Introduction
The mammalian Dickkopf genes (DKK) encode a class of extracellular signalling molecules that control cell fate during embryonic development and regulate tissue homeostasis in adults 12. Four DKK gene members have been identified so far. DKK1, DKK2 and DKK4 antagonise canonical Wnt/β-catenin signalling by interaction with LDL-receptor-related proteins (LRP5 and LRP6) 3. In contrast, DKK3 does not sequester LRPs or Wnt ligands 245. Its function in antagonising nuclear β-catenin levels, designated as the hallmark of an activated Wnt pathway often found in human tumour tissues 6, has received conflicting reports 789. Most evidence suggest DKK3 exerts a tumour suppressive function by inhibiting a non-canonical Wnt signalling branch referred to as the planar cell polarity (PCP) pathway. The PCP pathway is characterised by the activation of c-Jun kinase (JNK) via recruitment of small GTPases of the Rho/Rac family 10. It results in changes in cell adhesion, motility and polarity 11 rather than interfering with the networks of proliferation and differentiation, which is mediated by canonical Wnt/β-catenin signalling 6.
In agreement with its putative tumour-suppressive function 9121314DKK3 is commonly downregulated in human cancers such as lung cancer 151617, renal clear cell carcinoma 18, pancreatic cancer 19, leukaemia 20, prostate cancer 721, bladder cancer 22, melanoma 23 and gastrointestinal tumours 24. In many of these diseases transcriptional loss is tightly associated with methylation of the DKK3 promoter 15161820212224, whereas in other malignancies the cause of downregulation remains to be elucidated or is not related to 5'-cytosine methylation 23. A study on lung cancer revealed that the rate of DKK3 methylation increased steadily from normal lung tissue, to low-grade and high-grade atypical adenomatous hyperplasia to invasive adenocarcinoma 25, suggesting a potential role of DKK3 methylation in lung cancer progression. In mouse cancer models, DKK3 has proved a promising therapeutic agent capable of repressing tumour progression, for example, in testicular germ cell cancer 14 and prostate cancer 13. More recently, a breast cancer xenotransplantation model demonstrated that a single adenoviral-mediated intra-tumoural injection of a DKK3 expression vector efficiently discontinued tumour growth, with the induction of apoptosis in these cells 26. This suggests that DKK3 may have an important tumour-suppressive function that either prevents tumour initiation or attenuates cancer progression. Interestingly, loss of DKK3 expression was first observed in numerous immortalised tumour-derived cell lines 27. Immortalisation, that is escape from cellular senescence, is an early event in malignant transformation 28, so DKK3 could act as a tumour suppressor gene by mediating the effects of senescence stimuli. In concordance with this hypothesis, DKK3 expression was found to be elevated in organs with predominantly growth-arrested post-mitotic cells, for example in the heart and brain 29 and also in senescent prostate epithelial cells 30.
However, to the authors' knowledge, a comprehensive study on DKK3 gene regulation and its implication in breast cancer has not yet been published. In our study we investigated DKK3 mRNA expression, DKK3 protein expression and DKK3 promoter methylation in breast cell lines as well as in normal and malignant primary breast tissues. Our results demonstrate for the first time that DKK3 expression is frequently downregulated in human breast cancer as a consequence of aberrant DNA methylation within the DKK3 gene promoter.
Materials and methods
Patient material
Nineteen matched tumour and normal tissue samples from breast cancer patients and 131 tissue samples from breast carcinomas were obtained from patients treated by primary surgery for breast cancer at the Departments of Gynecology at the University Hospitals of Aachen, Jena, Regensburg and Düsseldorf, Germany, between 1991 and 2005. The selection of cases was based on availability of tissue, and the sample was recruited in a non-selective, consecutive manner. Female patients presenting with unilateral, invasive breast cancer with no individual breast cancer history were included in the study. Exclusion criteria were: neo-adjuvant chemotherapy before surgery; presentation with secondary breast cancer; or peritumourous carcinoma in situ present in the tumour sample. Patient characteristics are shown in Table 1.
<p>Table 1</p>
Demographic and clinical patient characteristics of primary breast carcinomas (n = 150)
Variable
Categorisation
n
1
%
Clinicopathological factors
Age at diagnosis
median: 57 years (range 28 to 86 years)
<57 years
74
49.3
= 57 years
76
50.7
Tumour size2
pT1
59
39.3
pT2
70
46.7
pT3
8
5.3
pT4
10
6.7
pTx
3
2.0
Lymph node status2
pN0
72
48.0
pN1 to 3
71
47.3
PNx
7
4.7
Histological grade
G1
13
8.7
G2
75
50.0
G3
62
41.3
Histological type
Ductal
122
81.3
Lobular
19
12.7
Other
9
6.0
Immunohistochemistry
Oestrogen receptor
Negative (IRS3 0 to -2)
47
31.3
Positive (IRS 3 to 12)
98
65.3
n.a.
5
3.3
Progesterone receptor
Negative (IRS3 0 to 2)
51
34.0
Positive (IRS 3 to 12)
94
62.7
n.a.
5
3.3
1Only female patients with unilateral invasive breast cancer were included. 2According to International Union Against Cancer: TNM Classification of Malignant Tumours 32.3IRS = immunoreactivity score 35. n.a. = not available.
All patients gave informed consent for retention and analysis of their tissue for research purposes and the Institutional Review Boards of the participating centres approved the study.
Tumour histology was determined according to the criteria of the World Health Organization 31, while disease stage was assessed according to International Union Against Cancer 32. Tumours were graded according to Bloom and Richardson, as modified by Elston and Ellis 33. After surgery, tumour material was immediately snap-frozen in liquid nitrogen. Sections stained with haematoxylin and eosin were prepared for assessing the percentage of tumour cells; only samples containing more than 70% tumour cells were selected. Samples were dissolved in lysis buffer followed by DNA isolation using the QIAamp DNA Mini Kit (Qiagen, Hilden, Germany) according to the manufacturer's recommendations.
Breast cell lines
The cancerous breast cell lines BT20, Hs578T, MCF7, MDA-MB231, SKBR3, T47D and ZR75-1 and the non-cancerous lines HMEC and MCF12A were obtained from the American Type Culture Collection (ATCC) (Rockville, MA, USA) and cultured under recommended conditions.
RNA expression analysis
RNA isolation, RT-PCR and realtime PCR were performed as previously described 34. To ensure experiment accuracy, all quantitative measurements were performed in triplicate. Intron-spanning primer sequences and cycling conditions are given in Table 2.
<p>Table 2</p>
Oligonucleotide primers used in the study
Sequence (5' to 3')
TA [°C]
Primer [nM]
Cycles
Product size (bp)
RT-PCR
GAPDH
Forward: TGGTCACCAGGGCTGCTT
59
400
35
510
Reverse: GTCTTCTGGGTGGCAGTGAT
DKK3
Forward: AAGGCAGAAGGAGCCACGAGTGC
59
400
35
182
Reverse: GGCCATTTTGGTGCAGTGACCCCA
Semiquantitative realtime PCR
GAPDH
Forward: ATGGCCAGCGGGAAGAC
60
500
40
289
Reverse: ATGGCCAGCGGGAAGAC
DKK3
Forward: ACAGCCACAGCCTGGTGTA
60
400
40
123
Reverse: CCTCCATGAAGCTGCCAAC
Methylation-specific PCR
DKK3 unmethylated
Forward: TTAGGGGTGGGTGGTGGGGT
58
320
34
126
Reverse: CTACATCTCCACTCTACACCCA
DKK3 methylated
Forward: GGGCGGGCGGCGGGGC
58
320
34
120
Reverse: ACATCTCCGCTCTACGCCCG
TA = annealing temperature.
Bisulphite-modification and methylation-specific PCR
About 1 μg of genomic DNA was bisulphite-modified using the EZ DNA Methylation Kit (Zymo Research, Orange, CA, USA) according to the manufacturer's recommendations. Methylation-specific PCR (MSP) was performed as previously described 34. Primers and cycling conditions are listed in Table 2. Specificity of MSP primers in detecting the DKK3 methylation status were demonstrated using universal unmethylated and universal polymethylated DNA as a template (Epi Tect Control DNA Set; Qiagen, Hilden, Germany).
5-aza-2'-deoxycytidine and trichostatin A treatment
DNA demethylating treatment of breast cancer cell lines was performed with 5-aza-2'-deoxycytidine as described elsewhere 34, modified by the addition of 300 nM of the histone deacetylase inhibitor trichostatin A (Sigma-Aldrich, Deisenheim, Germany) on day three (incubation for 24 hours). Drug concentrations were adjusted in advance to warrant viability and replication of all cell lines.
Immunohistochemistry
Formalin-fixed, paraffin-embedded 2 μm tissue sections were subjected to immunostaining using the Advance Kit (Dako, Hamburg, Germany) following the manufacturer's instructions. Antigen retrieval was performed by pre-treatment with citrate buffer (pH 7) in a microwave oven (20 minutes at 200 W). Sections were incubated for 30 minutes with the primary antibody (AP1523a, Abgent, San Diego, CA, USA; 1:50), washed and incubated for 10 minutes with the secondary antibody (biotinylated polylink; Dako, Hamburg, Germany). Diaminobenzidin (Dako, Hamburg, Germany) was used for antibody detection. An experienced breast cancer pathologist (N.B.) scored the immunohistochemical staining according to the scoring system suggested by Remmele and Stegner 35. The tissue specimens for immunohistochemical analysis are characterised in Table 3.
<p>Table 3</p>
Immunohistochemical analysis of DKK3 protein expression in breast cancer samples (n = 16) in relation to clinicopathological parameters
Age
Size1 (pT)
Node status1 (pN)
Grade
Histology
ER2
PR2
DKK3 methylation
DKK3 IRS tumour3
DKK3 IRS normal4
49
1
0
3
IDC
-
-
-
9
12
85
2
1
3
IDC
-
-
n.a.
3
n.a.
69
2
1
2
ILC
-
-
-
9
12
82
3
1
3
IDC
-
-
+
6
n.a.
45
1
1
3
IDC
-
-
+
4
12
60
3
0
3
IDC
-
-
n.a.
8
n.a.
61
1
0
2
IDC
-
-
+
0
n.a.
72
1
0
2
IDC
-
-
n.a.
4
n.a.
44
1
1
3
IDC
-
-
-
12
12
86
2
n.a.
3
IDC
-
-
-
8
n.a.
60
1
1
3
IDC
+
-
+
2
9
66
1
0
2
IDC
+
+
+
3
n.a.
54
2
0
3
IDC
+
-
+
6
12
83
1
0
2
IDC
+
+
-
9
n.a.
79
2
0
3
IDC
+
+
-
8
12
62
4
1
3
IDC
+
-
+
3
9
1According to International Union Against Cancer: TNM Classification of Malignant Tumours 32. 2According to Remmele and Stegner 35. 3According to Remmele and Stegner 35 as a continuous variable. 4Matched normal breast epithelial tissue. IRS = immunoreactivity score. IDC = invasive ductal carcinoma. ILC = invasive lobular carcinoma. n.a. = not available.
Statistical evaluations
Statistical analyses were completed using SPSS 14.0 (SPSS, Chicago, IL, USA). Differences were considered significant when p < 0.05. A non-parametric Mann-Whitney U-test and a Kruskal-Wallis test were applied to examine expression levels among normal tissues, DKK3 unmethylated tumours and DKK3 methylated tumours. A student's t-test was applied on the expression of paired normal and tumour samples. To study statistical associations between clinicopathological factors and DKK3 methylation status contingency tables and a two-sided Fisher's exact test were used.
Results
Differential DKK3 mRNA expression in breast cell lines
To start our analysis of DKK3 expression in breast cancer patients we analysed mRNA expression in non-malignant and malignant breast cell lines using realtime PCR. Strong DKK3 expression could be detected in non-malignant HMEC and MCF12A cells (Figure 1a) exhibiting expression levels comparable with human placental tissue, which is known to abundantly express DKK3 22. Among the malignant cell lines, Hs578T and SKBR3 cells revealed abundant DKK3 mRNA levels comparable with benign breast cells. In five further breast cancer cell lines (BT20, MCF7, MDA-MB231, T47D and ZR75-1) DKK3 expression was substantially reduced.
<p>Figure 1</p>
DKK3 mRNA expression and DKK3 promoter methylation analysis in breast cell lines
DKK3 mRNA expression and DKK3 promoter methylation analysis in breast cell lines. (a) DKK3 mRNA expression is differentially expressed in breast cell lines. Non-cancerous cell lines (HMEC and MCF12A) and cancerous breast cell lines (Hs578T, SKBR3, BT20, MCF7, MDA-MB231, T47D and ZR75-1) were analysed by realtime PCR and related to DKK3 mRNA expression in human placental tissue (set to 1). Grey bars = samples expressing abundant DKK3 mRNA; black bars = samples showing strong downregulation of DKK3 expression. (b) Hypermethylation of the DKK3 promoter in breast cell lines. Methylation specific PCR (MSP) was performed with bisulphite-treated DNA from benign and malignant breast cell lines. DNA bands in lanes labelled with U indicate PCR products amplified with primers recognising unmethylated DKK3 promoter sequence. DNA bands in lanes labelled with M represent amplificate generated with methylation-specific primers; water served as 'no template control' (NTC). MSP controls demonstrate the specificity of the DKK3 primers used. Universal poly-methylated bisulphite-converted DNA (UMD) exclusively yields amplification products with primers specific to methylated DKK3 promoter sequence; universal unmethylated bisulphite-converted DNA (UUD) yields exclusive amplification products with primers recognising the unmethylated DKK3 promoter sequence.
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Methylation of the DKK3 promoter in breast cell lines
Aberrant promoter hypermethylation of tumour suppressor genes during carcinogenesis is an effective mechanism resulting in downregulation and functional inactivation of these genes 3637. Knowing that DKK3 expression was downregulated in most malignant breast cell lines we performed promoter methylation analysis in these cells. By using MSP 38 we found a methylated DKK3 promoter sequence in all cell lines showing reduced DKK3 expression, BT20, MCF7, MDA-MB231, T47D and ZR75-1 (Figure 1b). In contrast to this, all DKK3 expressing cell lines (HMEC, MCF12A, Hs578T and SKBR3) as well as human placental tissue lacked DKK3 promoter methylation in the analysed promoter region.
In vitro demethylation of the DKK3 promoter
To prove a direct association of DKK3 promoter methylation with loss of DKK3 mRNA expression we treated seven breast cell lines sequentially with the DNA-methyltransferase inhibitor 5-aza-2'-deoxycytidine and the histone deacetylase inhibitor trichostatin A. Subsequently, we determined DKK3 promoter methylation and DKK3 mRNA expression before and after the drug treatment. MSP analyses after the treatment (Figure 2a) confirmed that promoter demethylation had occurred in all methylated cell lines by the appearance and enhancement of signals indicative of unmethylated DNA sequences. Those cell lines initially bearing a methylated DKK3 promoter showed elevated DKK3 mRNA expression after treatment (BT20, MCF7, MDA-MB231, T47D and ZR75-1; Figure 2b), whereas no DKK3 mRNA gain was achieved in unmethylated MCF12A and only a marginal DKK3 mRNA gain in SKBR3 cells. The induction of DKK3 mRNA transcription after the treatment as determined by realtime PCR ranged from 4.7-fold to 29-fold higher than in originally methylated breast cancer cells.
<p>Figure 2</p>
DKK3 mRNA expression after in vitro DNA demethylation
DKK3 mRNA expression after in vitro DNA demethylation. (a) In vitro demethylation of the DKK3 promoter. Methylation specific PCR of seven breast cell lines was performed with DNA from cells either untreated (-) or treated with 1 μM 5-aza-2'-deoxycytidine (DAC) and 300 nM trichostatin A (TSA) (+). (b) Re-expression of DKK3 mRNA in breast cell lines after treatment with DAC/TSA. All cell lines initially exhibiting low DKK3 mRNA restored expression of DKK3 compared with the untreated control cells. Induction level (fold change) of DKK3 mRNA expression was determined by realtime PCR.
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Differential DKK3 mRNA expression in primary breast carcinomas
DKK3 mRNA expression in primary breast tissues was then examined by realtime PCR. In the first step, 19 pairs of breast carcinoma tissues and corresponding normal breast tissue were analysed. A significant downregulation of DKK3 mRNA expression in tumour tissue compared with its adjacent normal tissue was detected in 14 (74%) of the 19 pairs (Figure 3a), as defined by an expression fold change of two or more (FC2).
<p>Figure 3</p>
DKK3 mRNA expression analysis in primary breast carcinomas
DKK3 mRNA expression analysis in primary breast carcinomas. (a) Realtime PCR of DKK3 mRNA expression in 19 matched pairs (normal vs. tumour). Arrowheads indicate downregulation in the tumour by an expression fold change of more than two (FC2). (b) Relative DKK3 mRNA expression in 40 additional breast cancer specimens. Mean expression of 19 normal breast tissues (N) was set to 1. Based on a FC2, grey bars represent tumour specimens (T) showing normal expression, black bars represent tumour specimens with reduced DKK3 mRNA expression.
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To further support this data set we analysed 40 additional breast carcinomas with no corresponding normal breast tissue and referred each individual DKK3 mRNA expression level to the mean DKK3 expression of the previously analysed 19 normal breast tissues (Figure 3b). The frequency of DKK3 mRNA downregulation measured in this tumour cohort (27 of 40, 68% by FC2) is in good agreement to the result achieved with the 19 matched pairs. Therefore downregulation of DKK3 mRNA in breast cancer is considered to affect about 70% of patients.
DKK3 promoter methylation in primary breast carcinomas
To address the question of whether DKK3 promoter methylation occurs in primary breast carcinomas, we analysed 150 mammary tumour samples by MSP. Corresponding normal breast tissue was available for 19 tumours. In total, 92 of 150 tumours (61.3%) revealed DKK3 promoter methylation (for example, #7 in Figure 4) whereas in 58 of 150 tumours (38.7%) the DKK3 promoter was unmethylated. In these cases, MSP amplification signals were obtained exclusively in the U-reaction (for example, #5 in Figure 4). Of the normal breast tissues, only a single sample (5.3% of 19 samples) gave a very weak methylation signal (data not shown) in contrast to all other normal tissues that lacked DKK3 promoter methylation. As an additional control that infiltrating immune cells do not contribute to methylation signals in mammary tumours, bisulphite-converted DNA from human peripheral blood lymphocytes were assayed and revealed an unmethylated DKK3 promoter, consistent with results from a previous study 39.
<p>Figure 4</p>
DKK3 promoter methylation analysis in primary breast carcinomas
DKK3 promoter methylation analysis in primary breast carcinomas. Methylation specific PCR results from 10 representative matched pairs of primary breast tumour (T) and corresponding normal breast tissue (N) are shown. DNA from human placenta (Plc) as well as from peripheral blood lymphocytes (Lyc) reveals an unmethylated DKK3 promoter. DNA from breast carcinoma cell line BT20 served as positive control. NTC = no template control.
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Correlation of DKK3 promoter methylation with loss of DKK3 mRNA expression
For all breast carcinoma samples analysed for DKK3 mRNA expression (n = 59) we determined the DKK3 promoter methylation status at the same time. Thus, we were able to directly compare DKK3 methylation and mRNA expression in primary human breast carcinomas. A boxplot (Figure 5) illustrates the distribution and medians of DKK3 RNA expression among normal breast tissues, DKK3 unmethylated tumours and DKK3 methylated tumours. The median DKK3 expression level (exp) of unmethylated tumours (exp = 0.87; FC = 1.2) was comparable with that of normal breast tissues (set to exp = 1). In contrast, DKK3 methylated tumours showed a significant mRNA downregulation (exp = 0.17; FC = 5.9) compared with DKK3 unmethylated tumours and normal breast tissue (global p < 0.001).
<p>Figure 5</p>
Correlation analysis of DKK3 promoter methylation with DKK3 mRNA expression in primary breast carcinomas
Correlation analysis of DKK3 promoter methylation with DKK3 mRNA expression in primary breast carcinomas. Tumours that are unmethylated in the DKK3 promoter express DKK3 mRNA comparable with DKK3 mRNA expression normal breast tissue, whereas in DKK3 methylated tumours DKK3 mRNA expression is significantly reduced. Horizontal lines = group medians; boxes = 25 to 75% quartiles, range, peak and minimum.
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Differential DKK3 protein expression in primary breast carcinomas
Immunohistochemical staining was used to investigate DKK3 protein expression in normal (n = 8) and malignant (n = 16) breast tissues. DKK3 was strongly expressed in non-malignant luminal and basal epithelial cells, achieving a mean (sd) immunoreactivity score (IRS) 34 of 11.3 (1.4) (Figure 6a) and a median IRS of 12 (range 9 to 12). DKK3 protein was not detectable in stromal cells in the normal breast tissue. Of the breast carcinomas, four of 16 (25%) revealed abundant DKK3 protein expression (IRS = 9 to 12; Figure 6b) in contrast to seven of 16 tumours (44%), which showed partial loss (IRS = 4 to 8; Figure 6c), and five of 16 tumours (31%) with substantial loss of DKK3 protein (IRS = 0 to 3; Figure 6d and Table 3). The mean protein staining intensity in breast carcinomas was determined to have an IRS of 5.9 (3.3) and the median to have an IRS of 6 (range 0 to 12). DKK3 expression levels in the tumour and normal tissue groups were shown to be significantly different (p = 0.002; U-test), and DKK3 protein was also differentially expressed within the eight matched pairs (p < 0.001; t-test). As a continuous variable, a lower IRS in breast carcinoma was significantly associated with the presence of DKK3 promoter methylation (p = 0.001; Fisher's exact test).
<p>Figure 6</p>
DKK3 protein expression in primary breast carcinomas as determined by immunohistochemical staining
DKK3 protein expression in primary breast carcinomas as determined by immunohistochemical staining. (a) Normal mammary tissue without (left) and with application (right) of DKK3 antibody. Abundant DKK3 protein expression is detectable in luminal and basal epithelial cells. (b) Breast carcinoma with unmethylated DKK3 promoter reveals abundant DKK3 protein expression. (c) and (d) Breast carcinomas with a methylated DKK3 promoter exhibit substantial loss of DKK3 protein expression. Original magnifications are given in upper right-hand corner.
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Association of DKK3 promoter methylation with clinicopathological factors
For descriptive data analysis clinicopathological patient characteristics were correlated with the DKK3 promoter methylation status. In a bivariate analysis, DKK3 promoter methylation was significantly associated with advanced patient age at diagnosis (p = 0.007). Furthermore, DKK3 promoter methylation was not associated with tumour size, lymph node status, histological grade, histological type, and oestrogen receptor or progesterone receptor positivity (data not shown).
Discussion
It was previously reported that expression of the putative Wnt antagonist DKK3 was downregulated in several tumour entities as a consequence of epigenetic DNA modification 15161820212224. Our study is the first to analyse DKK3 gene regulation in human breast cancer. Malignant breast cell lines showed strong reduction of DKK3 mRNA in association with DKK3 promoter methylation. Consistently, DKK3 mRNA expression was induced after promoter DNA demethylation in these cells. In primary breast carcinomas, DKK3 mRNA expression was downregulated in 68% of invasive tumours with significant association with methylation of the DKK3 gene promoter (p < 0.001). The total frequency of DKK3 methylation was 61% in breast carcinomas, whereas corresponding normal breast tissues were unaffected by this epimutation. We further showed that a loss of DKK3 protein in breast carcinomas is also associated with DKK3 promoter methylation (p = 0.001) whereas protein expression is abundant in epithelial cells of the normal breast. In summary, our data demonstrate for the first time that promoter methylation-mediated downregulation of DKK3 expression is a frequent and tumour-related epigenetic alteration in the development of human breast cancer.
The implication of aberrant canonical Wnt/β-catenin signalling in the pathogenesis of human cancer has become widely accepted 40. Its oncogenic effect is mediated by uncontrolled activation of target genes that for example, enhance cell proliferation, such as c-myc and cyclin D1. In breast cancer, several genes encoding inhibitors of canonical Wnt/β-catenin signalling have been reported to be frequently hypermethylated, for example, SFRP1 3441, SFRP2 42, SFRP5 43, WIF1 44 and DKK1 42. We suggest that disruption of a non-canonical Wnt signalling branch, the PCP pathway, may also be implicated in human carcinogenesis by pathologically altering the networks of cellular adhesion, motility and cell polarity, because it has been shown that expression of the putative PCP pathway inhibitor DKK3 is commonly downregulated in malignant tissues. As a consequence, loss of DKK3 may promote hyperactivation of the PCP pathway, thereby potentially enhancing tumour aggressiveness.
Recent in vivo experiments support a hypothesis that the loss of DKK3 expression promotes an aggressive cancer phenotype. In a mouse model, DKK3 proved to be a promising therapeutic agent to significantly inhibit tumour growth in testicular germ cell cancer 14. In an orthotopic prostate cancer model a similar treatment resulted in tumour regression, decreased metastasis and prolonged survival of the host 13. The most recent findings from a breast cancer study revealed that DKK3 not only attenuates tumour growth in a xenotransplantation mouse model, it also re-sensitised multidrug-resistant MCF7/ADR cells to doxorubicin treatment in a JNK-c-Jun dependent manner 26. This highlights its potential utility as a gene therapeutic agent in human breast cancer. Our study adds important information to this aspect, because it so far remained unknown if methylation-mediated loss of DKK3 expression also occurred in primary breast cancer, and, if so, how many patients were affected by this epimutation. We have shown that a large proportion (61%) of breast cancer patients have DKK3 promoter methylation in the carcinoma tissue, leading to a functional inactivation of the tumour-protective protein. Therefore, we conclude that a potential gene therapeutic treatment with DKK3 might be of benefit for a large target population of breast cancer patients.
In contrast to other studies, DKK3 promoter methylation in our cohort was not associated with clinicopathological factors indicative of a progressive cancer subtype, such as tumour size, node status or histological grade. The existence of such an association has been demonstrated in prostate cancer 712, in which expression of DKK3 was predominantly lost in high-grade prostatic tumours. Moreover, siRNA-mediated downregulation of DKK3 expression in prostate epithelial cells disrupted acinar morphogenesis 7, which taken with its prevalent expression in growth-arrested cells suggests a functional role of DKK3 in post-mitotic tissue differentiation processes. Whether DKK3 is also involved in maintaining glandular morphology in the normal mammary gland will be elucidated in a further study.
In human breast cancer, hypermethylation of Wnt antagonist genes was reported to be of clinical relevance. Both SFRP1 and SFRP5 methylation were shown to occur frequently and be tumour specific with a strong association to poor clinical patient outcome 3443. An impact of DKK3 promoter methylation on cancer patient survival has been repeatedly found. It was shown to be associated with reduced disease-free survival in acute lymphoblastic leukaemia 20, and also with shorter overall survival in kidney cancer 45 and lung cancer 46. Due to its functional properties as a potential tumour suppressor in human cancers including breast cancer 26, together with the finding that DKK3 methylation is a significant prognostic factor in three human malignancies, we speculate that DKK3 methylation might also bear prognostic power in breast cancer. This hypothesis is currently being approached in our laboratory in a further study.
In summary, we demonstrate for the first time that the Wnt antagonist gene DKK3 is a frequent target of epigenetic inactivation in human breast cancer, leading to downregulation of DKK3 mRNA and DKK3 protein expression in tumourous tissues. These results suggest a causative implication of DKK3 in the development of human breast cancer. Since DKK3 is believed to negatively regulate Wnt signalling, these results underline the pivotal role of a deregulated Wnt signalling pathway commonly found in this disease.
Conclusion
This study shows that the putative Wnt antagonist DKK3 is frequently downregulated in human breast cancer due to promoter methylation, whereas it is abundantly expressed and unmethylated in normal breast cell epithelium. Since promoter methylation is a primary cause to functionally inactivate tumour suppressor genes, DKK3 may act as a tumour suppressor in the human mammary gland. DKK3 is believed to particularly regulate non-canonical Wnt signalling. Therefore, we conclude that disruption of this Wnt pathway branch may add further tumour growth advantages to those already conferred by canonical Wnt/β-catenin signalling.
Abbreviations
DKK3: Dickkopf-3; FC: fold change; IRS: immunoreactivity score; JNK: c-Jun-kinase; LRP: LDL-receptor related protein; MSP: methylation-specific polymerase chain reaction; PCP: planar cell polarity pathway; RT-PCR: reverse transcription polymerase chain reaction; SD: standard deviation; siRNA: small interfering ribonucleic acid; TSA: trichostatin A.
Competing interests
Edgar Dahl has declared that he has submitted a patent application on the use of DKK3 promoter methylation. The other authors have no competing interests.
Authors' contributions
JV carried out the gene expression analyses, immunohistochemical studies, methylation experiments and statistical evaluations, participated in the conception and design of the study, and wrote the manuscript. NB participated in the immunohistochemical analysis, performed data interpretation and critically revised the manuscript. AH provided clinical samples and clinicopathological data, performed data interpretation, supported in statistical analyses and critically revised the manuscript. GK provided clinical samples and clinicopathological data, performed data interpretation and critically revised the manuscript. UH provided clinical samples and clinicopathological data, participated in data interpretation and critically revised the manuscript. RK participated in the design and co-ordination of the study and critically revised the manuscript. ED planned and co-ordinated the study, and critically revised the manuscript. All authors have given final approval of the text to be published.