Histone deacetylases (HDACs) are known to be associated with an overexpression in different types of cancer such as colon and prostate cancer. In this study we aimed to evaluate the protein expression of class I HDACs in urothelial carcinoma of the bladder.
Methods
A tissue microarray containing 348 tissuesamples from 174 patients with a primary urothelial carcinoma of the bladder was immunohistochemically stained for HDAC 1, 2 and 3. Intensity of staining was evaluated and the association with clinico-pathological features and prognosis was assessed.
Results
High HDAC expression levels were found in 40 to 60% of all investigated urothelial carcinomas (HDAC-1: 40%, HDAC-2: 42%, HDAC-3: 59%).
HDAC-1 and HDAC-2 were significantly associated with higher tumour grades.
Although all three markers could not predict progression in univariate analyses, high HDAC-1 expression was associated with a trend toward poorer prognosis. Patients with high-grade tumours and high expression levels of HDAC-1 were more likely to progress compared to all other patients (p < 0.05).
Conclusions
High-grade noninvasive papillary bladder tumours are associated with high expression levels of HDAC-1 and HDAC-2. High grade tumours in combination with high expression of HDAC-1 showed a worse prognosis than the other tumours. The high expression levels of HDACs observed particularly in high grade urothelial bladder cancer clearly warrant subsequent studies on the potential use of HDAC inhibitors as a novel therapeutic approach.
The online version of this article (doi:10.1186/1472-6890-14-10) contains supplementary material, which is available to authorized users.
Cédric Poyet, Bastian Jentsch contributed equally to this work.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
CP coordinated the study, performed statistical analyses and wrote the paper. BJ performed immuno-histological analyses and wrote the paper. TH, HHS, TS coordinated the study and revised essential parts of the paper. CP, DS and MS provided clinicopatholocial data for the study. PJW and HM supported the study coordination, assisted in technical questions and statistical support. GK conceived and coordinated the study, performed statistical analyses, wrote and revised the paper. All authors read and approved the final manuscript.
Abkürzungen
HDACs
Histone deacetylases
HDAC-i
HDAC-inhibitors
TMA
Tissue microarray
IRS
Immunoreactivity scoring
PFS
Progression free survival.
Background
The majority of bladder cancer patients (75-80%) initially present with papillary noninvasive (pTa) or superficially invasive (pT1) urothelial carcinoma, whereas the remaining 20-25% of primary tumours are already muscle invasive (≥ pT2) at first diagnosis [1, 2].
Among superficial tumours, almost 70% recur after transurethral resection and up to 25% of them show progression into a muscle invasive disease [3]. Bladder cancer patients have to be monitored closely for disease recurrence and progression, which contributes to the high costs of this disease. Therefore there is a great interest in identifying markers that can diagnose superficial cancer with a high risk of progression and allow for more specific surveillance strategies [4]. So far no established marker allows prediction of tumour progression.
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Histone deacetylases (HDACs) constitute a family of enzymes that deacetylate histones and other cellular proteins. They are major regulators of transcription and are also important in other cellular processes [5]. HDACs are classified into four different classes based on the phylogenetic analysis of their structure and homology to yeast enzymes [6]. Class I HDACs are divided into four isoforms (HDAC-1, -2, -3 and -8) and are known to be associated with an overexpression in different types of cancer such as colon and prostate cancer [7, 8]. Published expression array data for urothelial cancer could demonstrate an overexpression of different class I HDACs compared to normal urothelium. Especially, the first three isoforms HDAC-1, -2 and -3 were found to be overexpressed. Contrary to HDAC-8, for which no overexpression was found [2, 9‐12]. In contrast to these findings, a more recent study of Xu and colleagues reported no difference of expression in the expression levels of HDAC-2 between normal urothelial and bladder cancer tissue as assessed by immunohistochemistry [13]. Few studies have found an effect for HDAC-inhibitors (HDAC-i) in urothelial cancer cell lines [12, 14‐17], however, a broad expression analysis of HDACs in urothelial carcinomas has not been conducted so far. In addition, there is no study available on the prognostic relevance of class I HDACs in bladder cancer. We aimed to analyse the expression patterns of the most promising class I HDACs (HDAC-1, -2 and -3) in a representative cohort of primary bladder cancers and correlated these to clinico-pathological parameters including tumour stage, grade, multifocality, adjacent carcinoma in situ, growth pattern and finally clinical follow-up data.
Methods
Bladder cancer tissue microarray (TMA)
Tissue microarrays (TMA) contained 348 formalin-fixed, paraffin-embedded urothelial bladder cancer tissues from 174 patients and were constructed as previously described [18]. All tumour samples were represented in duplicate tissue cores (1 mm). The TMA consisted of tumour tissues only, normal urothelial samples were not available. Specimens were collected between 1990 and 2006 by the Institute of Surgical Pathology, University of Zurich, Switzerland. The TMA includes a series of 174 consecutive (non-selected) primary urothelial bladder tumours. Finally, the TMA contained 90 pTa, 68 pT1 and 16 ≥ pT2 tumours. Hematoxylin and eosin–stained slides of all specimens were reevaluated by two experienced pathologists (BJ, GK).
Tumour stage and grade were assigned according to UICC and WHO criteria.
Retrospective clinical follow-up data were available for all of 174 patients (100%). The median follow-up period for the entire cohort was 110.6 months (range 32.4 to 266.8 months). Clinico-pathologic data are summarized in Table 1. The study was approved by the local scientific ethics committee Kantonale Ethikkommission Zürich (http://www.kek.zh.ch/, approval no.: StV-Nr. 25/2007).
Table 1
Patient and tumor characteristics and results of molecular and immunohistochemical analyses
Variable
Categorization
n analyzable
%
Total n = 174
Clinico-pathologic data:
Age at diagnosis (median, range)
69,5 years (32–92)
<70 years
87
50.0
≥70 years
87
50.0
Sex
Female
43
24.7
Male
131
75.3
Tumor stage (WHO 1973a)
pTa
90
51.7
pT1
68
39.1
pT2
13
7.5
pT3
2
1.1
pT4
1
0.6
Histologic grade (WHO 1973a)
G1
44
25.3
G2
87
50.0
G3
43
24.7
Histologic grade (WHO 2004b)
Low grade
101
58.0
High grade
73
42.0
Adjacent carcinoma in situ
No
158
90.8
Yes
16
9.2
Multiplicity
Solitary
124
71.3
Multifocal
50
28.7
Growth pattern
Papillary
159
91.4
Solid
15
8.6
Immunohistochemistry (IHC):
HDAC-1
Low expression
104
59.8
High expression
70
40.2
HDAC-2
Low expression
101
58.0
High expression
73
42.0
HDAC-3
Low expression
71
40.8
High expression
103
59.2
aStaging and grading according to the 1973 WHO classification system.
bStaging and grading according to the 2004 WHO classification system.
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Immunohistochemistry
The TMA was freshly cut (3 μm). For immunohistochemical detection of HDAC-1, -2 and -3 isoforms on tissue samples, prediluted polyclonal rabbit IgG antibody directed against HDAC-1 (1:11, Abcam, Cambridge, UK), monoclonal mouse IgG antibody directed against HDAC-2 (1:5000, Abcam) and monoclonal mouse IgG antibody directed against HDAC-3 (1:500, Becton Dickinson, Franklin Lakes, NJ, USA) was used on 3 μm paraffin sections, as described [19]. Ki-67 was detected with clone MIB-1 (Dako, Glostrup, Denmark; dilution 1:50).
Immunohistochemical studies utilised an avidin-biotin peroxidase method with a diaminobenzidine (DAB) chromatogen. After antigen retrieval (microwave oven for 30 min at 250 W) immunohistochemistry was carried out in a NEXES immunostainer (Ventana, Tucson, AZ) following manufacturer’s instructions.
Evaluation of Immunohistochemistry
One surgical pathologist (BJ) evaluated the slides under the supervision of the senior author. Nuclear staining of HDAC isoforms was scored applying a semiquantitative immunoreactivity scoring (IRS) system that incorporates the percentual area and the intensity of immunoreactivity resulting in a score ranging from 0 to 12, as described previously [19]. For statistical analysis, the intensity of HDAC expression was grouped into low vs. high rates of expression. Cases exhibiting an IRS from 0–8 were pooled in a HDAC low expression group whereas cases with a higher IRS (9–12) were designated HDAC high expression group. The percentage of Ki-67 positive cells of each specimen was determined as described previously [20]. High Ki-67 labelling index was defined as more than 10% of positive tumour cells [21].
Statistical analysis
Statistical analyses were performed with SPSS version 20.0 (SPSS Inc, Chicago, IL). Differences were considered significant if p < 0.05. To study statistical associations between clinicopathologic and immunohistochemical data, contingency table analysis and 2-sided Fisher’s exact tests were used. Univariate Cox regression analysis was used to evaluate statistical association between clinicopathologic/immunohistochemical data and progression free survival (PFS). PFS curves were calculated using the Kaplan–Meier method with significance evaluated by 2-sided log-rank statistics. For the analysis of PFS, patients were censored at the date when there was a stage-shift (from Ta to T1-4, respectively from T1 to T2-T4), or if there was distant metastatic disease.
Results
Staining patterns of HDAC1-3
HDAC 1–3 protein expression in bladder cancer tissue samples was investigated by immunohistochemical analysis of the TMA containing 174 specimens from patients with a primary urothelial carcinoma of the bladder. All 174 (100%) patients could be evaluated for HDAC immunostaining. All three investigated HDACs showed high expression levels in 40 to 60% of all tumours. Figures 1, 2 and 3 represent examples of typical exclusively nuclear staining patterns of HDAC-1, -2 and -3 (low - and high expression). For HDAC-1 40% of the tumours showed high expression levels, for HDAC-2 42% and for HDAC-3 even 59% (Table 1).
Figure 1
Immunohistochemical staining with HDAC-1. (A) low expression HDAC-1 staining pattern in a low-grade urothelial tumour; (B) high expression HDAC-1 staining pattern in a typically high-grade urothelial tumour.
Figure 2
Immunohistochemical staining with HDAC-2. (A) low expression HDAC-2 staining pattern in a low-grade urothelial tumour; (B) high expression HDAC-2 staining pattern in a typically high-grade urothelial tumour.
Figure 3
Immunohistochemical staining with HDAC-3. (A) low expression HDAC-3 staining pattern in a low-grade urothelial tumour; (B) high expression HDAC-3 staining pattern in a typically high-grade urothelial tumour.
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×
×
Correlations to clinico-pathological parameters
HDAC-1 to 3 and Ki-67 were correlated with clinico-pathologic characteristics (stage, grading, adjacent carcinoma in situ, multiplicity and growth pattern) of the tumours (Table 2). Strong staining of HDAC-1 and HDAC-2 was associated with higher grading (both WHO 1973 and 2004), additionally tumours with high expression levels of HDAC-2 presented more often with adjacent carcinoma in situ compared to tumours with weak HDAC-2 staining. High expression levels of HDAC-3 were only associated with higher tumour grade according the new WHO 2004 grading system. Ki-67 showed a significant correlation with all clinico-pathologic characteristics (p < 0.05), except for tumour multiplicity. The expression levels of all three tested HDAC proteins were significantly associated with each other (data not shown). Furthermore, strong staining of all three HDACs correlated with high Ki-67 labelling index (for HDAC-1: Spearmans Rho rs = 0.325, p < 0.001, for HDAC-2: rs = 0.271, p < 0.001; for HDAC-3: rs = 0.191, p < 0.05).
Table 2
Associations of the HDAC-1, -2 and 3 and Ki-67 with pathologic characteristics (n = 174)
Variable
Categorization
HDAC-1 expression
HDAC-2 expression
HDAC-3 expression
Ki-67 expression
Low
High
p
Low
High
p
Low
High
p
Low
High
p
Tumor stage (WHO 1973)a
pTa
59
31
0.162
55
35
0.811
37
53
0.257
71
19
<0.001
pT1
37
31
37
31
30
38
35
33
pT2
5
8
7
6
2
11
2
11
pT3
2
0
1
1
1
1
0
2
pT4
1
0
1
0
1
0
0
1
Histologic grade (WHO 1973)a
G1
29
15
0.022
32
12
0.026
20
24
0.425
39
5
<0.001
G2
57
30
50
37
37
50
61
26
G3
18
25
19
24
14
29
8
35
Histologic grade (WHO 2004)b
Low grade
71
30
0.001
68
33
0.005
49
52
0.019
87
14
<0.001
High grade
33
40
33
40
22
51
21
52
Adjacent carcinoma in situb
No
96
62
0.432
96
62
0.032
65
93
1.00
105
53
<0.001
Yes
8
8
5
11
6
10
3
13
Multiplicityb
Solitary
79
45
0.124
77
47
0.093
49
75
0.587
86
38
0.003
Multifocal
25
25
24
26
22
28
22
28
Growth patternb
Papillary
97
62
0.278
94
65
0.416
65
94
1.00
107
52
<0.001
Solid
7
8
7
8
6
9
1
14
aChi-Square Pearson (2-sided); bold face representing p-values < 0.05.
bFisher’s exact test (2-sided); bold face representing p-values < 0.05.
Univariate progression analyses
A total of 158 patients underwent TUR for a primary Ta or T1 urothelial carcinoma of the bladder and were followed for a median of 110.7 month (range: 32.4 - 245.9 month). In this group, only high expression levels of Ki-67 were significantly associated with increased risk of progression (p < 0.01). Increased expression of HDAC-1 showed a tendency for higher progression rates, however this was not statistically significant (p = 0.085). Beside growth pattern none of the clinicopathological parameters were associated with PFS. Table 3 shows p-values for the pathological data and the molecular markers.
Table 3
Univariate analyses of disease progresssion (n =158)
Variable
Categorization
Tumor progression
na
events
pb
Pathologic data:
Tumor stage (WHO 1973c)
pTa
85
10
0.412
pT1
68
12
Histologic grade (WHO 1973c)
G1
43
3
0.093
G2
82
12
G3
28
7
Histologic grade (WHO 2004d)
Low grade
95
10
0.092
High grade
58
12
Adjacent carcinoma in situ
No
141
20
0.570
Yes
12
2
Multifocality
Unifocal tumor
111
15
0.486
Multifocal tumor
42
7
Growth pattern
Papillary
146
17
<0.0001
Solid
7
5
Immunohistochemistry:
HDAC-1
Low expression
92
9
0.085
High expression
61
13
HDAC-2
Low expression
88
12
0.628
High expression
65
10
HDAC-3
Low expression
65
8
0.754
High expression
88
14
Ki-67 IHC
Low expression
101
9
0.004
High expression
52
13
aOnly primary pTa and pT1 tumours are included.
bLog Rank test (2-sided); bold face representing p-values <0.05.
cStaging and grading according to the 1973 WHO classification system.
dStaging and grading according to the 2004 WHO classification system.
To test whether the combination of high expression levels of HDAC-1 & HDAC-2 with different known clinico-pathological parameters can predict prognosis we performed an univariate cox-regression analysis. The combination of high-grade tumours and high expression levels of HDAC-1 was a predictor of PFS (hazard ratio [HR], 1.640; 95% confidence interval [95% CI], 1.021-2.636; p = 0.044). However, this combination did not outperform tumor growth pattern or Ki-67 as a predictor of outcome. Both parameters were able to predict prognosis in univariate analysis (Table 3). The combination of HDAC-1 and growth pattern or HDAC-1 and Ki-67 were of no additional value to predict prognosis. In both cases the p-values were higher than for growth pattern or Ki-67 alone (data not shown).
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Kaplan-Meier analyses for PFS are depicted in Figures 4, 5, 6, and show that bladder cancer patients with the combined feature of high grade tumours and high expression pattern of HDAC-1 have a significantly shorter progression free survival than all other patients (Figure 4). High HDAC-1 expression alone showed a tendency for shorter PFS, although not statistically significant (Figure 5). In addition, patients with high expression levels of Ki-67 have a significantly shorter PFS (Figure 6).
Figure 4
Kaplan-Meier analyses for progression-free survival for group of high-grade tumours in combination with high expression levels of HDAC-1 vs. high- and low-grade tumours with low expression levels of HDAC-1. For statistical analysis for survival curves Log-Rank test was used.
Figure 5
Kaplan-Meier analyses for progression-free survival for HDAC-1 staining. For statistical analysis for survival curves Log-Rank test was used.
Figure 6
Kaplan-Meier analyses for progression-free survival for ki-67 staining. For statistical analysis for survival curves Log-Rank test was used.
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×
×
Discussion
This is the first comprehensive immunohistochemical analysis of the expression of several class I HDAC proteins (1, 2 and 3) in urothelial carcinoma. In our study, we found all three isoforms in a relevant amount of all investigated urothelial tumours. HDAC-1 and HDAC-2 were highly associated with high-grade superficial papillary bladder tumours. Additionally, high expression levels of HDAC-1 showed a tendency towards a shorter PFS.
So far, little was known about class I HDAC expression pattern in urothelial cancer [5]. According to the Proteinatlas (http://www.proteinatlas.org), HDAC-1 to -3 expression levels are moderate at most in urothelial cancer [22]. In previous expression arrays HDAC-2 and -3 showed higher expression levels in urothelial cancer than in normal urothelial tissue [2, 9, 11]. Expression array data from another study by Wild et al. demonstrated an upregulation of HDAC-1 in bladder cancer compared to normal urothelial tissue [23]. On the contrary, published data from other groups did not reveal any difference of class I HDAC expression between urothelial cancer and normal urothelium in microarray data [24, 25]. In accordance with these findings a study from Xu reported no difference in immunohistochemical expression of HDAC-2 in human bladder cancer tissue (142 cases) compared to normal urothelial tissue (23 cases) [13].
In a recent study, Niegisch and colleagues were able to show upregulation of HDAC-2 mRNAs in a subset of tested tumours compared to normal urothelium [9, 11, 17]. However, only 24 tumour tissues and 12 normal samples were tested.
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Our study is the first attempt to test the immunohistochemical expression of class I HDACs in a large cohort of patients with bladder cancer. As class I HDACs can be detected in a relevant group of urothelial cancer, they may therefore be relevant in pathophysiology and as target proteins for treatment.
Besides the distinct presence of class I HDACs in urothelial cancer, high expression levels of HDAC-1 and -2 were associated with stage and grade of this tumours. Overexpression of HDACs has been found in several other solid tumours such as prostate and colon cancer [7, 26, 27]. High expression levels of class I HDACs correlated with tumour dedifferentiation and higher proliferative fractions (measured by Ki-67) in urothelial carcinoma, which is in line with in vitro studies showing that high HDAC activity leads to tumour dedifferentiation and enhanced tumour cell proliferation [28‐30]. Despite the growth inhibitory effects of HDAC-i demonstrated in various cell lines including bladder cancer cells, a broad expression analysis of this attractive target has not been conducted yet [12‐16, 31, 32].
To the best of our knowledge, this is the first study analysing HDAC-1, -2 and -3 expression in bladder cancer and its association to prognosis. In our study HDAC-1 was found to be of rough prognostic relevance in pTa and pT1 tumours. High expression levels of class I HDACs have been found to be of prognostic relevance in other tumour entities before. Other study groups previously reported the association of class I HDACs with more aggressive tumours and even shortened patient survival in prostate and gastric cancer [7, 33]. Our findings suggest that HDAC-1 may have a role in prognosis of superficial urothelial tumours.
In our work the rate of Ki-67 positive tumour cells was highly associated with tumour grade, stage, and a shorter PFS. A substantial amount of research has demonstrated the prognostic role of Ki-67 in urothelial cancer; its prognostic value and its association with pathological parameters and prognosis could be shown in several studies [34‐36]. These findings are in line with our work and confirm the representativeness and validity of this TMA-construct. Furthermore, we observed a strong correlation between the proliferation index (Ki-67) and all three investigated HDACs. The connection between HDAC expression and Ki-67 observed in urothelial carcinoma has already been demonstrated for prostate, renal and colorectal cancer in previous studies [7, 19, 37].
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Additionally, intravesical instillation of HDAC-i may have a potential as chemopreventive agent to treat superficial bladder cancer, as up to 50% of superficial tumours showed high expression levels of HDACs. However, it is not clear whether HDAC protein expression as assessed by immunohistochemistry is a predictor for treatment response to HDAC-i. Thus, additional studies are needed to clarify the role HDAC-i in non-invasive urothelial cancer.
Our study has several limitations, including its retrospective design and the use of immunohistochemical methodology, which has inherent limitations, including scoring of staining. We used a standardized and well-established semiquantitative scoring method in accordance with previous publications to reduce variability. In addition, the proportion of muscle-invasive bladder cancer was limited and as a consequence we cannot draw any conclusion for this subgroup of tumours. Therefore future research should also try to assess whether class I HDACs have a prognostic value in locally advanced invasive or metastatic urothelial cancer.
Conclusion
High levels of class I HDACs showed a significant correlation with cellular proliferation and tumor grade. Non-invasive (pTa) and pT1 bladder tumours with high expression levels of HDAC-1 showed a tendency towards shorter PFS in our cohort. However, further prospective studies and bigger cohorts including muscle-invasive bladder cancer patients are needed to evaluate the prognostic value of HDACs. Moreover the high expression levels of HDACs in urothelial bladder cancer might be indicative for a treatment response to HDAC-i which ought to be evaluated in further studies.
Acknowledgements
The authors thank the Institute of Pathology, University of Zurich, for providing material and technical assistance to construct the TMA. Furthermore CP would like to thank Damina Balmer for her corrections and comments on the final manuscript.
Open Access
This article is published under license to BioMed Central Ltd. This is an Open Access article is distributed under the terms of the Creative Commons Attribution License (
https://creativecommons.org/licenses/by/2.0
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
CP coordinated the study, performed statistical analyses and wrote the paper. BJ performed immuno-histological analyses and wrote the paper. TH, HHS, TS coordinated the study and revised essential parts of the paper. CP, DS and MS provided clinicopatholocial data for the study. PJW and HM supported the study coordination, assisted in technical questions and statistical support. GK conceived and coordinated the study, performed statistical analyses, wrote and revised the paper. All authors read and approved the final manuscript.
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