Figure 1.
Reduction of glucose in the culture medium sensitizes breast cancer cells to metformin treatment but not human mammary epithelial MCF10A cells.
All cells were treated with different concentrations of metformin (0, 2, 4, 8, 16 mM) in medium containing different levels of glucose (0, 2.5, 5, 10, 15, 25 mM) for one day. Percentage of dead cells was determined using Sytox Green staining. Metformin significantly increased percentage of dead cells with decreasing glucose concentration in (A) MDAMB231 cells, (B) MCF7 cells, and (C) SKBR3 cells but not in (D) MCF10A cells. Data were presented as mean ± standard deviation.
Figure 2.
Metformin treatment of ovarian cancer cells is enhanced by low glucose conditions.
A. After 48 hour treatments with metformin (5 mM, +) or control vehicle (H2O, –), live OVCAR3 cell number was determined by counting trypan blue negative cells and dead cell number was determined by counting trypan blue positive cells. B. PA-1 cell death was determined as described in A. Phase contrast images (40x) of the cells cultured with (lower image) or without (upper image) metformin treatment. Bar graphs represented mean ± standard deviation. All metformin treated groups in medium containing low glucose (1 mM) were significantly different from their control groups. *Indicates significant difference between groups.
Figure 3.
Metformin decreases ATP levels in medium containing low glucose (2.5 mM).
MDAMB231 (A) and (B) MCF7 cells were treated with metformin (8 mM) in either 25 mM glucose or 2.5 mM glucose for one day and ATP levels were measured and fold change of ATP compared with control was plotted. C. ATP measurements in PA-1 cells after 12 hours with or without metformin. This time point was chosen because of the rapid rate of PA-1 growth under control culture conditions. Data were presented as mean ± standard deviation. All metformin treated groups in medium containing low glucose (2.5 mM) were significantly different from their control groups. *Indicates significant difference between groups.
Figure 4.
Metformin inhibits oxidative phosphorylation and increases glycolysis in 25 mM glucose containing medium in an AMPK-dependent manner.
A. MCF7 cells were treated with metformin (8 mM) for 15 hours in either 25 mM or 2.5 mM glucose containing media. Oxygen consumption rate (OCR) was determined using the FX24 instrument for metabolic flux analysis. Metformin treated groups were significantly different from their control groups. B. MCF7 cells were treated with metformin (8 mM) for 15 hours. Extracellular acidification rate (ECAR) was determined using the FX24 instrument for metabolic flux analysis. Metformin treated groups were significantly different from each other and their control groups. C. MCF7 cells were treated with metformin (8 mM) for 15 hours, and medium lactate levels were measured as an indicator of glycolytic flux. Metformin treated groups were significantly different from each other. D. Extracts of MCF7 and MDAMB231 cells harvested one day treatment with metformin in either 25 or 2.5 mM glucose were used for Western blotting detection of phosphorylated AMPK and total AMPK. β-Actin was detected as a loading control. Densitometry of p-AMPK/AMPK or p-AMPK/Actin for MCF7 cells is presented as a bar graph. Cleaved capsase 7 in MCF7 cells was detected with western blotting. β-Actin was detected as a loading control. E. MCF7 cells in high glucose were treated with metformin (8 mM) and compound C (10 µM) as indicated for 15 hours. DMSO is the vehicle control for compound C. ECAR was determined as described in B. Metformin treated groups were significantly different from each other. F. MCF7 cells in high glucose were treated with metformin (8 mM) and compound C (10 µM) as indicated for 15 hours. Medium lactate levels were determined as in C. Metformin treated groups were significantly different from each other. All bar graphs represent mean ± standard deviation. *Indicates significant difference between groups.
Figure 5.
In low glucose medium metformin inhibits AKT phosphorylation and mTOR activation.
MCF7 and MDAMB231 cells were treated with metformin in DMEM containing either 25 mM glucose or 2.5 mM glucose for one day. Western blotting was used to estimate the levels of p-AKT (Thr308), p-AKT (Thr473), total AKT, p-S6K, total S6K, 4EBP1 (lower bands represent hypophosphorylated and higher bands represent hyperphosphorylated), and β-actin as loading control.
Figure 6.
Replacement of glucose with fructose or galactose does not prevent metformin induced cell death or metformin induced ATP reduction.
MCF7 (A) and MDAMB231 (B) cells were treated with metformin in DMEM without glucose, with 25 mM glucose, with 25 mM galactose, 25 mM fructose, or 12.5 mM fructose plus 12.5 mM galactose for 1.5 days. Percentage of dead cells was determined by Sytox Green staining. Metformin treated groups in 25 mM galactose, 25 mM fructose and 12.5 mM fructose plus 12.5 mM galactose were significantly different from metformin treated groups in 25 mM glucose. MCF7 (C) and MDAMB231 (D) cells were treated in the indicated medium with or without metformin (8 mM) for one day and ATP levels were measured. Metformin treated groups in 2.5 mM glucose, 25 mM galactose and 25 mM fructose were significantly different from their control groups. Results were displayed as fold change compared with control. Data are presented as mean ± standard deviation. *Indicates significant difference between groups.
Figure 7.
High fructose (25 mM) and galactose (25 mM) do not support metformin enhanced glycolysis as observed in high glucose medium (25 mM).
MCF7 cells were treated with metformin (8 mM) in medium containing 25 mM glucose, 25 mM fructose or 25 mM galactose for 15 hours. OCR and ECAR were measured. A. OCR in either high glucose or fructose conditions, metformin treated groups were significantly different from their control groups, B. ECAR in either high glucose or fructose conditions, metformin treated groups were significantly different from each other, C. OCR in either high glucose or galactose containing media, metformin treated groups were significantly different from their control groups, D. ECAR in either high glucose or galactose conditions, metformin treated groups were significantly different from each other. Data are presented as mean ± standard deviation. *Indicates significant difference between groups.
Figure 8.
Ketogenic diets reduced serum glucose concentration and enhanced metformin effects on reducing 4T1 breast tumor growth in Balb/c mice.
A. Serum glucose was measured and demonstrated as bar graph. Data are presented as mean ± standard deviation. Groups on Ketogenic diets are significant different from groups on control diets. B. Tumor growth was measured at indicated time for CD (control diet), CD+Met (control diet plus metformin), KD (ketogenic diet) and KD+Met (ketogenic diet plus metformin). CD+Met treatment group was significantly different from KD+Met treatment group after day 11. C. Tumor volume at day 23. Data are presented as mean ± standard deviation (**indicates significant difference between groups).