The upregulation of tribbles homolog 3 (TRB3), a pseudokinase in mammals, has been observed in several types of malignant cancer, including thyroid, ovarian, liver and colorectal cancer. However, the pathological role and the regulatory mechanism of TRB3 in cancer remain unknown. In the current study, we demonstrated that the expression of TRB3 was upregulated in non-small cell lung cancer (NSCLC), correlating with tumor metastasis, disease recurrence and poor survival in patients. Knocking down TRB3 in aggressive lung cancer cell lines was demonstrated to significantly inhibit their malignant behaviors, including in vitro invasion and cell proliferation, as well as in vivo metastasis and tumor growth. The correlation between TRB3 and Notch 1 expression revealed that Notch 1 was downregulated by the knockdown of TRB3 in the lung adenocarcinoma cell lines. These results have provided insights into the correlation between TRB3 expression and lung cancer progression, and thus may have potential for the prognosis and therapy of lung cancer.
Tribbles homolog 3 (TRB3), a pseudokinase, is essential for the catalytic activity that is performed by 10% of the kinase superfamily members (1). TRB3 was also demonstrated to be a key factor in complementary kinome small interfering-RNA (siRNA) function, as a regulator of mitogen-activated protein kinase (MAPK) signaling (2). Previous studies have demonstrated that this occurs through the control of the MAPK-extracellular signal-related kinase (MAPK-ERK) and transforming growth factor β (TGFβ) pathways. Furthermore, TRB3 regulates JAG1 expression and is required for the proliferation of breast cancer cells (3). In addition, TRB3 is required in normal tissues during conditions of hypoxic/endoplasmic reticulum stress or nutrient deprivation, as it is upregulated and counteracts the effects of stress (4,5). TRB3 is also upregulated in cancer as a response to hypoxia (4,6) and is associated with a poor outcome (7) as it promotes the activation of key cancer signaling pathways (such as MAPK-ERK, TGFβ and jagged 1 protein (JAG1)/Notch). TRB3 expression and molecular function has rarely been demonstrated in cancer cell lines, with the exception of breast cancer cell lines (2).
The most understood function of the Notch family is cell fate regulation. This function has been regarded to be linked to the homeostasis of stem cell compartments (8–11) and thus, Notch signaling has been implicated in human cancer (10). Cell-autonomous oncogenic activation of Notch was identified in T-cell acute lymphoblastic leukemia/lymphoma (T-ALL). Notch 1 may be activated through chromosomal translocations and/or mutations (10,12). Downregulated expression of Notch-related factors, including Notch receptors, ligands and targets, has also been observed in solid tumors (10,13), including breast (13) and lung (14) cancer. To the best of our knowledge, no studies with regard to the correlation between cell-autonomous activation of Notch and TRB3 expression in lung cancer have been published to date. Furthermore, the loss of NUMB expression in breast cancer may contribute to increased Notch activity and Notch-dependent proliferation (15,16).
JAG1/Notch signaling has been considered to be a mediator of cancer progression and metastasis associated with the basal-like subtype (17,18). The majority of lung cancer patients have basal-like disease, and despite initial responses to systemic cytotoxic chemotherapy, the disease follows an aggressive clinical course with early recurrence (19). Therefore, JAG1/Notch signaling and regulators of this pathway are attractive therapeutic targets in this lung cancer subtype. TRB3 influences the tumor cell biology and may be regulated by the JAG1/Notch pathways. Tumor-initiating cells represent a small population of cells within certain types of tumors, which possess the unique ability to self-renew and to produce derivatives that maintain the tumor. The TRB3 target pathways, including Notch, MAPK-ERK and TGFβ (20,21), have been implicated in tumor-initiating cell maintenance, suggesting that through the control of these pathways, TRB3 may regulate the initiation of tumor formation. The metastatic potential of epithelial tumors is likely to depend on a process known as epithelial-to-mesenchymal (EMT) transition, where epithelial cells acquire a migratory mesenchymal phenotype (22). The Notch, TGFβ and MAPK-ERK pathways interact and have a synergistic effect on the production of factors that promote EMT and metastasis (23–25). The Notch and TGFβ pathways have been demonstrated to facilitate metastasis, and also have a role in determining the location of metastatic sites (26); TGFβ released from bone metastases induces JAG1 expression in tumor cells, which contributes to paracrine Notch activation in osteoblasts and preosteoclasts, and thus leads to bone invasion. This suggests that TRB3 may potentiate the initiation of tumor formation and the metastatic capacity of lung cancer cells through the regulation of JAG1/Notch activation. Additionally, the activation of these pathways and processes may result in reduced survival associated with tumors, and elevated TRB3 levels.
We hypothesized that the abnormal expression of TRB3 may participate in lung cancer development. By transfection analysis, we demonstrated the effect of knocking down TRB3 on human lung adenocarcinoma cells and the underlying molecular mechanism. The aim of the current study was to investigate the therapeutic potential of the knockdown of TRB3 in lung cancer.
Materials and methodsReagents and antibodies
Rabbit antibodies against human TRB3 (T8076) and Notch (SAB2101618) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Mouse antibody against human β-actin (sc-8432) and the secondary antibodies conjugated with horseradish peroxidase against mouse and rabbit IgG (sc-2005 and sc-2030, respectively) were purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA).
Clinical specimens, cells, plasmids and transfection
Clinical samples for quantitative PCR (Q-PCR) and immunohistochemistry (IHC) were obtained from Xiangya School of Medicine, Central South University (Changsha, Hunan, China) with informed patient consent and approval of the institutional review board (Xiangya School of Medicine Research Ethics Committee). Human lung adenocarcinoma cell lines were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA). The recombinant expression plasmid of pcDNA3.1(t) (pc3.1) expressing TRB3 was constructed. Briefly, the open reading frame of TRB3 (GenBank accession: BC027484) was cloned into plasmid pcDNA3.1(t) (Invitrogen Life Technologies, Carlsbad, CA, USA) between the XhoI and BamHI sites to build the pc3.1-shTRB3 recombinant plasmid. The A549 cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM; Gibco-BRL, Carlsbad, CA, USA) supplemented with 10% fetal bovine serum (FBS; Gibco-BRL) at 37°C in an incubator with an atmosphere of 5% CO2. The cells were transfected with pc3.1-shTRB3 using LipofectamineTM 2000 (Invitrogen Life Technologies) according to the manufacturer’s instructions.
Semi-quantitative RT-PCR
Total RNAs were isolated using TRIzol reagent (Invitrogen Life Technologies), according to the manufacturer’s instructions. The first-strand complementary DNA (cDNA) was reverse transcribed from 2 μg RNA in a final volume of 20 ml, using SuperScript II Reverse Transcriptase (Invitrogen Life Technologies). The primers were designed in accordance with GenBank. The quantity of cDNA used for each PCR reaction was 20 ng in a 50 ml reaction volume. The PCR was performed with the Applied Biosystems 7500 Real-Time PCR system (Invitrogen Life Technologies). The protocol was as follows: one cycle at 94°C for 4 min and 40 cycles at 94°C for 30 sec, 60°C for 30 sec and 72°C for 30 sec. The PCR products were assayed by a dissociation curve to verify a single product generation at the end point of the assay.
Western blot analysis
The cells were lysed in radioimmunoprecipitation assay (RIPA) buffer on ice and centrifuged at 12,000 × g for 30 h to obtain the supernatant. The extracted protein samples were separated by 12% SDS-PAGE and transferred onto polyvinylidene difluoride (PVDF) membranes (GE Healthcare, Amersham, UK). The membranes were blocked in 5% skimmed milk for 1 h and subsequently incubated with primary antibodies at 4°C overnight. Following washing with PBS three times, the samples were probed by secondary antibodies conjugated with horseradish peroxidase for 1 h at room temperature. The signals were detected using a chemiluminescence system SuperSignal West Pico Chemiluminescent Substrate (Pierce Biotechnology, Inc., Rockford, IL, USA). The three independent experiments were repeated to assess the relative protein levels.
Cell invasion assay
The cell invasion assay was performed in 24-well FluoroBlok cell culture inserts with 8-μm pore-size polyethylene terephthalate (PET) membranes (BD Biosciences, Franklin Lakes, NJ, USA). The insert was coated with 200 μl of 1 μg/μl Matrigel matrix (BD Biosciences) at 4°C overnight. Following starvation for 6 h in serum-free DMEM, the cells were harvested from one subconfluent 10 cm dish by cell dissociation buffer (Invitrogen Life Technologies), centrifuged at 300 × gh for 5 min and resuspended in DMEM. Cells (1×105, in 500 μl DMEM) were seeded onto the insert and 250 μl DMEM with 10% FBS was added into the lower chamber of the transwells. Following incubation for 18 h at 37°C, the medium inside the insert was removed and the insert was then placed in a novel 24-well plate. The invaded cells on the reverse side of the insert were labeled with a fluorescent dye, calcein acetoxymethl ester (4 μM in PBS; BD Biosciences), for 1 h at 37°C. The fluorescence was measured with 494/517 nm (excitation/emission wavelength) by a DU®-8 UV-Vis spectrophotometer (Beckman Coulter, Miami, FL, USA).
Statistical analysis
Data are presented as the mean ± standard error of the mean of independent experiments. One-way analysis of variance (ANOVA) was used to determine the differences among the groups. The normality and constant variance for experimental data were tested by the Levene’s test. Data without homogenous variance were log-transformed to meet the necessary assumptions of the analysis of variance. P<0.05 was considered to indicate a statistically significant difference. When the F value exceeded the critical value (P<0.05), the Newman-Keuls post hoc test was performed to compare the groups.
ResultsElevated expression of TRB3 in lung cancer
We assessed the differential expression of TRB3 in lung cancer specimens. The mRNA levels of TRB3 in tumor lesions of patients with non-small cell lung cancer (NSCLC) were determined by Q-PCR. Fifty-six of the sixty tumor samples showed a higher expression level of TRB3 compared with their respective adjacent, normal tissues (Fig. 1A). The upregulation of TRB3 was associated with distal metastasis and disease recurrence (Table I). Furthermore, the Kaplan-Meier survival curves revealed that TRB3 expression was inversely correlated with overall survival (Fig. 1B) and disease-free survival (Fig. 1C). The IHC results demonstrated that TRB3 was upregulated in the two types of NSCLC investigated, particularly in adenocarcinoma; however, TRB3 upregulation was not observed in normal lung tissues (Fig. 1D). The TRB3 expression was significantly correlated with tumor size and lymph node or distal metastasis status in NSCLC patients (Table I). These results suggested that the upregulation of TRB3 correlated with poor prognosis in patients with NSCLC.
TRB3 knockdown results in apoptosis in human lung adenocarcinoma cells
To elucidate the effect of knocking down TRB3 on human lung adenocarcinoma cells, A549 cells were transfected with a TRB3 interference vector and their proliferation and characteristics were detected. The expression level of TRB3 was significantly lower following shTRB3 transfection compared with the control groups (Fig. 2A). Additionally, the knockdown of TRB3 exhibited a positive effect on cell growth (Fig. 2B). The shTRB3 groups had the lowest transwell level compared with the remaining groups.
To understand whether TRB3 is biologically significant in the aggressiveness of lung cancer cells, A549 cells were subjected to TRB3 knockdown and examined for their aggressiveness in vitro. Knockdown of TRB3 was revealed to significantly decrease the invasive and migratory abilities of the A549 cells (Fig. 2C and D, respectively).
Correlation between TRB3 and Notch expression in the lung adenocarcinoma cell lines
Following determination of the elevated expression of TRB3 in lung cancer and the apoptotic effect of the TRB3 knockdown on the adenocarcinoma cells, the underlying mechanism of this effect was investigated. The results demonstrated a positive correlation between TRB3 and Notch 1 expression, at both the gene and protein level, in the lung adenocarcinoma cell lines (Fig. 3).
Discussion
The tribbles gene family was initially identified in Drosophila and considered as an inhibitor of mitosis that regulates cell proliferation, migration and morphogenesis during development (27,28). The three tribbles homologs, TRB1, TRB2 and TRB3, are considered to be members of the pseudokinase family, which contain a Ser/Thr protein kinase-like domain; however, lack the ATP binding pocket and catalytic residues. TRB3 is the most widely studied member of the mammalian tribbles family. The molecules which interact with TRB3 include transcription factors, such as ubiquitin ligase and the BMP type II receptor, which are members of the MAPK and PI3K signaling pathways (29,30). Hua et al demonstrated that TRB3 interacts with SMAD3 and promotes tumor cell migration and invasion (30). The authors suggested that TRB3 is a novel partner of SMAD3 and may be involved in retaining SMAD3 in the nucleus by physical interaction, and maintaining the mesenchymal status of tumor cells. These studies suggested that TRB3 may be a potential therapeutic target for the treatment of human tumor metastasis. In the present study, it was identified that TRB3 exhibits an abnormally abundant expression in lung cancer tissues in patients with NSCLC, and that the upregulation of TRB3 was correlated with an increased number of tumor metastases, a higher recurrence of tumors and poorer survival. According to these results, we hypothesized that TRB3 was a significant factor in promoting the malignant progression of tumors.
Our results demonstrated that suppressing TRB3 expression significantly inhibited tumor metastasis in A549 human lung adenocarcinoma cells. The knockdown of TRB3 affected cell growth and metastatic ability. The cells transfected with shTRB3 remained in the G1 stage compared with those in the non-treated group. This suggested that following the suppression of TRB3, the cell cycle was altered to remain in the G1 stage, as opposed to passing into the S and G2 stages. In addition, the invasive ability of the A549 cells was significantly decreased following the suppression of TRB3 expression. There are a limited number of studies concerned with the effects of TRB3 on the cell cycle regardless of the fact that studies in neuronal PC6-3 cells have demonstrated that TRB3 is involved in neuronal apoptosis evoked by nerve growth factor withdrawal. TRB3 is also a multi-functional adaptor in a number of signaling pathways (31). For example, TRB3 has been demonstrated to inhibit insulin-induced S6 kinase activation (31). Furthermore, it has been revealed that TRB3 binds to ATF4 and regulates its transcriptional activity (32). The expression of TRBs is regulated by inflammatory stimulation and is cell type specific (33). TRB3 mRNA may be upregulated by various stresses. Also, TRB3 is the transcriptional target of several factors, including PPARα, ATF4-CHOP and PI-3K (34–36). These studies indicated that TRB3 participates in multiple cellular processes and pathways.
JAG1/Notch signaling is a mediator of cancer progression and metastasis, which is associated with the basal-like cancer subtype (17). Therefore, the components of the Notch 1 pathway are attractive therapeutic targets for this cancer subtype. Whether TRB3 affects tumor cell biology may be inferred from data concerning the pathways it regulates. Tumor-initiating cells (TIC), a small population of cells within certain types of tumors, are able to produce derivatives that maintain the tumor. The pathways that TRB3s target, such as the Notch pathway, have been implicated in TIC maintenance. This suggests that through the control of these pathways, TRB3 may regulate tumor initiation. The metastatic potential of epithelial tumors likely depends on a process known as EMT, where epithelial cells acquire a migratory mesenchymal phenotype. The Notch 1 pathways interact with each other and have a synergistic effect on the production of factors that promote EMT and metastasis (24). In addition, the locations of metastases have been shown to be influenced by the Notch pathways (37). It has been demonstrated that the release of TGFβ stimulates JAG1 expression in tumor cells and enhances Notch activation in osteoblasts and preosteoclasts, which may promote bone invasion (38). Collectively, these findings predict that TRB3 may potentiate the initiation of tumor formation and the metastatic capacity of cancer cells, through its regulation of JAG1/Notch activation. However, whether the activation of these pathways and processes are regulated by TRB3, and whether reduced survival time is associated with tumors with an elevated level of TRB3, have not yet been identified. In this study, we demonstrated that Notch 1 gene expression was positively correlated with TRB3 in A549 cells.
The current study indicated that TRB3 expression was elevated in lung cancer tissues in patients with NSCLC. In addition, loss of TRB3 induced an apoptotic effect in the A549 lung adenocarcinoma cell lines. The cell cycles were held in the G1 stage and the invasive ability of the cells decreased significantly. The results also identified a positive correlation between TRB3 and Notch 1 in the A549 cells. Thus, this interaction may provide potential therapeutic targets for human NSCLC.
Acknowledgements
This study was supported by funding from the Hunan Provincial Department of Science and Technology (grant no. 2012SK3249) and the Hunan Provincial Department of Health (grant no. B2012-098), China.
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TRB3 expression in NSCLC and its correlation with survival rates. (A) Transcripts levels of TRB3 mRNA expression in normal and tumor tissues. (B) Overall survival and (C) disease-free survival in low (relative expression, 1 and 2) and high (relative expression, 3 and 4) TRB3 expression levels. (D) Immunohistochemistry of TRB3 in different types of lung cancer tissues (adenocarcinoma and squamous cell carcinoma) as well as in normal lung tissue. TRB3; tribbles homolog 3; NSCLC, non-small cell lung cancer.
Cell biological activites following transfection of A549 cells with either the shTRB3 vector or empty vector control. (A) TBR3 mRNA levels and (B) cell viability at different time points following vector transfection. (C) Invaded cells and (D) migrated cells following vector transfection. TRB3; tribbles homolog 3; shTRB3, short hairpin-tribbles homolog 3.
Correlation between Notch 1 and TRB3 expression in A549 cells transfected with either the shTRB3 vector or the empty control vector. NOTCH1 is downregulated following shTRB3 vector transfection at the mRNA and protein levels by (A) real time PCR; (B) western blot analysis and (C) immunofluorescence, respectively. TRB3, tribbles 3 homolog; shTRB3, short hairpin-tribbles homolog 3.
Correlation between TRB3 expression and clinicopathological factors in the 60 patients with NSCLC.
TRB3 expression
Characteristic
Low (0 and 1)
High (2 and 3)
P-valuea
Age
Years, mean ± SD
61.5 ± 5.1
60.87 ± 7.5
0.4782
Gender
Male
16
17
0.5712
Female
13
14
Smoking status
Smoker
17
15
0.8575
Non-smoker
12
16
Histological type
Adenocarcinoma
14
21
0.0280
Squamous cell carcinoma
20
10
Large cell carcinoma
3
5
Stage
I and II
18
10
0.0352
III and IV
11
21
Tumor status
T1 and T2
14
17
0.2782
T3 and T4
15
14
Lymph node metastasis
N0
18
9
0.0168
N1-N3
11
21
Distal metastasis status
M0
19
9
0.0316
M1
10
21
Recurrence status
Yes
11
23
0.0013
No
18
7
Statistical significance of the differences between groups in all the characteristics, with the exception of histological type, was analyzed by a two-sided Fisher’s exact test. The P-value for histological type was analyzed by the χ2 test. TRB3, tribbles homolog 3; NSCLC, non-small cell lung cancer.