Compound anti-cancer drug combining statin cholesterol-lowering drugs with thiazine antihypertensive drugs
An anti-cancer drug and thiazide technology, which can be used in drug combinations, pharmaceutical formulations, active ingredients of heterocyclic compounds, etc., can solve problems such as toxic side effects of life, endangering patients, and increasing toxic and side effects
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Embodiment 1
[0021] Example 1: The effect of administration of atorvastatin and hydrochlorothiazide on NF-κB of prostate cancer VCaP-N cells
[0022] Prostate cancer VCaP / N cells were inoculated at a density of 0.01×106 cells / ml and cultured for 24 hours. Then treated with atorvastatin and hydrochlorothiazide for 24h. The activity of NF-κB protein was detected by the method of luciferase reporter gene. The luciferase gene was introduced into PC-3 cells to form a stable clone, and then administered alone or in combination for 24 hours; then the luciferase detection kit was used to detect the activity of NF-kB luciferase, which indirectly reflected NF- kB level.
[0023] deal with Luciferase activity (% control group) Control group100 Atorvastatin group (10μM)89.2 Hydrochlorothiazide group (10μM)90.3 Atorvastatin (10μM) + Hydrochlorothiazide (10μM) group66.5
[0024] As can be seen from the table, the luciferase activity (% of the control group) of the atorvastatin (10μM) and hydr...
Embodiment 2
[0025] Example 2: The effect of administration of atorvastatin and hydrochlorothiazide on prostate cancer PC-3 cells
[0026] PC-3 cells were seeded in a 35mm petri dish at a density of 0.02x106 cells / ml and cultured for 24h. Then treated with 10 μM atorvastatin and hydrochlorothiazide for 96h. The number of live and dead cells was measured by trypan blue exclusion test. After an appropriate incubation time, collect the cells, stain them with trypan blue, count the blue-stained and non-stained cells under an inverted microscope, and use the formula "live cell rate (%) = total live cells / (total live cells + total dead cells) ×100%" to calculate cell survival rate.
[0027] deal with Number of living cells (1x104) Cell death rate (%) Growth inhibition rate (%) Control group37.22.9- Hydrochlorothiazide group (10μM)32.87.511.8 Atorvastatin group (10μM)35.34.05.1 Hydrochlorothiazide (10μM) + Atorvastatin (10μM) group 24.322.634.7
[0028] It can be seen from the table th...
Embodiment 3
[0029] Example 3: Effect of administration of atorvastatin and hydrochlorothiazide on prostate cancer CWR cells
[0030] CWR cells were seeded in 35mm petri dishes at a density of 0.02x106 cells / ml and cultured for 24h. Then treated with hydrochlorothiazide and atorvastatin at a concentration of 10 μM for 96 h. The number of live and dead cells was measured by trypan blue exclusion test. After an appropriate incubation time, collect the cells, stain them with trypan blue, count the blue-stained and non-stained cells under an inverted microscope, and use the formula "live cell rate (%) = total live cells / (total live cells + total dead cells) ×100%" to calculate cell survival rate.
[0031] The effects are as follows:
[0032]
[0033] It can be seen from the table that the PC-3 cell growth inhibition rate (% of the control group) in the atorvastatin (10μM) and hydrochlorothiazide (10μM) groups alone was 33.1% and 28.1%, while the combined administration group (A The torvast...
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