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Introduction

The vast majority of cellular activities are executed by coordinated gene expression. Precise regulation of the transcription factors that control gene expression is necessary to accomplish specific tasks and to maintain cellular homeostasis. Various endogenous and exogenous stimuli induce changes in gene expression, and dynamic changes of gene expression profiles are observed during all processes maintaining life. Deregulated gene expression by either genetic or epigenetic alterations on the other hand can cause a broad range of diseases and is important for the development of cancer. The transcription factor NFκB plays a central role in many biological processes such as inflammation, differentiation, cell death and tumorigenesis (1). In glioblastoma (GBM), the most malignant human brain tumor in man, overexpression or aberrant constitutive activation of NFκB contributes to survival (2), radio- and chemoresistance (3–5), elevated glioma cell motility (6,7), enhanced angiogenesis (8) as well as chronic inflammation (9). On the other hand it has been described that, under some circumstances and dependent on the cooperation of NFκB with a variety of other, yet mainly unidentified factors and modulators of its activity, NFκB is mandatory for the induction of cell death, even in GBM cells (10–12). Until today it has not been unraveled in detail by which mechanisms NFκB provides its dual function, either serving as an oncogene triggering survival, but also exerting, via induction of cell death, its function as a tumor suppressor. Plenty of suggestions exist as to how and by which factors the dual function of NFκB is regulated, but there are still many questions left.

In unstimulated cells, the inhibitor of NFκB (IκB) proteins sequester NFκB into inactive complexes in the cytoplasm. A variety of different stimuli such as hypoxia, stress or tumor necrosis factor α (TNFα) can induce, via different pathways, the phosphorylation of cytoplasmic IκB protein family members by the IκB kinase complex leading to IκB proteasomal degradation, this resulting in the nuclear translocation of NFκB and induction of target gene expression (13). Whereas the predominantly cytoplasmic family members IκBα, IκBβ and IκBɛ exclusively act as inhibitors of NFκB, the atypical and mainly nuclearly localized IκB protein IκBζ, coded by the NFKBIZ gene and being a primary response target gene of NFκB (14), is able to bind to NFκB, is postulated to work as a (co)-transcription factor, and in this way seems to modulate the expression of a subset of NFκB target genes. Modulation of gene expression is at least partially mediated by the intrinsic transactivation activity of IκBζ and its interaction with the NFκB subunit p50 (15,16). Moreover, IκBζ is associated with histone deacetylases suggesting that chromatin remodeling is important for the transcriptional activity of IκBζ (17). In this report we demonstrate that IκBζ is upregulated in glioma specimens, in primary low passage glioma cells as well as in most established glioma cell lines. In a glioma cell line resistant towards NFκB-dependent cell death that is induced by overexpression of a dominant active p53 variant the chimeric tumor suppressor-1 (CTS-1) (12,18), IκBζ is highly upregulated. In this regard we were interested whether IκBζ might be a candidate that regulates the switch between the dual functions of NFκB: serving as an oncogene or acting as a cell death inductor and tumor suppressor.

Recently it has been described that IκBζ is an important regulator of radiation induced cellular senescence in breast cancer cells (19). Subsequently, senescence associated proteins such as interleukins, chemokines or growth factors can signal to the tumor environment and could potentially promote tumor progression by promoting proliferation, invasion or angiogenesis (20) or by induction of detrimental chronic inflammatory immune responses (21). Additionally, IκBζ has been described as a regulator of chemokine (C-C motif) ligand 2, recruiting circulating monocytes to inflammatory regions (14). Radiation is a common approach in the treatment of glioma. In this regard it is postulated that irradiation, via induction of necrosis, might lead to (chronic) inflammatory processes in the tumor micro-milieu and subsequent induction of resistance towards radiation (reviewed in ref. 22). We were also interested whether in glioma IκBζ expression is regulated by γ-irradiation and if in this context IκBζ serves as a transcriptional inducer of inflammatory chemokine and cytokine secretion, this way putatively inducing a more malignant tumor phenotype by modulating the tumor micro-milieu. Our data provide novel information on the role of IκBζ in tumorigenesis and tumor progression in glioma.

Materials and methods

Cell lines, reagents

The LN-229 (here named LNT-229P) cell line is a human malignant glioma cell line and was kindly provided by N. de Tribolet (Lausanne, Switzerland). Generation of CTS-1 resistant cell line LNT-229R was previously described (12). GBM primary cells were established from human GBM tissue and used at passages 5–8. All cells were maintained in Dulbecco's modified Eagle's medium (DMEM; Gibco Life Technologies, Eggenstein, Germany) containing 10% tetracycline-approved fetal calf serum (Tet-FCS; Gibco), penicillin (100 U/ml) and streptomycin (100 μg/ml) in a humidified atmosphere containing 5% CO2. Cell culture growth and cellular density was determined by crystal violet staining as described. For irradiation, the cells were seeded in 6-well plates and irradiated using the Nordion GC40 Gammacell irradiator (Ottawa, ON, Canada). For generation of supernatants, the cells were treated as indicated, serum-free medium was added and cellular supernatants were harvested 24 or 48 h later. The protein content in supernatants was analyzed according to Bradford.

Transfection of cells with shRNA constructs

For transfection with shRNA contructs, the cells were seeded at 3×105 cells. After attachment, the cells were transfected with plasmid constructs coding for either IκBζ specific shRNA, or coding for scrambled shRNA unspecific for any known mRNA using Metafectene PRO (Biontex, Martinsried, Germany). shRNA plasmid constructs were a kind gift of Klaus Schulze-Osthoff (Interfaculty Institute for Biochemistry, University of Tübingen, Germany).

RNA preparation and quantitative RT-PCR

Total RNA was prepared using the High Pure RNA Isolation kit (Roche, Mannheim, Germany). RNA (5 μg) was reverse transcribed using Superscript II reverse transcriptase (Invitrogen, Carlsbad, CA, USA). Target gene expression was determined using SYBR green master mix (Thermo Fisher Scientific, MA, USA), on an ABI 7200 system. Relative mRNA expression was quantified using comparative 2−ΔΔT method {[EΔCT (TARGET)/EΔCT (GAPDH)]}. The following primers were used: IκBζ-frwd (TCTGGAACTCATTCGCCTCT), IκBζ-rev (TCAACCGATACTGCAAGCTG), IL-6-frwd (CGGGAACGAAAGAGAAGCTCTA), IL-6-rev (GGCGCTTGTGGAGAAGGAG), IL-8-frwd(GTGGAGAAGTTTTTGAAGAGGGC), IL-8-rev (CACTTCATGTATTGTGTGGGTCTG), CXCL-1-frwd (GCAGGGAATTCACCCCAAGA), CXCL-1-rev (GAT GCAGGATTGAGGCAAGC), GAPDH-frwd (TGCACCACCAACTGCTTAGC), GAPDH-rev (GGCATGGACTGTGG TCATGA). GAPDH was used for internal normalization and did not vary between cell types or treatments.

Construction of adenoviral vectors and adenoviral infection

A replication-deficient recombinant and tetracycline-inducible adenovirus expressing IκBζ was constructed using the Ad-Easy system (23). In brief, IκBζ cDNA was inserted into pTRE-tight (Takara Bio Europe SAS, Saint-Germain-en-Laye, France) downstream of the tetracycline-responsive promoter element. The inserted cDNA was completely sequenced, compared to the NCBI database and found to be correct. The expression cassette consisting of the CMV-minimal promoter, the Tet-responsive element and IκBζ cDNA was cloned into pAdTrack, containing an additional expression cassette for enhanced green fluorescence protein (EGFP), which was later used to monitor virus production and infection load. After recombination with the viral genome containing plasmid Ad-Easy1, recombinant adenoviral genomes were transfected into HEK-293 cells (ATCC). Ad-ON expresses the reverse TET-repressor (rtTA) and was a kindly gift of G. Thomas (Portland, OR, USA), Ad-CTS1, coding for a dominant active version of p53, has been previously described (18), Ad-Co#4, which serves a control virus, is based on the Ad-Easy-System, but lacks both EGFP and expression of the gene of interest. All viruses were CsCl-purified, dialyzed and titrated using the Clontech Adeno-X Rapid Titration System. Transgene expression and inducibility were tested by quantitative RT-PCR (qPCR) of infected LNT-229P cells. Infection with recombinant adenovirus was accomplished by exposing cells to adenovirus at a defined moiety of infection (MOI) in serum-free medium for 30 min followed by addition of serum-containing medium of the mentioned time periods.

NFκB luciferase reporter assay

LNT-229P cells grown in microtiter plates were transfected with 150 ng pNFκB-Luc expressing firefly luciferase and 20 ng pRL-CMV expressing renilla luciferase as an internal standard. As a positive control of NFκB activation, the cells were cotransfected with 40 ng pMEKK. At 24 h after transfection, the cells were infected with 100 MOI of Ad TET-IκBζ + 100 MOI of Ad-ON in the absence or presence of doxycycline (2 μg/ml) for 48 h. NFκB activity was assessed using the dual luciferase assay (24).

Detection of cytokine expression

Relative cytokine expression was analyzed using the RayBiotech Human Cytokine Array (RayBiotech, Norcross, GA, USA) according to the manufacturer's protocol. Cell culture supernatants were harvested at indicated time points and stored at −20°C. In parallel, RNA was harvested from the cells for cDNA synthesis and subsequent qPCR analysis of cytokine mRNA expression. Intensity of the spots on the array was normalized to the mean intensity of the internal control spots and relative intensity was measured from duplicate dots representing single cytokines. For the analysis of absolute amounts of IL-6, the cells were treated as indicated and IL-6 secretion was measured using an IL-6 immunoassay kit (RayBiotech).

TCGA and REMBRANDT analyses

IκBζ gene expression was analyzed in primary glioma and normal brain samples by assessing the TCGA data portal. The mRNA profiles were determined using the Agilent 244K G4502A micro-array (http://cancergenome.nih.gov/; accessed Dec. 2014). Statistical significance between GBM and normal CNS tissue was assessed using a t-test (p<0.05). The calculations were performed using GraphPad Prism Software 6.0 (GraphPad Software, CA, USA). Survival correlation analyses were done using the REMBRANDT database containing probes from the Affymetrix 223218_s_at and 223217_s_at dataset (National Cancer Institute; 2005; REMBRANDT version 1.5.9, http://rembrandt.nci.nih.gov). At the time of accession (Dec. 2014), the database contained mRNA data of 228 glioblastomas, 148 grade II/III astrocytomas, 67 grade II/III oligodendrogliomas, 11 mixed gliomas and 28 non-tumor control tissues. Kaplan-Meier survival curves were generated by analyzing the glioma cohort (WHO grade II–IV; n=138) as well as the GBM cohort (WHO grade IV; n=84) separately. IκBζ up- or down-regulation was defined as a twofold (or greater) difference from the mean expression level within a given dataset. p-values for differences in patient survival curves were obtained by using the log-rank or Wilcoxon test. The ‘Highest Geometric Mean Intensity’ of IκBζ expression was used as the reporter for relative IκBζ expression within the database.

Statistical and correlation analysis

The figures show data obtained in at least three independent experiments as indicated. Statistical analyses were performed using GraphPad Prism version 6.0 (GraphPad Software, CA, USA). Quantitative data were assessed for significance by paired t-test (*p<0.05; **p<0.01; ***p<0.001). Patient survival was analyzed by Kaplan-Meier life table and for comparison of survival Wilcoxon and log-rank test were used (significance level α = 0.05, JMP 11.0 software, SAS, Cary, NC, USA).

Results

IκBζ mRNA is upregulated in low passage glioma cell lines, established cell lines and glioma specimens

We generated a cell line (LNT-229R) completely resistant to NFκB-dependent cell death induction upon overexpression of a dominant-positive p53, chimeric tumor suppressor (CTS)-1 (12). In a microarray mRNA expression analysis, IκBζ was upregulated in LNT-229R cells (12) suggesting that in GBM IκBζ might be involved in the development of resistance and malignancy. By quantitative RT-PCR we validated IκBζ expression in LNT-229P and LNT-229R cells and found IκBζ mRNA to be 3-fold higher in LNT-229R compared to LNT-229P cells (Fig. 1A). In contrast to normal brain where IκBζ is barely expressed (15), the analysis of NFKBIZ gene expression data of the TCGA database revealed that mean IκBζ mRNA expression was 0.65-fold (log2 scale) higher in glioblastoma samples as compared to non-neoplastic CNS control tissues (Wilcoxon test, p<0.05) (Fig. 1B). Analyses of the REMBRANDT database also exhibited an enhancement in mean IκBζ expression in the GBM dataset, while other glioma subgroups such as astrocytoma or oligodendroglioma showed no induction of IκBζ mRNA expression levels as compared to normal CNS tissue (data not shown). In GBM cells, IκBζ expression was also upregulated in 3/3 tested low passage primary GBM cell lines (Tu120, Tu132, Tu140) as well as in 8/12 established glioma cell lines (Fig. 1C). In glioma specimens, IκBζ mRNA expression is highly variable, ranging from 1.5- (G-431) to 107-fold (G-409) compared to non-tumor brain tissue (Fig. 1D).

Figure 1 IκBζ mRNA expression is upregulated in most glioma cells. (A) Basal IκBζ mRNA expression in LNT-229P and CTS-1 resistant sibling LNT-229R cells (n=3, SEM, ***p<0.001). (B) Analysis of the TCGA glioma dataset (AgilentG4502A_07). Log2 scaled tumor/normal ratio of NFKBIZ. IκBζ mRNA expression was found to be 0.65 (log2)-fold increased in glioblastoma compared to non-tumor brain tissue (Wilcoxon test, *p<0.05). (C and D) Comparison of IκBζ mRNA expression in established and primary glioma cell lines (C) and glioma specimen (D) showed increased IκBζ mRNA in 8/12 established cell lines, 3/3 primary glioma cell lines and in 7/8 glioma specimens.

Overexpression of IκBζ does not influence CTS-1-induced, NFκB-dependent cell death

In CTS-1 sensitive LNT-229P, but not in resistant LNT-229R glioma cells, NFκB is activated upon adenovirally mediated expression of CTS-1, a dominant and constitutively active version of p53 (12). In LNT-229P cells CTS-1 mediated cell death is dependent on the activity of NFκB and could be largely inhibited by blocking NFκB activation (12). Since in LNT-229R cells IκBζ mRNA is upregulated (Fig. 1A) and since it is known that IκBζ is a direct target of NFκB and a modulator of NFκB activity, we analyzed whether in LNT-229P and LNT-229R cells IκBζ mRNA expression is regulated by CTS-1 and whether enhanced IκBζ expression influences the CTS-1-induced cell death in these cells. As shown in Fig. 2A, IκBζ expression is upregulated in Ad-CTS-1 infected LNT-229P cells that show a low basal level of IκBζ expression, but is not further enhanced in Ad-CTS-1 infected LNT-229R cells which per se show elevated IκBζ expression, indicating that in parental, but not in resistant cells, IκBζ, putatively via induction of NFκB, might be also regulated by CTS-1, a dominant version of p53.

Figure 2 IκBζ overexpression neither modulates NFκB activity nor protects glioma cells from CTS-1 induced cell death. (A) IκBζ mRNA expression in LNT229P and LNT229R cells after infection with Ad-CTS-1. AdCo#4 served as a negative control (n=4, SEM, **p<0.01). (B) Upon adenoviral infection and induction of transgene expression by addition of DOX, IκBζ mRNA increased after 12–24 h and stayed elevated at least up to 48 h (n=3, SEM, *p<0.05, ***p<0.001) (C) Induction of IκBζ mRNA expression does not prevent Ad-CTS-1 induced cell death in LNT-229P cells. The cells were infected with Ad-TET-IκBζ + Ad-ON in the presence (+DOX) or absence (−DOX) of doxycycline. After 24 h, the cells were infected with increasing MOI of Ad-CTS-1. Cell density was assessed by crystal violet staining 72 h later (n=3, SEM, **p<0.01). (D) NFκB reporter gene assay of LNT229P cells infected with Ad-TET-IκBζ + Ad-ON in the absence or presence of doxycycline (n=4, SD).

IκBζ has been described, at least in fibroblasts, to bind to the NFκB p50 subunit and to interfere with p65, modulating NFκB activity and mediating the induction of several NFκB responsive genes (15). In this context, enhanced expression of IκBζ in LNT-229R cells might be the reason why these cells are resistant to CTS-1-induced cell death. To test this, we generated a tetracycline/doxycycline (DOX)-inducible adenoviral system that allows us to transiently induce IκBζ expression. After infection of glioma cells with Ad-TET-IκBζ plus Ad-ON and addition of DOX, elevated IκBζ expression is detected 12 h after infection, increasing up to 48 h and then stable for at least 72 h (Fig. 2B and data not shown). Nevertheless, DOX-mediated induction of IκBζ expression neither changed basal NFκB activity which is known to be enhanced in LNT-229 cells nor the sensitivity of these cells towards CTS-1 induced cell death (Fig. 2C and D), indicating that IκBζ overexpression is not responsible for the NFκB- dependent resistance against CTS-1-induced cell death in LNT-229R cells.

IκBζ mRNA expression is induced by irradiation and serves as an activator for the expression of inflammation-associated cytokines IL-6, IL-8 and CXCL1

There are several hints that in glioma IκBζ might be a tumor promoting transcription factor, translating its oncogenic activity via induction of (chronic) inflammation. First of all, in glioma the NFκB signaling cascade is involved in processes of inflammation and resistance towards gamma-irradiation (25). Secondly, IκBζ as a direct target of NFκB is upregulated in fibroblasts by irradiation induced senescence and, in this regard, induces the expression of a variety inflammatory cyto- and chemokines such as interleukin (IL)-6, IL-8 and CXCL1 (19). Thirdly, IL-6 and IL-8 are upregulated in glioma cells upon irradiation (26), and last but not least, it has been described that IL-6 producing glioma cells were not affected by irradiation (27). We therefore investigated whether in glioma IκBζ might be a modulator of radiation induced expression of inflammatory cytokines. We first analyzed whether irradiation induces IκBζ expression. As shown in Fig. 3A, IκBζ mRNA expression was elevated in LNT-229P cells after irradiation. In a similar time frame, also IL-6, IL-8 and CXCL1 mRNA expression was induced (Fig. 3B–D). To validate whether irradiation-induced expression of inflammatory cytokine mRNA in glioma cells also translates into protein expression, we exemplarily analyzed IL-6 secretion in LNT-229P cells. As shown in Fig. 3E, IL-6 secretion was upregulated by irradiation in a dose- and time-dependent manner.

Figure 3 Irradiation of glioma cells induces the expression of IκBζ and inflammatory cytokines. (A–D) mRNA expression in LNT-229P cells at different time points after irradiation. (A) IκBζ, (B) IL-6 (C) IL-8 and (D) CXCL1 (n=3, SEM). (E) IL-6 protein concentration in cellular supernatants of irradiated LNT-229P cells analyzed by ELISA (n=3, SEM). *p<0.05, **p<0.01, ***p<0.001.

We were interested whether IκBζ is directly responsible for the induction of IL-6, IL-8 and CXCL1 cytokine expression or if IκBζ served as a modulator NFκB activity as described by Totzke et al (15). For this, we infected LNT-229P cells with Ad-TET-IκBζ + Ad-ON and induced IκBζ expression by addition of DOX. We used qPCR to measure cytokine mRNA expression as well as a membrane based microarray assay that allows the detection of 48 different cyto- and chemokines in cellular supernatants. We found that IL-6 and CXCL1 were upregulated after induction of IκBζ expression both at the level of mRNA and protein, whereas IL-8 expression was only marginally enhanced (Fig. 4). To validate that IκBζ is an inducer of inflammatory cytokine expression in glioma cells, we downregulated IκBζ expression in irradiated LNT-229P cells by transient transfection using three different IκBζ specific shRNA plasmid constructs. We found IκBζ being downregulated to 29 (#32), 36 (#29) and 64% (#30) compared to the level of irradiated cells transfected with an unspecific shRNA plasmid construct (scrambled shRNA, Fig. 5A). By transfection of the cells using the most efficient shRNA construct (#32), we next analyzed whether downregulation of IκBζ expression leads to a reduction in the expression of IL-6, IL-8 and CXCL1. Indeed, paralleled by the knockdown of IκBζ, IL-6, IL-8 and CXCL1 mRNAs were downregulated. Interestingly, even if IL-8 mRNA expression was not significantly induced by the induction of IκBζ expression (Fig. 4F), IL-8 mRNA was significantly reduced in IκBζ knockdown LNT229P cells (Fig. 5C). Additionally, we analyzed the concentration of IL-6 in supernatants of both, non- and irradiated LNT-229P cells transfected with either scrambled or the IκBζ-specific shRNA containing plasmids (#32). Fig. 5E demonstrates that decreased IL-6 mRNA expression in IκBζ knockdown cells is paralleled by the reduction of IL-6 protein in the supernatants of these cells. Our results indicate a direct role of IκBζ in the regulation of the expression of IL-6, IL-8 and CXCL1.

Figure 4 Overexpression of IκBζ in LNT229P cells enhances the secretion of IL-6 and CXCL-1. (A and B) Semi-quantitative detection of 48 tumor-associated cytokines in supernatants of Ad-TET-IκBζ + Ad-ON infected LNT-229P cells in the presence (+DOX) or absence (−DOX) of doxycycline. (C) Quantification of cytokine expression depicted from (A) and (B). (D) IκBζ mRNA expression in LNT-229P cells after adenoviral infection with Ad-TET-IκBζ + Ad-ON and cultivation in the absence (−DOX) or presence (+DOX) of doxycycline. (D–G) mRNA expression of IκBζ (D), IL-6 (E), IL-8 (F) and CXCL1 (G) 48 h after induction of IκBζ expression by adenoviral infection of LNT-229P cells with Ad-TET-IκBζ + Ad-ON and cultivation in absence (−DOX) or presence (+DOX) of doxycycline (n>3, SEM, *p<0.05, **p<0.005).

Figure 5 Downregulation of IκBζ results in the reduction of IL-6, IL-8 and CXCL1 mRNA. (A) LNT-229 cells were transiently transfected with shRNA containing plasmids targeting IκBζ (#29, #30, #32) or containing non-specific ‘scrambled’ shRNA (scr). Twenty-four hours after transfection the cells were irradiated with 30 Gy. IκBζ mRNA expression was significantly reduced in cells transfected with plasmids containing shRNA constructs targeting IκBζ. (B–D). Expression of IL-6 (B), IL-8 (C) and CXCL1 mRNA (D) was significantly reduced in irradiated LNT-229 cells transfected with the IκBζ shRNA containing plasmid #32. (E) IL-6 concentration in supernatants of irradiated LNT-229 cells transfected with the IκBζ shRNA containing plasmid #32 as detected by ELISA (n=3, SEM, *p<0.05, **p<0.01,***p<0.001).

Expression of IκBζ and its target genes IL-6, IL-8 and CXCL1 is correlated with a poor outcome of GBM patients

To evaluate a potential association of IκBζ expression, the expression of its inflammatory cytokine targets and patients survival, we used the REMBRANDT database IκBζ expression data and grouped either all glioma WHO grade II– IV (Fig. 6A) or GBM grade IV (Fig. 6B) with low or high IκBζ expression. IκBζ up- or down-regulation was defined as a twofold or greater difference from the mean expression level within a given dataset. Both on the early and late phase of survival analysis, patients with low IκBζ expression levels exhibit significantly longer survival times (glioma: p<1×10−7; GBM p<1×10−11). This analysis was repeated with a second REMBRANDT dataset revealing similar results (data not shown). These findings indicate a tumor promoting role of IκBζ. Similar survival data were obtained for IL-6, IL-8 and CXCL1. Again, glioma patients with lower expression of either IL-6, IL-8 or CXCL1 in the tumor tissue significantly showed longer survival than patients with higher cytokine expression (Fig. 6C–E).

Figure 6 In glioma, enhanced IκBζ or inflammatory cytokine expression correlates with poor outcome of the patients. (A and B) REMBRANDT survival analysis for glioma samples showed significantly longer survival times for patients with low expression of IκBζ in a mixed cohort of gliomas WHO grade II–IV (A) as well as in GBM grade IV patients only (B). (C–E) Significantly longer survival times for glioma (WHO II–IV) patients with low IL-6 (C), IL-8 (D) and CXCL1-expression (E).

Discussion

Patients with GBM currently undergo standard treatment consisting of maximal surgical resection and combined radiation and chemotherapy (28,29). Radiation has been a mainstay of GBM treatment for decades. Besides the therapeutic effect of radiation, side effects of this therapy approach have also been described. These unwanted and more or less tumor-driving side effects include radiation-induced glioma cell migration and invasion (30–32), modulation of NFκB activity, and, in this context, induction of resistance towards radiation and conversion of GBM into its most aggressive mesenchymal type subgroup (33,34). Moreover, tumor irradiation can lead to cytokine and chemokine expression such as vascular endothelial factor (VEGF), IL-8, IL-6, CXCL1 and CCL2 (19,26,32,35) in the tumor microenvironment, factors known to be involved in glioma progression and enhancement of the malignancy.

Our study demonstrates that the expression of the inflammatory and tumor promoting signaling molecules IL-6, IL-8 and CXCL1 is regulated by the atypical IκB protein IκBζ, a direct target of NFκB. Even if it was described that IκBζ inhibits transactivation of p65 and its DNA binding in HEK293 cells (15) this seems not to be the case for glioma, since no alterations of NFκB activity was detectable upon IκBζ over-expression in LNT-229P glioma cells (Fig. 2D), indicating a more direct effect of IκBζ on the expression of IL-6, IL-8 and CXCL1 and confirming the data of Yamazaki et al who have shown that IκBζ independent from NFκB, can directly serve as a transcription modulator of inflammatory genes (17).

Using inducible overexpression and shRNA mediated downregulation of IκBζ we were able to demonstrate that in glioma cells IκBζ serves as a transcriptional modulator of the cytokines IL-6, IL-8 and CXCL1. IL-6 is an inflammatory cytokine that is produced by human GBM cells (36), its expression is associated with the progression of glioma malignancy, putatively via induction of signal transducer and activator of transcription (STAT)-3 (37,38). IL-8, also named CXCL8, is known to drive tumorigenicity. In glioma, IL-8 is expressed both in vitro and in vivo. IL-8 plays an important role in infection and inflammation processes and it is known that its presence in the micro-milieu of glial tumors is crucial in regard to their vascularization as well as in the progression of these tumors (39). CXCL1, also known as the oncogene GRO, binds to the G-protein coupled chemokine (C-X-C motif) receptor 2. In embryogenesis, CXCL1 regulates spinal cord development by blocking the motility of oligodendrocyte precursor cells. In adults, this cytokine is involved in processes of inflammation, angiogenesis, but also wound healing (40,41). In glioma CXCL1 is highly expressed, and overexpression of CXCL1 in glioma possesses tumor cell motility and confers increased malignancy (42,43).

In recent centuries, and even after the development of more efficient treatment strategies, the median survival of glioblastoma patients has only marginally improved. In this regard, novel therapeutic strategies are urgently needed to treat glioma. There are suggestions that inhibition of chronic inflammation in the tumor micro-milieu as well as reduction of glioma associated angiogenesis by inhibiting the function of glioma secreted cytokines might be successful strategies to treat glioblastoma. We have shown in this study that in GBM cells IκBζ is a transcriptional modulator of several pro-tumorigenic, inflammatory or pro-angiogenic cytokines such as IL-6, IL-8 and CXCL1. Besides its function as a transcriptional activator of inflammatory cytokine expression, enhanced IκBζ has been demonstrated, via a transcription-independent mechanism, to also protect GBM cells towards necroptotic cell death, whereas knockdown of IκBζ in these cells induces necroptosis and delays tumor growth in mice (44). Furthermore, it has been described recently that IκBζ, at least in macrophages, regulates the expression of the monocyte chemoattractant protein (MCP)-1 (14), a cytokine that is also expressed by glioma cells, recruits microglia cells into and promotes the aggressiveness of this tumor (45).

One could think that targeting IκBζ in the GBM micro-milieu after or during radiation therapy might be an interesting novel idea for the treatment of glioma patients. However, one should also keep in mind that there might be disadvantageous effects blocking IκBζ in glioma: IκBζ has been described to regulate for the development of (glioma infiltrating) T(H)17 cells (46). T(H)17 cells are a subset of T cells important for the development of an efficient attack of GBM cells by immune cells, but also a subset of immune cells that are known to be inactivated by GBM released factors (reviewed in ref. 47). Therefore, a strategy targeting IκBζ in GBM cells exclusively might be more feasible than inhibiting IκBζ activity in the complete GBM micro-milieu.

Acknowledgements

We thank D.G. Hildebrand and K. Schulze-Osthoff for providing us with IκBζ-specific shRNA containing plasmids. This study was supported by the Interdisciplinary Center for Clinical Research of the University of Tübingen.

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References