Vesnarinone, a differentiation inducing drug, directly activates p21^waf1 gene promoter via Sp1 sites in a human salivary gland cancer cell line

Abstract

We previously demonstrated that a differentiation inducing drug, vesnarinone induced the growth arrest and p21^waf1 gene expression in a human salivary gland cancer cell line, TYS. In the present study, we investigated the mechanism of the induction of p21^waf1 gene by vesnarinone in TYS cells. We constructed several reporter plasmids containing the p21^waf1 promoter, and attempted to identify vesnarinone-responsive elements in the p21^waf1 promoter. By the luciferase reporter assay, we identified the minimal vesnarinone-responsive element in the p21^waf1 promoter at −124 to −61 relative to the transcription start site. Moreover, we demonstrated by electrophoretic mobility shift assay that Sp1 and Sp3 transcription factors bound to the vesnarinone-responsive element. Furthermore, we found that vesnarinone induced the histone hyperacetylation in TYS cells. These results suggest that vesnarinone directly activates p21^waf1 promoter via the activation of Sp1 and Sp3 transcription factors and the histone hyperacetylation in TYS cells.

British Journal of Cancer (2002) 87, 1042–1046. doi:10.1038/sj.bjc.6600592 www.bjcancer.com

© 2002 Cancer Research UK

We have previously demonstrated that a differentiation inducing drug, vesnarinone inhibits the growth of a human salivary gland cancer cell line, TYS, and induces the expression of p21^waf1, a potent inhibitor of cyclin dependent kinase (Sato et al, 1997a; Kawamata et al, 1998). Vesnarinone is currently used as a chemotherapeutic agent for head and neck cancer combined with radiation in several countries, such as Japan (Sato et al, 1997b,c), the United States and India. p21^waf1 is a gene functioning as a cell cycle blocker, and its expression is usually regulated at transcriptional level. p21^waf1 is known to inhibit cyclin dependent kinase activity in p53-mediated cell cycle arrest induced by DNA damage (El-Deiry et al, 1993). Further studies have indicated that p21^waf1 is also regulated by other transcription factors during cell differentiation and growth arrest (Dulic et al, 1994; Jiang et al, 1994). p21^waf1 promoter contains not only p53-binding sites but also several transcription factor responsive elements (Datto et al, 1995; Nakano et al, 1997). One of the responsive elements is for a transcription factor, Sp1. Sp1 responsive elements are located on the upstream of TATA box of p21^waf1 promoter. It is reported that several extracellular stimuli including butyrate (Nakano et al, 1997), transforming growth factor-β (Datto et al, 1995), phorbol esters (Biggs et al, 1996), okadaic acid (Biggs et al, 1996) and retinoic acid (Liu et al, 1996) activate the transcription of p21^waf1 gene through the Sp1 responsive elements.

Because TYS cells are reported to have a mutated p53 gene (Sato et al, 1997a), the expression of p21^waf1 gene and the growth arrest induced by vesnarinone may be conducted by the p53-independent pathway in TYS cells. In order to use vesnarinone more effectively on the patients with several malignancies, including head and neck cancer, the molecular mechanisms of the growth inhibitory effect of vesnarinone should be studied. In this experiment, we attempted to identify the vesnarinone-responsive elements in the p21^waf1 promoter, and clarify the molecular mechanisms of transcriptional activation of p21^waf1 gene by treatment with vesnarinone in a human salivary gland cancer cell line, TYS.

MATERIALS AND METHODS

Cell culture and reagents

TYS cells (Yanagawa et al, 1986) were grown in Dulbecco's modified Eagle medium (DMEM; Life Technologies, Inc., Gaithersburg, MD, USA) supplemented with 10% foetal calf serum (FCS; Bio-Whittaker, Walkersville, MD), 100 μg ml⁻¹ streptomycin, 100 U ml⁻¹ penicillin (Life Technologies, Inc.), and 0.25 μg ml⁻¹ amphotericin B (Life Technologies, Inc.) in a humidified atmosphere of 95% air and 5% CO₂ at 37°C. Vesnarinone (Otsuka Pharmaceutical Company, Tokyo, Japan) was dissolved in dimethyl sulphoxide (DMSO; Sigma, St. Louis, MO, USA) at a concentration of 10 mg ml⁻¹ as the first stock solution, and the first stock solution was diluted with the complete culture medium described above. Trichostatin A (TSA; Wako, Osaka, Japan) was dissolved in ethanol at a concentration of 1 mg ml⁻¹, and diluted with the complete culture medium at 10 μg ml⁻¹.

Plasmid preparation

The human wild-type p21^waf1 promoter luciferase fusion plasmid, WWP-Luc (El-Deiry et al, 1993), was a kind gift from Dr B Vogelstein (The Johns Hopkins Oncology Center). The 2.4-kilobase pair genomic fragment was subcloned into HindIII (Takara Biomedicals, Kusatsu, Japan) site of the luciferase reporter vector, pGL3-Basic (Promega, Madison, WI, USA) to generate pGL3-WWP (Kawamata et al, 1999) (Figure 1). pGL3-WWP was digested with PstI (Takara Biomedicals) and BglII (Takara Biomedicals), and re-ligated to generate pGL3-WWP-0.2 (Figure 1). pWP124 and pWPdel-SmaI (Nakano et al, 1997) (Figure 1) were kind gifts from Dr Toshiyuki Sakai (Kyoto Prefectural University of Medicine).

Figure 1.

Plasmid construction. pGL3-WWP is a reporter construct containing 2.3 kb p21^waf1 promoter sequence. pGL3-WWP-0.2, pWP124 and pWPdel-SmaI are 5′-deletion constructs of the p21^waf1 promoter. pGL3-WWP-0.2 contains 225 bp of p21^waf1 promoter sequence. pWP124 contains 134 bp and pWPdel-SmaI contains 70 bp of p21^waf1 promoter sequence.

Transient transfection and luciferase assay

TYS cells (5×10⁵ cells dish⁻¹) were seeded in 35 mm culture dish (Falcon; Becton Dickinson Labware, Lincoln Park, NJ, USA) in DMEM supplemented with 10% FCS. Twenty-four hours later, the cells were transfected with 5 μg of reporter plasmid DNA by using Superfect reagent (QIAGEN, Hilden, Germany). Fifteen hours after transfection, vesnarinone (50 μg ml⁻¹) was added, and 20 h later, cell lysates were collected. Luciferase activities were measured by Promega luciferase assay Kit (Promega). The luciferase activities were normalised by the amount of protein. Each experiment was repeated at least three times.

Electrophoretic mobility-shift assay

TYS cells (1.5×10⁶ cells dish⁻¹) were seeded in 100 mm culture dish (Falcon) in DMEM supplemented with 10% FCS. Twenty-four hours later, cells were treated with vesnarinone (50 μg ml⁻¹) for 15, 30 and 45 min. Cell lysates were prepared according to the method described by Chin et al (1996). In brief, cells were lysed with 50 mM HEPES-KOH (pH 7.9) buffer containing 400 mM NaCl, 0.2% NP-40, 10% glycerol, 0.1 mM EDTA, 1 mM dithiothreitol (DTT), 1 mM sodium orthovanadate, 0.5 mM phenylmethanesulphonyl fluoride (PMSF), 1 μg ml⁻¹ of aprotinin, 1 μg ml⁻¹ of leupeptin, and 1 μg ml⁻¹ of pepstatin A. The protein concentrations of samples were determined with a Bio-Rad protein assay kit (Bio-Rad, Hercules, CA, USA). Double stranded oligonucleotides, (Sp1-A: 5′-GAG GGC GGT CCC GGG CGG CG-3′, and Sp1-B: 5′-GAG GCG GGC CCG GGC GGG GCG GTT G-3′) (Figure 2) were labelled with [γ-³²p]ATP (Amersham Pharmacia Biotech., Uppsala, Sweden) by T4 polynucleotide kinase (Promega), and purified by a spin column system (Amersham Pharmacia Biotech.). Sp1-A contains two Sp1 sites, and Sp1-B contains three Sp1 sites (Figure 2). The binding reaction mixtures consisted of 12 μg of cell lysates and 1 μl of the radiolabelled probe (approximately 5×10⁴ c.p.m.) in a binding buffer of 10 mM HEPES-KOH (pH 7.9), 0.1 mM EDTA, 0.01% NP-40, 100 μg ml⁻¹ of poly (dI-dC) (Amersham Pharmacia Biotech.), and 5% glycerol. The reaction was allowed to proceed for 20 min at room temperature before loading on 6% polyacrylamide gel at a low-ionic-strength buffer (0.5×TBE). The gels were run at 100 V on ice for approximately 1 h and dried. The dried gels were exposed to X-ray film. For supershift experiments, anti-Sp1 and/or anti-Sp3 antibody (Santa Cruz Biotechnology, Santa Cruz, CA, USA) was added to the reaction mixture, and the mixture was incubated for 20 min at room temperature before addition of the radiolabelled oligonucleotide.

Figure 2.

Human p21^waf1 promoter sequence located between −215 bp and +19 bp. The transcription start site is indicated by the number 0 on the sequence. Sp1 binding sites tentatively termed Sp1-1, Sp1-2, Sp1-3, Sp1-4, Sp1-5 and Sp1-6 from the upstream are indicated by underlining and shown below the sequence. Sp1-A contains Sp1-1 and Sp1-2 sites, and Sp1-B contains Sp1-4, Sp1-5 and Sp1-6 sites. TATA box is also indicated by underlining.

Histone acetylation in TYS cells by vesnarinone treatment

TYS cells were seeded in 100 mm culture dishes. Twenty-four hours later, vesnarinone (50 μg ml⁻¹) or TSA (10 μg ml⁻¹) was added to the medium. Sixteen hours later, the cells were collected and the nuclear extracts were prepared as follows; cells were suspended in 400 μl of hypotonic buffer (20 mM HEPES-KOH (pH 7.9) containing 1 mM EDTA, 1 mM DTT, 20 mM NaF, 1 mM sodium orthovanadate, 0.5 mM PMSF, 0.2% NP-40, 1 μg ml⁻¹ leupeptin, 10 units ml⁻¹ aprotinin, and 1 μg ml⁻¹ pepstatin A). Samples were centrifuged at 15 000 r.p.m. and the pellets were resuspended in 200 μl of hypertonic buffer (20 mM HEPES-KOH (pH 7.9) containing 1 mM EDTA, 1 mM DTT, 20 mM NaF, 1 mM sodium orthovanadate, 0.5 mM PMSF, 0.2% NP-40, 420 mM NaCl, 20% glycerol, 1 μg ml⁻¹ leupeptin, 10 units ml⁻¹ aprotinin, and 1 μg ml⁻¹ pepstatin A). Samples were incubated on ice for 20 min and were centrifuged at 15 000 r.p.m. for 15 min. The supernatants were used as nuclear extracts. The protein concentrations of samples were determined with a Bio-Rad protein assay. Samples were electrophoresed on SDS-polyacrylamide gel. Proteins from gels were transferred to nitrocellulose (Bio-Rad) and were detected with an anti-acetylated Histone H3 antibody (Upstate Biotechnology, Lake Placid, NY, USA) and an Amersham ECL kit (Amersham Pharmacia Biotech.).

RESULTS

Effect of vesnarinone on the activation of p21^waf1 promoter

Several reporter plasmids (Figure 1) were transiently transfected in TYS cells, and luciferase activity was examined. Vesnarinone apparently enhanced the luciferase activity from the pGL3-WWP reporter plasmid in TYS cells when compared with untreated control or DMSO treatment (Figure 3). Vesnarinone also enhanced the luciferase activity from the pGL3-WWP-0.2 plasmid, which contained a 215 bp promoter fragment lacking two p53 binding sites (Figure 3). Surprisingly, vesnarinone also enhanced the luciferase activity from the pWP124 containing only a 124 bp promoter fragment. However, vesnarinone did not activate a 60 bp promoter fragment of p21^waf1 in pWPdel-SmaI reporter plasmid (Figure 3).

Figure 3.

Luciferase assay. TYS cells were seeded in 35 mm dishes in DMEM supplemented with 10% FCS. Twenty-four hours later, the cells were transfected in triplicate with 5 μg of the several reporter plasmids by use of the Superfect reagent. Fifteen hours after transfection, vesnarinone (50 μg ml⁻¹) was added, and 20 h later, cell lysates were collected. The luciferase activities of the cell lysates were measured with a Promega luciferase assay kit. Luciferase activities were normalized by the amount of protein in cell lysates. Data are shown as means (bars, s.d.), and are representative of three separate experiments with similar results.

Electrophoretic mobility-shift assay

According to the results from the luciferase assay, the vesnarinone-responsive element exists within 77 bp region relative to the TATA element. This 77 bp region harbours four independent and two overlapping nearly consensus binding sites for transcription factor Sp1. They are tentatively termed Sp1-1, Sp1-2, Sp1-3, Sp1-4, Sp1-5 and Sp1-6 from the upstream (Figure 2). To determine if Sp1 or other proteins can interact with the vesnarinone-responsive element, electrophoretic mobility-shift assay was performed using the oligonucleotides containing the Sp1-binding sites. The Sp1-A contains Sp1-1 and Sp1-2 sites, and the Sp1-B contains Sp1-4, Sp1-5 and Sp1-6 sites (Figure 2). After treatment with vesnarinone for 30 min, we detected the shifted band when using the Sp1-A as a probe (Figure 4A). However, when we used the Sp1-B, we could not detect any shifted bands after vesnarinone treatment (Figure 4A). As shown in Figure 4B, the mobility shift was detectable at 30 min after treatment with 50 μg ml⁻¹ vesnarinone, and the intensity of the shifted band increased at 45 min after treatment. Moreover, this band completely disappeared by adding excess unlabelled Sp1-A oligonucleotide (data not shown).

Figure 4.

Electrophoretic mobility-shift assay (A, B) and supershift assay (C). Nuclear extracts prepared from vesnarinone (50 μg ml⁻¹)- or DMSO-treated TYS cells were incubated with a ³²P-labelled Sp1-A probe or Sp1-B probe (A). Nuclear extracts from TYS cells after treatment with vesnarinone for 15, 30, 45 min and a labelled Sp1-A probe were incubated in the binding buffer (B). Protein samples were prepared from TYS cells after treatment with vesnarinone for 45 min. Polyclonal antibody against Sp1 and/or Sp3 was added to the binding reaction and incubated for 20 min at room temperature before addition of a labelled Sp1-A probe (C).

Supershift assay

To elucidate whether the retarded bands represent the binding of Sp1 or Sp3, supershift assay was performed by the nuclear extracts pre-incubated with anti-Sp1 or anti-Sp3 antibody (Figure 4C). In the presence of anti-Sp1 or anti-Sp3 antibody, the intensity of the shifted band was markedly reduced. The shifted band completely disappeared in the presence of anti-Sp1 and anti-Sp3 antibody together. When pre-immune rabbit-IgG was added as a negative control, the intensity of the band was slightly reduced. However, the effect of pre-immune IgG was much weaker than that of anti-Sp1 or anti-Sp3 antibody. Thus, the effect of pre-immune IgG was probably due to non-specific interference of the IgG protein with the binding of Sp1 or Sp3 protein and DNA.

Histone acetylation in TYS cells induced by vesnarinone

We investigated whether or not vesnarinone induced histone acetylation in TYS cells. Vesnarinone clearly induced histone acetylation in TYS cells like as TSA did (Figure 5).

Figure 5.

Histone acetylation in TYS cells induced by vesnarinone. Nuclear extracts were prepared from TYS cells after treatment with 50 μg ml⁻¹ vesnarinone or 10 μg ml⁻¹ TSA for 16 h. Protein samples were subjected to SDS–PAGE, transferred to nitrocellulose, and detected with an anti-acetylated Histone H3 antibody and Amersham ECL kit.

DISCUSSION

In this study, we examined the molecular mechanisms of the transcriptional regulation of p21^waf1 gene by a differentiation inducing drug, vesnarinone. We identified the minimal vesnarinone-responsive element in the p21^waf1 promoter at −124 to −61 relative to the transcription start site, and demonstrated that vesnarinone enhanced the binding of the transcription factors Sp1 and Sp3 to the vesnarinone-responsive element. Furthermore, we found that vesnarinone induced the histone acetylation in TYS cells.

Sp1 is a ubiquitously expressed nuclear protein that is initially identified as a protein that binds and stimulates transcription of simian virus 40 early promoter (Dynan and Tjian, 1983). Sp1 protein binds to the GC-rich sequences present in a variety of cellular and viral promoters and stimulates their transcriptional activity (Lania et al, 1997). Sp3 belongs to the same family of Sp1 related transcription factor, and it also binds to the GC-rich sequences (Sp1 binding sites) (Lania et al, 1997). In the p21^waf1 promoter, there are four independent Sp1 binding sites (Sp1-1–Sp1-4) and two overlapping Sp1 binding sites (Sp1-5, Sp1-6) (Figure 2). We identified the Sp1-1 and Sp1-2 site as main vesnarinone-responsive elements of the p21^waf1 promoter. Generally, eukaryotic transcription is regulated by more than one transcription factor, and these transcription factors form a complex in specific promoter elements via interaction with various cofactors (Struhl and Moqtaderi, 1998). Sp1 and Sp3 are likely to be transcription factors that have low specificity to the extra-cellular stimuli, but they would be indispensable factors in p53-independent pathway on the p21^waf1 gene transcriptional activity in our system.

Vesnarinone induced histone acetylation in TYS cells. Recent studies demonstrated that there were various kinds of histone acetyltransferase (HAT) and histone deacetylase (HDAC) in mammalian cells, and the level of histone acetylation was controlled by equilibrium of the activities of HAT and HDAC (Grunstein, 1997). The transcriptional coactivators, p300 and CREB binding protein (CBP) are known to possess the HAT activity, and interact with a wide range of DNA binding proteins, including Sp1, p53, the RelA (p65) nuclear factor κB subunit, E2F, MyoD, activator protein 1, several nuclear receptors, and many others (Yuan et al, 1996; Avantaggiati et al, 1997; Gu and Roeder, 1997; Lee et al, 1998; Ikeda et al, 2000). Although data was not shown, we confirmed the expressions of p300, CBP and HDAC1 proteins in the nucleus of TYS cells.

Several histone acetylation inducing drugs show the growth-inhibitory effect or differentiation-inducing effect, and are used as a chemotherapeutic agent on several human malignancies (Chen et al, 1997; Dion et al, 1997; Mccaffrey et al, 1997). The molecular targets for the differentiation inducing drugs (or histone acetylation inducing drug) may be different from those for DNA-damaging drugs. Moreover, activating pathway of the target molecules by differentiation inducing drugs may also be different from those by DNA-damaging drugs. Thus, the differentiation inducing drugs, such as vesnarinone may act synergistically on the induction of p21^waf1 gene with the DNA-damaging therapy, such as radiation and the administration of conventional chemotherapeutic drugs. These informations are useful for creating new strategy for differentiation-inducing-therapy.