Epipolythiodiketopiperazines from the Marine Derived Fungus Dichotomomyces cejpii with NF-κB Inhibitory Potential

The Ascomycota Dichotomomyces cejpii was isolated from the marine sponge Callyspongia cf. C. flammea. A new gliotoxin derivative, 6-acetylmonodethiogliotoxin (1) was obtained from fungal extracts. Compounds 2 and 3, methylthio-gliotoxin derivatives were formerly only known as semi-synthetic compounds and are here described as natural products. Additionally the polyketide heveadride (4) was isolated. Compounds 1, 2 and 4 dose-dependently down-regulated TNFα-induced NF-κB activity in human chronic myeloid leukemia cells with IC50s of 38.5 ± 1.2 µM, 65.7 ± 2.0 µM and 82.7 ± 11.3 µM, respectively. The molecular mechanism was studied with the most potent compound 1 and results indicate downstream inhibitory effects targeting binding of NF-κB to DNA. Compound 1 thus demonstrates potential of epimonothiodiketopiperazine-derived compounds for the development of NF-κB inhibitors.


Introduction
The secondary metabolism of fungi gives rise to chemically most diverse structures, some of which have proven useful in drug development. A promising source for new secondary metabolites are organisms isolated from special habitats, like marine-derived fungi and bacteria [1]. Accordingly, fungal secondary metabolites have gained popularity due to their newly discovered pharmaceutical potential as anti-inflammatory, cytotoxic or cytostatic agents.
A number of gliotoxin derivatives have been isolated inter alia from fungus Penicillium sp. strain JMF034, from Japanese deep-sea sediments. These marine-derived drug candidates display epigenetic and anti-cancer activities against P388 murine leukemia cells. Compounds containing a disulfide bond including gliotoxin G, 5a,6-didehydrogliotoxin and gliotoxin showed potent in vitro inhibitory activity against the recombinant H3K9 histone methyl transferase G9a. The presence of a disulfide bond is usually accompanied by distinct toxic effects that limit the therapeutic usage of this compound group. Here, the Ascomycete Dichotomomyces cejpii, isolated from the marine sponge Callyspongia cf. C. flammea, allowed isolation of new gliotoxin derivatives devoid of a disulfide bridge. Along with the likewise isolated polyketide heveadride these compounds were investigated as anti-inflammatory, cytotoxic or cytostatic agents [2].
Several gliotoxins have been identified as potent inhibitors of cancer associated inflammatory signaling pathways [3]. One of the crucial pathways linking cancer and inflammation is nuclear factor kappa B (NF-κB). Growing evidence indicates the involvement of this transcription factor in many inflammatory diseases and cancer progression. NF-κB became a promising therapeutic target of both hematological malignancies and solid tumors [4]. Many risk factors related to life style activate inflammatory pathways via NF-κB. Aberrantly activated NF-κB leads to expression of target genes involved in all steps of tumorigenesis. Moreover, constitutively active NF-κB serves as a useful prognostic indicator.
NF-κB is an inducible factor that acts as a dimer of pair-wise combinations of proteins from the Rel family [5]. This family comprises five members, RelA (p65), Rel (c-Rel), RelB, NF-κB1 (p105/p50) and NF-κB2 (p100/p52), which require dimerization prior to activation. Preferential dimer-binding is conditional for DNA affinity. In comparison to most eukaryotic transcription factors, the p50/p65 heterodimer presents a particularly high DNA affinity, which is why this dimer interacts with DNA more frequently than other NF-κB dimers [6]. Upon pathway activation through ligand binding, the natural inhibitor of kappa B (IκB), which is sequestering the inactive p50/p65 dimer in the cytoplasm, is phosphorylated, ubiquitinated and degraded by the proteasome. Active dimer translocates to the nucleus, binds to corresponding DNA sequences in promoter or enhancer regions and is responsible for the expression of pro-inflammatory genes [7].
In the present study we investigated the inhibitory effect of newly isolated natural epipolythiodiketopiperazines on anti-proliferative mechanisms via TNFα-induced p50/p65 NF-κB activity to understand cytostatic effects of these marine-derived drug candidates.

Structure Elucidation
Compound 1 was obtained from the marine sponge-derived fungus D. cejpii and its structure was elucidated via intensive analysis of spectroscopic data. A Ultraviolet (UV) maximum at 262 nm evidenced the presence of a conjugated π-π* system. A broad Infrared (IR) absorption at 3425 cm −1 pointed toward a hydroxyl group, while a strong IR absorption at 1722 cm −1 , arising from C=O stretching frequencies, indicated an ester moiety (Figures S1.1 and S1.2). The molecular formula of compound 1 was deduced from the results of an accurate mass measurement using high-resolution electrospray ionisation mass spectrometry (HRESIMS), m/z = 359.0672 [M + Na] + as C15H16N2O5S, implying nine degrees of unsaturation ( Figure S1.11). The 13 C Nuclear Magnetic Resonance (NMR) and Distortionless Enhancement by Polarization Transfer-135 (DEPT-135) spectra denoted the presence of 15 resonances for two methyl groups, two sp 3 methylene groups, three sp 2 methine, two sp 3 methine, and six quaternary carbons in the molecule (Table 1, Figures S1.3-S1.9). The first substructure was deciphered as a cyclohexadiene by interpreting 1 H-1 H Correlation Spectroscopy (COSY) correlations from H-5a through to H-9, and Heteronuclear Multiple Bond Correlation (HMBC) cross peaks between the resonances for H-9 and C-9a, C-5a, C-6, C-7 and C-8.
The two conjugated carbon-carbon double bounds within this substructure could be assigned as ∆ 7,8 and ∆ 9,9a due to the 13 C NMR chemical shifts of the respective carbon atoms (127.1/125.7, 119.5/137.4 ppm). The methine group CH-6 resonated at δH 5.79 and δC 74.9, indicating a substitution with oxygen at this site. Due to its 13 C NMR chemical shift (δC 170.5) C-12 was part of a carbonyl group. HMBC correlations arising from the resonance of CH3-13 to C-12, as well as to CH-6 established that an acetyl group was linked via the oxygen atom at CH-6. An extension of this first substructure was possible taking HMBC cross peaks between the resonances for the methylene group CH2-10 to C-9a on one side, and to C-10a and C-1 on the other side into account. The 13 C NMR chemical shifts of C-10a (δC 80.4) and of the protons and carbon atoms of the methine group CH-5a (δH 4.57, δC 61.6), indicated a substitution with a heteroatom at these sites, whereas C-1 was a carbonyl (δC 174.2). CH3-11 resonating at 2.98 and 27.8 ppm, respectively had to be linked to nitrogen. HMBC cross peaks between the resonances for this methyl group to the carbonyl carbon atom C-1 thus revealed an amide bond. A second amide was obvious when considering the 13 C NMR chemical shift (δC 171.3) for C-4. 1 H NMR chemical shifts of δH 4.30 and 4.17 for the geminal methylene protons 3a′ and 3a″ indicated the presence of a CH2OH moiety. Regarding HMBC cross peaks between the resonances for these methylene group protons CH2-3a to carbons C-3 and C-4, and of CH3-11 to C-1 and C-3, the second substructure from C-1 through to C-4 (including C-11) could be deduced, which was linked via N-5 to the first substructure.
Thus compound 1 is a diketopiperazine with a dihydro-indoline moiety. The molecular formula indicated the presence of one single sulphur atom within the molecule. As this point of the structure elucidation also two double bond equivalents were still to be accounted for. In accordance with the MS data, the sulphur atom was thus assigned to form a sulphur bridge between carbon C-10a and C-3, due to the 13 C NMR chemical shift of the respective carbons (C-3: 82.5 ppm, C-10a: 80.4 ppm). This is comparable to the disulfide bridge in the related compound gliotoxin (C-10a and C-3: δC 77.3 and 77.5, respectively) [8][9][10]. Overall, this structural arrangement of 1 is consistent with the established structures of gliotoxin-type metabolites and with recent biosynthetic evidence for this class of compounds [11,12].
The relative configuration was deduced on the basis of a Nuclear Overhauser Effect Spectroscopy (NOESY) experiment and the magnitude of significant 1 H-1 H coupling constants ( Figure S1.10). The coupling constant of JH-5a/H-6 = 13.5 Hz indicated that both protons are orientated 180° to each other, i.e., H-6 is axial and α-orientated whereas the axial H-5 is β-orientated. NOESY correlations between H-3a″, H-5a and H-10′ indicated that these protons are located on the same side, of the molecule, whereas NOESY correlations between H-3a′, H-6 and H-10″ proved the opposite orientation for these substituents. This again confirmed that proton H-5a and H-6 are trans orientated to each other. The configuration at the quaternary carbon C-10a could not be determined. We assume it to be as that of the co-occurring 6-acetylbisdethiobis(methylthio)gliotoxin (2) with the same basic structural arrangement [13,14]. Furthermore the fungus D. cejpii is a known producer of gliotoxin for which the absolute configuration had been determined and confirmed by biosynthetic evidence, the latter demonstrating the necessity of this configuration [8,10,11,13]. Fungal metabolite 1 is thus a naturally occurring gliotoxin derivative with the untypical feature of a single sulphur atom bridge. We suggest the trivial name 6-acetylmonodethiogliotoxin for 1.
Aside from 1, a further gliotoxin derivative, an acetylated dithiodiketopiperazine with two methylthio substituents, i.e., 6-acetylbisdethiobis(methylthio)gliotoxin (2) was isolated for the first time as a natural product. The structure of 2 was elucidated on the basis of detailed 1 H and 13 C NMR data (Figures S2.3-S2.10) and comparison with literature values of the semi-synthetically obtained compound [14] (Table 1). 1 H NMR values of 2 match very well with literature data. There were slight differences, however between the here observed 13 C NMR resonances for carbon C-3 and literature values (+3.6 ppm). These differences may be explained by the fact that reported 13 C NMR data had been determined only indirectly via HMBC correlations. Furthermore, it is known that NMR data of gliotoxin and its derivatives are strongly influenced by temperature and solvent [10]. Mass spectrometric data are according to the here shown structure and literature data.

Epipolythiodiketopiperazines Dose-Dependently Inhibit TNF Alpha-Induced NF-κB Activation
Compounds 1, 2 and 4 were analyzed in order to assess their inhibitory potential on TNFα-induced NF-κB activity in K562 cells. Considering the low amount of compound 3 available, we were unable to include this compound in biological assays. We determined compounds inhibition potential on TNFα-induced activation of a luciferase gene under the control of canonical NF-κB response elements. We treated transiently transfected K562 cells at different concentrations of compounds 1, 2 and 4, respectively, followed by the stimulation with TNFα. Results show that TNFα-induced NF-κB reporter gene activity was dose-dependently decreased by compounds 1, 2 and 4 compared to control with IC50 values of 38.5 ± 1.2 µM (compound 1), 65.7 ± 2.0 µM (compound 2) and 82.7 ± 11.3 µM (compound 4) ( Figure 2). IC50 values were calculated using XY scatter dependency chart. The 50% inhibition activity on NF-κB expression was established by using the best fitting model and calculated by trend formulas. The average value of at least 3 independent experiments was applied. Molecular mechanism of compound 1 (6-acetylmonodethiogliotoxin) was investigated in more detail.

6-Acetylmonodethiogliotoxin Down-Regulates the Expression of NF-κB Target Genes
NF-κB signaling results in activation of a large battery of target genes. Many of these genes have been associated with different steps of tumorigenesis [17]. In order to further validate the previously observed inhibition of NF-kB reporter gene activity we investigated whether 6-acetylmonodethiogliotoxin affects ICAM-1 gene transcription. K562 cells were transiently transfected with ICAM-1 plasmid followed by treatment with 6-acetylmonodethiogliotoxin at IC50 concentration, and then exposed to TNFα. Our results show that TNFα induced ICAM-1 promoter-driven reporter gene activity and 6-acetylmonodethiogliotoxin significantly inhibited this induction by 53% compared to control (Figure 3).  We further analyzed the molecular mechanism underlying the inhibition potential of 6-acetylmonodethiogliotoxin on TNFα-induced NF-κB activation. Here, we focused on degradation of IκBα, the natural inhibitor of NF-κB as well as on translocation of p50 and p65 subunits to the nucleus. As shown in Figure 4, 6-acetylmonodethiogliotoxin did neither prevent IκBα degradation, nor p50/p65 nuclear translocation. These results indicate that 6-acetylmonodethiogliotoxin mediated downstream inhibition of NF-κB pathway. As both subunits p50 and p65 translocated to the nucleus, 6-acetylmonodethiogliotoxin could either prevent their binding to DNA or abrogate NF-κB transcriptional activity.
In order to validate our hypothesis we investigated whether 6-acetylmonodethiogliotoxin is able to interfere with the binding affinity of NF-κB to its consensus response element. Figure 5 showed that 6-acetylmonodethiogliotoxin at IC50 concentrations significantly decreased binding affinity of p65 to the NF-κB consensus and this effect was further more pronounced at the higher concentration, whereas p50 was not affected by 6-acetylmonodethiogliotoxin treatment (data not shown). Altogether, these results provide evidence that 6-acetylmonodethiogliotoxin acts as a downstream inhibitor of NF-κB pathway altering binding of p65 to DNA.   (1) reduces binding affinity of p65 to DNA in a dose dependent manner. Dose-dependent effects of 6-acetylmonodethiogliotoxin (Compound 1) on p65 binding affinity to DNA. Jurkat cells were pre-incubated with 6-acetylmonodethiogliotoxin at indicated concentrations for 4 h and treated with TNFα (20 ng/mL) for 30 min, and then subjected to TransAM assay. Negative control (Co−) corresponds to nuclear extracts of DMSO treated cells, without TNFα activation, positive control (Co+) corresponds to nuclear extracts of DMSO treated cells activated by TNFα, wild-type (WT) and mutated type (MT) corresponds to nuclear extracts of DMSO treated cells activated by TNFα loaded on plate comprising wild-type or mutated consensus oligonucleotide, respectively. Goniothalamin (GTN) at concentration 7 μM was used as a positive inhibitory control. Shown data are mean ± SD of three independent experiments. Asterisks indicate a significant difference compared to control positive as analyzed by t-test (* p < 0.05; ** p < 0.01; *** p < 0.001).
As the NF-κB pathway is known to regulate a large battery of genes involved in cell proliferation and survival, we investigated the effects of compound 1 (6-acetylmonodethiogliotoxin) ( Figure 6A,B), compound 2 (6-acetylbisdethiobis(methylthio)gliotoxin) ( Figure 6C,D) and compound 4 (heveadride) ( Figure 6E,F) on K562 cell viability and proliferation. Importantly, any of the tested compounds decreased cancer cell viability after 8 h of treatment used for the investigation of NF-κB mechanisms, reflecting that down-regulation of NF-κB activation was not due to cell death induction. At later time points (24 h, 48 h and 72 h), 6-acetylmonodethiogliotoxin dose-dependently inhibited cancer cell proliferation ( Figure 6B). At 50 μM, compound 1 (6-acetylmonodethiogliotoxin) induced cytostatic effects and at higher concentrations of 70 μM and 100 μM a moderate cytotoxicity was observed reaching a maximum of 20% and 30% at 72 h, respectively. These observations could be the secondary consequences of early NF-κB inhibition.
However, compound 2 (6-acetylbisdethiobis(methylthio)gliotoxin) and compound 4 (heveadride), are weaker NF-κB inhibitors compared to compound 1 (6-acetylmonodethiogliotoxin) and did not significantly decrease K562 cell viability at any concentration or measured time point ( Figure 6C,E, respectively). On the other hand, 100 μM of both compounds reduced K562 proliferation compared to control. Whether these effects could be directly linked to the observed NF-κB down-regulation will be object of future studies.

Discussion
Our data indicate strong anti-proliferative potential on chronic myeloid leukemia cells, as 6-acetylmonodethiogliotoxin dose-and time-dependently inhibited K562 cell proliferation.
Importance of inflammation in cancer initiation and progression is nowadays well established. Many epidemiological, experimental and clinical studies strengthen the tight relationship between cancer and inflammation [18]. During past decades, NF-κB, as a crucial player in inflammatory signaling, became a popular target in cancer therapy. Abnormal NF-κB signaling can be detected in as much as 95% of all cancer cases and is responsible for aberrant expression of huge battery of genes involved in cancer onset and progression [17]. Natural compounds have been shown to counteract with NF-κB signaling and down-regulate its activity, thus acting as potent agents in both, cancer prevention and treatment [3,[19][20][21][22][23].
A transannular sulfur bridge as present in compound 1 seems to be essential for the observed NF-κB pathway interfering activity, as the related compound 2 without this feature did not display any activity. The finding of 6-acetylmonodethiogliotoxin with a monosulfide bridge is of importance, as this compound may serve as lead for the development of more potent and selective ligands for this therapeutically interesting drug target.
It is interesting to note, that monosulfides of gliotoxin derivatives have been obtained semi-synthetically from disulfid gliotoxin derivatives by reaction with tervalent phosphorus compounds, e.g., triphenylphosphine [24]. The investigated marine derived strain of Dichotomomyces cejpii however constantly produced 6-acetylmonodethiogliotoxin (1) under different cultivation conditions that was isolated directly from the fungal extract as a natural product. To our knowledge there are only sirodesmin H, isolated from the fungus Phoma lingam and emestrin-G, isolated from the fungus Armillaria tabescens, respectively, where such a bridged monosulfid was obtained directly by isolation as a natural product [25,26]. However these compounds solely possess the same epimonothiodioxopiperazine moiety while the rest of the structural backbone is quite different.

General Procedures for Natural Products Chemistry
Optical rotations were measured with a Jasco DIP 140 polarimeter (Jasco Inc., Easton, CA, USA). UV and IR spectra were obtained employing Perkin-Elmer Lambda 40 (PerkinElmer, Inc., Waltham, MA, USA) and Perkin-Elmer Spectrum BX instruments (PerkinElmer, Inc., Waltham, MA, USA), respectively. 1 H and 13 C NMR spectra were recorded on a Bruker Avance 300 DPX spectrometer (Bruker Corporation, Billerica, MA, USA). NMR spectra were referenced to residual solvent signals of acetone and methanol at δH/C 2.04/29. 8

Cultivation of Fungus, Extraction and Isolation
The marine-derived fungus Dichotomomyces cejpeii was isolated from a sample of the sponge Callyspongia sp. cf. C. flammea (collected at Bare Island, Sydney, Australia). The isolation of the fungus was carried out using an indirect isolation method. Sponge samples were rinsed three times with sterile H2O. After surface sterilization with 70% EtOH for 15 s the sponge was rinsed in sterile artificial seawater (ASW). Subsequently, the sponge material was aseptically cut into small pieces and placed on agar plates containing isolation medium: agar 15 g/L, ASW 800 mL/L, glucose 1 g/L, peptone from soymeal 0.5 g/L, yeast extract 0.1 g/L, benzylpenicillin 250 mg/L, and streptomycin sulfate 250 mg/L. The fungus growing out of the spongeal tissue was separated on biomalt medium (biomalt 20 g/L, agar 10 g/L, ASW 800 mL/L) until the culture was pure. The isolated fungus was identified by P. Massart and C. Decock, BCCM/MUCL, Catholic University of Louvain, Louvain-la-Neuve, Belgium.
A specimen is deposited at the Institute for Pharmaceutical Biology, University of Bonn, isolation number "293K09", strain number 225.
The fungus was cultivated on cultivation medium MPY: 10 L of malt, peptone, yeast solid agar medium (malt extract 20 g/L, peptone 2.5 g/L, yeast extract 2.5 g/L and 15 g/L agar) supplemented with demineralized water in 40 Fernbach flasks at room temperature (RT) for 30 days.

Transient Transfection and Luciferase Reporter Gene Assay
K562 cells were transiently transfected as described previously [28]. For each electroporation, we used 5 µg of a luciferase reporter gene construct containing 5 repeats of a consensus NF-κB site (Stratagene, Genomics Agilent, Diegem, Belgium) and 5 µg of a Renilla luciferase plasmid (Promega, Leiden, The Netherlands). The ICAM-1 LUC reporter plasmid was a generous gift from Wim Vanden Berghe (University of Antwerp, Antwerp, Belgium). The full-length ICAM-1 promoter construct contains approximately 1.4 kb of ICAM-1 5′-flanking DNA linked to the firefly luciferase (LUC) gene. Promoter sequences between 393 and 176 bp upstream of the gene, containing binding sites for C/EBP and NF-κB. After electroporation, cells were re-suspended in RPMI 1640 culture medium (Lonza, Verviers, Belgium), 10% FCS, 1% AB and cultured at 37 °C and 5% CO2 for 24 h. Afterwards, cells were harvested and re-suspended in fresh growth medium (RPMI 1640, 0.1% FCS, 1% AB) to a final concentration of 1 × 10 6 cells/mL and pre-treated for 2 h with 6-acetylmonodethiogliotoxin at indicated concentrations, followed by TNFα activation (20 ng/mL) for 6 h. After incubation, 75 µL of Dual-Glo ™ Luciferase Reagent (Promega, Leiden, The Netherlands) was added to 75 µL of the cellular suspension for a 10 min at 22 °C before luciferase activity measurement. Subsequently, 75 μL of Dual-Glo ™ Stop&Glo ® Reagent (Promega, Leiden, The Netherlands) was added for 10 min at 22 °C to the cell suspension to measure Renilla activity. An Orion microplate luminometer (Berthold Technologies, Bad Wildbad, Germany) was used to measure luciferase and Renilla activity. The results are expressed as a ratio of arbitrary units of firefly luciferase activity to Renilla luciferase activity.

Cell Viability Assessment
To assess percentage of viable K5562 cells within sample and to determinate K562 cells proliferation trypan blue exclusion test was used. Trypan blue is a vital stain that belongs to the family of azo compounds. It is a selective dye that stains only dead cells, passing through their plasma membrane. Viable cells are unstained as they can actively extrude this dye. Briefly, 20 μL of cell suspension was mixed with 20 μL of trypan blue solution and evaluated by Malassez cell counting chamber (Fisher Scientific, Erembodegem, Belgium). In order to assess the cell viability, the percentage of unstained cells to the total amount of cells within the sample was calculated and normalized to 100% of control cells viability. In order to assess cell proliferation the concentration of unstained cells was determined and normalized to 100% of control cells concentration.

Extraction of Cellular Proteins
After the indicated incubation times with 6-acetylmonodethiogliotoxin and TNFα, Jurkat cells were lysed, and the nuclear and cytoplasmic extracts were prepared according to Duvoix et al. [28]. Briefly, cell pellets (10 7 cells per sample) were suspended in ice-cold hypotonic lysis buffer containing protease inhibitor cocktail (Complete ® , Roche, Prophac, Luxembourg) and incubated on ice for 15 min. After incubation, 10% Igepal (Sigma-Aldrich BVBA Diegem, Belgium) was added to the cell suspension and each microcentrifuge tube was vigorously mixed by Vortex for 10 s to lyse cells followed by centrifugation in a refrigerated microcentrifuge tube at 18,000 rcf for 1 min. The cytoplasmic extract (supernatant) was aliquoted and stored at −80 °C until use. Cell pellets were additionally washed with 100 μL of hypotonic lysis buffer and after centrifugation at 4 °C, 18,000 rcf for 2 min the supernatant was removed. The ice-cold nuclear extraction buffer was added to each pellet and the cell suspension was gently mixed on an orbital shaker for 15 min at 4 °C following centrifugation at 10,500 rcf for 7 min at 4 °C. Then nuclear extracts (supernatant) were transferred to pre-chilled microcentrifuge tubes and stored at −80 °C until use. Protein content was determined for each sample using the Bradford assay (Bio-Rad protein Assay, Biorad, Nazareth, Belgium).

TransAM Assay
Jurkat cells were seeded at concentration 3 × 10 5 cells/mL and 10 7 cells were treated with Alterporriol E for 4 h followed by activation with TNFα (20 ng/mL) for 30 min. Subsequently, nuclear proteins were extracted from the cells according to manufacturer's protocol (Active motif, Nuclear extract kit, La Hulpe, Belgium). Nuclear protein extracts were submitted for TransAM assay, which was conducted according to the manufacturer' instruction (Active motif, TransAM NFκB family, La Hulpe, Belgium) and luminescent signal was measured by Luminometer (CentroLB 960, Berthold Technologies, Bad Wildbad, Germany).

Statistical Analysis
Data are expressed as mean ± SD Significance was determined by the Student's t-tests. p-Values below 0.05 were considered as statistically significant. IC50 values were calculated using XY scatter dependency chart. The 50% inhibition activity on NF-κB expression was established by using the best fitting model and calculated by trend formulas. The average value of at least 3 independent experiments was applied. Data are expressed as mean ± SD Significance was determined by the Student's t-tests. p-Values below 0.05 were considered as statistically significant.

Conclusions
Overall the described monosulfid production seems to be a special feature of this particular marine derived strain of D. cejpii. Moreover, our study validates the inhibitory effects of newly isolated natural epipolythiodiketopiperazines on anti-proliferative mechanisms via inhibition of TNFα-induced NF-κB activity. Especially, 6-acetylmonodethiogliotoxin as a most potent NF-κB inhibitor presenting the strongest anti-proliferative effects within the evaluated compounds represents a promising future marine-derived cytostatic drug candidate.