Introduction
Pancreatic cancer (PanCa) remains a lethal disease [
1]. There is increasing evidence suggesting that many factors such as smoking, stress, chronic depression and a high-fat diet, with cardiovascular disease and stress patients may contribute to PanCa genesis and development but the underlying mechanisms are not clear [
2‐
4]. Previous studies indicate that the enhanced tumour progression by smoking-stimulated nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) production and stress-stimulated autonomic activation of nervous system [
5,
6]. The autonomic activation of nerve system results in the release of catecholamines from the adrenal gland and sympathetic nerve terminals. Further studies suggest that both NNK and constantly high level of catecholamines modulate the activity of multiple components of the tumour microenvironment and consequently promote tumour-cell growth via β-adrenoceptors [
4,
7‐
9].
β-adrenoceptors are members of the superfamily of G protein-coupled adrenergic receptors, which mediate actions of the endogenous catecholamines in a variety of target cells [
10,
11]. β
1- and β
2-adrenoceptors have been found to be expressed in the BxPC-3, MIA PaCa-2, and Panc-1 cell lines [
12‐
14]. NNK functions as a β-adrenergic agonist and it has been shown that the binding of NNK or catecholamines to the β-adrenoceptors induce PanCa cell proliferation by activating the cyclic adenosine monophosphate (cAMP)/protein kinase A (PKA) pathways in PanCa cells [
15]. The consequence of PKA signalling leads to the transcriptional activation of proteins involved in proliferation via cAMP response element binding protein (CREB), activator protein 1 (AP-1) or NF-κB [
15‐
17]. Recent reports have shown that the agonists of the β
2-adrenoceptor stimulate the activation of Ras and Src tyrosine kinases via the mitogen-activated protein kinase (MAPK) pathway in cancer cells and fibroblasts [
18‐
20]. Ras activates several signalling pathways that lead to transcriptional activation of genes related to cell proliferation and antiapoptotic signalling cascades, including the Raf/MEK/extracellular signal-regulated kinase (ERK) and phosphatidylinositol 3-kinase (PI
3K)/ATP-dependent tyrosine kinases (Akt)/Phosphatase and tensin homolog deleted on chromosome 10 (PTEN) pathways and NF-κB [
17,
21].
Previous studies suggested that β-adrenergic antagonists may suppress cell proliferation and invasion and induce apoptosis in PanCa [
14,
22], and also β
2-adrenergic agonist can stimulate the production of cAMP and activation of G-protein effectors Gs [
23]. However, the mechanism of PanCa cell death induced by β
2-adrenergic antagonist is not clear. In this study, we determined the effects of β
2-adrenergic antagonist ICI118,551 on PanCa tumor growth and the underlying mechanism
in vitro and
in vivo.
Materials and methods
Tumor tissues, Cell lines and cell culture
Forty-eight pancreatic carcinoma specimens were obtained from the Department of Hepatobiliary and Pancreas Surgery, the First Affiliated Hospital of Xi'an Jiaotong University. The protocol was approved by The Human Research Review Committee at the University Hospital. The human ductal pancreatic adenocarcinoma cell lines, MIA PaCa-2 and the BxPC-3 were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA). The MIA PaCa-2 cell line harbours an activating point mutation in codon 12 of the k-ras gene, whereas BxPC-3 does not have that k-ras mutation [
24]. The cells were cultured in DMEM (Gibco, Grand Island, NY, USA) with 10% (v/v) heat-inactivated FBS (Gibco, Grand Island, NY, USA), penicillin (100 U/ml) and streptomycin (100 mg/ml)at 37°C with 5% CO
2 and 95% relative humidity. Before each experiment, cells were seeded at a density of 5 × 10
4 cells/cm
2.
Immunohistochemistry staining
Immunohistochemical staining for β1-adrenoceptor and β2-adrenoceptor were performed using the SABC kit according to the manufacturer's instruction (Abfrontier, Korea). The sections were incubated with primary antibodies (Abcam, Cambridge, MA, USA) overnight at 4°C and then incubated with the appropriate biotinylated secondary antibody (Abcam, Cambridge, MA, USA) for 30 min at room temperature. Sections were then incubated with avidin/biotin complexes for 30 min at room temperature. Following washing in PBS, immunoreactivity was visualized by using DAB reaction followed by hematoxylin counter staining. For evaluation of protein expression, the staining intensity was graded as 0 (negative), 1 (weak), 2 (medium) or 3 (strong). The slides were graded by two investigators. The densitometry analysis of immunohistochemical staining was performed using the Image-Pro Plus 4.5 software.
Cell cycle analysis
The cells after treatment were stained with propidium iodide (PI) and then analysed using flow cytometry for cell cycle according to the manufacturer's protocol. After stimulation for 24 h with ICI118,551 (100 μM) [
13,
14,
25] (Sigma Chemical, St. Louis, MO, USA), MIA PaCa-2 and BxPC-3 cells were fixed in ice-cold 70% ethanol at 4°C. On the day of analysis, the cells were then centrifuged (400 × g for 5 min) and washed once in staining buffer. After centrifugation, the cells were resuspended in 100 μL of staining buffer. The cells were then treated with RNase A and incubated for 30 min at 37°C. After RNase A digestion, the cells were stained for 30 min at room temperature (protected from light) with 10 μg of PI in a final volume of 0.5 mL of staining buffer. The samples were then analysed by flow cytometry. The percentages of cells in G0-G1, S, and G2-M were calculated using the ModFit computer program.
Animal studies and subrenal capsular assay
BALB/c athymic nude mice, 4 to 6 weeks old (Shanghai Experimental Animal Center (Chinese Academy of Sciences, China) were used for the subrenal capsule assay. PanCa xenografts were generated by implantation of MIA PaCa-2 and BxPC-3 cells into one flank of athymic nude mice. Each group contains n ≥ 8 male athymic nude mice (10 mice each group). On the day of the experiment, mice were anesthetized, and the left kidney was exposed. The same number of cells (1 × 108) in 25 μl was then injected into each mouse under the left renal capsule. After three days, a 5 mg/kg/dose of ICI118,551 was intraperitoneally injected into the mice every day. After inoculation with the tumor cells, mice were observed and sacrificed on day ten, when their left kidneys were excised. The left renal capsule were fixed in 10% neutral buffered formalin and processed in paraffin. Sections were cut on a microtome and mounted on glass slides. For histopathology, routine H&E staining was carried out. Animal care and experiments were carried out in accordance with the guidelines of the Xi'an Jiaotong University.
Electron microscopy
To evaluate the morphological features of cell death, the cells in the control group or cells treated with or without ICI118,551 (100 μM) were processed for transmission electron microscopy (TEM). Briefly, cells were pelleted by centrifugation and fixed with 2.5% glutaraldehyde in 0.1 M cacodylate buffer, pH 7.4 for 1 h at 4°C. After rinsing with cacodylate buffer, the specimens were fixed in 1% cacodylate-buffered osmium tetroxide for 2 h at room temperature, dehydrated in a graded series of ethanol, briefly transferred to propylene oxide and embedded in Epon-Araldite. Ultrathin sections (60-80 nm thick) were cut with a diamond knife, placed on formvar-carbon coated copper grids (200 mesh), stained with uranyl acetate and lead citrate and observed with a Jeol 100 SX TEM.
Determination of cell apoptosis by hoechst 33342 fluorescent staining
The cell death was assessed using Hoechst staining. Briefly, cells were seeded in 24-well plates at 5 × 104 cells/well and treated with ICI118,551 (100 μM) for 24 h. After treatment, cells were stained with 10 μg/ml Hoechst 33342 dye (Sigma Chemical, St. Louis, MO, USA). Fixed cells were incubated overnight at 4°C and visualized under a 365 nm UV light microscope. Quantitative analysis was performed by counting the blue fluorescent (apoptosis positive) cells from three independent fields at 400× magnification. Values were expressed as the percentage of apoptotic cells relative to the total number of cells per field.
Analysis of the apoptosis rate by Annexin V-FITC/PI
The apoptosis rate was measured using Annexin V-FITC/PI double staining followed by flow cytometry (FCM) according to the instructions (BD Biosciences, San Jose, CA, USA). After treatment with metoprolol (25-200 μM) and ICI118,551 (25-200 μM) for 24 h, MIA PaCa-2 and BxPC-3 cells were washed once with ice-cold PBS and resuspended in binding buffer at a concentration of 1 × 106 cells/ml. A total of 5 μL of Annexin V-FITC and 10 μL of 20 mg/mL PI were added to the cells, and the mixture was incubated for 15 min in the dark prior to the addition of 400 μl of PBS. Quantitative analysis of the apoptotic level was performed using a flow cytometer (BD Biosystems, CA, USA).
Electrophoretic mobility shift assays (EMSA)
The activity of NF-κB in PanCa cells was determined using An EMSA. Binding reaction mixtures (20 μl) containing 3 μl of nuclear extract protein (2-5 μg/μl), 1 μl of poly (dI-dC) in 10 mM Tris and 1 mM EDTA (1 μg/μl), 1 μl of MgCl2 (100 mM), 2 μl of 25 mM DTT/2.5% Tween-20, 1 μl of 1% NP-40, 2 μl of 10 × Binding Buffer (100 mM Tris, 500 mM KCl, 10 mM DTT, pH 7.5), 1 μl of IRDye™ end labelled oligo probe (50 nM) (LI-COR Biosciences, Lincoln, NE, USA) and 9 μl of Ultra Pure water were incubated for 30 minutes at room temperature. Proteins were separated by electrophoresis in a native 5% polyacrylamide gel at 4°C in running buffer (12.5 mM Tris borate, 0.25 mM EDTA; pH 8.0), then imaged using the LI-COR Bioscience Odyssey Imaging System according to the manufacturer's instructions. The sequence of the NF-κB-specific probe was 5'-AGT TGA GGG GAC TTT CCC AGG C-3'.
Western blotting analysis
The MIA PaCa-2 and BxPC-3 cells were treated with metoprolol (100 μM) and ICI118,551 (100 μM) for 24 h. The proteins were then extracted from the treated cells. The supernatant was collected and the total protein concentration was measured using the BCA assay kit (Pierce, Rockford, IL, USA) according to the manufacturer's instructions. The total proteins were used for Western blotting analysis using specific antibodies against caspase-3, caspase-9, Bcl-2, Bax, cyclin D1, cyclin E (Abcam, Cambridge, MA, USA), pERK, ERK, pAkt, and Akt (Cell Signal Technology, Beverly, MA, USA). Thirty μg of total protein each sample was separated by 12% SDS-polyacrylamide gel electrophoresis (SDS-PAGE), and the protein was electrically transferred onto a nitrocellulose membrane (Millipore, Bedford, MA, USA). The membrane was then blocked with TBST (10 mM Tris-HCl, pH 7.4, 150 mM NaCl, 0.1% Tween-20) containing 5% w/v non-fat dry milk and incubated with the primary antibody in TBST at 4°C overnight. The membrane was washed three times and was then incubated with the secondary antibody for 2 h at room temperature. After washing three times for 10 min each with 15 ml of TBST, signallings were visualised by enhanced chemiluminescence (Pierce, Rockford, IL, USA) associated fluorography.
Statistical analysis
The data were analysed by one-way ANOVA, and by the nonparametric Kruskal-Wallis test. The relationship between β-AR expression and clinical-pathologic character were analysed by Chi-square test. Values were expressed as the mean ± SEM and the differences were considered statistically significant at P < 0.05.
Discussion
In this study, we have demonstrated that β-adrenoceptors are expressed in PanCa cells. Our data suggested that the β-adrenergic antagonists were associated with the inhibition of PanCa cell proliferation and the induction of apoptosis and G1/S phase arrest. In addition, these effects mediated by the β2-adrenergic antagonist were associated with the decreased expression of pERK1/2, pAkt, and the activation of NF-κB. Furthermore, we have found that the β2-adrenergic antagonist ICI118,551 significantly increased PanCa cell apoptosis and G1/S phase arrest. The effects of ICI118,551 on the rate of apoptosis and on G1/S phase arrest were stronger than the β1-adrenoceptor antagonist metoprolol.
The G
1/S phase transition is a particularly important cell cycle control point. The cyclin D1 is a critical cell cycle regulatory protein and required for the progression through G1 to S phase [
17,
26]. The growth stimulatory signals in the form of increasing levels of cyclin D1 are received by the cells in the early stage of G
1, which are then followed by increasing levels of cyclin E at the later stage [
26]. ICI118,551 could remarkably down-regulate cyclin D1 and cyclin E expression, indicating that the negatively regulatory effect of the ERK and Akt pathway on the PanCa cell might be associated with the inhibition of NF-κB activation, a decrease in cyclin D1 expression and a delay in the G
1/S transition, and cell cycle process. Our data has demonstrated that ICI118,551 could disengage the prevention of apoptosis in PanCa cells via suppression of the ERK and Akt pathways and NF-κB activation, and consequently limited the activation of Bax, caspase-9, and caspase-3. The ERK and Akt pathway can phosphorylate Bad, which allows Bcl-2 to form homodimers that result in the generation of an antiapoptotic response. This phosphorylation allows Bcl-2, Bcl-XL, and Mcl-1 to bind Bax and prevent its activation [
27‐
29].
The Ras pathway is commonly altered in PanCa. Activating point mutations in the
K-ras gene are common in ductal pancreatic carcinomas. NNK induces activating point mutations in the
ras gene, so it is conceivable that the binding of NNK to β
2- adrenoceptors may stimulate this pathway via further activation of the Src tyrosine kinase and Ras. The effects of the β
2-adrenergic antagonist ICI118,551 on the G
1/S phase arrest and apoptosis are stronger in the BxPC-3 cells (expressing wild-type k-ras) than in the MIA PaCa-2 cells containing a k-ras mutation. Therefore, it suggests that k-ras may be a key molecule involved in the blockage of the β-adrenoceptor resulting in G
1/S arrest and apoptosis in PanCa cells. Previous study suggested that β
2-adrenergic receptor antagonist induces cell death by inhibiting the Ras/Raf/Erk1/2 and PI3K/Akt pathways and mitochondrial death pathway [
30]. Our results demonstrated that β
2-adrenergic receptor antagonist induced cell death in MIA PaCa-2 and BxPC-3 cells is independent of the mitochondrial Apaf-1/caspase-9 pathway.
Strategies to block β-adrenoceptors might be used to prevent cancer in smokers and stress patients, and for the prevention of cancer relapse and metastasis after conventional chemotherapy or surgical resection [
4,
15]. Considering that the β
2-adrenergic antagonists could be developed as therapeutic and preventive agents, we suggest that understanding the relationship between β
2-adrenoceptor signalling and G
1/S phase arrest and apoptosis may provide a new strategic therapy for pancreatic cancer.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
DZ, ZW, MZ, and KG carried out the experimental work, FW provided data analysis, QM provided tumor samples, clinical information, and histopathological analysis, DZ, ZW, QM, FW, and EW designed the study and participated in writing the paper. All authors read and approved the manuscript.