Comparative analysis of 14-3-3 isoform expression and epigenetic alterations in colorectal cancer

Background The 14-3-3 family is a group of intracellular proteins found in all eukaryotic organisms. Humans have seven isoforms that serve as scaffolds to promote interactions of regulatory phospho-proteins involved in many vital cellular processes and previous studies have shown that disturbances in native 14-3-3 levels can contribute significantly to the development of various cancers. Methods DNA and RNA was extracted from frozen tissue samples collected by the Human Cooperative Tissue Network. RNA samples were reverse transcribed and subjected to qRT-PCR analysis using fluorescently labelled probes. Genomic DNA was treated with bisulfite and cloned into bacterial vectors for subsequent high-resolution sequencing. Mammalian NIH3T3 cells were transformed with 14-3-3 eta and Ras expression vectors synthesized from cDNA. Colonies were counted and transforming capability assessed after 21 days of growth. Cell lysates were analyzed by western blot to verify protein expression. Results Here we examined normal and cancerous 14-3-3 expression levels of all seven isoforms in a cohort of sporadic colorectal adenocarcinomas and in a group of tumors and their matched normals using qRT-PCR analysis. We found a statistically significant decrease in the levels of 14-3-3 sigma, eta, and zeta observed among adenocarcinomas compared to normal tissue. A parallel analysis of microarray data from the TCGA dataset confirmed that expression of sigma and eta were down-regulated in colon tumors. To explore the mechanisms behind 14-3-3 expression changes, we examined the methylation status of the sigma, eta, and zeta gene promoters in selected samples. Our data identified novel CpG methylation sites in the eta promoter consistent with epigenetic silencing of both 14-3-3 sigma and eta isoforms during colon tumorigenesis. Because epigenetic silencing is the hallmark of a tumor suppressor we tested eta in focus formation assays and found that it is capable of suppressing ras-induced transformation of NIH3T3 cells. Conclusion To our knowledge, this is the first study to identify the 14-3-3 eta gene as a tumor suppressor and that its expression is suppressed in colon tumors by DNA hypermethylation. These data suggest a link between 14-3-3 expression levels and the development of colon cancers. Electronic supplementary material The online version of this article (doi:10.1186/s12885-015-1856-y) contains supplementary material, which is available to authorized users.


Background
The 14-3-3 proteins are a family of small, highly conserved, acidic proteins with molecular masses of 28-33 kDa. They are found in all eukaryotic species. There are seven different 14-3-3 proteins in mammalian cells, each designated by a Greek letter (β-beta, γ-gamma, δ-delta, ε-epsilon, ζ-zeta, θ/τ-theta/tau, η-eta) and each protein is nearly 80 % similar in their amino acid sequences. There is a highly conserved ligand-binding domain that interacts with phosphorylated serine residues on cellular proteins which targets two high-affinity binding motifs: RSXpSXP (mode1) and RXXXpSXP (mode 2). The ligandbinding domains are the most highly conserved regions of 14-3-3 proteins and all have uniformly high affinity for the binding motifs [1]. It is through these interactions that 14-3-3 proteins exert their biological activity since they have no enzymatic or transcriptional activity of their own.
Although very similar in structure, 14-3-3 proteins serve a number of diverse functions throughout human tissues. Individual regulation of 14-3-3 family members is tightly controlled in many tissues including dermal and epidermal layers [9], bones [14], and developing neurons [2,17]. Several studies have also shown 14-3-3 proteins play critical roles as signal integration points for cell cycle control, apoptosis, and mitogenic signal transduction [4,5]. Dysregulation of these proteins has also been linked to several human diseases and that 14-3-3s have even been proposed as potential therapeutic drug targets [31].
14-3-3 proteins have recently come to prominence due to new evidence suggesting they may play a role in human tumorigenesis [29]. For example several studies have shown that 14-3-3 sigma acts as a tumor suppressor and that its expression is often suppressed during the development of breast cancers [12]. Consistent with these findings, 14-3-3 sigma expression is induced by p53 [8] and can suppress the formation of foci induced by ras and myc in rodent cell transformation assays [24]. The expression of other 14-3-3 isoforms, such as gamma and zeta, appears to be upregulated in a number of human tumors [23,27], suggesting they may exhibit oncogenic properties. Studies in lung and breast cancers have identified a dysregulation of 14-3-3 gene expression in these tumors compared to normal tissue [18,22]. Loss of 14-3-3 sigma expression remains one of the most consistently observed molecular changes in both breast and colon cancers [3,20].
To date, only a few studies of human tumors in lung [22], in astrocytomas [30], and in meningiomas [15] have simultaneously characterized the expression levels of all seven 14-3-3 isoforms. The expression levels of the 14-3-3 isoforms have not been characterized in colorectal cancers. Our objective was to determine whether there is a change in expression in relation to normal colonic tissue as well as to identify 14-3-3 genes who's expression is altered during colon tumorigenesis.

Clinical characteristics of patients and samples
A total of 123 tissue samples were analyzed, taken from 113 patients of varying background: 48 male, 75 female, average age 63 years (range, 15-89 years), 10 black, 99 white, 14 unspecified. Sample set consisted of 71 malignant adenocarcinomas and 52 non-tumor controls including 11 patient-matched pairs. All adenocarcinomas (56 Grade II and 15 Grade III) were confirmed by pathological evaluation and contained a minimum density of 51 % lesion/49 % stroma. Stromal tissue does not appear to contribute significantly to a tissue's 14-3-3 expression when analyzed by immunohistochemistry [23]. The dataset included patients with varying stages of colorectal cancer (14 Stage I, 28 Stage II, 28 Stage III, and 4 Stage IV). The control group included various diagnoses: 12 diverticulosis, 5 polyps, and 32 non-tumor. Deidentified tissue samples were provided by the Cooperative Human Tissue Network (CHTN Western Division, Vanderbilt University, Nashville, TN) which is funded by the National Cancer Institute. Other investigators may have received specimens from the same subjects. Samples were kept frozen at −70°C until needed. These studies were reviewed by and designated as exempt by the University of Arizona Human Subjects Protection Program.

RNA extraction and purification
Total RNA was extracted from tissue samples using the RNeasy® Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's guidelines. To preserve RNA integrity, all tissue samples were maintained over dry ice prior to sample disruption using a VDI 12 Tissue Homogenizer (VWR, Radnor, PA). RNA concentration and quality were determined using a NanoDrop® ND-1000 Spectrophotometer (Thermo Fisher Scientific, Waltham, MA).

DNA extraction and purification
Genomic DNA was extracted from fresh-frozen tissue samples using the QIAamp® DNA Mini Kit (Qiagen), according to manufacturer's guidelines. Samples were digested with 25 units each of bovine pancreas ribonuclease A (Sigma, St. Louis, MO) for five minutes to remove residual RNA. DNA concentration and quality were determined using a NanoDrop® ND-1000 spectrophotometer (Thermo Fisher Scientific).

Bisulfite treatment of methylated human DNA
Four matched pairs of tumor and non-tumor genomic DNA (eight samples total) were subjected to bisulfite treatment using EpiTect® Bisulfite Kit (Qiagen), according to the manufacturer's guidelines. Following column purification, samples were eluted into 10 μL buffer TE (10 mM Tris, pH 8.0; 1 mM EDTA).

Single-copy isolation of 14-3-3 promoter regions by subcloning
Purified fragments of 14-3-3 promoter regions were ligated into bacterial cloning vectors using pGEM®-T Easy Vector System I (Promega, Madison, WI) according to the manufacturer's guidelines. Ligated constructs were immediately used to transform DH5α competent cells and grown on IPTG/β-Gal/Ampicillin positive agar plates for 24 h. Twelve white colonies were randomly selected from each plate and grown in 2 mL liquid cultures overnight. Plasmid DNA was then extracted and purified using AxyPrep Easy-96 Plasmid DNA Kit (Axygen, Union City, CA) according to the manufacturer's guidelines.

Sequencing and analysis of bisulfite-treated 14-3-3 promoter DNA
Sequencing of 14-3-3 promoter constructs was conducted by The University of Arizona Genetics Core Facility using an Applied Biosystems 3730 DNA Analyzer. Cloned sequences for each 14-3-3 isoform were aligned against established gene sequences using a ClustalW alignment algorithm and BioEdit © Software (Ibis Biosciences, Carlsbad, CA).

Cell culture and transfection conditions
NIH3T3 cell line was obtained from ATCC (American Type Culture Collection). Cells were grown in Dulbecco's modified minimal essential medium (Cellgro, VA) supplemented with 100 U of penicillin, 100 mg of streptomycin, and 5 % fetal bovine serum (Sigma) and maintained in a humidified atmosphere of 5 % CO 2 .

Transformation assay
Early passages of NIH3T3 cells were plated in 30 mm, 6-well plates at a density of 300,000 cells/well. 1 μg of each plasmid mixed in FuGene 6 transfection reagent (Promega) was slowly added to culture plates under gentle agitation. After 24 h, the transfected cells were trypsinized and counted. About 5,000 cells were plated into 100 mm dishes, each. Cells were grown in DMEM with 5 % fetal calf serum, changed every 84 h. After 21 days, cells were stained with 0.05 % crystal violet solution (Thermo Scientific #88101) and foci were counted using a ColCount colony counter (Oxford Optronix, UK).

Western blotting
To verify exogenous protein expression, cell lysates were collected 96 h after transformation. Total protein was extracted and analyzed by SDS-PAGE. Two rabbitprimary antibodies were used to probe for total Ras (Cell Signaling antibody #3339) and Flag peptide (Cell Signaling antibody #2368), incubated overnight in 5 % BSA at a dilution of 1:800. Uniform protein loading was verified using mouse anti-β-actin primary antibody (Sigma #A3853), also incubated overnight in 5 % BSA at a dilution of 1:800. Anti-rabbit HRP-conjugated secondary antibody (Jackson ImmunoResearch antibody #111-035-003) and anti-mouse HRP-conjugated secondary antibody were both used at a 1:10,000 dilution in 5 % blotting-grade blocker (Bio-Rad #170-6404).

Statistical analysis
Statistics were calculated using R © version 2.13.2 software (R Foundation for Statistical Computing, Vienna, Austria). A two-tailed Student's t-test and Mann-Whitney U-test were used to compare differences in 14-3-3 mRNA expression between tumor and non-tumor sample groups. P-values less than 0.01 were considered significant.

Results & discussion
Previous studies have examined changes in the expression of several 14-3-3 isoforms in lung, head and neck, breast, and gastric cancers [10,13,22,27]. Analysis of all seven 14-3-3 family members by immunohistochemistry showed an increase in epsilon, zeta, and theta isoforms in human meningiomas [15] however, there have been no equivalent studies in colon tumors.
In order to characterize 14-3-3 expression in human colorectal adenocarcinomas we began with a cohort of samples that consisted of 71 cancerous and 52 noncancerous colonic tissues. The relative levels of mRNA expression of each of the 14-3-3 isoforms were determined using primers specific to each isoform in quantitative real-time PCR reactions. The cycle-threshold values (ΔC t ) were normalized to a GAPDH control. In order to test the quality of our qRT-PCR reactions we also randomly selected the RNA from 24 patients (19 tumor, 5 non-tumor) and performed independent duplicate reactions to test for reproducibility and found that there was less than 1 % variation on average. The expression results were pooled and are graphed in Fig. 1. Statistical analysis revealed that three 14-3-3 isoforms, zeta, eta, and sigma, showed a statistically significant decrease (p < 0.001) in mRNA expression in tumor tissue when compared to non-tumor samples whereas little or no change was seen in the other isoforms. In both tumor and non-tumor samples, 14-3-3 isoforms zeta and epsilon exhibited the highest overall expression, consistent with previous 14-3-3 expression data collected in lung tissues [22]. We further analyzed our expression results by calculating the fold differences in mRNA expression in tumor verses non-tumor groups using the mean ΔC t values. The results, graphed in Fig. 2a, reveal that cancerous tissues showed a nearly 1.4 fold drop in expression of 14-3-3 sigma. This is consistent with what has been reported for breast cancers and suggests that depression of 14-3-3 sigma expression may also be important in the development of colorectal tumors. Similarly, the depression of 14-3-3 eta expression suggests that suppressed expression of this isoform is also associated with colorectal tumorigenesis.
For comparison and further evaluation we also analysed a subset of eleven tumors along with their matched normal tissues. Fold differences in expression were calculated for each matched pair individually and averaged (Fig. 2b). We found that 14-3-3 eta and sigma showed a 1.3 and a 4.4 fold decrease in the expression of these genes in tumor compared with their matched normal. Indeed, the magnitude of the fold change in expression of all of the isoforms was increased when tumor samples were compared with matched normals suggesting that using matched normals increases the sensitivity of detection of changes in gene expression. We saw no correlation between expression changes and the patient's age, sex, or race.
We further analyzed the TCGA microarray data set by examining 14-3-3 gene expression levels and tumor stage. For this analysis we grouped tumor stages I and II together into the early stage group and grouped tumor stages III and IV together into the late stage group. Next we plotted the level of expression for each of the 14-3-3 isoforms for early and late stage tumor groups and compared these to the levels of expression in normal samples. The results are depicted in Fig. 3. As might be expected from previous reports, 14-3-3 sigma showed a statically significant drop in average expression in both early and late stage tumors. Interestingly the magnitude of the level of the decrease in sigma expression became more pronounced in late stage tumors compared to early stage tumors suggesting that repression of this gene increases during tumor development. 14-3-3 eta expression also decreased but did not reach significance and appeared bimodal. That is the drop in expression was more pronounced in some tumors over others. In contrast 14-3-3 epsilon and gamma expression showed a significant increase in both early and late stage tumors. Notably, the average expression level of 14-3-3 beta was reduced in early stage tumors relative to normal cells, but was elevated in late stage tumors. Moreover, change in direction of the expression of this gene (eg. decreased in early stage tumors but increased in late stage tumors) explains why no statistically significant change in expression was observed when the expression results from all tumors was pooled together as was done in Fig. 1.
Having observed decreases in mRNA levels of several isoforms among colorectal tumors, we sought to explore the mechanisms responsible for driving 14-3-3 depletion. Previous studies have indicated that silencing of gene transcription through promoter hypermethylation is a primary mechanism of dysregulation for 14-3-3 sigma in many cancers. Aberrant methylation of the YWHAS gene's 5'-regulatory region has been reported in cancers of prostate, bladder, and liver tissues [7,19,21]. Epigenetic alteration of sigma has shown clinical significance, and hypermethylation correlates strongly with the development of melanomas and squamous cell carcinomas of the vulva [26,28]. Hypermethylation and down-regulation of 14-3-3 sigma has been consistently observed in a large portion of breast cancers for over a decade and remains a promising biomarker for the disease today [3,6]. The nature of epigenetic alteration of 14-3-3 and its relationship to cancer, however, appears to be tissue specific. Hypomethylation of 14-3-3 sigma and subsequent up-regulation of the gene has been observed in non-small cell lung carcinomas [25]. The large body of evidence supporting an epigenetic mechanism for regulation of 14-3-3 prompted us to examine the methylation status of the promoter regions of zeta, eta, and sigma.
Although the promoter region and the CpG islands that are methylated in the sigma gene are well documented [16], the promoters and potential methylation sites for zeta and eta are not known. Hence, we began with a computational analysis of all seven of the 14-3-3 promoter sequences using EMBOSS Cpgplot (http://www.ebi.ac.uk/). The predicted methylation sites for all seven of the 14-3-3 genes are shown in supplemental Additional file 1: Figure  S1. The predicted CpG islands for eta, zeta, and sigma are displayed in Fig. 3 as dashed lines and represent likely regions of methylation based on GC density. Potential CpG islands predicted to occur in the promoter regions of each of the three 14-3-3 isoforms were used to guide our bisulfite-coupled genomic sequencing efforts. Importantly, the individual CpG methylation sites predicted by EMBOSS and subsequently observed in the bisulfite sequencing of the 14-3-3 sigma gene match previously reported methylation positions [16].
To conduct the analysis genomic DNA was extracted from patient-matched pairs of tumor and non-tumor tissues and subjected to bisulfite treatment to differentiate methyl-cytosines from unmethylated cytosines [11]. PCR amplification of a roughly 650 bp region centered near the  Fig. 4) was conducted for 14-3-3 zeta, eta, and sigma genes. Bacterial subcloning was then used to isolate single copies of the promoter regions for subsequent sequencing and analysis. Figure 4 shows the location of each methylated CpG site that was observed along all three targeted genes. Vertical bars represent average changes in the proportion of methylpositive clones for matched tumor/non-tumor clones.
Positive values indicate an increase in percent methylation of adenocarcinomas compared to their nontumor controls.
Of the three 14-3-3 genes examined two, sigma and eta, showed significant hypermethylation. The sigma promoter exhibited an overall hypermethylated state (14.0 % methylation of CpG sites in non-tumor tissues versus 34.9 % methylation in tumors), consistent with the epigenetic changes of 14-3-3 established in other cancers [3,6,16]. The eta promoter displayed a large number of methylation sites within a roughly 250 basepair region centered on the gene's start of transcription. The proportion of methyl-positive CpG sites within 100 bp of the gene's transcriptional start site was higher in tumor tissues (29.8 %) compared to non-tumor tissues (18.2 %). Such a large shift in promoter methylation suggests that the eta isoform may be dysregulated in a manner similar to 14-3-3 sigma. The zeta isoform did not exhibit strong methylation in either tumor or nontumor groups, suggesting its observed down-regulation in colon cancers is the result of some unidentified mechanism. To our knowledge, this is the first study that identifies individual CpG methylation sites in the 14-3-3 zeta and eta genes.
14-3-3 sigma's established role in colorectal cancers as a tumor suppressor and the similarities in dysregulation of expression of 14-3-3 eta prompted us to test whether eta could also act as a tumor suppressor. A mammalianexpression vector containing full-length 14-3-3 eta was constructed and used to transform human NIH3T3 cell lines. A 900 bp segment of cDNA comprising the entire coding region of 14-3-3 eta was generated (see Methods) and ligated into an FNpCDNA3 vector containing an Nterminal FLAG tag. The multiple cloning site was sequenced to confirm the construct's integrity and reading frame continuity. The expression plasmid was used in focus formation assays to test whether eta could suppress Ras-induced transformation of NIH3T3 cells. The resultant foci were counted according to the Methods section, results are shown in Fig. 5. H-ras transformants exhibited a statistically-significant increase (p < 0.05) in foci count, as compared to non-treated NIH3T3 controls (Fig. 5a & c). This transforming potential of H-ras was significantly suppressed by cotransfection with 14-3-3 eta, a result that is similar to what we observed previously when we cotransfected with 14-3-3 sigma [24]. Cells derived from expanding foci from each transformation assay were grown and collected on day 4 and lysates parepared and analyzed by western blot (see Methods) to confirm exogenous expression of FLAG-14-3-3 eta and H-ras (Fig. 5d). Overexpression of 14-3-3 eta did not increase foci count over the control group, further supporting 14-3-3 eta's potential role as a tumor suppressor. To verify that the FNpCDNA3 vector alone was not responsible for the tumor suppressor effects seen in the 14-3-3 eta plus H-ras groups, another focus formation assay was run comparing H-ras transformants and Hras plus empty FNpCDNA3 vector cotransformants (shown in panels b, c, and e of Fig. 5). Ras and Ras plus vector groups showed an equivalent amount of Ras expression by western blot and significantly higher expression than endogenous levels of Ras seen in the vector alone group. Ras and Ras plus empty FNpCDNA3 did not show a statistically significant

Conclusions
Dysregulation of specific 14-3-3 isoforms has been detected in a number of tumor types suggesting that these proteins play a role in maintenance of the normal cell phenotype but can promote tumorigenesis if expression of these genes is altered. Here we examined the expression levels of all seven of the 14-3-3 family members in colorectal adenocarcinomas and found that, in general, the expression of most of the 14-3-3 genes was down regulated in the tumors analyzed by quantitative rtPCR. Of these we found that a statistically significant decrease in 14-3-3 zeta, eta, and sigma expression occurred in tumor samples using rtPCR as compared to non-tumor controls. Comparison of the fold change values obtained for our tumor cohort and the fold change values for the TCGA data set confirm that the expression of sigma and eta are indeed suppressed in colon tumors. However, we found that normalizing using matched controls increased the sensitivity for detecting changes in gene expression. This suggests that the expression level of 14-3-3 genes varies between individuals.
Importantly, analysis of the expression values for colon tumors in the TCGA data set revealed that the change in expression of 14-3-3 genes is complex that we first realized. When compared with tumor stage several 14-3-3 genes exhibited a diverse change in expression. For example, 14-3-3 sigma expression levels, a putative tumor suppressor, decreased in late stage tumors relative to early stage tumors. In contrast the expression of 14-3-3 gamma, an oncogenic 14-3-3 family member, increases in more advanced tumors. However, the most dynamic change in expression was shown by 14-3-3 beta. Here we found that expression of the beta gene was depressed in early stage tumors but increased in late stage tumors. The significance of this change in direction of expression is unclear. However, one possible explanation is that the contribution of this gene to colon tumorigenesis changes with tumor stage. Overall the level and direction of the change in 14-3-3 expression appears to correlate with the degree of advancement of the tumor and appears to be associated with the biological function of the protein.
The expression of some 14-3-3 genes in tumors is thought to be regulated epigenetically. Consequently, prompted by the well documented hypermethylation of the sigma promoter we examined the promoter methylation status of eta and zeta using bisulfite-coupled genomic sequencing and found that the eta promoter was also extensively hypermethylated in colorectal tumors. Indeed the extent of methylation at the eta promoter was considerably more extensive than what we observed for 14-3-3 sigma. Hence, as with 14-3-3 sigma, the expression of 14-3-3 eta is also negatively regulated epigenetically in human tumors suggesting that it may be a tumor suppressor. Consistent with this, 14-3-3 eta could also suppress focus formation induced by an activated Ras oncogene confirming that eta can act as a tumor suppressor.
Overall, our studies show that 14-3-3 gene expression is altered in colon tumors, but that the direction of the change in expression levels varies with each gene and may be a reflection of the role that individual proteins play in the tumorigenic process. Further analysis of how 14-3-3 expression is regulated and how these proteins can influence tumor development is warranted.