Introduction
Breast cancer is one of the most common types of cancer in women and accounts for 7–10% of all diseases. Approximately 40 million people succumb to the disease each year (1). The incidence of breast cancer is rising in China (2) and is threatening to become a severe public health problem. Of patients with breast cancer 60–80% will develop bone metastases during the course of the disease (3). More than half of these patients will experience persistent and increasing bone pain, which seriously impairs the patient’s quality of life.
Radiation therapy is a common option for the treatment of breast cancer. Such therapeutic options include external beam radiation therapy and internal radionuclide therapy. In most breast cancer patients with bone metastases, pain in the bone can be relieved through radiation therapy. However, the benefits of radiation therapy can be limited by damage repair mechanisms, cell repopulation, and radiation-resistant hypoxic tumor cells. The radiosensitivity of tumor cells is an important factor that affects the efficacy of radiotherapy. In 1963, Adams et al (4) used nitroacetophenone to radiosensitize rat hypoxic cells. Following this initial report, many researchers have been developing radiation-sensitizing drugs to improve the efficacy of radiotherapy.
Radiation sensitizing agents are defined as any chemicals or biological reagents that selectively enhance the lethality of radiation on tumor cells or that reduce the radiation resistance of tumor cells. Thus, they improve the effect of radiation therapy. The ideal radiation sensitizer should meet the following criteria (5): (i) the agent should be stable and should not easily react with other substances; (ii) the effective dose should not be toxic or at least tolerable; (iii) the agent should be soluble in water for easy delivery; (iv) even at low doses, the drug should have radiation sensitizing effects in conventional fractionated treatment. However, it is difficult to find radiation sensitizers that fully meet all these criteria. In practice, drugs that enhance radiotherapy and show limited toxicity are often used as radiation sensitizers.
Chemotherapy drugs are the best studied agents for promoting radiosensitivity. However, chemotherapeutic drugs are toxic to normal cells and can have synergistic effects with radiation, often making them intolerable for patients. Therefore, there is still a clear need for novel radiation sensitizers in the clinic.
Arsenic trioxide (As2O3) was first used for the treatment of acute promyelocytic leukemia (APL) in 1970, and it was approved by the U.S. Federal Food and Drug Administration (FDA) in 2000. Previous studies (6-8) found that, in addition to APL, As2O3 is also effective against a number of solid tumors, including esophageal, liver, breast and gastric cancer. Although high doses of As2O3 may show significant toxicity, low doses can have notable antitumor effects, including changing tumor cell cycle distribution, promoting cell differentiation and apoptosis, reducing glutathione levels, directly damaging DNA, and inhibiting tumor angiogenesis (9–12). It is possible that As2O3 may also have radiosensitizing effects. In the present study, we examined whether As2O3 could sensitize human MCF-7 breast cancer cells to 89SrCl2 β-ray irradiation in vitro and we also investigated the underlying molecular mechanisms.
Materials and methods
Cell line
Human breast cancer MCF-7 cell line was obtained from the experimental center of clinical laboratory diagnostics at Bengbu Medical College. They were cultured in RPMI-1640 medium (Gibco, CA, USA) supplemented with l0% FBS (Gibco) in an incubator with 5% CO2 and saturated humidity at 37°C.
MTT assay evaluation of the effects of As<sub>2</sub>O<sub>3</sub> on cell proliferation
MCF-7 cells (1.0×104 cells per well) were seeded in 96-well plates and cultured for 24 h. The medium was then replaced with the same medium containing As2O3 (Sigma, MO, USA) at concentrations of 0, 0.5, 1, 2, 5, 10, 20, 50 and 100 μM for 24 h (6 wells at each concentration). Following incubation, the medium was removed and 200 μl of fresh medium containing 50 μg/μl MTT (Sigma) was added into each well and incubated for an additional 4 h. Medium was then discarded and 150 μl dimethyl sulfoxide (DMSO, Sigma) was added. Optical density (OD) at 570 nm was measured by DG3022A type Microplate Reader (State-run East China Electronic Tube Factory). The rate of cell proliferation was calculated as follows: (experimental OD value/control OD value) ×100%. The experiment was repeated 6 times. Growth curves were plotted; the ordinate and abscissa represent the concentration of As2O3 and the rate of cell proliferation, respectively. According to the curve, the 50% inhibiting concentration (IC50) was calculated.
<sup>89</sup>SrCl<sub>2</sub> irradiation and the calculation of absorbed dose
Cells were cultured for 24 h, medium was removed, and fresh medium containing 740, 1480 or 2960 kBq/ml of 89SrCl2 (Chengdu Gaotong Isotope Co., Ltd.) was added to the wells for another 48 h. Cumulative absorbed doses from 89Sr internal irradiation were computed according to the formulation (13), D = AEt/m (where A, E, m and t represent radioactivity of 89SrCl2, mean energy of β-ray from 89Sr, mass of irradiated cells and irradiating time, respectively).
Cell grouping and treatment
MCF-7 (5×104) cells per well were seeded in 6-well plates and incubated for 24 h. Cells were then randomly divided into four groups: control, As2O3, 89SrCl2 and As2O3+89SrCl2 group (combination group). Each treatment was performed in triplicate. The As2O3 and the combination group were treated with 1 or 2 μmol/l of As2O3 for 24 h. 89SrCl2 was added into both the 89SrCl2 and the combination group for another 48 h. Medium was then removed and fresh medium was added into each well. Cells were cultured for another 24 h. The experiment was repeated 6 times.
Morphological observations
The morphological changes of MCF-7 cells in each group were observed under an inverted microscope and images were captured with a digital camera.
Colony formation assay to detect the effects of <sup>89</sup>SrCl<sub>2</sub> on cell proliferation
Cells were detached from culture dishes with 0.25% trypsin (Sigma) and adjusted to 5×104/ml with fresh medium. Various treatments, including 0, 370, 740, 1480, 2960, 4440 and 5920 kBq/ml of 89SrCl2 were added to 100, 150, 200, 400, 1000, 2000 and 10000 cells. Cells were seeded in triplicate in different wells of 6-well plates for 24 h. Cells in the As2O3 group and the combination group were treated with 1 or 2 μM of As2O3 for 24 h. 89SrCl2 was added into the 89SrCl2 group and the combination group for another 48 h. Medium was then discarded and fresh medium was added into each well. Cells were cultured for a total of 12 days. Subsequently, cells were rinsed with phosphate-buffered saline (PBS), and colonies were fixed with 95% ethanol for 15 min. They were then stained with crystal violet for 20 min and counted under the microscope. Surviva1 fraction, SF = no. of colonies formed/(no. of cells seeded × plating efficiency of the control). The cell survival curve was plotted by the multi-target one hit model (14). Mean lethal dose (D0), quasi-threshold dose (Dq), extrapolation number (N) and radiosensitivity enhancing ratio (SER) were calculated.
Cell cycle analysis
Cells were harvested and rinsed with PBS. They were fixed with 70% ethanol at 4°C overnight. The following day, cells were centrifuged and the supernatant was discarded. Pellets were rinsed twice with PBS and incubated with 1.5 μl 25 mg/ml RNase A (Sigma) at 37°C for 30 min. They were then stained with 12 μl 50 μg/ml PI and protected from light at 4°C for 30 min. Cell cycle distribution was measured by FACSCalibur type flow cytometer (Becton-Dickinson).
Cell apoptosis analysis
Buffer was prepared according to instructions provided for the Annexin V-FITC/PI apoptosis detection kit (BD Biosciences, USA). Cells were harvested, mixed with 300 μl buffer, incubated in the dark with 5 μl Annexin V-FITC for 15 min, and then mixed with 5 μl PI for 5 min. Cell apoptosis was analyzed by flow cytometry (FCM).
Expression of Bcl-2 and Bax mRNA measured by RT-PCR
Total RNA was isolated with TRIzol reagent (Invitrogen, CA, USA) according to the manufacturer’s instructions. cDNA was synthesized at 42°C for 1 h and at 70°C for 10 min from 4 μg of total RNA using the SuperScript II Reverse Transcriptase (Invitrogen) following the manufacturer’s protocol. cDNA was subsequently amplified using Hot-StarTaq DNA Polymerase (Qiagen, Australia) and primers at MyCycler™ type PCR (Bio-Rad, CA, USA). Sequences of the primers are as follows (Shanghai Sangon Biological Engineering Technology and Services Co., Ltd.): GAPDH: 5′-GGGAAGGTGAAGGTCGGAGTC-3′ (sense primer), 5′-AGCAGAGGGGGCAGAGATGAT-3′ (antisense primer); Bcl-2: 5′-CAGCTGCACCTGACGCCCTT-3′ (sense primer), 5′-GCCTCCGTTATCCTGGATCC-3′ (antisense primer); Bax: 5′-ACCAAGAAGCTGAGCGAGTGTC-3′ (sense primer), 5′-TGTCCAGCCCATGATGGTTC-3′ (antisense primer).
The PCR program consisted of initial denaturation at 95°C for 3 min, followed by 30 cycles of denaturation at 95°C for 45 sec, annealing for 45 sec at 55°C (Bcl-2), 58°C (Bax) or 63°C (GAPDH) and extension at 72°C for 1 min. A final extension step at 72°C for 10 min was included for all primers. PCR products were stored at 4°C and electrophoresed in agarose gel buffered by 1X TBE at 100 V. Images were captured with an ultraviolet analyzer. The electrophoretic pattern was semi-quantitatively analyzed with SmartView image software, and the ratio of sample intensity to intensity of GAPDH was determined.
Western blot analysis
Protein was extracted from cultured cells and subjected to western blot analysis using specific antibodies to Bcl-2 and Bax. The cells were harvested and rinsed with PBS. Cell extracts were prepared with pre-chilled lysis buffer (50 mM Tris-HCl, 150 mM NaCl, 1% Triton X-100, 0.5% deoxycholate, 1 mM EDTA, 1 mM Na3VO4, 1 mM NaF, 2% Cocktail) and cleared by centrifugation at 12,000 g for 30 min at 4°C. The supernatant was collected and total protein concentration was measured using the BCA assay kit (Sigma) according to the manufacturer’s instructions. Cellular extract containing 30 μg of total protein was separated by 12% sodium dodecylbenzene sulfonate-polyacrylamide gel electrophoresis (SDS-PAGE), and the protein was transferred to PVDF membrane (Millipore, MA, USA). The membrane was then blocked with TBST (10 mM Tris-HCl, pH 7.4, 150 mM NaCl, 0.1% Tween-20) containing 5% w/v non-fat dry milk at 37°C for 1 h. It was then incubated with mouse anti-human Bcl-2 or Bax antibodies (1:200; Santa Cruz Biotechnology, CA, USA) or β-actin antibody (1:800; Santa Cruz Biotechnology) in TBST at 4°C overnight. The membrane was washed three times and hybridized with horseradish peroxidase-conjugated sheep anti-mouse IgG (1:2000; Millipore) for 2 h at room temperature. After washing three times for 10 min each with 15 ml TBST, protein bands specific for the antibodies were visualized by enhanced chemiluminescence (Amersham Pharmacia Biotech, NJ, USA) associated with fluorography. The intensity of bands for Bcl-2 and Bax proteins were analyzed with Smart view image software and the relative values of Bcl-2/Bax in different groups were calculated.
Statistics
Data are presented as the mean ± SD. Differences between two groups were determined by a t-test between independent samples using SPSS 11.5 software. The relationship between cell viability and As2O3 concentration was assayed using curvilinear regression and correlation analysis.
Results
Suppression of MCF-7 cell proliferation by As<sub>2</sub>O<sub>3</sub>
We measured MCF-7 cell proliferation 24 h after treatment with multiple concentrations of As2O3 and found that the proliferation of cells was suppressed to varying degrees (Fig. 1). As2O3 doses below 2 μM slightly inhibited (reduced by only 20%) cell proliferation; at As2O3 concentrations above 5 μM, proliferation was much more significantly inhibited. Markedly, the degree of inhibition increased in a dose-dependent manner. The curvilinear regression equation Y=91.7C−0.225 (r2=0.983, P<0.05) between the percentage of cell proliferation (Y, %) and As2O3 concentration (C, μM) was plotted, and the IC50 at 24 h was calculated to be 11.7 μM. To prevent the killing of MCF-7 cells by As2O3, only 1 and 2 μM doses of compound were used to investigate the radiosensitizing effects of As2O3 on cells treated with 89SrCl2.
Cumulative absorbed dose of MCF-7 cells exposed to <sup>89</sup>SrCl<sub>2</sub>
MCF-7 cells were exposed for 48 h to 370, 740, 1480, 2960, 4440 and 5920 kBq/ml of 89SrCl2. Cumulative absorbed doses of 89SrCl2 were 0.5, 1, 2, 4, 6 and 8 Gy, respectively.
Morphological changes of MCF-7 cells treated with As<sub>2</sub>O<sub>3</sub> and <sup>89</sup>SrCl<sub>2</sub>
MCF-7 cells were observed under an inverted microscope. Cells in the control group were adhered to the culture dish and grew normally. They displayed a typical polygon or spindle shape, clear cell profile, and intact nuclei. However, cells in the As2O3 group experienced morphological changes, including partly condensed chromatin and the appearance of vacuoles. Morphological changes of cells in the 89SrCl2 group were also apparent. With the increase of 89SrCl2 concentration, cells gradually became round and unattached. They showed decreased refractive indexes, increased particles in crystal, vacuole-like structures and partly ruptured nuclear membranes. Additionally, debris appeared around cells, some dead cells were found floating in the medium, soma became round in shape, the chromatin condensed and karyopyknosis and fragmentation occurred. The proliferation of cells in the combination group was significantly suppressed, with increased cell debris, incomplete nuclear membranes and smaller shapes and sizes (Fig. 2).
Clone formation assay evaluating the radiosensitizing effects of As<sub>2</sub>O<sub>3</sub> on MCF-7 cells treated with <sup>89</sup>SrCl<sub>2</sub>
MCF-7 cell survival curves in different groups are shown in Fig. 3. Curve equations were as follows: 89SrCl2 group, SF1=1−(1−e−D/2.89)2.18; 1 μM As2O3+89SrCl2 group, SF2=1− (1−e−D/2.32)2.10; 2 μM As2O3+89SrCl2 group, SF3=1− (1−e−D/1.61)1.95. For the formulas, SF represents cell survival rate and D is irradiated dose. The shoulder zone of the cell survival curve in the combination group became narrow, with an increased slope of the linear part, reduced mean lethal dose (D0) and quasi-threshold dose (Dq) (compared with those in the 89SrCl2 group, P<0.05). It showed that As2O3 may radiosensitize MCF-7 cells exposed to β-rays from 89SrCl2. Radiosensitization effects were enhanced with increased As2O3 concentrations in the low level range. Clones are shown in Fig. 4.
Effects of As<sub>2</sub>O<sub>3</sub> and <sup>89</sup>SrCl<sub>2</sub> on the distribution of MCF-7 cell cycle
Cells in the control group were found mostly in phases G0/G1 or S of the cell cycle. Cells in the treatment groups were mostly found to be in the G2/M phase. In both the As2O3-treated and 89SrCl2-treated groups, the percentage of cells in G2/M phase increased in a dose-dependent manner (compared with control, P<0.05). The percentage of cells in G2/M phase in the combination group increased dramatically. This increase was most apparent in the 2 μM As2O3 and 4 Gy 89SrCl2 group; 45.8% of the cell population was in G2/M. Of note, cells in S phase decreased compared with those in the 89SrCl2 group (P<0.05) (Table I).
Effects of As<sub>2</sub>O<sub>3</sub> and <sup>89</sup>SrCl<sub>2</sub> on MCF-7 cell apoptosis
Annexin V-FITC/PI double staining flow cytometry was used to discriminate among live cells, dead cells, and cells during early or late apoptotis (Fig. 5). Cells were divided into four subpopulations: live cells with low levels of Annexin V and PI (LL zone), cells in the early apoptotic phase with high levels of Annexin V and low levels of PI (LR zone), cells in the late apoptotic phase, and dead cells with high levels of Annexin V and PI (UR zone). We were also able to identify cells that had experienced mechanical injury during the experiment as having low levels of Annexin V and high levels of PI (UL zone). The spontaneous apoptotic rate of MCF-7 cells in the control was low. MCF-7 cells in the early apoptotic phase could be increased by As2O3. 89SrCl2 increased the percentage of dead MCF-7 cells and increased the number of cells in the late apoptotic phase from (2.1±0.7%) in the control to (20.5±4.3%) in the 4 Gy 89SrCl2 group. There was only a limited effect in the early apoptotic phase. In the combination groups, cells in both the early and late apoptotic phases as well as dead cells were all significantly increased. The rate of cells in the early apoptotic phase increased from (6.7±1.8%) in the 4 Gy 89SrCl2 group to (32.6±4.5%) in the 2 μM As2O3 and 4 Gy 89SrCl2 group (P<0.01). The number of cells in the late apoptotic phase and dead cell groups increased from (20.5±4.3%) in the 4 Gy 89SrCl2 group to (25.7±6.2%) in the 2 μM As2O3 and 4 Gy 89SrCl2 group (P<0.05) (Fig. 5, Table II).
Effects of As<sub>2</sub>O<sub>3</sub> and <sup>89</sup>SrCl<sub>2</sub> on the expression of Bcl-2 and Bax mRNA in MCF-7 cells
The expression of Bcl-2 mRNA was lower in the 2 μM As2O3 group and the 4 Gy 89SrCl2 group, compared to control. However, expression of Bax mRNA was unchanged by treatment (Fig. 6).
Data was analysed by Smart view image software, and the relative values (the ratio of the sample intensity to the intensity of GAPDH) of expression of Bcl-2 mRNA in the 4 Gy 89SrCl2 group and in the combination group were (27.25±3.56%) and (11.47±2.32%) (P<0.05), respectively. There were no differences in Bax mRNA (P>0.05). Despite this, the ratio of Bcl-2/Bax was significantly altered compared to control (P<0.05). Thus, As2O3 represses Bcl-2 mRNA expression caused by 89SrCl2 without affecting the expression of Bax mRNA (Fig. 6, Table III).
Effects of As<sub>2</sub>O<sub>3</sub> and <sup>89</sup>SrCl<sub>2</sub> on the expression of Bcl-2 and Bax proteins in MCF-7 cells
Bcl-2 and Bax proteins were both expressed in all MCF-7 control cells. Bcl-2 protein levels decreased in the 2 μM As2O3, the 4 Gy 89SrCl2 and the combination group. However, Bax protein was unchanged by treatment. The relative expression of Bcl-2 protein in the combination group was less than that in the 4 Gy 89SrCl2 group (P<0.05). There was no significant difference between the relative expression of Bax protein in each group (P>0.05) when analyzed by Smart view image software. It showed that As2O3 can inhibit the expression of Bcl-2 protein, without evident effects on the expression of Bax protein. Thus, the ratio of Bcl-2/Bax was decreased, which is in accordance with the effects of 89SrCl2 (Fig. 7, Table IV).
Discussion
Breast cancer is one of the most common types of cancer in women and it is often associated with bone metastases (2,3). Currently, the common approach for the treatment of bone metastasis is external beam radiation therapy. While this method is relatively effective for a single large metastasis, it is quite poor for the treatment of multiple lesions. Systemic medication (analgesic drug therapy and chemotherapy) has some advantages for patients with multiple bone metastases, but there are other toxic side-effects associated with such therapies. Systemic radionuclide therapy has drawn much attention in the clinic. It is a relatively simple and economical procedure that effectively relieves pain and can target multiple bone metastases with few side-effects.
89SrCl2 has been widely and successfully used for the treatment of bone metastases (15–17). Similar to calcium, 89Sr is a nuclide that is commonly found in bone. It is estimated that 30–80% of intravenously injected 89Sr will aggregate in the bone, especially at sites of active bone formation. Thus, its accumulation within bone metastases is about 2–25 times higher than it is in normal bone (18). The physical half-life of 89Sr is 50.56 days, and its biological half-life in normal bone is 14 days. However, 12–90% of 89Sr is still retained within bone metastases 3 months after 89Sr injection. The long-term accumulation of 89Sr within the bone metastatic lesion is a significant advantage for 89Sr to treat bone metastases. Physically, 89Sr emits pure β-rays with an average energy of 1.46 MeV, producing an average range in the bone of only 3 mm. Therefore, 89Sr can effectively kill tumor cells while limiting its effect on the surrounding bone. This results in the shrinkage or elimination of bone metastases and relief of bone pain. Nevertheless, there are still some patients who do not respond due to radioresistance of tumor cells (19,20). Thus, searching for safe and effective radiation sensitizers to improve the efficacy of radiation therapy has become a hot topic in radiation biology.
In recent years, arsenic and some Chinese herbs have been found to have radiosensitizing effects. As2O3 is the main component of Chinese medicine arsenic, which was first used for the treatment of patients with APL; in these patients, the treatment had a beneficial effect. In addition, other studies (21–24) have shown that As2O3 can induce tumor cell apoptosis and inhibit the growth of some solid tumors, including esophageal and liver cancers. This effect is partly due to regulation of cell cycle progression, induction of apoptosis and differentiation, blockage of tumor cell sub-lethal DNA damage repair, reduction of telomerase activity and glutathione content in tumor cells, and inhibition of angiogenesis (25). Such mechanisms can also enhance the radiosensitivity of tumor cells (26), providing the theoretical basis for the clinical application of As2O3 as a radiation sensitizer. In this study, we demonstrated that As2O3 dose-dependently inhibits the proliferation of MCF-7 cells in vitro (with IC50 at 11.7 μM, Fig. 1). In our radiosensitizing experiment, we found that there were no significant morphological changes of MCF-7 cells treated with low doses of As2O3, but obvious changes were observed for the cells exposed to 89SrCl2 for 48 h, which was accompanied by cell growth inhibition. When cells were treated with the combination of As2O3 and 89SrCl2 treatment, significant cell death, apoptosis and growth inhibition were observed.
Radiation dose-survival curves reflect irradiated cell survival in vitro and accurately determine proliferation and cell death. The parameters D0, Dq and N can be calculated from the radiation dose-survival curve. The D0 is the average lethal dose needed to cause cell death; this reflects the degree of cell sensitivity to radiation. The greater the D0 value, the lower the cell sensitivity to radiation. The threshold dose Dq value reflects the repair capacity of cells to sublethal damage and negatively correlates with radiation sensitivity. The N is the extrapolation number, reflecting the number of radiation-sensitive areas within the cell or required number of target hits. Any two of the three parameters can be used to reflect the extent of radiation sensitivity of cells (14).
In our study, we found that compared to 89SrCl2 radiation alone, the addition of As2O3 significantly decreased the D0 and Dq values of MCF-7 cells (P<0.05). This translated into radiosensitization ratios of 1.25 and 1.79, respectively, indicating that pretreatment with As2O3 significantly reduces the average lethal dose of MCF-7 cells to 89SrCl2 irradiation. Thus, As2O3 significantly increases the radiosensitivity of MCF-7 cells to 89SrCl2 irradiation in a dose-dependent manner.
Uncontrolled cell proliferation is one of the prominent features of cancer cells, which may result from deregulated cell cycle control. There are a few key phase regulatory sites that play key roles in the regulation of cell cycle progression. Of these, the regulatory sites at the G1/S and G2/M phases are the most important (27,28). Many anticancer drugs cause cell cycle arrest in the G1/S or G2/M phases to inhibit tumor proliferation (29). The radiosensitivity of tumor cells is closely related to both their capacity to repair DNA and their phase in the cell cycle. Cells in the G2/M phase are most sensitive to radiation; cells in early S phase and G1 phase are moderately sensitive, and cells in late S phase are least sensitive to radiation (30). Therefore, an important consideration to improving radiosensitivity and radiotherapy efficacy involves promoting tumor cells to enter the cell cycle but to remain in the G2/M phase. In our study, we found that 89SrCl2 or As2O3 treatment dose-dependently increased the percentage of MCF-7 cells in G2/M phase, but there was no significant effect on G0/G1 phase. This suggested that 89SrCl2 or As2O3 treatment could cause MCF-7 cells to arrest in G2/M phase. Compared to 89SrCl2 treatment alone, addition of As2O3 significantly increased the percentage of cells in G2/M phase (and decreased in G0/G1 phase). The percentage of cells in radioresistant S phase reached its lowest proportion. These results suggest that the G2/M phase arrest and decrease of cell number in S phase might be one mechanism by which As2O3 sensitizes MCF-7 cells to 89SrCl2 irradiation. These results are consistent with previous studies (31–33) showing that As2O3 can upregulate cyclin B, CDK-1 and p21, but downregulate CDK-6, CDC-2 and cyclin A expression. This correlated with an effect on G2/M cell cycle arrest.
Radiation-induced apoptosis is an important mechanism to kill tumor cells. Thus, inducing apoptosis in tumor cells has become a new strategy in radiation oncology. Apoptosis is also the common pathway by which many antitumor drugs exert their effects. FCM is a common method for studying apoptosis, and it can sensitively and accurately distinguish between early and late phases of apoptotic cells via double staining for Annexin V/PI (34). In the present study, we found that 89SrCl2 irradiation significantly induced late phase apoptosis and cell death but had little effect on early phase apoptosis of MCF-7 cells. However, addition of As2O3 significantly induced not only late phase apoptosis and cell death but also early phase apoptosis of MCF-7 cells (P<0.01; P<0.05 vs. 89SrCl2 treatment only). These results suggest that increasing the sensitivity of MCF-7 cells to 89SrCl2-induced apoptosis might be one of the mechanisms by which As2O3 sensitizes cells to 89SrCl2 irradiation.
Numerous factors affect the response of tumor cells to radiation, including the ability to repair DNA double strand breaks, transmembrane signal transduction and apoptosis-related gene expression (35). Previous studies (36–40) showed that Bcl-2 and Bax play significant roles in the regulation of apoptosis after irradiation. For example, it has been reported that knockdown of Bcl-2 expression significantly sensitized human PC-3 prostate cancer cells to irradiation (38). In this study, we found that the expression of Bcl-2 and Bax at both the mRNA and protein levels can be detected in MCF-7 cells without any treatment. Treatment with 2 μM As2O3 or 4 Gy 89SrCl2 irradiation reduced the antiapoptotic gene Bcl-2 at both the mRNA and protein levels. This reduction was more significant in the combination group (P<0.05 vs. 4 Gy 89SrCl2 group). We did not detect significant changes in Bax expression, but the overall Bcl-2/Bax ration did decrease in the individual experimental groups compared to control. This suggests that the radiosensitizing effect of As2O3 might be due to inhibition of Bcl-2 expression and subsequent reduction of the ratio of Bcl-2/Bax, which increases the sensitivity of MCF-7 cells to 89SrCl2 irradiation. Another study showed that with the reduction of the Bcl-2/Bax ratio, the formation of Bax homodimers increases, resulting in an increase of the permeability of the mitochondrial membrane in tumor cells (41). This leads to the release of cytochrome c, activation of downstream signaling pathways, and activation of caspase family members and apoptosis. Kumagai et al (42) have consistently found that As2O3-induced apoptosis is correlated with downregulation of Bcl-2 and Bcl-xL expressions in NB4 cells.
In summary, we found that low doses of As2O3 (below 20% of the IC50) significantly enhance the sensitivity of MCF-7 cells to 89SrCl2 β-ray irradiation in vitro, which is, at least in part, through inducing G2/M cell cycle arrest, downregulating Bcl-2 gene expression, and reducing the ratio of Bcl-2/Bax. Consequently, the overall effect is an increase in cell apoptosis. Further understanding of the underlying molecular mechanisms and exploring the possibility of As2O3 radiosensitization in vivo may have significant clinical implications and provide experimental evidence to improve the radionuclide therapeutic efficacy on malignant bone metastasis.
In conclusion, we demonstrated that 1–2 μM of As2O3 could increase the radiosensitivity of human breast cancer MCF-7 cell line by inducing G2 phase delay. The lethal effect of 89SrCl2 on MCF-7 cells thus was enhanced concomitantly with As2O3 pretreatment. The mechanism could be involved in the raising of the apoptosis rate of cells owing to the reduction of the Bcl-2/Bax rate.