Notch1 binds and induces degradation of Snail in hepatocellular carcinoma
© Lim et al; licensee BioMed Central Ltd. 2011
Received: 13 October 2011
Accepted: 30 November 2011
Published: 30 November 2011
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© Lim et al; licensee BioMed Central Ltd. 2011
Received: 13 October 2011
Accepted: 30 November 2011
Published: 30 November 2011
Hepatocellular carcinoma (HCC) is a common, highly invasive malignant tumor associated with a high mortality rate. We previously reported that the aberrant expression of Snail via activation of reactive oxygen species contributes to the invasive property of HCC, in part by downregulation of E-cadherin through both transcriptional repression and epigenetic modification of the E-cadherin promoter. Having demonstrated the ability of Snail to bind and recruit histone deacetylase 1 and DNA methyltransferase 1 in this context, we set out to look for other interactions that could affect its ability to promote oncogenic transformation and cancer cell invasion.
Using cells that stably expressed Snail, we characterized Snail protein interactors by tandem affinity purification and mass spectrometry. Immunoprecipitation and subcellular colocalization studies were performed to confirm our identification of the Notch1 intracellular domain (NICD) as a novel Snail-binding partner. NICD interaction with Snail was found to induce ubiquitination and MDM2-dependent degradation of Snail. Interestingly, NICD inhibited Snail-dependent invasive properties in both HCC cells and mouse embryonic fibroblasts.
Our study demonstrates that NICD can oppose Snail-dependent HCC cell invasion by binding and inducing proteolytic degradation of Snail. Although Notch signaling and Snail are both widely considered tumor-promoting factors, our findings indicate that the individual oncogenic contribution of Notch1 and Snail in malignant systems should be interpreted carefully, particularly when they are conjointly expressed.
Hepatocellular carcinoma (HCC) is a common, highly invasive malignant tumor associated with a high mortality rate [1, 2]. The resistance of HCC to existing antineoplastic agents and the limited effectiveness of chemotherapies due to underlying liver disease contribute to the poor prognosis for patients with HCC . Although surgical resection is the preferred standard of care for patients with HCC, few patients are suitable candidates for this treatment and recurrence is common even after radical curative resection [3, 4]. Given the inadequate impact of conventional therapies and the rising incidence of HCC, elucidation of the oncogenic mechanisms underlying HCC development is critical for identifying potential therapeutic targets or modalities.
Snail is a well-known zinc finger (ZF) transcriptional repressor responsible for epithelial-to-mesenchymal transitions (EMTs) and metastasis in several cancers [5, 6]. We previously reported that upregulation of human SNAI1 (Snail) expression by reactive oxygen species contributes to the invasive nature of HCC, in part by inducing the expression of matrix metalloproteinases and downregulating E-cadherin expression through both transcriptional repression and epigenetic modification of the E-cadherin promoter . Other recent reports have revealed that Snail induces broad epigenetic modifications of target genes by interacting with tumor-associated proteins (including HDAC1, DNMT1 and p53) [7–9]. Taken together, the ability of Snail to promote oncogenic transformation and cancer cell invasion is likely mediated by its interactions with other proteins in addition to its transcriptional activity.
The Notch signaling pathway regulates embryonic cell determination and differentiation as well as postnatal development [10, 11]. Although alterations in the Notch pathway are associated with malignant processes, there is also evidence that supports a tumor-suppressive role for Notch signals . Activation of the Notch pathway is initiated through juxtacrine ligand-receptor interactions and the proteolytic cleavage of Notch1 by γ-secretase, which liberates the Notch1 intracellular domain (NICD) from the membrane, allowing NICD to translocate to the nucleus . Nuclear NICD then associates with CSL (CBF1/RBPJk in vertebrates, Suppressor of hairless in Drosophila, Lag-1 in Caenorhabditis elegans) transcriptional factors to inhibit CSL transcriptional repression of Notch target genes . Of note, though both NICD and Snail proteins are known to play a central role in cancer cell growth, invasion and metastasis, Notch signaling is also capable of inhibiting HCC tumor growth through the induction of cell-cycle arrest and apoptosis [5, 13–15].
In this study, we have identified NICD as a novel Snail binding partner by using tandem affinity purification and mass spectrometry (MS/MS) in HCC cells. Using HCC cell lines and mouse embryonic fibroblasts (MEFs), we demonstrate that NICD can induce Snail degradation and impede Snail-dependent cell invasion. Although Snail is known to be degraded by the β-TrCP1 and FBXL14 E3 ubiquitin ligases, our data indicate that NICD-mediated Snail degradation may instead be dependent on MDM2 [16, 17].
Coimmunoprecipitation experiments showed that Myc-NICD can interact with MDM2 (Figure 4D). In a previous report, we found that Snail may also bind MDM2 (Figure 4D) . These data support the notion that NICD induces degradation of the Snail protein via MDM2-mediated ubiquitination because NICD has no known intrinsic E3 ligase function. Indeed, in Hep3B cells cotransfected with Myc-NICD and MDM2 siRNA, NICD-induced Snail degradation was decreased compared to control siRNA-transfected cells (Figure 4E). Glycogen synthase kinase 3β (GSK-3β) is known to induce Snail phosphorylation and degradation through the E3 ubiquitin ligase β-TrCP1 . To determine whether NICD-induced Snail degradation is reliant on GSK-3β/β-TrCP1, we analyzed the protein level of the Snail 2SA mutant, which has two point mutations in the β-TrcP motif, in cells cotransfected with Snail 2SA mutant and NICD. We found that both the Snail WT and 2SA mutant proteins were uniformly degraded by NICD, implying that NICD-induced Snail degradation is a β-TrcP-independent phenomenon (Figure 4F).
To test whether NICD specifically inhibits Snail-induced cell invasion, we performed invasion assays in NICD and/or Snail siRNA-transfected Hep3B cells after treatment with H2O2. As portrayed in Figure 6E, we found that H2O2-treated cells ectopically expressing NICD were less invasive than H2O2-treated control cells, which correlates with the ability of NICD to inhibit H2O2-dependent upregulation of Snail expression (Figure 3E). However, in H2O2-treated cells cotransfected with Snail siRNA, NICD expression lacked any effect on cell invasion (Figure 6E and Additional file 3). Taken together, these results demonstrate that NICD can inhibit Snail-induced cell invasion.
Previously, Notch1 was shown to cooperate with the Snail pathway by upregulating Snail transcription, inducing EMT and promoting hypoxia-induced tumor cell invasion . However, we found that NICD, which is an intracellular functional molecule liberated from Notch1, can suppress Snail protein via direct binding. This suggests that the Notch1-Snail pathway includes not only the single functional pathway but also a reciprocal interrelationship. Although both NICD and Snail protein play a central role in cancer cell growth, invasion and metastasis [5, 13–15], their physical interaction has not been described previously. Given the highly invasive phenotype of HCC and the overexpression of Snail in HCC tissue , we utilized HCC cell lines as a model cell system in which to study the functional involvement of NICD-Snail interaction in disease development.
Notch1 is known to regulate Snail and Slug mRNA levels, but efforts have not been made to examine alternative functions of NICD and Snail expression in the same cancer cell line [19–21]. In this study, we have demonstrated the ability of NICD to associate with Snail to induce its ubiquitination and proteasomal degradation. NICD has been reported to upregulate Snail activity by inducing Snail mRNA expression under hypoxic conditions . In addition, Notch1 is related to the mesenchymal program by activating Snail expression in cardiac development [22, 23]. Our findings appear to be inconsistent with these previous results. However, because Notch signals and cellular functions vary according to cell type and cellular environment, these inconsistencies could be caused by the different cell types and conditions. Although ectopic expression of NICD slightly induced Snail transcription, we postulate that the genetic interaction between Snail and NICD and their physical association may be physiologically exclusive events, which may account for their contrasting cellular effects. In our previous study, ROS stress upregulated Snail mRNA and protein expression . In the ROS-treated cells, Myc-NICD downregulated the Snail protein level, not the mRNA level (Figure 3). These latter data indicate that, under conditions of exogenous Snail expression or endogenous Snail upregulation by ROS stress, NICD reduces Snail protein levels by inducing Snail degradation without affecting Snail transcription. Because the NICD ΔANK mutant failed to induce ubiquitination and degradation of Snail, it appears that the physical interaction of NICD and Snail is required for the degenerative process. NICD is not known to have inherent E3 ligase functions, indicating that NICD may initiate or serve as a cofactor of the degradation signal. We have shown that Myc-NICD interacts with MDM2 (Figure 4D), but the NICD ΔANK mutant did not (data not shown). In addition, in MDM2 siRNA-transfected cells, NICD-induced Snail degradation was decreased compared to control siRNA-transfected cells (Figure 4E), suggesting that MDM2 has a role in NICD-induced Snail degradation.
We attempted to improve the transient transfection conditions with a stably NICD-expressing cell line based on a retroviral expression system. In these cells, the expression levels of NICD were much lower than those found with transient transfection. As shown in Figure 5 and Additional file 3 NICD-induced Snail degradation occurred in our stably NICD-expressing cells. In addition, to show that ligand-stimulated, NICD-induced Snail degradation took place, we used the cell line that expressed the exogenous Jagged1 ligand. In these cells, NICD induced Snail degradation (Figure 5C). Moreover, Notch1 siRNA upregulated endogenous Snail protein levels, as shown in Figure 5A. These data suggest that NICD-induced Snail degradation occurs in certain physiological conditions.
In this study, NICD-induced degradation of Snail inhibited Snail-dependent invasive behavior, as expected. Consistent with these invasion data, E-cadherin expression decreased in Snail-overexpressed cells, but it did not in Snail- and NICD-coexpressed cells compared to control cells (Additional file 3). In our previous study, we reported p53-induced Snail degradation via MDM2 . Notch1 expression and signaling were regulated differently, depending on p53 status [13, 24]. In other systems, Notch1 related to the mesenchymal program by activating Snail expression [19, 22, 23]. In another previous study, we showed that Notch1 and Snail differentially regulate invasion of HCC cells depending on p53 status . The inhibition of invasion by NICD and Snail coexpression was observed in both Hep3B cells (p53-null) and Huh7 cells (p53-mutant). On the other hand, in p53 WT cells such as HepG2, NICD and Snail coexpression promotes invasiveness . In the present study, we showed NICD regulated invasion via Snail degradation in p53-null or p53-mutant status. On the basis of these reports, we suspect that the interactions among p53, MDM2, Notch1 and Snail play an important role in EMT. Furthermore, these data explain the context-dependent regulation of EMT by the Notch signaling system. Our study provides one clue for understanding the complex regulation mechanism of p53, MDM2, Notch1 and Snail in the EMT process. The regulation of these proteins and their physiological contribution to HCC development and malignant behavior require further investigation. However, the mechanism that we have described presents substantial evidence of cross-interference between the Notch and Snail signaling pathways, which is mediated by their direct binding.
Herein we have identified NICD as a novel binding partner of Snail. Our results indicate that the interaction between NICD and Snail promotes Snail ubiquitination and degradation through an MDM2-dependent mechanism. Accordingly, we have shown that NICD impairs Snail-associated cell invasion in a conserved manner between MEFs and HCC cells. These findings collectively suggest that in the instance in which Notch1 and Snail are conjointly present, Notch signaling may serve as an antagonist of Snail function. The results of our research ultimately support caution in the use of genetic or pharmacological strategies that solely target the Notch pathway for therapeutic treatment in Snail-associated HCC. Further investigation is warranted to fully determine the precise cellular processes disrupted by Notch inhibition and thus to better assess the therapeutic value and clinical implications of Notch pathway antagonists.
Hep3B human hepatoma cells, Huh7 human hepatoma cells, HT-29 human colorectal carcinoma cells, Panc-1 human pancreatic cancer cells, MDA-MB231 human breast carcinoma cells and 293T cells were cultured in DMEM with 10% fetal bovine serum (FBS). In some experiments, cells were incubated with 10 μM MG132 for 6 hours. To establish stable 293T lines expressing human triple-tagged Snail, we inserted the Snail cDNA sequence into the pIRES2-EGFP/SFB vector and transfected the 293T cells with either pIRES2-EGFP/SFB as a control or pIRES2-EGFP/SFB-Snail with FuGENE 6 transfection reagent (Roche Applied Science, Penzberg, Germany). G418 sulfate (Geneticin; Invitrogen, Carlsbad, CA, USA) or puromycin (InvivoGen, San Diego, CA, USA) were used to select colonies. Primary MEFs obtained from embryos of p53-/- mice at day 13.5 were cultured in DMEM supplemented with 10% FBS. For siRNA experiments, cells were transfected with Notch1, Snail, MDM2 and control siRNA (ON-TARGETplus siRNA reagents; Dharmacon/Thermo Fisher Scientific, Lafayette, CO, USA) using Oligofectamine transfection reagent (Invitrogen/Life Technologies). After a 72-hour transfection or transduction, protein expression was analyzed by immunoblotting. All other reagents were purchased from Sigma-Aldrich (St Louis, MO, USA).
For purification, cells stably expressing Snail tagged with S protein-Flag-SBP (streptavidin-binding peptide) (SFB) were lysed with 50 mM Tris·HCl, pH 8.0, 150 mM NaCl, 5 mM ethylenediaminetetraacetic acid (EDTA) and 0.5% Nonidet P-40 (NP-40) (NTEN) lysis buffer supplemented with protease and phosphatase inhibitors. Streptavidin Sepharose (first purification) followed by S-beads (second purification) were used to bind SFB-tagged Snail. Snail complexes were reduced, alkylated and digested overnight with trypsin. Peptides were characterized using MS/MS (Thermo Fisher Scientific, Inc, Waltham, MA, USA). The resulting peptide tandem mass spectra were searched against a comprehensive nonredundant protein database using SEQUEST Cluster software (Thermo Fisher Scientific, Inc).
Human SNAI1 and NICD were obtained from the Huh7 cell line and cloned into pCMV/HA, pCMV/Myc and/or p3 × Flag/CMV expression vectors. Using pCMV/HA-Snail as a template, a SNAG domain-deleted Snail construct (ΔSNAG), ZF region-deleted Snail construct (ΔZF) and ZF region construct were developed by performing PCR with the following primers: 5'-AGAATTCGGAAGCCCTCCGAC-3' (forward for ΔSNAG), 5'-AGCGGCCGCTCAGCGGGGACATCC-3' (reverse for ΔSNAG), 5'-AGAATTCCGCGCTCTTTCCTC-3' (forward for ΔZF), 5'-AGCGGCCGCTCAT CGAGCCTGGAGATCCTTGGC-3' (reverse for ΔZF), 5'-AGAATTCCGAAGGCCTTCAACTGCAAATAC-3' (forward for ZF) and 5'-AGCGGCCGCTCAGCGGGGACATCC-3' (reverse for ZF). Using pCMV/Myc-NICD as a template, RAM domain-deleted (ΔRAM), ANK domain-deleted (ΔANK), TAD domain-deleted (ΔTAD), OPA domain-deleted (ΔOPA) and PEST domain-deleted (ΔPEST) mutant constructs were developed by site-directed mutagenesis. All constructs were confirmed by sequencing. HA-tagged ubiquitin and human Jagged1 constructs were kindly provided by Dr C Chung and Dr L Nie, respectively. Flag-Snail WT and 2SA mutant constructs were obtained from Addgene, Inc (Cambridge, MA, USA).
Flag-Snail and Myc-NICD were cloned into pMSCV. To generate MSCV-expressing Flag-Snail or Myc-NICD, we transfected GP293 cells with pMSCV (for control virus), pMSCV/Flag-Snail or pMSCV/Myc-NICD with FuGENE 6 transfection reagent. Twenty-four hours after transfection the medium was changed, then the medium was collected at 12-hour intervals. The collected medium containing retrovirus was filtered and stored at -20°C. Before the retrovirus was used, we titrated it using the QIAamp Viral RNA Mini Kit (QIAGEN, Valencia, CA, USA) and the One Step SYBR PrimeScript RT-PCR Kit II (TaKaRa Bio Inc, Shiga, Japan). Cells were seeded at 30% confluence 12 hours before infection, and the media were replaced with medium containing MSCV. After infection for 24 hours, the medium was replaced with fresh medium and the infected cells were selected with puromycin (InvivoGen).
In this study, we used the following antibodies: rat and mouse anti-Snail mAb (Cell Signaling Technology, Inc, Danvers, MA, USA), rabbit anti-Snail pAb (Abcam, Cambridge, MA, USA), rabbit anti-Notch1 mAb (Epitomics, Inc, Burlingame, CA, USA), goat anti-Notch1 pAb (Santa Cruz Biotechnology, Santa Cruz, CA, USA), rabbit anti-Jagged1 pAb (Santa Cruz Biotechnology), rabbit anti-p21 pAb (Cell Signaling Technology, Inc, and Santa Cruz Biotechnology), mouse anti-E-cadherin mAb (BD Biosciences, Franklin Lakes, NJ, USA), mouse anti-Myc mAb (Santa Cruz Biotechnology), mouse anti-Flag mAb (Sigma-Aldrich), mouse anti-HA mAb (Sigma-Aldrich), rabbit anti-HA pAb (Abcam) and mouse anti-β-actin mAb (Sigma-Aldrich).
Tissue and cell lysates were prepared, and immunoblot analysis was performed as described previously . Band intensity was determined using ImageMaster 2D Elite version 4.01 software (Amersham/GE Healthcare, Uppsala, Sweden). For immunoprecipitation, Hep3B cells were transfected with Flag-Snail, Myc-NICD and MDM2. After 48 hours, the cells were lysed in buffer (50 mM Tris·HCl, pH 8.0, 150 mM NaCl, 5 mM ethylenediaminetetraacetic acid (EDTA) and 0.5% Nonidet P-40 (NP-40)) and centrifuged at 16, 000 × g for 15 minutes to remove debris. Cleared lysates were subjected to immunoprecipitation with antibodies. For immunocytochemistry, cells were fixed in 4% paraformaldehyde at room temperature for 15 minutes, permeabilized in 5% Triton X-100 for 5 minutes, and then stained using pAbs. The secondary antibodies used were anti-mouse Alexa Fluor 594 dye conjugate and anti-rabbit Alexa Fluor 488 dye conjugate (Molecular Probes/Life Technologies, Carlsbad, CA, USA). Nuclei were stained with 4', 6-diamidino-2-phenylindole (DAPI blue) (Molecular Probes/Life Technologies). After mounting, the cells were visualized using a multiphoton confocal laser-scanning microscope (Carl Zeiss, Thornwood, NY, USA).
Twenty-four hours after transfection the cells were treated with 10 μM MG132 for 6 hours. The treated cells were then harvested with PBS containing 10 mM N-ethylmaleimide (NEM) and 1 mM dithiothreitol (DTT). The cells were washed with PBS, centrifuged and subjected to one freeze-thaw cycle. Cell pellets were then resuspended in 200 μl of buffer 1 (10 mM Tris·HCl, pH 7.5, 10 mM NaCl, 0.5% NP-40, 5 mM EDTA, 1 mM ethylene glycol tetraacetic acid (EGTA), 10 mM NEM, 1 mM DTT, 5 mM NaF, 1 mM Na3VO4 and protease inhibitor cocktail) and sonicated in a water bath (Bioruptor; Diagenode, Denville, NJ, USA). Next 500 μl of buffer 2 (20 mM Tris·HCl, pH 7.5, 0.5 M NaCl, 0.5% NP-40, 5 mM EDTA, 1 mM EGTA, 10 mM NEM, 1 mM DTT, 5 mM NaF, 1 mM Na3VO4 and protease inhibitor cocktail) were added, and the extracts were subjected to a 30-minute rotation at 4°C. Extracts were then centrifuged. We added 2 μg of anti-Flag M2 antibody and protein A/G beads to the supernatant and incubated it for 2 hours. The beads were then washed three times, resuspended in loading buffer and boiled. Immunoblotting was performed as described above.
Real-time PCR analysis of cDNA samples was performed with specific primers designed using Primer Express software (Applied Biosystems, Foster City, CA, USA). The primers used for Snail were 5'-AAGGATCTCCAGGCT CGAAAG-3' (forward) and 5'-GCTTCGGATGTGCATCTTGA-3' (reverse) and the primers used for β-actin were 5'-GCAAAGACCTGTACGCCAACA-3' (forward) and 5'-TGCATCCTGTCGGCAATG-3' (reverse). Total RNA was extracted from cultured cells using an RNeasy kit (QIAGEN) according to the manufacturer's protocol. cDNA was synthesized using 1 μg of RNA with avian myeloblastosis virus reverse transcriptase (Promega, Madison, WI, USA) and oligo(dT) primers. Transcript levels were assessed by quantitative real-time PCR (ABI 7300; Applied Biosystems), and all experiments were normalized to β-actin.
Cell invasion was measured at 96 hours as described by the manufacturer (Oris Cell Invasion and Detection Assay Kit; Platypus Technologies, LLC, Madison, WI, USA). In the invasion assay, fluorescence was monitored at an excitation of 492 nm and an emission of 530 nm using a multiplate reader (EnVision Multilabel Reader; PerkinElmer, Inc, Waltham, MA, USA).
The Duolink II fluorescence assay was used to analyze Hep3B, HT-29, Panc-1 and MDA-MB231 cells. Cells were seeded at 30% confluence on a cover glass and treated with 10 μM MG132 and 300 μM H2O2 for 6 hours. Huh7 cells were fixed with 4% paraformaldehyde and permeabilized with 0.5% Triton X-100 for 15 minutes each, then blocked and incubated with mouse anti-Snail Ab (1:100 dilution; Cell Signaling Technology) and rabbit anti-Notch1 Ab (1:100 dilution; Epitomics, Inc) for 30 minutes. The Duolink II PLA probe protocol was used to detect the signals. After mounting, the cells were visualized using a multiphoton confocal laser-scanning microscope (Carl Zeiss).
Bacterial lysate expressing GST-Snail proteins (WT, ΔZF and ZF mutants) was purified by immobilization on glutathione Sepharose beads (Pharmacia Biotech/GE Healthcare, Uppsala, Sweden). The beads were thoroughly washed with wash buffer (20 mM Tris·HCl, pH 8.0, 1 mM EDTA, 1 mM DTT, 150 mM NaCl, 1% Triton X-100) containing protease inhibitor mixture. The bound proteins were incubated with Myc-NICD-transfected cell lysate, washed with the wash buffer and eluted by boiling in the SDS sample buffer for 10 minutes. The sample was then analyzed by immunoblotting.
The data in the bar graphs of Figure 3 and 6 are expressed as the means (± SD) of three independent experiments. All results shown in the bar graphs are expressed as the fold ratio relative to untreated or control cells. Statistical analysis was performed using SPSS version 12 statistical software (SPSS Inc, Chicago, IL, USA).
6 ankyrin/cdc10 repeat
CBF1/RBPJk in vertebrates: Suppressor of hairless in Drosophila: Lag-1 in Caenorhabditis elegans
Dulbecco's modified Eagle's medium
mouse embryonic fibroblast
murine stem cell virus
tandem affinity purification and mass spectrometry
Notch1 intracellular domain
polymerase chain reaction
proline-: glutamic acid-: serine- and threonine-rich region
reactive oxygen species
reverse transcriptase polymerase chain reaction
small interfering RNA
divergent N-terminal region
transcriptional transactivation domain
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (MEST) (no. 2010-0014611).
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