Application of combination of zoledronic acid and organic selenium compound in preparation of antitumor drugs
An anti-tumor drug, zoledronic acid technology, applied in the field of tumor treatment, can solve the problems of tumor cell apoptosis, DNA damage, cell cycle arrest, etc., and achieve the effect of efficiently inducing tumor cell apoptosis
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Embodiment 1
[0036] Example 1 Study on anti-prostate tumor activity in vitro of ZOL and organic selenium compounds
[0037] In this experiment, we studied the in vitro antitumor activity of organic selenium compounds and ZOL on prostate cancer PC-3 cells. We look forward to the development of novel synergistic chemotherapy strategies for the treatment of tumors.
[0038] (1) Prostate cancer cells in logarithmic growth phase (PC-3 cells; purchased from American Type Culture Collection) were taken at a density of 2×10 4 cells / mL were seeded in 96-well plates (100 μL / well) and allowed to grow for 2 hours. PC-3 cells were pretreated with 20 μM ZOL for 8 h, and then 2 μM organic selenium compounds SeC and SeD (100 μL) were added to a 96-well plate, and no addition of ZOL and organic selenium compounds was used as a blank control, and the incubation was continued for 64 hours. After the time was up, 25 μL of MTT solution (5 mg / mL, PBS buffer) was added to each well and incubated for 4 hours. ...
Embodiment 2
[0055] Example 2 Study on the Effects of ZOL and Organoselenium Compounds on ROS Levels of Prostate Tumors
[0056] The excessive accumulation of reactive oxygen species ROS in cells is an important initial signal to cause cell damage, so we detected the effect of ZOL combined with organic selenium compounds (SeC, SeD) on prostate cancer cells after staining with DHE probes. Impact. The specific method is as follows:
[0057] The cells were inoculated in a 96-well plate at a density of 200,000 cells / mL. After the cells adhered to the wall for 24 hours (the medium used for culturing cells was DMEM medium), 50 μL of 20 μM ZOL was added to incubate for 2 to 8 hours as required. Afterwards, the DMEM medium was replaced with 20 μM, 100 μL DHE probe per well, incubated in the dark for 30 min, and SeC and SeD were added after ZOL incubation according to the requirements of each group (the concentration of SeC and SeD can be 0.25-8 μM; this paper The concentration of SeC and SeD use...
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