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Murakami et al. BMC Cancer (2018) 18:680 https://doi.org/10.1186/s12885-018-4588-y RESEARCH ARTICLE Open Access Dual effects of the Nrf2 inhibitor for inhibition of hepatitis C virus and hepatic cancer cells Yuko Murakami1†, Kazuo Sugiyama2*†, Hirotoshi Ebinuma3, Nobuhiro Nakamoto2, Keisuke Ojiro2, Po-sung Chu2, Nobuhito Taniki2, Yoshimasa Saito1, Toshiaki Teratani2, Yuzo Koda4, Takahiro Suzuki2, Kyoko Saito5, Masayoshi Fukasawa5, Masanori Ikeda6, Nobuyuki Kato7, Takanori Kanai2 and Hidetsugu Saito1* Abstract Background: We previously showed that knockdown of nuclear factor E2-related factor 2 (Nrf2) resulted in suppression of hepatitis C virus (HCV) infection. In this study, whether brusatol, an Nrf2 inhibitor, has dual anti-HCV and anticancer effects was explored. Methods: The anti-HCV effect of brusatol was investigated by analyzing HCV RNA and proteins in a hepatic cell line persistently-infected with HCV, HPI cells, and by analyzing HCV replication in a replicon-replicating hepatic cell line, OR6 cells. Then, dual anti-HCV and anticancer effects of brusatol and enhancement of the effects by the combination of brusatol with anticancer drugs including sorafenib, which has been reported to have the dual effects, were then investigated. Results: Brusatol suppressed the persistent HCV infection at both the RNA and protein levels in association with a reduction in Nrf2 protein in the HPI cells. Analysis of the OR6 cells treated with brusatol indicated that brusatol inhibited HCV persistence by inhibiting HCV replication. Combination of brusatol with an anticancer drug not only enhanced the anticancer effect but also, in the case of the combination with sorafenib, strongly suppressed HCV infection. Conclusions: Brusatol has dual anti-HCV and anticancer effects and can enhance the comparable effects of sorafenib. There is therefore the potential for combination therapy of brusatol and sorafenib for HCV-related hepatocellular carcinoma. Keywords: Hepatitis C virus, Hepatocellular carcinoma, Nuclear factor E2-related factor 2, Chemotherapy, Brusatol, Sorafenib, Anticancer, Anti-HCV Background Chronic infection with hepatitis C virus (HCV) has been a worldwide health problem for decades, frequently leading to serious liver diseases such as liver cirrhosis and hepatocellular carcinoma (HCC) [1, 2]. For a long period, an interferon-based regimen has been the major therapy for * Correspondence: sygiyamkz@a8.keio.jp; hsaito@a2.keio.jp † Yuko Murakami and Kazuo Sugiyama contributed equally to this work. 2 Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University, Shinanomachi 35, Shinjuku-ku, Tokyo 160-8582, Japan 1 Division of Pharmacotherapeutics, Faculty of Pharmacy, Keio University, Minato-ku, Tokyo 105-8512, Japan Full list of author information is available at the end of the article HCV despite various adverse effects. Recently, several kinds of direct-acting antivirals (DAAs), which target proteins of the replication complex of HCV, including the nonstructural protein (NS)3, NS5A, and NS5B, have been developed, and combination regimens of such DAAs have achieved a sustained viral response more than 90% of the patients without using interferons [3]. It is known that reduction of persistent HCV infection reduces the incidence of HCC in HCV patients [4]. However, DAA treatments for HCV patients complicated with HCC are controversial because HCC as well as decompensated liver cirrhosis is a stronger prognostic factor than elimination of HCV for such patients [5]. We considered that one feasible © The Author(s). 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. Murakami et al. BMC Cancer (2018) 18:680 resolution for this issue is the development of a drug that has dual effects, i.e., a drug that has both anti-HCV and anti-HCC effects. Regarding agents with such dual effects, it has been demonstrated that the anti-tumor drug sorafenib, a kinase inhibitor that blocks the RAF kinase [6], also suppresses HCV replication, albeit in vitro [7–9]. Clinically, sorafenib has been approved and used for systemic anti-HCC therapy [10, 11]. However, sorafenib has not achieved a satisfactory cure of HCC [12]. Additionally, sorafenib did not affect the HCV RNA level during its clinical use in HCC patients with HCV [13]. Therefore, development of another agent with such dual effects is desirable for use as a monotherapy or as a combination therapy with existing anticancer drugs such as sorafenib. Recently, we established a cell line persistently-infected with HCV, HPI cells, and showed that higher expression of nuclear factor E2-related factor 2 (Nrf2) contributes to persistent HCV infection, and that knockdown of Nrf2 suppresses its persistent infection [14]. Nrf2 is a transcriptional regulator of an array of genes including genes involved in the regulation of cell proliferation, redox homeostasis [15, 16] and cell metabolism such as glucose and glutamine metabolism [17]. Under normal conditions, Nrf2 is constantly degraded via ubiquitination by the association with Kelch-like ECH-associated protein 1 (Keap1) in the cytosol. Nrf2 is activated via dissociation with Keap1 by stress, such as reactive oxygen species. Nrf2 is also activated by phosphorylation independent of the Keap1 pathway in some tumors. Once it is activated in either way, Nrf2 or phosphorylated Nrf2 (p-Nrf2) is translocated into the nucleus and transactivates its target genes [18, 19]. Clinical studies have shown that Nrf2 is related to cell proliferation and invasion, as well as chemo-resistance of various human cancers [20–26], and that it is also involved in the progression and prognosis of HCC [20, 23, 24]. Indeed, somatic mutations of Nrf2 and Keap1 are detected in HCC [27], and a recent exome analysis showed that both Nrf2 and Keap1 are driver genes for carcinogenesis in HCC [28]. In addition, it has been reported that HCV activates Nrf2 [29], and that p62/Sqstm1 pathways were facilitated in HCV-positive HCC (C-HCC), leading to Nrf2-dependent metabolic reprogramming and promotion of HCC [30]. Based on these data, we expected that inhibition of Nrf2 could exert dual effects against HCV infection and proliferation of C-HCC. Thus, to explore such dual effects by an Nrf2 inhibitor in vitro, we chose the quassinoid, brusatol, a compound derived from a natural product, which has been shown to inhibit the Nrf2 pathway and to reduce tumors in vivo and in vitro [31, 32]. Two cell lines, the HPI cell line and the OR6 cell line, were mainly used. The OR6 cell line is a full-length HCV replicon replicating cell line in which Page 2 of 14 HCV replication can be easily determined by luciferase assay [33]. In these studies, it was demonstrated, for the first time, that brusatol has dual anti-HCV and anticancer effects. Methods Hepatocellular carcinoma tissue specimens A tissue array slide of HCV-positive hepatocellular carcinoma tissue specimens including control non-hepatocellular-carcinoma specimens without either HCV or HBV infection (code LV8013) was purchased (US Biomax, Rockville, MD). Cell culture The HPI cell line, which was established in our previous study [13], and the hepatoma cell lines Huh6 [34], Huh7.5 [35], and HepG2 (ATCC #HB-8065), were cultured in high-glucose DMEM (Life Technology, Carlsbad, CA) supplemented with 10% fetal calf serum. The OR6 cell line was cultured in the same medium with addition of 0.3 mg/ml geneticin (Life Technologies). Knockdown experiment Knockdown for Nrf2 expression in cultured cells was performed by transfection of siRNA against Nrf2, NEF2L2-HSS107128 (Life Technologies) and control RNA, stealth RNAi negative control medium GC duplex (Life Technologies). The transfection was done with Lipofectamine RNSiMAX transfection reagent (Life Technologies) according to the manufacturer’s protocol. Immunohistochemical staining A tissue array slide was deparaffinized and hydrated with xylene and a graded alcohol series. After antigen activation in 10 mM citrate at 120 °C for 10 min, non-specific binding was blocked with 5% bovine serum albumin and the slide was incubated overnight with a primary antibody at 4 °C. Subsequently, the slide was incubated with a secondary antibody for 1 h, and the signal was developed by staining with 3,3′-diaminobenzidine using the Vectastain Elite ABC Kit® (Vector Laboratories, Burlingame, CA) according to the manufacturer’s protocol. Positivity of p-Nrf2 was given an immunoreactivity score, which was determined by amplification of the intensity of nuclear staining score (0, negative; 1, weakly positive; 2, moderately to strongly positive) and the ratio of stained nuclei (0, no nuclei; 1, 1 to 50%; 2, more than 50%). The immunoreactivity scores were generated by a pathologist. Statistical analysis was done with the Mann-Whitney test using Graphpad (Prism, La Jolla, CA). Immunofluorescence staining Cultured cells were seeded on a chamber slide 24 h prior to the administration of a reagent or 48 h prior to immunofluorescence staining without administration of a Murakami et al. BMC Cancer (2018) 18:680 reagent. For immunofluorescence staining, the cells were fixed with 4% paraformaldehyde, permeabilized with 0.05% Triton X-100 solution and blocked with 5% bovine serum albumin. Subsequently they were incubated with primary antibodies (mixed) and then with secondary antibodies (mixed) against the respective primary antibody. Finally, the cells were mounted with Vectashield containing 4′,6-diamidino-2-phenylindole (Vector Laboratories). Immunofluorescence was detected and processed by using a fluorescence microscope, EVOS AMF-4302 (Thermo Fisher Scientific, Waltham, MA), and Photoshop CS (Adobe Inc., San Jose, CA). Subcellular localization, nuclear or cytosol, of the protein was determined by merging images of the protein and DAPI. Immunoblot analysis For immunoblot analysis, cultured cells were harvested in RIPA buffer (Thermo Fisher Scientific, Waltham, MA). After the addition of an equal volume of 2X Laemmli sample buffer (Bio-Rad, Hercules, CA) containing 5% β-mercaptoethanol, the cell lysates were heat-denatured at 95 °C for 5 min and then sonicated for 10 min. The protein concentration of the sample was determined using the Pierce 660-nm Protein Assay kit (Thermo Fisher Scientific) according to the manufacturer’s protocol, and equal amounts (protein content) of samples were subjected to SDS-PAGE (Bio-Rad). Proteins in the gels were transferred to the PVDF membrane, Immobilon (Merck Millipore, Darmstadt, Germany), blocked with 5% milk powder, and incubated with a primary antibody at the concentration recommended by the manufacturer at room temperature for 1 h or at 4 °C overnight. Then, after incubation with horseradish peroxidase-conjugated secondary antibody (GE Healthcare, Little Chalfont, UK) for 1 h, the protein signals were detected by using ECL Prime (GE Healthcare). Relative intensity of the immunoblot band for the proteins to that of b-actin was calculated with the image analyzer at each time point and concentration. It was calculated with the values for no drug at 0 h as 1.00. Primary and secondary antibodies for immunohistochemical staining, immunofluorescence staining and immunoblot analysis Primary antibodies used were against HCV core (Institute of Immunology, Tokyo, Japan), HCV NS5A (Virogen, Watertown, MA), β-Actin (Abcam, Cambridge, UK), Nrf2 (Santa Cruz, Dallas, TX), and p-Nrf2, phospho-serine 40, (Abcam). For immunoblot analysis, HRP-labeled secondary antibodies against mouse IgG, rabbit IgG, and goat IgG (GE Healthcare) were used depending on the primary antibodies used for immunoblotting. For immunofluorescence staining, Alexa-fluor-488-labeled goat anti-mouse Page 3 of 14 and Alexa-fluor-568-labeled goat anti-rabbit (Life Technologies) secondary antibodies were used. Quantitative reverse transcription polymerase chain reaction (qRT-PCR) qRT-PCR assays were performed with the Thermal Cycler Dice TP800 (Takara, Shiga, Japan) to measure RNA of 2 regions of the HCV genome: the 5′ untranslated region (5’UTR) and the NS5A region. Primer sets (forward / reverse) used were: 5’-AAGCGTCTAGCCAT GGCGTTAGTA / 5’-GGCAGTACCACAAGGCCTT TCG, 5’-CCGCGACGTGTGGGACTGGGTTTGCAC / 5’-CTCCGAGGCCGCCACCCTCCAGATGGC and 5’-GCACCGTCAAGGCTGAGAAC / 5’-TGGTGAAGA CGCCAGTGGA for the 5’UTR, the NS5A region and control GAPDH, respectively. The reverse transcription reaction was done at 37 °C for 15 m, and then at 85 °C for 5 s with the Primescript RT Master Mix (Takara). The polymerase chain reaction was done first at 95 °C for 30 s and then with 40 cycles of 95 °C for 5 s and 60 ° C for 30 s, followed by 95 °C for 15 s, 60 °C for 30 s and 95 °C for 15 s, using the KAPA SYBR® FAST qPCR Kit (Kapa Biosystems, Boston, MA). Relative quantification was performed using the 2-ΔΔCT method, and each value was normalized by the value of GAPDH. PCR amplifications were performed in triplicate, and statistical analysis was performed by using Student’s t-test. Luciferase assay For luciferase assays, OR6 cells were seeded on a 24 well culture plate. The assay was performed in triplicate using a Renilla Luciferase Assay System (Promega, Madison, WI) according to the manufacturer’s protocol. Luminescent signals were measured with a spectrometer (Promega). Transcriptome analysis At 24 h after plating the HPI cells onto a 10 cm-diameter dish, 160 nM brusatol or 25 nM siRNA against Nrf2 together with control (DMSO and scrambled RNA, respectively) were added to the culture medium. The concentration of brusatol and siRNA corresponded to that which provides twice the 50% growth inhibition (GI50) and 14% inhibition of Nrf2 expression (based on the previous study), respectively. Forty-eight hours later, total RNA was prepared from the cultured cells using the RNeasy extraction kit (Qiagen, Germantown, MA). For transcriptome analysis, cDNA microarray analysis of the extracted RNA was performed using Human Oligo Chip 25 K (Toray, Tokyo, Japan) and 3D-Gene scanner 3000 (Toray). Microarray data were deposited in Gene Expression Omnibus (https://www.ncbi.nlm.nih.gov/geo/). Murakami et al. BMC Cancer (2018) 18:680 Cell viability assay Cell viability was determined using the MTS assay kit, Celltiter 96® Aqueous One Solution Cell Proliferation Assay (Promega) according to the attached protocol. The absorbance of each well was measured with the microplate reader Model 680 (Bio-Rad). At 48 h after the administration of the drug, a curve was created by plotting the logarithm of the concentration of the drug on the X-axis and the percentage of cell growth, determined with the MTS assay, to that of no drug on the Y-axis. Then, the concentration of the drug corresponding to 50% growth inhibition (GI50) was estimated by using Graphpad (Prism). As for viable cell counting with trypan blue, the HPI cells were seeded onto a 24-well plate. At indicated time points, the cells were washed, treated with trypsin-EDTA solution and stained with 0.2% trypan blue, and then non-stained cells were counted. Measurements for MTT assay and the trypan blue method were done in triplicate at each time point, and statistical analysis was performed by using Student’s t-test. Results Expression of p-Nrf2 in C-HCC and cultured hepatoma cell lines First, we explored the expression status of the active form of Nrf2, p-Nrf2, was explored in C-HCC clinical specimens using a tissue array slide and cultured hepatoma cell lines including a HCV-positive cell line (HPI cell line) and HCV-negative cell lines (Huh7.5, Huh6 and HepG2 cell lines). Figure 1a shows representative features of p-Nrf2 expression in C-HCC clinical specimens as determined by immunohistochemistry. In this analysis, p-Nrf2 was expressed exclusively in the nuclei of 45% (9/20) of the C-HCC specimens on the array examined, whereas only 5% (1/20) of the non-HCC specimens without either HCV or HBV infection were positive for p-Nrf2. Positivity of p-Nrf2 as represented by an immunoreactivity score was significantly greater in C-HCC specimens (0, 55%; 1, 10%; 2, 25%; 10%; 4, 10%) than in non-HCC specimens (0, 95%; 1, 5%) (p = 0.003). As shown in the immunofluorescence analysis (Fig. 1b), p-Nrf2 was expressed exclusively in the nuclei of the HPI cells, in which HCV core protein was also positively stained in cytosol. p-Nrf2 was also exclusively expressed in the nuclei of the HCV-negative hepatoma cell lines, although relatively few of the HepG2 cells were p-Nrf2-positive. Expression of Nrf2 itself was not clearly recognized by immunofluorescent analysis owing to non-specific signals in the cytosol. Instead, we performed immunoblot analysis of Nrf2 after knockdown with siRNA against Nrf2 was performed, and it was confirmed that Nrf2 expression in the hepatoma cell lines was suppressed with siRNA against Nrf2 (Fig. 1c). Page 4 of 14 These results confirmed that p-Nrf2 was expressed in a considerable number of C-HCC clinical specimens as well as in the hepatoma cell lines including the HCV-positive hepatoma cell line, supporting the concept that p-Nrf2 plays an important role in the pathogenesis of C-HCC. Brusatol reduced the HCV RNA level in the HPI cells To determine if brusatol affects the persistence of HCV infection, the effect of brusatol administration on the RNA levels in the 5’UTR and the NS5A region of HCV in the HPI cells was analyzed by qRT-PCR. Brusatol reduced HCV RNA levels in a dose-dependent manner from 24 to 72 h after its administration (Fig. 2a). This effect was diminished at 48 h and 72 h compared to 24 h after the administration of brusatol, possibly because of recovery of RNA replication at the later time, especially in a lower concentration of brusatol. To further explore this effect, this effect of brusatol was compared with that of anticancer drugs such as cis-diamminedichloro-platinum (CDDP), mitomycin C (MMC), and sorafenib. In order to adjust the effects on cell toxicity, they were administered at a concentration corresponding to GI50 (determined in Fig. 6a to d): 80 nM, 4.3 μg/ml, 2.0 μg/ml and 8.0 μM, for brusatol, CDDP, MMC and sorafenib, respectively. The extent of HCV RNA reduction by brusatol was comparable to that by sorafenib whereas CDDP and MMC did not induce a reduction in HCV RNA (Fig. 2b). These results indicated that the potency of brusatol for suppression of the persistence of HCV infection at the RNA level was similar to that of sorafenib. Brusatol reduced the level of the Nrf2 protein and the HCV proteins in the HPI cells To investigate the inhibitory effect of brusatol on HCV infection and Nrf2 at the protein level, the Nrf2 protein and the HCV proteins in the HPI cells were analyzed after the administration of brusatol using immunoblot analysis (Fig. 3a and Additional file 1: Table S1). In the absence of brusatol, the level of the Nrf2 protein increased gradually over the first 24 h, possibly reflecting robust cell proliferation early after cell seeding prior to contact inhibition. However, the increase in the Nrf2 protein during this period was suppressed by brusatol. As to the HCV proteins, the core and NS5A proteins were also suppressed by brusatol in a dose-dependent manner, especially from 24 h to 72 h after its administration, whereas in the absence of brusatol, their levels increased markedly for up to 72 h after the administration of DMSO (control). Next, to explore the subcellular expression status of p-Nrf2 and the HCV proteins in the HPI cells after the administration of brusatol, immunofluorescent staining of these proteins was performed at 6 and 48 h after its Murakami et al. BMC Cancer (2018) 18:680 siNrf2 C-HCC #1 - + .5 Hu h6 He pG 2 c h7 HE Hu p-Nrf2 HP I a Page 5 of 14 - + - + - + Nrf2 -Actin C-HCC #2 Non-HCC b p-Nrf2 Core DAPI Merged HPI Huh7.5 Huh6 HepG2 Fig. 1 Expression of p-Nrf2 in C-HCC samples and in cultured hepatoma cell lines. a Immunohistochemical analysis of the expression of p-Nrf2, and hematoxylin-eosin (HE) staining in C-HCC specimens (#1 and #2) and a non-HCC specimen without either HCV or HBV infection. Bars, 50 μm. b Immunofluorescent analysis of the p-Nrf2 and the HCV core protein with nuclear staining (DAPI), and their merged images in the cell lines. c Immunoblot analysis of the Nrf2 protein in the cultured hepatoma cell lines after knockdown with siRNA against Nrf2 or control RNA. Beta-actin was used for validation of sample loading administration (Fig. 3b and c, respectively). In accordance with the immunoblotting analysis, the cytosolic expression of the HCV core protein was suppressed at 48 h after brusatol administration albeit with a lower level of suppression at 6 h. However, the nuclear expression of p-Nrf2 with brusatol administration did not differ much from that of control at either time point. In contrast, pNrf2 was markedly reduced on immunofluorescence in OR6 cells after the administration of brusatol (Fig. 4c). This difference could be attributed to the characteristics of the both cells; while they were originated from Huh7.5 cells, OR6 cells and HPI cells were established after a few months and around 2 years, respectively. We speculated that the total amount of the Nrf2, as shown in Fig. 3a, is more crucial than the nuclear expression of p-Nrf2 in the HPI cells, and further study will be needed to explain this phenomenon. These combined experiments, we verified that brusatol suppressed the persistence of HCV infection at the protein level, as well as at the RNA level, in association with reducing the Nrf2 protein level. Murakami et al. BMC Cancer (2018) 18:680 Page 6 of 14 a b Fig. 2 Effect of brusatol and anticancer drugs on the HCV RNA level. a-b qRT-PCRs for HCV RNA in the HPI cells. The value for HCV RNA was normalized by the value for GAPDH RNA and is presented as fold change to that of control. Statistical significance *: p < 0.01, **: p < 0.001, ***: p < 0.0001 versus 0 nM or control. a qRT-PCRs after the administration of brusatol. b qRT-PCRs after the administration of agents at a concentration for the GI50 (80 nM, 4.3 μg/ml, 2.0 μg/ml and 8.0 μM for brusatol, CDDP, MMC and sorafenib, respectively) Brusatol inhibited replication of HCV replicon The infection cycle of HCV consists of multi-steps, such as viral entry, uncoating, translation, and replication and production of virus particles. Of these steps, we focused on the replication step as a candidate of a target of brusatol to suppress persistent infection of HCV, since the replication step is the most crucial step for persistence of HCV infection. To evaluate the effect of brusatol on HCV replication, luciferase activity of the OR6 cells was measured after the administration of brusatol. Brusatol dramatically reduced luciferase activity in a dose-dependent manner from 48 h to 72 h after its administration (Fig. 4a). However, early after brusatol administration (at 43 h), suppression of HCV replication in OR6 cells was not as great as suppression of HCV RNA levels in the HPI cells (Fig. 2a). It is likely that this difference is related to the delay in brusatol-induced change in luciferase protein compare to brusatol-induced primary change in HCV RNA. To explore the effect of brusatol on HCV replication at the HCV protein level in the OR6 cells, the expressions of the HCV proteins and the Nrf2 protein were analyzed by immunoblot analysis after the administration of brusatol using immunoblot analysis (Fig. 4b and Additional file 3: Table S2). While the Nrf2 protein level increased gradually over 24 h in the absence of brusatol, the Nrf2 protein level was suppressed by brusatol, although the suppression level was not as intense as was observed in the HPI cells. As to the HCV proteins, the core and NS5A proteins were markedly suppressed by the administration of brusatol in a dose-dependent manner from 24 h to 72 h, whereas the core and NS5A proteins increased in the absence of brusatol. Next, to explore the subcellular expression status of p-Nrf2 and the HCV proteins in the OR6 cells after the administration of brusatol, immunofluorescent staining of these proteins was performed at 6 h and 48 h after its Murakami et al. BMC Cancer (2018) 18:680 a Time Brusatol (nM) 0h Page 7 of 14 2h 4h 0 40 80 160 0 40 80 160 0 40 80 160 6h 24h 0 40 80 160 0 40 80 160 48h 72h 0 40 80 160 0 40 80 160 Nrf2 Core NS5A -Actin b p-Nrf2 Core DAPI Merged p-Nrf2 Core DAPI Merged Control Brusatol (80 nM) c Control Brusatol (80 nM) Fig. 3 Effect of brusatol on expression and subcellular distribution of Nrf2 and HCV proteins. a Immunoblot analysis of Nrf2 and HCV proteins in HPI cells after administration of brusatol. Beta-actin was used for validation of sample loading. b-c Immunofluorescent staining for p-Nrf2 and the HCV core protein in the HPI cells with nuclear staining (DAPI) at 6 (b) and 48 (c) h after the administration of brusatol administration (Fig. 4c and d). Nuclear expression of p-Nrf2 was remarkably suppressed at 6 h after brusatol administration, but it had almost recovered by 48 h. On the other hand, cytosolic expression of the core protein was suppressed at 48 h, in accordance with the result of the immunoblot analysis. These results suggest that suppression of persistent HCV infection by brusatol was due to its inhibition of HCV replication, although there remains a possibility that other steps of the infection cycle might also be involved. Comparison of the transcriptome of the HPI cells treated with brusatol and that of the cells treated with siRNA against Nrf2 We predicted that brusatol could affect expression of a wider range of genes than siRNA against Nrf2, which also suppresses persistent HCV infection in the HPI cells [32], because siRNA more specifically targets gene expression in general. To clarify this difference, the transcriptomes of the HPI cells treated with brusatol and that of the cells treated with siRNA against Nrf2 were compared. This analysis showed that 97 genes were commonly down-regulated by the two agents. The total number of genes down-regulated (less than 0.5-fold vs. control) by brusatol was greater than that of genes down-regulated by the siRNA against Nrf2 (820 vs. 458) (Fig. 5a). On the other hand, 169 genes were commonly up-regulated (more than 2-fold vs. control) by the two reagents. The total number of genes up-regulated by brusatol was greater than that of genes down-regulated by the siRNA against Nrf2 (822 vs. 502) (Fig. 5b). The categories of gene function of the commonly affected genes are shown in Table 1. Notably, 33 of the 97 commonly down-regulated genes belonged to categories Murakami et al. BMC Cancer (2018) 18:680 Page 8 of 14 a b c d Fig. 4 Effect of brusatol on replication of the HCV replicon. a Luciferase activity of OR6 cells after administration of brusatol. Statistical significance *: p < 0.01, **: p < 0.001, ***: p < 0.0001 versus 0 nM. b Immunoblot analysis of Nrf2 and HCV proteins in OR6 cells after administration of brusatol. Beta-actin was used for validation of sample loading. c-d Immunofluorescent staining of p-Nrf2 and the HCV core protein in OR6 cells with nuclear staining (DAPI) at 6 (c) and 48 (d) h after the administration of brusatol related to metabolisms including lipid metabolism (10 genes), cholesterol metabolism (6 genes), glutamine/glutamate metabolism (5 genes) and other types of metabolism (12 genes), while 54 of the 163 commonly up-regulated genes belonged to categories including transcription (30 genes), signal transduction (10 genes) and cell proliferation/growth (14 genes). These transcriptome analyses showed that brusatol affected a wider range of gene expression than siRNA against Nrf2, and that a considerable number of genes were commonly affected by the two agents especially in categories related to metabolisms, of which cholesterol metabolism is known to be of great importance for the infection cycle of HCV. Murakami et al. BMC Cancer (2018) 18:680 a siRNA against Nrf2 Page 9 of 14 Brusatol 820 458 361 97 723 b siRNA Brusatol against Nrf2 822 502 339 169 659 Fig. 5 Venn-diagram of genes down-regulated and up-regulated by brusatol or by the siRNA against Nrf2. a-b Venn-diagrams of affected genes based on the transcriptome of the HPI cells treated with brusatol or with siRNA against Nrf2. The microarray data were deposited in Gene Expression Omnibus (accession numbers: GSE52321 and GSE98920). a The numbers of genes down-regulated (< 0.5-fold vs. control) by the siRNA or by brusatol are shown in the circles. The number of genes commonly down-regulated is shown in the overlapped region of the circles. The number of genes downregulated exclusively by each agent is shown in the non-overlapped region; b The numbers of genes up-regulated (> 0.5-fold vs. control) by the siRNA or by brusatol are shown in the circles. The number of genes commonly up-regulated is shown in the overlapped region of the circles. The number of genes up-regulated exclusively by each reagent is shown in the non-overlapped region Inhibition of the proliferation of the HPI cells by brusatol and anticancer drugs To confirm the inhibitory effect of brusatol on the proliferation of the HPI cells and to determine the concentration of brutasol required for 50% growth inhibition (GI50), the viability of the HPI cells after administration of brusatol (Fig. 6a) and, for comparison, after administration of anticancer drugs such as CDDP, MMC and sorafenib (Fig. 6b-d, respectively) was measured. Brusatol time-dependently and dose-dependently reduced cell viability, and the concentration for GI50 was calculated as 80 nM, 4.3 μg/ml, 2.0 μg/ml, and 8.0 μM for brusatol, CDDP, MMC and sorafenib, respectively. With trypan blue staining as well, brusatol time-dependently and dose-dependently reduced cell viability (Additional file 2: Figure S1), and the concentration for GI50 at 48 h was calculated as 91 nM, which almost corresponded to the value with the MTS assay (80 nM). However, the inhibition of cell proliferation by brusatol was not as potent as that of anticancer drugs even with a higher brusatol concentration (320 nM, data not shown), possibly due to the difference in the mechanism of inhibition of proliferation between brusatol and the anticancer drugs. The inhibition of cell proliferation of the other cell lines including Huh7.5, Huh6 and HepG2 cells by brusatol was confirmed (data not shown). These results showed that brusatol has anticancer effect against hepatoma cell lines, although the effect was not as potent as the other anticancer drugs. Combination of brusatol and sorafenib simultaneously enhanced anticancer and anti-HCV effects It is of clinical use to combine anticancer drugs with different mechanisms of action in order to enhance the total anticancer effect and to reduce the dosage of individual drugs to decrease adverse effects. Therefore, the effects of a combination of brusatol with an anticancer drug on both cell proliferation and HCV infection were investigated. Proliferation of the HPI cells was inhibited by the combination of an anticancer drug with brusatol more effectively than by a single administration of the anticancer drug (Fig. 7a). Moreover, the combination of brusatol with an anticancer drug reduced the HCV RNA level in the HPI cells to the same extent as that of a single administration of brusatol at 24 h after their administration (Fig. 7b). However, at later time points, from 48 h and 72 h after the drug administration, only the combination of brusatol and sorafenib dramatically reduced the HCV RNA level, whereas the combination of brusatol with the anticancer drugs did not further reduce the HCV RNA level. These data showed that the combination of brusatol with an anticancer drug enhanced the anticancer effect of the anticancer drugs. Most importantly, the combination of brusatol and sorafenib dramatically suppressed HCV infection in addition to enhancing the anticancer effect and, at least based on the value at 72 h (lanes 4, 5 and 8 in Fig. 7b), this effect of the combination could be synergistic on HCV suppression. Murakami et al. BMC Cancer (2018) 18:680 Page 10 of 14 Table 1 Categoly of genes down-regulated and up-regulated in the HPI cell commonly by the treatment with brusatol and by the treatment with siRNA for Nrf2 Category of gene function Corresponding GO numbera Number of genes commonly Number of genes commonly down-regulated (less than 0.5 fold) up-regulated (more than 2 fold) Lipid metabolism GO:0006629, GO:0016042, GO:0030497 10 2 Cholesterol metabolism GO:0006695, GO:0008203, GO:0016125 6 1 Glutamine/glutamate metabolism GO:0006536, GO:0006542, GO:0006749 5 0 Other metabolisms GO:0008152, GO:0005975 12 4 Oxidation reduction GO:0055114, GO:0045454, GO:0006979 11 6 Inflammatory/immune response GO:0006954, GO:0006955 3 4 Transcription GO:0006810, GO:0015031 5 30 Signal transduction GO:0007165, 6 10 Translation GO:0006412 4 2 Protein/amino acids modification GO:0006468, GO:0006470, GO:0006486, GO:0006493, GO:0006464 6 11 Transport GO:0006810, GO:0015031 7 4 Biologiacal process GO:0008150 2 5 Cell proliferation/ growth GO:0008285, GO:0008283, O:0007049, GO:0001558 5 14 Apoptosis GO:0006917, GO:0042981, GO:0006917, GO:0043065 3 7 Cell adhesion GO:0007155 3 6 Multicellular organismal GO:0007275 development 3 9 Other functions 12 25 Unknouwn functions 21 54 Totalb 97 a 163 b gene ontology (GO) number based on Gene Ontology Consortium (http://www.geneontology.org/) some genes were overlapped as to category Discussion The present study showed that 35% (7/20) of C-HCC samples were positive for p-Nrf2. Although this percentage was less than the 55% (11/20) in HCC with HBV infection (data not shown), activation of Nrf2 is attributed to the pathogenesis of C-HCC. For clinical application of brusatol, however, the relationship between Nrf2 or p-Nrf2 expression status and clinicopathological features of HCC such as stage, histology, susceptibility and prognosis must be clarified. Since the results in the present study were obtained using only tissue array analysis, we are planning to conduct a cohort study of Nrf2 or p-Nrf2 expression in C-HCC. We hypothesized that inhibition of Nrf2 could inhibit both HCV infection and proliferation of hepatoma cells based on our previous study and on previous reports that are described in the introduction. To date, a small number of Nrf2 inhibitors has been described including brusatol [31, 32], retinoic acid receptor α agonists [36], leutolin [37], and trigonelline [38]. Of them, we preliminary explored the anti-HCV effect via Nrf2 inhibition by using brusatol and all-trans retinoic acid (ATRA), which is known to have an anti-HCC effect [39]. We chose brusatol for the present study because only brusatol showed an anti-HCV effect but ATRA did not, although reason for this difference was not unclear. Brusatol has been shown to have an anti-proliferation effect on cancer cells including chemoresistant cells. Although the precise mechanism by which brusatol inhibits Nrf2 is not fully understood, it was shown that brusatol and related compounds inhibits protein synthesis [40]. Furthermore, brusatol selectively inhibits the Nrf2 pathway, and the reduction of Nrf2 is through enhancement of ubiquitination and degradation of Nrf2 [31]. Therefore, the alteration of mRNA expression observed in the present study could be a secondary phenomenon after reduction of Nrf2 protein caused by brusatol. A recent study demonstrated that brusatol reduced the Nrf2 protein level in a post-translational manner, since this reduction appeared very early (from 30 min to 12 h) after its administration, with maximal inhibition at around 2 h [32]. The present study using the HPI cells similarly