Application of chloroquine or pharmaceutically acceptable salt thereof in preparation of medicine for treating or/and preventing liver cancer
A technology for inhibiting liver cancer and drugs, applied in the application field of preparing drugs for treating or/or preventing liver cancer, can solve the problems of inability to remove the cause, the molecular mechanism of the cause and pathogenesis is not completely clear, and there is no satisfactory prevention.
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Embodiment 1
[0057] Embodiment 1, chloroquine enhanced the anti-liver cancer activity of 7-deoxynarcicycline
[0058] 1. Preparation of the medicine named 7-deoxynarcicycline+CQ for the treatment or / and prevention of liver cancer
[0059] This embodiment provides a drug for treating or / and preventing liver cancer (abbreviated as 7-deoxynarcicycline+CQ), the active ingredients of which are chloroquine phosphate and 7-deoxynarcicycline, which can treat or / and prevent liver cancer In the medicine, the mass ratio of chloroquine phosphate and 7-deoxynarcicycline is 1:20. The preparation method of the medicine for treating or / and preventing liver cancer is as follows:
[0060] 1.1 Preparation of 7-deoxynarcicycline solution
[0061] 7-Deoxynarcicycline was prepared as a 10 mM stock solution by dissolving in dimethyl sulfoxide (DMSO), and stored in aliquots at -20°C, and diluted to the corresponding concentration with normal saline to obtain 7-deoxynarcicycline solution.
[0062] 1.2 Preparat...
Embodiment 2、7
[0075] Example 2, 7-deoxynarcicycline anti-liver cancer activity
[0076] 1. 7-Deoxynarcicycline inhibits the growth of hepatocellular carcinoma and promotes the apoptosis of hepatocellular carcinoma
[0077] Cell viability was measured by MTT assay, and the growth inhibitory effect of 7-deoxynarcicycline on two typical human liver cancer cell lines (HepG2, Huh-7) was analyzed. The HepG2 and Huh-7 cells were planted in the logarithmic growth phase, and then treated with 10 μM 7-deoxynarcicycline. After 0, 12, 24, 48, and 72 hours, the cell viability was measured by the MTT method. The results showed that 10 μM 7-deoxynarcicycline was treated for 0, 12, 24, 48, and 72 hours, and the viability of liver cancer cells had a time-dependent downward trend ( Figure 4 ). The HepG2 and Huh-7 treated with 7-deoxynarcicycline for 48 hours were tested for monoclonal formation experiments. The results showed that 7-deoxynarcicycline treated HepG2 and Huh-7 for 48 hours could significantl...
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