Nobiletin acts as a potential anticancer agent against osteosarcoma by regulating ERK and AKT signaling pathways
Abstract
The current study was aimed to evaluate the antiproliferative activity of nobiletin, a flavonoid, on osteosarcoma cell line, SaOS-2. Furthermore, we attempted to investigate the signaling pathways involved in the cell growth inhibition mechanism. Upon exposure, nobiletin showed significant cell inhibitory effect on SaOS-2 cells in a dose-dependent manner as evidenced by MTT assay and LDH assay. Moreover, flow cytometric analysis demonstrated that upon treatment with nobiletin, SaOS-2 cells underwent apoptosis and showed increased number of cells arrested in G2/M phase. Activation of caspase-9 and -3 indicate the activation of apoptotic signaling pathway in SaOS-2 cells. Additionally, it was observed that the cell inhibitory effect was regulated by the activation of ERK signaling pathway while AKT signaling pathway was down regulated in SaOS-2 cells after 24 hours of Nobiletin treatment.
Introduction
Skeletal integrity is maintained by equilibrium between osteoblasts mediated bone formation and osteoclasts mediated bone resorption. Any imbalance in this equilibrium leads to osteoblastic lesions and other severe clinical consequences often termed as bone cancer or osteosarcoma. Commonly, bone cancer is resulted by invasion of different cancers to bone tissue, phenomenon known as bone metastases. American cancer society estimates nearly 3,020 new cases of bone cancer and 1,460 deaths due to bone cancer in 2014 (American Cancer Society, 2014). Although, many chemotherapeutic drugs are currently employed for the treatment of bone cancer, yet there is demand for safe and novel drugs having minimum side effects. Over the past few years, the development of natural compounds as anticancer agents has been revealed (Newman and Cragg, 2007). Intensive efforts for discovering new drugs based on natural products has proven beneficial, with nearly 47% drugs of natural origin been approved as anticancer agents. Flavonoids are a group of natural polyphenols widely present in plants and well known to play significant role in various pharmacological activities (Harborne and Williams, 2000; Kim et al., 2013). Recent studies highlighted the anticancer potential of these flavonoids and explored as therapeutic drugs in clinics (Neuhauser, 2004).
Nobiletin (5,6,7,8,3',4'-hexamethoxy flavone), a flavonoid, is present in citrus fruits and found to possess anti-inflammatory (Murakami et al., 2005) and antitumor potential (Tang et al., 2007; Sato et al., 2002). Previous studies showed the antiproliferative effect of nobiletin on various cell lines including lung adenocarcinoma cell line A549 cells (Luo et al., 2008) and hepatic cancer cell line, SMMC-7721 (Ma et al., 2014). However, the antiproliferative effect of nobiletin on osteosarcoma cells has not been studied till date. Furthermore, the mechanism of anticancer action exerted by nobiletin is also rarely reported. Therefore, this study aims to characterize the inhibitory effect of nobiletin on osteosarcoma cell line and delineate the signaling mechanism involved.
Materials and Methods
Materials
Nobiletin (purity ≥98%), 3-(4,5-dimethlthiazol-2-yl)-2,5-diphenyl-tetrazoliumbromide (MTT), bovine serum albumin (BSA), fetal bovine serum (FBS), phosphate buffer saline (PBS), DMSO, sodium dodecyl sulfate (SDS), EDTA, Tris-HCl, was purchased from Sigma-Aldrich (USA). Cytotoxicity detection kit was purchased from Takara Bio Inc., Shiga, Japan. Caspase-3 colorimetric assay kit and caspase-9 colorimetric assay kit was obtained from Biovision, Inc. Protein assay reagent was purchased from Bio-Rad Laboratories (Hercules, USA). Antibody against AKT, ERK, β-catenin and β-actin were purchased from Cell Signaling Technology, Danvers, MA.
Cell culture
Human osteosarcoma cell line, SaOS-2, was cultured in 10% fetal bovine serum (FBS), 100 U/mL penicillin and 100 µg/mL streptomycin (Lonza, Switzerland) supplemented α-MEM medium (Invitrogen, USA). The cells were grown at 37°C in humidified chamber with 95%air and 5%CO2. The confluence level of SaOS-2 cell line was maintained at 70-80%. SaOS-2 cell line was chosen because it is known to be depicting osteosarcoma characteristics and is being widely used for cell proliferation and differentiation studies (Hunt et al., 1996).
Cell viability assay (MTT assay)
The antiproliferative effect of nobiletin on SaOS-2 cell line was performed by MTT assay. Cell viability assay was achieved by plating 2 x 104 cells/well in 96 well plate at 37°C for 24 hours followed by treatment with different doses of nobiletin (0.5, 1, 2.5, 5 and 10 µM). After incubating the cells at predetermined time points i.e. 24, 48 and 72 hours, 3-(4,5-dimethlthiazol-2-yl)-2,5-diphenyl-tetrazoliumbromide (MTT) solution (20 µL) was added in each well and again incubated for 3 hours at 37°C to facilitate the production of MTT formazan by mitochondrial succinate. After removal of supernatant, DMSO was added to each well to dissolve MTT formazan. Cell viability was calculated after measuring optical density using UV-Vis spectrophotometer at 570 nm wave length. Each experiment set was done in triplicate for accuracy and data are expressed as mean ± SD.
LDH assay
Cell cytotoxicity was determined by evaluating the release of lactate dehydrogenase enzyme from the damaged cells using cytotoxicity detection kit according to manufacturer’s protocol. Lactate dehydrogenase enzyme is found in the cytoplasm of cells and is commonly used as a marker to detect cell membrane damage (Legrand et al., 1992). Briefly, SaOS-2 cells were seeded in 96 wells plate at cell density of 2 x 104 cells/well and further incubated at 37°C. After 24 hours, cells were treated with various doses (0.5, 1, 2.5, 5 and 10 µM) of nobiletin for 0, 24, 48 and 72 hours. From each well, cell culture medium was collected and mixed with PBS and LDH reagent in ratio of 1:4:5 and kept in dark for 1 hour at 25°C. Following the addition of 50 μL of stop solution, absorbance was measured at 490 nm.
Flow cytometric study for apoptosis evaluation
After SaOS-2 cells were treated with nobiletin at 0.5, 1 , 2.5, 5 and 10 µM doses for 24 hours, cells were harvested and collected as pellet (1,000 rpm for 5 min). Subsequently, cells were fixed with 70% ice cold ethanol and washed twice with PBS. Cells were further treated with Triton X-100 (1% v/v) and incubated at 37°C for 10 min. 50 µg/mL of propidium iodide solution was then added to the cells at 4°C for 15 min in the darkto stain the cellular DNA. The distribution of cells in the phases of cell cycle and apoptotic rate was then determined using FACScan flow cytometer (BD Biosciences, San Jose, CA, USA)
Western blot analysis
Total cell lysate was collected fromSaOS-2 cells treated with nobiletin for 24 hours in ice cold RIPA buffer containing protease inhibitor cocktail (Roche). Thereafter, samples were vortexed and centrifuged at 12,000 rpm for 30 min to collect the supernatant. Total protein amount was determined using protein assay reagent (Bio-Rad) to normalize the protein content. Equal amount of proteins were separated on 10-12% sodium deodecyl sulfate-polyacrylamide gel electrophoresis and then electrophoretically transferred to nitrocellulose membrane. Tween 20-tris buffered saline (TBST) including nonfat dry milk (5%) was spread on the membrane at room temperature for 1 hour to block non-specific sites and then the membrane was incubated overnight with primary antibodies (pAKT, pERK, ERK, AKT and β-actin) at 4°C. The membrane was washed again with TBST three times and then incubated with appropriate horseradish peroxidase (HRP) conjugated rabbit anti-mouse secondary antibody (Santa Cruz Biotech, USA) for 1 hour at room temperature. Again after three times washing the membrane with TBST, bands were visualized by enhances chemiluminescence detection system (FUJFILM Las-3000 mini, Tokyo, Japan).
Caspase-3 and -9 activity assay
To confirm the apoptotic activity, caspase-3 and -9 were determined using caspase-3 and -9 colorimetric assay kit, according to manufacturer’s protocol. After the treatment of SaOS-2 cells with nobiletin, total cells were collected as pellet by centrifuging at 12,000 x g for 10 min. Pellet was then resuspended in 50 µL of ice cold lysis buffer for 10 min at 4°C and centrifuged again at 10,000 x g for 1 min to collect supernatant. After the quantification of total protein in the supernatant, respective substrates were added to equal amount of proteins and incubated at 37°C for 30 min. Activity was determined by reading the samples at 400 nm in a microtiter plate reader.
Over expression of AKT allele
SaOS-2 Cells were plated at 3.5 X 104 cells/well in a 48-well dish and transfected with 0.75 μg of myrAktdeltaPH plasmid DNA (Addgene, Cambridge, MA:10841), encoding Myr-Akt, or empty plasmid pECE (Addgene:26453),as control, with Fugene HD (Promega, Sunnyvale, CA)transfection reagent according to the manufacturer’s protocol. After 8 hours of transfection, cells were treated with nobiletin for 24 hours. MTT assay was performed to assess the cell viability of treated cells as described above.
Inhibition of ERK signaling pathway
SaOS-2 Cells plated at a density of 3.5 X 104 cells/well in a 48-well dish were treated with nobiletin, with or without PD98059 (5 μM) for 24 hours. Cell viability of SaOS-2 cells was analyzed by MTT assay.
Statistical analysis
GraphPad Prism 5.0 (San Diego, CA) was utilized for evaluating statistical analysis of obtained data by using two-tailed Student t-test. Statistical significance was considered at a value of p<0.05.
Result and Discussion
The antiproliferative effect of nobiletin on osteosarcoma cell line was determined following 24, 48 and 72 hours treatment of SaOS-2 cells with nobiletin at various doses of 0.5, 1.0, 2.5, 5.0 and 10.0 µM using MTT assay. Results demonstrated growth inhibitory effect of nobiletin on SaOS-2 cells in a dose-dependent manner at all the time points (Figure 1A). After 24 hours of treatment, SaOS-2 cell viability was decreased to 50 and 70% of control by nobiletin at a dose of 5 and 10 µM, respectively. Even low doses of nobiletin (0.5, 1 and 2.5 µM) showed significant growth inhibitory effect on SaOS-2 cells compared to control at 72 hours. In agreement to MTT assay, dose-dependent cell cytotoxicity exerted by nobiletin was also demonstrated by LDH assay (Figure 1B).
Figure 1: Antiproliferative effect of nobiletin at different concentrations on SaOS-2 cells (A) MTT assay (B) LDH assay
To examine whether nobiletin treatment could affect cellcycle progression and apoptosis in osteosarcoma cells, SaOS-2 cells were treated with different concentrations of nobiletin. Rate of apoptosis and phase of cell cycle arrest induced by nobiletin on SaOS-2 cells was analyzed using flow cytometry after 24 hours of treatment. As shown in Table I, 28.2 ± 2.2% increase in rate of apoptosis was observed after treatment with 10 µM of nobiletin (Figure 2A). In addition, cells treated with lower doses of nobiletin also showed increased rate of apoptosis in a dose-dependent manner. An increase in the number of cells arrested at G2/M phase in SaOS-2 cells was observed after treatment of nobiletin in a dose-dependent manner (Figure 2B).
Figure 2: Effect of nobiletin treated for 24 hours at different concentration (0, 0.5, 1, 2.5, 5 and 10 μM) on apoptosis and cell cycle arrest. (A) Nobiletin induces apoptosis ratio in SaOS-2 cells; (B) Cell cycle distribution after treatment of SaOS-2 cells with varying doses of nobiletin. Three independent experiments were performed and data is expressed as their mean ± SD (ap<0.01, bp<0.001)
Following 24 hours treatment of SaOS-2 cells with different doses of nobiletin, caspase-9 and -3 activities were determined. Results demonstrated a significant increase of caspase-9 and -3 activities after stimulation with nobiletin (Figure 3). A dose-dependent increase in activities was observed for both, caspase-9 and -3, after 24 hours of stimulation with nobiletin in SaOS-2 cells (Figure 3A and B). An increment in the caspase-9 and -3 activity points toward a caspase-9 and -3 dependent signaling in SaOS-2 cells for inducing apoptosis by nobiletin.
Figure 3: Activation of caspase activity after 24 hours of treatment with varying doses of nobiletin, (A) Caspase-9 and (B) Caspase-3 activity. Three independent experiments were performed and data is expressed as their mean ± SD (ap<0.01, bp<0.001)
Results from Western blotting showed (Figure 4) that the protein levels of p-ERK were upregulated in SaOS-2 cells after treatment with nobiletin, but that of p-AKT was down-regulated. Phosphorylation of ERK molecules were in a dose-dependent manner after 24 hours of treatment. Similarly, a dose-dependent suppression of phosphorylation of AKT molecule was observed after 24 hours of treatment.
Figure 4: Nobiletin regulated expression of pAKT, AKT, pERK, ERK and β-actin in SaOS-2 cells
In order to substantiate our results that nobiletin mediates it antiproliferative effect through activation of ERK signaling pathway and suppression of AKT signaling, we tried to inhibit the activation of ERK pathway by PD 98059 and restore AKT signaling in SaOS-2 by constitutive expression of AKT molecule in presence of nobiletin. ERK signaling pathways was inhibited by well-known MEK inhibitor, PD98059 (5 μM), for 30 min prior to the treatment of nobiletin (5 μM) to SaOS-2 cells. After 24 hours of treatment, MTT assay was performed to assess the cell viability of the treated cells. As shown in Figure 5A, nobiletin (5 μM) was able to induce 50% decrease in cell viability compared to control whereas prior blocking of ERK signaling by PD98059 dramatically reversed the cytotoxicity induced by nobiletin in comparison to only nobiletin treated SaOS-2 cells. To deduce the role AKT signaling pathway, SaOS-2 cells were transiently transfected with myrAkt delta PH plasmid DNA followed by treatment of nobiletin for 24 hours. Expression of constitutive form of AKT inside the SaOS-2 cells nullified the antiproliferative effect of nobiletin (Figure 5B), restoring proliferative character of SaOS-2 cells.
Figure 5: Antiproliferative effect of nobiletin (5 μM) on SaOS-2 cells after 24 hours of treatment (A) After blocking ERK signaling pathways by PD98059 (B) After transfecting SaOS-2 cells by myr Akt delta PH plasmid DNA. Three independent experiments were performed and data is expressed as their mean ± SD (ap<0.05, bp<0.01, cp<0.001)
Acknowledgement
This work was supported by Natural Science Foundation of Shandong Province: ZR2009CL027; Science and Technology Bureau of Jinan, Science and technology star fund project: 20100118; Shandong Academy of Medical Sciences Medical Foundation：201023
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