Bangladesh J Pharmacol. 2015; 10: 183-190
Available Online: 6 March 2015; DOI: 10.3329/bjp.v10i1.21096
Alpha-naphthyl isothiocyanate triggering G2/M phase arrest and apoptosis in human brain malignant glioma U87MG cells via mitochondrial pathway
Qiang Zhang, Yu-Ting Wang, Shi-Mei Jing, Jian-Yong Chang and Jin-Peng Wang
Department of Neurosurgery, Brain Hospital of Weifang People’s Hospital, Weifang 261 041, China.
Cancer protective effect of cruciferous vegetables is partly attributed to organic isothiocyanates (ITC) with an –N = C = S functional group. Elucidation of the mechanism by which ITCs impart protection against cancer has been the topic of intense research in the past few decades. In this study, we demonstrate that ANIT significantly decreased proliferation and viability of human brain malignant glioma U87MG cells in a dose-dependent manner. The cell cycle analysis showed that ANIT induced significantly G2/M arrest and sub-G1 phase (apoptotic population) in U87MG cells. CDK1 activity assay and Western blot analysis showed that there observed marked reduction in the CDK1/cyclin B activity and protein levels. Pretreatment with specific inhibitors of caspase-3 (Z-DEVE-FMK) and -9(Z-LEHD-FMK) significantly reduced caspase-3 and -9 activity in U87MG cells. Western blot analysis and colorimetric assays also displayed that ANIT caused a time-dependent increase in cytosolic cytochrome c, pro-caspase-9, Apaf-1, AIF, Endo G and the stimulated caspase-9 and -3 activity.
Phenethyl and benzyl isothiocyanates inhibited carcino-genesis induced by carcinogens such as diethyl nitrosamine (DEN), dimethyl benzo(a)anthracene (DMBA) or benzo(a)pyrene (BP) (Wattenberg et al., 1987). The mechanism involved in the inhibition of carcinogenesis by ITCs is most likely due to the blocking of the activation of carcinogens through the inactivation of P450 enzymes and activation of Phase II enzy-mes (Wattenberg et al., 1987).
We hypothesized that resonance structure of naphthyl moiety would result in more effective anticancer agents based on the observation that in comparison to the phenyl and benzyl derivatives, naphthyl structure provides more electron donation. In addition, no previous study exists addressing whether the ANIT inhibits cell proliferation, promotes cell cycle arrest and induces apoptosis in human brain malignant glioma cells. The aim of the present study is to determine and explore ANIT-triggered G2/M phase arrest and cell death in U87MG cells via a mitochondria-dependent apoptotic signaling.
Reagents and chemicals: Alpha-naphthylisothiocyanate (ANIT), [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetra-zolium bromide] (MTT),propidium iodide (PI), Triton X-100, RNase A, dimethylsulfoxide (DMSO) were purchased from Sigma Chemical Co. (St.Louis, MO, USA). RPMI-1640 medium, fetal bovine serum (FBS), L-glutamine, penicillin-streptomycin and trypsin-EDTA were obtained from Gibco BRL/Invitrogen Corp (Grand Island, NY, USA). Caspase-9 inhibitor (Z-LEHDFMK),caspase-8 inhibitor (Z-IETD-FMK) and caspase-3inhibitor (Z-DEVD-FMK) were obtained from Invitrogen (R&D Systems, Minneapolis, MN,USA)
Cells, culture method and cell morphology identification: U87MG cell lines (human brain malignant glioma) were purchased from the Food Industry Research and Development Institute (Hsinchu, Taiwan). Cells were plated onto 75 cm2 tissue culture flasks in RPMI-1640 medium supplemented with 10% FBS, 100 U/mL penicillin, 100 μg/mL streptomycin and 2 mM L-glutamine and grown at 37˚C under a humidified 5% CO2 and 95% air at one atmosphere. U87MG cells of about 2 x 105 cells/well in a 12-well plate were treated with different concentrations (0, 10, and 20 μM) ANIT and incubated for 24 and 48 hours. Cells were directly examined and were photographed under contrast-phase microscope (Yang et al., 2009).
MTT assay: U87MG cells of about 1 x 104 cells/well in 96-well plates were treated with to 4, 8, 16, 32, and 64 μM of ANIT and DMSO, 0.1% in media served as a vehicle control. After a 24 hours incubation, 100 μL of 0.5 mg/mL MTT solution was added to each well, and the plate was incubated at 37˚C for 3 hours. An aliquot of 100 μL of 0.04 N HCl in isopropanol was added and the absorbance at 570 nm was measured for each well with the cell survival ratio expressed as % of control.
Cell cycle distribution analysis: The U87MG cells were seeded onto 12-well culture plates at 2 x 105 cells/well then incubated with 10 μM of ANIT for 24 hours. The cells were harvested and washed by centrifugation. For cell cycle and apoptosis determination, cells were fixed by 70% ethanol in -20˚C overnight and then re-suspended in PBS containing 40 μg/mL PI and 0.1 mg/mL RNase A and 0.1%. Triton X-100 in dark room for 30 min. The cell cycle distribution and apoptotic nuclei were determined by flow cytometry (FACSCalibur™, Becton Dickinson, Franklin Lakes, NJ, USA).
DAPI staining for apoptosis: About 2 x 105 cells/well of U87MG cells in a 12-well plate were treated with 0, and 10 μM of ANIT and 0.1% DMSO as the control. Cells were incubated and grown for 24 hours. Cells were stained by 4'-6-diamidino-2-phenylindole (DAPI) and were photographed under fluorescence microscopy.
CDK1 kinase assay: U87MG cells of about 1 x 107 density were suspended in a buffer containing a final volume of 0.2 mL, 50 mM Tris-HC1(pH 7.5), 1 mM phenylmethyl-sulfonyl fluoride, 50 pg/mL leupeptin, 2-mercaptoethanol (10 mM), MgCl2 (1 mM), EGTA (2 mM), dithiothreitol (0.5 mM), Brij (350.01%), b-glycerophosphate (25 mM), and NaCl (0.5 M). Cell suspensions were sonicated and centrifuged for 30 min. To determine the CDK1 kinase assay condition using MV Peptide, its absorbance was measured at 492 nm (Yang et al., 2004; Kuo et al., 2009). Assay was carried out according to the protocol of Medical and Biological Laboratories CDK1 kinase assay kit (MBL, Nagoya, Japan).
Western blot: U87MG cells of about 1 x 107 density in a 75-T flask were treated with 10 μM of ANIT for 0, 6, 12, 24 and 48 hours. The examined cells were harvested and washed with cold PBS for detecting the changes of protein levels correlated with G2/M phase-modulated and apoptotic signaling. The total proteins were collected from ANIT-treated U87MG cells before the CDK1, cyclin B and cyclin A were detected and measured. The level of cytosolic fraction proteins such as cytochrome c, Apaf-1, pro-casepase9, AIF, and Endo G were determined and isolated according to the mitochondria/cytosol fractionation kit manufacturer's protocol (BioVision, Inc. Mountain View, CA, USA). U87MG cells after exposure to ANIT were harvested, disrupted and then centrifuged to isolate cytosolic fractions. The total or cytosolic protein (40 μg) from each sample was resolved on 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) and transferred to nitrocellulose membrane. The blot was soaked in blocking buffer (5% non-fat dry mik/0.05% Tween-20 in 20 mM TBS at pH 7.6) at room temperature for 1 hour and then incubated with anti-CDK1, anti-cyclin B, anti-cyclin A, anti-cytochrome c, anti-Apaf-1, antipro-casepase-9, anti-AIF, and anti-Endo G antibodies (SantaCruz Biotechnology, Inc.) in blocking buffer at 4˚C overnight. A secondary antibody horseradish peroxidase conjugate was added and detected by chemiluminescence and autoradiography using X-ray film. To ensure equal protein loading, each membrane was stripped and reprobed with anti β-actin antibody.
Assays for caspase-3, -8 and -9 activities: Caspase-3, -8 and -9 activities were assessed according to the manufacturer’s instructions (Caspase colorimetric kit, R&D-System Inc.). U87MG cells of about 1 x 107 density in a 75-T flask were pretreated with or without the selective inhibitors (Z-DEVE-FMK forcaspase-3, Z-IETD-FMK for caspase-8 and Z-LEHD-FMK for caspase-8) and then treated with 10 μM ANIT were incubated for 24 hours to detect caspase-3, -8 and -9 activities. Briefly, cells were harvested and lysed in 50 μL lysis buffer containing 2 mM DTT for 10 min. After centrifugation, the supernatants containing 100 μg proteins were incubated with caspase-3, -8 and -9 substrate in reaction buffer. Samples were incubated in a 96-well flat bottom micro-plate at 37˚C for 1 hour. Levels of released pNA (Z-DEVEpNA, Z-IETD-pNA and Z-LEHD-pNA for cas-pase-3, -8 and -9, respectively) were measured with an ELISA reader (AnthosLabtec Instruments) at an absorbance of 405 nm.
Statistical analysis: Student's t-test was used to analyze the differences between the ANIT-treated and control groups. All data were expressed as mean ± SD from at least three independent experiments. P<0.05, p<0.01 and p<0.001 were indicative of significant difference.
The cell viability of ANIT on a human brain malignant glioma cell line U87MG was investigated by the MTT assay. The results shown in Figure 1A indicated that ANIT significantly reduced the percentage of viable cells when compared to that of control cells. These effects were found to be in a dose-dependent manner. The IC50 of ANIT was 8.3 ± 0.6 μM after 24 hours treatment. In addition, the examined cells exhibited morphological changes, including rounding and shrinkage after 24 and 48 hours-incubation with 10 and 20 μM of ANIT (Figure 1B). Viable cells were determined by MTT assay. The cell morphological changes were examined and photographed under phase-contrast microscopy (x200) as described in Materials and methods. There was a significant difference (***p<0.001) when compared with the control group by Student's t-test analysis.
Figure 1: Effects of ANIT on cell viability (A) and morphology (B) of U87MG cells. Cells were cultured with 0, 4, 8, 16, 32 and 64 μM of ANIT for 24 hours
Cells were treated with 10 μM of AITC for 24 hours and then were analyzed and determined for cell cycle distribution by PI staining and flow cytometric analysis. AITC induced chromatin condensation (an apoptotic characteristic) in U87MG cells. Cells were incubated with 10 μM of AITC for 24 hours and apoptotic cells were determined by DAPI staining and were photographed by fluorescence microscopy (x200) as described in Materials and Methods. ANIT induced reduction of cell viability could be due to apoptosis (sub-G1 population) mediated by cell cycle arrest which were determined. Representative profiles of cell cycle progression and percentage of each phase are presented in Figure 2A. Significant arrest was seen at G2/M phase at 10 μM of ANIT and it significantly increased apoptotic cells (sub-G1groups) (Figure 2A). Apoptotic chromatistic (nuclear and chromatin condensation) in GBM8401 cells occurred with or without ANIT (10 μM) treatment for 24 hours determined by DAPI staining (Figure 2B).
Figure 2: Effects of ANIT on cell cycle distribution (A) and chromatin condensation (B) in U87MG cells
This experiment was carried out to prove ANIT-induced accumulation of G2/M population in U87MG cells and it was regulated associated proteins. U87MG cells were incubated with 10 μM AITC for 0, 6, 12, 24 and 48 hours, harvested from each sample and then relative protein levels were determined by Western blot analysis. The levels of CDK1, cyclin B and cyclin A were examined, and ß-actin as an internal control using SDS-PAGE and Western blotting as described in Materials and Methods. ***p<0.001, was significantly different compared to the control group. The results are shown in Figure 3a and Figure 3b. U87MG cells after exposure to AITC showed that a significant decrease of CDK1 activity (Figure 3A) and down-regulated the protein levels, including CDK1, cyclin B and cyclin A as shown in Figure 3B.
Figure 3: ANIT alters the levels of CDK1 activity (A), and the CDK1, cyclin (A) and cyclin (B) proteins of G2/M phase arrest in U87MG cells. Cells were incubated with 10 μM AITC for 0, 6, 12, and 24 hours for CDK1 activity
To assess the ANIT-induced apoptotic cell death, the results of Western blot analysis from 10 μM of ANIT co-incubation with U87MG cells for 0, 6, 12, 24 and 48 hours are shown in Figure 4A. The raise in protein levels of cytochrome C, Apaf-1, pro-caspase-9, AIF, and Endo G in cytosolic fractions may contribute to the occurrence of ANIT-triggered mitochondrial apoptosis and this signaling was found to be time dependent. Figure 4B, showed that ANIT induced a significant rise in caspase-3 and -9 activities rather than influence of caspase-8 response. This stimulation of activity of the caspases cascade in U87MG cells was reduced after pre-incubation with specific inhibitors of caspase-3 and -9, respectively. Based on these results, ANIT-induced cell death was correlated with caspase-dependent and -independent mitochondrial apoptotic pathways.
Figure 4: ANIT affects the relative protein levels of apoptosis (A) and caspase-3, -8 and -9 activities (B) in U87MG cells. ap<0.001, significant difference
Isothiocyanates ITCs (R-N=C=S) are electrophilic compounds and are known to react predominantly with thiols, and to a much lesser extent with NH2 and OH groups (Drobinica et al., 1965; Brusewitz et al., 1977). Therefore, the major route of metabolism and elimination of ITCs from the body is the mercapturic acid pathway i.e. by formation of non-enzymatic and enzymatic conjugation with reduced glutathione (GSH) to give thiol conjugates. TCs was extensively studied in cancer cell lines originating from various tissues (Xu et al., 2000; Srivastava et al., 2004). However, there is no report on ANIT in having anti-cancer activity against human brain malignant glioma.
The experimental results showed that ANIT induced cytotoxic responses in a dose dependent manner. It stimulated morphological changes such as rounding and shrinkage in U87MG cells after 24 and 48 hours-treatment. Cell growth and proliferation of mammalian and tumor cells occur through cell cycle progression. The inhibition of cell cycle distribution has been recognized as a target for anticancer agents (Schwartz et al., 2005; Kim et al., 2008). The results in the present study showed that U87MG cells when treated with 10 μM of ANIT for 24 hours resulted accumulation in the G2/M phase by flow cytometric analysis, suggesting the sequential events of cell cycle arrest followed by apoptosis. It is known that the CDK1/Cyclin B complex is one of the major regulators leading the G2/M progression or apoptosis. Hence, we investigated the U87MG cells after ANIT treatment determining the G2/M phase regulated protein levels and the data showed that a decrease in the protein levels of CDK1, cyclin B and cyclin A by Western blot analysis, and CDK1 kinase assays revealed reduction of CDK1 activity at 6, 12 and 24 hours after 10 μM of AITC treatment.
Apoptotic cell death induction is one of the best strategies for cancer treatment (Batista et al., 2009; Sanchez-Munoz et al., 2009). Our results indicated that ANIT induced apoptosis in U87MG cells. This was demonstrated by flow cytometric analysis and DAPI staining was applied to confirm cell apoptosis in examined U87MG cells. The results from the Western blot analysis showed that AITC increased protein levels of cytochrome C, Apaf-1, pro-caspase-9, AIF, and Endo G, suggesting that analyses of protein abundance indicated that AITC induced apoptosis through a mitochondria-dependent pathway. Also, AITC stimulates the loss of mitochondrial membrane potential resulting from the mitochondria dysfunction (data not shown). In this study, we observed the ANIT-induced caspase-9 and -3 activities in U87MG and the specific inhibitors (Z-DEVEFMK for caspase-3 and Z-LEHD-FMK for caspase-9) individually prevented ANIT-induced caspase-3 and -9 activities, respectively in U87MG cells. ANIT-induced G2/M phase arrest and apoptosis in U87MG cells is shown in Figure 5.
Figure 5: The proposed model of ANIT-induced G2/M phase arrest and apoptosis in U87MG cells
In conclusion, we studied ANIT triggered G2/M phase arrest and apoptosis in U87MG cells. The experimental results showed that ANIT induced morphological changes on U87MG cells, decreased the percentage cell viability, increased G2/M phase arrest, and stimulated the levels of caspase-9, -3, AIF and Endo G through a mitochondria dependent apoptotic pathway.
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