Chemically induced mouse liver tumors are resistant to treatment with atorvastatin
BMC Cancer volume 14, Article number: 766 (2014)
Atorvastatin is a potent inhibitor of the mevalonate pathway and widely used as a hypolipidemic drug. Some epidemiological studies and animal experiments indicate that the long-term use of atorvastatin and structurally related drugs might be associated with a reduced risk of developing hepatocellular carcinoma (HCC), the most common hepatocellular malignancy in humans. However, the potential of atorvastatin to inhibit HCC formation is controversially discussed.
Hepatocellular tumors were chemically induced by treatment of C3H/He mice with 10 μg/g body weight N-nitrosodiethylamine and the ability of atorvastatin to interfere with tumor formation was investigated by treatment of mice with 0.1% atorvastatin in the diet for 6 months. Tumor size and tumor multiplicity were analyzed, as were tissue levels of cholesterol and atorvastatin.
Atorvastatin treatment efficiently reduced serum cholesterol levels. However, the growth of tumors driven by activated MAPK (mitogen-activated protein kinase) signaling was not attenuated by the presence of the drug, as evidenced by a lack of reduction of tumor volume or tumor multiplicity by atorvastatin. Levels of the atorvastatin uptake transporters Oatp1a4 and Oatp1b2 were down-regulated at the mRNA and protein levels in chemically induced mouse liver tumors, but without striking effects on atorvastatin concentrations in the tumor tissue.
In summary, the present data provide substantial evidence that atorvastatin does not beneficially influence tumor growth in mouse liver and thereby challenge the hypothesis that statin use might protect against hepatocellular cancer.
Statins are an important and widely used class of hypolipidemic drugs. Their pharmacological efficacy is based on their ability to competitively inhibit 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMGCR), an important and rate-limiting enzyme in the isoprenoid- and cholesterol-synthesizing mevalonate pathway. Apart from their lipid-lowering properties, several epidemiological studies evidence that the long-term use of statins in humans might be causally linked to a reduced risk of developing different types of cancer. For recent review articles about this topic see for example [1–4]. However, there are also studies available which negate the beneficial effects of statin use on cancer incidence or mortality [5, 6]. Another meta-analysis of published data came to the conclusion that there is only weak, inconclusive evidence for a beneficial effect of statin use regarding cancer development .
One organ, for which anti-cancer effects of statins have been discussed quite often, is the liver. A number of epidemiological studies and meta-analyses have been published linking statin treatment to a diminished risk for hepatocellular carcinoma (HCC) [8–15]. However, epidemiological evidence for the inhibition of HCC formation by statins is controversial, due to potential confounders, bias, controversies about study design, mechanistic issues, and absence of a duration-risk relationship [10, 16–20]. In vitro, different statins are able to inhibit the growth and to induce apoptosis and cell cycle arrest of hepatoma cell lines [21–23]. Atorvastatin was shown to inhibit the growth of HUH-7-derived xenograft tumors . Several genetic or chemical experimental HCC models have been used to analyze potential tumor-inhibiting properties of statins in rodents: transgenic, MYC-driven HCC development was diminished by treatment with atorvastatin , as rosuvastatin did in mice developing HCC due to transgenic SV40-T antigen expression . Diethylnitrosamine (DEN)-induced liver tumors in obese mice were suppressed by treatment with pitavastatin , and similar effects were observed in DEN-treated rats when lovastatin was co-administered . By contrast, no tumor-inhibitory effect of atorvastatin was detectable on the development of murine TSC2-associated liver hemangiosarcomas .
In consideration of ambiguous epidemiological data and of the fact that different statins produce highly divergent effects on hepatoma cells , further animal experiments with different statins and HCC models are needed. Therefore, in the present study, we analyzed potential protective effects of atorvastatin treatment on the growth of chemically induced mouse liver tumors harboring an activated Ras/Raf/MAPK (mitogen-activated protein kinase) signaling pathway. This type of tumors was chosen because the MAPK is frequently overactivated in human HCC  and because previous studies by our group revealed that enzymes of cholesterol biosynthesis, namely Hmgcs1 (3-hydroxy-3-methylglutaryl-CoA synthase) and Lss (lanosterol synthase), are transcriptionally up-regulated in chemically induced mouse liver tumors with an activated Ras/Raf/MAPK pathway. In addition, a down-regulation of Cyp7a1, encoding the rate-limiting enzyme in the cholesterol-metabolizing bile acid synthesis pathway, was observed in these tumors and accordingly, tumors with activated MAPK signaling contained significantly higher levels of cholesterol [32, 33]. Assuming the observed changes in the tumor’s metabolic profile being advantageous for its growth or survival, inhibitors of cholesterol biosynthesis might be especially suited as a treatment option for this particular liver tumor phenotype.
Male inbred C3H/HeN mice (Janvier Labs, Saint-Berthevin, France) were injected with a single i.p. dose of 10 μg/g body weight of the genotoxic tumor inducer DEN (dissolved in 0.9% NaCl) at 12–14 days of age. In the course of hepatic DEN metabolism, ethyl cations are formed which form covalent adducts with the DNA, thus giving rise to gene mutations. This procedure follows an established protocol as used e.g. in [32–34], and the resulting tumor phenotype has been extensively studied [33, 34]. One week later, animals were stratified into two groups: one group (25 mice) received standard control diet (Ssniff, Soest, Germany), the second group (24 mice) was fed a modified diet (Ssniff) containing 0.1% wt/wt atorvastatin (Ca2+ salt, catalog no. A2476; TCI, Tokyo, Japan). Atorvastatin was chosen because it is the most commonly prescribed and also one of the most potent statins on the market. The selected concentration of the drug has proven to be efficacious to reduce cholesterol levels in mice without exerting toxic effects . Mice had access to food and tap water ad libitum and were kept on a 12 h dark/light cycle. After 6 months of continuous atorvastatin treatment, the mice were killed; livers were excised and immediately frozen on dry ice for immunohistochemistry. Aliquots of livers and serum samples to be used for cholesterol determination were snap-frozen in liquid nitrogen. All animals received humane care and protocols complied with institutional guidelines. Ethical approval for the animal study was obtained from the Regierungspräsidium Tübingen (permission no. TO6/10).
Cryostat sections (10 μm thickness) were fixed in 4% paraformaldehyde and stained with hematoxylin/eosin or immunohistochemically for glutamine synthetase, E-cadherin, and phosphorylated ERK1/2 (extracellular signal-regulated kinase) using the antibodies and methodology described in previous papers [33, 35]. For staining of OATP1A4 and OATP1B2, primary antibodies against the two transporters (Santa Cruz Biotechnology, Santa Cruz, CA, USA; catalog no. sc-47270 and sc-18436) were used at 1:50 dilution in combination with horseradish peroxidase-conjugated donkey-anti-goat secondary antibodies (1:50 dilution; Santa Cruz Biotechnology; catalog no. sc-3851) and the substrates 3-amino-9-ethylcarbazole/H2O2. Histochemical staining for glucose-6-phosphatase activity was performed according to  on glutaradehyde-fixed slices.
Whole cell extracts were denatured in Laemmli buffer at 40°C, separated by sodiumdodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE; 50 μg of protein per lane) and transferred to PVDF membranes. Antibodies against E-cadherin (1:100; Becton Dickinson, Heidelberg, Germany; catalog no. 610181), OATP1A4 and OATP1A2 (see above; 1:200 dilution), and glyceraldehyde-3-phosphate dehydrogenase (1:1,000; Millipore, Chandler’s Ford, UK; catalog no. MAB374) were used in combination with alkaline phosphatase-conjugated secondary antibodies directed against mouse (1:10,000; Tropix, Weiterstadt, Germany; catalog no. AC32ML) or goat immunoglobulins (1:5,000; Santa Cruz Biotechnology; catalog no. sc-2022), with CDP-Star (Tropix) as a substrate. Chemiluminescence was monitored on a charge-coupled device (CCD) camera system (Raytest, Straubenhardt, Germany).
Extraction of cholesterol and 4β-hydroxycholesterol
Serum cholesterol was determined by GC-MS as described previously  with minor modifications: briefly, 10 μl of serum were spiked with 10 μg of [2H5]-cholesterol as internal standard. After saponification with 0.5 ml 1 M NaOH in 90% ethanol at 70°C for 1 h, 250 μl H2O were added and the samples extracted with 2 ml n-hexane. A 50 μl aliquot of the extract was evaporated to dryness and derivatized with 20 μl N,O-bis(trimethylsilyl)trifluoroacetamide for 30 min at room temperature.
Sample preparation for 4β-hydroxycholesterol analysis was performed as previously published  with minor modifications. Briefly, liver tissue (10–30 mg) was homogenized in 400 μl phosphate buffer (0.1 M potassium phosphate, 2 mM EDTA, 11 μg/ml butylhydroxytoluene (BHT), pH 7.4) using a pestle. After addition of 10 μg BHT and 50 ng of the internal standard [2H4]-4β-hydroxycholesterol, the homogenate was saponified with 2.5 ml 1 M NaOH in 90% ethanol at 70°C for 1 h under argon and then extracted with 1 ml H2O and 5 ml CHCl3. The organic phase was evaporated to dryness in a stream of N2 and the residue dissolved in 1 ml toluene. Samples were purified by solid phase extraction on silica cartridges (Isolute Si 100 mg; Biotage, Uppsala, Sweden) preconditioned with n-hexane. Cartridges were washed with 1 ml n-hexane and 10 ml 2-propanol in n-hexane (0.5% v/v), and then eluted with 2 ml 2-propanol in n-hexane (30% v/v). The eluate was evaporated to dryness in a stream of N2 and derivatized as described above.
Cholesterol and 4β-hydroxycholesterol quantification
A 5975C inert XL MSD in the EI mode, coupled to a 7890A gas chromatograph (GC; Agilent Technologies, Waldbronn, Germany) was used. GC was performed on a J&W DB-5MS column (25 m, 0.2 mm i.d., 0.33 μm film thickness; Agilent) in the splitless mode. For cholesterol analysis, the GC oven program started at 150°C and was held for 1 min. Temperature was increased with 20°C/min to 300°C, with a total run time of 18.5 min. The trimethylsilyl derivatives of cholesterol and the internal standard [2H5]-cholesterol were detected in SIM mode at m/z 458 and 463, respectively. For the analysis of 4β-hydroxycholesterol, the GC oven program started at 150°C and was held for 1 min. Temperature was increased with 10°C/min to 250°C, then with 30°C/min to 300°C. The trimethylsilyl derivatives of 4β-hydroxycholesterol and the internal standard [2H4]-4β-hydroxycholesterol were quantified in SIM mode at m/z 366 and 370, respectively, using m/z 456 and 460 as qualifier ions.
Calibration samples for cholesterol were prepared in isooctane with 10% 2-propanol in the concentration range from 1 μg to 30 μg. Calibration samples for 4β-hydroxycholesterol were prepared in isooctane with 0.8% 2-propanol from 5 ng to 100 ng.
Calibration samples were worked up as the samples, and analyzed together with the unknown samples. Calibration curves based on internal standard calibration were obtained by weighted (1/×) linear regression for the peak area ratio of the analyte to the respective internal standard against the amount of the analyte. The concentration in unknown samples was obtained from the regression line.
Atorvastatin and 2-hydroxy-atorvastatin quantification
Tissue samples (50 to 150 mg) were homogenized in a total volume of 600 μl of acetate buffer (0.1 M, pH 5) and internal standard (100 pmol each of 2H5-atorvastatin and 2H5-2-hydroxyatorvastatin) in a FastPrep 24 homogenizer (MP Biomedicals, Santa Ana, USA) for 40s at speed 6.0 using lysing matrix D. The homogenate was extracted with ether:2-propanol 9:1 (v/v), and the organic phase evaporated in a stream of nitrogen. The residue was dissolved in aqueous ammonium acetate (10 mM with 1% formic acid):acetonitrile 60:40 (v/v) and determined by LC/MS-MS analysis as described .
Quantification of tumor burden
Tumor burden was quantified as the area fraction (corresponding to the volume fraction) of glucose-6-phosphatase-altered lesions on an Axio Imager light microscope (Imager.M1; Zeiss, Göttingen, Germany). AxioVision software Rel.4.5 (Zeiss) was used to determine tumor and normal tissue areas. The calculation of the number and size of glucose-6-phosphatase lesions per cm3 of liver tissue was performed according to . For each mouse, three liver lobes were examined (right lobe, left lateral lobe, and caudate lobe) using three slices per liver lobe with at least 20 sections distance between the individual slices. Hematoxylin/eosin staining of the tumors and immunohistochemical staining for glutamine synthetase and E-cadherin was assessed on parallel slices.
Tumor tissue samples from mice of both treatment groups were punched out of liver slices (20 μm thickness) by a sharpened cannula. Following proteinase K digestion, genomic DNA was amplified by polymerase chain reaction (PCR) using the following primer pairs: Ha-ras_fwd 5′-GAGACATGTCTACTGGACATCTT-3′, Ha-ras_rev 5′-GCTAGCCATAGGTGGCTCACCTG-3′; B-raf_fwd 5′-TCAAAATGCTTTCTCTAATAGGA-3′, B-raf_rev 5′-TGTTCTGGAACTATATAGACAG-3′. PCR products were analyzed for mutations in Codon 61 of Ha-ras and Codon 637 of B-raf by restriction fragment length polymorphisms analysis as previously described .
Cell culture and in vitroassays
Mouse hepatoma cell lines 53.2b, 55.1c, 70.4 and Hepa1c1c7  were grown in D-MEM/F-12 medium (Invitrogen, Darmstadt, Germany) supplemented with 1% fetal bovine serum and antibiotics. For cytotoxicity testing, 9000 cells were seeded per well of a 96-well plate and treated with the indicated concentrations of atorvastatin for 24 h starting 24 h after seeding. Plates were analyzed using the neutral red uptake and Alamar Blue tests as previously described . For the analysis of growth behavior, cells were seeded on 96 well-plates at a density of 5000 cells/well and treated with the indicated concentrations of atorvastatin starting 12 h after seeding. Solvent controls received medium containing 0.4% dimethyl sulfoxide. Medium was changed after 48 h. Following different incubation periods, cells were fixed by 10% trichloroacetid acid and analyzed photometrically after staining with sulforhodamine B according to .
Gene expression analysis
Total RNA was isolated and reverse transcribed from cell cultures or liver tissue as previously described , using Trizol reagent (Invitrogen) and avian myeloblastosis virus reverse transcriptase (Promega, Mannheim, Germany). SYBR green I-based analyses of target gene expression were conducted on a LightCycler instrument (Roche) as previously described  using the following primer pairs: Hmgcr_fwd 5′-AGCAAGTGATTACCCTGAGTTTAG-3′, Hmgcr_rev 5′-CAGACATTCTTCATTAGGTCGTG-3′; Hmgcs1_fwd 5′-TTGGGGACGTTAAATTAGAAGAT-3′, Hmgcs1_rev 5′-CCAAGCCAGAACCGTAAGAG-3′; Oatp1a4_fwd 5′- GAAACAGTATTCCTCCACCATC-3′, Oatp1a4_rev 5′-TTGATAAGCCCAACTACAGACG-3′; Oatp1b2_fwd 5′-ATCCCGTGACTAATCCAACA-3′, Oatp1b2_rev 5′- ACCAAACTGCTGCTCTATAAACT-3′; 18S rRNA_fwd 5′-CGGCTACCACATCCAAGGAA-3′, 18S rRNA_rev 5′-GCTGGAATTACCGCGGCT-3′. The Mm_Cyp7a1_1_SG QuantiTect Primer Assay (Qiagen, Hilden, Germany) was used for Cyp7a1 determination. Expression was normalized to the housekeeping gene 18S rRNA using the Pfaffl method .
Calculation of statistical significance
Statistical significance was calculated using an unpaired t-test with Welch’s correction. Homogeneity of variances was tested for using Bartlett’s test. The Shapiro-Wilk test was used to analyze normal distribution of values. Differences were considered significant when p < 0.05.
Growth inhibition of murine tumor cell lines by atorvastatin in vitro
First, studies with mouse hepatoma cell lines were conducted to prove the in vitro efficacy of atorvastatin treatment of murine liver tumor cells. Mouse hepatoma cell lines 53.2b, 55.1c, 70.4, and Hepa1c1c7 were screened for their expression of Hmgcs1 and Hmgcr, encoding the first and rate-limiting steps in cholesterol biosynthesis. All cell lines expressed the two mRNAs at levels comparable or slightly higher than normal mouse liver. Cyp7a1 expression was not detectable (data not shown). A moderate therapeutic dose of 40 mg atorvastatin per day results in maximum human plasma levels of 66 ng/ml, corresponding to a plasma concentration of ~118 nM of the drug . However, hepatic concentrations are ~50-fold higher than in plasma, as measured in atorvastatin-treated rats, resulting in an estimated liver concentration of ~6 μM . Therefore, the ability of atorvastatin to interfere with hepatoma cell growth in vitro was tested at concentrations ranging from 1 μM to 20 μM, in order to meet the expected in vivo concentration of atorvastatin in mouse liver tumor cells. After 24 h of treatment, 55.1c cells appeared to be rather resistant to atorvastatin treatment up to the maximum concentration of 20 μM, while cells from lines 70.4 and Hepa1c1c7 showed the greatest sensitivity (Figure 1A). Long-term growth of atorvastatin-treated cells was monitored using the sulforhodamine B assay. Again, 55.1c cells were most resistant, with only the highest concentration of atorvastatin causing a remarkable inhibition of cell growth (Figure 1B). Hepa1c1c7 cells showed diminished growth already at 1 μM atorvastatin, while 53.2b cells were inhibited at concentrations ≥5 μM. In summary, atorvastatin was able to interfere with the viability and/or growth of different mouse hepatoma cell lines at in vivo-relevant concentrations.
Effects of atorvastatin on hepatoma growth in vivo
Chemically induced mouse liver tumors were generated by a single injection of DEN at 2 weeks of age according to . Starting one week later, mice were stratified into a control (standard diet) and an atorvastatin group (0.1% atorvastatin in the diet). Atorvastatin feeding slightly but significantly inhibited weight gain of the animals in the atorvastatin group during the 6 months period of the experiment (Figure 2A). Atorvastatin-fed mice possessed larger livers and had an increased liver to body weight ratio (Figure 2B). In line with its expected pharmacological effects, atorvastatin significantly reduced serum cholesterol and liver 4β-hydroxycholesterol levels (Figure 2C). None of the animals died during the study or had to be sacrificed ahead of schedule.
At the end of the experiment, livers were isolated and the occurrence of hepatocellular tumors was analyzed. Three liver lobes were analyzed for each mouse (see Methods section). Tumor incidence was 100% in both groups and multiple tumors were detected per animal. This is in line with previous results from comparable experiments with DEN as a tumor inducer [32–34]. For a detailed list of the number of tumors analyzed per animal, please refer to the Additional file 1: Table S1. As also expected from previous studies, the vast majority (>95% by number and volume fraction) of the resulting tumors after 6 months were basophilic, E-cadherin-expressing and glutamine synthetase-deficient hepatocellular adenoma (data not shown; for representative immunostainings see Figure 3A). These characteristics are hallmarks of mouse liver adenoma with activated MAPK signaling; e.g. see . Accordingly, mutation analyses revealed that 20 out of 26 analyzed tumors (77%) contained activating mutations in either Codon 61 of Ha-ras or Codon 637 of B-raf (Table 1), encoding key players in the MAPK cascade. Accordingly, Ha-ras-mutated tumors were strongly positive for the phosphorylated active MAPK downstream kinase ERK1/2 (data not shown).
Quantification of the hepatic tumor volume fractions (Figure 4A) as well as the calculation of liver tumor multiplicities (Figure 4B) in the two groups revealed that no significant differences were present between atorvastatin-treated and control mice (for details please also refer to the Additional file 1: Table S1). However, variances of tumor volume fractions were not equal in the two groups, with the significantly higher variance in the atorvastatin group (p = 0.002; Bartlett’s test). Therefore, some differences were visible when mice were grouped into “responder classes”, according to their individual tumor burden (Figure 4C): with atorvastatin treatment, there were, on the one hand, comparably many weak responders with a hepatic tumor volume fraction of <15%. On the other hand, very strong responders with a hepatic tumor volume >50% were exclusively present in the atorvastatin-treated group. Similarly, tumors of the biggest size class, with a diameter of >6.5 mm, were observed in atorvastatin-treated livers only (Figure 4D). Tumor volume fraction values were normally distributed within the control group, but not in the atorvastatin group (p = 0.026; Shapiro-Wilk test). Altogether, this indicates a broader distribution of tumorigenic response in mice treated with atorvastatin, as compared to control mice. However, these effects of atorvastatin did not alter the overall mean tumor response of the population, which was not distinguishable from controls.
Expression of atorvastatin uptake transporters and atorvastatin levels in tumors
Atorvastatin is taken up into hepatocytes by means of the organic anion transporters OATP1A4 and OATP1B2 . To check whether inefficient uptake of atorvastatin might have caused the lack of efficacy of the drug on tumor development, the expression of these two transporters in normal liver and liver tumors was analyzed by immunohistochemistry, Western blotting, and real-time RT-PCR. The results are presented in Figure 3 and demonstrate a marked reduction of both transporters in liver tumor tissue, as compared to surrounding normal hepatocytes. Of note, OATP1B2 immunoreactivity was preferentially located in perivenous hepatocytes surrounding the central veins (Figure 3A). Our results are therefore in line with previous findings that mouse liver tumors with activated MAPK lack the expression of many ‘perivenous’ genes . The down-regulation of the two transporters might indicate that the uptake of atorvastatin into tumor cells is reduced. Thus, the levels of atorvastatin and its major metabolite 2-hydroxyatorvastatin were analyzed by mass spectrometry in normal liver and tumor tissue (Figure 3D). Levels of both the drug and its metabolite were reduced in the tumors, but the effect slightly failed our criteria for statistical significance (p = 0.052 for atorvastatin and p = 0.068 for hydroxyatorvastatin, respectively).
Mouse liver tumors with an activated MAPK signaling pathway have been extensively characterized; they show high expression levels of cholesterol-synthesizing enzymes along with a down-regulation of the main cholesterol-metabolizing enzyme and possess elevated levels of cholesterol [32, 33]. Assuming that the metabolic pathways active in a certain type of tumor are beneficial for their growth, these tumors appear suited for a preventive approach based on a cholesterol-lowering compound such as atorvastatin. Possible beneficial effects of statin treatment regarding the formation of HCC are controversially discussed (see Background section). The present data conclusively show that DEN-induced tumor development in male C3H/HeN mice is not beneficially affected by treatment with atorvastatin. This is in line with the lack of tumor-inhibiting properties of atorvastatin in a mouse model of TSC2-related liver hemangioma , but not with data obtained with a MYC-driven HCC mouse model where atorvastatin acted as a tumor-preventive compound .
In principle, a lack of treatment efficacy might always be related to a too low dose of the respective agent. In the present study, 0.1% atorvastatin in the diet was able to slightly reduce the weight gain of the mice and to induce elevated liver weights, indicating that the maximum tolerated dose of the drug has been chosen for the experiment and that results obtained with higher dosing would always be questionable due to unspecific toxicity of the compound. Moreover, pharmacological efficacy of the drug was shown by a significant reduction of cholesterol levels in the treated population. The observed degree of serum cholesterol reduction is within the range of what is expected at therapeutic statin doses in humans . Moreover, the in vitro experiments, where the different cell lines showed variable responses to atorvastatin treatment despite similar levels in cholesterol-synthesizing enzymes, suggest that effects other than HMGCR inhibition might contribute to the growth-inhibitory effect of the drug. Of note, it has been published that tumor-inhibitory effects of lovastatin even occur in the absence of measurable effects on cholesterol levels .
The daily food intake has not been measured during the present study. However, when calculating with published average values of a food intake of 5 g per mouse of 30 g body weight , the total oral uptake of atorvastatin in our experiment was approximately 167 mg/kg body weight/day. This is considerably higher than in the MYC-HCC experiment by , where the drug had been administered three times per week at 100 mg/kg body weight, which led to an inhibition of tumor growth. In synopsis, all these parameters indicate that the selected atorvastatin dose was not too low to produce relevant effects. The differences between our results and the previous study with MYC-induced HCCs  might result from the differences between the physiology of transgenic MYC-driven HCCs and our chemically induced tumors. Differences between mouse strains might also play a role in the response to atorvastatin treatment. Unfortunately, no information about the genetic background of the mice is provided in . Moreover, the low number of only 5 animals per group in the previous study  hampers statistical evaluation and interpretation of these results.
In humans, atorvastatin is mainly metabolized by cytochrome (CYP) P450 3A4 . Accelerated metabolism of the drug in the tumor cells might also be responsible for the lack of treatment efficacy in our experimental system. Mouse liver tumors with an activated MAPK pathway show de-regulated, mostly diminished, mRNA expression of various CYPs. Enzymes from the Cyp3a family, however, are not significantly altered in MAPK-activated mouse liver tumors, as compared to normal tissue [32, 33]. This indicates that major alterations in the metabolism of atorvastatin are not to be expected in the tumor cells.
An inefficient uptake of the drug into the tumor cells might explain also the lack of atorvastatin efficacy in our experiment. We show that organic anion transporters involved in the uptake of atorvastatin, namely Oatp1b2 (Slco1b2) and Oatp1a4 (Slco1a4) , are strongly down-regulated in the tumors at the mRNA and protein levels. Studies with human HCC samples have revealed the down-regulation of OATP1B1 [53, 54], the human atorvastatin-transporting protein . In view of this fact, it is tempting to speculate that human hepatocellular tumors might exhibit a reduced ability to take up atorvastatin and probably also other structurally related statins. This scenario implies that statins might not be effective in tumor cells when administered at the therapeutic dose, thus arguing against the proposed protective effect of statins, given the fact that the putative tumor-inhibiting properties of statins are based on direct effects of the drug on tumors cells, not on indirect effects involving statin effects on tumor-surrounding non-tumorous cells. However, the observed reduction of atorvastatin levels in mouse liver tumors is not very pronounced. Therefore, it seems rather unlikely that the apparent lack of tumor inhibition in our experiment can be solely explained by a diminished uptake of the drug into the tumors.
In summary, present data challenge the idea that atorvastatin inhibits tumor development in the liver. Nonetheless, it has to be noted that results from animal experiments cannot be transferred to the situation in humans with absolute certainty, in this particular case for example due to possible species differences in tumor genetics and biology, and/or due to the much higher interindividual variability in the human population, as compared to inbred mouse strains. However, in the absence of unequivocal epidemiological data, results from animal experimentation are an important and indispensable source of information.
The present data provide substantial evidence that atorvastatin does not beneficially influence tumor growth in mouse liver and thereby challenge the hypothesis that statin use might protect against hepatocellular cancer.
- Hmgcs :
Mitogen-activated protein kinase
Organic anion transporting peptide
(Real time) polymerase chain reaction
Sodiumdodecylsulfate-polyacrylaminde gel electrophoresis.
Osmak M: Statins and cancer: current and future prospects. Cancer Lett. 2012, 324 (1): 1-12. 10.1016/j.canlet.2012.04.011.
Singh PP, Singh S: Statins are associated with reduced risk of gastric cancer: a systematic review and meta-analysis. Ann Oncol. 2012, 24 (7): 1721-1730.
Zeichner S, Mihos CG, Santana O: The pleiotropic effects and therapeutic potential of the hydroxy-methyl-glutaryl-CoA reductase inhibitors in malignancies: a comprehensive review. J Cancer Res Ther. 2012, 8 (2): 176-183. 10.4103/0973-1482.98967.
Thurnher M, Nussbaumer O, Gruenbacher G: Novel aspects of mevalonate pathway inhibitors as antitumor agents. Clin Cancer Res. 2012, 18 (13): 3524-3531. 10.1158/1078-0432.CCR-12-0489.
Emberson JR, Kearney PM, Blackwell L, Newman C, Reith C, Bhala N, Holland L, Peto R, Keech A, Collins R, Simes J, Baigent C: Lack of effect of lowering LDL cholesterol on cancer: meta-analysis of individual data from 175,000 people in 27 randomised trials of statin therapy. PLoS One. 2012, 7 (1): e29849-10.1371/journal.pone.0029849.
Bonovas S, Filioussi K, Tsavaris N, Sitaras NM: Statins and cancer risk: a literature-based meta-analysis and meta-regression analysis of 35 randomized controlled trials. J Clin Oncol. 2006, 24 (30): 4808-4817. 10.1200/JCO.2006.06.3560.
Kuoppala J, Lamminpaa A, Pukkala E: Statins and cancer: A systematic review and meta-analysis. Eur J Cancer. 2008, 44 (15): 2122-2132. 10.1016/j.ejca.2008.06.025.
Tsan YT, Lee CH, Ho WC, Lin MH, Wang JD, Chen PC: Statins and the risk of hepatocellular carcinoma in patients with hepatitis C virus infection. J Clin Oncol. 2013, 31 (12): 1514-1521. 10.1200/JCO.2012.44.6831.
Tsan YT, Lee CH, Wang JD, Chen PC: Statins and the risk of hepatocellular carcinoma in patients with hepatitis B virus infection. J Clin Oncol. 2012, 30 (6): 623-630. 10.1200/JCO.2011.36.0917.
Pradelli D, Soranna D, Scotti L, Zambon A, Catapano A, Mancia G, La Vecchia C, Corrao G: Statins and primary liver cancer: a meta-analysis of observational studies. Eur J Cancer Prev. 2013, 22 (3): 229-234. 10.1097/CEJ.0b013e328358761a.
Leung HW, Chan AL, Lo D, Leung JH, Chen HL: Common cancer risk and statins: a population-based case–control study in a Chinese population. Expert Opin Drug Saf. 2013, 12 (1): 19-27. 10.1517/14740338.2013.744392.
Lai SW, Liao KF, Lai HC, Muo CH, Sung FC, Chen PC: Statin use and risk of hepatocellular carcinoma. Eur J Epidemiol. 2013, 28 (6): 485-492. 10.1007/s10654-013-9806-y.
Lonardo A, Loria P: Potential for statins in the chemoprevention and management of hepatocellular carcinoma. J Gastroenterol Hepatol. 2012, 27 (11): 1654-1664. 10.1111/j.1440-1746.2012.07232.x.
El-Serag HB, Johnson ML, Hachem C, Morgana RO: Statins are associated with a reduced risk of hepatocellular carcinoma in a large cohort of patients with diabetes. Gastroenterology. 2009, 136 (5): 1601-1608. 10.1053/j.gastro.2009.01.053.
Singh S, Singh PP, Singh AG, Murad MH, Sanchez W: Statins are associated with a reduced risk of hepatocellular cancer: a systematic review and meta-analysis. Gastroenterology. 2013, 144 (2): 323-332. 10.1053/j.gastro.2012.10.005.
Bonovas S, Nikolopoulos G, Sitaras NM: Statins and reduced risk of hepatocellular carcinoma in patients with hepatitis C virus infection: further evidence is warranted. J Clin Oncol. 2013, 31 (32): 4160-
Lund JL, Montomoli J: Common flaws in pharmacoepidemiologic study design and analysis. J Clin Oncol. 2013, 31 (32): 4161-4162. 10.1200/JCO.2013.51.5593.
Clement S, Peyrou M, Foti M, Negro F: Statins may protect against hepatocellular carcinoma development in patients infected with hepatitis C virus, but what are the mechanisms?. J Clin Oncol. 2013, 31 (32): 4160-4161.
Carrat F: Statin and aspirin for prevention of hepatocellular carcinoma: What are the levels of evidence?. Clin Res Hepatol Gastroenterol. 2014, 38 (1): 9-11. 10.1016/j.clinre.2013.09.007.
Singh PP, Singh S: Statins and risk reduction in hepatocellular carcinoma: fact or fiction?. J Clin Oncol. 2012, 30 (20): 2569-2570. 10.1200/JCO.2012.43.2179. author reply 2570–2571
Kah J, Wustenberg A, Keller AD, Sirma H, Montalbano R, Ocker M, Volz T, Dandri M, Tiegs G, Sass G: Selective induction of apoptosis by HMG-CoA reductase inhibitors in hepatoma cells and dependence on p53 expression. Oncol Rep. 2012, 28 (3): 1077-1083.
Relja B, Meder F, Wilhelm K, Henrich D, Marzi I, Lehnert M: Simvastatin inhibits cell growth and induces apoptosis and G0/G1 cell cycle arrest in hepatic cancer cells. Int J Mol Med. 2010, 26 (5): 735-741.
Zhang W, Wu J, Zhou L, Xie HY, Zheng SS: Fluvastatin, a lipophilic statin, induces apoptosis in human hepatocellular carcinoma cells through mitochondria-operated pathway. Indian J Exp Biol. 2010, 48 (12): 1167-1174.
Yang PM, Liu YL, Lin YC, Shun CT, Wu MS, Chen CC: Inhibition of autophagy enhances anticancer effects of atorvastatin in digestive malignancies. Cancer Res. 2010, 70 (19): 7699-7709. 10.1158/0008-5472.CAN-10-1626.
Cao Z, Fan-Minogue H, Bellovin DI, Yevtodiyenko A, Arzeno J, Yang Q, Gambhir SS, Felsher DW: MYC phosphorylation, activation, and tumorigenic potential in hepatocellular carcinoma are regulated by HMG-CoA reductase. Cancer Res. 2011, 71 (6): 2286-2297. 10.1158/0008-5472.CAN-10-3367.
Tijeras-Raballand A, Hainaud-Hakim P, Contreres JO, Gest C, Le Henaff C, Levy BI, Pocard M, Soria C, Dupuy E: Rosuvastatin counteracts vessel arterialisation and sinusoid capillarisation, reduces tumour growth, and prolongs survival in murine hepatocellular carcinoma. Gastroenterol Res Pract. 2010, 2010: 640797-
Shimizu M, Yasuda Y, Sakai H, Kubota M, Terakura D, Baba A, Ohno T, Kochi T, Tsurumi H, Tanaka T, Moriwaki H: Pitavastatin suppresses diethylnitrosamine-induced liver preneoplasms in male C57BL/KsJ-db/db obese mice. BMC Cancer. 2011, 11: 281-10.1186/1471-2407-11-281.
Bjorkhem-Bergman L, Acimovic J, Torndal UB, Parini P, Eriksson LC: Lovastatin prevents carcinogenesis in a rat model for liver cancer. Effects of ubiquinone supplementation. Anticancer Res. 2010, 30 (4): 1105-1112.
Finlay GA, Malhowski AJ, Polizzi K, Malinowska-Kolodziej I, Kwiatkowski DJ: Renal and liver tumors in Tsc2(+/-) mice, a model of tuberous sclerosis complex, do not respond to treatment with atorvastatin, a 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor. Mol Cancer Ther. 2009, 8 (7): 1799-1807. 10.1158/1535-7163.MCT-09-0055.
Leszczynska A, Gora M, Plochocka D, Hoser G, Szkopinska A, Koblowska M, Iwanicka-Nowicka R, Kotlinski M, Rawa K, Kiliszek M, Burzynska B: Different statins produce highly divergent changes in gene expression profiles of human hepatoma cells: a pilot study. Acta Biochim Pol. 2011, 58 (4): 635-639.
Schmidt CM, McKillop IH, Cahill PA, Sitzmann JV: Increased MAPK expression and activity in primary human hepatocellular carcinoma. Biochem Biophys Res Commun. 1997, 236 (1): 54-58. 10.1006/bbrc.1997.6840.
Jaworski M, Ittrich C, Hailfinger S, Bonin M, Buchmann A, Schwarz M, Kohle C: Global gene expression in Ha-ras and B-raf mutated mouse liver tumors. Int J Cancer. 2007, 121 (6): 1382-1385. 10.1002/ijc.22801.
Unterberger EB, Eichner J, Wrzodek C, Lempiainen H, Luisier R, Terranova R, Metzger U, Plummer S, Knorpp T, Braeuning A, Moggs J, Templin MF, Honndorf V, Piotto M, Zell A, Schwarz M: Ha-ras and beta-Catenin oncoproteins orchestrate metabolic programs in mouse liver tumors. Int J Cancer. 2014, 135 (7): 1574-1585. 10.1002/ijc.28798.
Moennikes O, Buchmann A, Romualdi A, Ott T, Werringloer J, Willecke K, Schwarz M: Lack of phenobarbital-mediated promotion of hepatocarcinogenesis in connexin32-null mice. Cancer Res. 2000, 60 (18): 5087-5091.
Singh Y, Braeuning A, Schmid A, Pichler BJ, Schwarz M: Selective poisoning of Ctnnb1-mutated hepatoma cells in mouse liver tumors by a single application of acetaminophen. Arch Toxicol. 2013, 87 (8): 1595-1607. 10.1007/s00204-013-1030-8.
Wachstein M, Meisel E: Histochemistry of hepatic phosphatases of a physiologic pH; with special reference to the demonstration of bile canaliculi. Am J Clin Pathol. 1957, 27 (1): 13-23.
Czubayko F, Beumers B, Lammsfuss S, Lutjohann D, von Bergmann K: A simplified micro-method for quantification of fecal excretion of neutral and acidic sterols for outpatient studies in humans. J Lipid Res. 1991, 32 (11): 1861-1867.
Dzeletovic S, Breuer O, Lund E, Diczfalusy U: Determination of cholesterol oxidation products in human plasma by isotope dilution-mass spectrometry. Anal Biochem. 1995, 225 (1): 73-80. 10.1006/abio.1995.1110.
Podszun MC, Grebenstein N, Hofmann U, Frank J: High-dose supplementation with natural alpha-tocopherol does neither alter the pharmacodynamics of atorvastatin nor its phase I metabolism in guinea pigs. Toxicol Appl Pharmacol. 2013, 266 (3): 452-458. 10.1016/j.taap.2012.11.018.
Campbell HA, Pitot HC, Potter VR, Laishes BA: Application of quantitative stereology to the evaluation of enzyme-altered foci in rat liver. Cancer Res. 1982, 42 (2): 465-472.
Buchmann A, Karcier Z, Schmid B, Strathmann J, Schwarz M: Differential selection for B-raf and Ha-ras mutated liver tumors in mice with high and low susceptibility to hepatocarcinogenesis. Mutat Res. 2008, 638 (1–2): 66-74.
Braeuning A, Menzel M, Kleinschnitz EM, Harada N, Tamai Y, Kohle C, Buchmann A, Schwarz M: Serum components and activated Ha-ras antagonize expression of perivenous marker genes stimulated by beta-catenin signaling in mouse hepatocytes. Febs J. 2007, 274 (18): 4766-4777. 10.1111/j.1742-4658.2007.06002.x.
Braeuning A, Vetter S, Orsetti S, Schwarz M: Paradoxical cytotoxicity of tert-butylhydroquinone in vitro: What kills the untreated cells?. Arch Toxicol. 2012, 86 (9): 1481-1487. 10.1007/s00204-012-0841-3.
Skehan P, Storeng R, Scudiero D, Monks A, McMahon J, Vistica D, Warren JT, Bokesch H, Kenney S, Boyd MR: New colorimetric cytotoxicity assay for anticancer-drug screening. J Natl Cancer Inst. 1990, 82 (13): 1107-1112. 10.1093/jnci/82.13.1107.
Pfaffl MW: A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001, 29 (9): e45-10.1093/nar/29.9.e45.
Bellosta S, Paoletti R, Corsini A: Safety of statins: focus on clinical pharmacokinetics and drug interactions. Circulation. 2004, 109 (23 Suppl 1): III50-III57.
Paine SW, Parker AJ, Gardiner P, Webborn PJ, Riley RJ: Prediction of the pharmacokinetics of atorvastatin, cerivastatin, and indomethacin using kinetic models applied to isolated rat hepatocytes. Drug Metab Dispos. 2008, 36 (7): 1365-1374. 10.1124/dmd.107.019455.
Hailfinger S, Jaworski M, Braeuning A, Buchmann A, Schwarz M: Zonal gene expression in murine liver: Lessons from tumors. Hepatology. 2006, 43 (3): 407-414. 10.1002/hep.21082.
Lau YY, Okochi H, Huang Y, Benet LZ: Multiple transporters affect the disposition of atorvastatin and its two active hydroxy metabolites: application of in vitro and ex situ systems. J Pharmacol Exp Ther. 2006, 316 (2): 762-771.
Stone NJ, Robinson JG, Lichtenstein AH, Bairey Merz CN, Blum CB, Eckel RH, Goldberg AC, Gordon D, Levy D, Lloyd-Jones DM, McBride P, Schwartz JS, Shero ST, Smith SC, Watson K, Wilson PW: 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults: A Report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. J Am Coll Cardiol. 2014, 63 (25 Pt B): 2889-2934.
Bachmanov AA, Reed DR, Beauchamp GK, Tordoff MG: Food intake, water intake, and drinking spout side preference of 28 mouse strains. Behav Genet. 2002, 32 (6): 435-443. 10.1023/A:1020884312053.
Park JE, Kim KB, Bae SK, Moon BS, Liu KH, Shin JG: Contribution of cytochrome P450 3A4 and 3A5 to the metabolism of atorvastatin. Xenobiotica. 2008, 38 (9): 1240-1251. 10.1080/00498250802334391.
Wlcek K, Svoboda M, Riha J, Zakaria S, Olszewski U, Dvorak Z, Sellner F, Ellinger I, Jager W, Thalhammer T: The analysis of organic anion transporting polypeptide (OATP) mRNA and protein patterns in primary and metastatic liver cancer. Cancer Biol Ther. 2011, 11 (9): 801-811. 10.4161/cbt.11.9.15176.
Tsuboyama T, Onishi H, Kim T, Akita H, Hori M, Tatsumi M, Nakamoto A, Nagano H, Matsuura N, Wakasa K, Tomoda K: Hepatocellular carcinoma: hepatocyte-selective enhancement at gadoxetic acid-enhanced MR imaging–correlation with expression of sinusoidal and canalicular transporters and bile accumulation. Radiology. 2010, 255 (3): 824-833. 10.1148/radiol.10091557.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/14/766/prepub
The authors thank Claudia Eser, Britta Klumpp, Johanna Mahr, Monika Seiler, and Elke Zabinsky for skillful technical assistance. This work was in part supported by the Medical Faculty of the University of Tübingen (Fortüne program) and by the Robert Bosch Foundation Stuttgart. We acknowledge support by Deutsche Forschungsgemeinschaft and Open Access Publishing Fund of Tuebingen University.
The authors declare that they have no competing interests.
ABr: conception and design of the study, animal experimentation, data analysis and interpretation, manuscript writing; PB: data acquisition; UH: LC-MS and GC analyses; ABu: statistical evaluation of data; MS: conception and design of the study. All authors read and approved the final manuscript.
Electronic supplementary material
About this article
Cite this article
Braeuning, A., Bucher, P., Hofmann, U. et al. Chemically induced mouse liver tumors are resistant to treatment with atorvastatin. BMC Cancer 14, 766 (2014). https://doi.org/10.1186/1471-2407-14-766
- Chemical carcinogenesis
- Hypolipidemic drug