Overexpression of AKT decreases the chemosensitivity of gastric cancer cells to cisplatin in vitro and in vivo

Introduction

Gastric cancer is a prevalent health issue and remains a leading cause of cancer-related mortality worldwide (1). Cisplatin (CDDP) is an antineoplastic agent used for the treatment of several types of human cancer (2,3), including gastric cancer. However, the efficacy of these drugs is limited by CDDP resistance. To date, a number of mechanisms have been proposed to explain CDDP resistance, including AKT overexpression (4–7). A better understanding of the processes and mechanisms leading to CDDP resistance in gastric cancer cells is necessary to develop effective therapies which may provide a pharmacological intervention for acquired CDDP resistance in cancer.

AKT is a serine/threonine kinase and consists of a family of proteins, which include AKT1, AKT2 and AKT3 (8). The AKT pathway regulates diverse cellular processes, including cell proliferation, cell cycle progression and cell survival (9). AKT is additionally important in survival when cancer cells are exposed to various stress stimuli, including cytotoxic anticancer drugs (6). Previous studies have shown that AKT hyperactivation may correlate with the resistance of cancer cells to CDDP (10–12). In the present study, we observed that AKT expression levels were significantly increased when cells were treated with CDDP. Further experiments demonstrated that AKT activation may be associated with the Janus kinase 2 (JAK2)/signal transducer and activator of transcription 3 (STAT3) pathway. The data presented in this study may provide useful information with regard to the development of potential new therapeutic approaches for the treatment of gastric cancer by targeting the JAK2/STAT3/AKT pathway to overcome CDDP resistance.

Materials and methods

Cell lines and animals

BGC823 gastric cancer cells were obtained from the Cell Bank of Chinese Academy of Sciences (Shanghai, China) and maintained in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS), 100 mg/l penicillin and 100 mg/l streptomycin at 37°C in a humidified atmosphere of 5% CO2. The following antibodies were used: anti-AKT, anti-STAT3, anti-phospho-JAK2, anti-phospho-STAT3, STAT3 inhibitor (Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA), anti-phospho-AKT (Millipore, Billerica, MA, USA), anti-JAK2 (Cell Signaling Technology, Inc., USA), dichlorodihydrofluorescein diacetate (DCFDA; Sigma, St. Louis, MO, USA) and N-acetylcysteine (NAC; Sigma).

A total of 9 BALB/c-nu mice, 4–5 weeks old and 18–20 g in weight, provided by Beijing HFK Bioscience Co., Ltd. (Beijing, China), were bred in laminar flow cabinets and kept at a constant humidity and temperature (25–28°C) according to standard guidelines outlined in a protocol approved by Wuhan University, Wuhan, China.

Measurement of reactive oxygen species (ROS) production

BGC823 cells were treated with CDDP for 6 h. After washing with PBS, the cells were incubated with 33 mg/ml DCFDA in PBS for 30 min at 37°C. The excess probe was washed off and the labeled cells were measured using a microscope.

JAK2 siRNA transfection

BGC823 cells were transfected with JAK2 siRNA and control siRNA (Santa Cruz Biotechnology) according to the manufacturer’s instructions. Fresh medium without antibiotics was applied following 8 h of incubation, and following an additional 48 h, the medium was replaced with 10% FBS, 100 mg/l penicillin and 100 mg/l streptomycin. Cell growth was maintained.

Western blot analysis

The cells were solubilized in ice-cold lysis buffer (1X PBS, 1% Igepal CA-630, 0.5% sodium deoxycholate, 0.1% SDS and 10 mg/ml phenylephrine). Following 30 min of centrifugation at 13,000 g at 4°C, the supernatants were transferred to new microcentrifuge tubes and the protein concentration of the supernatant was measured using the BCA protein assay (Pierce Biotechnology, Inc., Rockford, IL, USA) and then stored at −80°C. Cell lysate (50 μg) was separated on an SDS-polyacrylamide gel. Following SDS-PAGE, the proteins were transferred onto nitrocellulose membranes. For detection of the proteins, the membranes were blocked using 10% non-fat dry milk in Tris-buffer containing 0.1% Tween (TBS-T) and then incubated at 4°C overnight with anti-AKT, anti-phospho-JAK2, anti-phospho-STAT3, anti-phospho-AKT antibodies (Millipore), which were diluted in TBS-T containing 5% non-fat dry milk.

In vivo tumor growth assay

All animal experiments were conducted with the approval of the Beijing HFK Bioscience Co., Ltd. Following alcohol preparation of the skin, the nude mice (4 weeks of age) were subcutaneously inoculated with 200 μl of cell suspension (2×106 cells/ml) into the dorsal flank using a sterile 22-gauge needle. The animals were monitored daily and tumor volume (mm3) was calculated as follows: volume = (shortest diameter)2 x (longest diameter)/2. When the diameters of the tumors were >10 mm, the mice were treated by an intraperitoneal (i.p.) injection of 1 mg/kg CDDP, 2 g/kg NAC, and solvent once a week for 14 days. The nude mice were divided into the following groups: treated with solvent (control), CDDP and CDDP/NAC. Each group contained 3 mice. Bidimensional tumor measurements were analyzed with calipers 3 times a week; the mice were euthanized on the 7th day following drug treatment. The expression levels of AKT were examined by immunohistochemistry as previously described (13,14).

Statistical analysis

Statistical analyses were performed using SPSS version 11.3 software (SPSS, Inc. Chicago, IL, USA). Values are expressed as the means ± SD. Differences were analyzed by the χ2 test for incidence data and by the Student’s t-test for comparison of the means. P<0.05 was considered to indicate a statistically significant difference.

Results

Expression levels of AKT in gastric cancer cells

The AKT protein levels in the cancer cells were measured by western blot analysis. The cells were treated with various concentrations of CDDP for different periods of time (Fig. 1).

Figure 1 (A and B) Detection of AKT protein expression levels in gastric cancer cells (BGC823) by immunoblotting. Actin is used to show equal amounts of protein loading in each lane.

ROS production in gastric cancer cells

BGC823 cells were treated with 30 mg/ml CDDP for 6 h and the production of ROS was measured by flow cytometry. (Fig. 2A). BGC823 cells were then treated with CDDP, control siRNA and JAK2 siRNA. After washing with PBS, the cells were incubated with 33 mg/ml DCFDA in PBS for 30 min at 37°C to measure the prodution of ROS (Fig. 2B).

Figure 2 (A) CDDP induces ROS production. BGC823 cells were treated with 30 mg/ml CDDP and the production of ROS was measured by flow cytometry. (B) BGC823 cells were treated with CDDP, control siRNA and JAK2 siRNA and the production of ROS was measured using DCFDA. ROS, reactive oxygen species; DCFDA, dichlorodihydrofluorescein diacetate; CDDP, cisplatin. *P<0.05 versus control.

Effect of downregulation of the JAK2/STAT3 signaling pathway in gastric cancer cells

To determine whether the AKT-induced CDDP resistance is dependent on the activation of the JAK2/STAT3 signaling pathway, the cells were treated with 33 mg/ml NAC and 30 mg/ml CDDP. This significantly suppressed the activation of the JAK2/STAT3 signaling pathway (Fig. 3A). The expression of AKT was also decreased in the cells treated with CDDP in combination with WP1066, a STAT3 inhibitor (Fig. 3B). These results demonstrate that NAC increases the sensitivity of BGC823 cells to CDDP and that the JAK2/STAT3 pathway is involved in the AKT-induced CDDP resistance of cancer cells. Combination treatment with NAC and CDDP also decreased the levels of phospho-JAK2 and phospho-STAT3 in the BGC823 cells (Fig. 3A).

Figure 3 (A) CDDP causes the rapid tyrosine phosphorylation of JAK2 and STAT3. Growth-arrested BGC823 cells were treated with 30 mg/ml CDDP and 33 mg/ml NAC. Following incubation for 6 h, western blots were probed with phosphotyrosine-specific anti-JAK2 and phosphotyrosine-specific anti-STAT3 antibodies. (B) Growth-arrested BGC823 cells were treated with 30 mg/ml CDDP and 5 μM WP1066 (STAT3 inhibitor). Following incubation for 12 h, western blots were probed with anti-AKT antibody. CDDP, cisplatin; NAC, N-acetylcysteine.

In vivo studies

Tumor development was induced by an injection of 200 μl of cell suspension (2×106 cells/ml) into the dorsal flank of athymic nude mice at 4 weeks of age. When the diameters of the tumors were >10 mm, the mice were treated by an intraperitoneal (i.p.) injection of 1 mg/kg CDDP, 2 g/kg NAC and solvent once a week for 14 days. The mice were sacrificed at 6 weeks post inoculation and tumors were excised and photographed to measure tumor size. The tumors from the mice treated with CDDP and NAC were significantly smaller in size compared to those from the mice treated with CDDP alone or solvent (control) (Fig. 4A). These results supported those obtained by immunohistochemistry assay, which showed that combination treatment with NAC and CDDP exerted a significantly greater inhibitory effect on AKT activation in gastric cancer cells compared to treatment with CDDP alone (Fig. 4B)

Figure 4 The mice were sacrificed and tumors were excised and photographed to measure tumor size at 6 weeks post-inoculation according to the guidance of the Animal Experimental Ethics Committee of Wuhan University. (A) Tumor sizes and tumor volumes of the nude mice in CDDP and CDDP/NAC groups. Data are presented as the means ± SD (n=3, P<0.05). (B) Immunohistochemical expression of AKT in tumors from mice treated with CDDP or CDDP/NAC. CDDP, cisplatin; NAC, N-acetylcysteine.

Discussion

Previous studies have demonstrated that the upregulation of AKT is a potential target for chemoresistance and AKT is overexpressed in certain types of cancer cells following treatment with CDDP (15–17). AKT is considered as an attractive target for chemotherapy and it has been postulated that the inhibition of AKT may preferentially kill cancer cells (18). Certain studies have reported the association of AKT gene amplification with drug resistance (19–22). In this study, we demonstrated that the AKT gene is amplified in BGC823 gastric cancer cells following treatment with CDDP (Fig. 1). These data suggest that the AKT gene is a potential target for CDDP resistance in BGC823 human gastric cancer cells.

The present data indicate that treatment with CDDP significantly increases AKT expression in BGC823 gastric cancer cells, as shown by western blot analysis. Furthermore, our data demonstrate that AKT expression notably reaches a plateau in BGC823 gastric cancer cells. This indicates that AKT may be a positive regulator of drug resistance in human gastric cancer cells. Previous studies have reported that CDDP is capable of inducing ROS production (16). Our results were consistent with these findings. Thus, we hypothesized that ROS may be an important component of the cellular stress signal transduction network. In the present study, we demonstrated that the inhibition of ROS activation inhibits AKT activation, while no changes in the levels of ROS were observed when the cells were treated with JAK2 siRNA (Fig. 2B), suggesting that the decreased expression of ROS renders AKT inactive at upstream signaling pathways. Thus, the production of ROS induced by CDDP activates AKT, thus promoting the development of resistance to chemotherapeutic agents, indicating the important role of AKT in BGC823 cells.

We also determined whether the AKT-induced CDDP resistance is dependent on the activation of the JAK2/STAT3 signaling pathway. The combined treatment of the BGC823 cells with NAC and CDDP significantly decreased the activation of the JAK2/STAT3 (Fig. 3A). In addition, AKT activation was decreased when the cells were treated with CDDP and WP1066, a STAT3 inhibitor (Fig. 3B). These results indicate that NAC increases the sensitivity of the BGC823 cells to CDDP. Thus, the JAK2/STAT3 pathway is involved in the AKT-induced CDDP resistance of cancer cells. This is consistent with AKT activation through phosphorylation that is dependent on JAK2/STAT3 activity. NAC and CDDP combination treatment decreased the levels of phospho-JAK2 and phospho-STAT3 in BGC823 cells (Fig. 3A).

However, we have not demonstrated the mechanism underlying acquired drug resistance. Evidence suggests that the JAK2/STAT3 signaling pathway is involved in drug resistance and the regulation of AKT signaling, which may subsequently be associated with the resistance of cancer cells. By contrast, inhibiting the activity of ROS may improve the sensitivity and efficacy of chemotherapeutic drugs in the treatment of gastric cancer as it may result in the downregulation of the JAK2/STAT3 pathway and AKT, thus increasing the sensitivity of the cancer cells to treatment. Thus, it can be hypothesized that the overexpression of the AKT gene may induce drug resistance in gastric cancer via a multitude of mechanisms and AKT may be a potential molecular therapeutic target in gastric cancer.

In conclusion, our results indicate that the JAK2/STAT3 signaling pathway regulates AKT expression by ROS and is thus involved in the resistance of gastric cancer cells to chemotherapeutic agents in vitro and in vivo. The AKT gene may provide a promising therapeutic target, which may be targeted to overcome CDDP resistance in human tumors.

Acknowledgements

The authors would like to thank Mr. Hong Xia for administrative support and technical assistance in this study. This study was supported by grants from the National Natural Science Foundation of China (no. 30770967) and the Fundamental Research Funds for the Chinese Central Universities (no. 201130202020016 and no. 201130202020017).

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References