Application of doxycycline in preparing antitumor drugs
An anti-tumor drug, doxycycline technology, applied in the direction of anti-tumor drugs, drug combinations, tetracycline active ingredients, etc., can solve the problems of endangering life safety and quality of life, low anti-tumor activity, low cure rate, etc. Low cost, wide range of sources, and the effect of inhibiting tumor metastasis
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Embodiment 1
[0042] Embodiment 1: Doxycycline is to the inhibitory effect of human tongue cancer, laryngeal cancer, choriocarcinoma, salivary gland tumor, human gallbladder cancer, human thymoma cell growth
[0043] (1) Cell Recovery and Culture
[0044] The cryopreserved tumor cells were taken out from the liquid nitrogen and immediately put into a 37°C water bath to thaw the cells. In a biosafety cabinet, suck the cell suspension into a centrifuge tube with an appropriate amount of medium, centrifuge at 800rpm / min for 5 minutes; discard the supernatant, suspend the cells with 1mL of medium, and suck it into a cell culture dish with an appropriate amount of medium Place the cells at 37°C, 5% CO 2 , under saturated humidity conditions. Subculture when the cells reach 80%-90% contact confluence, digest into a single cell suspension with 0.2% trypsin, and centrifuge at 800rpm / min for 5 minutes; discard the supernatant, add 1-2mL medium to suspend the cells, and transfer the cells to 2 -Co...
Embodiment 2
[0056] Example 2: Inhibitory effect of doxycycline on cell migration of human tongue cancer, laryngeal cancer, choriocarcinoma, salivary gland tumor, human gallbladder cancer, and human thymoma
[0057] (1) Cell Recovery and Culture
[0058] The frozen cells were taken out of the liquid nitrogen and immediately put into a 37°C water bath to thaw the cells. In a biosafety cabinet, suck the cell suspension into a centrifuge tube with an appropriate amount of medium, centrifuge at 800rpm / min for 5 minutes; discard the supernatant, suspend the cells with 1mL of medium, and suck it into a cell culture dish with an appropriate amount of medium Cells were cultured at 37°C, 5% CO2, and saturated humidity. Subculture when the cells reach 80%-90% contact confluence, digest into a single cell suspension with 0.2% trypsin, and centrifuge at 800rpm / min for 5 minutes; discard the supernatant, add 1-2mL medium to suspend the cells, and transfer the cells to Continue culturing in 2-3 Petri ...
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