Butein induces cell apoptosis and inhibition of cyclooxygenase‑2 expression in A549 lung cancer cells

Introduction

The flavonoid butein may be isolated from the bark of Rhus verniciflua Stokes and the flowers of Butea monosperma. It is a biologically active flavonoid, and a number of studies have reported its anticarcinogenic activities (1–3). The organic extract purified from Rhus verniciflua Stokes inhibits the growth of transformed hepatic cells, but not the untransformed parent cells (4), whereas butein alone may introduce G(2)/M phase arrest in hepatic cells (5). Its anti-proliferative or pro-apoptotic effects may be induced through downregulating STAT3-related gene expression (6) and inhibiting telomerase activity (7). The flavonoid may also re-sensitize the tumor necrosis factor α-related apoptosis-inducing ligand (TRAIL) resistant leukemia cells undergoing apoptosis following TRAIL treatment (8), and may reduce clonogenic growth of human breast cancer cells (9). These experiments indicated the potential anticarcinogenic effect of butein on different cell types.

Prostaglandins may be produced from arachidonic acid with the enzyme cyclooxygenase (COX) in tumor tissues. Increased expression of COX-2 in the neovasculature of breast tumors has been observed, which suggests that the enzyme may be involved in the later stage of cancer development. In the estrogen receptor-positive MCF-7 cells, COX-2 overexpression increases the growth rate and colony formation in soft agar, and promotes movement across the Matrigel basement membrane (10). By contrast, overexpressing COX-2 in the Hs578T estrogen receptor-negative breast cancer cell line also activates matrix metalloproteinase-2 (11). These activities may encourage the invasiveness of cancer cells and facilitate metastasis. Altered gene expression in cell cycle and apoptosis, or their regulatory signals may also support tumorigenesis. Notably, COX-2 may increase the expression of the epidermal growth factor receptor, aromatase, and Bcl-2, which may be integrated into these processes (12).

COX-2 inhibitors have shown a degree of protection against breast carcinogenesis in animal models. Celecoxib inhibits the onset and progression of 7,12-dimethylbenz[a]anthracene-induced mammary tumorigenesis in rats, while nimesulide reduces tumor incidence induced by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (13). These experimental results have demonstrated that COX-2 inhibition may protect against cancer. Therefore, the inhibition of COX-2 has been suggested to be a promising therapeutic strategy for human cancer, thus, indicating the importance of overcoming the therapeutic resistance of cancer and the possible role of COX-2 in cancer. In the current study, the effect of butein on COX-2 expression in human lung cells was investigated. Furthermore, the effects of butein on proliferation and apoptosis in A549 lung cancer cells were evaluated.

Materials and methods

Chemicals and drugs

Butein was obtained from Jilin University (Changchun, China), dimethylsulfoxide (DMSO), Tris-HCl, EDTA, SDS, phenylmethylsulfonyl fluoride (PMSF), bovine serum albumin (BSA), leupeptin, Nonidet P-40, deoxycholic acid, sodium orthovanadate, aprotinin and a polyclonal antibody against β-actin were purchased from Sigma-Aldrich (St. Louis, MO, USA). Protein assay kits were obtained from Bio-Rad Laboratories (Hercules, CA, USA). Dulbecco’s modified Eagle’s medium (DMEM) and fetal-bovine serum (FBS) were obtained from Gibco-Life Technologies (Carlsbad, CA, USA). COX-2 polyclonal antibodies were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). Anti-mouse secondary antibodies were purchased from Qiagen (Hilden, Germany).

Cell culture

The A549 non-small cell lung carcinoma (NSCLC) cell line was obtained from the Cell Bank of the Chinese Academy of Sciences (Shanghai, China) and cultured in DMEM supplemented with heat-inactivated FBS (10%), L-glutamine (2 mM), penicillin (100 IU/ml), and streptomycin (100 μg/ml) in a humidified incubator aerated with 5% CO2 and 95% at 37°C. When cells reached 70–80% confluency, they were trypsinized, counted and treated with celastrol in complete cell medium. Control cells were treated with vehicle (DMSO) for the same duration.

Cell viability assay

Cells were plated in 96-well culture plates at an initial density of 1×104 cells/well and allowed to adhere to the plates. The culture medium was replaced by fresh medium containing butein at concentrations ranging between 0 and 20 μmol/l and incubated for 48 h. The cell proliferation kit I (MTT) from Roche Applied Science (Mannheim, Germany) was used to measure cell viability. Briefly, 10 μl labeling solution was added to each well of the 96-well plates. After 2 h in the CO2 incubator, 100 μl solubilization solution was added to dissolve the purple crystals, which were the products of the MTT substrates. The absorbance was measured at 570 nm by a plate reader (Perkin-Elmer, Waltham, MA, USA). Absorbance measured in the MTT assays is expressed as a percentage of the control (defined as 100%).

Cell cycle analysis

Cells were seeded in 25 cm2 flasks and incubated overnight to allow cells to adhere to the plate. A549 cells were treated with 10 and 20 μmol/l butein for 24 h. Following treatment, control (untreated) and treated floating and adherent cells were collected by trypsinization. The cells (1×106 cells/ml) were washed twice with cold phosphate-buffered saline (PBS) and fixed in 70% ethanol. Immediately prior to the analysis, the cells were washed with PBS and stained with a solution containing propidium iodide (PI; 0.2 mg/ml) for 1 h at 4°C and with RNase A (0.1 mg/ml) for 30 min at 37°C. The distribution of cells in the cell cycle was measured by flow cytometry (Becton-Dickinson, Franklin Lakes, NJ, USA). Percentages of cells in the cell cycle phases were calculated using the Cell Quest software (Becton-Dickinson).

Measurement of apoptosis by ELISA

The induction of apoptosis by butein was assayed by the Nucleosome ELISA kit (Fitzgerald Industries International, Acton, MA, USA). This kit uses a photometric enzyme immunoassay to quantitatively determine the formation of cytoplasmic histone-associated DNA fragments (mono and oligonucleosomes) following apoptotic cell death. Apoptosis was determined by ELISA and the A549 cells (1×105) were treated with butein at 0, 10 and 20 μmol/l for 12, 24 and 48 h in a 96-well plate. The induction of apoptosis was evaluated by assessing the enrichment of nucleosome in the cytoplasm, and determined as described in the manufacturer’s instructions for the nucleosome ELISA kit.

Quantitative polymerase chain reaction (qPCR) assay

Cells were seeded in 6-well plates for one day prior to treatment. The medium was removed and cells were cultured in fresh DMEM containing 20 μmol/l butein. Following 6 h treatment, total RNA was extracted from the cells using TRIzol reagent (Invitrogen Life Technologies, Carlsbad, CA, USA). The concentration and purity of RNA were determined by absorbance at 260/280 nm. DNA strands were synthesized from 3 μg total RNA by oligo-dT primers and M-MLV Reverse Transcriptase (Takara Bio, Inc., Shiga, Japan). Target fragments were quantified by real-time PCR, and an ABI prism 7700 Sequence Detection system (Applied Biosystems, Foster City, CA, USA) was employed for this assay. Taqman®/VIC® MGB probes and primers for COX-2 [Assay ID (NM_000963.1): HS00153133_M1] and β-actin, and Real-time PCR Taqman Universal PCR Master mix were obtained from Applied Biosystems. PCR reactions were set up as described in the instructions, which was validated by the company. The signal obtained for β-actin was used as a reference housekeeping gene to normalize the quantity of total RNA amplified in each reaction. Relative gene expression data were analyzed using the 2−ΔΔCt method.

Western blot analysis

Cells were washed once with PBS (pH 7.4) and harvested into a 1.5 ml microtube with 0.5 ml lysis buffer (PBS, 1% NP-40, 0.5% sodium deoxycholate, 0.1% SDS). The lysis buffer contained protease inhibitors (40 mg/l PMSF, 0.5 mg/l aprotinin, 0.5 mg/l leupeptin, 1.1 mmol/l EDTA and 0.7 mg/l pepstatin). The harvested cells were then lysed with a cell disruptor (Branson Ultrasonics Corp., Danbury, CT, USA) on ice for 30 sec. The protein concentration of the cell lysate was determined by a Dc protein assay (Bio-Rad, Richmond, CA, USA). Lysate protein (50 μg) was separated on 10% SDS-PAGE and transferred onto an Immobilon polyvinylidene difluoride membrane (Millipore, Billerica, MA, USA). Anti-COX-2 (Cayman Chemicals, Ann Arbor, MI, USA), and secondary anti-mouse IgG antibodies conjugated with horseradish peroxidase (HRP; Santa Cruz Biotechnology, Inc.) were used for protein detection. An enhanced chemiluminescence detection kit (Amersham Pharmacia Biotech, Piscataway, NJ, USA) provided the chemiluminescence substrate for HRP, and the targeted protein was visualized by autoradiography (Xue Wang, The First Hospital of Jilin University, Changchun, China).

Statistical analysis

Values are expressed as the mean ± standard deviation. The data were analyzed by one-way analysis of variance. P<0.05 was considered to indicate a statistically significant difference.

Results

Butein inhibits the growth of human lung cancer cells

To evaluate the antiproliferative activities of butein on A549 cells, the MTT assay was applied. As shown in Fig. 1, exposure of A549 cells to increasing concentrations of butein (0–20 μmol/l) for 72 h resulted in a dose-dependent growth inhibition. The lower butein concentrations (2.5–5 μmol/l) did not affect A549 cell viability significantly, whereas concentrations between 10 and 20 μmol/l significantly reduced cell viability. The IC50 for the 48 h incubation time was ~14.18 μM. Therefore, 15–20 μmol/l doses were selected for further butein treatment studies.

Figure 1 Effect of butein on the growth of A549 cells. A549 cells were treated with butein (0–20 μmol/l) for 48 h. Viability was determined by the MTT assay. The data are presented as the percentages relative to the control (defined as 100%). The data are expressed as the mean ± standard deviation of triplicate samples from three independent experiments. *P<0.05 and **P<0.01, vs. control.

Butein-induced cell cycle arrest and apoptosis in A549 cells

The results on the effect of butein on cell cycle progression of A549 are shown in Fig. 2A. As compared with the control, 10 μmol/l butein increased the population of G1 phase from 35.3 to 42.4%. This effect was enhanced when A549 cells were treated with 20 μmol/l butein (61.5% cell population in G1 phase).

Figure 2 Butein-induced cell cycle arrest and apoptosis in A549 cells. (A) The effects of butein cell cycle distribution in A549 cells. A549 cells following treatment with 0, 10 and 20 μmol/l of butein for 24 h were fixed and stained with PI and cell cycle distribution was analyzed by flow cytometry. (B) Induction of apoptosis in A549 cells by butein. A549 cells were cultured with 0, 10 and 20 μmol/l of butein for 12, 24 and 48 h. Cells were harvested and lysed with lysis buffer. Cell lysates containing cytoplasmic oligonucleosomes of apoptotic cells were analyzed by means of Nucleosome ELISA. Each value is the mean ± standard deviation of three determinations. *P<0.05 and **P<0.01, vs. control. PI, propidium iodide.

Fig. 2B shows the time course of DNA fragmentation in continuous treatment with 10 and 20 μmol/l butein. DNA fragmentation of A549 was found at 12 h and maximized at 48 h following the addition of butein. In contrast to the control, when cells were treated with butein, the number of cells undergoing apoptosis increased between ~3.3 and 8.2-fold at 10 and 20 μmol/l butein, respectively, at 48 h.

mRNA expression of COX-2 following butein treatment

qPCR was performed to detect the mRNA expression of COX-2 in A549 cancer cells following butein treatment. As shown in Fig. 3, mRNA levels of COX-2 was significantly reduced following butein treatment as compared with the control group (P<0.05), which showed that mRNA expression of COX-2 was downregulated by butein treatment in A549 cancer cells.

Figure 3 The mRNA expression of COX-2 in A549 cancer cells following butein treatment for 48 h by qPCR. ##P<0.01, vs. control. COX-2, cyclooxygenase-2; qPCR, quantitative polymerase chain reaction.

Protein expression of COX-2 in A549 cells following butein treatment

A549 cells were treated with 20 μmol/l butein, and cultured for 24 h. Protein lysates were prepared for western blot analysis. As shown in Fig. 4, protein levels of COX-2 were significantly reduced in A549 cells following butein treatment compared with the control (P<0.05), which was in agreement with the result that butein treatment may downregulate COX-2 mRNA expression in A549 cancer cells.

Figure 4 The protein expression of COX-2 in A549 cancer cells following butein treatment for 48 h by western blotting. **P<0.01, vs. control. COX-2, cyclooxygenase-2

Discussion

Lung cancer is the leading cause of cancer-related mortality worldwide. NSCLC accounts for ~75–85% of lung cancer. NSCLCs commonly develop resistance to radiation and chemotherapy, and often present at stages beyond surgical respectability. Since current treatment modalities are inadequate, novel therapies are required to reduce the effects of the increasing incidence in pulmonary neoplasm (14,15). Butein is a polyphenolic compound, which may be extracted from the stem bark of cashews and Rhus verniciflua Stokes, and used as a food additive and a traditional herbal medicine. Previous studies suggested that butein exhibits anticancer activity and that butein may induce apoptosis in human promyelocytic leukemia (16) and B16 melanoma cells (17). In vitro, butein may suppress the proliferation of the majority of human cancers, including breast and colon carcinomas, osteosarcoma, prostate tumor and hepatic stellate cells (3,9,18–21). The present study indicated that butein inhibits cell proliferation of lung cancer in a dose-dependent manner, which is in agreement with previous studies (3,18–21).

COX-2 is inducible by inflammatory stimuli, including cytokines, growth factors, and tumor promoters, and is upregulated in a variety of malignancies and favors the growth of malignant cells by stimulating proliferation and angiogenesis (22,23). In previous years, a large number of studies demonstrated that COX-2 is overexpressed in ovarian cancer (24–26). Furthermore, Arico et al (27) found that COX-2 is capable of inducing angiogenesis via the vascular endothelial growth factor and prostaglandin production and may also inhibit apoptosis by inducing the antiapoptotic factor Bcl-2, as well as activating antiapoptotic signaling through Akt/protein kinase B. These results suggest that COX-2 is important in the generation and progression of solid tumors, and that inhibition of COX-2 may inhibit the growth of a variety of solid malignancies. In the present study, butein mediated the downregulation of COX2 expression in human lung cancer cells and induced cancer cell apoptosis, which may be a key molecular mechanism of butein in anticancer therapy.

In conclusion, butein was observed to decrease COX-2 expression in cancerous lung cells in the current study. Considering the importance of COX-2 in lung carcinogenesis, the findings may provide the scientific basis for potential pharmaceutical application of butein.

Acknowledgements

This study was supported by grants from the National Natural Science Foundation of Jilin (Project no. 83657488).

References