Interferon-λ1 induces G1 phase cell cycle arrest and apoptosis in gastric carcinoma cells in vitro
- Zhitao Gao
- Moli Zhu
- Yaping Wu
- Pan Gao
- Zhihai Qin
- Hui Wang
- Published online on: May 15, 2014 https://doi.org/10.3892/or.2014.3185
- Pages: 199-204
Interferon-λ (IFN-λ), type III IFNs, the newest IFN family, includes 3 subtypes, IFN-λ1, -λ2 and -λ3, also known as interleukin-29 (IL-29), IL-28A and IL-28B. All of the IFN-λs bind the same heterodimeric receptor complexes composed of the IL-10 receptor β (IL-10Rβ) and a novel IL-28 receptor α (IL-28Rα) (1,2). Interferons (IFNs) have been described as agents mediating antiviral responses for many years. Type I IFNs, IFN-α/β, have been clinically applied for treating certain types of malignancies for more than 30 years, yet a wide range of adverse effects hampered further clinical applications (3,4). However, further investigations are required to clarify the biological properties and the mechanisms responsible for their functions. Type III IFNs, IFN-λs, have similar signaling pathways as IFN-α/β and inhibit the proliferation of tumor cells through cell cycle arrest or apoptosis.
Gastric carcinoma is an intractable disease, with a high incidence and mortality rate, as it frequently develops in the aged (5–7). Extensive surgery decreases the quality of life of patients, and radical chemotherapy and radiotherapy are not often appropriate for aged patients (8). A novel therapeutic strategy is thereby required to improve prognosis. More effective, preventive and therapeutic approaches are urgently needed. Type I IFNs have been clinically examined in various types of malignanies including gastric carcinoma. Yet, type I IFNs are associated with numerous serious adverse effects, e.g. major depression. Type III IFNs have various immunological actions similar to type I IFNs. However, IFN-λ-mediated growth suppression has not yet been well explored.
Research has shown that the IFN-λs may have unique cellular functions distinct from their role as secreted cytokines (9). Yan et al found that the IFN-λs could inhibit lung carcinoma cell growth and produce antitumor effects (10). The same observation was also made by Steen et al that IFN-λs could sharply inhibit the proliferation of gastric carcinoma cells (11). These results indicate that IFN-λs may be a new therapeutic option for tumors. However, whether IFN-λs inhibit the growth of gastric carcinoma cells remains unknown.
In the present study, we examined the potential antitumor action of IFN-λ1 in human gastric carcinoma cell lines and the possible interaction between IFN-λ1 and human gastric carcinoma cells. The results indicated that IFN-λ1 plays a crucial role in inhibiting gastric carcinoma cells and provide the foundation for the use of IFN-λ1 in tumor therapy.
Materials and methods
Antibodies and reagents
Mouse anti-human monoclonal primary antibodies for β-actin, Bax, cytochrome c, apoptosis-inducing factor (AIF), p21, p27 and horseradish peroxidase-conjugated goat anti-mouse IgG antibodies were purchased from Cell Signaling (Beverly, MA, USA). RPMI-1640 and fetal bovine serum (FBS) were purchased from Gibco (Invitrogen, USA). Propidium iodide (PI) was purchased from Sigma-Aldrich (St. Louis, MO, USA). IFN-λ1 was purchased from R&D Systems (Minneapolis, MN, USA). Viable cells were measured with a cell proliferation assay kit [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; MTT] (Roche, USA). The Annexin V-FITC/PI apoptosis kit was purchased from Biosea Biotechnology Co. Ltd. (Beijing, China). All other reagents were purchased from Sigma-Aldrich unless otherwise mentioned.
Human gastric carcinoma HGC-27 and SGC-7901 cells were obtained from the Chinese Type Culture Collection (Institute of Cell Biology, Chinese Academy of Science, Shanghai, China) and cultured in RPMI-1640 medium containing 10% FBS, 100 IU/ml penicillin and 100 mg/ml streptomycin at 37°C in a humidified atmosphere of 5% CO2 and 95% air. After reaching 80–90% confluency, cells were collected by 0.25% trypsin detachment and centrifugation and then replanted into 96- or 6-well plates at an appropriate density according to the different experimental requirements. After a 48-h culture, all experiments were performed.
Cell viability assay
Cell viability was evaluated using the MTT assay. Cells were seeded in a 96-well plate at a density of 5×103 cells/well. The total volume was adjusted to 200 μl with growth medium. At 24 h after the seeding, cells were treated with different concentrations of IFN-λ1 (0, 10, 100, 1000 ng/ml). Cell viability was examined after 48 h using a standard MTT method. Drug effect was expressed as a percentage relative to the controls. The rate of cell viability was calculated as follows: (absorbance of treated group - absorbance of blanks)/(absorbance of control - absorbance of blanks) × 100 expressed as a percentage.
Flow cytometry and cell cycle analysis
The apoptotic cells were detected using the Annexin V-FITC apoptosis kit. Briefly, the treated cells were collected by 0.25% trypsin and centrifuged, then washed with ice-cold phosphate buffer solution and resuspended in 200 μl binding buffer at a density of 1×106/ml. Ten microliters of Annexin V-FITC antibody was added, and cells were incubated for 30 min at room temperature and supplemental 300 μl of binding buffer was added and cells were stained with 5 μl PI for 5 min. The apoptotic cells were measured by flow cytometry (FACScan, Becton-Dickinson, Mountain View, CA, USA). For synchronization at G1 phase, cells were cultured with IFN-λ1 and fixed in ice-cold 70% ethanol, treated with RNase (50 μg/ml) and stained with PI (50 μg/ml). Cell cycle distribution was analyzed with FACScan and Cell Quest software.
Detection of mitochondrial membrane potential (ΔΨm)
The mitochondrial membrane potential ΔΨm was determined using the KeyGEN mitochondrial membrane JC-1 kit (KeyGEN, China) according to the manufacturer’s instructions (12). Briefly, after cells were infected with viral particles for the indicated times, the cells were pelleted, washed with PBS and resuspended in 0.5 ml of diluted JC-1 reagent (1 μmol/ml in incubation buffer) for 20 min. Then 0.2 ml of incubation buffer was added, and the cells were centrifuged, washed and resuspended in 1 ml PBS for laser scanning confocal microscopy (Olympus, Japan) and flow cytometry.
Western blot analysis
Cells were treated with IFN-λ1 for 48 h and washed with phosphate-buffered saline and then resuspended in RIPA buffer (25 mM Tris-HCl, pH 7.6, 150 mM NaCl, 1% Nonidet P-40, 1% sodium deoxycholate, 0.1% SDS) with a protease inhibitor cocktail (Sigma-Aldrich). SDS-PAGE was performed with 12% polyacrylamide gels, and portions (25 μg) of protein of the cell lysate were used. After electrotransfer, membranes were blocked for 1 h at room temperature with 6% Quick-Blocker (Chemicon, Temecula, CA, USA) dissolved in TBST [20 mM Tris-HCl, 137 mM NaCl, 0.1% (v/v) Tween-20, pH 7.6], then incubated overnight at 4°C with the different primary antibodies at the appropriate dilution in TBS-T buffer. The following monoclonal antibodies were used: anti-p21 antibody (Ab), anti-p27 Ab, anti-Bax Ab, anti-Bcl-2 Ab, anti-caspase-3 Ab, anti-caspase-9 Ab, anti-cytochrome c Ab and anti-apoptosis-inducing factor (AIF) Ab (Cell Signaling, Beverly, MA, USA), followed by incubation with a horseradish peroxidase-conjugated secondary antibody. The membranes were developed with the ECL system (GE Healthcare, Little Chalfont, UK) and exposed to X-ray film. The anti-β-actin antibody was used as an internal control for sample loading.
The results from the in vivo studies are representative of at least 2–3 independent experiments and are expressed as mean ± SD. The differences between the groups were examined using one-way analysis of variance (ANOVA) using the Statistical Package for the Social Sciences (SPSS) 14.0 software (SPSS Inc., Chicago, IL, USA). Statistical significance was assumed at P<0.05 in all cases.
IFN-λ1-mediated growth suppression
We examined whether IFN-λ1 could suppress the growth of the gastric carcinoma cells. We treated the HGC-27 and SGC-7901 cells with IFN-λ1 and examined the viability and the cell proliferation rates. Compared with the control group, IFN-λ1 treatment significantly inhibited the proliferation of the gastric carcinoma cells in a concentration-dependent manner (Fig. 1).
IFN-λ 1 inhibits cell proliferation in the HGC-27 and SGC-7901 cells. (A) HGC-27 and (B) SGC-7901 cells were incubated with the indicated concentrations of IFN-λ 1 for 48 h, and cell proliferation was determined by the MTT assay. The values shown are the mean ± SD from five replicated wells for each treatment and are expressed as a percentage of the control cells. Significance of the differences to the control cells was analyzed using one-way ANOVA (*P<0.05;**P<0.01). IFN-λ1, interferon-λ1.
G1 phase arrest induced by IFN-λ1
To explain the mechanism of cell growth inhibition by IFN-λ1 concerning cell cycle change, we analyzed the effects of IFN-λ1 treatment on the cell cycle. As shown in Table I, the percentage of cells in the G1 phase increased, whereas the percentage of cells in the G2 and S phases decreased (Fig. 2). These results demonstrated that IFN-λ1 induced G1 phase arrest in the gastric carcinoma cells.
Cells were infected with the indicated concentrations of IFN-λ1 and cultured for 48 h. Cell cycle profiles of (A) HGC-27 and (B) SGC-7901 cells were analyzed using flow cytometry, and the data are shown in mean percentages with s.e.s (n=3). *P<0.05, **P<0.01, comparison between IFN-λ1-treated and control cells. IFN-λ1, interferon-λ1.
Mitochondrial membrane potential ΔΨm
To confirm the effects of IFN-λ1 on gastric carcinoma cell mitochondria in vitro, gastric carcinoma cells were treated with different concentrations of IFN-λ1. Changes in mitochondrial membrane potential of the cells were detected using laser scanning confocal microscopy (Fig. 3A and 3B) and flow cytometry (Fig. 3C). It was obvious that the mitochondrial membrane potential was decreased after treatment with IFN-λ1 (Fig. 3D). Based on the results above, we hypothesized that IFN-λ1 may induce apoptosis through pathways that downregulate mitochondrial membrane potential.
Measurement of mitochondrial membrane potential (MMP) was determined using JC-1 probe. JC-1 is widely used to monitor mitochondrial membrane depolarization. (A and B) In the IFN-λ1 untreated cells (Con) with high mitochondrial membrane potential, JC-1 spontaneously formed complexes known as J-aggregates with intense red fluorescence. Whereas, in the IFN-λ1-treated or apoptotic cells with low mitochondrial membrane potential, JC-1 remained in the monomeric form, which shows only green fluorescence. Thus mitochondrial depolarization was indicated by a decrease in red/green fluorescence intensity ratio. (C) Flow cytometric analysis of mitochondrial membrane potential in the HGC-27 and SGC-7901 cells. (D) Data are expressed as mean ± SEM (n=3). Columns not sharing the same superscripted letter differ significantly; aP<0.05 and bP<0.01. IFN-λ1, interferon-λ1.
Apoptosis induction by IFN-λ1 treatment
Apoptosis was confirmed by Annexin V and PI staining. As shown in Fig 4, the Annexin V+/PI fraction and subsequently the Annexin V+/PI+ fraction of the gastric carcinoma cells were increased following IFN-λ1 treatment. These data collectively suggest an apoptotic effect of IFN-λ1 in gastric carcinoma cells.
Flow cytometric analysis of apoptosis. (A) HGC-27 and (B) SGC-7901 cells were treated with IFN-λ1 for 48 h or left untreated (Con). (C and D) The cell apoptosis rates were increased in both cell lines in a dose-dependent manner. Data are expressed as mean ± SEM (n=3). (*P<0.05;**P<0.01).
Expression of proteins involved in cell cycle progression and apoptosis
To understand the mechanism by which IFN-λ1 caused G1-phase cell cycle arrest, we examined the effects of IFN-λ1 on the induction of p21 and p27, which regulate the G1-phase checkpoint (13–15). IFN-λ1 treatment induced p21 and p27 expression in a concentration-dependent manner (P<0.05) (Fig. 5), suggesting that IFN-λ1 may regulate cell cycle arrest through p21 and p27.
Expression levels of apoptosis-linked proteins in the HGC-27 and SGC-7901 cells following IFN-λ1 treatment for 48 h. Expression levels of caspase-3, caspase-9, the respective cleaved forms, Bax, Bcl-2, cytochrome c and AIF in the cytoplasmic fraction were analyzed by western blot analyses. Actin expression is shown as a loading control for total cytoplasmic protein, respectively. IFN-λ1, interferon-λ1.
Disruption of the mitochondrial membrane potential is a critical event in triggering mitochondrial-mediated apoptosis. Mitochondrial dysfunction is induced by various cellular stimuli, causing the translocation of Bax from the cytosol to the mitochondria, which subsequently triggers the release of cytochrome c and AIF from the mitochondria into the cytosol and finally induces apoptosis via either caspase-dependent or caspase-independent pathways. To further clarify the mechanisms of apoptosis in the gastric carcinoma cells triggered by IFN-λ1, we targeted apoptotic proteins in the mitochondrial pathway. IFN-λ1 significantly increased Bax expression in the mitochondria (Fig. 5). IFN-λ1 also concentration-dependently upregulated the expression of cytochrome c and AIF proteins (P<0.05).
In recent years, increasing research has focused on the relationship between cytokines and tumorigenesis. It has been suggested that cytokines may be a new therapeutic option for tumors (16–20). In our experiments, we demonstrated that IFN-λ1 inhibited the growth of gastric carcinoma cells in a concentration-dependent manner. These data suggest that IFN-λ1 may be a potential antitumor agent for the treatment of gastric cancer.
Impaired apoptotic induction and dysregulated cell cycle progression are important factors in cancer development. Accordingly, inhibition of cell cycle regulation is particularly useful in the treatment of cancer. In our in vitro study, we demonstrated the apoptosis-inducing effects of IFN-λ1 in gastric carcinoma cells using PI cell cycle analysis, Annexin V and PI staining as well as activated caspase-3. Our study showed that IFN-λ1 induced G1 phase arrest and apoptosis in the gastric carcinoma cells.
Experimental evidence suggests that apoptosis can be mediated by several different pathways and that there are numerous regulatory molecules associated with these pathways. Proteins of the Bcl-2 family include both pro- and anti-apoptotic members that elicit opposing effects on mitochondria (21–23) Enhancement of pro-apoptotic Bax over Bcl-2 proteins can enhance the permeability of the mitochondrial membrane, which in turn results in the release of apoptogenic factors. Repression of anti-apoptotic members of this family, including Bcl-2 and Bcl-xl, preserves the integrity of the mitochondria. This blocks the release of soluble inter-membrane factors such as cytochrome c that activate effectors of apoptosis. In the present study, we found that treatment of gastric carcinoma cells with IFN-λ1 upregulated pro-apoptotic Bax protein and downregulated anti-apoptotic protein Bcl-2.
The alteration in the Bax/Bcl-2 ratio is critical for apoptosis and causes the release of cytochrome c from mitochondria into the cytosol after loss of mitochondrial membrane potential. Cytosolic cytochrome c can bind to Apaf-1 and activate caspase-9 in the apoptosomes in response to diverse inducers of cell death. Caspase-9 is activated and finally an increase in the activation or cleavage of caspase-3 results (24,25). It has been recognized that control of cell cycle progression in cancer cells is an effective strategy to inhibit tumor growth as the molecular analyses of human cancers have revealed that cell cycle regulators are frequently deregulated in most common malignancies. Our in vitro data demonstrated that treatment of gastric carcinoma cells with IFN-λ1 induced G1 phase arrest of cell cycle progression, indicating that one of the mechanisms by which IFN-λ1 inhibits the proliferation of gastric cancer cells is inhibition of cell cycle progression.
Regulation of the cell cycle at the G1 checkpoint is complex and involves multiple molecular processes. p21 appears to be important since introduction of nonfunctional p21 or a p21 antisense oligonucleotide diminished the G1 arrest in a variety of cancer cells (26,27). Apart from directly inhibiting cyclin-dependent kinase activity to promote cell cycle arrest, p21 interacts with proliferating cell nuclear antigens. Our results demonstrated elevated p21 and p27 levels in gastric carcinoma cells in response to IFN-λ1. It is possible that G1 arrest upon IFN-λ1 treatment here was caused by p21 and p27. Exposure to IFN-λ1 elevated the Bax level in the mitochondria, and stimulated the release of cytochrome c and AIF from the mitochondria into the cytosol, suggesting that IFN-λ1-induced apoptosis in gastric carcinoma cells is mediated by the mitochondrial pathway.
In conclusion, we demonstrated that IFN-λ1 induced G1 phase arrest and apoptotic cell death in gastric carcinoma cells through the activation of p21/p27 and the mitochondrial-mediated apoptotic pathway. In the present study, although the exact mechanism remains unclear, IFN-λ1 as a chemotherapeutic agent induces cell death and may be a potential therapeutic option for gastric cancers.
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