Introduction
Breast cancer is one of the most common female malignancies, as well as one of the leading causes of cancer-associated morbidity and mortality in women (1,2). The standard and classical treatments for breast cancer, including surgical resection, radiotherapy and chemotherapy, are far from satisfactory due to limited efficacy and high rates of recurrence (3). Thus, the development of new therapeutic strategies is urgently needed for the treatment of breast cancer. Arsenic compounds, such as arsenic trioxide (ATO), which has been used in standard treatment strategies for acute promyelocytic leukemia (APL) (4,5), and sodium arsenite, have been reported to show cytotoxic effects against breast cancer cell lines (6–9). However, such arsenic compounds are commonly regarded as toxic compounds with adverse effects, including visceral organ damage, serious acute toxicity, and potential carcinogenicity, which consequently limit their clinical applications (10–12).
Arsenic disulfide (As2S2), as the predominant active ingredient of realgar, also known as ‘Xiong-Huang’ in traditional Chinese medicine, is considered to be a candidate for the treatment of several types of malignancies; it exhibits relatively low toxicity, and has the advantage of being orally administered (10,13–15). A series of basic and clinical studies have reported the antitumor effects of As2S2 in different types of malignancies, particularly hematopoietic tumors such as APL (13,16–19). Recently, there is increasing evidence to support that As2S2 has the ability to induce apoptosis and inhibit the growth of hematopoietic and solid tumor cell lines, such as human lymphoma cell lines (20), cervical cancer cell lines (21), human hepatocellular carcinoma cells (22), and human osteosarcoma cell lines (23). However, although the cytocidal effect of realgar nanoparticles has been demonstrated (24), the effects of As2S2 on breast cancer cells, and the underlying mechanisms, have yet to be fully investigated.
In recent decades, studies on the development of three-dimensional (3D) cell culture systems to generate multi-cellular tumor spheroids have attracted much attention. The findings of such studies suggest that the natural manner in which solid tumor cells grow in vivo is in 3D, indicating that growing cancer cells in 3D culture mimics more closely the in vivo environment compared with traditional two dimensional (2D) cell culture systems (25–28). In this sense, 3D-cultured breast cancer cells are able to provide more accurate evidence of the drug’s activity in development of novel therapeutics (25). The actual tumor microenvironment in the human body consists of cancer cells, fibroblasts, endothelial cells and extracellular matrix (26). In comparison with 2D cell-culture systems, the specific characteristics of 3D-culture systems include tight cell-cell interactions, cell-microenvironment interactions, and special internal and external cellular structures (27,28).
The aim of the present study was to investigate the effects of As2S2 on MCF-7 cells (a human breast cancer cell line), and to further disclose the possible molecular mechanisms underlying the action of the drug. In the present study, 2D- and 3D-cell culture systems were introduced in order to observe and compare the cell formation, cellular architecture, and drug responses between the two culture systems, and to evaluate the effects of As2S2 on MCF-7 cells cultured in the two systems.
Materials and methods
Reagents
The cell counting kit-8 (CCK8) was obtained from Dojindo Molecular Technologies, Inc. (Tokyo, Japan). The fluorescein isothiocyanaste (FITC) Annexin V Apoptosis Detection kit was from BD Biosciences (San Diego, CA, USA). The ECL™ Western Blotting Analysis system and ECL™ Prime Western Blotting Detection reagent were purchased from GE Healthcare (Buckinghamshire, UK). As2S2 and mouse anti-human Bcl-2-associated X protein (Bax) were purchased from Sigma-Aldrich (Merck KGaA, Darmstadt, Germany). The Pro-Survival Bcl-2 Family Antibody Sampler kit, rabbit anti-human phosphoinositol 3-kinase (PI3K), rabbit anti-human Akt, and rabbit anti-human mammalian target of rapamycin (mTOR) were obtained from Cell Signaling Technology, Inc. (Danvers, MA, USA). Mouse anti-human caspase-7 was purchased from BD Pharmingen (BD Biosciences, San Jose, CA, USA). Mouse anti-human p53 was obtained from BioLegend, Inc. (San Diego, CA, USA).
Cell lines and cell culture
The human breast cancer cell line, MCF-7, and the human normal breast cell line, 184B5, were purchased from the American Type Culture Collection (Manassas, VA, USA). MCF-7 cells were cultured in Alpha-MEM medium (Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA) supplemented with penicillin, streptomycin and 10% fetal bovine serum (Merck KGaA, Darmstadt, Germany). 184B5 cells were cultured in DMEM/F12 medium supplemented with 5% FBS, 1x Insulin, Transferrin and Selenium (ITS; Lonza Group Ltd., Anaheim, CA, USA), 100 nM hydrocortisone (Merck KGaA), 2 mM sodium pyruvate (Lonza Group, Ltd., Chiba, Japan), 20 ng/ml epidermal growth factor, 0.3 nM trans-retinoic acid (both from Merck KGaA), 100 U/ml penicillin and 100 μg/ml streptomycin. Cells were maintained as attached cells at 37°C in 5% carbon dioxide in a humidified atmosphere.
2D cell-culture assay
MCF-7 cells were seeded at a density of 10,000 cells/well in 500 μl cell culture media into 48-well plates (Iwaki Co., Ltd., Tokyo, Japan), and then incubated for 24 h. Vehicle for controls (cell culture media) and different concentrations of As2S2 were subsequently added into the corresponding wells to adjust the final drug concentrations of As2S2 to 0, 4, 8 and 16 μM. MCF-7 cells were allowed to grow for 72 h in the presence of the drug. This was followed by a cytotoxicity assay and other downstream applications, including apoptosis detection and western blotting.
3D cell-culture assay
3D spheroids were formed using DSeA 3D micro-plates (International Frontier Technology Laboratory, Inc., Tokyo, Japan) with thermo-reversible gelatin polymer (TGP), as described previously (29). Briefly, TGP powder in each well was dissolved in Alpha-MEM medium (Thermo Fisher Scientific, Inc.) and incubated at 4°C overnight to develop the aqueous solution (the sol phase). MCF-7 cells were subsequently seeded into cold Alpha-MEM medium with TGP on ice at a density of 10,000 cells/well, followed by incubation at 37°C to develop the gel form. Vehicle and the drug were applied in the identical manner as described above for the 2D cell culture. MCF-7 cells were incubated in the gel at 37°C for 72 h to develop spheroids (Fig. 1).
Microscopy
The cellular morphological structures of MCF-7 cells in both 2D- and 3D-cultures were observed on the fourth day following seeding using an IX70® inverted microscope (Olympus Corporation, Tokyo, Japan). A series of bright-field images were recorded and examined with 10×, 20× and 40× objectives (original magnifications: x100, x200 and x400, respectively).
Cytotoxicity assay
Cell cytotoxicity was analyzed using a CCK-8 assay (Dojindo Molecular Technologies, Inc.). A total of 1×104 cells/well MCF-7 cells were seeded into 48-well plates (the cell density was 1×104 cells/500 μl), and As2S2 was added at final concentrations of 0, 4, 8 and 16 μM. The plate was subsequently incubated at 37°C in a humidified atmosphere of 95% air and 5% CO2 for 72 h. Following incubation, 25 μl CCK-8 reagent was added into each well, followed by an additional incubation for 3 h at 37°C in a humidified atmosphere. The optical density (OD) value of each well was measured using a Corona MT P-32 micro-plate reader (Corona Electric Co., Ltd., Ibaraki, Japan) at 570 nm. The cell viability rate was calculated according to the following equation: Cell viability rate = (OD sample value − OD blank value)/(OD control value − OD blank value) ×100%.
Assessment of apoptosis
Apoptotic rates of the MCF-7 cells were analyzed using an Annexin V-FITC Apoptosis Detection kit (BD Biosciences). MCF-7 cells (2×105 cells/well) were seeded in 24-well plates (cell density, 2×105 cells/ml; volume, 1 ml cell suspension/well), and treated with serial concentrations of As2S2 (final concentrations: 0, 4, 8 and 16 μM); this was followed by incubation for an additional 72 h. Subsequently, the staining procedure was performed according to the manufacturer’s protocol. A total of 1×104 cells was analyzed using a flow cytom-eter (BD Biosciences). The cells were subsequently assessed for viable (Annexin V−/PI−), early apoptotic (Annexin V+/PI−), late apoptotic (Annexin V+/PI+) and necrotic (Annexin V−/PI+) cells.
Western blotting
A western blotting protocol was utilized in order to evaluate the protein expression levels of Bcl-2, Bax, p53, caspase-7, PI3K, Akt and mTOR in both monolayers and spheroids. Total protein was extracted from the MCF-7 cells treated with various final concentrations of As2S2 (0, 4, 8 and 16 μM) in both 2D and 3D cell-culture systems. Briefly, cell lysates were separated by SDS-PAGE and transferred into a polyvinylidene difluoride (PVDF) transfer membrane (Immobilon-P; Merck Millipore, Darmstadt, Germany). Membranes were blocked with 5% skimmed milk for 1 h. The membranes were washed with Tris-buffered saline/0.1% Tween-20 (TBST), and then incubated overnight at 4°C with 1:500 anti-mouse p53 specific antibody (cat. no. 628201; BioLegend, Inc.), 1:500 anti-mouse Bax-specific antibody (cat. no. B8429; Merck KGaA), 1:1,000 anti-mouse caspase-7-specific antibody (cat. no. 551238; BD Biosciences), 1:1,000 anti-rabbit Bcl-2-specific antibody (cat. no. 9941), 1:1,000 anti-rabbit PI3K p85 subunit-specific antibody (cat. no. 4228), 1:1,000 anti-rabbit Akt-specific antibody (cat. no. 4691), and 1:1,000 anti-rabbit mTOR-specific antibody (cat. no. 2983) (all from Cell Signaling Technology, Inc.). Membranes were also probed with mouse anti-human β-actin (cat. no. ab49900; Abcam, Tokyo, Japan) at 1:1,000 dilution as the internal control. The membranes were incubated overnight with the primary antibodies listed above at 4°C. The following day, the blots were incubated with 1:1,000 anti-mouse (cat. no. 7076) or 1:1,000 anti-rabbit (cat. no. 7074) (both from Cell Signaling Technology, Inc.) specific polyclonal secondary antibodies for 1 h at room temperature. The membranes were washed three times with TBST. Signals were detected with an ECL Western Blot detection kit in a luminescent image analyzer (Fujifilm; LAS-3000; Fujifilm, Tokyo, Japan). The images obtained were subsequently quantitatively analyzed using the ImageJ software program (Rasband, W.S., ImageJ, U.S. National Institutes of Health, Bethesda, MD, USA; http://rsb.info.nih.gov/ij/).
Statistical analysis
Data are presented as the mean ± standard error of the mean. One-way analysis of variance (ANOVA) followed by Tukey’s post-hoc test was performed for multiple comparisons, whereas Student’s t-test was used for the comparison of two groups. P<0.05 was considered to indicate a statistically significant difference. Each experiment was repeated independently at least three times.
Results
Human normal breast cells 184B5 are less sensitive to As<sub>2</sub>S<sub>2</sub> in comparison to MCF-7 cells
In order to determine the cytotoxic selectivity of As2S2, a normal human breast epithelial cell line (184B5) was used as a normal control (30,31), and the cytotoxic effect of As2S2 on both the breast cancer cell line (MCF-7) and 184B5 cells was examined using a CCK-8 assay. As shown in Fig. 2, dose-dependent inhibition was observed in the two cell lines following exposure to different concentrations of As2S2 (2-16 μM) for 72 h. In comparison with 184B5 cells, however, the MCF-7 cells exhibited significantly higher sensitivity to As2S2, with increased inhibitory ratios in cell viability (Fig. 2A) and decreased IC50 values of As2S2 (Fig. 2B). These results suggested that As2S2 is less cytotoxic to normal breast epithelial cells than it is to breast cancer cells.
Microscopic imaging of 2D cultured and 3D cultured MCF-7 cells
Following treatment with various concentrations (0, 4, 8 and 16 μM) of As2S2 for 72 h, the bright-field images of MCF-7 cells in both 2D and 3D cultures were recorded using an inverted microscope (Olympus Corporation) with original magnifications of ×100, ×200 and ×400 (objectives: 10×, 20× and 40×, respectively). As shown in Fig. 3, MCF-7 cells attached simply to the bottom of the wells in a monolayer manner in the 2D culture plates, whereas they formed multicellular spheroids (MCSs) in the 3D culture plates. The morphological changes of MCF-7 cells cultured as 2D monolayers and 3D spheroids following exposure to 0, 4, 8 and 16 μM As2S2 were examined. Exposure to a relatively high concentration (i.e., 8 or 16 μM) of As2S2 caused substantial morphological defects in both the 2D and 3D culture systems. Specifically, following treatment with As2S2 for 72 h, the MCF-7 monolayers in the 2D plates clearly decreased in a dose-dependent manner, whereas the structural integrity of the MCF-7 spheroids in the 3D plates deteriorated and fragmented, with a destructive configuration (Fig. 3). In contrast, treatment with 4 μM As2S2 (a relatively low concentration) led to a modest decrease in 2D-cultured MCF-7 cells, whereas it failed to cause any morphological changes in the 3D spheroids.
Cytotoxic effects of As<sub>2</sub>S<sub>2</sub> on 2D- and 3D-cultured MCF-7 cells
CCK-8 assays were performed to assess the viability of cells (in both the 2D- and 3D-cell culture systems) exposed to 0–24 μM of As2S2 for 72 h. As shown in Fig. 4A, a significant decrease in cell viability was observed in 2D-cultured MCF-7 cells following treatment with various concentrations of As2S2; this occurred in a dose-dependent manner. Specifically, in comparison with the control group (0 μM As2S2), cell viability was markedly reduced to 77.32±3.92 and 15.24±1.04% after exposure to 2 and 24 μM As2S2, respectively. In contrast, relatively higher concentrations (≥8 μM) of As2S2 were observed to have a significant dose-dependent inhibitory effect on 3D-cultured MCF-7 cells. There were significant differences between the 2D- and 3D-cultured systems in cell viability following exposure to As2S2 with the final drug concentrations of 4, 8, 12 and 16 μM. Although similar dose-dependent growth inhibition was observed in 3D-cultured MCF-7 cells, the growth inhibition rates were much lower compared with those observed in the 2D culture system. In particular, the growth inhibition rates induced by a relatively high concentration (≥8 μM) of As2S2 in the 2D-culure system were more than two times higher compared with those observed in the 3D culture system, indicating that the MCF-7 spheroids in the 3D culture system were more resistant to the cytotoxicity of As2S2 in comparison to the monolayers in the 2D culture system.
The growth inhibition curves were obtained using the probit regression analysis method (Fig. 4B), and the half-maximal inhibitory concentration (IC50 value) of As2S2 in the 2D and 3D culture systems was further calculated from their respective inhibition curves. As shown in Fig. 4C, the mean IC50 value of As2S2 in the 3D culture system was approximately three times higher compared with that in the 2D culture system (5.11±0.69 μM in the 2D culture system; 15.65±2.12 μM in the 3D culture system; P=0.0091). These results suggested that the monolayer cells were more sensitive to As2S2 in comparison with the spheroid cells.
As<sub>2</sub>S<sub>2</sub> treatment induced apoptosis of 2D- and 3D-cultured MCF-7 cells
To explore whether the induction of apoptosis was involved in the cytotoxicity of As2S2 in MCF-7 cells cultured in the 2D and 3D cultured systems, an Annexin V-FITC/PI dual staining assay was performed. The MCF-7 cells of monolayers and spheroids were exposed to 0, 4, 8 and 16 μM As2S2 for 72 h. The number of apoptotic MCF-7 cells was measured by an Annexin V-FITC/PI dual staining assay, followed by flow cytometry, which was based on the probe of the early (Q4) and late apoptosis (Q2) of MCF-7 cells (Fig. 5A).
As shown in Fig. 5B, the early apoptosis of MCF-7 cells was induced by As2S2 in a dose-dependent manner in the 2D- and the 3D-culture system. Without any drug exposure, MCF-7 cell spheroids seemed to be more susceptible to early apoptosis than the 2D monolayers, and the median values of the Annexin V+/PI− (early apoptosis) cells in the 2D monolayers and the 3D spheroids were 6.65±1.60 and 19.68±1.81%, respectively. The number of early apoptotic cells in the drug-free 3D culture was signifi-cantly increased in comparison with the 2D culture (P=0.0017). Following treatment with 4, 8 and 16 μM of As2S2 for 72 h in the 2D culture monolayers, the percentages of cells in early apop-tosis were 13.38±3.25% (P=0.5439), 22.40±5.24% (P=0.0340), and 31.08±2.86% (P=0.0017), respectively, in comparison with control (0 μM As2S2). By contrast, following treatment with 4, 8 and 16 μM of As2S2 for 72 h in 3D culture spheroids, the percentages of cells in early apoptosis were 25.63±2.03% (P=0.1628), 30.23±2.29% (P=0.0082), and 34.63±1.10% (P=0.0005), respectively, in comparison with the control.
In the absence of As2S2, the 3D spheroids were more susceptible to early apoptosis in comparison with the 2D monolayers. The pro-early apoptotic effects of As2S2 between the 2D and 3D systems were therefore compared by evaluating the apoptotic index, i.e., the ratio of apoptotic cell percentages between the drug treatment groups and the control. As shown in Fig. 5C, the early apoptotic indices in the 2D-cultured MCF-7 cells treated with 4, 8 and 16 μM of As2S2 for 72 h increased 2.22±0.50-fold (P=0.8209), 3.95±1.20-fold (P=0.2107), and 5.67±1.51-fold (P=0.0275), respectively, in comparison with the control (1.00). In 3D-cultured spheroids, the early cell-apoptotic indices following treatment with 4, 8 and 16 μM of As2S2 increased 1.33±0.16-fold (P=0.4645), 1.57±0.16-fold (P= 0.0988), and 1.82±0.22-fold (P= 0.0140), respectively, in comparison with the control (1.00). These data demonstrated that MCF-7 cells cultured as spheroids were more resistant to As2S2 in terms of the early induction of apoptosis, in comparison with cells cultured as monolayers, with statistically significant differences in the presence of 8 (P=0.0457) and 16 μM (P=0.0448) As2S2.
As shown in Fig. 5D, late apoptosis of the MCF-7 cells was induced by As2S2 in a dose-dependent manner, particularly in 2D monolayers. In 2D culture monolayers, following treatment with 4, 8 and 16 μM of As2S2 for 72 h, the percentages of cells in late apoptosis (Annexin V+/PI+) were 0.53±0.23% (P=0.9568), 1.17±0.58% (P=0.3166), and 3.60±0.06% (P=0.0005), respectively, in comparison with the control. By contrast, the MCF-7 spheroids were more resistant to As2S2-induced late apoptosis, without any significant increases in those cells in the presence of any concentration of As2S2.
As shown in Fig. 5E, the late apoptotic index of MCF-7 cells was induced by As2S2 in a dose-dependent manner in both 2D- and 3D-culture systems. In 2D culture monolayers, following treatment with 4, 8 and 16 μM As2S2 for 72 h the late cell-apoptotic index increased 2.72±0.49-fold (P=0.8894), 4.48±0.49-fold (P=0.5016), and 8.99±4.52-fold (P=0.0458), respectively, in comparison with the control (1.00). In the 3D-cultured spheroids, following As2S2 treatment at concentrations of 4, 8 and 16 μM for 72 h, the late cell-apop-totic index increased 0.98±0.38-fold (P>0.99), 1.65±0.35-fold (P=0.5419), and 2.63±0.42-fold (P=0.0352), respectively, in comparison with the control (1.00). Therefore, the data in the present study demonstrated that MCF-7 cells cultured as spheroids were more resistant to As2S2 in terms of the late induction of apoptosis, in comparison with cells cultured as monolayers, with statistically significant differences in the presence of 4 (P=0.0206) and 8 (P=0.0231) μM As2S2, respectively.
Effects of As<sub>2</sub>S<sub>2</sub> on the expression of apoptosis-associated proteins in 2D- and 3D- cultured MCF-7 cells
To further investigate the mechanism underlying As2S2-induced apoptosis in MCF-7 monolayers and spheroids, the expression levels of apoptosis-associated proteins were evaluated. To accomplish this, the levels of pro-apoptotic proteins, such as Bax, p53 and caspase-7, as well as of the anti-apoptotic protein, Bcl-2, were assessed by western blotting. As shown in Fig. 6A, C and D, the expression levels of the pro-apoptotic proteins, Bax, p53 and caspase-7, were significantly upregulated by As2S2 in MCF-7 monolayers. The protein levels of Bax were markedly increased following treatment with 4 (P=0.004), 8 (P=0.0032) and 16 (P=0.0258) μM As2S2, in comparison with the control (0 μM As2S2) (Fig. 6A). For p53, the protein levels increased in a dose-dependent manner, following exposure to 4, 8 and 16 μM As2S2 (in comparison with the control). A statistically significant increase was observed following treatment with 16 μM As2S2 (P=0.0045) (Fig. 6C). The protein expression of caspase-7 was significantly upregulated after incubation with 8 (P=0.0003) and 16 (P=0.0009) μM As2S2, in comparison with the control (Fig. 6D). By contrast, a similar increase in the expression level of Bax was confirmed in treated 3D spheroids after treatment with 4, 8 and 16 μM As2S2 (P= 0.0026, P=0.0265, P=0.0226 vs. control, respectively), and As2S2 treatment tended to induce the increased expression of p53; however, the expression of caspase-7 was not significantly increased in the 3D culture system (Fig. 6A, C and D).
As shown in Fig. 6B, following treatment with As2S2 for 72 h, the expression of the anti-apoptotic protein, Bcl-2, was down-regulated in both MCF-7 monolayers and spheroids. Following treatment with 16 μM As2S2, statistically significant decreases were observed in MCF-7 monolayers (P=0.0221 vs. control) and spheroids (P=0.0051 vs. control) (Fig. 6B).
Effects of As<sub>2</sub>S<sub>2</sub> on the expression of pro-survival proteins in 2D- and 3D- cultured MCF-7 cells
Since the PI3K/Akt/mTOR pathway serves an essential role in cell growth, proliferation, and survival (32,33), the protein expression of these pro-survival mediators were detected in both 2D monolayers and 3D spheroids of MCF-7 cells. Following 72 h of exposure to 4, 8 and 16 μM As2S2, the protein levels of PI3K in 2D- and 3D-cultured MCF-7 cells were decreased in a dose-dependent manner in comparison with their untreated counterparts (Fig. 7A). At a concentration of 16 μM, As2S2 had a significant inhibitory effect on 2D monolayers (P=0.01). As2S2 also induced a significant downregulation of PI3K in 3D spheroids at final concentrations of 8 (P=0.0066) and 16 (P=0.0001) μM, respectively. As shown in Fig. 7B, subsequently to treatment with As2S2 for 72 h, the Akt protein expression levels were downregulated in MCF-7 monolayers and spheroids. After treatment with 16 μM As2S2, statistically significant decreases were observed in MCF-7 monolayers (P=0.0031) and spheroids (P=0.0028) (Fig. 7B). Following exposure to 4, 8 and 16 μM As2S2, the protein levels of mTOR decreased in a dose-dependent manner in both 2D and 3D MCF-7 cells, in comparison with their untreated counterparts; after treatment with 16 μM As2S2, statistically significant differences were observed in both 2D monolayers (P<0.0001) and 3D spheroids (P=0.0004) (Fig. 7C).
Discussion
Several arsenic compounds have been investigated for their antitumor potency and efficacy against different breast cancer cell lines (7–9). For instance, ATO, as a Food and Drug Administration (FDA)-approved drug, was reported to have the potential to suppress cell growth, inhibit cell migration, induce apoptosis and cell cycle arrest, and downregulate cancer pro-coagulant activity in breast cancer cell lines (34–37). However, ATO is regarded as a toxic agent that must be carefully monitored after its intravenous administration. ATO is known to cause severe adverse effects, including liver damage and QT prolongation (10–12). As2S2, which shows similar efficacy and fewer adverse effects (14,15), is much less toxic than arsenic trioxide and other common arsenic compounds, including sodium arsenite and arsenate (14,38), and has been considered as an alternative oral arsenic agent for cancer treatment. In China, As2S2 has already been approved for clinical use in the treatment of leukemia (16–18,39). A series of clinical studies and trials proved that treatment with As2S2 was well tolerated, with only moderate side-effects in patients suffering from APL (13,39,40). Recent studies have also reported the potent anti-tumor properties of As2S2 in various solid cancer cell lines, along with a marked reduction in cytotoxic effects in human normal cell lines (41–43). However, there have been very few studies on the anti-tumor effects of As2S2 in breast cancer cells (24), and fewer studies on the underlying mechanisms. Therefore, the present study was performed to investigate the anticancer effects of As2S2, and the underlying mechanisms in 2D- and 3D-cultured MCF-7 cells. To the best of our knowledge, this is the first report to show the mechanism underlying the cytotoxicity induced by As2S2 in MCF-7 cells cultured in 2D and 3D culture systems.
In the present study, an in vitro cell culture method was adapted to create 3D spheroids of MCF-7 cells. The 3D cell-culture system established in the present research was based on the adoption of TGP, in which the sol-gel transiting phase is reversibly regulated by temperature (44). By way of comparison, the effects of As2S2 on MCF-7 cells cultured as a 2D monolayer were also investigated. The results demonstrated that As2S2 decreased the cellular viability of MCF-7 cells by inducing cellular apoptosis in both 2D and 3D cell cultures. These effects were also associated with the activation of pro-apoptotic signals, such as executioner caspase-7, p53 and Bax, and the inhibition of Bcl-2 (associated with anti-apoptotic signaling), as well as the pro-survival PI3K/Akt/mTOR pathway. In addition, the microscopic observations revealed that 2D cells simply attach to the bottom of the wells in a traditional monolayer cell distribution, whereas the 3D cells form multicellular spheroids via cell-cell interactions. The data from the cell viability assays and apoptosis detection experiments revealed that 3D spheroids exhibited a certain degree of drug resistance, in comparison with the 2D monolayer cell culture. This could be attributed to the specific morphological structure of 3D spheroids (Fig. 3), which is similar to the features that studies have previously reported (45,46).
Unregulated cell survival and uncontrolled cell growth may result in excessive cellular proliferation and the loss of controlled cell death, which are two typical phenotypes of cancer cells (47,48), including breast cancer cells. The results obtained from the WST cell proliferation assays demonstrated that As2S2 strongly inhibited the cellular viability of MCF-7 cells in a dose-dependent manner, in both 2D monolayers and in 3D spheroids. Consistently with these findings, the data revealed that As2S2 is able to induce apoptosis in 2D- and 3D-cultured MCF-7 cells in a concentration-dependent manner. Since 3D cell-culture models enable cells to form structures that mimic the in vivo architecture in a more physiologically relevant condition compared with traditional 2D monolayers (49–51), the present study provided a more reliable method for investigating the actual function of As2S2 in MCF-7 cells. In addition, the data of the present study demonstrated the increased drug resistance of MCF-7 cells cultured in a 3D system in comparison with those cultured in a 2D system, either through the inhibition of cell viability or the induction of apoptosis by As2S2. Notably, it was revealed that, in the absence of any drug treatment, MCF-7 cell spheroids were more susceptible to apoptosis than the 2D monolayers, which is consistent with observations made by other researchers (52–54). This might be associated with the specific hypoxic and endocrinal changes in the 3D spheroid microenvironment. This phenomenon was different from anoikis (55,56), since the MCF-7 spheroids developed in the present study demonstrated cell-cell interactions and interacted with each other, with the extracellular matrix, and with their microenvironment.
Emerging evidence has demonstrated that arsenic compounds such as arsenic trioxide exert anti-tumor effects by inducing apoptosis in hematological cancer and in solid tumors (6,57,58). The molecular mechanisms underlying arsenic-mediated apoptosis include the activation of intrinsic and extrinsic apoptosis pathways, as well as the suppression of pro-survival pathways in various cancer cell lines. In the current study, the results demonstrated that As2S2 induced the expression of pro-apoptotic proteins and inhibited the levels of pro-survival proteins, suggesting the possible pathways responsible for the cytotoxicity of As2S2 in MCF-7 cells. Caspases-3 and -7 play critical roles as effectors in the execution phase, namely, the final phase of apoptosis (59,60). Although the expression of caspase-3 was not detected in either 2D monolayers or 3D spheroids (data not shown), the results of the present study indicated that As2S2 significantly increased the protein expression of caspase-7 in 2D-cultured MCF-7 cells in a dose-dependent manner. In that respect, the MCF-7 cell apoptosis that was induced by As2S2 in the present study might be mediated via the activation of caspase-7 instead of caspase-3, which is congruent with the findings of previous studies showing that the MCF-7 cell line does not express caspase-3, but that it may undergo apoptosis through the activation of caspases-7 and -6 (61,62). The tumor suppressor p53 is capable of inducing cell apoptosis via activation of the mitochondrial and death receptor-induced apoptotic pathways (63,64). The results of the present study revealed that As2S2 increased the protein level of p53 in a dose-dependent manner in 2D- and 3D-cultured MCF-7 cells, which is consistent with the results showing that As2S2 induced the expression of activated caspase-7 expression in 2D culture. Furthermore, As2S2 activated Bax (a pro-apoptotic protein), but inhibited Bcl-2 (an anti-apoptotic protein from the Bcl-2 family), in MCF-7 monolayers as well as in spheroids, indicating the significant role that As2S2 exerted in stimulating the intrinsic pathway of apoptosis. The PI3K/Akt/mTOR pathway, which is thought to promote cellular proliferation and survival and which has been shown to be associated with inactivation of the apoptotic signals, is the most frequently activated signaling pathway in breast cancer (32,33,65,66). Blocking the expression of PI3K/Akt/mTOR simultaneously inhibits cell survival and promotes pro-apoptotic activity. In the present study, the decrease in PI3K/Akt/mTOR expression that occurred in MCF-7 monolayers and spheroids following treatment with As2S2 revealed the possible inhibitory role of the arsenic compound in the downregulation of cancer cell-survival signals, which suggests the activation of pro-apoptotic signaling.
In conclusion, the present study has provided evidence that As2S2 may be a potential therapeutic agent to be applied in the treatment of breast cancer. The in vitro results in the present study suggested that As2S2 inhibited the viability of MCF-7 cells and induced cell apoptosis in both 2D monolayers and 3D spheroids in a concentration-dependent manner. Activation of the mitochondrial apoptosis pathway may be involved in this mechanism, since the upregulation of the pro-apoptotic mediators, Bax, p53, caspase-7, as well as the downregulation of the anti-apoptotic mediator, Bcl-2, were observed following exposure to As2S2. In addition, the inhibition of the pro-survival PI3K/Akt/mTOR pathway by As2S2 treatment contributed to the suppression of cell viability and the induction of apoptosis in 2D- and 3D-cultured MCF-7 cells. Furthermore, the present study has revealed that 3D spheroids of MCF-7 cells had a higher rate of cell viability and reduced cell apoptosis in comparison with 2D monolayer cells following treatment with As2S2, indicating the drug resistance of 3D spheroids. However, the present study focused on delineating the pro-apoptotic effect of As2S2 in breast cancer cells, and therefore it was confined to one of the cell death mechanisms. Further studies will be performed to elucidate other potential mechanisms involved in the anti-tumor function of As2S2, particularly with respect to the induction of cell cycle and autophagy. Furthermore, the mechanism of drug resistance in 3D spheroids also requires further investigation.