Application of adenosine monophosphate-activated protein kinase (AMPK) inhibitor Compound C to drug for treating tumors
A technology of tumor drugs and inhibitors, applied in the field of medicine, can solve the problems of drug resistance, tumor recurrence, and side effects, and achieve the effect of inhibiting tumor cell activity and induction, promoting tumor cell apoptosis, and reducing harm
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 11
[0037] Effect of Different Concentrations of Compound C on Viability of Blood Tumor Cells by MTS
[0038] S11: Cell pretreatment
[0039] 1) Two kinds of lymphoma cells (Jurkat, K562) were resuspended to 5×10 4 Cells / mL, seeded in 96-well plates respectively;
[0040] 2) Add Compound C to the 96-well plate respectively, and set the concentration gradient of 0 μM, 0.5 μM, 1 μM, 5 μM, 10 μM and 20 μM, and after culturing for 48 hours, detect the cell survival;
[0041] S12: MTS detection of cell viability
[0042] 1) Gently mix 2mL MTS and 100μL PMS evenly;
[0043] 2) Add 20 μL of MTS mixture to each well, mix thoroughly, place in a carbon dioxide cell incubator, and incubate for 3 hours in the dark;
[0044] 3) Use a microplate reader to detect the wavelengths at OD490nm and OD630nm;
[0045] 4) Using the OD value at the Compound C concentration of 0 μM as a control, analyze the cell viability at each concentration gradient.
[0046] Using Rapamycin reagent as a control,...
Embodiment 12
[0048] Effect of Compound C on tumor cell apoptosis analyzed by flow cytometry
[0049] S11: Cell pretreatment
[0050] 1) Lymphoma cells (Jurkat, K562) were resuspended to 3×10 5 Cells / mL, seeded in 12-well plate;
[0051] 2) After adding Compound C and culturing for 48 hours, detect cell apoptosis;
[0052] S12: Analysis of cell apoptosis by flow cytometry
[0053] 1) Collect the cell suspension;
[0054] 2) Centrifuge the cell suspension at 800 g at 4°C for 5 min, discard the supernatant, and collect the cells in the pellet;
[0055] 3) Wash the cells twice with pre-cooled PBS, and then resuspend the cells with 100 μL 1×AnnexinV Binding Buffer;
[0056] 4) Add 5 μL Annexin V-FITC and 5 μL PI staining solution to each sample, mix gently, and react in the dark at room temperature for 15 minutes; pay attention to setting single staining and blank control, and follow-up flow cytometry adjustment needs to be compensated;
[0057] 5) After the incubation, add 400 μL pre-coo...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


