Background
Nasopharyngeal carcinoma (NPC) remains endemic among ethnic Chinese and the Inuits of Alaska. It is a distinct entity of head and neck cancers because of its characteristic epidemiology, pathogenesis, and association with the Epstein-Barr virus [
1]. Metastasis of cancer cells to the neck lymph nodes, which can occur in up to 75% of NPC patients, represents an adverse prognostic factor of the disease [
2]. Distant metastases, such as those to the lungs, liver, and bone, remain a major cause of treatment failure [
3]. Metastasis is a phenomenon composed of multiple sequential cascades and various cyto-physiologic changes, including reduction of tumor cell adhesion, degradation of extracellular matrix (ECM), enhancement of cell motility, and promotion of neo-vascularization [
4]. Thus, a degradation of the ECM and components of the basement membrane caused by the concerted action of proteinases like matrix metalloproteinases (MMPs), cathepsins, and plasminogen activators (PA) play an important role in tumor invasion and metastasis [
5,
6]. Among these enzymes, MMP-2 and MMP-9 can degrade most ECM components and are profoundly involved in the development of cancer invasion and metastasis [
7,
8]. Therefore, the inhibition of MMP-2 or MMP-9-mediated migration or invasion may be a preventive method of limiting cancer metastasis.
Selaginella tamariscina (Beauv.) is a traditional Chinese herbal medicine for chronic trachitis. Its major constituents are flavonoids (e.g. amentoflavone, hinokiflavone, sotetsuflavone, and apogenin) and saccharides (e.g. trehalose, d-glucose, dfructose and d-rhamnose) [
9‐
11]. Previous studies have demonstrated that
Selaginella tamariscina possesses anti-bacterial, anti-hypertensive, and anti-hyperglycemic effects [
10,
12,
13]. Moreover,
Selaginella tamariscina has been shown to have anti-tumor activities, probably via an expression of the p53 tumor suppressor gene and an induction of G1 arrest in the cell cycle against certain tumor cell lines [
14]. Recently, Yang et al. found that
Selaginella tamariscina extract (STE) can down-regulate the expression of MMPs and u-PA, and inhibit the invasion and metastatic activities of lung cancer cells [
15]. There is, however, no data about the anti-metastatic potential of STE on NPC cancer cells. Thus, this study examined the effects of aqueous extracts of
Selaginella tamariscina with potential anti-metastatic properties in 12-O-tetradecanoylphorbol-13-acetate (TPA)-treated human NPC HONE-1 cells
in vitro to investigate the signaling pathway of the process.
Methods
Preparation of Selaginella tamariscina extracts
Selaginella tamariscina (Beauv.) leaves were purchased from herb stores in Taichung, Taiwan and the
Selaginella tamariscina extracts (STE) were prepared as described previously [
16]. The plant material was identified at the Department of Biochemistry of Chung Shan Medical University in Taichung and a voucher specimen is deposited. Briefly, 100 g of air-dried leaves were boiled at 70°C for 24 hours with 500 mL of 50% ethanol. The extraction procedure was repeated twice. The solvent was removed from the combined extract using a vacuum rotary evaporator. The filtrate was then lyophilized and stored at −20°C until further studies were to be conducted. A voucher specimen was deposited in the National Research Institute of Chinese Medicine, Taiwan [
16].
The extraction yield was 2.8% (w/w) and the chemical profile of STE was analyzed using high-pressure liquid chromatograms (HPLC)-mass spectrometer. Briefly, the STE was analyzed by Hitachi L-6200 with an L-4500 Diode Array detector with a PE Sciex Qstar Pulsar ESI-TOF mass spectrometer. Samples (10 μl) were injected onto a Merck LiChrospher 100 RP-18 column (4mm×250 mm). The column was equilibrated in 0.05% acetic acid/water (solution A) and elution of the components was achieved by increasing the concentration of solution B (100% acetonitrile) from 0 to 100% in 30 min at a flow rate of 1 ml/min. Absorbance was monitored at 254 nm. The molecular masses of the peaks were determined from electro-spray ionization mass spectra using a multiply-charged ion profile based on the modified method of Chang et al. [
17]. For subsequent experiments, the STE powder was dissolved in dimethyl sulfate (DMSO) to achieve designed concentrations (0, 25, 50, 75, and 100 μg/mL).
Cell and cell culture
A human nasopharyngeal carcinoma cell line from ATCC (Manassas, VA), HONE-1 cells, was cultured in RPMI-1640 medium (Life Technologies, Grand Island, NY), 10% fetal bovine serum, 2 mM glutamine, 100 U/ml penicillin, and 100 μg/ml streptomycin. All cell cultures were maintained at 37°C in a humidified atmosphere of 5% CO2. For STE treatment, appropriate amounts of stock solution of STE were added into the culture medium to achieve the indicated concentrations. The cells were then incubated for the indicated time periods. Dimethyl sulfoxide solution without STE was used as blank reagent.
Analysis of cell viability (MTT assay)
To evaluate the cytotoxicity of STE, an MTT colorimetric assay was performed to determine cell viability [
18]. Cells were seeded in 24-well plates at a density of 1×10
5 cells per well and treated with 0, 25, 50, 75, 100, 150 and 200 μg/mL of STE at 37°C in 5% CO
2 for 24 h and 48 h. At the end of the exposure period, the cells were washed with PBS and incubated with 0.8 mL of MTT (Sigma chemical Co., St. Louis, MO, USA) per well (final concentration, 0.5 mg/mL) at 37°C in 5% CO
2 for 4 h. The viable cell number was directly proportional to the production of formazan following solubilization with isopropanol, which was measured spectrophotometrically at 563 nm (Beckman Spectrophotometer DU640, Beckman Instruments, Fullerton, CA, USA).
Cell migration and invasion assays
Cell migration and invasion were assayed according to the methods described by Chu et al. [
19]. After treatment with STE for 24 h, the surviving HONE-1 cells were harvested and seeded to a Boyden chamber (Neuro Probe, Cabin John, MD, USA) at 10
4 cells per well in serum-free medium, and then incubated for 24 h at 37°C. To determine cell migration, the cells were seeded into the Boyden chamber on membrane filters that were not coated with Matrigel. The filters were then air-dried for 5 h in a laminar flow hood. The migrating cells were fixed with methanol and stained with Giemsa. The cell numbers were counted by light microscopy.
For the invasion assay, 10 μL Matrigel (25 mg/50 mL; BD Biosciences, MA, USA) was applied to 8 μm pore size polycarbonate membrane filters. The bottom chamber contained standard medium. The invasion of cells treated or untreated with STE was measured as in the migration assay.
Determination of MMP-9 activity by zymography
The activities of MMP-9 in the conditional medium were measured by gelatin zymography protease assays as previously described [
20]. Briefly, collected media of an appropriate volume were prepared with SDS sample buffer without boiling or reduction, and subjected to 0.1% gelatin-8% SDS-PAGE electrophoresis. After electrophoresis, the gels were washed with 2.5% Triton X-100 and incubated in a reaction buffer (40 mM Tris–HCl, pH 8.0; 10mM CaCl2 and 0.01% NaN3) at 37°C for 12 h. The gel was stained with Coomassie brilliant blue R-250 for visualization.
RNA preparation and TaqMan quantitative real-time PCR
Total RNA was isolated from cancer cells using Trizol (Life Technologies, Grand Island, NY) according to the manufacturer’s instructions. Quantitative real-time PCR analysis was performed using TaqMan one-step PCR Master Mix (Applied Biosystems). Total cDNA (100 ng) was added per 25 μl reaction with MMP-9 or GAPDH primers and TaqMan probes. The MMP-9 and GAPDH primers and probes were designed using commercial software (ABI PRISM Sequence Detection System; Applied Biosystems). The oligonucleotide sequences of TaqMan probes and primers were described in Table
1. Quantitative real-time PCR assays were conducted in triplicate on a StepOnePlus sequence detection system. Threshold was set above the non-template control background and within the linear phase of target gene amplification to calculate the cycle number at which the transcript was detected [
21].
Table 1
Primers list for real-time PCR assay
MMP-9 (Hs00957562_m1) | (FAM)- GGCGCTCATGTACCCTATGT |
GAPDH ( Hs99999905_m1) | (FAM)-GGCGCCTGGTCACCAGGGCTGCTTT |
The HONE-1 cells were seeded at a concentration of 5 x10
4 cells per well in 6-well cell culture plates. After 24 h of incubation, pGL3-basic (vector) and MMP-9 promoter plasmid were co-transfected with a β-galactosidase expression vector (pCH110) into cells using Turbofect (Fermentas, Carlsbad, CA) as previously described [
20]. After 12 h of transfection, the cells were treated with vehicle or STE (0~50 μg/mL) for 24 h. The cell lysates were harvested and luciferase activity was determined using a luciferase assay kit. The value of the luciferase activity was normalized to transfection efficiency and monitored by β-galactosidase expression.
Western blot analysis for determining molecular pathway
Total cell lysates or nuclear extracts were prepared as previously described [
22]. The cell lysates were separated in a 10% polyacrylamide gel and transferred onto a nitrocellulose membrane. The blot was subsequently incubated with 5% non-fat milk in Tris-buffered saline (20 mM Tris, 137 mM NaCl, pH 7.6) for 1 h to block non-specific binding, and then overnight with polyclonal antibodies against three MAPKs (ERK 1/2, JNK ½, and p38), Src, FAK, and β-actin with the specific antibodies for unphosphorylated or phosphorylated forms. The blots were then incubated with horseradish peroxidase goat anti-rabbit or anti-mouse IgG for 1 h.
Signal was detected by using an enhanced chemi-luminescence (ECL) commercial kit (Amersham Biosciences). The relative photographic density was quantitated by scanning the photographic negatives on a gel documentation and analysis system (AlphaImager 2000, Alpha Innotech Corporation, San Leandro, CA, USA).
Statistical analysis
Statistically significant differences were calculated using the Student’s t-test (Sigma-Stat 2.0, Jandel Scientific, San Rafael, CA, USA). Significance was set at p<0.05. The values are the means ± standard deviation (SD) of at least three independent experiments.
Discussion
The nasopharynx is situated over the base of the skull where lymphatic tissues and circulation are rich. Metastases of nasopharyngeal cancer cells to the neck lymph nodes and distant organs are common in NPC patients, even in the early stage of the disease. Herbal medicines are a popular practice of healthcare in eastern countries. Numerous studies have shown that they are beneficial in the treatment of many diseases, including cancers [
23]. Although the anti-tumor activities of several herbal medicines against human NPC cells have been demonstrated previously [
24,
25], there is no data in current literature regarding the anti-metastatic activity of herbal medicine for NPC cells. The present study demonstrates that the extract of
Selaginella tamariscina can significantly inhibit the migration and invasion ability of HONE-1 cancer cells, suggesting a potential role in the treatment of metastatic NPC.
A degradation of the ECM and components of the basement membrane by MMPs play a crucial role in the development of cancer metastasis.
In vivo evidence from chicken chorio-allantoic membrane (CAM) assay shows that MMP-9 is inter-dependent in tumor invasion, while tumor cells show only low levels of invasion in the absence of MMP-9 [
26]. Itoh et al. also report that metastatic colonies are seldom observed in MMP-9-deficient mice injected intravenously with melanoma or lung carcinoma cells [
27]. Clinically, the positive relationships between MMP-9 and metastasis in patients with NPC have been reported [
28,
29]. The results in the present study demonstrate that STE inhibits the migration and invasion of human NPC HONE-1 cells via decreasing the MMP-9 protein levels (Figure
3). To date, this is the first scientific report related to the inhibitory effect of STE on NPC invasiveness via decreased production of tumor metastasis-related proteins. Since several studies have indicated that inhibition of MMP expressions or enzyme activities can be used as early targets for preventing cancer metastasis [
30‐
32],
Selaginella tamariscina may be a potential candidate for cancer treatment.
The expression of MMP-9 can be regulated by an inflammatory cytokine, a growth factor, or an oncogene through activation of different intracellular-signaling pathways [
33]. Among these stimulators, TPA is a well-known substitute for diacylglycerol as a high affinity ligand for conventional protein kinase C (PKC). It can induce MMP-9 expression and result in an increase in invasion in various malignant cell lines [
34]. FAK, one of the major kinases of focal adhesions, is a vital regulator involved in focal adhesion assembly and cell migration. FAK becomes activated when it is phosphorylated at tyrosine 397 (Y397). It is associates with Src and forms a dual kinase complex [
35]. Activated Src phosphorylates FAK, thereby creating a signaling cascade through the Ras and mitogen-activated protein kinase (MAPK) [
36].
Moreover, the activation of one or more MAPK pathways (e.g. ERK1/2, JNK and p38) is known to be important for the MMP-9 induction by TPA in various cell types [
37‐
40]. The present study shows that the TPA-induced MMP-9 expression of HONE-1 cells is accompanied by an increase of phosphorylation of Src, FAK, ERK1/2, JNK and p38. The MAPKs inhibitors test suggests that TPA induces MMP-9 expression through the ERK1/2 and p38, but not the JNK, pathways. It can be assumed that the inhibitory effects of STE on TPA-induced MMP-9 activity of HONE-1 cells may be through the inactivation of the signaling pathways of TPA induction. The results here reveal that STE treatment of TPA-induced HONE-1 cells inhibit MMP-9 expression and ERK1/2 phosphorylation without affecting JNK and p38 phosphorylation (Figure
6). This indicates that participation of the Src/FAK/ErK 1/2 pathway is the putative mechanism for the inhibition of MMP-9 synthesis by STE in human NPC HONE-1 cells.
Several flavonoid compounds have been isolated from
Selaginella tamariscina, including amentoflavone, apigenin, hinokiflavone, and sotetsuflavone [
9,
10,
41]. Previous studies have shown that amentoflavone can reduce histamine release from rat peritoneal mast cells [
42], while apigenin can inhibits the production of MMPs in various malignant tumors [
43,
44]. Oozes et al. report that pro-inflammatory signals are mediated by TNF-α via pathways of nuclear factor-κB (NF-κB) and Akt [
45]. Ruiz and Haller have demonstrated that apigenin inhibits the pro-inflammatory gene expression in intestinal epithelial cells by blocking Akt phosphorylation/activity [
46]. These findings suggest that flavonoids may be the active compounds responsible for the anti-metastatic activity of
Selaginella tamariscina. Further investigations on the exact effective components of STE are warranted to determine its potential use in oncology.
Conclusions
In conclusion, extract of Selaginella tamariscina prevents the metastasis of HONE-1 cells by the transcriptional inhibition of the MMP-9 expression and activity through a down-regulation of ERK1/2 signaling pathways. These results suggest that Selaginella tamariscina has the ability to exert inhibitory effects on critical steps in metastasis, including cellular mobility, migration and invasion. However, the interpretation of this study is limited because the lack of an in vivo animal study. Selaginella tamariscina should be further tested by an in vivo model to determine if it is effective in the prevention of nasopharyngeal carcinoma invasion or metastasis.
Competing interests
The authors have no competing interests.
Authors’ contributions
CHH, CWL, and MKC conceived and designed the study. BCW, SFY and CYC performed the experiments. YHH, HYH and HPL analyzed the data. CWL and MKC drafted the manuscript. CWL revised the manuscript. MKC provided comments and editorial review of the manuscript. All authors read and approved the final manuscript.