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Abstract
Obesity and related metabolic disorders, such as diabetes mellitus, raise the risk of liver carcinogenesis. Metformin, which is widely used in the treatment of diabetes, ameliorates insulin sensitivity. Metformin is also thought to have antineoplastic activities and to reduce cancer risk. The present study examined the preventive effect of metformin on the development of diethylnitrosamine (DEN)-induced liver tumorigenesis in C57BL/KsJ-+Leprdb/+Leprdb (db/db) obese and diabetic mice. The mice were given a single injection of DEN at 2 weeks of age and subsequently received drinking water containing metformin for 20 weeks. Metformin administration significantly reduced the multiplicity of hepatic premalignant lesions and inhibited liver cell neoplasms. Metformin also markedly decreased serum levels of insulin and reduced insulin resistance, and inhibited phosphorylation of Akt, mammalian target of rapamycin (mTOR), and p70S6 in the liver. Furthermore, serum levels of leptin were decreased, while those of adiponectin were increased by metformin. These findings suggest that metformin prevents liver tumorigenesis by ameliorating insulin sensitivity, inhibiting the activation of Akt/mTOR/p70S6 signaling, and improving adipokine imbalance. Therefore, metformin may be a potent candidate for chemoprevention of liver tumorigenesis in patients with obesity or diabetes.
Citation: Ohno T, Shimizu M, Shirakami Y, Baba A, Kochi T, Kubota M, et al. (2015) Metformin Suppresses Diethylnitrosamine-Induced Liver Tumorigenesis in Obese and Diabetic C57BL/KsJ-+Leprdb/+Leprdb Mice. PLoS ONE 10(4): e0124081. https://doi.org/10.1371/journal.pone.0124081
Academic Editor: Raul M. Luque, University of Cordoba, SPAIN
Received: September 19, 2014; Accepted: March 3, 2015; Published: April 16, 2015
Copyright: © 2015 Ohno et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Data Availability: All relevant data are within the paper.
Funding: These authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Diabetes mellitus, a major complication of obesity, is a serious healthcare problem worldwide due to its high prevalence; the International Diabetes Federation estimated in 2008 that 246 million adults worldwide had diabetes and that the prevalence was expected to reach 380 million in 2025 [1]. Many diabetic patients die of cardiovascular and cerebrovascular events and infectious diseases. Cancer is also a major cause of death in patients with diabetes as obesity and diabetes significantly raise the risk of several types of malignancies, especially hepatocellular carcinoma (HCC) [2–5].
HCC is one of the most frequently occurring cancers worldwide, causing 0.7 million deaths each year [6]. Several pathophysiological mechanisms linking obesity, diabetes, and liver carcinogenesis have been demonstrated, including the development of insulin resistance and adipokine imbalance [7–9]. Hyperinsulinemia may directly contribute to the development of HCC because insulin, which plays a key role in the oncogenesis signal transduction network [10], induces HCC cells to proliferate and resist apoptosis [11–13]. Activation of the phosphatidylinositol 3-kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) pathway induced by unrestrained insulin is also associated with hepatocarcinogenesis [14]. Excessive activation of the Akt/mTOR pathway has a crucial role in obesity-associated insulin resistance [15], and is critically important in liver carcinogenesis [14, 16]. In addition, increased levels of leptin, but decreased levels of adiponectin, are involved in the progression of steatosis and related liver tumorigenesis [17–20]. These findings suggest that targeting insulin resistance and adipokine imbalances such as hyperleptinemia and hypoadiponectinemia might be an effective strategy for preventing obesity- and diabetes-related liver carcinogenesis [8, 9].
Metformin is one of the most widely used drugs for the treatment of type 2 diabetes mellitus. The drug improves insulin sensitivity, especially in skeletal muscles, decreases hepatic gluconeogenesis, and inhibits glycogenolysis [21]. Furthermore, both clinical and experimental studies have demonstrated that metformin exerts beneficial effects on cancer prevention and treatment in various organs, including liver [22–25]. Several potential mechanisms have been proposed to explain the anticancer and cancer preventive properties of metformin. For instance, metformin exerts antineoplastic effects through the activation of the energy sensor AMP-activated protein kinase (AMPK) [26, 27]. Inhibition of the Akt/mTOR signaling pathway is also a critical mechanism for the suppression of cancer cell proliferation by metformin [28]. Moreover, metformin has direct effects on adipocyte and cardiac muscle, resulting in reduction of leptin secretion [29] and induction of adiponectin secretion [30].
In a recent study, administration of metformin prevented chemically-induced liver tumorigenesis in mice [22]. Metformin also inhibits proliferation of HCC-derived cells via induction of cell cycle arrest at G0/G1 phase [31], and treatment of the mouse HCC xenograft model with metformin shows suppressed tumor growth [32]. Another study demonstrated that metformin treatment up-regulates the expression of p21CIP and p27KIP, but down-regulates cyclin D1 levels, which are shown both in HCC cell lines and in tumor xenograft tissues [33]. In addition, Saito and colleagues [34] reported using flow cytometric analysis that metformin treatment significantly reduces the number of tumor-initiating epithelial cell adhesion molecule (EpCAM)-positive HCC cells, which are considered as hepatic cancer stem cells.
These findings suggest that metformin might be a useful agent for preventing HCC development; however, detailed studies clarifying the chemopreventive effects of metformin on obesity- and diabetes-related liver tumorigenesis have not yet been conducted. In the present study, we examined the preventive effects of metformin on hepatic carcinogen diethylnitrosamine (DEN)-induced liver tumorigenesis in C57BL/KsJ-+Leprdb/+Leprdb (db/db) mice, which exhibit obesity and diabetes, focusing on improvements in insulin resistance, inhibition of the Akt/mTOR signaling pathway, and amelioration of adipokine imbalance.
Materials and Methods
Animals and chemicals
Male and female C57BL/KsJ-m+/+Leprdb (+/db) mice were obtained from Japan SLC (Shizuoka, Japan) and were housed in plastic cages (2–3 mice per cage) with free access to drinking filtered tap water and a pelleted basal diet CRF-1 (Oriental Yeast Co., Ltd., Tokyo, Japan) under controlled conditions of humidity (50±10%), light (12/12 h light/dark cycle) and temperature (23±2°C). Mice were maintained in the specific pathogen free (SPF) facility at Gifu University Life Science Research Center in accordance with Institutional Animal Care Guidelines. The protocol was approved by the Committee on the Ethics of Animal Experiments of Gifu University (the authorization number is 25–8). DEN was purchased from Sigma Chemical Co. (St. Louis, MO, USA) and dissolved in phosphate buffered saline to make 1% (w/v) solution, according to manufacturer’s instruction. Metformin was supplied by Dainippon Sumitomo Pharma Co. (Tokyo, Japan). The maximum solubility of metformin is 346 mg/ml in water.
Experimental procedure
Newborn db/db mice were obtained by mating male and female +/db mice. Female db/db mice were planned to be randomly divided into the following 4 experimental and control groups: no treatment control group (group 1); metformin alone group (group 2); DEN alone group (group 3); and DEN plus metformin group (group 4). Some mice, which would be in groups 3 and 4, received a single intraperitoneal injection of DEN (25 mg/kg body weight) at 2 weeks of age. Originally, groups 1 and 2 would have 5–6 mice as DEN-free control groups and groups 3 and 4 would have 10–20 mice as DEN-injected groups. Finally, DEN-free 11 mice and DEN-injected 32 mice were separated as follows: group 1 (n = 6), group 2 (n = 5), group 3 (n = 19), and group 4 (n = 13). At 4 weeks of age, mice in groups 2 and 4 were given tap water containing metformin (300 mg/kg/day) until the end of the experiment. Although water consumption was not measured in this study, previous report showed that db/db mice drink about 30 ml/100g/day of water [35], and then mice were supplied with 1.0 mg/ml of metformin. This concentration of metformin was also established according to previous chemopreventive studies [22, 36]. Mice in groups 1 and 3 were given tap water without metformin. At 24 weeks of age (after 20 weeks of metformin treatment), all mice were sacrificed to analyze the development of liver neoplasms and preneoplastic lesions, foci of cellular alterations (FCA). The histological definition of FCA is indicated by Popp and Goldsworthy [37].
Histopathological analysis
At sacrifice, livers were immediately removed and maximum sagittal sections of 3 lobes (left lateral lobe, left medial lobe, and right medial lobe) were used for histopathological examination. For all experimental groups, 4-m thick sections of formalin-fixed, paraffin-embedded livers were stained with hematoxylin and eosin (H&E) for histopathology. The presence of HCC, liver cell adenoma, and FCA was judged according to previously described criteria [38]. The multiplicity of FCA was assessed on a per unit area (cm2) basis [17]. The histological features of the livers were evaluated by using the non-alcoholic fatty liver disease (NAFLD) activity score (NAS) system [39].
Protein extraction and western blot analysis
Total protein was extracted from non-tumorous areas of liver samples (30 mg) using 500 μl lysis buffer [50 mM Tris–HCl (pH 8.0), 150 mM NaCl, 0.1% sodium dodecyl sulfate (SDS), 0.5% deoxycholic acid, 1% NP-40] containing protease inhibitors (Protease Inhibitor Cocktail Set I; Calbiochem) and Mini-BeadBeater-1 (BioSpec Products). Proteins (20 μg/lane) were separated by SDS–polyacrylamide gel electrophoresis and transferred onto nylon membranes (Immobilon-P Transfer Membranes; Millipore). Immunoblots were performed using primary antibodies. Primary antibodies for Akt (#9272), phosphorylated Akt (p-Akt; Ser473, #9271), mTOR (#2972), phosphorylated mTOR (p-mTOR; Ser2448, #2971), AMPK-α (#2603), phosphorylated AMPK-α (p-AMPK-α; Thr172, #2535), p70S6 (#9202), phosphorylated p70S6 (p-p70S6; Thr389, #9205), STAT3 (#9132), phosphorylated STAT3 (p-STAT3; Tyr705, #9231), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH, #2118) were obtained from Cell Signaling Technology (Beverly, MA, USA). GAPDH was served as a loading control. Membranes were incubated with an appropriate horseradish peroxidase-conjugated secondary antibody (GE Healthcare). Each membrane was developed using an enhanced chemiluminescent substrate for the detection of horseradish peroxidase (Thermo Scientific), followed by densitometric scanning using NIH image software version 1.45 [40].
Clinical chemistry
Blood samples, which were collected from inferior vena cava at sacrifice after 6 hours of fasting, were used for chemical analyses. Serum concentrations of insulin, leptin, and high molecular weight adiponectin were determined by an enzyme immunoassay according to the manufacturer’s protocols (Shibayagi, Gunma, Japan). Serum levels of glucose were measured using a glucose CII-test kit (Wako, Osaka, Japan). Insulin resistance and insulin sensitivity were determined by calculating the homeostatic model assessment of insulin resistance (HOMA-IR) and the quantitative insulin sensitivity check index (QUICKI), respectively [7, 17]. HOMA-IR index was calculated according to the formula: HOMA-IR = [fasting glucose (mmol/l)]*[fasting insulin (μU/ml)]/22.5. QUICKI was determined as follows: QUICKI = 1 ⁄ [log(I0) + log(G0)], where I0 is the fasting insulin (μU/ml) and G0 is the fasting glucose (mg/dl), which correlates with the glucose clamp method [41].
Statistical analysis
The results are presented as the means ± SD, and were analyzed using JMP software version 10 (SAS Institute, Cary, NC, USA). Differences among the 4 groups were analyzed by one-way ANOVA. When the ANOVA showed a statistically significant effect (P < 0.05), each experimental group was compared by Tukey-Kramer’s multiple comparisons test. The differences were considered significant at P values of less than 0.05.
Results
General observations
No significant differences were observed in body weights or relative weights of the livers and white adipose tissue (periorchis and retroperitoneum) among the 4 groups at the end of the experiment (Table 1). During the experiment, no clinical symptoms of metformin toxicity were seen. Histopathological examination also did not show metformin toxicity in important organs including the liver, kidney, and spleen.
Effects of metformin on DEN-induced liver tumorigenesis in db/db mice
Macroscopically, whitish and nodular tumors were observed only in the livers of mice treated with DEN alone group at the end of the study (Fig 1A). As listed in Table 2, hepatic neoplasms, including liver cell adenoma (Fig 1B) and HCC (Fig 1C), developed only in the livers of mice that received DEN alone; however, metformin treatment completedly inhibited the occurence of adenoma and HCC. Hepatic preneoplastic lesions, FCA (Fig 1D) developed in the livers of all mice that received DEN. Metformin treatment significantly reduced the multiplicity of FCA (Fig 1E; P < 0.001).
(A) The whitish and nodular tumors (HCC; arrowheads) are present in the liver of DEN-treated db/db mouse. (B, C, and D) Paraffin-embedded sections stained with H&E. Representative histopathology of (B) liver cell adenoma, (C) HCC, and (D) FCA. Bars are (B) 200 μm and (C and D) 100 μm. (E) Average numbers of FCA in all groups [untreated control group (n = 6), metformin alone group (n = 5), DEN alone group (n = 19), and DEN plus metformin group (n = 13)]. Each column represents the mean ± SD. * P < 0.001.
Effects of metformin on serum levels of glucose and insulin, insulin resistance, and insulin sensitivity
Since insulin resistance plays a critical role in liver carcinogenesis, the effects of metformin treatment on serum levels of glucose and insulin and on improvements in insulin resistance were examined. There were no significant differences in serum glucose levels among groups, irrespective of DEN and metformin treatment (Fig 2A). However, in the DEN-treated groups, administration of metformin markedly decreased serum levels of insulin and HOMA-IR (Fig 2B and 2C; P < 0.05). The value of QUICKI, which indicates the degree of insulin sensitivity, was also significantly increased by metformin treatment in DEN-treated mice (Fig 2D; P < 0.05).
Serum levels of glucose (A) and insulin (B) were measured by the mutarotase/glucose oxidase method or enzyme immunoassay, respectively. The values of the HOMA-IR (C) and the QUICKI (D) were calculated to evaluate insulin resistance or insulin sensitivity, respectively. Values are the means ± SD. * P < 0.05.
Effects of metformin on phosphorylation of Akt, mTOR, p70S6, and AMPK-α in the livers of experimental mice
Activation of the Akt/mTOR pathway has a crucial role in obesity-associated insulin resistance, and is critically important in liver carcinogenesis. Therefore, the effects of metformin treatment on inhibition of Akt, mTOR, and downstream p70S6 phosphorylation in the liver were examined. As shown in Fig 3, western blot analysis revealed that hepatic expression levels of p-Akt and p-mTOR, which were increased by DEN treatment (P < 0.05), were significantly decreased by metformin administration (P < 0.001). Metformin also reduced hepatic expression of p-p70S6, irrespective of DEN treatment (P < 0.01). Levels of p-AMPK-α were unaltered by metformin administration in the present study, regardless of DEN treatment.
(A) Total protein was extracted from the livers of experimental mice and expression of Akt, p-AKT, mTOR, p-mTOR, p70S6, p-p70S6, AMPK-α, and p-AMPK-α was examined by western blot. Repeat western blots gave similar results. (B) Blot intensities were quantified using densitometry. Columns and lines indicate means and SD of triplicate assays. * P < 0.05, ** P < 0.01, and *** P < 0.001.
Effects of metformin on serum levels of leptin and adiponectin
As adipokine imbalance is associated with liver tumorigenesis, we examined the effects of metformin on serum levels of leptin and adiponectin in the experimental mice. Among the DEN-treated groups, serum leptin levels were decreased significantly by metformin administration (Fig 4A; P < 0.05). Conversely, metformin administration significantly increased serum adiponectin levels in DEN-treated db/db mice (Fig 4B; P < 0.05).
Serum levels of leptin (A) and adiponectin (B) were measured by enzyme immunoassay. Values are the means ± SD. * P < 0.05.
Discussion
Obesity and diabetes mellitus, which have become more prevalent in the majority of developed countries, are significant risk factors for the development of HCC [2–5]. Reports have suggested that pathophysiological disorders associated with obesity and diabetes, such as insulin resistance and adipokine imbalance, may be promising targets in the prevention of HCC, especially in obese and diabetic patients [8, 9]. The results of the present study show for the first time, that metformin, an anti-diabetic agent used worldwide, effectively prevents the development of DEN-induced liver tumorigenesis in obese and diabetic db/db mice probably by ameliorating insulin resistance and adipokine imbalance. Of note, metformin administration completely suppressed development of liver cell neoplasms. Recent clinical reports have also indicated that metformin lowers the risk of several types of cancers, including HCC, in patients with diabetes [23–25]. These clinical findings [23–25], together with the results of the present study, suggest that metformin should be evaluated as a powerful candidate for preventing HCC development in obese individuals, and especially in obese individuals with diabetes.
Recently, a similar effect of metformin has reported by Tajima et al. [36], demonstrating its preventive effect on obesity-related liver tumorigenesis using C57Bl/6 mice fed high-fat diet. The db/db mice were selected in the present study because it is a well-known model with high susceptibility to DEN-induced liver tumorigenesis and is thought to be suitable for investigating the development of diabetes- and obesity-related live cancer [17, 20, 42, 43]. Our previous reports have indicated that this high susceptibility might be, at least in part, due to insulin resistance and adipokine imbalance [17, 20, 42, 43]. Another similar literature [22] has shown that metformin prevents DEN-induced liver carcinogenesis in C57BL/6J mice. This is thought interesting since metformin exerts its anti-cancer effects even in lean rodents which appear to have normal state of insulin and adipokine secretions. In our present study, we try to investigate whether metformin is useful to suppress the susceptibility to hepatocarcinogenesis in obese and diabetic mice, which is thought to mimic diabetes- and obesity-related live cancer in human. In addition, metformin is clinically used for diabetic patients, therefore it is considered that clinical trial can be relatively easily conducted in the future with employing not lean but obese and diabetic patients whom metformin is approved to prescribe.
In this study, only female mice were employed. Male rodents are considered to be susceptible to the development of DEN-induced liver cancer compared to female, namely, Naugler et al. [44] have reported that male wild-type mice displayed 100% incidence of DEN-induced liver cancer while females had only 20%. This literature suggested that if we employed male mice in our protocol, the incidence of liver tumor was expected to be too high to compare metformin treated- with untreated-group. In addition, because of the high susceptibility to DEN-induced liver tumorigenesis in db/db mice, the tumor incidence would be much higher than that in wild-type mice even for a shorter experimental duration. Therefore, we thought female mice were suitable for the present study.
We considered reduction of serum insulin levels and improvement of insulin sensitivity as one of the most important mechanisms of metformin in the suppression of liver tumorigenesis in obese and diabetic mice, due to the oncogenic properties of insulin on HCC cells, including stimulation of cell growth and anti-apoptotic activity [11–13]. Several animal studies have suggested that targeting higher serum insulin levels and insulin resistance is an effective strategy for inhibiting obesity- and diabetes-related liver tumorigenesis [17, 42, 43]. For instance, dietary supplementation with branched-chain amino acids (BCAA), which improves insulin resistance and glucose tolerance in chronic liver disease patients [45], significantly suppresses liver tumorigenesis in obese and diabetic mice by decreasing serum insulin levels as well as improving insulin sensitivity [17]. Moreover, BCAA supplementation reduced the risk of HCC in obese patients with chronic viral liver disease [46], demonstrating the clinical significance of lowering insulin levels and attenuating insulin resistance in the prevention of liver carcinogenesis in obese and diabetic patients.
It is unclear why serum insulin and leptin levels were higher in DEN-treated db/db mice in the present study (Figs 2 and 4). DEN is known as a hepatocarcinogen and has a carcinogenic potency to induce DNA-adducts after being mediated by several enzymes [47, 48]. No literature can be found showing that the serum levels of insulin or leptin differ between DEN-treated and control rodents and that DEN and its metabolite DNA-adduct have direct effects on insulin or leptin levels. According to the previous report, the pro-inflammatory cytokines in chronic hepatitis leads insulin resistance [49], therefore DEN treatment also induced acute and chronic liver injury and might led to production of pro-inflammatory cytokines, resulting in higher serum insulin levels and insulin resistance.
We assessed insulin resistance only by HOMA-IR and QUICKI in this study, since several reports have indicated the validity and reproducibility of those to evaluate insulin resistance [50–52]. Another study, however, suggests that the predictive accuracy of these surrogate indices in mice is not as substantial as those in humans [53]. Therefore, additional studies, such as glucose tolerance, insulin tolerance, and/or euglycemic-hyperinsulinemic clamp tests, should be conducted to confirm whether metformin indeed ameliorates insulin resistance and glucose metabolism in the mouse model. Since the report from Tajima et al. [36] has indicated that metformin restored insulin sensitivity which was examined by insulin tolerance test in mice fed high-fat diet, it is assumed that similar effect of metformin would be observed in the present study. The serum glucose levels were very high (over 800 mg/dl) in accordance with previous reports [17, 54, 55]. Another report [56], however, have shown the glucose level of db/db mice can be over 700 mg/dl. There was a possibility that the measuring instrument we use in this study tended to show relatively higher levels of glucose. There was no reports investigating long-term effect of metformin on glucose levels in db/db mice, whereas a recent report has shown that short-term administration of metformin does not ameliorate glucose levels in db/db mice [57].
Activation of insulin signaling strongly triggers induction of the PI3K/Akt/mTOR pathway in hepatic preneoplastic and neoplastic lesions in rats [14]. Activation of the Akt/mTOR signaling is also involved in HCC development [16]. In the present study, hepatic expression of p-Akt, p-mTOR, and p-p70S6, a protein downstream of mTOR, was significantly decreased by metformin. We presume therefore that metformin inhibits activation of the PI3K/Akt/mTOR pathway, primarily by lowering serum insulin, and that this may suppress liver tumorigenesis in obese and diabetic mice.
In addition to inhibiting activation of the insulin-dependent PI3K/Akt/mTOR pathway, several studies have shown that metformin inhibits mTOR activation through activation of AMPK, which is also a critical mechanism of metformin in exerting its anti-tumor effects [26, 27]. In similar DEN-induced liver carcinogenesis studies using db/db mice, due to administration of a synthetic retinoid [42] or a component of green tea catechins [43] the levels of phosphorylated (i.e., activated) AMPK-α were increased, which was considered as one mechanism of suppressing liver tumorigenesis by these agents. In the present study, however, phosphorylated (i.e., activated) AMPK-α was not increased by metformin administration. These findings suggest that AMPK-dependent activity plays a minimal role in suppressing liver tumorigenesis in this mouse study. These findings are also consistent with those of a recent study showing that metformin prevents DEN-induced liver tumorigenesis in mice via AMPK-independent mechanism [22]. It also could be thought that metformin exerted its ameliorating effect on glucose metabolism through activating AMPK rather in muscle than in liver, which might lead to antitumor effect via decreasing serum insulin levels.
Moreover, adipokine imbalance, such as increased serum leptin levels and decreased serum adiponectin levels, is critically involved in obesity- and diabetes-related liver tumorigenesis [17–20], indicating that improving adipokine imbalance may be effective in preventing liver tumorigenesis. The serum leptin levels in DEN-treated group seem to be higher than those in the control group without respective changes in fat mass. The finding appears consistent with a previous study demonstrating that post-hepatitis cirrhotic patients had significantly higher serum leptin levels than healthy control without significant differences in BMI [58]. Although the underling mechanism is still unclear, the differences in serum leptin levels in the present study might be due to chronic liver damage caused by DEN stimulation.
In a previous study, BCAA supplementation effectively suppressed hyperleptinemia and this inhibition was associated with reduced liver carcinogenesis in db⁄db mice [17]. Pitavastatin, a lipid-lowering drug, also reduced the development of DEN-induced hepatic preneoplastic lesions in db⁄db mice via increasing serum adiponectin levels [20]. Leptin inhibits induction of apoptosis in HCC cells, whereas adiponectin induces apoptosis even in the presence of leptin by inhibiting leptin-induced Akt phosphorylation [19]. Therefore, in the present study, the effects of metformin on amelioration of adipokine imbalance, such as decreasing leptin but increasing adiponectin in serum, may prevent obesity- and diabetes-related liver tumorigenesis. Increased levels of adiponectin in serum and adipose tissue of db/db mice due to metformin have also been reported in a previous report [59].
The signaling pathways of leptin and its receptors still remain fully unclear. Among them, the major pathway appears via long-form of leptin receptors (Ob-RL) with activating JAK2/STAT, while leptin modulates, directly and indirectly, other signaling pathways, including PI3K and mTOR [60]. The literatures have demonstrated that leptin also functions via JAK2/STAT3 signaling pathway through short-form leptin receptors (Ob-RS) [61] and that both Ob-RL and Ob-Rs are expressed in the brain and liver [62, 63], while only Ob-RL is non-functional in db/db mice. These appear to indicate that leptin also activates STAT3 via Ob-RS, which still functions in db/db mice. We assumed that leptin could mediate its signaling even in db/db mice and, in this study, the difference of serum leptin levels might affect the pathophysiology of the experimental mice, but protein levels of STAT3 and p-STAT3 showed no significant difference among groups (S1 Fig). Since we here focus on insulin and leptin signaling and related protein levels, and the mechanisms of liver carcinogenesis is considered to be complicated, future studies might be needed to address the association of metformin with liver tumorigenesis by investigating other proteins and signaling pathways, and ideally conducting kinome-wide study, related to liver carcinogenesis in addition to insulin and leptin signaling and proteins examined in this study.
Hepatic steatosis, which is often observed in obese individuals and diabetic patients, may also be involved in liver tumorigenesis as hepatic lipid accumulation can induce hepatocyte proliferation and hepatic hyperplasia [64]. Previous studies have also shown that metformin prevents liver tumorigenesis induced by DEN [22] or by a high-fat diet [36] in mice by inhibiting pathways driving hepatic lipogenesis and by reducing fat accumulation in the liver. In the present study, however, improvements by metformin in hepatic steatosis as well as other histopathological findings assessed with NAS were not observed (S2 Fig). We believe this is likely due to the duration of the experiment (20 weeks) as the previous study [36] showing effects of metformin on liver steatosis was a short-term study (8 weeks). Therefore, future studies should be conducted using short-term studies to confirm that metformin reduces hepatic lipid accumulation in this liver tumorigenesis model using db/db mice.
In summary, the present study indicates that treatment with the anti-diabetic agent metformin, which has a preventive effect on HCC development based on case-control studies and meta-analyses of human trials [23–25], suppresses DEN-induced liver tumorigenesis in db/db mice probably by improving insulin resistance, inhibiting excess activation of the Akt/mTOR signaling, and ameliorating adipokine imbalance. The results of the present study, together with those of previous reports [17, 20, 42, 43], also suggest that targeting obesity- and diabetes-related metabolic abnormalities, including insulin resistance and adipokine imbalance, by either pharmaceutical or nutritional interventions, may be a promising strategy for preventing liver carcinogenesis in obese and diabetic patients who are at an increased risk of HCC development.
Supporting Information
S1 Fig. Effect of metformin on protein levels of STAT3 and phosphorylated STAT3.
https://doi.org/10.1371/journal.pone.0124081.s001
(TIF)
Author Contributions
Conceived and designed the experiments: TO MS. Performed the experiments: TO AB TK MK. Analyzed the data: TO YS TT HT. Contributed reagents/materials/analysis tools: AB TK MK. Wrote the paper: TO MS HM.
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