The anti-cancer effects of metformin, the most widely used drug for type 2 diabetes, alone or in combination with ionizing radiation were studied with MCF-7 human breast cancer cells and FSaII mouse fibrosarcoma cells. Clinically achievable concentrations of metformin caused significant clonogenic death in cancer cells. Importantly, metformin was preferentially cytotoxic to cancer stem cells relative to non-cancer stem cells. Metformin increased the radiosensitivity of cancer cells in vitro, and significantly enhanced the radiation-induced growth delay of FSaII tumors (s.c.) in the legs of C3H mice. Both metformin and ionizing radiation activated AMPK leading to inactivation of mTOR and suppression of its downstream effectors such as S6K1 and 4EBP1, a crucial signaling pathway for proliferation and survival of cancer cells, in vitro as well as in the in vivo tumors. Conclusion: Metformin kills and radiosensitizes cancer cells and eradicates radioresistant cancer stem cells by activating AMPK and suppressing mTOR.
Metformin (1, 1-dimethylbiguanide hydrochloride) is the most widely used drug to treat type 2 diabetic patients. Metformin reduces blood glucose levels by suppressing gluconeogenesis in the liver and increasing glucose uptake by skeletal muscle1,2,3. Metformin decreases blood insulin levels, increases insulin sensitivity, suppresses synthesis of proteins, fatty acids and cholesterol, and increases free fatty acid utilization1,2,3. In addition, metformin has been shown in the last several years to possess strong anti-cancer effects3,4,5,6,7. Use of the drug by type 2 diabetic patients significantly suppressed development of cancers in breast8, pancreas9, and lung10, while diminishing cancer-related mortality. Furthermore, the response of diabetic patients with breast cancer to neoadjuvant chemotherapy was markedly better in those treated with metformin rather than other anti-diabetic drugs11. In a number of recent preclinical studies, metformin reduced proliferation of cancer cells and induced apoptotic and clonogenic death of cancer cells in vitro4,12,13,14,15, caused cell cycle arrest13,15 and reduced incidence and growth of experimental tumors in vivo16,17. These impressive epidemiological and preclinical results led to the recent commencement of several clinical trials evaluating the anti-cancer properties of metformin in combination with conventional chemotherapeutic drugs3,4,5,6.
The PTEN/PI3K/Akt/mTOR signaling pathway plays a central role in survival and proliferation of cancer cells18,19,20,21,22,23. This pathway is frequently mutated in cancer cells, leading to dysregulation of cell proliferation, differentiation, and survival. Metformin disrupts mitochondrial respiration leading to an imbalance of the AMP:ATP ratio. Increase in the level of AMP relative to ATP activates 5' AMP-activated protein kinase (AMPK), which then suppresses the activity of mTOR12,13,14,15,16,17,24. Therefore, suppression of mTOR through AMPK activation is believed to constitute the major mechanism underlying the anti-cancer activities of metformin12,13,14,15,16,17,21,22. Metformin has also been reported to directly inactivate mTOR in certain cell lines3. It has been reported recently that ionizing radiation activates AMPK25,26,27, and that metformin enhances the radiation-induced AMPK activation and cancer cell death25. Metformin has also been demonstrated to amplify chemotherapy-induced AMPK activation24.
Recent evidence unequivocally indicates that a small proportion of cells in human cancers are cancer stem cells (CSCs) (also termed tumor-initiating cells)28,29,30,31, and CSCs are both chemoresistant31,32,33,34,35 and radioresistant35,36,37,38 compared with non-cancer stem cells (non-CSCs). Importantly, it has been reported that metformin markedly improved the response of human tumor xenografts to conventional chemotherapy drugs by eradicating CSCs in the tumors39,40,41.
In the present report, we show that metformin is potentially effective to enhance the response of cancers to radiotherapy by killing cancer cells preferentially CSCs, and by radiosensitizing cancer cells. Our preliminary results have previously been reported42,43.
Metformin is cytotoxic to cancer cells
Metformin reduced the clonogenic survival of FSaII mouse fibrosarcoma cells and MCF-7 human breast cancer cells in dose and time-dependent manner as shown in Fig. 1. In FSaII cells (Fig. 1A), incubation with 1.0 mM metformin for 1 h reduced the clonogenic survival of cells to 65.1%, and incubation for 24 h or 48 h reduced the survival to 49.3% and 28.7%, respectively. Incubation of MCF-7 cells with 1.0 mM metformin for 24 or 48 h decreased the cell survival to 81.7% and 71.0%, respectively (Fig. 1B). We investigated the effects of a long-term exposure of cells to clinically relevant concentrations of metformin (6–30 μM)15,22. on the survival of cancer cells. Figure 1C shows that culturing FSaII cell in media containing 5 µM metformin reduced the clonogenic survival to 66.4%, and culturing FSaII and MCF-7 cells with 30 µM metformin decreased the survival to 64.1% and 71.9% respectively. When cells were cultured in the presence of metformin in the above mentioned studies, the size of resultant colonies and the cell density in the colonies were found to be reduced as compared with the colonies formed in regular medium. It was thus clear that metformin not only killed cancer cells so that the number of colonies formed were reduced, but it also suppressed the proliferation of surviving cells. We also studied whether metformin causes apoptotic death by flow cytometric determination of sub-G1 cells, annexing V staining and Western blot analysis of PARP and caspase-3 cleavage. The incubation for 48 h with 1–5 mM metformin caused little apoptosis in both MCF-7 and FSaII cells (see Supplementary Fig. S1 online). It thus appeared that apoptotic death did not contribute significantly to the total cell death, i.e. clonogenic cell death, caused by metformin in the present study.
Metformin sensitizes cancer cells to radiation
The radiation survival curves of FSaII and MCF-7 cells treated with metformin for 24 h before and 24 h after irradiation were steeper than the radiation survival curves of control cells (Figs. 1D and E). The radiosensitization caused by metformin was statistically significant at radiation doses higher than 3 Gy (P<0.05).
Metformin and irradiation activate AMPK and suppress mTOR, S6K1 and 4EBP1
Figure 2A shows that, in MCF-7 cells incubated with 5 mM metformin, the levels of p-AMPK gradually increased becoming significant after incubation for 16 h whereas the levels of p-mTOR and its downstream targets p-S6K1 and p-4EBP1 decreased after incubation with 5 mM metformin for 24 h. The levels of p-ACC, a substrate of p-AMPK, also increased as a result of activation of AMPK. These changes in the signals were further amplified when the incubation with 5 mM metformin was prolonged to 48 h. Irradiation of MCF-7 cells with 4 Gy gradually increased p-AMPK levels and slightly decreased the levels of p-mTOR, p-S6K1 and p-4EBP1 from 16 h post-irradiation. The levels of p-AMPK, p-mTOR, p-S6K1 and p-4EBP1 at 48 h after irradiation were almost similar to those at 16 h post-irradiation (Fig. 2A). As shown in Fig. 2B, the treatment of MCF-7 cells for 48 h with 1 or 5 mM metformin in combination with 4 Gy irradiation was far more effective than metformin or irradiation alone to increase p-AMPK and p-ACC and to decrease p-mTOR, p-S6K1, and p-4EBP1. Similar results were observed with FSaII cells (Fig. 2C): incubation with 1 mM metformin for 24–48 h increased p-AMPK and p-ACC levels and decreased p-mTOR, p-S6K1 and p-4EBP1 levels, and the combination of metformin with irradiation were far more effective than metformin or irradiation alone in activating AMPK and decreasing the phosphorylation of mTOR, S6K1 and 4EBP1. Detailed analysis on the changes in p-AMPK and p-mTOR in MCF-7 cells caused by metformin alone, radiation alone and combined are shown in Supplementary Fig. S2 online.
Inhibition of AMPK reduces the cytotoxic and radiosensitizing effect of metformin
Transfection of MCF-7 and FSaII cells with siRNA for AMPK markedly suppressed the AMPK level (Fig. 3A). The metformin-induced cell death (Fig. 3B) and the metformin-induced radiosensitization (Fig. 3C) were also significantly reduced by the transfection of the cells with AMPK siRNA.
Metformin is preferentially toxic to CSCs or CS-like cells relative to non-CSCs
It is well established that CSCs of human breast cancer cells such as MCF-7 cells are characterized with CD44high/CD24low surface markers28,31,37,39,40,41,44. In a representative experiment (Fig. 4A), 2.78% of MCF-7 cells were CD44high/CD24low cells, i.e. CSCs, and a 48 h treatment with 1 mM or 5 mM metformin reduced the fraction of CD44high/CD24low cells to 2.20% and 1.29%, respectively. The results of 7 experiments are summarized in Fig. 4B. The fraction of CD44high/CD24low cells before treatment was 3.4% and the fraction of CD44high/CD24low cells in the surviving cells after 48 h metformin treatment decreased in dose-dependent manner. For example, the fraction of CD44high/CD24low cells in the cell population which survived the 48 h treatment with 1 mM metformin was only 2.0% (P<0.05).
It has been shown that CSCs in various cancers express high-level of aldehyde dehydrogenase (ALDH1) activity, and thus ALDH1-positive CSCs can be isolated by flow cytometry44,45,46. Representative results of the effect of metformin on the proportion of ALDH1-positive cells, putative CSCs or CS-like cells, in the FSaII cells are shown in Fig. 4C. The proportion of ALDH1-positive FSaII cells was initially 2.72%, and it decreased to 1.66 and 0.80% after an 48 h incubation with 0.1 and 1 mM metformin, respectively. The means of 5–7 determinations are shown in Fig. 4D. Before the treatment, 1.92% of FSaII cells were ALDH1-positive, and incubation with 0.1 mM metformin for 48 h reduced the proportions of ALDH1-positive cells in the surviving cells to 1.08% (P<0.05).
The activities of ATP-binding cassette (ABC) transporters including the ABCG2 transporter are markedly elevated in CSCs32. Therefore, when cells are incubated with certain dyes such as the fluorescent Hoechst 33342, CSCs expel the dye whereas non-CSCs do not, thus making it possible to identify CSCs as side population (SP) cells by flow cytometry44,47. Representative data on the metformin-induced changes in the fraction of SP cells (putative CSCs) of FSaII cells are shown in Fig. 4E: proportion of SP cells decreased from 2.15% in the control to 0.88% after a 48 h incubation with 5 mM metformin. Given that CD44high/CD24low cells are CSCs of breast cancer28,31,37,39,40,41,44, and ALDH1-positive cells are putative CSCs or CS-like cells44,45,46 and SP cells are also putative CSCs of many different cancer cell lines44,47, the decreases in the proportion of CD44high/CD24low cells, ALDH1-positive cells and SP cells by metformin clearly indicated that metformin is preferentially cytotoxic to CSCs or CS-like cells relative to non-CSCs in MCF-7 and FSaII cells, as observed in other cell lines39,40,41, We have observed similar results in human MIAPaCa-2 pancreatic cancer cells and human A549 human cancer cells42,43.
Metformin impedes sphere formation
CSCs grow as spheres (tumor-spheres) upon incubation in non-adherent conditions39,40,44. When 1,000 MCF-7 cells were incubated for 8 days in metformin-free sphere medium, 44 ± 3 spheres with > 50 µM diameter were formed while 32 ± 2 and 13 ± 2 spheres were formed when incubated with 0.1 mM or 0.5 mM metformin, respectively. The numbers of FSaII spheres also declined when cultured with metformin. In addition to the decline in the number of sphere formed, the size of spheres formed upon incubation with 0.1 mM metformin was clearly smaller than those in the medium without metformin (Fig. 5A).
CSCs or CS-like cells are radioresistant
Figure 6A shows that, in a representative study, 3.14% of MCF-7 cells were CD44high/CD24low cells, i.e. CSCs, and irradiation with 3 or 5 Gy followed by a 48 h incubation increased the fraction of CD44high/CD24low cells to 4.82% and 6.05%, respectively. Such an increase in the fraction of CD44high/CD24low cells after irradiation indicated that CSCs are more radioresistant than non-CSCs. Importantly, maintaining MCF-7 cells with 1 mM metformin for 48 h after irradiation reduced the radiation-induced increase in the fraction of CSCs. The means of 5 experiments (Fig. 6B) showed that 1 mM metformin significantly suppressed the increase in the CSCs fraction caused by 3–7 Gy irradiation in MCF-7 cells. As shown in Fig. 5C, irradiation with 3 or 5 Gy significantly increased the fractions of ALDH1-positive FSaII cells, and metformin attenuated the radiation-induced increase in the fraction of ALDH1-positive cells.
Metformin enhances the efficacy of radiation to suppress tumor growth
Figure 7A shows that the treatment of C3H mice bearing FSaII tumors in the hind legs (s.c.) with metformin at 25 mg/kg twice a day (i.p.) slightly reduce the tumor growth. On the other hand, irradiation of tumors with 20 Gy markedly suppressed the tumor growth starting about 12 days post-irradiation. When host mice were treated with 25 mg metformin/kg twice a day, and tumors were irradiated 1 h after the first metformin treatment, tumor growth was markedly suppressed. Consequently, the days required for 4-fold increase in tumor volume were 17 ± 3 days after 20 Gy irradiation whereas it was 28 ± 4 days after the combined treatment with irradiation and metformin. The difference i.e. 17 v.s. 28 days, was statistically significant (P<0.001). The appearance of skin over the tumors treated with radiation alone and those treated with metformin in combination with radiation were similar.
To reveal whether AMPK/mTOR signaling pathway plays any role in the response of tumors to metformin and irradiation, we investigated the expression of p-AMPK and p-mTOR in the tumors using immunohistological method (Figs. 7B–E). In the FSaII tumors treated with 25 mg metformin/kg twice a day for 6 days, the level of p-AMPK significantly increased. The level of p-AMPK also significantly increased 6 days after 20 Gy irradiation. When tumors were irradiated 1 h after the first metformin treatment, the increase in p-AMPK expression was more pronounced than that occurred by metformin or irradiation alone (Figs. 7B and C). In contrast to the increase in p-AMPK levels, p-mTOR levels was markedly suppressed by metformin and irradiation alone or combined (Figs. 7D and E). Similar results were obtained with MCF-7 tumors grown in nude mice (see Supplementary Fig. S3 online).
This study has shown that metformin is cytotoxic to cancer cells at clinically achievable concentrations. Importantly metformin was preferentially cytotoxic to CSCs or CS-like cells relative to non-CSCs. Furthermore metformin increased the radiosensitivity of cancer cells in vitro and it markedly enhanced the response of experimental tumors to irradiation suggesting that the anti-diabetic drug metformin is potentially useful to enhance the efficacy of radiotherapy of cancer. Activation of AMPK and suppression of mTOR appeared to play an important role for the cytotoxic and radiosensitizing effect of metformin in vitro as well as in vivo.
Treatment of FSaII and MCF-7 cells with metformin at concentrations as low as 0.5 mM for 1–48 h significantly reduced clonogenic survival of the cells (Fig. 1). The plasma concentrations of metformin of type 2 diabetic patients treated with metformin are elevated to 6–30 µM range15,22. As shown in Fig. 1C, the long-term incubation of MCF-7 or FSaII cells with media containing 5–30 µM metformin reduced the clonogenic survival of cells by about 30% (Fig. 1C). In addition to inducing clonogenic death, the prolonged exposure to 5–100 µM of metformin markedly reduced the size of colonies formed and decreased the cell density in the colonies (data not shown) indicating that metformin not only kills cancer cells but it also suppresses the proliferation of surviving cancer cells, in agreement with the reports by other investigators14,21. The mode of cell death caused by metformin is unknown, but our studies indicated that apoptotic death contribute little to the total clonogenic cell death. It appeared that cells undergo necrotic death rather than apoptosis upon treatment with metformin (see Supplementary Fig. S1 online). Another potentially important feature of metformin was that 48 h treatment of cancer cells with 1 mM or 5 mM metformin significantly increased their radiosensitivity (Fig. 1D).
Increasing evidence indicates that the P13K/Akt/mTOR pathway plays crucial role in the survival and proliferation of cancer cells3,4,5,18,19,20. Metformin has been shown to inactivate mTOR via activation of AMPK, thereby causing cell cycle arrest, apoptosis, and clonogenic death, and inhibition of tumorigenesis3,5,12,13,14,15,16,17,21. In the present study, in excellent agreement with the previous reports, metformin markedly activated AMPK and inactivated mTOR, thereby decreasing the levels of downstream effectors p-S6K1 and p-4EBP1 in MCF-7 and FSaII cells in vitro (Fig. 2). Importantly, as reported by others25,26,27, irradiation also activated AMPK leading to reduction of p-mTOR, p-S6K1 and p-4EBP1 in the present study (Fig. 2). Combination of metformin and irradiation was more efficient than either radiation or metformin alone to activate AMPK and inactivate mTOR and its targets S6K1 and 4EBP1 (Figs. 2B and C). Similar to our observation, metformin markedly enhanced the radiation-induced activation of AMPK in cancer cells25. However, other investigators reported that ionizing radiation caused mTOR activation rather than mTOR inactivation in various cell lines27,48,49 particularly in the absence of AMPK activity27. In these studies, mTOR activation was observed in 1–6 h after irradiation, while in our study, inactivation of mTOR occurred from 16 h after irradiation. In a recent study, mTOR was activated for 6 h after irradiation and then inactivated thereafter50. Such an increase in mTOR activity after irradiation may be attributed to radiation-induced activation of Akt26. We may then speculate that mTOR activity is transitorily increased after irradiation, but the increase is eventually subdued as a result of progressive increase in AMPK activity. These observations are of interest since inhibition of mTOR activity with rapamycin or RAD100 markedly increased the cellular radiosensitivity48,49. As shown in Fig. 3, inhibition of AMPK activity with AMPK siRNA significantly reduced the cytotoxic and radiosensitizing effects of metformin against MCF-7 and FSaII cells, in agreement with the report by others24. Together, it may be reasonable to conclude that the metformin-induced cell death and radiosensitization of cancer cells (Fig. 1) are caused by the metformin-induced activation of AMPK and resultant inactivation of mTOR.
The significant decline in the fraction of CD44high/CD24low cells, i.e. CSCs, of MCF-7 cells and ALDH1-positive cells and SP cells of FSaII (Fig. 3) by metformin indicated that metformin is preferentially cytotoxic to CSCs or CS-like cells compared with non-CSCs. Our results are in excellent agreement with the recent observations by others that metformin selectively killed CSCs in various cell lines39,40,41. We have previously observed similar results in other human cancer cell lines including MIAPaCa-2 pancreatic cancer and A549 lung cancer cells42,43. CSCs have been known to grow as spheres (tumor-spheres) when incubated in non-adherent conditions39,40,44. Metformin at concentrations as low as 0.01 mM could suppress the number and size of spheres derived from both MCF-7 cells and FSaII cells (Fig. 5) further supporting the conclusion that CSCs or CS-like cells are more vulnerable to metformin than non-CSCs. As pointed out above, inactivation of mTOR may be a major mechanism for the anti-cancer effects of metformin. The PI3K/Akt/mTOR pathway has been reported to be activated in more aberrant manner in CSCs than non-CSCs18,19,20,29,30 so that CSCs are more sensitive than non-CSCs to suppression of mTOR. Indeed, suppression of Akt or mTOR was preferentially toxic to CSCs relative to non-CSCs19,22,23. Therefore, we may conclude that the metformin-induced suppression of mTOR via AMPK activation is more toxic to CSCs or CS-like cells than non-CSCs.
In contrast to the effect of metformin, ionizing radiation increased the relative proportion of CSCs or CSC-like cells (Fig. 6) indicating that CSCs or CS-like are radioresistant as compared with non-CSCs. Other investigators also reported that CSCs were radioresistant35,36,37,38 although the mechanism for the radioresistance of CSCs has not yet been clearly defined. Importantly, metformin significantly reduced the radiation-induced increase in the fraction of CSCs or CS-like cells (Fig. 6), which may be attributed to metformin-induced death of CSCs or CS-like cells. It is also possible that metformin sensitized CSCs or CS-like cells to radiation. Further studies are needed to reveal this intriguing and potentially important question.
Treatment of mice bearing FSaII tumors (s.c.) in the legs with metformin at 50 mg/kg/day (i.p.) slightly suppressed the growth of tumors (Fig. 7), in agreement with the reports by others33,51,52. Although the inhibition of tumor growth by metformin alone was small in the present study (Fig. 7), the drug markedly enhanced the response of tumors to irradiation. Such a marked suppression of tumor growth by the combined treatment may be attributed, at least in part, to the pronounced suppression of mTOR activity as a result of AMPK activation in the tumor cells (Fig. 7). Based on the results of in vitro studies, we may further speculate that metformin caused death of cancer cells, suppressed the proliferation of cancer cells, radiosensitized cancer cells, and eradicated or radiosensitized CSCs. Further studies are warranted to reveal the exact mechanisms by which metformin causes the remarkable increase in the radioresponse of tumors. The maximum safe dose of metformin for human is 2,550 mg/day for average size person of 60 kg53. In the present study, the dose of metformin given to mouse was 50 mg/kg/day, which is equivalent to 240 mg/day for 60 kg person according to a formula suggested by the National Institute of Health (U.S.A.)53. Therefore, the dose used for mouse in the present study was only about one-tenth that for the recommended safe dose for human.
It would be of interest to determine the proportion of CSCs in the tumors before and after treatment. The present study on the combined effect of metformin and a large single dose of radiation against tumor is relevant to the current trend of hypofractionated radiotherapy with high-dose per fraction using stereotactic techniques. However, the efficacy of metformin to enhance the response of tumors to conventional fractionated radiotherapy remains to be determined. Nevertheless, our results clearly indicated for the first time that metformin is potentially effective to enhance the efficacy of radiotherapy.
FSaII fibrosarcoma cells of C3H mice and MCF-7 human mammary adenocarcinoma cells obtained from the American Type Culture Collection (Manassas, VA) were used. We have previously used FSaII cells for various radiobiological research54.
Clonogenic survival of cancer cells
Cells in exponential growth phase were treated with metformin at 37°C for various lengths of time. Cells were then washed twice, cultured in drug-free regular medium (10–12 days for FSaII cells and 20 days for MCF-7 cells), colonies formed were fixed and stained51. The numbers of colonies containing more than 50 cells were counted and the surviving fractions wee calculated.
Effect of metformin on the radiation-induced death of cancer cells
Cells were incubated with metfomin for 24 h before and 24 h after irradiation, and their clonogenic survival was determined. Cells treated with metformin for 48 h without exposure to radiation or those exposed to irradiation only were used as controls. Irradiation of cells were performed with 250 kV orthovoltage X-rays (Philips Medical System).
Effect of AMPK siRNA on the cytotoxic and radiosensitizing effects of metformin
Cells were transfected with AMPK siRNA and then investigated the response of cells to metformin and irradiation alone or combined. siRNA duplexes targeting human AMPK was purchased from Dharmacon (Lafayette, CO). siRNA duplexes targeting mouse AMPK was purchased from Santa Cruz. AccuTarget™ negative control siRNA (Invitrogen, Carlsbad, CA) was used as a negative control. LipofectAMINE 2000 (Invitrogen) was used to transfect siRNA duplexes at final concentrations of 50 nM according to the manufacturer’s recommendations.
Analysis of signaling pathway by Western blot
Cells were lysed, proteins were separated by SDS-polyacrylamide gel electrophoresis (PAGE) and transferred to nitrocellulose membranes. The membranes were blocked with 1% (v/v) nonfat dry milk in Tris-buffered saline with 0.05% Tween20 and incubated with antibodies against proteins of interest(Antibodies against p-AMPK (Thr172), p-ACC (Ser79), p-mTOR (Ser2448), p-S6K1 (Thr389), p-4EBP1(Thr37/46), AMPK, ACC, mTOR, S6K1, 4EBP1 and β-actin were obtained from Cell Signaling Technology (Beverly, MA))51. The blots were labeled with goat anti-rabbit or anti-mouse IgG conjugated with horseradish peroxidase, and visualized with chemiluminescence (SUPEX, NeuroNex, Korea). The band intensities were measured using ImageJ 1.41 software (NIH, Bethesda, MD).
Effect of metformin on CSCs or CS-like cells. MCF-7 cells
MCF-7 cells were incubated with metformin for 24 or 48 h, enzymatically dispersed into single cells, washed, and suspended in PBS. Cells were next incubated for 20 min with anti-CD44 antibody (FITC-conjugated 555478, BD Biosciences, Franklin Lakes, N.J.) followed by incubation with phycoerythrine-conjugated anti-CD24 antibody (BioLegend, San Diego, CA) for 20 min in the dark at 4°C, washed with PBS containing 1% (v/v) FCS, and then CD44high/CD24low cells were identified using flow cytometry37,39,40. FSaII cells. The CSCs or CS-like cells of FSaII cells were identified using the Aldefluor assay method and also the Side population assay method44,45,46. Aldefluor assay44,45,46: FSaII cells were treated with metformin for 24 or 48 h and washed. The cells were then dispersed into single cells, and the ALDH activity was determined following the manufacturer’s instruction (BODIPY-aminoacetaldehyde, Stemcell Technology, Vancouver, Canada). Side population assay: FSaII cells were treated with metformin for 24 or 48 h and washed. The cells were then dispersed into single cells, incubated with Hoechst 33342 (Sigma, St Louis, MO) at 50 µmol/mL either alone or in combination with the ABC transporter inhibitors verapamil (50 µmol/mL) (Sigma, St Louis, MO) and FTC (10 µM) for 90 min at 37°C. After washing, SP cells were identified using flow cytometry44,46.
Effect of metformin on sphere formation
FSaII and MCF-7 cells were plated in six-well ultralow attachment plates (Corning, Lowell, MA) at a density of 1000 cells/plate in serum-free RPMI medium supplemented with 20 ng/mL BGF, 20 ng/mL EGF, 5 μg/mL bovine insulin and 2% (v/v) B27, and containing no or various concentrations of metformin. After incubation for 8 days, the numbers of spheres with diameter > 50 µM were counted under a microscope39,40,44.
Radiosensitivity of CSCs or CS-like cells
MCF-7 cells or FSaII cells in exponentially growth phase were irradiated and incubated with or without 1 mM metformin for 48 h. The fraction of CD44high/CD24low cells in MCF-7 cells and that of ALDH1-positive cells or side population cells in FSaII cells were assessed using the methods described above.
About 2.0 × 105 FSaII cells in 0.05 mL of serum-free medium were subcutaneously injected into right hind legs of 7–8 weeks-old male C3H mice. When tumors grew to about 150 mm3 in volume, mice were randomly divided into the following four groups: (a) control, (b) metformin, (c) irradiation, (d) metformin plus irradiation. The groups (b) and (d) animals were treated twice a day with metformin by i.p. injection of 25 mg/kg drug dissolved in 0.1 mL saline (50 mg/kg/day). The irradiation only group (group c) received i.p injection of 0.1 mL saline twice a day. For the irradiation of tumors (group c and d), mice were anesthetized by i.p. injection of a mixture of 100 mg/kg ketamine and 10 mg/kg xylazine, the body was covered with a 2 mm thick lead sheet, and tumor-bearing legs were locally exposed to 20 Gy of radiation in a single dose with 250 kV orthovoltage X-ray machine (Philips Medical System). Tumor diameter was measured using a caliper, and tumor volume was calculated53. At the end of the study, mice were euthanized by CO2 asphyxiation. All the animal experiments were performed following a protocol approved by the University of Minnesota Institutional Animal Care and Use Committee (Protocol number 0112A13064).
Tumors treated with metformin and radiation alone or combined were excised, snap frozen in liquid nitrogen and subsequently cut in 5 µm sections. Preparation and procedures for the frozen tumor sections were performed as described earlier with some slight modifications55,56,57. Briefly, sections were incubated for 30 min with PBS/5% BSA/3% FBS, and subsequently incubated with either p-AMPK, or p-mTOR antibody (Cell Signaling). After one hour incubation the slides were washed thoroughly with PBS/5% BSA/3% FBS and the secondary antibody anti-rabbit IgG fluorescein iso-thiocyanate (FITC) was added (Sigma, St Louis, MO)56. One hour later, after a thorough wash, images of the sections were acquired on an Olympus IX70 Inverted Microscope at 200x magnification and digitally analyzed and differentially quantified by morphometric analysis57.
The means of each group were compared with one-tail student’s t-test. P < 0.05 was considered significant.
We greatly thank Drs. Seymour Levitt, Kathryn Dusenbery and Douglas Yee for their interest in the present work and encouragement. This work was supported by Joseph Wargo Fund from the Minnesota Medical Foundation, Komen for the Cure Fund from the University of Minnesota Cancer Center, R&D Program of KOSEF (2009-0093747 and 2011-0015230) and Korea Health 21 R&D Project (A062254).
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Current Treatment Options in Oncology (2017)