- Open Access
The Runx transcriptional co-activator, CBFβ, is essential for invasion of breast cancer cells
© Mendoza-Villanueva et al; licensee BioMed Central Ltd. 2010
Received: 23 April 2010
Accepted: 30 June 2010
Published: 30 June 2010
The transcription factor Runx2 has an established role in cancers that metastasize to bone. In metastatic breast cancer cells Runx2 is overexpressed and contributes to the invasive capacity of the cells by regulating the expression of several invasion genes. CBFβ is a transcriptional co-activator that is recruited to promoters by Runx transcription factors and there is considerable evidence that CBFβ is essential for the function of Runx factors. However, overexpression of Runx1 can partially rescue the lethal phenotype in CBFβ-deficient mice, indicating that increased levels of Runx factors can, in some situations, overcome the requirement for CBFβ. Since Runx2 is overexpressed in metastatic breast cancer cells, and there are no reports of CBFβ expression in breast cells, we sought to determine whether Runx2 function in these cells was dependent on CBFβ. Such an interaction might represent a viable target for therapeutic intervention to inhibit bone metastasis.
We show that CBFβ is expressed in the metastatic breast cancer cells, MDA-MB-231, and that it associates with Runx2. Matrigel invasion assays and RNA interference were used to demonstrate that CBFβ contributes to the invasive capacity of these cells. Subsequent analysis of Runx2 target genes in MDA-MB-231 cells revealed that CBFβ is essential for the expression of Osteopontin, Matrixmetalloproteinase-13, Matrixmetalloproteinase-9, and Osteocalcin but not for Galectin-3. Chromatin immunoprecipitation analysis showed that CBFβ is recruited to both the Osteopontin and the Galectin-3 promoters.
CBFβ is expressed in metastatic breast cancer cells and is essential for cell invasion. CBFβ is required for expression of several Runx2-target genes known to be involved in cell invasion. However, whilst CBFβ is essential for invasion, not all Runx2-target genes require CBFβ. We conclude that CBFβ is required for a subset of Runx2-target genes that are sufficient to maintain the invasive phenotype of the cells. These findings suggest that the interaction between Runx2 and CBFβ might represent a viable target for therapeutic intervention to inhibit bone metastasis.
CBFβ is a transcriptional co-activator that is recruited to promoters by members of the Runx family of transcription factors. Runx transcription factors are defined by the presence of a conserved DNA-binding domain, termed the Runt domain, that recognises the consensus sequence ACC(A/G)CA . The Runt domain also interacts with CBFβ. CBFβ binds to the non-DNA-binding surface of the Runt domain to induce structural changes in the DNA-recognition surface, thereby increasing its affinity for DNA [2, 3]. CBFβ is essential for haematopoiesis and the development of the skeleton, by virtue of its interaction with Runx proteins [4–6]. Indeed, CBFβ is essential for most of the known functions of Runx proteins. However, there is evidence that in some situations Runx proteins can regulate gene expression independently of CBFβ. In the sea urchin, CBFβ is not required for expression of the Runx target gene PKC1 [7, 8]. Moreover, overexpression of Runx1 partially rescued the lethal phenotype in CBFβ-deficient mice, indicating that overexpressed Runx1 can regulate gene expression in the absence of CBFβ .
Runx2 is overexpressed in breast cancer cell lines that metastasize to bone where it has an established role in invasion. When Runx2 function was inhibited in metastatic breast cancer cells transplanted to bone, tumorigenesis and osteolysis were prevented . Runx2 regulates the expression of several genes known to be involved in cell migration and metastasis including, Matrixmetalloproteinase-13 (MMP-13) and Matrixmetalloproteinase-9 (MMP-9), Vascular Endothelial Growth Factor (VEGF) and Bone Sialoprotein (BSP)[11–13]. Ablation of Runx2 expression in metastatic breast cancer cells, MDA-MB-231, resulted in down-regulation of metastatic genes and reduced the invasive capacity of the cells . However, it is not known if the increased expression of Runx2 observed in metastatic breast cancer cells is sufficient to regulate gene expression independently of CBFβ. Indeed, it is not known if CBFβ is expressed in metastatic breast cancer cells.
Here we demonstrate that CBFβ is expressed in metastatic breast cancer cells and that it is essential for cell invasion. We also show that several Runx2-target genes, known to be involved in cell invasion, require CBFβ. However, whilst CBFβ is essential for invasion not all Runx2 target genes require CBFβ. We conclude that CBFβ is required for a subset of Runx2-target genes that are sufficient to maintain the invasive phenotype of the cells. These findings suggest that the interaction between Runx2 and CBFβ might represent a viable target for therapeutic intervention to inhibit bone metastasis.
CBFβ is associated with Runx2 in the metastatic breast cancer cell line MDA-MB-231
To establish if CBFβ is associated with Runx2 in MDA-MB-231 cells, endogenous Runx2 was immunoprecipitated with an anti-Runx2 antibody followed by western blotting with an anti-CBFβ antibody (Fig. 1D). CBFβ co-precipitated with Runx2 in both MDA-MB-231 and UMR-106 (Fig. 1D, lanes 3 & 6). The association was specific, as CBFβ did not co-precipitate with a non-specific IgG antibody (Fig. 1D, lanes 2 & 5). These data demonstrate that the Runx2/CBFβ complex is present in MDA-MB-231 cells.
Depletion of CBFβ in MDA-MB-231 cells reduces their invasive capacity
CBFβ is essential for expression of invasion genes in MDA-MB-231 cells
We subsequently used chromatin immunoprecipitation (ChIP) to determine whether CBFβ was selective for individual promoters by comparing the presence of CBFβ on the OPN and Galectin-3 promoters. Real-time PCR was used to amplify the OPN and Galectin-3 promoters after immmunoprecipitation of fragmented chromatin with either CBFβ-specific or Runx2-specific antibodies. Compared to non-specific IgG controls the OPN and Galectin-3 promoters were enriched approximately 3.5-fold with the CBFβ-specific antibody and 5-fold with the Runx2-specific antibody (Figs. 4D & 4E). Taken together, these findings demonstrate that CBFβ is recruited to both OPN and Galectin-3 promoters but is not essential for Galectin-3 activation.
Re-expression of CBFβ restores invasion capacity and OPN expression
To examine the effect of CBFβ* on gene expression we measured OPN and MMP-13 mRNA levels. When CBFβ* was expressed in cells transfected with CBFβ siRNAs, OPN mRNA levels were restored to similar levels observed in the non-specific siRNA transfectants (Fig. 5C). We also examined the effect of CBFβ* on the activity of the OPN promoter in CBFβ-depleted MDA-MB-231 cells (Fig. 5D). MDA-MB-231 cells transfected with siCBFβ or siNS were transfected with a plasmid containing the WT human OPN promoter or a mutant OPN promoter in which the Runx2-binding sites were mutated. The relative reporter activity was obtained by comparison of the WT promoter activity with the mutant promoter activity. In the absence of CBFβ the activity of the OPN promoter decreased by 35% compared to the non-specific siRNA controls and was restored to similar levels as the controls when CBFβ* was expressed (Fig. 5D). CBFβ* also restored MMP-13 mRNA expression and stimulated activity of the MMP-13 promoter (Figs. 5E & 5F). Taken together, these data show that CBFβ is a positive regulator of metastatic-gene expression and cell invasion.
In this study we established that CBFβ is expressed in MDA-MB-231 cells and that it is essential for cell invasion. We subsequently demonstrated that CBFβ participates in the activation of genes implicated in cell invasion. Importantly, re-expression of CBFβ in the CBFβ-knockdown cells restored the invasive capacity. The restored invasive capacity was also accompanied by an increase in CBFβ-target gene expression, as exemplified by the increased expression of OPN. We also demonstrated that the metastatic genes OPN and Galectin-3 are Runx2-targets in metastatic breast cancer cells. However, whilst CBFβ was essential for the expression of OPN, MMP-13, MMP-9 and OC it was not required for Galectin-3 expression, despite the fact that CBFβ is recruited to the Galectin-3 promoter. CBFβ is therefore functionally redundant with respect to Galectin-3 expression in MDA-MB-231 cells. Together, our data demonstrate that CBFβ is essential for invasion of metastatic breast cancer cells and that the expression level of Runx2 is not sufficient to overcome the requirement for CBFβ, at least at a subset of Runx2-target genes.
The finding that CBFβ was present on the promoter of Galectin-3 was surprising, given that CBFβ is not required for Galectin-3 expression. One explanation for this might be that whilst CBFβ can be recruited to the Galectin-3 promoter it is not essential for Runx2 binding, possibly due to the presence of other cooperating transcription factors. Precedence for such a scenario has been demonstrated for Runx1, whereby the DNA-binding activity of Runx1 is enhanced by the cooperating transcription factor Ets-1 [23, 24].
Our finding, that not all Runx2-target genes require CBFβ for their expression, is consistent with the observation that in CBFβ-deficient mice overexpression of Runx1 can only partially overcome the requirement for CBFβ. However, in MDA-MB-231 cells the genes that are dependent on CBFβ must be required for invasion since this process is inhibited in the absence of CBFβ. Presumably in the Runx1 mouse model the high expression of Runx1 is sufficient to activate a subset of genes in some cells that enables the partial rescue. The primary function of CBFβ is to enhance DNA-binding of Runx proteins and so in the absence of CBFβ, binding of Runx proteins to their target genes will be compromised. We envisage that in some cases overexpression of Runx proteins is sufficient to raise the intracellular concentration to a level that enables them to bind to a subset of target genes independently of CBFβ. Indeed, in addition to the experimental overexpression of Runx1 there are examples in nature where Runx proteins appear to function in the absence of CBFβ. In the sea urchin, CBFβ is not required for expression of the Runx-target gene PKC1, nor is it recruited to the promoter [7, 8]. In the chicken, Runx1 is highly expressed in the dorsal pharyngeal region but CBFβ is not , and in C. elegans CBFβ is restricted to the hypodermis whereas the Runx protein, RNT-1, is expressed in the intestine . However, it is not clear at present whether a high intracellular concentration of Runx proteins in these situations is the determining factor that enables them to bind to their target genes in the absence of CBFβ.
Perturbation of Runx2 regulatory function by mutagenesis in MDA-MB-231 cells has been shown to abolish their capacity to form osteolytic lesions in the bone, suggesting that modulating Runx2 function might be a viable means of inhibiting bone metastases . Thus, our finding that CBFβ is required for Runx2 to regulate metastatic genes indicates that disruption of this interaction would also inhibit the formation of metastases. Indeed, previous work has shown that proliferation of the human leukemia cell line ME-1 can be inhibited by compounds that disrupt the interaction between Runx1 and CBFβ . Such compounds may also be able to disrupt the Runx2/CBFβ interaction in metastatic breast cancer cells. The Runx2/CBFβ interaction might therefore represent a viable therapeutic target in metastatic breast cancer.
CBFβ is expressed in metastatic breast cancer cells and is essential for cell invasion. CBFβ is required for expression of several Runx2-target genes known to be involved in cell invasion. However, whilst CBFβ is essential for invasion, not all Runx2-target genes require CBFβ. We conclude that CBFβ is required for a subset of Runx2-target genes that are sufficient to maintain the invasive phenotype of the cells.
Cell lines and cell culture
The non-metastatic MCF-7 and metastatic MDA-MB-231 human breast cancer cell lines were cultured in alpha minimal essential medium (α-MEM) containing 10% fetal bovine serum, 100 U/mL penicillin and 100 μg/mL streptomycin. Human cervical carcinoma (HeLa) cells were cultured and maintained in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% FBS, 100 U/ml penicillin and 100 μg/mL streptomycin. UMR-106 rat osteosarcoma cell line was cultured in DMEM supplemented with 10% fetal bovine serum, 1 mM sodium pyruvate, 100 U/mL penicillin and 100 μg/mL streptomycin.
Stable CBFβ knockdown MDA-MB-231 cell line
These cell lines were established by a method described previously , using SureSilencing shRNA plasmids for human CBFβ (SABiosciences). Transfected cells were selected by the addition of 1 μg/mL puromycin into the media. Surviving cells were then assessed for the relative expression of CBFβ compared with the nonspecific-transfected control cell line by western blot, and the clones with the greatest degree of knockdown were selected for subsequent experiments.
Nuclear and cytoplasmic extracts
Nuclear extracts from mammalian cells were routinely prepared as previously described . The nuclear and cytoplasmic extracts were subjected to a SDS-PAGE followed by western blot.
Immunoprecipitation and Western Blot
Whole cell extract preparations were incubated with 3 μg of Runx2 antibody (MBL) followed by incubation with Protein G agarose beads. Normal mouse IgG was used as a control. Washed beads were boiled with 50 μl of loading buffer ([0.625 M] Tris-Cl pH 6.8, 50% glycerol, 10% SDS, 10% β-mercaptoethanol, 0.05% bromophenol blue). For western blot, the samples were denatured with loading buffer and heated at 100°C prior to loading onto 12% SDS polyacrylamide gel. Proteins were detected with a mouse monoclonal anti-Runx2 (MBL), whole serum anti-Runx2 or rabbit polyclonal anti-CBFβ antibodies (Abcam). Goat anti-mouse IgG or anti-rabbit IgG conjugated with horseradish peroxidase (Pierce), were used as secondary antibodies. Immune complexes were detected by Supersignal West Dura Extended Duration Substrate (Pierce) as described previously .
Luciferase constructs and plasmids
Genomic DNA from MDA-MB-231 cells was isolated following standard protocols. The human OPN promoter from -170/20 was cloned using primers 5'-GGCGGGCTCGAGGTGTGTGTGCGTTTTTGTTTTTT-3' and 5'-CCCGCCAAGCTTTGCCTCCTCCTGCTGCTGCT-3'. The 5' and 3' primers contain a XhoI and a HindIII site respectively. The amplified OPN promoter fragment was cloned into the promoter-basic luciferase reporter plasmid pGL3B (Promega). The mutant OPN promoter reporter was generated by site directed mutagenesis (Stratagene), changing the Runx2-binding site, ACCACA, to ACAGCA. The pGL3MMP-13 promoter reporter plasmid encoding the wild-type promoter sequence has been described previously . pGL3MMP-13mut was generated by mutating the distal Runx2 site in the pGL3MMP-13 promoter already harbouring a mutation in the proximal Runx-binding site . The subsequent plasmid has both proximal and distal Runx2-binding sites mutated. The plasmid Flag-CBFβ-HA (CBFβ*) was generated by introducing the CBFβ mouse cDNA into pcDNA3 flanked by Flag and HA tags at the N-terminus and C-terminus, respectively.
Transient transfections and siRNAs
Cells were cultivated in 6-well plates at a concentration of 1.5 × 105 cells/well at 37°C and 5% CO2 atmosphere, 24 hours before transfection. Transfections were performed using lipofectamine 2000 (Invitrogen). For the luciferase assays the cells were transfected with 350 ng of the luciferase plasmids and 50 ng of Renilla luciferase plasmid and cotransfected with 400 ng of plasmid CBFβ* or pCDNA3, DNA was maintained in equal amounts. After 48 h, cells were harvested and lysates were measured for luciferase activity and normalized for transfection efficiency to Renilla luciferase activity (dual-luciferase reporter assay system, Promega). The relative reporter activity was obtained by comparison to mutant promoter activity. All readings were performed in triplicate and in three separate experiments. Data are presented as mean ± standard deviation (S.D.). MDA-MB-231 cells transfected with siRNA against CBFβ (siCBFβ), Runx2 (siRunx2), or a nonspecific siRNA (siNS) (Santa Cruz Biotechnology), were performed with oligofectamine (Invitrogen). 24 hrs after a second transfection the cells were used for mRNA extraction or invasion assays.
Total mRNA was isolated from cell pellets using an RNeasy mini kit (QIAGEN); genomic DNA was removed using the RNase-free DNase set (QIAGEN). mRNA expression of the selected genes was determined by real-time PCR using one-step QuantiTect SYBR Green RT-PCR kit (QIAGEN) according to the manufacturer's protocol. Nucleotide sequences of specific primers for the different genes were: Acidic ribosomal phosphoprotein P0 (RPLO), forward 5'-GGCGACCTGGAAGTCCAA-3' and reverse 5'-CCATCAGCACCACAGCCTT-3'; Runt-related transcription factor 2 (Runx2), forward 5'-AGCCCTCGGAGAGGTACCA-3' and reverse 5'-CGGAGCTCAGCAGAATAATTTTC-3'; Core binding factor beta (CBFβ), forward 5'-CTTAGAAAGAGAAGCAGGCAAGG-3' and reverse 5'-AACTCCAGACAGCCCATACCA-3'; Matrix metalloproteinase 13 (MMP-13), forward 5'-AAATTATGGAGGAGATGCCCATT-3' and reverse 5'-TCCTTGGAGTGGTCAAGACCTAA-3'; Osteopontin (OPN), forward 5'-TTGCAGCCTTCTCAGCCA-3' and reverse 5'-CAAAAGCAAATCACTGCAATTCT-3'; Matrix metalloproteinase 9 (MMP-9), forward 5'-ACCACAACATCACCTATTGGATC-3' and reverse 5'-ACCAAACTGGATGACGATGTCT-3'; Osteocalcin (OC), forward 5'-GTGCAGAGTCCAGCAAAGGTG -3' and reverse 5'-CAGCCAACTCGTCACAGTCC-3'; Galectin-3, forward 5'-GGGCCACTGATTGTGCCT-3' and reverse 5'-TGTTGTTCTCATTGAAGCGTGG-3'. Thermocycler conditions included an initial reverse transcription at 50°C for 30 minutes, then 95°C for 15 minutes; this was followed by a PCR program: 94°C for 30 seconds, 60°C for 45 seconds and 72°C for 45 seconds for 40 cycles. Data were collected and analysed on a Chromo4 Real-Time PCR sequence detection system (Biorad). Data are presented as mean ± standard deviation (S.D.).
Cells were analyzed for invasion through Matrigel 24 well plates according to the manufacturer's protocol (BD Biosciences). Briefly, cells were placed in Matrigel inserts at 1.8 × 104 cells/ml in serum-free medium and were allowed to migrate for 22 hrs at 37°C. Non-migrating cells were removed from the top of the filter by scrubbing with a cotton swab. Cells that migrated were fixed and stained with DAPI (ProLong Gold, Invitrogen). Cells that migrated through the Matrigel were counted manually. Data are presented as mean ± standard deviation (S.D.).
Chromatin immunoprecipitation (ChIP) assays were performed according to the published method with modifications . Briefly, MDA-MB-231 cells were cross-linked with 1% formaldehyde-phosphate-buffered saline for 10 minutes at room temperature and quenched by the addition of glycine to a final concentration of 250 mM. The cells were washed twice with cold phosphate-buffered saline and harvested. The cell pellet was resuspended in lysis buffer (50 mM Tris-Cl, pH 8.0, 10 mM EDTA, 1% sodium dodecyl sulfate). Samples were then sonicated for 15 minutes at high power with a Diagenode sonicator. After sonication, the samples were centrifuged in a benchtop microcentrifuge at 4°C, and the supernatants were diluted with ChIP dilution buffer (0.01% sodium dodecyl sulfate, 1.1% Triton X-100, 1.2 mM EDTA, 16.7 mM Tris-Cl, pH 8.0, 167 mM NaCl). For immunoprecipitation, the samples were pre-cleared using 10 μl Dynabeads protein A (Invitrogen). Four micrograms of each antibody (CBFβ or Runx2 or control IgG) was added to the sample, and the samples were incubated overnight at 4°C, followed by the addition of 10 μl Dynabeads protein A and incubation for 1 h at room temperature. The remainder of the procedure was followed according to the method described previously . The DNA was isolated with Qiagen DNA purification kit. Real time PCR was performed with Osteopontin promoter primers (forward: 5'-TGAATGCCCATCCCGTAAA-3'; reverse: 5'-ATGCCCATCCCGTAAATGA-3'); 18S gene primers (forward: 5'-GTAACCCGTTGAACCCCATT-3' reverse: 5'-CCATCCAATCGGTAGTAGCG-3') and Galectin-3 as previously reported . The relative enrichment of target DNA was determined by calculating the ratio of DNA from specific antibody to that from control IgG, and normalized by 18S non-specific genomic DNA within the same sample. Data are presented as mean ± standard deviation (S.D.).
One-way analysis of variance was used to determine statistical differences between groups using SPSS software (Chicago, IL). A p value < 0.05 was considered statistically significant. Multiple comparisons between individual groups were assessed by the method of Tukey. Comparisons of multiple groups to a single control were done according to the method of Dunnett. For comparison of mRNA, statistical evaluation of significant differences was performed using the Student's t-test. Asterisk (*) indicates P < 0.05 when compared to control and were considered statistically significant.
This work was funded by the Wellcome Trust and the Association for Cancer Research (AICR). D. M-V and C. L-C are recipients of PhD scholarships from the Mexican National Council on Science and Technology (CONACYT) and the General Direction of International Relations of the Mexican Ministry of Public Education (SEP). Thanks to Elisa Aguilar-Martinez for her comments on the manuscript.
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