Skip to main content

Significance of decoy receptor 3 (Dcr3) and external-signal regulated kinase 1/2 (Erk1/2) in gastric cancer

Abstract

Background

Decoy receptor 3 (DcR3), a member of the tumor necrosis factor receptor (TNFR) superfamily, is associated with anti-tumor immunity suppression. It is highly expressed in many tumors, and its expression can be regulated by the MAPK/MEK/ERK signaling pathway. The MAPK/MEK/ERK pathway has been reported to be a regulator in tumor occurrence, development and clonal expansion. External-signal regulated kinase (ERK) is a vital member of this pathway.

Results

The expression of DcR3 and ERK1/2 in tumor tissues of gastric cancer patients was significantly higher than the non-cancerous group (Pā€‰<ā€‰0.05). There was no statistical difference among tumor tissues from patients with different ages or gender, and even of different differentiation (Pā€‰>ā€‰0.05). However, in patients with stage I gastric cancer, the DcR3 and ERK1/2 levels were significantly lower than patients with more advanced stages.

Conclusions

DcR3 and ERK1/2 play a vital role in the development of gastric cancer, and they may be new markers for indicating the efficiency of gastric cancer treatment in the future.

Background

Decoy receptor 3 (DcR3) is a member of the tumor necrosis factor receptor (TNFR) superfamily. It has been shown to be the decoy receptor for Fas ligand (FasL), LIGHT and TL1A [1ā€“3], also known as TR6 [4]. DcR3 is mostly expressed in tumor cells and competitively inhibits TNF signaling. Overexpression of DcR3 in tumor cells protects them from apoptosis. DcR3 protects tumor cells from immune surveillance as it contributes to the suppression of the host anti-tumor immunity.

DcR3 mRNA and protein are amplified in various malignant tissues, such as lung cancer, colon cancer, gastric cancer, oesophageal carcinoma, pancreas cancer and malignant melanoma [1, 5, 6]. Wu et al.[7] reported that DcR3 could not be detected in non-tumor patients, but could be detected in 98.8% (82/83) of patients with malignant cancers.

This phenomenon demonstrates that the elevated DcR3 expression is significantly correlated with tumorigenesis and tumor progression. Wu et al.[8] reported that DcR3 was highly expressed in human gastric cancer (GC), and positively correlated with the development and metastases of gastric lesions. Gastric cancer patients with a high DcR3 expression presented a more advanced pN2-3 disease than those with a low DcR3 expression.

The DcR3 for FasL may be involved in the progression of gastric cancer. Further evaluation of the possible roles of DcR3 and the regulation of DcR3 expression in malignant cells is very important for the development of new strategies for controlling the growth of malignant cells that escape the host immune surveillance.

At the early stage, the MAPK/ERK pathway is activated in tumors, which is a notable sign for many kinds of cancers in humans. Recently, several lines of evidence suggested that ERK could be a parameter for predicting the prognosis of various cancers such as breast cancer, colon cancer, pancreas cancer and cholangiocarcinoma. Wang et al.[9] reported that the expression of ERK1/2 was high in cholangiocarcinoma, which correlated with the TNM stages.

Kim et al.[10] found that LPS induced DcR3 release in human intestinal epithelial cells (IEC), which appeared to be via the activation of mitogen-activated protein kinases (MAPK), such as extracellular signal-regulated kinase 1 and 2 (ERK1/2) and c-Jun NH2-terminal protein kinase (JNK). LPS-induced DcR3 release in SW480 cells was abolished by ERK1/2 and JNK inhibitors. Furthermore, Yang et al.[11] reported that 3ā€‰g/ml DcR3 markedly induced the phosphorylation of ERK and p38.

In accordance with these reports, we propose that DcR3 and ERK1/2 are closely related. The DcR3 genes closely correlated with the occurrence and development of many kinds of tumors. In this study we investigated the expression level and location of DcR3 and ERK1/2 in gastric cancer patients of different ages, gender, stage and differentiation, to explore the relationship between DcR3/ERK1/2 and gastric cancer occurrence and development. Furthermore, we provide suggestions for clinical diagnosis of gastric cancers.

Methods

Clinical samples

Tumors were from gastric cancer patients who were undergone endoscopic biopsy or curative operations in Zhongshan hospital affiliated with Xiamen university. Tumor tissues from which DNA and protein were isolated were from fresh specimen of resection surgery. All samples were obtained with patient consent and approval of the Committee on Medical Ethics of Zhongshan Hospital Xiamen University.

Mice

All the experiments were performed using 6ā€“8ā€‰weeks male nude mice purchased from Model Animal Research Center of Medical College Xiamen University. All the animals were housed under specific pathogen free conditions with constant access to water and chow. All experimental procedures were carried out following the approval of the Animal Care and Use Committee of Xiamen University.

Cell culture

The human gastric cancer cell line BGC823 was maintained in our laboratory, which was cultured in flasks with Dulbeccoā€™s modified Eagleā€™s medium (DMEM) supplemented with 10% fetal bovine serum (FBS), and 1% penicillin-streptomycin at 37Ā°C in an humidified atmosphere of 5% CO2.

Reagents

DMEM, FBS and penicillin-streptomycin were purchased from Hyclone Corporation (Utah, USA). Hematoxylin-and-eosin (H&E) assay kit were purchased from Chemicon International, Inc (Temecula, CA, USA). ERK1/2 and DcR3 Abs were purchased from Santa Cruz Bio technology. RT-RCR reagents were purchased from TaKaRa (Dalian, China). The primer sequence was synthesized from Sangon (Shanghai, China).

In vivo animal tumor models

Tumors were generated in male nude mice by intramuscular (i.m.) injection of BGC823 cells (1.0ā€‰Ć—ā€‰105 cells in 100Ī¼L PBS) into the right flank. Tumor measurements were converted to tumor volume (V) by the formula (Lā€‰Ć—ā€‰W2ā€‰Ć—ā€‰0.52), where L and W are the length and width, respectively. Measurements were made with a vernier caliper. All tumor-bearing mice were divided randomly into groups (2 mice/group).

RT-PCR and Western blotting analysis for examining the expression of DcR3/ERK

Total RNA of DcR3 and ERK1/2 was extracted from stimulated cells using Trizol. To measure ERK/DcR3 gene copy number, DNA from fresh tumor samples was analyzed with RT-PCR. The upstream and downstream primers for ERK1 mRNA were 5'-CCTGCTCATCAACACCACC-3ā€™ and 5'-CGTAGCCACATACTCCGTCA-3ā€™, and for ERK2 mRNA were 5'-TCTTCC AGCCCTCCTTCCTG-3' and 5'-CGTTTCTGCGCCGTTAGGT-3'. The samples were denatured at 95Ā°C for 4ā€‰min, followed by 35 cycles of amplification (95Ā°C, 45ā€‰sec; 55Ā°C, 45ā€‰sec; and 72Ā°C, 60ā€‰sec). The products were 300-bp and 400-bp fragments respectively. For DcR3 mRNA, the upstream primer was 5'- GCAAAGCCAAGGATTCCCCCTG -3ā€™ and the downstream primer was 5'-GGCACTGCTCTGAGCTGGAGCTG-3ā€™. The samples were denatured at 95Ā°C for 4ā€‰min, followed by 30 cycles of amplification (95Ā°C, 45ā€‰sec; 55Ā°C, 45ā€‰sec; and 72Ā°C, 60ā€‰sec). The product was a 921-bp fragment.

BGC823 cells were harvested and lysed in cell lysis buffer (1% (v/v) Nonidet P-40, 150ā€‰mM NaCl, 50ā€‰mM Trisā€“HCl (pH 8), 1ā€‰mM PMSF, 2ā€‰g/ml aprotinin, and 2ā€‰g/ml leupeptin) which could release DcR3 and ERK1/2 proteins. Twenty-five micrograms of total lysate was fractionated by SDS-PAGE and subjected to Western blotting analysis using the anti-ERK or anti-DcR3 mAb (clone 3ā€‰H5).

Western blotting and ELISA assay for examining the expression of DcR3/ERK after inhibitors treatment

BGC823 cells culture supernatants were collected at various intervals, and levels of U0126, PD98059, APDC, MEK1/2 and ERK1/2 interferences were quantified using commercial ELISA kits, according to the vendorā€™s instructions. Cells treated with ERK1/2 shRNA (5:2, 6:2), U0126/PD98059 (0ā€‰Ī¼mol/L, 5ā€‰Ī¼mol/L, 10ā€‰Ī¼mol/L, 20ā€‰Ī¼mol/L, 40ā€‰Ī¼mol/L) and APDC (0ā€‰Ī¼mol/L, 10ā€‰Ī¼mol/L, 20ā€‰Ī¼mol/L, 40ā€‰Ī¼mol/L, 80ā€‰Ī¼mol/L), respectively. After a 5- or 7-day incubation, cells were subjected to the cytokines as indicated assay. Twenty-five micrograms of total lysate was fractionated by SDS-PAGE and subjected to Western blotting analysis using the anti-ERK or anti-DcR3 mAb (clone 3ā€‰H5).

Immunohistochemistry analysis for the expression of DcR3 and ERK1/2

Tumor tissues were fixed in a formaldehyde medium and embedded in paraffin. Sections 6 mm thick were mounted on glass slides pretreated with 0.1% poly-L-Lysine. They were then deparaffinaged in xy-lene, dehydrated in graded ethanol and soaked in 3% H2O2 for 10ā€‰min to eliminate endogenous peroxidase activity. Next, the slides were submerged in citrate buffer (pH 6.0) and boiled at 92ā€“98Ā°C in a microwave oven for 10ā€‰min. Subsequently, they were rinsed 3 times with PBS for 10ā€‰min each and blocked with 10% normal goat serum in PBS for 1ā€‰hr at room temperature. The slides were then reacted with the affinity-purified rabbit anti-TR6 Ab (1.67ā€‰g/ml) at room temperature for 2ā€‰hr. After washing, the slides were incubated with biotinylated goat-anti-rabbit antibody for 10ā€‰min. TR6 signal was revealed by streptavidin-peroxidase using DAB as a substrate according to instructions from the Histostain-Plus kit (Zymed Laboratories, South San Francisco, CA). DcR3 signals were revealed in brown. Finally, the slides were counterstained with hematoxylin and sealed with Aqueous Mounting Media (Zymed).

Statistical analysis

Data were presented as meanā€‰Ā±ā€‰SD. The significance of the difference between the groups was assessed by Student`s two-tailed t-test. Probability value of less than 0.05 was considered significant. All means were calculated from at least three independent experiments.

Results

Cancer patients have elevated DcR3 levels

To study the correlation between DcR3 expression and tumor occurrence and development, tumors from 50 gastric cancer patients were collected and tested for DcR3 mRNA and protein levels. As shown in Figure 1a, the 921ā€‰bp DcR3 bands were generated by RT-PCR from the tumor tissues of most patients (36/50), compared with the non-cancerous tissues (2/50) from the same organs of these patients. These results demonstrate that DcR3 levels were significantly increased (eight randomly picked clinical samples are shown in Figure 1a). To further confirm our results, the DcR3 protein levels were examined by western blotting. The results demonstrate that DcR3 protein could be detected in most cancer patients; DcR3 protein was detected in 74% (37/50) of the tumor tissues, but only in 6% (3/50) of the non-cancerous tissues (Table 1 and Figure 1b; eight randomly picked clinical samples are shown in Figure 1b).

Figure 1
figure 1

The expression of DcR3 in gastric cancer and non-cancerous tissues analyzed by RT-PCR (Figure1a) and Western blotting (Figure1b). a: Lane M, DNA markers; lanes1-7, tumor tissues; lane 8, non-cancerous tissues; DcR3 mRNA was positive in 36 of 50 tumor tissues (1ā€“7) and negative in non-cancerous tissues (8). b: lanes1-7, tumor tissues; lane 8, non-cancerous tissues. DcR3 protein was positive in 37 of 50 samples of tumor tissue (1ā€“7), which only 3 of 50 in non-cancerous tissues (8).

Table 1 Analysis of gastric cancer patients with DcR3 and ERK1/2 expression in tumor and normal tissues

Expression of ERK1/2 in Clinical samples

To identify the signaling molecules related to DcR3, the expression levels of ERK1/2, JNK and p38 were tested. We found that only ERK1/2 could be detected in tumor samples (data not shown for JNK and p38). ERK1 mRNA was detected in 74% of the samples (37/50), and ERK2 mRNA was detected in 64% of the samples (32/50; Table 1 and Figure 2a). At the protein level, ERK1 was detected in 84% (42/50) and ERK2 in 74% (37/50) of the tumor tissues (Table 1 and Figure 2b). These results indicate that patients with gastric cancer tumors have a higher ERK1/2-positive occurrence compared with the non-cancerous tissues (Pā€‰<ā€‰0.05). There was a positive correlation between the mRNA and protein levels, as in 42 of 50 tumor tissues the ERK1 protein level was elevated, of which 36 cases were consistent with the mRNA expression. In contrast, ERK1 protein expression was detected only in five normal tissues. When examining ERK2, 37 of 50 cases of tumor tissues were positive for ERK2 protein expression, of which 27 cases were consistent with the ERK2 mRNA expression, while only ten cases showed positive protein expression in normal tissues. The eight randomly picked samples are shown in Figure 2.

Figure 2
figure 2

The expression of ERK1/2 in gastric cancer and non-cancerous tissues analyzed by RT-PCR (Figure 2a) and Western blotting (Figure 2b). a: Lane M, DNA markers; lanes1-7, tumor tissues; lane 8, non-cancerous tissues; ERK1 and ERK2 mRNA were positive in tumor tissues. b: ERK1 and ERK2 protein were positive in tumor tissues (1ā€“8).

Location of ERK1/2 in gastric cancer patients

To examine ERK1/2 distribution, tumors from 50 patients were tested by immunohistochemistry. The results show that ERK1/2 were expressed in tumor tissues from most of the patients. ERK1 expression was found in the cytoplasm. ERK2 positive expression was found in some tumor cells (Figure 3).

Figure 3
figure 3

The location of ERK1/2 protein in gastric cancer tissues analyzed by immunohistochemistry. A: Control, B: ERK1, C: ERK2.

DcR3 and ERK1/2 levels correlate with tumor invasion but not with age, gender or differentiation

The positive incidence of DcR3 mRNA in tumor tissues of gastric cancer patients was 72.0% (36/50), and of DcR3 protein 74.0% (37/50), which was significantly higher than in non-cancerous tissues showing only 4% (2/50) and 6% (3/50), respectively (Pā€‰<ā€‰0.05; Table 1). The positive occurrence of ERK1/2 mRNA expression was 74.0% (37/50) and 64.0% (32/50), and of protein expression 84.0% (42/50) and 74.0% (37/50). Both of them were significantly higher than the non-cancerous tissues, showing 12.0% (6/50) and 18.0% (9/50), and 10.0% (5/50) and 20.0% (10/50), respectively (Table 1). These results suggest that DcR3 and ERK1/2 expression levels correlated with tumor occurrence and development.

As shown in Tables 2, 3 and 4, there was no significant difference between tumor tissues from different ages, gender groups and patients with different differentiation stages of gastric cancer (Pā€‰>ā€‰0.05). However, DcR3 and ERK1/2 expression levels were significantly high in TNM stage II-IV (Table 5). Thus, the expressions of DcR3 and ERK1/2 correlated with tumor invasion and TNM stage, but not with age, gender or differentiation.

Table 2 Correlation of expression of DcR3 and ERK1/2 with age in gastric cancer patients
Table 3 Correlation of expression of DcR3 and ERK1/2 with gender in gastric cancer patients
Table 4 Correlation of expression of DcR3 and ERK1/2 with tumor differentiation in gastric cancer patients
Table 5 Correlation of expression of DcR3 and ERK1/2 with pathologic stages of tumour in gastric cancer patients

Expression levels of DcR3 and ERK1/2 are amplified in animal models

As shown in Table 6, after injecting BGC823 cells into the right flank of nude mice, the tumors grew each day. RT-PCR was used to test DcR3 and ERK1/2 mRNA levels in the tumors and western blot analysis was used to examine protein levels. In gastric cancer animal models, DcR3, ERK1 and ERK2 were detected at 921ā€‰bp, 300ā€‰bp and 400ā€‰bp, respectively. In these tumor tissues DcR3 mRNA was detected from day six, peaked on day 10, and remained detected on day 12. DcR3 was also detected from day six to day 12 in liver, while it was only detected on day 12 in heart and lung (Figure 4a). ERK1/2 mRNA expressions were detected from day four in tumor tissues, and ERK1 mRNA peaked on day 10 (Figure 4a and Table 7).

Table 6 Weight of BGC823 tumor in nude mouse ( xā€‰Ā±ā€‰s, nā€‰=ā€‰6)
Table 7 Expression of DcR3 and ERK1/2 mRNA in tumor tissues of animal models analyzed by RT-PCR
Figure 4
figure 4

The expression of DcR3 and ERK1/2 in mouse models analyzed by RT-PCR (Figure 4a) and Western blotting (Figure 4b). a: Lane M, DNA marker; lanes1-6, hearts, livers, spleens, lungs, kidneys and tumor tissues of mouse models on the fourth day; lanes7-12, which on the eighth day ; lanes13-18, on the twelfth day; ERK1 mRNA was positive in lane2,8,9,12,14,15,18, ERK2 mRNA was positive in lane1,2,6,9,10,12,13,14,15,17,18. DcR3 mRNA was detected in lane8, 12, 13, 14, 15, 16, 17, 18. b: lane 1, heart; lane2, liver; lane3, spleen; lane4,lung; lane5, kidney; lane6, tumor tissues; The expression of ERK1 protein increased in tumor tissues as time went on, in heart, liver and kidney persisted for 12ā€‰days, The expression of ERK2 could be detected in spleen and tumor from the second day which was positive in tumor tissues till the fourth day and all of five organs to the twelfth day. The expression of DcR3 protein was positive in tumor tissues and liver on the sixth day and in spleen on the tenth day, which was negative in heart, lung, kidney until the twelfth day.

DcR3 protein was detected on day six in tumor tissues and liver, and the expression remained until day 12. DcR3 protein was detected on day 10 in spleen and by day 12 in heart, kidney and lung. ERK1 protein was detected on day four in tumor tissues, and continued to increase each day. ERK1 protein remained at a stable level in heart, liver and kidney, but it decreased in lung and spleen on day 10, after reaching the peak. ERK2 was detected on day two in spleen and tumor tissues. From day four, ERK2 protein was detected in all six samples, and continued to increase till day 12. These results suggest that ERK1 and ERK2 might have different effects on tumor occurrence, development and clonal expansion.

DcR3 expression decreased after inhibiting the expression or phosphorylation of ERK1/2 in BGC823 cells

To investigate the effect of ERK1/2 expression and phosphorylation on DcR3 expression, BGC823 cells were treated with ERK1/2 shRNA or with inhibitors that specifically regulate the ERK pathway. Western blot analysis confirmed that the inhibitors efficiently blocked the phosphorylation of the MEK/ERK pathway molecules, and that the shRNA significantly reduced the expression of ERK1/2 (Figure 5). As shown in Figure 5A, when BGC823 cells were treated with ERK1/2 shRNA, ERK1/2 and P-ERK1/2 levels declined compared with the control.

Figure 5
figure 5

The expression of ERK1/2 and P-ERK1/2 in BGC823 cell line with plasmid interference and inhibitor detected by Western blotting. a: The expression levels of ERK1/2 and P-ERK1/2 declined compared with the control. 1) control group; 2) 5:2 (plasmid: reagent); 3) 6:2 (plasmid: reagent). b: ERK1/2 phosphorylation gradually declined as the concentrations of the inhibitor U0126, PD98059 increased, but total ERK1/2 protein expression hardly changed. 1) 0ā€‰Ī¼mol/L; 2) 5ā€‰Ī¼mol/L; 3) 10ā€‰Ī¼mol/L; 4) 20ā€‰Ī¼mol/L; 5) 40ā€‰Ī¼mol/L. c: ERK1/2 phosphorylation gradually declined as the concentrations of the inhibitor APDC. 1) 0ā€‰Ī¼mol/L; 2) 10ā€‰Ī¼mol/L; 3) 20ā€‰Ī¼mol/L; 4) 40ā€‰Ī¼mol/L; 5) 80ā€‰Ī¼mol/L. d: PD98059 can obviously inhibit the MEK1/2 phosphorylation level, but it did not alter MEK1/2 or NF-ĪŗB expression levels. 1) 0ā€‰Ī¼mol/L; 2) 5ā€‰Ī¼mol/L; 3) 10ā€‰Ī¼mol/L; 4) 20ā€‰Ī¼mol/L; 5) 40ā€‰Ī¼mol/L.

U0126 is a very effective MEK inhibitor, resulting in the inhibition of ERK phosphorylation, as does PD98059. ERK phosphorylation gradually declined as the concentrations of the drugs increased, although total ERK1/2 protein expression hardly changed (Figure 5B).

APDC can inhibit NF-ĪŗB cell activation in a variety of cells. Through the degradation of IĪŗB, APDC can decrease the translocation of NF-ĪŗB, thus blocking NF-ĪŗB activation. As shown in Figure 5 C, under different concentrations of APDC, changing the level of NF-ĪŗB inhibition can significantly attenuate ERK1/2 phosphorylation levels. However, the specific mechanism requires further investigation.

To examine the effect of these inhibitors and shRNA on DcR3 expression we used ELISA analysis, which demonstrated that secreted DcR3 in the supernatant decreased after the different treatments (Figure 6). Statistical analysis showed that DcR3 secretion levels were significantly different between the experiment groups and control groups (Pā€‰<ā€‰0.05). As shown in Figure 6, interference with ERK1/2 in BGC823 cells led to decreased DcR3 protein expression compared with the control group. The trend matches the ERK expression level in Figure 5 and proves that the two are positively correlated. Furthermore, DcR3 and P-ERK expression levels decreased when cells were treated with different concentrations of U0126, PD98059 and APDC. This data indicates that secretion of DcR3 positively correlated with P-ERK1/2 expression levels in BGC823 gastric cells. It is worth noting that in the U0126 group, DcR3 secretion levels increased when the drug concentration reached 40ā€‰Ī¼mol/L; however, the specific mechanism requires further investigation. In the APDC group, DcR3 levels did not change significantly at concentrations higher than 20ā€‰Ī¼mol/L.

Figure 6
figure 6

The expression of DcR3 protein with plasmid interference and inhibitor by ELISA analysis. a: DcR3 expression levels in BGC823 culture supernate decreased when cells were treated with ERK1 interference plasmid. b: DcR3 expression levels decreased when cells were treated with ERK2 interference plasmid. c: DcR3 expression levels decreased when cells were treated with different concentrations of U0126, PD98059 and APDC Ī¼mol/L.

Discussion

It has been demonstrated that the DcR3 gene is expressed at a low level in human embryo, lung, brain, liver, spleen, stomach, colon, lymph nodes and spinal cord, whereas it was expressed at a high level in cancers such as gastrointestinal cancer, hepatocellular carcinoma and pancreatic cancer [1, 12].

Wu et al.[8] reported that the expression of DcR3 in gastric cancer patients was significantly higher than normal. DcR3 expression in the well-differentiated gastric cancer was significantly lower than that of poorly differentiated specimens (Pā€‰<ā€‰0.05).

The DcR3 expression level was significantly associated with lymph node metastasis and pathological stage, but did not correlate with tumor size, metastatic status, or histological types. When patients were followed-up for 63ā€‰months, DcR3 overexpression was found to be associated with a significantly shortened survival rate [13, 14].

Many reports have shown that high expression levels of ERK1/2 closely correlated with breast, colorectal and pancreatic cancer, as well as malignant melanoma, leukemia and myxoma [15ā€“18].

Our research showed that in patients with gastric cancer, the positive incidence of DcR3 and ERK1/2 mRNA was higher than that in the non-cancerous tissues (Pā€‰<ā€‰0.05). RT-PCR and western blotting showed that the mRNA and protein expression levels of DcR3 and ERK1/2 in tumor tissues were significantly higher than those in non-cancer tissues, suggesting that DcR3 and ERK1/2 levels correlate with tumor development but not with age, gender or differentiation (Pā€‰>ā€‰0.05).

Our results showed that the positive incidence of expression of DcR3 and ERK1/2 mRNA and DcR3 and ERK1/2 protein matched each other. The immunohistochemistry results also demonstrated that in gastric tumors, ERK1/2 was highly expressed.

Chen et al.[19] reported that the positive rate of DcR3 expression was 74.4% (32/43) in hepatocellular carcinoma, and that there was a significant correlation between DcR3 expression and metastasis as well as recurrence and differentiation.

In the mouse gastric model, RT-PCR showed that DcR3 mRNA could be detected in tumors from day six. ERK1/2 mRNA and protein were also detected in tumors, and ERK1 levels gradually increased in gastric tumors. Furthermore, they were also detected in heart, liver, spleen, lung and kidney of the gastric cancer animal model, suggesting that they have an important role in tumor progression. ERK1/2 mRNA was detected from day four in tumor tissues, and ERK1 mRNA peaked on day 10. ERK1 protein could also be detected on day four in tumor tissues, and continued to increase every day. ERK1 remained at a stable level in heart, liver and kidney, but it decreased in lung and spleen on day 10, after reaching the peak. ERK2 was detected on day two in spleen and tumor tissues. From day four, ERK2 was detected in all six tissues, and continued to increase till day 12. ERK2 could not be detected in heart, lung and spleen by RT-PCR on day 12 in animal models, but protein levels could be detected. These results suggest that ERK1 and ERK2 might have different effects on tumor occurrence, development and clonal expansion. Many studies indicated that the expression of ERK1/2 mRNA and protein varies in different tumors and cells [20, 21]. Some recent reports suggested they could be entirely opposite in some cases. Thus, the effects of ERK1 and ERK2 on the tumors are unlikely to be the same.

Conclusions

In conclusion, high expression of DcR3 and ERK1/2 may suppress tumor cell apoptosis and play an influential role in gastric cancer occurrence and development, which is an important mechanism in tumorigenesis [22]. In our study, DcR3 and ERK1/2 presented an overexpression tendency, and participated in the tumor immunity. We infer that in the tumor occurrence and developing process, the expression of ERK1/2 and DcR3 may be related to each other. Understanding the role of ERK1/2 in DcR3 expression might shed light on gastric cancer's diagnosis and identify a factor that regulates the expression of DcR3. It might be a new marker for early diagnosis of gastric cancer. DcR3 is a secreted protein, which can be detected in blood serum. Thus it could serve as a reliable index for clinical malignant tumor diagnosis, treatment and prognosis. Therefore, DcR3 has the potential of becoming a novel tumor marker in the future.

References

  1. Pitti RM, Marsters SA, Lawrence DA: Genomic amplification of a decoy receptor for Fas ligand in lung and colon cancer. Nature. 1998, 396: 699-703. 10.1038/25387.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  2. Yu KY, Kwon B, Ni J: A newly identified member of tumor necrosis factor receptor superfamily (TR6) suppresses LIGHT-mediated apoptosis. J Biol Chem. 1999, 274: 13733-13736. 10.1074/jbc.274.20.13733.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  3. Migone TS, Zhang J, Luo X: TL1A is a TNF-like ligand for DR3 and TR6/DcR3 and functions as a T cell costimulator. Immunity. 2002, 16: 479-492. 10.1016/S1074-7613(02)00283-2.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  4. Roth W, Isenmann S, Nakamura M: Soluble decoy receptor 3 is expressed by malignant gliomas and suppresses CD95 ligand-induced apoptosis and chemotaxis. Cancer Res. 2001, 61: 2759-2765.

    PubMedĀ  CASĀ  Google ScholarĀ 

  5. Bai C, Connolly B, Metzker ML: Overexpreasion of M68P DcB3 human gastrointestinal tract tumors independent of gene amplification and its location in a fourgene cluster. Proc Natl Acad Sci USA. 2000, 97 (3): 1230-1235. 10.1073/pnas.97.3.1230.

    ArticleĀ  PubMedĀ  CASĀ  PubMed CentralĀ  Google ScholarĀ 

  6. Shoichiro TSUJI, Ryo Hosotani, Shin Yonehara: Endogenous Decoy Receptor 3 Blocks The Growth Inhibition Signals Mediated by Fas Ligand in Human Pancreatic Adenocarcinoma. Int J Cancer. 2003, 106: 17-25. 10.1002/ijc.11170.

    ArticleĀ  Google ScholarĀ 

  7. Yulian WU, Bing Han, Hongwei Sheng: Clinical significance of detecting elevated serum DcR3/TR6/M68 in malignant tumor patients. Int J Cancer. 2003, 105: 724-732. 10.1002/ijc.11138.

    ArticleĀ  Google ScholarĀ 

  8. Wu Y, Guo E, Yu J: High DcR3 expression predicts stage pN2 in gastric cancer. Hepatogastroenterology. 2007, 54 (79): 2172-2176.

    PubMedĀ  CASĀ  Google ScholarĀ 

  9. Jiangning Wang: Expression of ERK1/2 protein in cholangiocarcinoma relation with TNM stages. Shandong medicine. 2008, 48 (14): 60-61.

    Google ScholarĀ 

  10. Kim S, Fotladu A, Kotoula V: Increased expression of soluble decoy receptor 3 in acutely inflamed intestinal epithelia. Clini immunol. 2005, 115 (3): 286-294. 10.1016/j.clim.2005.02.014.

    ArticleĀ  CASĀ  Google ScholarĀ 

  11. Yang CR, Wang JH, Hsieh SL: Decoy receptor 3 (DcR3) induces osteoclast formation from monocyte/macrophage lineage precursor cells. Cell death differ. 2004, 11 (Suppl 1): S97-S107.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  12. Yu KY, Kwon B, Ni J: A newly identified member of tumor necrosis factor receptor super family (TR6) suppresses LIGHT-mediated apoptosis. T Biol Chem. 1999, 274 (20): 13733-13736. 10.1074/jbc.274.20.13733.

    ArticleĀ  CASĀ  Google ScholarĀ 

  13. Takahama Y, Yamada Y, Emoto K: The prognostic significance of overexpression of the decoy receptor for Fas ligand (DcR3) in patients with gastric carcinomas. Gastric Cancer. 2002, 5 (2): 61-68. 10.1007/s101200200011.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  14. Lin Wanwan, Hsieh SL: Decoy receptor 3: A pleiotropic immunomodulator and biomarker for inflammatory diseases, autoimmune diseases and cancer. Biochem Pharmacol. 2011, 81 (7): 838-847. 10.1016/j.bcp.2011.01.011.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  15. Hornberg Jorrit J, Bernd Binder, Bruggeman Frank J, Birgit Schoeber, Reinhart Heinrich, Westerhoff Hans V: Control of MAPK signalling: from complexity to what really matters. Oncogene. 2005, 24: 5533-5542. 10.1038/sj.onc.1208817.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  16. Kondoh K, Torii S, Nishida E: Control of MAP kinase signaling to the nucleus. Chromosoma. 2005, 114: 86-91. 10.1007/s00412-005-0341-9.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  17. Schmitz KJ, Wohlschlaeger J, Alakus H: Activation of extracellular regulated kinases (ERK1/2) but not AKT predicts poor prognosis in colorectal carcinoma and is associated with k-ras mutations. Virchows Arch. 2007, 450: 151-159. 10.1007/s00428-006-0342-y.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  18. Hayashi S, Nishiyama T, Miura Y: DcR3 induces cell proliferation through MAPK signaling in chondrocytes of osteoarthritis. Osteoarthr Cartil. 2011, 19 (7): 903-910. 10.1016/j.joca.2011.03.005.

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  19. Chen Gang, Luo Dianzhong, Wang yun, Liao Zhiling, Zhang Meiyan: DcR3 suppresses apoptosis of tumor cells in HCC. Chinese Journal of Net Pathology. 2007, 36 (2): 113-117.

    CASĀ  Google ScholarĀ 

  20. Yang H, Qu L, Ma H: Mycoplasma hyorhinis infection in gastric carcinoma and its effects on the malignant phenotypes of gastric cancer cells. BMC Gastroenterol. 2010, 10 (1): 132-10.1186/1471-230X-10-132.

    ArticleĀ  PubMedĀ  PubMed CentralĀ  Google ScholarĀ 

  21. Xi L, Xiao C, Bandsma RH: C-reactive protein impairs hepatic insulin sensitivity and insulin signaling in rats: Role of mitogen-activated protein kinases. Hepatology. 2011, 53 (1): 127-135. 10.1002/hep.24011. 2010 Sep; 24. [Epub ahead of print] 2011 Jan

    ArticleĀ  PubMedĀ  CASĀ  Google ScholarĀ 

  22. Tu HF, Liu CJ, Liu SY: Serum Decoy receptor 3 level:a predictive marker for nodal metastasis and survival among oral cavity cancer patients. Head and neck-journal for sciences and specialties of the head and neck. 2011, 33 (3): 396-402.

    Google ScholarĀ 

Download references

Acknowledgements

This study was financially supported by the 985 funds. Fujian Province nature science funds(2010D009).Science and Technology Department of Fujian province provincial public research institutes for basic scientific research special (2011R10020-2).

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Guohong Zhuang or Zhongchen Liu.

Additional information

Competing interest

The authors declare that they have no competing interest.

Authorsā€™ contributions

DY and XF carried out the molecular genetic studies, participated in the sequence alignment and drafted the manuscript. PY, QW carried out the immunoassays. FY, SY and BL participated in the sequence alignment. ZL participated in the design of the study and performed the statistical analysis. GZ conceived of the study, and participated in its design and coordination. All authors read and approved the final manuscript.

Donghai Yang, Xin Fan contributed equally to this work.

Authorsā€™ original submitted files for images

Rights and permissions

Open Access This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/2.0 ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Yang, D., Fan, X., Yin, P. et al. Significance of decoy receptor 3 (Dcr3) and external-signal regulated kinase 1/2 (Erk1/2) in gastric cancer. BMC Immunol 13, 28 (2012). https://doi.org/10.1186/1471-2172-13-28

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1471-2172-13-28

Keywords