Acyclic retinoid and angiotensin-II receptor blocker exert a combined protective effect against diethylnitrosamine-induced hepatocarcinogenesis in diabetic OLETF rats
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Insulin resistance (IR) is closely associated with the progression of hepatocellular carcinoma (HCC). Acyclic retinoid (ACR) targets retinoid X receptor α and reportedly prevents HCC recurrence in clinical practice. Angiotensin-II receptor blocker (ARB) can also inhibit experimental hepatocarcinogenesis and HCC development. These are reported to suppress IR-based hepatocarcinogenesis; however, limited data are available regarding the combined effects of both these agents. This study aimed to investigate the combined chemopreventive effect of ACR and ARB on liver tumorigenesis on rats with congenital diabetes.
Male diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) and non-diabetic Long-Evans Tokushima Otsuka (LETO) rats underwent 70% partial hepatectomy following a single intraperitoneal injection of diethylnitrosamine to induce hepatocarcinogenesis and the administration of ACR (peretinoin, 40 mg/kg/day), ARB (losartan, 30 mg/kg/day), and a combination of ACR and ARB. Six weeks thereafter, we assessed the size and number of the pre-neoplastic lesions (PNL) as well as the altered angiogenesis, oxidative stress, and chronic inflammation in the liver. Moreover, we assessed the effects exerted by ACR and ARB on in vitro cell growth in human HCC cell lines and human umbilical vascular endothelial cells (HUVECs).
OLETF rats showed increase in the size and number of PNLs compared to LETO rats. ACR suppressed the augmentation in size and number of PNLs in the OLETF rats with suppression of cell growth, intrahepatic angiogenesis, lipid peroxidation, oxidative DNA damage, and proinflammatory cytokine production. Combining ACR with ARB enhanced the tumor-suppressive effect and ameliorated intrahepatic angiogenesis, lipid peroxidation, and proinflammatory status; however, cell growth and oxidative DNA damage remained unchanged. IR-mimetic condition accelerated in vitro proliferative activity in human HCC cells, while ACR inhibited this proliferation with G0/G1 arrest and apoptosis. Furthermore, ACR and ARB significantly attenuated the HUVECs proliferation and tubular formation under the IR-mimetic condition, and a combination of both agents demonstrated greater inhibitory effects on HUVEC growth than each single treatment.
ACR and ARB exert a combined inhibitory effect against IR-based hepatocarcinogenesis by the inhibition of cell growth, intrahepatic angiogenesis, and oxidative stress. Thus, this combination therapy appears to hold potential as a chemopreventive treatment therapy against HCC.
KeywordsAcyclic retinoid ARB Hepatocarcinogenesis Chemoprevention Insulin resistance
Angiotensin-converting enzyme inhibitor
Angiotensin-II type1 receptor blocker
Branched-chain amino acids
Extracellular signal-regulated kinase
Placental glutathione S-transferase
- GST-P+ PNL
GST-P positive pre-neoplastic lesions
Homeostasis model assessment-insulin resistance
Human umbilical vascular endothelial cell
Long-Evans Tokushima Otsuka
Mitogen-activated protein kinase
Nonalcoholic fatty liver disease
Otsuka Long-Evans Tokushima Fatty
Quantitative insulin sensitivity check index
Retinoic acid receptor
Recombinant human insulin
Retinoid X receptor
Signal transducers and activators of transcription
Type2 diabetes mellitus
Tumor necrosis factor
Vascular endothelial growth factor
Hepatocellular carcinoma (HCC) is the fifth most common cancer and the third leading cause of cancer-related deaths worldwide . HCC prognosis is generally poor owing to the high recurrence rate; 50% of HCC patients experience recurrence following curative treatment, including surgical resection and ablation [2, 3]. Therefore, chemoprevention for either primary or secondary HCC development can be beneficial for improving prognosis.
Insulin resistance (IR) commonly develops in chronic liver diseases, including liver cirrhosis. Further, recent studies have demonstrated that Type 2 diabetes mellitus (T2DM) with IR is one of the most powerful risk factors for HCC progression [3, 4, 5, 6]. T2DM is associated with a two- to three-fold increased risk of HCC, irrespective of the etiology [7, 8]. In fact, basic experiments that have used congenitally diabetic rats revealed that the IR status, defined by the coexistence of high blood glucose and high insulin levels, directly accelerated diethylnitrosamine (DEN)-induced hepatocarcinogenesis . Moreover, recent epidemiological studies have shown an increased proportion of non-B/non-C HCC in keeping with the rising prevalence of non-alcoholic fatty liver diseases (NAFLD) during the previous decade [10, 11]. NAFLD is generally associated with IR and includes the spectrum of simple steatosis and non-alcoholic steatohepatitis (NASH), recognized as a potentially progressive disease that may lead to HCC. These basic and clinical evidences point to the strong need for new chemopreventive strategies against IR-based hepatocarcinogenesis.
Acyclic retinoid (ACR, NIK-333) was developed in Japan as an oral synthetic retinoid that targets retinoid nuclear receptors, including retinoid X receptor (RXR) and retinoic acid receptor (RAR) . Several clinical trials have demonstrated significant reduction in the post-therapeutic recurrence of HCC and improved survival rate in patients who were administered ACR [13, 14]. In addition, ACR reportedly exerts chemopreventive effects on hepatocarcinogenesis in some rodent models [15, 16, 17]. ACR leads to growth suppression in human HCC cells by inducing cell cycle arrest at G0/G1 phase and apoptosis. It is noteworthy that as per recent basic research, ACR treatment can prevent obesity-related liver tumorigenesis and alleviate IR, liver steatosis, and inflammation . Thus, ACR is expected to be a novel agent for reducing the HCC incidence in patients with liver cirrhosis. In fact, larger-scale clinical trials are currently ongoing to validate ACR efficacy in preventing HCC development; however, no satisfactory outcomes have been reported. This indicates that ACR monotherapy may not exert sufficiently strong inhibitory effects to enable HCC chemoprevention. Therefore, we postulated that the combination therapy of ACR and another agent with more potent anticancer effects, especially on IR-based hepatocarcinogenesis, would be more effective.
Angiotensin-converting enzyme inhibitor (ACE-I) and angiotensin-II type1 receptor blocker (ARB), key drugs for renin-angiotensin-aldosterone system (RAAS) blockade, are widely used in clinical practice for managing arterial hypertension, heart failure, myocardial infarction, and chronic kidney disease without any serious adverse effects. It is interesting to note that as per several researches, ACE-I and ARB possess strong antiangiogenic activity, and these agents could inhibit tumor growth in several types of cancers, including HCC using clinically comparable doses [19, 20]. ACE-I and ARB have also shown to subside IR in clinical practice . We previously reported that in addition to inhibiting HCC growth, ACE-I/ARB significantly suppressed hepatocarcinogenesis even in the presence of IR along with the inhibition of vascular endothelial growth factor (VEGF) in the liver .
Here, we examined whether the administration of a combined therapy of ACR and ARB significantly inhibited the occurrence and development of IR-based hepatocarcinogenesis in rats with congenital diabetes. Furthermore, we analyzed the underlying mechanisms of the therapeutic effects of both agents in relation to cancer cell survival, angiogenesis, and oxidative stress.
Animals and regents
Eight-week-old male diabetic Otsuka Long-Evans Tokushima Fatty (OLETF) rats and littermate Long-Evans Tokushima Otsuka (LETO) rats were procured from the Otsuka Pharmaceutical Co. (Tokushima, Japan). The rats were housed in stainless steel mesh cages under controlled conditions (temperature: 23 °C ± 3 °C, relative humidity: 50% ± 20%, 10–15 air changes/h, illumination: 12 h/d). The rats were permitted ad libitum access to tap water throughout the study period. Peretinoin (NIK-333), as an ACR, was provided by the Kowa Company Ltd. (Nagoya, Japan), and losartan potassium, as an ARB, was purchased from Merck Ltd. (Tokyo, Japan).
Intrahepatic triglyceride, 4-HNE, and 8-OHdG measurement
In order to determine the intrahepatic triglyceride content, the liver tissue homogenates were extracted using 2:1 (vol/vol) chloroform/methanol. Chloroform/methanol was added to the homogenate, and the mixture was then shaken for 15 min. Following centrifugation at 14,000 rpm for 10 min, the organic layer was collected. This extraction was repeated thrice. The collected sample was dried and resuspended in 1% Triton X-100/ethanol. The measurement was conducted using Triglyceride E-test Wako (Wako Pure Chemical Industries, Ltd., Osaka, Japan). The hepatic 4-Hydroxynonenal (4-HNE) content was measured using the 4 Hydroxynonenal ELISA Kit (MyBioSource, San Diego, CA, USA) as per the manufacturer’s protocol.
For determining the liver 8-hydroxy-2′-deoxyguanosine (8-OHdG) levels, DNA was extracted from the frozen liver tissue using a DNeasy mini kit (Qiagen, Tokyo, Japan) and purified as described previously . The 8-OHdG level in the extracted DNA solution was determined using the highly sensitive 8-OHdG check ELISA kit (Nikken Seil Co., Ltd.). The 4-HNE and 8-OHdG levels were indicated as a ratio to those of the negative control group.
Histological and immunohistochemical analyses
The liver sections were fixed with 10% formalin and embedded in paraffin. Then, 5-μm paraffin sections were stained with hematoxylin and eosin. For detecting the pre-neoplastic lesions, immunohistostaining was performed using anti-placental glutathione S-transferase (GST-P) polyclonal antibody (Medical & Biological Laboratories Co., Nagoya, Japan). Semi-quantitative analyses of the size of the GST-P positive pre-neoplastic lesions were conducted using the NIH ImageJ software (http://imagej.nih.gov/ij/).
Cell culture and proliferation assay
Two human liver cancer cell lines Huh7 (JCRB0403) and HLE (JCRB0404) and human umbilical vascular endothelial cells (HUVECs) (IFO50271) were obtained from the Japanese Collection of Research Bioresources Cell Bank (Osaka, Japan). Cells were cultured in Dulbecco’s modified Eagle’s medium (Thermo Fisher Scientific K.K., Kanagawa, Japan) supplemented with 10% fetal bovine serum and 1% ampicillin/streptomycin.
Cell proliferation was assessed using water-soluble tetrazolium salt − 1 assay as per the manufacturer’s protocol. Initially, for the validation of the inducible effects of insulin on cell proliferation, the cells were treated with different dilutions of recombinant human insulin (rh-insulin) (0, 5, 10, 20, 30, and 40 μU/mL) (Gibco, Tokyo, Japan). Thereafter, we compared the effects of ACR (peretinoin, 10 μM), ARB (losartan, 10 μM), and the combined treatment (each 10 μM) on cell proliferation of Huh7, HLE, and HUVECs that were cultured under high concentrations of D-(+)-glucose (Nacalai Tesque, Kyoto, Japan) and rh-insulin. The cells were seeded on 96-well uncoated plastic dishes at a density of 5 × 104 cells/mL, and each treatment was started 12 h after seeding and incubated for another 24 h. Three independent experiments were performed; the average values were calculated from five replicates of each experiment.
RNA extraction and quantitative real-time RT-PCR
Total RNA was extracted from the cultured human liver cancer cells, HUVECs, or frozen liver tissues using the RNeasy mini kit (QIAGEN, Tokyo, Japan) as per the manufacturer’s instructions. Total RNA from each sample was reverse transcribed into cDNA using the high-capacity RNA-to-cDNA kit (Applied Biosystems Inc., Foster City, Calif., USA) as per the manufacturer’s instructions. The mRNA expression was assessed with quantitative real-time PCR using the StepOnePlus real-time PCR system (Applied Biosystems, Foster City, USA) using Fast SYBR Green master mix (Applied Biosystems). Relative gene expression was measured with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as an internal control. The relative amount of target mRNA in each cycle was evaluated by applying a threshold cycle to the standard curve. The mRNA levels were indicated as a ratio to the negative control. All primers were purchased from Sigma Aldorich (Additional file 1: Table S1).
Protein extraction and western blotting
Whole cell lysates were prepared from 106 cultured human liver cancer cells using T-PER Tissue Protein Extraction Reagent supplemented with proteinase and phosphatase inhibitors (all Thermo Scientific, Rockford, IL, USA). Fifty micrograms of whole cell lysates were separated by SDS-PAGE; thereafter, they were transferred to a PVDF membrane that was subsequently blocked with 5% bovine serum albumin in Tris-buffered saline + Tween–20 for 1 h. Thereafter, each membrane was incubated overnight with an antibody against p44/42 mitogen-activated protein kinase (MAPK) [extracellular signal-regulated kinase (ERK) 1/2], Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204), Caspase-3, Cleaved caspase-3, and β-Actin (Cell Signaling Technology); washed; and incubated with Amersham ECL IgG and HRP-linked F(ab)2 fragment (GE Healthcare Life Sciences, Piscataway, NJ, USA; 1:5000 dilution). Finally, each membrane was developed using Clarity Western ECL Substrate (BIORAD, Hercules, CA, USA).
In vitro endothelial tubular formation
In vitro angiogenesis was defined as the formation of capillary-like structures in HUVECs co-cultures with human diploid fibroblasts, as previously described . In brief, 24-well tissue culture plates were coated with Matrigel (Collaborative Biochemical Products, Bedford, MA, USA; 150 mL/well) and allowed to set at 37 °C for 30 min. Thereafter, 2.5 × 104 HUVECs were added to each well and incubated at 37 °C for 20 h under 5% CO2 atmosphere and different conditions. Semi-quantitative analysis of tubule formation was performed using NIH ImageJ software (http://imagej.nih.gov/ij/).
The data were subjected to Student’s t-test or one-way analysis of variance followed by Bonferroni’s multiple-comparison test, as appropriate. Bartlett’s test was used for determining the homology of variance. Statistical analyses were performed using Prism, version 6.04 (GraphPad Software, La Jolla, CA, USA). All tests were two-tailed, and P-values < 0.05 were considered statistically significant.
Physical and serological findings in OLETF and LETO rats
Characteristic features of the experimental rats
ACR + ARB
Body weight (g)
410.0 ± 21.6
498.0 ± 27.3a
491.7 ± 33.4a
493.8 ± 32.9a
480.0 ± 25.0a
18.0 ± 4.0
83.8 ± 16.0a
74.0 ± 10.8ab
60.3 ± 2.0ab
59.0 ± 11.1ab
174.3 ± 17.1
199.6 ± 26.6a
189.8 ± 13.9a
184.2 ± 12.6a
184.3 ± 19.2a
8.5 ± 2.8
33.2 ± 13.1a
29.9 ± 22.3a
35.4 ± 24.3a
33.6 ± 15.0a
216.7 ± 10.6
239.6 ± 41.4a
232.9 ± 32.0a
237.4 ± 50.9a
242.8 ± 44.2a
51.5 ± 2.0
73.9 ± 14.4a
66.4 ± 8.4a
67.1 ± 11.1a
74.3 ± 6.9a
3.85 ± 0.15
4.11 ± 0.09
3.93 ± 0.11
3.87 ± 0.13
4.02 ± 0.1
Total bilirubin (mg/dL)
0.100 ± 0.02
0.103 ± 0.02
0.093 ± 0.017
0.095 ± 0.012
0.079 ± 0.017
According to the underlying characteristics, OLETF rats exhibited obesity, hypertriglyceridemia, hyperglycemia, and hyperinsulinemia along with mild elevation of aspartate and alanine aminotransferase (AST and ALT) as compared to the LETO rats. In the OLETF rats, HOMA-IR was notably higher. Correspondingly, QUICKI, a surrogate marker of insulin sensitivity, was lower than that in the LETO rats (Fig. 1b). Meanwhile, there was no significant difference between the two groups in terms of the serum albumin and total bilirubin levels. Among the OLETF groups, treatment of ACR and/or ARB reduced hypertriglyceridemia; however, the body weight, liver function, and glycemic status remained unchanged (Table 1 and Fig. 1b).
ACR and ARB ameliorate IR-enhanced growth of GST-P positive pre-neoplastic lesions in diabetic OLETF rats
Initially, in order to determine whether IR stimulates the augmentation of hepatocarcinogenesis, we conducted a histological comparison of the number and size of the DEN-induced GST-P positive pre-neoplastic lesions (GST-P+ PNL) between the LETO and OLETF rats (Fig. 1c). Semi-quantitative analyses revealed that both the number and size of hepatic GST-P+ PNL in the OLETF rats were higher than those in the LETO rats, indicating that IR promotes hepatocarcinogenesis (Fig. 1d). Then, we evaluated the effects of ACR and/or ARB on the IR-induced exacerbation of hepatocarcinogenesis. In non-diabetic LETO rats, either ACR or ARB significantly decreased the number and size of hepatic GST-P+ PNL in accordance with the previous reports (Additional file 2: Figure S1a, b). Interestingly, these suppressive effects were observed in diabetic OLETF rats with greater magnitude than those in LETO rats (Fig. 1c, d). Moreover, the individual administration of ACR or ARB demonstrated weaker effects than the combined administration of ACR and ARB (Fig. 1c, d).
Effects of ACR and ARB on proliferation, cell cycle, and apoptosis of the DEN-treated liver of OLETF rats and human liver cancer cells
Effects of ACR and ARB on intrahepatic angiogenesis in DEN-treated liver of OLETF rats and vascular endothelial in vitro growth
Effects of ACR and ARB on oxidative DNA damage and lipid peroxidation in the liver of OLETF rats
Currently, the increasing prevalence of obesity is recognized as one of the most serious global public health issues. Among all obesity-related medical abnormalities, IR is particularly closely associated with the progression of various types of malignancies, including breast, colorectal, and pancreatic cancers as well as HCC [4, 5, 6, 7, 8, 25, 26, 27]. Numerous evidences show that IR causatively plays a key role in HCC development. Although the insulin signaling pathway is known to be responsible for tumor initiation, it insufficiently contributes to hepatocarcinogenesis by itself. Actually, hepatocytes may acquire the capacity to adapt insulin-dependent mechanisms for their proliferation and survival during chronic liver injury, and sequentially may promote premalignant transformation and tumor growth . Moreover, the IR status fosters a hepatic microenvironment that favors the propagation of premalignant and malignant cells, such as angiogenesis, oxidative stress, and chronic inflammation [29, 30, 31, 32]. Our studies on mice models show that the IR status may facilitate hepatocarcinogenesis by stimulating hepatic neovascularization and VEGF expression; both high glucose and insulin could prime in vitro endothelial tubular formation via ERK1/2 phosphorylation . IR also plays a crucial role in the production of oxidative stress in the liver, thus upregulating the proinflammatory cytokines [31, 32, 33, 34]. These cytokines stimulate chronic liver inflammation with hepatic steatosis, and consequently lead to liver tumorigenesis. IR-stimulated oxidative stress also induces DNA adduct formation to initiate tumor formation. These mechanistic evidences suggest that IR and its related metabolic alterations could be crucial chemopreventive targets for obesity-related hepatocarcinogenesis.
The present study distinctly demonstrated that clinically equivalent doses of ACR or ARB successfully ameliorated DEN-induced hepatocarcinogenesis in diabetic OLETF rats. Recent researches have progressively demonstrated the mechanistic insights in the regulatory effects of ACR on RXRα. Therefore, ACR could activate RXRα not only directly by acting as its ligand, but also indirectly by inhibiting the Ras-ERK pathway that devitalizes RXRα by phosphorylating it . Thus, current in vitro results also revealed that ACR treatment inhibited human HCC cells growth with ERK1/2 dephosphorylation. In contrast, losartan, used as ARB, did not affect HCC cell growth in this study. It is noteworthy that telmisartan, another kind of ARB, reportedly exerts antiproliferative effect on human HCC cell lines by inducing cell cycle arrest . A major underlying reason for this discrepancy could be the difference in the pharmacological activity of losartan and telmisartan. For example, telmisartan is known to possess peroxisome-proliferator-activated-receptor (PPAR) γ-activating action; however, losartan does not possess it . PPARγ activation contributes, at least partially, to HCC cell growth inhibition; therefore, this additive action of telmisartan may be involved in HCC growth suppression.
It is noteworthy that the despite ineffectiveness of ARB on HCC cells, combined ACR and ARB treatment showed a marked synergistic inhibitory effect on the development of pre-neoplastic lesions in OLETF livers. Thus, to elucidate the underlying mechanism of this synergistic effect, we focused on the antiangiogenic properties of ACR and ARB. Different angiostatic agents, including ARB, are reported to frequently exert additive or synergistic antitumor effects in combination with each other . Therapies that target tumor vessels are proven beneficial for cancer treatment in experimental models . However, some studies suggest that treatment with a single antiangiogenic agent may be insufficient for complete suppression of tumor angiogenesis because the compensatory activation of proangiogenic factors was mostly found following treatment with a single angiostatic agent [38, 40]. Actually, our previous studies has demonstrated that monotherapy with an ACE-I or vitamin K2 could exert anticancer effect in rat hepatocarcinogenesis models, although either treatment alone did not prevent HCC recurrence in clinical practice. Remarkably, the combination treatment of both the agents exclusively achieved efficient prevention of cumulative HCC recurrence after curative therapy, along with VEGF suppression . In the current study, ARB treatment expectedly exerted antiangiogenic activities in the liver of OLETF rats, as in our previous reports. However, it was surprising to observe suppressed intrahepatic angiogenesis in ACR-treated rats. Our in vitro study also confirmed that ACR and ARB attenuated IR-induced vascular endothelial cell proliferation and tubular formation. A recent report demonstrated that bexarotene, a ligand of RXRα, significantly inhibited HUVEC morphogenesis, proliferation, and migration . Moreover, LGD1069 (Targretin®), a selective RXR ligand, also exerted antiangiogenic effects by suppressing the expression of Runx2, indicating that ACR attenuates vascular endothelial growth mainly by acting as an RXRα ligand in our model .
Intriguingly, the results from the present study show that ACR and ARB were likely to improve in vivo hepatocarcinogenesis more potently than in vitro cancer cell and HUVEC proliferation. Following such discrepant findings, we assessed the effects on hepatic lipid metabolism and oxidative stress to identify additional effects of both agents. ACR is reported to efficiently protect from the acceleration of lipogenesis independently of glucose metabolism in DEN-treated mice liver . In addition, several basic studies have demonstrated that ARB reduced hepatic steatosis [23, 45, 46]. According to these evidences, our data showed that ACR and ARB reduced hepatic triglyceride accumulation with reduced serum hypertriglyceridemia; however, it did not affect the glycemic status of OLETF rats. ACR and ARB also suppressed hepatic lipid peroxidation coincidently while inhibiting lipogenesis; however, only ACR reduced the oxidative DNA damage in the liver of OLETF rats. Further investigation is warranted for a deeper understanding of the functional mechanism underlying the differential antioxidant effects of ACR and ARB. IR and hepatic lipid accumulation also stimulate inflammatory changes in the liver. ACR and ARB reduced the hepatic expression levels of Tnfa, Il6, and Il1b mRNA in OLETF rats with improved hepatic steatosis. Tumor necrosis factor (TNF)-α is a key mediator of IR-induced interleukin (IL)-6 production and hepatocarcinogenesis, and IL-6 plays a crucial role in HCC development via STAT3 activation . Aberrant activation of Janus kinase (JAK)-STAT signaling pathways is critical for HCC development; therefore, the anti-inflammatory properties of ACR and ARB partially contribute toward protection from hepatocarcinogenesis in DEN-treated OLETF rats by blocking STAT3 activation. On the other hand, neither ACR nor ARB affected oxidative DNA damage, lipid peroxidation and inflammatory cytokine levels in LETO rats model. (data not shown). Thus, we speculate that ACR and ARB could potentiate their anticancer effects with improvement these microenvironmental status.
ACR and ARB have been demonstrated to exert multiple pharmacological activities for efficiently preventing hepatocarcinogenesis. Similar to ARB, ACR also commonly exerts synergistic effects in combination with other clinically available drugs, including interferon-β, valproic acid, vitamin K2, trastuzumab, and bevacizumab [48, 49, 50, 51]. In addition to these agents, recent xenograft analysis has demonstrated that branched-chain amino acids (BCAA) may also be used as a candidate partner for peretinoin-based cocktail therapy against HCC . Therefore, the combination of both agents is likely to be one of the best therapies for chemoprevention against HCC. However, we need to ponder over the effect of ACR and ARB on IR, because the IR status, as estimated using HOMA-IR and QUICKI, were not changed by treatment with ACR nor ARB in this study.
Nevertheless, further study with long-term administration of both agents may prove that the IR-modulating effect of this combination regimen plays a key role in the chemoprevention of IR-based hepatocarcinogenesis.
In sum, we elucidated that ACR and ARB exerted a combined inhibitory effect on hepatocarcinogenesis along with the inhibition of angiogenesis, oxidative stress, and chronic inflammation. It is noteworthy that these inhibitory effects were achieved at clinically relevant low doses without causing any serious adverse events. Therefore, this combination regimen may eventually emerge as a potential new therapeutic strategy for chemoprevention against IR-based hepatocarcinogenesis.
The authors would like to thank Enago (www.enago.jp) for the English language review.
This study was supported in part by a grant-in-aid for Scientific Research C (17 K09438) from the Japan Society for Promotion of Science. The funding body had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
N.N conducted most of the experiments and drafted the manuscript. K.K orchestrated all experimental data and drafted the manuscript. M.K, Y.A, S.S, K.S, Y.S, H.T, Y.O, H.K, K.M, T.N, and A.M offered the technical or material support. H.Y designed and supervised the study. All authors read and gave final approval for the manuscript.
Ethics approval and consent to participate
All the animal procedures were performed as per the recommendations of the Guide for Care and Use of Laboratory Animals (National Research Council). The study was approved by the animal facility committee of Nara Medical University (permit No. 10842).
Consent for publication
The authors declare that they have no competing interests.
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