Curcumin induces apoptosis in gallbladder carcinoma cell line GBC-SD cells
© Liu et al.; licensee BioMed Central Ltd. 2013
Received: 27 April 2013
Accepted: 23 June 2013
Published: 26 June 2013
Gallbladder carcinoma is a malignant tumor with a very low 5-year survival rate because of the difficulty with its early diagnosis and the very poor prognosis of the advanced cancer state. The aims of this study were to determine whether curcumin could induce the apoptosis of a gallbladder carcinoma cell line, GBC-SD, and to clarify its related mechanism.
First, the anti-proliferative activities of curcumin-treated and untreated GBC-SD cells were determined using the MTT and colony formation assays. Then, the early apoptosis of cells was detected by the annexin V/propidium iodide double-staining assay and Hoechst 33342 staining assay. Detection of mitochondrial membrane potential was used to validate the ability of curcumin on inducing apoptosis in GBC-SD cells. Cell cycle changes were detected by flow cytometric analysis. Finally, the expressions of the apoptosis-related proteins or genes caspase-3, PARP, Bcl-2, and Bax were analyzed by western blot and quantitative real time PCR assay. Statistical analyses were performed using the Student’s t-test for comparison of the results obtained from cells with or without curcumin treatment.
The MTT assay revealed that curcumin had induced a dose- and a time-dependent decrease in cell viability. Colony counting indicated that curcumin had induced a dose-dependent decrease in the colony formation ability in GBC-SD cells. Cells treated with curcumin were arrested at the S phase, according to the flow cytometric analysis. A significant induction of both the early and late phases of apoptosis was shown by the annexin V-FITC and PI staining. Morphological changes in apoptotic cells were also found by the Hoechst 33342 staining. After treatment with curcumin fluorescence shifted from red to green as ΔΨm decreased. Furthermore, western blot and quantitative real time PCR assays demonstrated that the curcumin induced apoptosis in GBC-SD cells by regulating the ratio of Bcl-2/Bax and activating the expression of cleaved caspase-3.
Taken together, the results indicate that curcumin may be a potential agent for the treatment of gallbladder cancer.
KeywordsCurcumin Gallbladder carcinoma GBC-SD cell Proliferation Apoptosis
Gallbladder carcinoma is one of the most common malignant tumors of the biliary system and is the fifth most common malignancy of the gastrointestinal tract [1, 2]. Early gallbladder carcinoma is asymptomatic or manifests only as an abdominal discomfort. Some patients can develop the symptom of acute or chronic cholecystitis, which is easy to ignore or miss. In the later period, patients can develop abdominal pain, jaundice, and angular, but most of the patients have no surgical opportunities. The prognosis of advanced gallbladder carcinoma is very poor, [3–5] and the 5-year survival rate is only about 5% . So far, surgical resection is the only treatment that offers a hope for cure . Moreover, the majority of patients have frequent recurrences following surgery and unsatisfactory results following chemotherapy or radiotherapy . Therefore, more research about the occurrence of gallbladder carcinoma and the mechanism of its development, as well as finding effective treatments and drugs, is an important need.
Curcumin, a phenolic compound present in Zingiberaceae Curcuma longa, rhizoma zedoariae, turmeric, etc., has been shown to have anticarcinogenic [9–11] and anti-inflammatory properties , including an inhibitory effect on the production of various cytokines. Curcumin has attracted much attention because of its low price and low toxicity, as well as its wide pharmacological and potential anticancer effects. It is believed that the anticancer mechanism of curcumin is mainly in inducing the apoptosis of cancer cells [13–15] and suppressing metastasis [16–18]. The apoptosis induced by curcumin is due to the activation of a multi-signal transduction pathway. Curcumin induces apoptosis in breast cancer cell lines, and the activation of apoptosis was confirmed by PARP-1 cleavage and by the increased ratio between the pro-apoptotic Bax and the anti-apoptotic Bcl-2 proteins . Moreover, apigenin and curcumin synergistically induced cell death and apoptosis and also blocked cell cycle progression at the G2/M phase of A549 cells . Although curcumin has been found to induce apoptosis in several types of cancers, the molecular apoptotic mechanisms of curcumin in the gallbladder carcinoma cell line GBC-SD have not previously been investigated.
The goals of this study were to determine whether curcumin could induce apoptosis in GBC-SD cells and to clarify the related mechanism, which may offer a promising new approach in the effective treatment of gallbladder carcinoma.
Effect of curcumin on the viability of GBC-SD cells
Effect of curcumin on cell cycle distribution in GBC-SD cells
Effect of curcumin on apoptosis in GBC-SD cells
Morphological changes in the apoptotic cells were revealed by the Hoechst 33342 staining, as shown in Figure 3(B). In the untreated GBC-SD cells, the nuclei were stained weak homogeneous blue, whereas in the group treated with curcumin, bright chromatin condensation and nuclear fragmentation were observed, the rates of which increased in a dose-dependent manner.
Effects of curcumin on mitochondrial membrane potential(ΔΨm)
To validate the ability of curcumin on inducing apoptosis in GBC-SD cells, we performed a cellular functional assay. JC-1 probe is a fluorescent cationic dye that can selectively accumulate into mitochondria by electrochemical gradient and changes color from red to green as ΔΨm decreases. As illustrated in Figure 3(C), untreated GBC-SD cells exhibited red fluorescence. After treatment with.
Effect of curcumin on the signal pathway of caspase and Bcl-2 family members in GBC-SD cells
To the best of our knowledge, this is the first study to reveal the ability of the natural compound curcumin to induce apoptosis in GBC-SD cells. In recent years, studies have shown that curcumin can inhibit the growth of a variety of tumor cells [9, 21, 22], as well as induce cell differentiation and apoptosis in some tumors [24–27]. Curcumin can also be used as a natural antitumor drug . Here, we have shown the biochemical and molecular mechanisms of apoptosis induction by curcumin in GBC-SD cells.
Curcumin manifests its antitumor effect through the induction of cell apoptosis in vitro. Our experiment showed a significant inhibition of cell proliferation in a dose- and time-dependent manner, thereby suggesting that treatment with curcumin inhibited the growth and reduced the viability of GBC-SD cells. The cell apoptosis experiment showed that curcumin had the biological activity of inducing tumor cell apoptosis. We used flow cytometry to detect the cell cycle, and the results showed a significant decrease in the number of cells in the proliferative G0/G1 phase and a significant increase in the number of cells in the S phase, after 48 h of treatment with curcumin. The result suggested that curcumin could block cells in the S phase, which prevented DNA from replicating properly, thus inhibiting tumor growth.
Cell apoptosis is an autonomous cell death process, which can be induced by a variety of drugs and physical and chemical factors. The induction of apoptosis has been described as a standard and best strategy in anticancer therapy [29, 30]. The family of cysteine-containing aspartate-specific proteases (caspase) contains many members that are closely related with cell apoptosis [31, 32]. So far, 10 members have been identified in humans. Caspase-3, a protein on the common path of cell apoptosis, is one of the most important members and the key executor of cell apoptosis. Caspase-3 usually exists in the cytoplasm in the form of an inactive zymogen. When activated by the many external apoptosis signals, caspase-3 can induce the inactivation of many key proteases in the cytoplasm, cell nucleus, and cytoskeleton, and finally cause the apoptosis of cells. In our study, the results showed that the change of caspase-3 expression was in accordance with the tendency of changes in cell apoptosis. The cleavage of PARP was increased accordingly. The Bcl-2 gene family is one of the best studied of the anti-apoptosis genes, and according to the members’ different biological effects, it is divided mainly into the Bax, Bcl-2, and Bid proteins. Among them, the apoptosis-promoting protein Bax and the anti-apoptotic protein Bcl-2 play an important role in regulating cell apoptosis [33, 34]. The occurrence and severity of apoptosis depends on the ratio of Bcl-2/Bax . When this ratio is reduced, the caspase apoptosis proteins can be activated. Through the western blot assay, it was found that the expression of Bcl-2 was reduced and that of Bax was promoted in GBC-SD cells treated with curcumin, thus decreasing the Bcl-2/Bax ratio significantly.
In conclusion, this study suggests that curcumin inhibits the proliferation of GBC-SD cells and arrests the cell cycle in the S phase. Curcumin induces GBC-SD cell apoptosis mainly by activating the Bcl-2 and caspase-3 pathways. Other apoptotic mechanisms remain to be researched further.
Cell lines and culture
GBC-SD cells were purchased from the Shanghai Cell Institute Country Cell Bank. The cells were cultured in high-glucose DMEM (Gibco, USA) supplemented with 10% fetal bovine serum (Gibco, USA), 100 μg/mL streptomycin and 100 U/mL penicillin (Hyclone, USA), at 37°C, under a 5.0% CO2 atmosphere.
Drugs and antibodies
3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium (MTT) assay
Colony formation assay
Cells in the logarithmic growth phase were digested into a single-cell suspension with a trypsin-EDTA (Gibco, USA) solution, and then 2 mL of the cell suspension was seeded onto 6-well plates (Corning, USA) at a density of 200 cells/mL. After adherence, the cells were treated with curcumin (0.75, 1.5, and 3 μmol/L) for 48 h and then cultured for 15 days. Thereafter, the cells were fixed with 10% formalin and stained with 0.1% crystal violet (Sigma-Aldrich). After washing, the plates were air dried, and digital images were taken of stained single clones observed under a microscope (Leica, Germany). The results represent the average of 3 independent experiments done over multiple days.
Cell cycle analysis
GBC-SD cells were treated with curcumin (3.75, 7.5, and 15 μmol/L) for 48 h. Then, the cells were collected and fixed with cold 70% ethanol and stored at −20°C. The cells were then washed and resuspended in cold PBS and incubated at 37°C for 30 min with 10 mg/mL RNase and 1 mg/mL propidium iodide (Sigma-Aldrich). DNA content analysis was performed by flow cytometry (BD, San Diego, USA). The percentage of cells in the different cell cycle phases was determined using the Cell Quest acquisition software (BD Biosciences).
Flow cytometric analysis of cell apoptosis
The annexin V/propidium iodide assay was performed according to the manufacturer’s recommendation (Invitrogen, USA). Briefly, GBC-SD cells were plated into 6-well plates (Corning, USA) and incubated for 48 h with curcumin (3.75, 7.5, and 15 μmol/L). In brief, the cells were collected and then were washed with cold PBS, centrifuged, resuspended in 100 ul of binding buffer containing 2.5 ul FITC conjugated annexin-v and 1ul 100 ug/ml PI and incubated for 15 mins at room temperature in the dark. A total of at least 10 000 events were collected and analyzed by flow cytometry (BD, San Diego, USA).
Detection of morphological apoptosis with Hoechst 33342 staining
After treatment with curcumin (3.75, 7.5, and 15 μmol/L) for 48 h, the GBC-SD cells were washed with PBS and fixed with methanol:acetic acid (3:1) for 15 min at room temperature. Fixed cells were washed with PBS and stained with 5 μg/mL of Hoechst 33342 stain for 10 min. Changes in the nuclei of cells after staining with Hoechst 33342 were observed using a fluorescence microscope (Leica, Germany).
Detection of mitochondrial membrane potential(ΔΨm) variation with fluorescence microscopy
The ΔΨm was analyzed by fluorescence microscopy using the 5,50,6,60-tetrachloro-1,10,3,30-tetraethylbenzimidazolcarbocyanine iodide (JC-1) probe. After treatment with curcumin (3.75, 7.5, and 15 μmol/L) for 48 h, 5ul of the JC-1 staining solution(Beyotime,China) per ml culture of medium was added to each well and samples were then incubated in 5% CO2 incubator at 37°C for 20 min protected from light. After washing twice with buffer solution, GBC-SD cells were analyzed by using a fluorescence microscope (Leica, Germany).
Reverse transcription and quantitative real-time polymerase chain reaction (qPCR)
Quantitative PCR was performed as previously described  qPCR was used to quantify the expression of BCL2 and Bax mRNA in the experimental groups. GBC-SD cells were treated with curcumin (3.75, 7.5, and 15 μmol/L) for 48 h. Total RNA was isolated using the RNA easy kit (Invitrogen, USA). First strand cDNA was synthesized from 500 ng total RNA using a PrimeScript® Reverse Transcriptase (TaKaRa, Japan). Quantitative real-time PCR was performed in a reaction volume of 20 μl including 2 μl cDNA. The primer sequences were as follows: BCL2 (forward-5’-CAA ATG CTG GAC TGA AAA ATT GTA-3’ , reverse-5’-TAT TTT CTA AGG ACG GCA TGA TCT-3’), BAX (forward-5’-GAC ACC TGA GCT GAC CTT GG-3’; reverse-5’-AGG AAG TCC AGT GTC CAG C-3’) and GAPDH (forward-5’-AAG CTC ATT TCC TGG TAT GACA-3’ , reverse-5’-TCT TAC TCC TTG GAG GCC ATGT-3’). PCR conditions were as follows: 95°C for 30sec followed by 40 cycles at 95°C for 5 sec, 60°C for 34 sec. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was used as an internal reference gene to normalize the expression of apoptotic genes. Relative quantification of apoptosis-related genes was analyzed by the comparative threshold cycle (Ct) method. For each sample, the Ct value of the apoptotic gene was normalized using the formula: ΔCt = Ct (apoptotic genes) - Ct (GAPDH). To determine relative expression levels, the following formula was used: ΔΔCt = ΔCt (treated) - ΔCt (control). The value was used to plot the expression of apoptotic genes using the formula 2−ΔΔCt.
Western blot analysis
Western blot was performed as previously described . Breafly, GBC-SD cells were treated with various concentrations of curcumin (3.75, 7.5, and 15 μmol/L) for 48 h and then lysed in a sample buffer, followed by denaturation. The total protein concentration of the cell extracts was determined using the bicinchoninic acid assay system (Beyotime, China) with BSA as a standard. Equal quantities (80 μg protein per lane) of total proteins were separated by SDS-PAGE (8%, 12% gels) under reducing conditions. The proteins were then electrophoretically transferred to nitrocellulose membranes. The membranes were blocked with 5% skimmed milk, and incubated with anti-caspase-3, anti-Bcl-2, anti-Bax, anti-PARP, anti-β-actin and anti-β-tubulin antibodies, respectively (1:1000; Cell Signaling Technology) at 4°C overnight. This was followed by an incubation with goat anti-rabbit/anti-mouse secondary antibody conjugated with horseradish peroxidase (1:5000; Abcam). An equal loading of each lane was evaluated by immunoblotting the same membranes with β-actin antibodies after the detachment of previous primary antibodies. Photographs were taken and the optical densities of the bands were scanned and quantified with the Gel Doc 2000 (BioRad, USA).
All values are expressed as the mean ± SD and they were analyzed by the Student’s t- test using SPSS version 13.0 software. A p-value of less than 0.05 was considered significant.
This study was supported by the National Natural Science Foundation of China (No. 81172026, 81272402, and 81172029), Foundation of Shanghai Outstanding Academic Leaders (No. 11XD1403800), National High Technology Research and Development Program (863 Program) (No. 2012AA022606), Post-doctoral Research Foundation of China (No. 2012M511107), Foundation for Interdisciplinary Research of Shanghai Jiaotong University (No. YG2011ZD07), Shanghai Science and Technology Commission Inter-governmental International Cooperation Project (No. 12410705900), and Post-doctoral Research Program of Shanghai (No. 12R21415300).
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