- Open Access
Epstein-Barr Virus encoded LMP1 regulates cyclin D1 promoter activity by nuclear EGFR and STAT3 in CNE1 cells
- Yang Xu†1, 2, 3, 4,
- Ying Shi†1, 2, 3, 5,
- Qi Yuan1, 2, 3, 4,
- Xuli Liu1, 2, 3, 4,
- Bin Yan1, 2, 3,
- Ling Chen1, 2, 3,
- Yongguang Tao1, 2, 3, 5Email author and
- Ya Cao1, 2, 3, 5Email author
© Xu et al.; licensee BioMed Central Ltd. 2013
- Received: 22 August 2013
- Accepted: 12 November 2013
- Published: 13 November 2013
The principal Epstein–Barr virus (EBV) oncoprotein, latent membrane protein 1 (LMP1) is strongly associated with nasopharyngeal carcinoma (NPC), a prevalent cancer in China. The epidermal growth factor receptor (EGFR) is important in carcinogenesis, as it is a ubiquitously expressed receptor tyrosine kinase. Signal transducer and activator of transcription 3 (STAT3) is a master transcriptional regulator in proliferation and apoptosis. Our previous study demonstrated that the nuclear EGFR could bind to the cyclin D1 promoter directly in the presence of LMP1, and the correlation between EGFR and STAT3 in NPC remains to be further explored. Here, we have shown that the interaction of EGFR and STAT3 increased in the nucleus in the presence of LMP1. LMP1 promoted both EGFR and STAT3 binding to the promoter region of cyclin D1, in turn, enhancing the promoter activity of cyclin D1. Furthermore, we demonstrated that both transcriptional activity and mRNA levels of cyclin D1 were decreased by small molecule interference of EGFR and STAT3 activity. These findings may provide a novel linkage between the EGFR and STAT3 signaling pathways and the activation of cyclin D1 by LMP1 in the carcinogenesis of NPC.
- Cyclin D1
- Epstein–Barr virus
- Latent membrane protein 1
- Nasopharyngeal carcinoma
Epstein-Barr virus (EBV) is a ubiquitous herpes virus that is linked to multiple malignancies, including Burkitt’s lymphoma, Hodgkin’s disease, gastric cancer esophageal cancer cervical cancer and prostate cancer and nasopharyngeal carcinoma (NPC)[1–9]. Latent membrane protein 1 (LMP1) encoded by EBV functions as an essential factor in EBV-induced cell transformation and is expressed in many of the malignancies associated with EBV. LMP1 protein is detected in approximately 60 percent of tissue samples from patients with NPC[10, 11], while LMP1 mRNA is detected in nasopharyngeal swabs in over 90% of NPC patients by RT-PCR[12, 13]. The frequent expression of LMP1 in undifferentiated NPC points to a role for this viral oncoprotein as a key molecule in NPC pathogenesis[14–19].
Elevated amounts of the epidermal growth factor receptor (EGFR) at both the protein and mRNA levels are detected in the epithelial cell carcinomas including NPC, and its expression correlates with the levels of LMP1. Our earlier research reports that LMP1 may increase both expression and phosphorylation levels of EGFR[21, 22] and that LMP1 could regulate the nuclear accumulation of EGFR in a dose-dependent manner quantitatively and qualitatively. We also showed that nuclear EGFR could bind to the cyclin D1 promoter directly and transactivate the cyclin D1 promoter by LMP1 in NPC. Many factors such as the epidermal growth factor, the DNA damage factor, ultraviolet irradiation, radiation and cetuximab increase EGFR translocation into the nucleus[24–29]. These findings clearly indicate that EGFR may act as a new factor that directly target genes related to cellular transformation, cell cycle regulation, DNA damage repair and replication.
Signal transducer and activator of transcription 3 (STAT3) is a member of the STAT family of cytoplasmic proteins that is constitutively active in many human cancers[30, 31]. Upon stimulation by cytokines or growth factors, STAT3 translocates into the nucleus to upregulate numerous target genes, such as cyclin D1, c-fos, c-Myc, Bcl-XL, and VEGF, stimulating cell proliferation and preventing apoptosis. Overexpression and activation of STAT3 is strongly associated with NPC[32–34]. Our previous finding showed that EBV LMP1 stimulates the phosphorylation of STAT3 at both tyrosine 705 (Tyr 705) and serine 727 (Ser 727). Furthermore, we demonstrated that LMP1 signals through the Janus kinase 3 (JAK3) and extracellular signal-regulated kinase 1/2 (ERK1/2) pathways upon the activation (or transactivation) of STAT3. LMP1 may induce vascular endothelial growth factor (VEGF) expression via the JAK/STAT and mitogen-activated protein kinase (MAPK)/ERK signaling pathways. The relationship between LMP1 regulated STAT3 and other target genes remain unclear.
Cyclin D1 is a key regulatory protein at the G1/S checkpoint of the cell cycle. A recent census concluded that cyclin D1 gene amplification and overexpression are present in breast cancer, lung cancer, melanoma and oral squamous cell carcinomas[30, 36, 37]. Our previous studies have shown that LMP1 can activate cyclin D1 gene expression, upregulate the promoter activity of cyclin D1 by inducing c-Jun/Jun B heterodimers and via EGFR transcriptional activity as well as transcriptional intermediary factor 2 (TIF2) interaction in NPC cell lines. Therefore, we explored whether LMP1 regulated transactivation of the cyclin D1 promoter via activated EGFR and STAT3 in NPC would provide a new link in understanding the mechanisms of carcinogenesis and progression of NPC.
In this study, we found that LMP1 promoted the interaction of EGFR and STAT3 in the nucleus. The nuclear EGFR and STAT3 could target the cyclin D1 promoter directly, in turn, upregulating the cyclin D1 promoter activity and mRNA level. Furthermore, knockdown of EGFR and STAT3 decreased cyclin D1 promoter activity. Our results provide a novel linkage between deregulated EGFR signaling and the activation of cyclin D1 gene expression induced by LMP1 in NPC tumorigenesis.
CNE1 is an LMP1-negtive, poorly differentiated NPC cell line. CNE1- LMP1 is a stably transfected cell line, established by introducing LMP1 cDNA into CNE1 cells, and the cell line stably expressing LMP1[17, 34, 41–43]. Two cell lines were grown in RPMI 1640 (GIBCO BRL, U.S.A.), containing 10% fetal calf serum and 100 U/ml penicillin/streptomycin, and all cell lines grew, at 37°C under 5% CO2 and 95% air at 99% humidity.
Plasmid (pCCD1-Luc), kindly provided by Dr. Strauss M, contained 3.9 kb of the human cyclin D1 promoter cloned into the multiple cloning sites of pBSK+, driving the gene expression for firefly luciferase. The pcDNA3.1-EGFR expression plasmid was constructed by cloning the whole EGFR coding fragment into XhoI sites of the pcDNA3.1 vector. Expression plasmid for dominant negative mutant of EGFR (EGFR-DN) had a deletion of 533 amino acids at the N terminus, which competitively inhibited the activation of EGFR, and was cloned into pcDNA3.1. The pSG5-STAT3 was obtained from whole STAT3 coding fragment cloned into XhoI sites of the pSG5 vector. Expression plasmid for dominant negative mutant of STAT3 (STAT3β) had a deletion of 55-residue in C-terminal transactivation domain of STAT3 and replaced by seven unique C-terminal residues (CT7). The EGFR and STAT3 motif mutation (designated as pD1-mut-Luc) from pCCD1-Luc were generated by PCR based on an overlap extension technique. The primers used for generating mutations were: 5′- CTCCACCTCACCCCCTAAAT-3′ and 5′-AGGGATGGCTTTTGGGCTCT -3′. PCR-amplified fragments carrying the desired mutations were then cloned into Xba I sites of the pBSK + vector. The construction of expected TAKARA Biotechnology completed mutations and the sequencing of integrity of the vector. DNAzyme 1 (DZ1) is an LMP1-targeted DNAzyme that binds and cleaves LMP1 RNA in a highly sequence-specific manner. And the control oligonucleotide of DZ1 (TAKARA, China) was designed by inverting the catalytic core sequence. To monitor transfection efficiency, pRL-SV40 (Promega, U.S.A) was used as an internal control.
Preparation of cell lysates and cell fractions
For whole cell lysates, 107/ml cultured cells were harvested and washed twice with ice-cold phosphate-buffered saline (PBS), and then lysed in the 500 μl lysis buffer [10 mM Tris–HCl, pH 8.0; 1 mM EDTA, 2% sodium dodecyl sulfate (SDS); 5 mM dithiothreitol (DTT); 10 mM phenylmethyl sulfonylfluoride (PMSF); 1 mM Na3VO4; 1 mM NaF; 10% (vol/vol) glycerol; protease inhibitors cocktail tablet (Roche, Switzerland)] for 30 min on ice and centrifuged at 15,000 × g for 10 min. The supernatant was collected and stored at -70°C until used.
For Preparation of cytoplasmic and nuclear fractions, 107/ml cells were washed with PBS and suspended in 200 μl of lysis buffer (10 mM Hepes, pH 7.9; 10 mM KCl; 0.1 mM EDTA; 0.1 mM EGTA; 1 mM DTT; 0.5 mM PMSF; and protease inhibitor cocktail). The cells were incubated on ice for 15 min, after which 6.5 μl of 12.5% NP-40 was added; the contents were mixed and then centrifuged for 1 min at 12,000 rpm. The supernatant was saved as cytoplasmic fraction. The pellet was resuspended in 12.5 μl of ice-cold nuclear extraction buffer (20 mM Hepes, pH 7.9; 0.4 M NaCl; 1 mM EDTA; 1 mM EGTA; 1 mM DTT; 1 mM PMSF; and protease inhibitor cocktail) and incubated on ice for 40 min with mixing every 10 min, then they were centrifuged for 5 min at 12,000 rpm at 4°C. The supernatant was saved as nuclear fraction. The cytosolic and nuclear fractions were stored at -70°C until used.
Western blot analysis
Fifty microgram (μg) of the total proteins from cell preparations were separated on 10% SDS- polyacrylamide gel electrophoresis and then electrotransfered onto the nitrocellulose membrane. The membranes were blocked with buffer containing 5% non-fat milk in PBS with 0.05% Tween-20 (PBST) for 2 hrs, and incubated with different primary antibodies (anti-EGFR or anti-STAT3) overnight at 4°C. After second wash with PBST, the membranes were incubated with anti-rabbit (sc-2004, Santa Cruz, U.S.A.) or anti-mouse (sc-2005, Santa Cruz, U.S.A.) horseradish peroxidase- conjugated secondary antibody for 1 hr. at room temperature and color was developed with the enhanced chemiluminescence detection kit (ECL, Pierce, U.S.A.), then, and followed by exposure to autoradiographic film. The antibodies used were as follows: EGFR (sc-03-G, Santa Cruz, U.S.A.), p-EGFR (sc-12351, Santa Cruz, U.S.A.), STAT3 (#9132, Cell Signaling Technology, U.S.A.), p-STAT3 (#9131, Cell Signaling Technology, U.S.A.), β-actin (sc-8432, Santa Cruz, U.S.A.), α-tubulin (sc-5286, Santa Cruz, U.S.A.), Nucleolin (sc-8031, Santa Cruz, U.S.A.), cyclin D1 (Cat# 2261–1, Epitomics, U.S.A.).
Co-immunoprecipitation analysis and immunoblotting analysis
Cell extracts were prepared with harvested cells from CNE1 and CNE1-LMP1 lysed in an immunoprecipitation (IP) lysis buffer (50 mM Tris–HCl, 150 mM NaCl, 10% NP-40, 1 mM EDTA, 10% glycerol, 10 mM NaF, 1 mM Na3VO4, 1 mM DTT, 1 mM PMSF, and protease inhibitor cocktail tablet). Two milligram (mg) of protein prepared were mixed with 40 μl of protein A-Sepharose beads (Sigma, U.S.A.) in the IP assay buffer (1× PBS, 0.5% Nonidet P-40, 0.5% sodium deoxycholate, 0.1% SDS), incubated at 4°C for 2 hrs with gentle agitation and centrifuged for 10 min at 2,000 rpm for preclearing. The recovered supernatant was incubated with either 2 μg of anti-EGFR or 2 μg of anti-STAT3in the presence of 1× protease inhibitors at 4°C overnight with mild shaking. Followed by addition of 50 μl of Protein A-Sepharose beads and the incubation were continued for 2 hrs at 4°C with gentle shaking. Then, Protein A-precipitated protein complex was recovered by centrifugation for 10 sec. at 12,000 rpm and followed washed three times with IP assay buffer, the harvested beads were resuspended in 30 μl of 2× SDS PAGE sample buffer were boiled for 5 min. to release the bound protein. A 20 μg aliquot of cell lysate was used as an input control. The samples were then analyzed by Western blot. Antibodies for Western blot detection were EGFR IgG antibody and STAT3 IgG antibody.
Transient transfection and luciferase assay
Cells were cultured in 24-well plates at a density of 1 × 105 per well overnight and were transfected with Lipofectamine™ 2,000 (Invitrogen, U.S.A.) as the manufacturer’s instructions. Each transfection contained 800 ng/well of pCCD1-Luc or pD1-mut-Luc firefly luciferase reporter and 80 ng/well of internal control pRL-SV40 or contained 400 ng/well of firefly luciferase reporter and 80 ng/well of internal control pRL-SV40 together with 200 ng/well of each expression plasmid or blank expression plasmid necessary to normalize the amount of DNA transfected. Twenty-four hrs. after transfection, cells were harvested at 36 hrs. after transfection and lysates were analyzed for luciferase activity using the Dual Luciferase Reporter assay (Promega, U.S.A.) according to the manufacturer’s directions with a GloMax™ Microplate Luminometer (Promega, U.S.A.). The luciferase reporter plasmids were co-transfected with pRL-SV40 to correct for variations in transfection efficiency. The relative luciferase activity normalized to the value of pRL-SV40 activity. Results were expressed as fold induction of pCCD1-Luc activity in CNE1 cells, which was assigned a value of 1. WHI-P131, PD98059 and AG1478 inhibited the activities of cyclin D1 induced by stable expression LMP1. CNE1-LMP1 cells were transfected with cyclin D1 promoter-reporter construct and Renilla luciferase plasmid as an internal control. The data represent the mean ± SD of the three independent experiments performed in triplicate.
To observe WHI-P131, PD98059 and AG1478 inhibiting the activities of cyclin D1 induced by stable expression LMP1, 24 hrs. after transfection, cells were treated with WHI-P131 (Calbiochem, U.S.A. ), PD98059 (Cell Signalling Technology, U.S.A. ), AG1478 (Cell Signalling Technolgoy, U.S.A.) or 0.1% DMSO for 2 hr. Cells were harvested at 26 h after transfection and subjected to the luciferase assay. Empty firefly reporter vector served as the negative control.
Electrophoretic mobility shift assay (EMSA)
EMSA for EGFR/STAT3 binding to cyclin D1 was performed using the LightShift™ Chemiluminesent EMSA kit (Pierce, U.S.A ) and was conducted according to the manufacturer’s protocol. Briefly, Double-stranded oligonucleotides, were labeled using the biotin 3′end labeling (Invitrogen, U.S.A ). Ten μg of nuclear extracts were incubated with 2 μl biotin-labeled probes in binding buffer for 20 min. at room temperature. Additionally, increasing concentrations of 200- fold of excess of a cold competitive oligonucleotide (biotin- unlabeled probe) and NF-κB biotin-unlabeled probe (as a nonspecific competitive probe) were added to confirm specificity of the interaction. The reaction mixture was then loaded onto 10% non- denaturing polyacrylamide gel containing 0.5× Tris borate (TBE) and electro- phoresed in 0.5× TBE at 4°C prior to visualization according to the manufacturer; Followed by transferred to BiodyneR B Nylon membrane, avidin-HRP to probes, and visualized and quantitated with a PhosphorImager (Bio Rad, U.S.A). All the double-stranded probes were synthesized as follows: for the putative binding site of EGFR in the cyclin D1 promoter: 5′-TCGCTGAGATTCTTT GGCCGTCTG-3′ (wild type) and 5′-TCGCTGAGATACTCG GGCCGTCTG-3′ (mutated type). For the STAT3 binding site in cyclin D1 promoter: 5′-GTGGCGTTCTTGGAA ATGCG- CCCA-3′ (wild type) and 5′-GTGGCGAGCTTGTGA ATGCGCCCA-3′ (mutated type).
To verify the involvement of EGFR, STAT3, LMP1 in the complex, DZ1, small molecular inhibitors AG1478, WHI-P 131and PD98059, was added to the mixture containing the nuclear extracts and biotin-labeled probes and incubated at room temperature or on ice for an additional 10 min.
We used EGFR siRNA and STAT3 siRNA to reduce EGFR and STAT3 gene expression. The siRNA sequences for EGFR (sc-29301, Santa Cruz, U.S.A) and STAT3 (sc-29493, Santa Cruz, U.S.A ), and the negative control siRNA (sc-37007, Santa Cruz, U.S.A ) (silencer negative control) were purchased from Santa Cruz. Cells were plated at 30% to 40% confluency, in RPMI 1640 and 10% FCS. The indicated siRNA (100 pmol EGFR siRNA; and/or 100 pmol of STAT3 siRNA) was transfected in six-well plates using 10 μl Lipofect AMINE as recommended (Invitrogen, U.S.A ) for 6 hrs. in serum-free medium. Medium containing serum was added to bring the concentrations of serum to those indicated above.
To study transcriptional activity of endogenous EGFR and STAT3, cells were transiently cotransfected with pCCD1-Luc, and 10 nM of the noncoding control siRNA as a control.
RT-PCR and quantitative real-time PCR
Cells were transfected with the specified siRNAs and placed in RPMI 1640 with 5% FCS. Forty-eight hours later, they were harvested for RNA isolation using Trizol (Invitrogen, U.S.A). RNA was reverse transcribed with random primers and SuperScript II reverse transcriptase according to Invitrogen’s protocol. The RT Real-Time SYBR/ROX PCR Master Mix was purchased from TAKARA; and PCR analysis was performed on an Applied Biosystems 7500 Real-Time PCR System, according to the instructions of the manufacturer. The RT-PCRs were performed in duplicates for four independent experiments and the results were normalized to the respective expression levels of actin. The primer sequences were for cyclin D1 (forward) 5′-CTCCACCTCACC- CCCTAAAT -3′ and (reverse) 5′-AGAGCCCAAAAGCCATCC-3′ and for actin (forward) 5′-TTCC- AGCCTTCCTTCCTGGG-3′ and (reverse) 5′-TTGCGC- TCAGGAGGAGCAAT-3′. The amplification product of cyclin D1 was 177 bp. The mean ± SD of three independent experiments is shown.
Flow cytometry was used to quantify cells in each phase of the cell cycle. Cells (2 × 105) were plated into 6-well plates and treated with the indicated siRNAs after 24 hrs. Cells were harvested after an additional 72 hrs, washed with PBS and fixed in 70% ethanol overnight at 4°C. To detect the fluorescent intensity of certain proteins, cells were counterstained in the dark with 50 μg/ml phosphatidyl inositol (PI) and 0.1% ribonuclease A (RNase A) in 400 μl of PBS at 25°C for 30 min. Stained cells were assayed and quantified using a FACSort Flow Cytometer (Becton Dickinson, U.S.A).
All statistical calculations were performed with the statistical software program SPSS ver.10.0. Differences between various groups were evaluated by the Student’s t test. The difference was of statistical significance, when p <0.05.
LMP1 promoted the interaction of EGFR with STAT3 in NPC cells
LMP1 induced EGFR and STAT3 nuclear translocation in NPC cells
LMP1 activated the activity of cyclin D1 promoter by the EGFR and STAT3 pathways
Inhibitors of both EGFR and STAT3 signaling pathways attenuated LMP1-augmented cyclin D1 promoter activities and protein levels
Nuclear accumulation of EGFR and STAT3 is dependent on the activation of the related signaling pathways. CNE1-LMP1 cells were treated with the small molecule inhibitor WHI-P131, a specific inhibitor of STAT3 phosphorylation at residue tyrosine 705 and serine 727. Both the promoter activity (Figure 4C) and the protein level (Figure 4D) of cyclin D1 decreased greatly upon WHI-P131 treatment. Treatment with PD98059, a chemical inhibitor that blocks the nuclear translocation of STAT3, also decreased cyclin D1 promoter activity (Figure 4C) and protein expression (Figure 4D). On the other hand, the data in Figure 4C and Figure 4D indicated that AG1478, an EGFR specific tyrosine kinase inhibitor, decreased the transcriptional activity of the cyclin D1 promoter and protein level. WHI-P131 was less efficient in the presence of PD98059 in cyclin D1 transcription (Figure 4C) but not cyclin D1 protein level (Figure 4D). siSTAT3 or WHI-P131 induced a stronger inhibition of cyclin D1 promoter activity than siEGFR or AG1478. Taken together, these data suggest that both EGFR and STAT3 signaling pathways are involved in the transcriptional activity of Cyclin D1 promoter and protein levels.
LMP1 regulated the nuclear EGFR and STAT3 binding to the cyclin D1 promoter region directly
To address whether nuclear EGFR is involved with the cyclin D1 promoter directly, we mutated the cyclin D1 promoter sequence such that no transcription factor binds. As shown in Figure 5C, biotin-labeled wild-type EGFR oligonucleotide and nuclear EGFR formed a specific complex in CNE1- LMP1 cells (Figure 5C lane 3). With a mutated EGFR probe, no specific complex band was present (Figure 5C lane 5), whereas a weak band was detected in CNE1 cells. Formation of this complex from CNE1- LMP1 cells was blocked by competition with the cold EGFR (Figure 5C lane 4) but not by the mutated EGFR or nonspecific nucleotide NF-κB (Figure 5C lanes 6 and 7). After blocking the EGFR signaling pathway with the small molecule inhibitor AG1478, the band indicating a complex was weaker in the CNE1-LMP1 nuclear proteins (Figure 5D). To confirm that LMP1 controlled the cyclin D1 promoter, the CNE1-LMP1 cells were treated with DZ1, which is a specific LMP1-targeted DNAzyme construct. Data in Figure 5E showed that the complex band of biotin-labeled EGFR nucleotide with nuclear protein weakened in CNE1-LMP1 cells after treatment with DZ1. Taken together, these results show that LMP1 regulates the binding capacity of EGFR, STAT3 to the cyclin D1 promoter region in vitro.
LMP1 induced EGFR and STAT3 to activate cyclin D1 gene expression
cyclin D1 over-expression is important in the development and progression of numerous cancers. Regulation of the cyclin D1 protein level is one of the critical aspects in cell proliferation and tumor development, indicating that cyclin D1 may be regarded as a therapeutic target in cancer. Cyclin D1 is upregulated expression in NPC. Overexpressed cyclin D1 in NPC increases the risk of tumor formation and local disease recurrence. Although cyclin D1 is known to be a target gene of EGFR and STAT3[46, 53–56], its transcriptional regulation remains elusive after the infection of virus. Our previous study reported that LMP1 encoded by EBV could regulate the nuclear accumulation of EGFR and that nuclear EGFR could bind to the promoters of cyclin D1 and cyclin E to accelerate the G1/S phase transition. Another report showed that EBV LMP1 signals through the Janus kinase 3 (JAK3) and ERK1/2 pathways upon the activation of STAT3 and STAT transactivation to induce expression of VEGF. Overexpressed EGFR could activate specifically and persistently STAT3 after the decrease TGF-beta signaling pathway. The key contribution of the present study is to provide a link between signaling via LMP1/EGFR and LMP1/STAT3, which is consistent with the previous findings that EBV LMP1 could promote the expression of EGFR[58, 59].
The mechanism by which EBV LMP1 induces EGFR and STAT3 to enhance the promoter activity and expression of cyclin D1 involves physical and functional interaction between EGFR and STAT3. This observation is in agreement with other reports that nuclear EGFR interacts with transcription factors, such as STAT3, E2F1, STAT5 and TIF2 to induce the expression of some target genes in various cancers[31, 40, 60–63]. Nuclear EGFR-targeted genes including cyclin D1[54, 64], iNOS, B-Myb, Aurora A and COX-2, have been reported, yet these studies did not support cyclin D1 as the target gene co-regulated by EGFR and other transcription factors after the infection of EBV, such as in the work of EGFR and STAT3 co-affecting on iNOS and STAT1 in breast cancer[31, 57]. Together, these findings suggest the EGFR-STAT3 axis signaling pathway is critical in regulating cellular transcriptional and biologic properties in different carcinomas in response to diverse carcinogens such as virus infection.
Our previous studies reported EBV LMP1 induces in both expression and phosphorylation of EGFR in a dose-dependent manner[21, 45], and other authors demonstrated EGFR that accumulated in the nucleus of breast carcinoma cell lines and esophageal cancer tissues was highly tyrosine-phosphorylated[54, 65]. Meanwhile, we found EBV LMP1 expressing cells exhibited more nuclear accumulation of Tyr 705-phophorylated STAT3 (pY-STAT3)[35, 45]. EGFR physically interacts and functionally cooperates with STAT3 at both the cytoplasmic and nuclear levels. As reported, EGFR and phosphorylated STAT3 were strongly expressed in the nucleus of cancer cells in surgical and biopsy specimens of nasopharyngeal tissues from NPC patients in southern China[35, 66], suggesting that EGFR- and STAT3-dependent mechanisms are important for carcinogenesis.
It has been shown that LMP1 induces cyclin D1 expression through EGFR in NPC cells. The present study show that the promoter activity and mRNA expression level of cyclin D1 in LMP1-expressing cells could be decreased by co-transfecting the plasmids of mutated EGFR/STAT3 or siRNA for EGFR and siSTAT3. However, we did not find the cooperative effect of siEGFR and siSTAT3 at both mRNA and protein levels of cyclin D1. We provide the evidence showing cyclin D1 might be modulated by STAT3 induced by EBV LMP1, illustrating the importance of the JAK/STAT signaling pathway on EBV LMP1 induced cyclin D1 transcription and expression.
The current standard therapy for NPC is radical radiotherapy for early stage disease and concurrent chemoradiotherapy for advanced disease[67, 68]. EGFR and STAT3 are good targets for cancers treatment. Thus, agents such as the anti-EGFR antibody cetuximab, the EGFR tyrosine kinase inhibitor gefitinib, and STAT3 inhibitors (such as S3I-201 or JSI-124) could be used in preclinical models or each phase of clinical trials[69–71]. Interestingly, a novel STAT3 inhibitor S3I-1747 selectively interrupt the interaction of EGFR and STAT3 directly. Those reports also suggested that either an anti-EGFR or anti-STAT3 agent might be a potent chemopreventive agent for patients with anti-invasion and anoikis-sensitizing activities. Therapies such as monoclonal antibodies and tyrosine kinase inhibitors targeting EGFR have demonstrated limited anti-tumor efficacy[71, 73]; however, reports of combined targeting of EGFR and STAT3 are few. Recently, EBV LMP1-specific DNAzyme, DZ1, inhibits the majority of oncogenic signaling pathways converging on sets of transcription factors that ultimately control gene expression patterns resulting in tumor formation, progression, and metastasis. Our data showed that DZ1 can inhibit EBV LMP1-induced promoter activity of cyclin D1 via EGFR or STAT3 and that DZ1 enhanced cyclin D1 promoter inhibition based on experiments with mutants of EGFR or STAT3. These results suggest that combining inhibitors for EGFR/STAT3 and DZ1 in LMP-expressing cancers may be a promising therapeutic strategy. The combination of Src and EGFR inhibition with Gemcitabine treatment in STAT3-mediated therapy-resistant pancreatic tumors was also effective at inhibiting the growth of xenografts of both therapy-sensitive and -resistant pancreatic cancer cells in vivo without increasing toxicity. It is possible that EGFR and STAT3, individually or as a pair, contribute to tumor progression. Alternatively, crosstalk between signaling pathways provides a potential route to overcome the blockade of a single or double targeted therapies, but this can be overcome by the blockade of multiple targets. Our data provide further evidence that the combination of three inhibitors may be efficacious for cancer, and more extensive investigation will be required.
In summary, we found that EBV LMP1 enhances the transcriptional activity and mRNA level of the cyclin D1 gene in CNE1 cells. This underlying mechanism for cyclin D1 regulation involves regulated binding of EGFR and STAT3 in the cyclin D1 promoter region as well as increasing the promoter activity of the cyclin D1 gene. Such a mechanism may partially contribute to the proliferation and growth of tumor cells with an LMP1-induced increase in the nuclear accumulation of EGFR and STAT3.
We would like to thanks members of the lab for critical discussions of this manuscript. This work was supported by the Fundamental Research Funds for the Central Universities [2011JQ019], the National Basic Research Program of China [Grant# 2011CB504300, 2009CB521801], the Program for New Century Excellent Talents in University [Grant# NCET-07-0863], and the National Natural Science Foundation of China [Grant# 30930101, 30772482, 81071755].
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