SIP1 is downregulated in hepatocellular carcinoma by promoter hypermethylation
© Acun et al; licensee BioMed Central Ltd. 2011
Received: 10 November 2010
Accepted: 6 June 2011
Published: 6 June 2011
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© Acun et al; licensee BioMed Central Ltd. 2011
Received: 10 November 2010
Accepted: 6 June 2011
Published: 6 June 2011
Smad interacting protein-1 is a transcription factor that is implicated in transforming growth factor-β/bone morphogenetic protein signaling and a repressor of E-cadherin and human telomerase reverse transcriptase. It is also involved in epithelial-mesenchymal transition and tumorigenesis. However, genetic and epigenetic alterations of SIP1 have not been fully elucidated in cancers. In this study, we investigated mutations and promoter hypermethylation of the SIP1 gene in human hepatocellular carcinomas.
SIP1 expression was analyzed in HCC cell lines and primary tumors in comparison to normal and non-tumor liver tissues by using semi-quantitative RT-PCR, quantitative real-time RT-PCR and immunohistochemistry. Mutation and deletion screening of the SIP1 gene were performed by direct sequencing in HCC-derived cells. Restoration of SIP1 expression was sought by treating HCC cell lines with the DNA methyl transferase inhibitor, 5-AzaC, and the histone deacetylase inhibitor, TSA. SIP1 promoter methylation was analyzed by the combined bisulfite restriction analysis assay in in silico-predicted putative promoter and CpG island regions.
We found that the expression of SIP1 was completely lost or reduced in five of 14 (36%) HCC cell lines and 17 of 23 (74%) primary HCC tumors. Immunohistochemical analysis confirmed that SIP1 mRNA downregulation was associated with decreased expression of the SIP1 protein in HCC tissues (82.8%). No somatic mutation was observed in SIP1 exons in any of the 14 HCC cell lines. Combined treatment with DNA methyl transferase and histone deacetylase inhibitors synergistically restored SIP1 expression in SIP1-negative cell lines. Analysis of three putative gene regulatory regions revealed tumor-specific methylation in more than half of the HCC cases.
Epigenetic mechanisms contribute significantly to the downregulation of SIP1 expression in HCC. This finding adds a new level of complexity to the role of SIP1 in hepatocarcinogenesis.
Hepatocellular carcinoma (HCC) is one of the most lethal cancer types worldwide and also the most common type of liver cancer [1–3]. The exact mechanisms that drive hepatocarcinogenic processes are not yet completely understood. Identification of genetic and epigenetic changes involved in hepatocellular carcinoma development is of high interest for a better understanding of this aggressive malignancy.
Smad interacting protein-1 (SIP1, also known as ZEB2) is encoded by ZFHX1B at chromosome 2q22 and is a two-handed zinc finger transcription factor that contains a central homeodomain as well as CtBP-binding and Smad-interacting domains. SIP1 has been shown to act predominantly as transcriptional repressor but can also act as transcriptional activator in vivo [4–8].
SIP1 was originally identified in a transforming growth factor-β/bone morphogenetic protein (TGF-β/BMP) signaling pathway by its binding to the MH2 domain of receptor-activated SMADs . SIP1 has been thoroughly studied for its role in repressing E-cadherin expression, which is a central event in the epithelial-to-mesenchymal transition (EMT) [5–7, 10, 11]. Accordingly, an elevated SIP1/E-cadherin ratio was shown to correlate with invasive disease and poor prognosis in gastric, pancreatic, esophageal and ovarian carcinomas [12–15]. Overexpressed SIP1 also caused resistance to DNA damage-induced apoptosis and correlated with poor survival in patients with bladder cancer . In contrast, only a few studies exist with regard to the role of SIP1 in suppressing tumorigenesis. For instance, repression of human telomerase reverse transcriptase (hTERT) expression in breast and liver cancer cells was shown to be partly mediated by SIP1 [17, 18]. Also, by directly inhibiting cyclin D1, SIP1 caused G1 arrest in squamous carcinoma cells .
SIP1 was strongly expressed in, and with another transcriptional repressor, SNAIL, increased invasion of HCC cells . We recently reported an immunohistochemistry study on tissue arrays and described decreased SIP1 levels in a group of tumors, including HCC . In mature hepatocytes in vitro, TGF-β induces EMT by downregulation of Claudin-1, which is also associated with upregulation of SIP1 and SNAIL and downregulation of E-cadherin . Our recent observations also implicated SIP1 as a candidate regulator of replicative senescence in HCC cells . Taken together, these findings indicate that SIP1 may play a role in hepatocarcinogenesis.
Epigenetic regulation of SIP1 expression by miRNAs [23–26] and a natural antisense transcript (NAT)  were recently described. Studies on the promoter methylation of SIP1 were also reported. The SIP1 gene was found to be hypermethylated and silenced in a poorly metastatic breast cancer cell line . In a more recent study, SIP1 downregulation in pancreatic cancer was shown to be mediated through promoter hypermethylation . However, genetic and epigenetic mechanisms regulating SIP1 expression have never been studied in HCC.
In the present study, we investigated the expression of SIP1 at genetic, epigenetic and protein levels in a series of HCC cell lines and primary tumors. Downregulation of SIP1 in HCC cell lines and tumors was found to be mediated by aberrant promoter methylation. Therefore, epigenetic inactivation of SIP1 may play a critical role in hepatocarcinogenesis.
DNA samples from 39 pairs of HCCs and tumor-adjacent normal tissues were used; these archival materials have previously been described . HCC-derived SNU449, SNU475, Mahlavu, SNU423, SNU398, SK-Hep1, Focus, SNU387, SNU182, Hep40, Huh7, PLC/PRF5, Hep3B and hepatoblastoma-derived HepG2 cell lines were studied.
TissueScan Liver Cancer Tissue qPCR Panel I was purchased from Origene Technologies (Rockville, MD). Each plate consisted of pre-normalized cDNAs derived from 48 liver samples covering eight tumor-adjacent normal, 23 HCC (grade I, II, IIIA, IV), three cholangiocarcinoma, one adenoma and 13 non-tumor lesions of the liver. (Additional file 1).
Fifteen formalin-fixed and paraffin-embedded liver tissues deriving from two normal, one HBV carrier, three chronic hepatitis B, three chronic hepatitis C, three cirrhosis and three HCC cases were obtained from the Department of Pathology of Gulhane Military Medical Academy in Ankara, Turkey, upon the favourable decision of ethics committee of Gulhane Military Medical Academy. An HCC tissue array consisting of 61 tumors and five normal cases was purchased from Biochain (Hayward, CA). A total cell lysate of a normal liver tissue was kindly provided by Dr KC Akcali.
Total RNA was isolated from cell lines using NucleoSpin RNA II (Macherey-Nagel, Germany) as indicated by the manufacturer. Reverse transcription was performed with Revert Aid First Strand cDNA Synthesis kit (Fermentas, Lithuania) according to the manufacturer's instructions. Multiplex semi-quantitative RT-PCR was performed by using SIP1-specific primers (SIP1-RTF and SIP1-RTR) and GAPDH-specific primers (GAPDH-RTF and GAPDH-RTR). Primer sequences are given in the supplementary information section (Additional file 2).
Quantitative analysis of SIP1 transcripts was performed by real-time RT-PCR on cDNAs from the TissueScan liver cancer tissue qPCR panel I (OriGene, Rockville, MD) according to the manufacturer's instructions and as previously described . Finnzymes DyNAmo™ HS SYBR Green qPCR kit (Finnzymes, Finland) was used and samples were run on a Stratagene MX3005P™ real-time PCR system (Stratagene, La Jolla, CA). The TBP gene was used as an internal control [32, 33] and relative levels of SIP1 transcripts were measured by a modified ΔΔCt formula [31, 34]. Statistical analyses were performed by the Student's t test.
Western blotting was performed as previously described . Briefly, total cell lysates from SNU398, Huh7, Hep40 and SNU182 cell lines were prepared in NP-40 lysis buffer [50 mM Tris-HCl pH 8.0, 150 mM NaCl, 1% Non-idet P40 (v/v) and a cocktail of EDTA-free protease inhibitors (Roche Diagnostics, Mannheim, Germany)]. Protein content was measured with the Bradford assay. Equalized lysates were run on 8% SDS-PAGE and then transferred onto polyvinylidene fluoride (PVDF) membranes using a wet transfer apparatus (Bio-Rad, Hercules, CA). 6E5 hybridoma supernatant was used as the primary antibody. Horseradish peroxidase (HRP)-conjugated donkey anti-mouse IgG (sc-2318; Santa Cruz, CA) was used as the secondary antibody at 1:2000 dilution. Protein bands were visualized using SuperSignal West Femto chemiluminescent substrate (Pierce, Rockford, IL).
Following a pathologist's review, immunohistochemistry (IHC) was performed on human liver tissues to determine the expression of SIP1, as previously described . In brief, tissue sections were deparaffinized and treated with 10 mM citrate buffer for antigen retrieval. Then, samples were incubated first with a homemade SIP1 monoclonal antibody (clone 6E5), and after washing, with a universal staining kit secondary reagent (LabVision, Fremont, CA). An IgG2a isotype antibody was used as the control (R&D Systems, MN). Diaminobenzidine (DAB) was used as the chromogen, and the slides were counterstained using Mayer's hematoxylin. Immunoreactivity was registered semi-quantitatively, and the immunostaining in each section was assessed independently by two observers (EO and TY). The staining intensity was graded relatively as: no staining (0), weak (+), moderate (++) or strong (+++) .
Except UTR, all exons of SIP1 were amplified in 14 HCC cell lines using 13 sets of primers (Additional file 2). PCR products were purified with the PCR96 Cleanup Kit (Millipore, Billerica, MA) and directly sequenced by the sequencing service company Iontek (Istanbul, Turkey). Mutation screening was performed using the Mutation Surveyor software package (v 3.10, SoftGenetics, LLC, State College, PA).
5-azacytidine (5-AzaC) and Trichostatin A (TSA) treatments were performed as described previously [36–38]. Briefly, cells were seeded in six-well plates at a density of 3 × 105 cells/well and treated after 24 h with 2.5 μM 5-AzaC (Sigma-Aldrich, St. Louis, MO) for 96 h. In the last 24 h, they were treated with 300 nM or 1 μM TSA (Sigma-Aldrich, St. Louis, MO) either alone or combined with 5-AzaC. The medium and 5-AzaC were refreshed every 24 h. Control cultures were left untreated or received a mock treatment with adequate volumes of DMSO (Sigma-Aldrich, St. Louis, MO) in the case of TSA treatment. At the end of the treatment, cells were harvested for DNA and RNA isolation.
The sequence of the human SIP1 gene was retrieved from the NCBI gene database and putative SIP1 promoters were predicted by Promoter2.0 software . The genomic region containing the SIP1 gene, starting from the third exon to 20 kb upstream of the first exon, was analyzed for CpG islands by MethPrimer software .
Genomic DNA was extracted from the cell lines using the Qiagen DNeasy Tissue kit (Hilden, Germany) and bisulfite treated with the Epigentek Methylamp™ DNA Modification kit (Brooklyn, NY) according to the manufacturers' instructions. Nested primer pairs targeted to SIP1 CpG islands were used to amplify bisulfite-treated DNAs (the list of primers is given in Additional file 2) and PCR products were restriction digested by BstUI or TaqI (New England BioLabs, Ipswich, MA) to detect methylation status, as previously described .
We expanded our analysis to clinical samples in order to detect the expression of SIP1 transcripts in a panel of human HCCs by quantitative real-time RT-PCR (Figure 1B). SIP1 expression was found to be significantly reduced in 17 of 23 (73.91%) HCC tumors, compared to eight normal liver tissues from the same panel (p = 0.01). Three of the remaining HCC samples displayed normal and the other three showed high SIP1 transcript levels. Decreased SIP1 expression was also observed in the majority of the non-HCC liver lesions - the cholangiocarcinomas and adenomas (data not shown).
Immunostaining of human liver tissues with SIP1 antibody.
SIP1 Expression (staining intensity)
HCC (n = 64)
Normal Liver (n = 7)
Cirrhosis (n = 3)
HBV Carrier (n = 1)
HBV (n = 3)
HCV (n = 3)
To investigate whether SIP1 is inactivated by allelic deletions and/or somatic mutations, we performed direct sequence analysis using genomic DNA from 14 HCC cell lines. Genomic PCR was carried out using 13 sets of primers that amplify the entire coding region, including splice acceptor and donor sites (exons 2-10) of SIP1. No somatic mutations leading to amino acid substitutions or frameshifts were found, indicating that mutational alterations of SIP1 are not main genetic events in hepatocarcinogenesis (data not shown).
SIP1 is a member of the ZEB family of transcription factors and, along with other E-cadherin repressors, it was repeatedly shown to induce the EMT phenotype both in vivo and in vitro and correlate with a poor prognosis in cancer patients [5, 12, 15, 19]. On the other hand, SIP1 was also shown to be a negative regulator of hTERT transcription in breast cancer cells . Consistent with this, we have recently reported that SIP1 was partly responsible for inducing senescence in hepatocellular carcinoma-derived cells through hTERT repression, and hypothesized that it may act as a tumor suppressor gene in HCC . In support of this hypothesis, a recent microarray study showed downregulation of SIP1 in early and advanced HCC . Also, induced expression of SIP1 has recently been shown to directly inhibit cyclin D1 in the A431 squamous carcinoma cell line, leading to the accumulation of cells in the G1 phase . Other studies described posttranscriptional regulation mechanisms, such as those mediated by miR-200 family [24–26] and SIP1 NAT , in the downregulation of SIP1 in different pathophysological contexts.
Obviously, DNA methylation and alterations of chromatin structure are predominant mechanisms that epigenetically inactivate tumor suppressor genes in tumors . For instance, SIP1 was found to be hypermethylated in poorly metastatic breast adenocarcinoma cells, but hypomethylated in a more aggressive variant of this cell line . Yet more recently, silencing of SIP1 expression was shown to be mediated by promoter hypermethylation in a substantial proportion of pancreatic cancer cell lines and tissues .
Herein, we explored the expression of SIP1 in HCC at the transcriptional and protein levels and provided a mechanistic insight by demonstrating that promoter hypermethylation operates as one of the mechanisms in the epigenetic regulation and downregulation of SIP1 in the majority of HCC samples.
Our initial expression studies in HCC cell lines revealed two groups of cells that differentially express SIP1. Most fibroblastoid-like cells displayed strong SIP1 transcripts, while cell lines with an epitheloid appearance had no or low expression. This in vitro expression pattern of SIP1 was in accordance with its role in inducing EMT, but was neither informative about a tumor versus normal comparison of SIP1 levels nor the behaviour of SIP1 in a liver tissue context. We therefore proceeded with normal liver and HCC tissues and found a significant decrease of SIP1 transcripts in 74% of tumors. By using a previously described anti-SIP1 monoclonal antibody, clone 6E5, an immunoblot was performed with the lysates of HCC cell lines . This assay not only proved the specificity of this antibody, but confirmed our initial observation that SIP1 is downregulated in tumors (Figure 2). Even a higher rate of SIP1 downregulation was observed in our IHC experiments. Compared to normal, 83% of HCC cases displayed no immunoreactivity and the remaining tumor samples were stained with only a weak intensity. This small difference between transcript and protein levels might be explained by the aforementioned posttranscriptional regulatory mechanisms of SIP1 expression. In fact, a miRNA profiling study that showed upregulation of miR-200c in HCCs but not in benign liver tumors could partly explain the downregulation of SIP1 in HCCs . It would be interesting to analyze the expression levels of these regulators in HCCs.
Genetic screening of cell lines did not reveal any mutational alterations in the SIP1 gene, suggesting the implication of epigenetic regulatory mechanisms for the silencing of SIP1 in HCC. Upon our observation that SIP1 mRNA expression was restored after treatment of cells with 5-azaC and TSA, we decided to explore promoter hypermethylation as a possible mechanism of SIP1 downregulation in HCC.
In vitro activities of three alternative SIP1 promoter regions have been previously described in experiments with mouse tissue and the one located around the first exon (P2) exhibited the highest activity. The other alternative promoter regions (P1 and P3) were of low, but detectable, activity . Studies in human cancer cell lines revealed a similar pattern of promoter activation, but this time in an AKT-dependent manner . In striking contrast to these findings, we detected only one methylated tumor sample among 26 paired tissues when we examined the P2 promoter region. However, nearly half of the HCC cases displayed tumor-specific hypermethylation at both the P1 and P3 putative promoter sites. In fact, the number of CpG sites were more restricted in P2 than in the P1 and P3 regions. We also noticed only one BstUI restriction site in P2 but two in the P1 region. P3 amplicons, which were devoid of BstUI sites, were digested with the TaqI enzyme. Hypermethylation in the P3 alternative promoter region (43%) might inhibit SIP1 translation in a different context. The regulation of SIP1 translation by a NAT has been previously shown . After the completion of EMT, a NAT is expressed and makes translation of SIP1 mRNA possible. This NAT expression was shown to be controlled by elements placed at the 5' site of the second exon, which corresponds to the P3 alternative promoter region . Therefore, hypermethylation at the P3 site might inhibit the expression of the NAT, which in turn negatively affects SIP1 translation. It would be interesting to study the expression of the NAT in HCC.
Downregulation of SIP1 in HCC is also in accordance with the dual role of TGF-β in tumorigenesis. The tumor suppressor role of TGF-β in the premalignant stage was shown to switch to an EMT-inducing role in the later stages of cancers, leading to metastasis . This former failsafe mechanism might partly explain higher levels of SIP1 expression in normal liver compared to HCCs. Despite our previous description that SIP1 is partly responsible for replicative senescence in liver cancer cells, its role in inducing apoptosis in distinct pathophysiolocal contexts should also be thoroughly investigated in HCC. Given the downregulation and possible tumor suppressor role of SIP1 in HCC, we also propose the assessment of this regulator as a prognostic factor for patients affected by this aggressive form of liver cancer.
The data presented here clearly demonstrate that SIP1 is downregulated and undergoes epigenetic silencing in a considerable proportion of HCCs. Taken with our previous findings that SIP1 represses hTERT and mediates senescence arrest in HCC-derived cells, our results suggest that SIP1 is regulated in and a potential tumor suppressor gene of hepatocarcinogenesis.
We thank Professor Mehmet Ozturk for kindly providing patient samples used in methylation analysis. This work was supported by Scientific and Technological Research Council of Turkey Grants 107S174 (to MC Yakicier) and 104S243 (to T Yagci).
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