In vitro evaluation of the antitumor effect of bismuth lipophilic nanoparticles (BisBAL NPs) on breast cancer cells.

AIM: The objective of this study was to evaluate the antitumor activity of lipophilic bismuth nanoparticles (BisBAL NPs) on breast cancer cells.
MATERIALS AND METHODS: The effect of varying concentrations of BisBAL NPs was evaluated on human MCF-7 breast cancer cells and on MCF-10A fibrocystic mammary epitheliocytes as noncancer control cells. Cell viability was evaluated with the MTT assay, plasma membrane integrity was analyzed with the calcein AM assay, genotoxicity with the comet assay, and apoptosis with the Annexin V/7-AAD assay.
RESULTS: BisBAL NPs were spherical in shape (average diameter, 28 nm) and agglomerated into dense electronic clusters. BisBAL NP induced a dose-dependent growth inhibition. Most importantly, growth inhibition was higher for MCF-7 cells than for MCF-10A cells. At 1 µM BisBAL NP, MCF-7 growth inhibition was 51%, while it was 11% for MCF-10A; at 25 µM BisBAL NP, the growth inhibition was 81% for MCF-7 and 24% for MCF-10A. With respect to mechanisms of action, a 24-hour exposure of 10 and 100 µM BisBAL NP caused loss of cell membrane integrity and fragmentation of tumor cell DNA. BisBAL NPs at 10 µM were genotoxic to and caused apoptosis of breast cancer cells.
CONCLUSION: BisBAL NP-induced growth inhibition is dose dependent, and breast cancer cells are more vulnerable than noncancer breast cells. The mechanism of action of BisBAL NPs may include loss of plasma membrane integrity and a genotoxic effect on the genomic DNA of breast cancer cells.

Introduction

Breast cancer continues to be a major challenge for modern medicine worldwide.1 Despite the efforts of the chemical and medicinal industry, breast cancer prevalence is expected to rise.2 Conventional treatments, including surgery, chemotherapy, and radiation, not only kill tumor tissue but also healthy tissue. Chemotherapy is the treatment of choice for localized and metastasized cancers. Cancer tissue distinguishes itself from normal tissue in the following aspects: sustained proliferative signaling, evasion of growth suppressors, resistance to cell death, replicative immortality, induction of angiogenesis, invasion, and metastasis.3 Traditional chemotherapy not only kills the tumor but also damages normal healthy tissue. There is an ongoing effort for developing selective antitumor agents that attack tumor tissue with a higher efficacy while sparing healthy tissue and diminishing side effects. Several metallic nanostructures, including silver, gold, and selenium nanoparticles (NPs), have been analyzed to inhibit the growth of breast cancer cells.4–6 Nonmetallic NPs have been used as a vehicle for “specific drug delivery” at the tumor site.7

Bismuth is the heaviest member of the pnictogen group and is often referred to as a “green” element.8 In medicine, bismuth subsalicylate (ie, Pepto-Bismol) is used to treat diarrhea, indigestion, and nausea. Although bismuth has no direct application against cancer cells, several bismuth-based compounds have potent anticancer activity, eg, thiosemicarbazone, hydrazone, and dithiocarbamate.9–12 Hydrazone derivatives are well-known to possess antimicrobial activity, but the Bi(III) hydrazine complex proved to be the most active form against several cancer cell lines (Jurkat, HL60, MCF-7, and HCT-116).13,14 A novel bismuth–sulfapyridine complex that inhibits the growth of leukemia cells (K562)15 and heterocyclic organobismuth(III) compounds, which were investigated as antimicrobial agents, turned out to have significant anticancer activity against several human cancer cell lines.16 Interestingly, the aforementioned bismuth compounds have both antimicrobial and anticancer activities. Recently, our group described the excellent antimicrobial properties of lipophilic bismuth NPs (BisBAL NPs) with a minimal inhibitory concentration of 5–10 µM against several oral pathogens.17 However, the potential anticancer activity of bismuth NPs has not been extensively explored. A recent report describes how tumor-targeted bismuth NPs enhanced X-ray radiation therapy against breast cancer cells.18

In this work, we report for the first time that BisBAL NPs selectively inhibit the growth of breast cancer cells in a dose-dependent way. BisBAL NPs seem a promising innovative alternative in cancer chemotherapy that deserves to be evaluated in other cancer cell lines and animal models.

Materials and methods

Synthesis and characterization of BisBAL NPs

To synthesize BisBAL NPs, the colloidal method according to Badireddy et al was used.17 Briefly, 0.485 g of Bi(NO3)3•5H2O was dissolved in 20 mL propylene glycol, heated to 80°C, and agitated for 2 hours to obtain a 50 mM Bi3+ solution. A 2:1 molar ratio of Bi3+ (Bis) to 2,3-dimercapto-1-propanol (BAL) was prepared by adding 25 µL 10 M BAL to 10 mL 50 mM Bi3+ solution. A stock suspension of 25 mM BisBAL NPs was prepared by adding 0.85 volumes (V) of ice-cold ultrapure water and 0.15 V of freshly prepared ice-cold 75 mM NaBH4 to 5 mL 50 mM BisBAL NP under continuous vigorous mixing; the pink-colored BisBAL solution instantly transformed to a black-colored suspension of BisBAL NPs. The distribution of BisBAL NP’s size and shape was analyzed with scanning electron microscopy (SEM; Nova NanoSEM 200, FEI Company, Eindhoven, the Netherlands; 15 kV). The presence of bismuth was corroborated by energy-dispersive X-ray spectroscopy (EDS) SEM. For structural analysis, X-ray diffractometry patterns were obtained from water-washed (three centrifugation cycles, 16,100×g, 30 seconds), air-dried BisBAL NPs (deposited several times on a glass slide overnight) using an X-ray dif-fractometer (Panalytical X’Pert PRO MRD) equipped with Cu Kα as an X-ray source (λ=1.541874 Å). The ultraviolet (UV)-visible spectrum of the BisBAL NP suspension was recorded using a spectrophotometer (SpectraMax Plus384 Absorbance Microplate Reader; Molecular Devices, LLC, Sunnyvale, CA, USA).

Cell culture

The human breast carcinoma cell line MCF-7 was obtained from the American Type Culture Collection (ATCC HTB-22; ATCC, Rockville, MD, USA). A fibrocystic mammary gland epithelial cell line, MCF-10A (ATCC CRL-10317; ATCC) was used as a nontumor control. MCF-7 cells were cultivated in DMEM/Ham’s F12 (DMEM/F12) supplemented with 10% FBS (Gibco-Invitrogen, Carlsbad, CA, USA) and 100 U/mL penicillin, 100 µg/mL streptomycin, and 0.25 µg/mL amphotericin B (Sigma-Aldrich Corporation, St Louis, MO, USA) in cell culture flasks (Corning Inc., Corning, NY, USA) at 37°C in a humidified atmosphere with 5% CO2.19 MCF-10A cells were cultivated in mammary epithelial cell growth medium supplemented with 100 ng/mL cholera toxin in cell culture flasks (Corning Inc.) at 37°C and 5% CO2. Cells of a confluent monolayer were harvested by scraping, washed three times with 10 mM PBS, pH 7.4 (PBS), and counted with a hemocytometer.

MTT cell viability assay

The effect of BisBAL NPs on MCF-7 and MCF-10A cell number was evaluated using the MTT cell viability assay (Biotium, Hayward, CA, USA).20 Then, 1×105 cells were incubated with 0, 0.125, 1, 10, 25, 50, and 100 µM of BisBAL NPs or 1,000 µM doxorubicin (Doxolem, Teva Lab, Madrid, Spain). The treatment was terminated by washing the cells with PBS. Next, cells were incubated with MTT (10 µL/well) at 37°C and 5% CO2 for 2 hours in the dark according to the manufacturer’s instructions. Next, the medium was removed, and 100 µL of dimethylsulfoxide (DMSO) was added to dissolve the reduced MTT formazan product. To quantify the reduced MTT, the absorbance at 570 nm (A570) was measured by microplate absorbance reader (BioTek, Winooski, VT, USA); DMSO served as a blank. The assay was performed in triplicate.

Cell membrane permeability by fluorescence microscopy

Calcein AM is an excellent tool to study cell membrane integrity. Calcein AM is membrane-permeant and can be introduced into cells via incubation. Once inside the cells, nonfluorescent calcein AM is hydrolyzed by endogenous esterase into a highly charged green fluorescent molecule that is retained in the cytoplasm of living cells. Therefore, intracellular calcein AM in living cells was interpreted as a signal of intact cell membrane. This assay was used to analyze the cell membrane permeability of MCF-7 cells after a 24-hour exposure to 0, 1, 10, and 100 µM BisBAL NP; 0 µM BisBAL NP, ie, cells exposed to pure culture medium, served as a growth control. After incubation, cells were washed three times with PBS and stained with 2 µM calcein AM (Biotium) for 30 minutes at 37°C.21 Nuclei of MCF-7 cells were stained with 1 µg/mL DAPI (Abcam Inc, Cambridge, UK).22 Next, cells were washed again with PBS and air-dried in the dark. Cell morphology was observed with fluorescein isothiocyanate (FITC) and DAPI filters at 485 and 358 nm, respectively (Thornwood, NY, USA). A degraded or amorphous nucleus was interpreted as a potential genotoxic effect.

Genotoxicity by comet assay and fluorescence microscopy

To determine the possible genotoxic effect of BisBAL NPs, MCF-7 cells were incubated overnight at 37°C/5% CO2 with 1 or 10 µM BisBAL NP, 100 µM etoposide (Sigma) as a positive control, or culture medium as a growth control. After incubation, cell damage was determined with the OxiSelect™ Comet Assay Kit (Cell Biolabs, Inc, San Diego, CA, USA) according to the manufacturer’s instructions.23 Briefly, cells were harvested by scraping and centrifugation (700×g, 2 minutes) and washed with PBS. Cell suspensions were mixed with liquefied Comet Agarose at a 1:10 ratio (v/v) and pipetted on an OxiSelect Comet Slide (75 µL/well). After a 15-minute embedding step (4°C, dark, horizontal position), cells were lysed (25 mL lysis buffer/slide, 30-minute incubation, 4°C, dark, horizontal position) and treated with an alkaline solution (25 mL/slide, 30 minutes, 4°C, dark) to relax and denature the DNA. Finally, the samples are electrophoresed in a horizontal chamber (300 mA for 30 minutes) to separate intact DNA from damaged fragments. Next, samples are washed with sterile MilliQ water, treated with 70% cold ethanol for 5 minutes, air-dried, and stained with the DNA dye DAPI (100 µL/well), and viewed with an epifluorescence microscope using a DAPI filter (Thornwood, NY, USA).

Apoptosis evaluation by phosphatidylserine-expressing plasma membrane by fluorescence microscopy

In healthy cells, phosphatidylserine is located in the inner leaflet of the plasma membrane. Apoptotic cells, on the contrary translocate phosphatidylserine to the outer leaflet of the plasma membrane to be recognized by phagocytes. In order to analyze whether BisBAL NPs promote apoptosis among cancer cell lines, the CF®488A Annexin V and 7-AAD Apoptosis Kit (Biotium) was used according to the manufacturer’s instructions. Briefly, cells (1×104/well in a 96-well plate) were cultured for 24 hours at 37°C/5% CO2 in DMEM/F12 and exposed for 3 hours to 1 or 10 µM BisBAL NP, 100 µM etoposide (Sigma) as positive control of cell death, or pure culture medium as a growth control. Next, cells harvested by scraping were washed three times with PBS, resuspended in 100 µL 1× annexin binding buffer, and incubated (30 minutes, on ice, dark) with 5 µL CF488A-Annexin V and 2 µL of 7-AAD working solution. Next, cells were observed with a fluorescence microscope using FITC and CY5 filters (Thornwood, NY, USA).

Statistical analysis

A multiple comparison 2-way ANOVA with Tukey’s correction was used to compare all groups. For all statistical tests, a significance level of α=0.05 was considered.

Results

Characterization of BisBAL NPs

The obtained BisBAL NPs were spherical in shape with an average diameter of 28 nm. The NPs were composed of rhombohedral crystallites (≈18 nm) with dithiols as lipophilic surface groups and the lattice spacing of individual crystallite was 0.325 nm. The specific presence of bismuth was confirmed by EDS-SEM. The BisBAL NPs formed electrodense clusters (Figure 1). UV-visible absorbance revealed that BisBAL NPs had a higher (≈70%) affinity for 1-octanol rather than for water, consistent with a lipophilic property of the dithiols bound to NP surface. BisBAL NPs resulted to be stable for at least 2 months at 4°C and room temperature.

Figure 1

Characterization of lipophilic bismuth nanoparticles (BisBAL NPs).

Notes: (A) Shape, size, and shape-and-size distribution of BisBAL NPs were obtained by scanning electron microscopy. (C) The presence of bismuth was confirmed by the emission lines characteristic of this element, as can be seen in the spectrum. The signal at 1.486 keV is due to the aluminum substrate where the sample was placed. (B) and (D) The UV-visible absorbance and the X-ray diffractometry pattern of BisBAL NPs.

Antitumor activity

MCF-7 tumor cells that had been exposed to 1 µM BisBAL NP grew 50% less than MCF-7 that had not been exposed to BisBAL NPs (Figure 2). Unlike tumor cells, the growth of control cells decreased only 10.5% (Figure 2). When exposed to a higher dose (25 µM BisBAL NP), tumor cell growth was 80.4% less and control cells grew 26% less than nonexposed cells. Exposure to 1,000 µM doxorubicin diminished MCF-7 cell growth by 98%. Thus, BisBAL NPs selectively inhibit tumor cell growth in a dose-dependent way.

Figure 2

Antitumor activity of BisBAL NPs on the human breast cancer cell line MCF-7.

Notes: Cell viability of MCF-7 (human breast cancer cell line) and MCF-10A (nontumor human breast cancer cell line) was determined by the MTT cell viability assay at A570 after a 24-hour exposure to 0, 0.125, 1, 10, 25, 50, and 100 µM BisBAL NP and 1,000 µM DOX (positive control of cytotoxicity). After a multiple comparison 2-way ANOVA with Tukey’s correction, all samples were significantly different (P<0.0001), except for: 1) 50 vs 100 µM BisBAL NP exposure for MCF-7 cells, 2) 0 vs 0.125 µM BisBAL NP exposure for MCF-10A cells, and 3) among 10 and 25 µM BisBAL NP, and 1,000 µM DOX exposure for MCF-10A cells. Bars indicate mean±SD (n=4 for MCF-7 and n=3 for MCF-10A).

Abbreviations: DOX, doxorubicin; BisBAL NPs, lipophilic bismuth nanoparticles.

Cell membrane permeability alteration after exposure to BisBAL NPs

After a 24-hour exposure to 1 µM BisBAL NP, MCF-7 morphology changed; cells rounded up and released calcein AM, indicating loss of cell membrane integrity (Figure 3). This effect was more pronounced after exposure to 10 µM BisBAL NP, whereas after exposure to 100 µM BisBAL NP only cell debris was observed. These results are consistent with the MTT cell viability assay results, where 95% of tumor cells died at 100 µM BisBAL NP.

Figure 3

Effect of BisBAL NPs on cell membrane integrity of breast cancer cells evaluated with the calcein AM assay.

Notes: Fluorescent (485 nm) calcein AM distribution (within or outside MCF-7 cells) after a 24-hour exposure to 1, 10, or 100 µM BisBAL NP for 24 hours. Red arrow indicates released calcein AM. Bar, 5 µm.

Abbreviation: BisBAL NPs, lipophilic bismuth nanoparticles.

Genotoxic assays

Possible damage to genomic DNA of breast cancer cells was analyzed with the comet assay and fluorescence microscopy, in which 100 µM etoposide served as a positive control of DNA break induction. As of 10 µM BisBAL NP, “comets” identical to the ones in the etoposide control were observed (Figure 4), suggesting that 10 µM BisBAL NP promotes DNA strand breaks. Interestingly, 1 µM BisBAL NP did not alter genomic DNA.

Figure 4

Genotoxic effect of BisBAL NPs on MCF-7 breast cancer cells.

Notes: MCF-7 cells were incubated for 24 hours with culture medium as a growth control of intact cells, 100 µM etoposide (positive control of genotoxic effect), and 1 or 10 µM BisBAL NPs. DNA damage was evaluated with the OxiSelect™ Comet Assay Kit, and DAPI-stained DNA was observed with an epifluorescence microscope with DAPI filter. Red arrow indicates the stellar morphology. Bar, 5 µm.

Abbreviation: BisBAL NPs, lipophilic bismuth nanoparticles.

Apoptosis assays

Programmed cell death is a response to different kinds of stimuli. To analyze if BisBAL NPs could induce apoptosis among MCF-7 cells, the Annexin V, 7-AAD assay, and fluorescence microscopy were used. BisBAL NPs at 1–10 µM yielded results that were very similar to the positive control of 100 µM etoposide (Figure 5). In contrast, no signals of programmed cell death were observed in the growth control. Altogether these results suggest that low concentrations of bismuth NPs promote apoptosis among breast cancer cells.

Figure 5

Detection of apoptosis in human breast cancer cells by BisBAL NPs.

Notes: Apoptosis induction in MCF-7 cells by BisBAL NPs was detected with the CF®488A Annexin V and 7-AAD apoptosis assay. Etoposide at 100 µM was used as a positive control of an apoptotic agent, whereas pure culture medium was used as a negative control; 1 and 10 µM BisBAL NPs were analyzed on MCF-7 cells. After treatments, cell cultures were observed with a fluorescence microscope using fluorescein isothiocyanate (green) and CY5 (red) filters. Bar, 5 µm.

Discussion

To claim antitumor property of any compound, it is fundamental to demonstrate cell death or loss of basic cell metabolism after exposure to the compound of interest. Programmed cell death is a highly complex process by which the cell activates its own machinery for self-destruction in response to a variety of stimuli, which has led to a classification of cell death subroutines that includes extrinsic and intrinsic apoptosis, regulated necrosis, autophagic cell death, and mitotic catastrophe.24 For each subroutine, measurable biochemical features have been defined.

Nanomedicine is a new discipline that offers the possibility to develop “smart drugs” that allows controlled target-specific, drug delivery controlled with less adverse effects than nontargetted drugs.25,26 Nanocomposites are applied in tissue engineering and imaging for diagnostic and therapeutic purposes, including cancer diagnosis and treatment. Different metal NPs (silver, gold, platinum, magnesium, copper, etc) are applied in the treatment of cancer. The NP may have direct or indirect antitumor activity. In direct antitumor activity, the NP itself may inhibit growth or survival of tumor cells, whereas the induction of heat would be an example of indirect antitumor activity of NPs (photothermal therapy).27 Several groups have reported anticancer activity of different types of metal NPs, such as silver, gold, platinum, magnesium, and copper NPs.18,28,29 Unfortunately, aforementioned metal NPs are toxic for human cells, which restricts their application in the clinic.30,31 As opposed to aforementioned metal and others such as aluminum and antimony, bismuth is considered to be nontoxic.32 In medicine, bismuth subsalicylate is used to treat diarrhea without cytotoxic reports.33 We previously reported the excellent bactericidal, antifungal, and antibiofilm activities of bismuth NPs.17 Furthermore, BisBAL NPs are not toxic for human epithelial and blood cells.32,34

In this work, we demonstrated the effectiveness of bismuth NPs to inhibit the growth of human tumor cells selectively because 1 µM of BisBAL NPs decreased the growth of tumor cell growth with 51%, while the growth of control cells was unaltered. Employing in vitro assays Wang et al (2012) described that cuprous oxide NPs selectively induce apoptosis of tumor cells.35 On the contrary, Deng et al reported the indirect antitumor activity of bismuth NPs. They used bismuth NPs as radiosensitizers to enhance X-ray radiation therapy and achieved a significant tumor reduction.18 In our study, the antitumor effect of BisBAL NPs was not only direct and selective but also dose-dependent. In our in vitro set up, the therapeutic range was 1–25 µM BisBAL NP. In these range, antitumor activity was selective as it hardly had adverse effects on healthy cells. The anticancer activity of silver NPs on the human colon adenocarcinoma cell line HT-29 is also dose-dependent.36 Apart from having anticancer activity, NPs in the form of polymeric carbon nanotubes have been proposed to serve as carriers of chemotherapeutic agents by facilitating an increased permeability and retention within the tumor.37,38

The anticancer potential of NPs was screened for against the MCF-7 cancer cell line and the MCF-10A normal cell line as a control with the calcein AM assay. The anticancer results were comparable with the anticancer drug (cisplatin), but without damaging the control cell line.39

Based on the calcein AM assay, we suggest that the possible anticancer action mechanism of BisBAL NPs is altering the cell membrane integrity of tumor cells. After a 24-hour exposure to 100 µM BisBAL NP, MCF-7 cells look completely destroyed; an effect not seen after exposure to 10 µM BisBAL NP. Similar results have been reported for silver NPs that had been synthetized with a “green method.” Copper ferrite NPs also decreased cell viability and caused membrane damage in a dose-dependent way in MCF-7 breast cancer cells.40 We hypothesize that the water solubility and lipophilicity of bismuth is enhanced when bismuth ions are complexed with small lipophilic molecules such as dimercaptopropanol. It is highly probable that the lipophilic character of BisBAL NPs is responsible for an increased affinity to cell membranes of breast cancer cells compared with nonlipophilic bismuth presentations. The cellular uptake of several anticancer composites has been improved after increasing the lipophilicity of the composites.41,42 Another strategy to improve drug delivery while protecting the drug is the encapsulation of the compound in liposomes.41

The genotoxicity experiments revealed that the genomic DNA of exposed tumor cells to 1–10 µM BisBAL NP was significantly more damaged than the DNA of nonexposed tumor cells. The genotoxicity of silver, gold, and platinum NPs on different cell lines is well-known.43 Using the same comet assay as we did, Lebedová et al recently reported DNA damage induced by silver NPs. The effect was independent of NP size.43 On the contrary, the DNA damage induced by gold and platinum NPs was NP size-dependent.43 Liu et al described the cytotoxic and genotoxic effects of a 24-hour exposure of liver cells to cobalt NPs. Interestingly, cobalt ions were less cytotoxic than cobalt nanostructures.44

Our results indicate that low concentrations of BisBAL NPs induced apoptosis among MCF-7 cells. Likewise, Banu et al reported that silver and gold NPs promote apoptosis and regulate p53 and Bcl-2 expression in human breast adenocarcinoma cells.45 Azizi et al described a cytotoxic effect, via apoptosis, of albumin-coated copper NPs on MCF-7 cells,46 suggesting that they could be a new chemotherapeutic agent against invasive breast cancer. Our results with BisBAL NPs suggest that concentrations up to 10 µM kill tumor cells selectively, probably by disrupting the cell membrane before causing damage to genomic DNA at higher concentrations. Altogether, our results suggest that BisBAL NPs could alter the plasma cell membrane during their entry and diminish its permeability. Once internalized, BisBAL NPs damage the genomic DNA by direct interaction.

In conclusion, BisBAL NPs inhibit human tumor cell growth selectively and in dose-dependent way. The possible action mechanisms of BisBAL NPs may be altering the membrane permeability of breast cancer cells and causing damage to the genomic DNA.