Loss of Runt-related transcription factor 3 induces resistance to 5-fluorouracil and cisplatin in hepatocellular carcinoma

Introduction

Hepatocellular carcinoma (HCC) is the sixth most common cancer and the third most frequent cause of cancer-related mortality worldwide (1,2). Although patients with early-stage HCC can receive curable treatment, the prognosis of patients with advanced disease is relatively poor. Drug resistance contributes to the poor prognosis in patients with advanced HCC, and elucidation of the molecular mechanisms underlying drug resistance would facilitate the development of more effective therapeutic strategies (3,4).

Drug efflux is a major molecular mechanism thought to affect drug resistance in patients with HCC. Increased drug efflux can decrease the accumulation of anticancer drugs (5). Multidrug resistance proteins (MRPs) are members of the ATP-binding cassette (ABC) transporter superfamily and are involved in drug efflux (6), contributing to the drug resistance observed in patients with HCC (5). Notably, MRPs are upregulated in 5-fluorouracil (5-FU)-resistant cancer cells, and MRP5 expression has been shown to influence 5-FU resistance in pancreatic carcinoma cells (7,8). Furthermore, various studies have shown that there is a significant association between MRPs and 5-FU sensitivity (9–12). Drug resistance to cisplatin (CDDP), another common anticancer agent used for HCC chemotherapy (13–16), is also mediated by MRPs (17–20).

Human Runt-related transcription factor 3 (RUNX3), a tumor suppressor expressed in gastric cancers (21), regulates cell growth and apoptosis as a downstream effector of transforming growth factor-β (TGF-β) signaling (22). RUNX3 was originally reported as a tumor suppressor in gastric cancer (21) and has been shown to function as a tumor suppressor in HCC as well (23,24). We and other researchers have reported that the protein and mRNA expression of RUNX3 are decreased in HCC and that loss of RUNX3 expression induces various effects in HCC, including prevention of apoptosis, induction of cancer stem cell-like changes, and promotion of the epithelial-mesenchymal transition (EMT) (24,25). Moreover, RUNX3 has been shown to regulate MRPs in pancreatic cancer (26). However, the mechanisms through which RUNX3 and MRPs may mediate drug resistance in HCC are not completely understood.

Therefore, in the present study, we assessed the relationship between RUNX3 and MRP expression in HCC. We also evaluated the effects of RUNX3 re-expression on drug resistance to 5-FU and CDDP in HCC.

Materials and methods

Cell lines and cell culture

The human HCC cell lines Hep3B, Huh7 and HLF were obtained from the American Type Culture Collection (ATCC; Manassas, VA, USA). The cells were maintained in Dulbecco's modified Eagle's medium (DMEM; Invitrogen, Carlsbad, CA, USA), supplemented with 10% heat-inactivated fetal bovine serum (FBS), 1% non-essential amino acids, 1% sodium pyruvate and 1% penicillin/streptomycin solution (all from Sigma, St. Louis, MO, USA). The cells were cultured at 37°C in an atmosphere containing 5% CO2 and 95% air. Cell growth was halted at subconfluency under restricted serum conditions with 0.1% dialyzed FBS for 36 h before the experiments, if needed.

Ectopic RUNX3 expression

A human RUNX3 construct was obtained by reverse transcription-polymerase chain reaction (RT-PCR)-based cloning of the gene from normal human hepatocytes (Sanko Junyaku, Co., Ltd., Tokyo, Japan). Human RUNX3 and/or chloramphenicol acetyltransferase (CAT; mock) constructs were transfected into Hep3B, Huh7 and HLF cells using FuGENE 6 transfection reagent (Roche Diagnostics, Basel, Switzerland). At least two independent transfections were performed for each cell line. The cells were incubated under serum-starved conditions for 24 h and used for the following experiments.

Immunoblot analysis

Cells were plated in 6-well plastic tissue culture dishes and grown to confluency. The cells were washed twice with cold phosphate-buffered saline (PBS) and lysed in 150 µl of sample buffer [100 mNM Tris-HCl (pH 6.8), 10% glycerol, 4% sodium dodecyl sulfate (SDS), 1% bromophenol blue and 10% β-mercaptoethanol]. The samples were resolved by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis and transferred to Immobilon-P polyvinylidene difluoride membranes (Millipore Corporation, Bedford, MA, USA). The membranes were blocked using Tris-buffered saline with Tween-20 (TBS-T; Sigma) containing 5% bovine serum albumin for 1 h. The membranes were then incubated with antibodies against RUNX3, MRP1 and MRP2 (all from Abcam, Cambridge, MA), MRP3 (Sigma), MRP5 (Abcam), and β-actin (Sigma) overnight at 4°C. The membranes were washed 3 times with TBS-T and probed with horseradish peroxidase-conjugated secondary antibodies before being developed with an enhanced chemiluminescence western blotting detection system (Amersham Biosciences, Piscataway, NJ, USA).

MTT assay

Cell proliferation was assessed using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assays. Briefly, cells were grown in 96-well plastic tissue culture dishes at a density of 1×104 cells/ml. After 24 h of quiescence, cells were cultured for the indicated period with or without 10% FBS. Then, 10 µl of MTT (5 mg/ml in PBS) was added to each well, and the cells were incubated for an additional 4 h at 37°C. The purple-blue formazan precipitate was dissolved in 100 µl of dimethyl sulfoxide (DMSO). Mitochondrial activity, which reflected cell viability, was evaluated by measuring the optical density at 570 nm on a microplate reader (Bio-Rad, Hercules, CA, USA).

To evaluate 5-FU and CDDP resistance, the cells were treated with various concentrations of 5-FU and/or CDDP for 72 h, and MTT assays were then performed as described above.

Gene silencing of RUNX3 with small interfering RNA (siRNA)

RUNX3-expressing Hep3B and Huh7 cells were transfected with either scrambled negative control siRNA or RUNX3 siRNA (Applied Biosystems, Foster City, CA, USA) using RNAiFect transfection reagent (Qiagen, Hilden, Germany). The cells were incubated for 24 h, and then serum starved for 48 h. MTT assays were then performed.

HCC tissues and immunohistochemistry

A group of 23 patients [18 men (age range, 52–78 years; average age 65.1 years) and five women (age range, 55–74 years; average age, 65.8 years)] were included in the present study. Resected HCC tissues were obtained after receiving written informed consent that adhered to the stringent ethical criteria of the Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences. Immunohistochemistry was performed on formalin-fixed paraffin-embedded sections prepared from the resected tissue. Sections were dewaxed and dehydrated; after rehydration, endogenous peroxidase activity was blocked for 30 min in a methanol solution containing 0.3% hydrogen peroxide. Following antigen retrieval in citrate buffer, the sections were blocked again overnight at 4°C. The sections were probed with anti-RUNX3 mouse monoclonal antibodies (ab40278), anti-MRP1 monoclonal antibodies (ab32574), anti-MRP2 monoclonal antibodies (ab15603) (all from Abcam), anti-MRP3 monoclonal antibodies (M6567; Sigma) and anti-MRP5 monoclonal antibodies (ab24107; Abcam). The primary antibody was detected using a biotinylated anti-rabbit antibody or a biotinylated anti-mouse antibody (both from Dako Japan). The signal was amplified by avidinbiotin complex formation and was developed with diaminobenzidine, followed by dehydration in alcohol and xylene. The sections were then mounted and scored for RUNX3, MRP1, MRP2, MRP3 and MRP5 using a four-point scale: 0, negative; 1, weak signal; 2, intermediate signal; and 3, strong signal. All sections were scored independently by two observers without prior knowledge of the clinical background. All discrepancies in scoring were reviewed, and a consensus was reached. Statistical analyses were performed using JMP software (SAS Institute, Inc., Cary, NC, USA).

Gene expression profiling analysis in human HCC

To further investigate correlations between RUNX3 and MRP expression in HCC, publicly available HCC data sets were evaluated using Oncomine (http://www.oncomine.org). In brief, mRNA expression profiles for RUNX3, MRP1, MRP2, MRP3 and MRP5 were evaluated using RUNX3/106_at, RUNX3/204197_s_at, RUNX3/204198_s_at, MRP1/34384_at, MRP2/206155_at, MRP3/209641_s_at, and MRP5/209380_s_at, respectively, in HCCs from the human liver data sets. Statistical analyses were performed using JMP software.

Results

Ectopic RUNX3 expression reduces MRP expression in HCC cell lines

Ectopic RUNX3 protein expression was regulated in 3 HCC cell lines exhibiting positive or negative endogenous RUNX3 expression (Hep3B, Huh7 and HLF cells) (24). RUNX3 protein expression was detected by immunoblot analysis after transfection with the RUNX3 plasmid (Fig. 1). Hep3B, Huh7 and HLF cells expressed MRP1, MRP2, MRP3 and MRP5. Ectopic RUNX3 protein expression generally decreased MRP expression levels in all 3 cell lines. Expression of MRP1, MRP2, MRP3 and MRP5 in the RUNX3-expressing Hep3B, Huh7 and HLF cells was weaker than that in the control CAT-expressing cells (Fig. 1).

Figure 1 Immunoblot analysis. Eukaryotic expression constructs for CAT (mock) and RUNX3 were introduced into Hep3B, Huh7 and HLF cells. Cell lysates were collected 48 h after transfection. Immunoblot analysis was performed using antibodies against RUNX3, MRP1, MRP2, MRP3, MRP5 and β-actin. Immunoblotting for β-actin was used to verify equal loading of cellular proteins. Representative blots of more than 3 independent experiments are shown.

Ectopic RUNX3 protein expression suppresses cell growth and increases 5-FU and CDDP sensitivity

Ectopic RUNX3 expression suppressed cell growth in the Hep3B and Huh7 cells compared with that in the control Hep3B and Huh7 cells at 3 days after transfection (Fig. 2). Next, we analyzed the effects of RUNX3 on chemosensitivity in the RUNX3- or CAT (mock)-transfected Hep3B and Huh7 cells. RUNX3 expression enhanced 5-FU sensitivity in both cell lines; the 50% inhibitory concentration (IC50) of 5-FU decreased from 8.16 to 4.84 nM and from 9.81 to 4.76 nM in the Hep3B and Huh7 cells, respectively (Fig. 2A). RUNX3 expression also enhanced CDDP sensitivity in both cell lines; the IC50 of CDDP decreased from 6.76 to 4.58 nM and from 9.28 to 4.57 nM in the Hep3B and Huh7 cells, respectively (Fig. 2B).

Figure 2 Cell growth activity and sensitivity to chemotherapeutic agents. Hep3B and Huh7 cells were treated with the indicated concentrations of 5-FU (A) and CDDP (B) for 3 days. Cell viability was measured by MTT assay. All results are expressed as ratios relative to the value on day 1. Data represent the mean ± SE of more than three independent experiments performed in triplicate.

MRP expression is inversely correlated with RUNX3 expression in human HCC tissues

Twenty-three HCC tissue samples were available for comparison of MRP and RUNX3 protein expression by immunohistochemistry. Representative images of tissues with different levels of MRP1 expression, i.e., negative (score 0), weak signal (score 1), intermediate signal (score 2) and strong signal (score 3), are shown in Fig. 3A–D. Correlation analysis showed that high MRP expression scores were generally observed in tissues with low RUNX3 expression (Fig. 4).

Figure 3 Immunohistochemical analysis of MRP expression. The images show the immunohistochemical staining of MRP1 (A, score of 0; B, score of 1; C, score of 2; and D, score of 3). Scale bar, 100 µm.

Figure 4 Correlation between RUNX3 expression and (A) MRP1, (B) MRP2, (C) MRP3 and (D) MRP5 expression scores in human HCC tissues. Plots of MRP expression scores are shown compared with RUNX3 expression scores.

Gene expression profiling analysis in human HCC

Lastly, we evaluated the effects of ectopic RUNX3 expression on MRPs in order to elucidate the mechanisms underlying RUNX3 expression-induced chemosensitivity. We analyzed Oncomine data sets to examine the correlation between the expression of RUNX3 and MRPs. The results revealed that RUNX3 mRNA expression was inversely correlated with MRP1, MRP2, MRP3 and MRP5 mRNA expression (MRP1, r=−0.6007, P=0.1538; MRP2, r=−0.55729, P<0.05; MRP3, r=−0.53741, P<0.05; MRP5, r=−0.36607, P<0.05; Fig. 5).

Figure 5 Correlation between RUNX3 and MRP expression in human HCC data sets. The correlation between RUNX3 and MRP expression was analyzed using publically available microarray data sets (http://www.oncomine.org). The correlation coefficients and P-values of the relationships among RUNX3, MRP1, MRP2, MRP3 and MRP5 expression are shown. The 95% tolerance ellipses for pairs of variables have been plotted.

Discussion

Chemoresistance is a major challenge encountered during the therapeutic treatment of HCC. In the present study, we evaluated the relationship between RUNX3 expression and chemosensitivity in HCC. RUNX3 was found to act as a tumor suppressor in HCC, consistent with previous studies showing that RUNX3 is frequently lost in HCC (23,27–29) and that loss of RUNX3 contributes to the malignant transformation of HCC (23–25).

In a previous study of pancreatic cancer, we reported that the RUNX3 expression status affects gemcitabine sensitivity by attenuating MRP expression (26). Therefore, we hypothesized that RUNX3 expression may influence chemosensitivity in HCC. Drug resistance can be induced by several cellular processes. For example, MRPs mediate drug efflux, which decreases the accumulation of drugs within cancer cells. In the present study, we found that MRP expression generally decreased following ectopic expression of RUNX3 in all 3 HCC cell lines examined. Moreover, these cells exhibited higher chemosensitivity to 5-FU and CDDP than control cells, further supporting the role of MRPs in drug resistance in these cells.

Consistent with a previous study in pancreatic cancer, we found that RUNX3 blocked MRP expression in HCC cells. Moreover, MRP expression varied in HCC tissues and was positively correlated with RUNX3 protein expression. Since the number of HCC tissues in the present study was relatively small, we also assessed the relationship between MRPs and RUNX3 expression using the Oncomine database; this analysis further supported the positive correlation between RUNX3 and MRP expression. These results indicated that RUNX3 expression may regulate MRP expression. Notably, RUNX3 expression has been shown to sensitize gastric cancer cells to chemotherapeutic drugs by downregulating MRP1 through inhibition of MRP1 promoter activity (30). Thus, our findings suggest that RUNX3 may regulate MRP expression by inhibiting promoter activity in HCC cells and that targeting of RUNX3 and related signaling molecules may be a potential treatment modality for HCC.

Although we assessed the relationship between MRPs and RUNX3 expression in the present study, other factors have also been implicated in 5-FU and CDDP resistance. Multidrug resistance 1 (MDR1/ABCB1) and other ABCB transporters are also involved in the resistance against 5-FU (10,31,32). CDDP resistance is established via a multifactorial mechanism including drug efflux and drug inactivation (33–35). In the present study, we did not evaluate the effects of RUNX3 protein expression on these mechanisms; thus, further studies are necessary.

In conclusion, the loss of RUNX3 expression may upregulate MRP expression, thereby contributing to 5-FU and CDDP resistance in patients with HCC. Moreover, re-expression of RUNX3 downregulated MRP expression and resensitized HCC cells to 5-FU and CDDP.

Acknowledgments

The authors thank Shin-ichi Nishina and Minoru Matsubara for their valuable suggestions.

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References