT method, and the western medicine control group was treated with 10 -5 mol / L paclitaxel liposomes were processed accordingly and detected by MTT. The result is as figure 1 shown, 10 -5 , 10 -6 , 10 -7 The cell viability of the mol / L SPRC treatment group was significantly lower than that of the normal control group, and SPRC could inhibit the cell viability of liver cancer and gastric cancer cells.
Embodiment 3
[0028] Example 3 SPRC promotes cell apoptosis experiment
[0029] SGC and HepG2 cells were seeded in culture dishes with 10 -5 mol / L SPRC for 24 hours, and with 10 -5 mol / L paclitaxel liposomes were treated accordingly. Hoechst staining results as figure 2 As shown, the observed results showed obvious morphological features of apoptosis such as nuclear condensation and nuclear fragmentation in SPRC-treated SGC and HepG2 cells.
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