SD118-Xanthocillin X (1), a Novel Marine Agent Extracted from Penicillium commune, Induces Autophagy through the Inhibition of the MEK/ERK Pathway

A compound named SD118-xanthocillin X (1) (C18H12N2O2), isolated from Penicillium commune in a deep-sea sediment sample, has been shown to inhibit the growth of several cancer cell lines in vitro. In the present study, we employed a growth inhibition assay and apoptotic analysis to identify the biological effect and detailed mechanism of SD118-xanthocillin X (1) in human hepatocellular carcinoma (HepG2) cells. SD118-xanthocillin X (1) demonstrated a concentration-dependent inhibitory effect on the growth of HepG2 cells and caused slight cellular apoptosis and significantly induced autophagy. Autophagy was detected as early as 12 h by the conversion of microtubule-associated protein 1 light chain 3 (LC3-I) to LC3-II, following cleavage and lipid addition to LC3-I. The pharmacological autophagy inhibitor 3-methyladenine largely attenuates the growth inhibition and autophagic effect of SD118-xanthocillin X (1) in HepG2 cells. Our data also indicated that the autophagic effect of SD118-xanthocillin X (1) occurs via the down-regulation of the MEK/ERK signaling pathway and the up-regulated class III PI3K/Beclin 1 signaling pathway.

death. Intriguingly, our study shows that SD118-xanthocillin X (1) induced slight cell apoptosis and significant autophagy in HepG2 cells. One proposed downstream effector of ERK involved in the regulation of autophagy is mTOR kinase, which inhibits autophagy by phosphorylating downstream substrates that are possibly analogous to other autophagy associated gene (ATG) products [16,17]. We found that class III PI3K/Beclin 1 and the MEK/ERK signaling pathway are involved in the SD118-xanthocillin X (1)-induced autophagy process in HepG2 cells, a process that was partially attenuated by 3-methyladenine. These data reveal that SD118-xanthocillin X (1) induced autophagy in HepG2 cells via a non-canonical signaling pathway [17].

Cytotoxic Activity of SD118-Xanthocillin X (1) in HepG2 Cells
HepG2 cells and a normal cell line L02 (human normal liver cell line cells) were chosen to evaluate the cytotoxic activity of SD118-xanthocillin X (1). Cell viability was examined by a formazan-based MTT cell viability assay as described in "Materials and Methods". A concentration-dependent inhibitory effect by SD118-xanthocillin X (1) on cellular growth was observed in the HepG2 cells, with the IC 50 at the 0-55.56 µM (0-16 μg/mL) dosage being 22.88 ± 4.76 µM (6.59 ± 1.37 μg/mL) after 48 h.
These data indicated that SD118-xanthocillin X (1) had a significant inhibitory effect on the proliferation of HepG2 cells ( Figure 1B). However, we observed that SD118-xanthocillin X (1) had no statistically significant effect on normal liver cells (L02 cells) ( Figure 1C).
Since cell viability was significantly inhibited by SD118-xanthocillin X (1), it was critical to classify which type of cell death was induced in HepG2 cells. An annexin V/PI assay was performed to detect the apoptosis and cell cycle distribution by SD118-xanthocillin X (1) treatment. Our data showed that SD118-xanthocillin X (1) slightly induced apoptosis ( Figure 2A) and did not alter the cell cycle distribution of the HepG2 cells ( Figure 2B). To explore the mechanism of the growth inhibitory effect of SD118-xanthocillin X (1) further, we assayed its autophagy effect, which has been shown to be a novel response to some anticancer agents that induce autophagy and trigger an autophagic cell death (ACD) response.

SD118-Xanthocillin X (1) Induces Apoptosis and Autophagy in HepG2 Cells
Using transmission electron microscopy (TEM), which is the standard method to detect autophagy reliably [12], we observed the formation of autophagosomes in the HepG2 cells after SD118-xanthocillin X (1) treatment ( Figure 3). As shown in Figure 3, the negative control cells exhibited normal nuclei, with uniform, dispersed chromatin and abundant microvilli on the plasmalemma ( Figure 3A). The detection of starvation-induced autophagy was used as a positive control ( Figure 3B). In contrast, SD118-xanthocillin X (1) treatment for 12 h resulted in indistinguishable organelles and a decrease in microvilli ( Figure 3C). After 24 h, the appearance of autophagic vacuoles containing degraded organelles was found ( Figure 3D), and the formation of these membranous vacuoles increased gradually over time ( Figure 3E). A higher magnification showed that the autophagic vacuoles contained the remnants of cellular organelles. These biological indicators demonstrated that SD118-xanthocillin X (1) results in the appearance of autophagosomes in HepG2 cells.

The Expression of Autophagy-Related Genes
LC3 has been shown to be an autophagosomal marker in mammals. LC3 usually exists in two forms: LC3-I (16 kDa) and LC3-II (14 kDa). The amount of LC3-II or the ratio of LC3-II/LC3-I correlates with the status of autophagosomes [18]. Beclin 1 is involved in both signaling pathways that activate autophagy and in the initial step of autophagosomal formation [19,20].
Our results showed that the mRNA expression of the LC3 ( Figure 4A) and Beclin 1 ( Figure 4B) genes were up-regulated after 12 h of SD118-xanthocillin X (1) treatment in a time-dependent manner in HepG2 cells by quantitative real-time PCR. Moreover, western blot analysis confirmed that SD118-xanthocillin X (1) altered the expression of autophagy-related genes at the protein level. We examined the expression of Beclin 1 and the conversion of LC3-I to LC3-II in the HepG2 cells after SD118-xanthocillin X (1) treatment at different time points; as shown in Figure 4C, the increased expression was time dependent and most notable after 12 h. Thus, the above data indicate that SD118-xanthocillin X (1) increased the expression of the autophagy-related genes, LC3, and Beclin 1. Beclin 1 (B). HepG2 cells were treated with 24.3 µM SD118-xanthocillin X (1) for indicated times, and relative mRNA expression of autophagic genes was measured by quantitative Real-Time PCR analysis. (** p < 0.001, *** p < 0.0001) compared to control group; (C) HepG2 cells were treated with 24.3 µM SD118-xanthocillin X (1) for indicated times. Western blot represents the conversion of LC3-I to LC3-II and time-dependent up-regulation of Beclin 1 following SD118-xanthocillin X (1) treatment. Protein contents were normalized with β-actin.

3-MA Partially Attenuates the Autophagic Effect of SD118-Xanthocillin X (1)
To investigate whether inhibition of autophagy would affect the cytotoxicity of SD118-xanthocillin X (1), we employed 3-MA, an autophagy inhibitor that acts via the suppression of class III PI3K activity [21], in our cell activity study. The cells were treated with 5 mM 3-MA, and the viability was examined by a cytotoxic activity test. As shown in Figure 5A, the activities of the cells in the control, 3-MA group, SD118-xanthocillin X (1) plus 3-MA group and SD118-xanthocillin X (1) group were 101 ± 1.3%, 80.18 ± 4.2%, 56.0 ± 3.2% and 24.5 ± 2.6%, respectively ( Figure 5A). In comparison to the SD118-xanthocillin X (1) plus 3-MA group, the activity of the cells decreased more in the SD118-xanthocillin X (1) group. We repeated the same experiments six times, and a similar tendency was detected; the effect was statistically significant. Through western blotting, we confirmed that 3-MA partially attenuated the effect of SD118-xanthocillin X (1) on autophagy-related gene expression ( Figure 5B). Taken together, our data indicate that SD118-xanthocillin X (1) may play a significant role in autophagy-induced cell death.

The Effect of SD118-Xanthocillin X (1) on Autophagy-Related Signaling Pathways
mTOR is a serine/threonine protein kinase that is involved in many pathways in the negative regulation of autophagy, acting as a convergence point [22,23]. In mammalian cells, phosphorylated mTOR (p-mTOR) correlates with the inhibition of autophagy. Rapamycin, an allosteric mTOR inhibitor, has been shown to induce autophagy in malignant glioma cells [24]. To identify the role of SD118-xanthocillin X (1) in related pathways, we investigated the mTOR activity by western blotting. As shown in Figure 6, SD118-xanthocillin X (1) treatment resulted in decreased levels of p-mTOR in the HepG2 cells, whereas the total mTOR levels were unaffected. It has been previously reported that autophagy is regulated by the MEK/ERK pathway [17]. Therefore, we tested whether p-ERK1/2 levels were regulated by SD118-xanthocillin X (1) and found a sustained decrease of p-ERK1/2 in the SD118-xanthocillin X (1) group, but not in the control cells. Bcl-2-mediated autophagy occurs through both Beclin 1 and mTOR signaling: Bcl-2 interacts with Beclin 1 and down-regulates autophagy, and it also positively regulates the mTOR signaling pathway, which can inhibit autophagic activity [25,26]. Thus, the above results show that SD118-xanthocillin X (1) induces autophagy in HepG2 cells by down-regulating Bcl-2 and inactivating the MEK/ERK pathway ( Figure 6). Previous studies demonstrated that SD118-xanthocillin X (1) exhibited effective anti-proliferative activity in the majority of cell lines derived from human solid tumors [15]. In the present study, we provided evidence that this compound slightly induced apoptosis and significantly induced autophagy in HepG2 cells, a process that was followed by autophagic cell death. Autophagy was morphologically and biochemically characterized and included the appearance of autophagic vacuoles in the cytoplasm of the treated HepG2 cells that contained the remnants of organelles, as shown by TEM. We also detected the up-regulated expression of autophagy-related genes and the increased conversion of LC3-I to LC3-II.
We further investigated the signaling pathways affected in SD118-xanthocillin X (1)-induced autophagy. Autophagy is positively regulated by the class III PI3K signaling pathway [27,28]. Beclin 1 is a Bcl-2-interacting coiled-coil protein that is a mammalian ortholog of yeast Atg6/Vps30 and is required for the formation of autophagosomes; Beclin 1 is monoallelically deleted in 40%-75% of sporadic breast and ovarian cancers [29]. The overexpression of Beclin 1, which forms a complex with class III PI3K to initiate autophagy, induces cell death in MCF cells [30]. In the present study, we found an increased expression of Beclin 1 and a decreased expression of Bcl-2 in HepG2 cells following SD118-xanthocillin X (1) treatment, and this SD118-xanthocillin X (1)-induced autophagy in the HepG2 cells was partially attenuated by 3-MA, indicating the involvement of SD118-xanthocillin X (1) in drug-induced autophagy.
Autophagy is also negatively regulated by the MEK/ERK signaling pathway [17]. ERKs are a widely conserved family of serine/threonine protein kinases implicated in many cellular processes, such as cell proliferation, differentiation, and apoptosis. ERK1/2 (p42/p44MAPK) can be activated by a great number of oncogenes and extracellular stimuli, including mitogens, growth factors, cytokines, and chemokines. An increasing number of studies have suggested that ERK1/2 plays a role in modulating autophagy [30][31][32][33][34][35] because the constitutive expression of Beclin 1 relies on the basal activity of MEK/ERK, and enhanced Beclin 1 is attributable to an inhibition of MEK/ERK activation. MEK1 and MEK2 activate p44 and p42 through the phosphorylation of activation loop residues Thr202/Tyr204 and Thr185/Tyr187, respectively. Indeed, ERKs require both Thr and Tyr phosphorylation for full activity [36]. Our study showed that SD118-xanthocillin X (1) induced autophagy by down-regulating p-Erk1/2 (Thr202/Tyr204 and Thr185/Tyr187) and its activity, which was followed by a reduction in p-mTOR. We found that the non-canonical MEK/ERK module regulates mutually antagonistic processes by regulating Beclin 1 levels. The basal activity of MEK/ERK protected mTOR [17]. As shown in the present study, SD118-xanthocillin X (1)-induced autophagy in HepG2 cells involves the inhibition of mTOR phosphorylation. Thus, our data indicated that SD118-xanthocillin X (1)-induced autophagy in HepG2 cells is associated with the suppression of the MEK/ERK signaling pathway and the enhancement of class III PI3K/Beclin 1 signaling. This is the first report characterizing the involvement of these signaling pathways in SD118-xanthocillin X (1)-induced autophagy. However, one limitation of our study is that we did not examine the upstream effectors of the ERK pathway or other autophagic pathways.
Since the apoptotic and autophagic response machineries share common pathways and cross-talk molecules, such as Bcl-2 and Bcl-xl [37,38], further studies on the signaling pathways of both responses are needed to better clarify the biological role of SD118-xanthocillin X (1). These investigations may help uncover the molecular mechanism by which SD118-xanthocillin X (1) confer its chemotherapeutic effect in cancer therapy.

Test Compound
SD118-Xanthocillin X (1) was isolated from a strain of Penicillium commune (SD-118) found in a deep-sea sediment. After incubation, the fermented broth was sterilized by adding EtOAc, and the mycelia were separated from the culture broth by filtration. The broth was extracted repeatedly with EtOAc (200 mL each flask) to yield an extract, and the mycelia were air-dried and soaked three times in acetone/water (4:1, v/v) for 3 days. To remove the acetone, the acetone/water extract was evaporated under vacuum and then extracted again with EtOAc to yield another extract. The combined extraction (27 g) was fractionated using silica gel vacuum liquid chromatography (VLC) with petroleum/EtOAc (from 1:0 to 1:1) and CHCl 3 /MeOH (from 20:1 to 0:1) gradient elution to produce 12 fractions (Fr. 1-Fr. 12) [15].

Drug Preparation
SD118-Xanthocillin X (1) was dissolved in DMSO and further diluted in PBS. The final solution used in the experiments was 7 g/L; the DMSO concentration was less than 0.1% and did not affect cellular function or the assay systems. 3-Methyladenine (3-MA, Sigma Chemical Co.) was dissolved in 50 °C PBS; upon cooling, the product precipitates out of the solution. The final concentration of 3-MA was 5 mM.

Cell Lines and Growth Inhibition Assay
HepG2 cells were cultured in RPMI 1640 medium and L02 cells were cultured in DMEM medium (HepG2 and L02 cells were purchased from the cell bank of Shanghai Institute of Cell Biology), both of them supplemented with 10% fetal bovine serum and 100 units/mL penicillin. All of the cultured cells were maintained under a humidified 5% CO 2 atmosphere at 37 °C. The cytotoxic activity of SD118-xanthocillin X (1) was determined using a standard MTT, a yellow tetrazole-based colorimetric assay. Briefly, the HepG2 cells were seeded at a density of 7 × 10 3 cells/well in 96-well microtiter plates. After 24 h, the cells were exposed to different concentrations of the test compounds; cell survival was determined by the addition of MTT solution, as described previously.

Flow Cytometry Analysis of Apoptosis
Cell apoptosis was examined using an Annexin V-FITC Apoptosis Detection Kit (KeyGEN Biotech, NanJing, China) that measures the externalization of phosphatidylserine in the plasma membrane. The cells were seeded in six-well plates at a density of 5 × 10 6 cells/mL and incubated overnight; SD118-xanthocillin X (1) was added at different time points (12 h, 24 h, and 48 h). The cells were then collected by trypsinization, washed twice with cold PBS and re-suspended in 500 µL of binding buffer (2.5 mM CaCl 2 , 140 mM NaCl and 10 mM Hepes/NaOH, pH 7.4), at a concentration of 1 × 10 6 cells/mL. Annexin V-FITC and PI were then added to the cells, which were analyzed using flow cytometry. The results were calculated using Cell Quest software and are shown as percentages. Early apoptotic cells were negative for PI and positive for annexin-V, whereas late apoptotic dead cells displayed both high annexin-V and PI labeling [39].

Transmission Electron Microscopy (TEM)
The HepG2 cells were collected after trypsin/EDTA treatment, washed twice with PBS and centrifuged at 800 r/min for 5 min. The cells were then fixed in 3% ice-cold glutaraldehyde for at least 3 h. After washing in cool PBS, the cells were postfixed in osmium tetroxide, and embedded in Spurr's resin. Thin sections were cut, and double stained with uranyl acetate and lead citrate. Ultrathin sections were observed using a HITACHI H7560 electron microscope.
The real-time PCR results were analyzed using the 7300 system software and normalized using the detection of β-actin. The relative expression levels of the target genes were compared to the levels of reference gene (β-actin) using the comparative cycle threshold (ct) method as the fold difference = 2 −(∆ct of target gene − ∆ct of reference) .

Western Blotting
Total protein was extracted from cultured cells using the whole protein extraction kit (containing pH 7.4 50 mM Tris, 150 mM NaCl, 1% Triton X-100, 1% sodium deoxycholate, 0.1% SDS and 1 mM PMSF), and the protein concentration was determined using the BCA Protein Assay Reagent (Beyotime, China). Equal amounts of protein were separated discontinuously on 6%-15% SDS-PAGE, transferred to a nitrocellulose membrane, and incubated with anti-human mono/polyclone antibodies overnight at 4 °C. After incubation of the secondary antibody at room temperature for 1 h, the immunoblots were visualized using an enhanced chemiluminescence (ECL) kit. The antibodies used were anti-LC3, anti-Beclin 1, anti-Bcl2, anti-mTOR, phosphorylated-mTOR, phosphorylated-ERK1/2, and anti-actin (Cell Signaling Technology, MA, USA).

Statistical Analysis
The data are reported as the mean ± SD of at least three independent experiments. Each treatment was performed in triplicate culture wells. Statistically significant values were tested by Dunnett's Tests, and p values less than 0.05 were considered statistically significant.

Conclusion
In summary, the findings presented here indicate that SD118-xanthocillin X (1) is highly effective in reducing cell viability and that the reduced survival of HepG2 cells is associated with the initiation of autophagy. SD118-Xanthocillin X (1)-induced autophagy resulted from the inhibition of the MEK/ERK-mTOR signaling pathway and the enhancement of the class III PI3K/Beclin 1 signaling pathway.