Susceptibility of hepatoma-derived cells to histone deacetylase inhibitors is associated with ID2 expression

Introduction

Hepatocellular carcinoma (HCC) is one of the most lethal malignancies worldwide (1,2). HCC is caused mainly by chronic liver inflammation due to hepatitis B virus, hepatitis C virus (HCV) or alcohol abuse (1). Despite curative resection and recent advances in treatments, the clinical course of HCC is variable and many patients suffer recurrence after surgery. Poor prognoses in cases of HCC can be explained largely by the high rate of intrahepatic recurrence (IHR), which results from metastatic spread of cancer cells (3).

Previously, we identified a gene, inhibitor of DNA binding 2 (ID2), that is significantly downregulated in HCCs, especially in advanced HCCs, relative to surrounding liver tissues (4,5). Moreover, we found that ID2 is a portal vein invasion-related gene in HCV-related HCC (6) and that ID2 negatively regulates the invasive potential of cancer cells (7). Therefore, HCC patients with low ID2 expression have poor prognoses (7). ID2 belongs to a protein family that comprises ID1 to ID4; these proteins have a helix-loop-helix structure and form heterodimers with basic helix-loop-helix transcription factors to act as dominant-negative inhibitors of transcription (8–10). IDs are involved in proliferation processes, differentiation, development, senescence and angiogenesis (11–15), and are linked to various malignant tumors (16–31).

In this study, we searched for antitumor drugs that are effective against cells with low ID2 expression because such antitumor drugs might be useful in the treatment of patients who have HCC and a poor prognosis. We found that alteration of ID2 expression affected the susceptibility of cells to histone deacetylase (HDAC) inhibitors and that HDAC inhibitors were the only antitumor drugs tested for which alteration of ID2 expression had an effect. HDAC inhibitors have emerged as a new class of antitumor agents (32–34). HDAC inhibitors can cause multiple epigenetic changes in aberrant cells. Treatment with HDAC inhibitors most frequently induces apoptosis (35–37). Although their precise mode of action remains uncertain, HDAC inhibitors can modulate the cell cycle, apoptosis, angiogenesis, invasion and metastases (32,33,38–40). Here, we aimed to investigate how and whether ID2 affected the anti-tumor activity of sodium butyrate (NaB), an HDAC inhibitor.

Materials and methods

Hepatoma cell lines

Human hepatoma-derived cell lines, HLE and HuH-7, were purchased from the Health Science Research Resources Bank (Osaka, Japan). Cells were cultured in DMEM (Nissui Pharmaceutical, Tokyo, Japan) containing 10% heat-inactivated fetal bovine serum (Life Technologies, Tokyo, Japan) and supplemented with penicillin (100 U/ml), streptomycin (100 μg/ml) and sodium bicarbonate (1.5 g/l) at 37°C in 5% CO2 in air. As in our previous report (7), ID2-knockdown and ID2-overexpression were accomplished by transfection of HuH-7 and HLE cells with ID2-specific small interfering RNAs (siRNAs) or an ID2-expression plasmid vector, respectively. HuH-7 and HLE cells transfected with control siRNA or empty pcDNA3.1(-) plasmid DNA were used as the respective control.

Administration of histone deacetylase inhibitors

NaB (Sigma-Aldrich, Tokyo, Japan), sodium 4-phenyl-butyrate (NaPB; Funakoshi, Tokyo, Japan), tricostatin A (TSA; Sigma-Aldrich), suberoylanilide hydroxamic acid (SAHA; Cosmo Bio, Tokyo, Japan), MS-275 (Sigma-Aldrich), apicidin (Sigma-Aldrich) and HC-toxin (Sigma-Aldrich) were each used as an HDAC inhibitor in this study. HDAC inhibitors were added to cultures 24 h after cells had been seeded; cultures were then further incubated with the inhibitor for defined periods at 37°C in 5% CO2 in air.

MTS assay

The CellTiter 96 AQueous One Solution Cell Proliferation Assay (Promega, Tokyo, Japan) which includes 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) was used according to the manufacturer’s instructions to evaluate cell survival. Cells (3×103) were seeded into the wells of 96-well plates and cultivated. At the appropriate time, MTS was added to the cells, which were then incubated for 2 additional hours at 37°C. The optical density of the culture medium at 492 and 650 nm were then measured by using an EnVision plate reader (PerkinElmer, Waltham, MA). Triplicate wells were analyzed in each assay.

Annexin V staining

The Annexin V-FLUOS Staining Kit (Roche Diagnostics, Tokyo, Japan), which includes Annexin V/propidium iodide (PI), was used according to the manufacturer’s instructions to detect apoptosis. The cultures were observed under a fluorescent microscope (IX71; Olympus, Tokyo, Japan). Simultaneously, Hoechst33342-positive cells were counted as total number of cells in cultures; Hoechst33342 was purchased from Sigma-Aldrich.

Semiquantitative real-time RT-PCR

Semiquantitative real-time RT-PCR (semi-qRT-PCR) was performed as described previously (7,41) with minor modifications. Real-time PCR amplification was performed using the LightCycler 480 Probe Master and Universal ProbeLibrary Probes in a LightCycler System Version 3 (all from Roche Diagnostics). Primers and probes that were used are listed in Table I. Amplification was performed according to a two-step cycle procedure consisting of 45 cycles of denaturation at 95°C for 10 sec and annealing/elongation at 60°C for 30 sec. We used the Δ/Δ threshold cycle method to semiquantitatively measure mRNA levels; glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and β-actin (ACTB) were both used as reference genes. All values of mRNA levels are expressed relative to control.

Table I The primers and hydrolysis probes used in this study.

Table I

The primers and hydrolysis probes used in this study.

Primers and probes	Sequence (5′→3′)
ID2
5′-primer	ATATCAGCATCCTGTCCTTGC
3′-primer	AAAGAAATCATGAACACCGCTTA
Hydrolysis probe	UPL Probe #5a
BCL2
5′-primer	TTGACAGAGGATCATGCTGTACTT
3′-primer	ATCTTTATTTCATGAGGCACGTT
Hydrolysis probe	UPL Probe #6a
BCL2L1 (BCL-XL)
5′-primer	GCTGAGTTACCGGCATCC
3′-primer	AGATTCTGAAGGGAGAGAAAGAGA
Hydrolysis probe	UPL Probe #83a
BAX
5′-primer	ATGTTTTCTGACGGCAACTTC
3′-primer	ATCAGTTCCGGCACCTTG
Hydrolysis probe	UPL Probe #57a
CDKN1A (P21)
5′-primer	TCACTGTCTTGTACCCTTGTGC
3′-primer	GGCGTTTGGAGTGGTAGAAA
Hydrolysis probe	UPL Probe #32a
GAPDH
5′-primer	AGCCACATCGCTCAGACAC
3′-primer	GCCCAATACGACCAAATCC
Hydrolysis probe	UPL Probe #60a
ACTB
5′-primer	CCAACCGCGAGAAGATGA
3′-primer	CCAGAGGCGTACAGGGATAG
Hydrolysis probe	UPL Probe #64a

a The number of Universal ProbeLibrary probes (Roche Applied Bioscience).

Statistical analysis

Data are presented as mean ± standard deviation. Dunnett’s test for multiple comparisons was used to evaluate the differences between three groups. Calculations were performed using SPSS Statics 17.0 software (IBM, Tokyo, Japan). P<0.05 was considered statistically significant.

Results

Susceptibility to histone deacetylase inhibitors in HCC-derived cell lines in which ID2 was knocked down or overexpressed

We used the MTS assay and previously established HCC-derived cell lines in which ID2 expression was suppressed or enhanced (7) to examine the susceptibility of HCC cells to antitumor drugs. Among the tested antitumor drugs, the antitumor activity of an HDAC inhibitor, NaB, was increased in ID2 knockdown cells and decreased in ID2-overexpressing cells (Fig. 1). Similar results were obtained with other HDAC inhibitors including TSA, SAHA, PBA, MS-275, apicidin and HC-toxin (Figs. 2 and 3). However, for other types of antitumor agents than HDAC inhibitors (e.g., 5-fluorouracil, cisplatin, docetaxel and etoposide), such results were not observed (Fig. 4).

Figure 1 ID2 levels and antitumor activity of NaB. Cells were subjected to an MTS assay 72 h after 20 mM NaB administration; NaB is one of several HDAC inhibitors that had an effect on survival of HCC-derived cells. Cell viability was lower in HCC-derived cells transfected with ID2 knockdown siRNAs than those transfected with control siRNA. Cell viability was higher in HCC-derived cells that overexpressed ID2 than in those transfected with an empty vector. *P<0.05 compared with HuH-7/siCont or HLE/pCont.

Figure 2 The antitumor activity of HDAC inhibitors in ID2 knockdown cells. Cells were subjected to an MTS assay to evaluate the effect of ID2 on the antitumor activity of HDAC inhibitors other than NaB. Each HDAC inhibitor had an effect similar to that of NaB (Fig. 1) on the ID2 knockdown cells. *P<0.05 compared with HuH-7/siCont.

Figure 3 The antitumor activity of HDAC inhibitors in cells that overexpressed ID2. Cells were subjected to an MTS assay to evaluate the effect of ID2 on the antitumor activity of HDAC inhibitors other than NaB. In cells that overexpressed ID2, each HDAC inhibitor, except SAHA, had an effect similar to that of NaB (Fig. 1). *P<0.05 compared with HLE/pCont.

Figure 4 ID2 levels and antitumor activity. Cells were subjected to MTS assay 72 h after administration of the indicated antitumor drugs,. †P<0.05 compared with HuH-7/siCont or HLE/pCont.

Influence of ID2 on NaB-induced apoptosis

In HLE derivatives treated with 20 mM NaB for 72 h, the number of cells positive for both Annexin V and PI (late apoptosis) was significantly lower among ID2-overexpressing cells than empty-vector control cells (approximately 44 vs. 87%, respectively) (Fig. 5B). For HuH-7 derivatives treated with 20 mM NaB for 72 h, the percentage of cells positive for both Annexin V and PI (late apoptosis) was 34% among ID2-knockdown cells and 25% among siRNA-transfected control cells (Fig. 5A). In both HLE and HuH-7 derivatives, Annexin V single-positive cells (early apoptosis) showed same tendency with the Annexin V and PI double-positive cells, although Annexin V single-positive cells were less than 10% of each cell type.

Figure 5 ID2 levels and apoptosis caused by NaB. Cells were stained with Annexin V/Propidium iodide (PI)/Hoechst 33342 after 20 mM NaB had been administered for 72 h; cells were then assessed by fluorescence microscope. Cells positive for both Annexin V and PI staining were considered to be in the late stage of apoptosis. Cultures containing ID2 knockdown cells had higher percentages of apoptotic cells than did cultures with control siRNA transfected cells. Cultures with ID2 overexpressing cells had lower percentages of apoptotic cells than did cultures containing cells transfected with empty vector. *P<0.05 compared with HuH-7/siCont or HLE/pCont.

We examined expression of apoptosis-related genes in HLE and HuH-7 cells that had been treated with NaB. Following addition of 20 mM NaB, about half of the HLE cells had died within 24 h and about half of the HuH-7 cells had died within 48 h. Treatment with NaB induce expression of BCL2 mRNA (an anti-apoptotic mRNA) in HuH-7 cells transfected with control siRNA and in HLE cells transfected with empty vector; however, this NaB-dependent induction was suppressed in HuH-7 cells transfected with ID2-specific siRNAs and enhanced in HLE cells that overexpressed ID2 (Fig. 6A and B). Levels of another anti-apoptotic mRNA, BCL2L1 (BCL-XL), decreased immediately after addition of NaB in control HuH-7 cells and in ID2-knockdown HuH-7 cells; 48 h after NaB addition, BCL2L1 levels had partially recovered in control cells, but they had not recovered in ID2-knockdown HuH-7 cells (Fig. 6C). HLE cells that overexpressed ID2 and control HLE cells did not differ significantly in BCL2L1 mRNA levels (Fig. 6D). The mRNA level of BAX, a pro-apoptotic gene, was not influenced by ID2 expression (Fig. 6E and F).

Figure 6 Changes in expression of anti-apoptotic genes following NaB administration. The mRNA levels of BCL2, BCL2L1 and BAX were measured after 20 mM NaB administration for 0, 6, 24 or 48 h. (A and B) BCL2 mRNA level was induced by NaB administration when compared to the induction in control cells, this NaB-dependent induction was suppressed in ID2 knockdown cells and enhanced in cells that overexpressed ID2. (C and D) The BCL2L1 mRNA level decreased immediately after NaB administration and was then partially restored. In ID2 knockdown cells, the restoration of BCL2L1 expression was largely suppressed relative to that in control cells. **Both ID2-targeted cells showed P<0.05 compared with control cells.

Discussion

In this study, ID2 negatively regulated the susceptibility of HCC-derived cells to HDAC inhibitors (Figs. 1–3). Several types of antitumor drugs were tested for their effects on HCC-derived cells with altered ID2 levels; cells became more susceptible HDAC inhibitors when ID2 was downregulated, but no other type of antitumor drug had this effect (Fig. 4). Previous reports showed that ID2 expression was linked to poor prognosis of HCC (5–7). ID2 expression is low in HCC samples that also exhibit other poor prognosis indicators such as poor differentiation or portal vein invasion. Therefore, we reasoned that HDAC inhibitors may be useful for treating HCC characterized by indicators of poor prognosis.

HDAC inhibitors have emerged as a new class of antitumor drugs that are intended to modulate epigenetic regulation and several clinical trials have been conducted (42,43). Although HDAC inhibitors act on HDACs specifically, genome-wide acetylation of chromatin as a result of HDAC inhibition cause changes in the expression of many genes (45–47). Interestingly, addition of NaB to HCC-derived cell lines induced expression of anti-apoptotic BCL2 and this induction of BCL2 was positively regulated by ID2 expression (Fig. 6). This finding indicates that ID2 may exert an anti-apoptotic function via regulation of anti-apoptotic genes in the presence of this HDAC inhibitor (Figs. 5 and 6), although a pro-apoptotic gene, BAX, was not influenced by ID2 expression (Fig. 6). Cyclin-dependent kinase inhibitor 1A (CDKN1A; p21, Cip1) is one of the genes activated by HDAC inhibitors and activated CDKN1A inhibits the transition from G1 to S phase (48). The activation of CDKN1A induced by HDAC inhibitors results in growth arrest and apoptosis in several malignant cell types (47,49,50). We also observed NaB-mediated induction of CDKN1A and this induction was significantly suppressed by ID2 overexpression (data not shown). In ID2 knockdown cells, however, that NaB-mediated CDKN1A induction was not affected. The expression of ID2 itself was gradualy induced following the addition of NaB (data not shown). This increase in ID2 expression might be an endogenous defensive effect in response to HDAC inhibitors. Because ID2 acts as a dominant-negative inhibitor of basic helix-loop-helix transcription factors by forming heterodimers (8–10), some of counter partners forming heterodimers with ID2 may responsible for HDAC susceptibility.

We suggest that ID2 could serve as a predictive marker of the response of HCC to HDAC inhibitors. ID2 influences the susceptibility of HCC cells to the HDAC inhibitor by regulating the expression of anti-apoptotic genes. Further investigation of the mechanism by which ID2 affects susceptibility to HDAC inhibitors, and of the influence of ID2 on DNA methylation are needed because histone acetylation and DNA methylation are each correlated with epigenetic regulation. Biomarkers for clinical response are strongly needed for improvement of patients’ quality of life and also medical economics. ID2 may be useful as a biomarker of the likely response of HCC to HDAC inhibitors; moreover, further research on ID2 expression in HCC may contribute to the identification of new molecular targets that can be altered to enhance the effects of HDAC inhibitors. Such advances may lead to the improvement of antitumor therapy that is based on HDAC inhibitors.

Acknowledgements

This study was partly supported by JSPS KAKENHI Grant Number 18390366, 24659610, Research Fellowships of the Japan Society for the Promotion of Science for Young Scientists (JSPS KAKENHI Grant Number 187616) and the New Frontier Project of Yamaguchi University School of Medicine.

References