Methylomics analysis identifies ZNF671 as an epigenetically repressed novel tumor suppressor and a potential non-invasive biomarker for the detection of urothelial carcinoma
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Chia-Ming Yeh1,2,*, Pi-Che Chen3,*, Hsiao-Yen Hsieh2,5, Yeong-Chin Jou3, Chang-Te Lin3, Ming-Hsuan Tsai1, Wen-Yu Huang1,2, Yi-Ting Wang1,2, Ru-Inn Lin1,6, Szu-Shan Chen1,2, Chun-Liang Tung4, Shu-Fen Wu1,2, De-Ching Chang1,2, Cheng-Huang Shen3, Cheng-Da Hsu5 and Michael W.Y. Chan1,2,*
1 Department of Life Science, National Chung Cheng University, Min-Hsiung, Chia-Yi, Taiwan
2 Institute of Molecular Biology, National Chung Cheng University, Min-Hsiung, Chia-Yi, Taiwan
3 Department of Urology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi, Taiwan
4 Department of Pathology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi, Taiwan
5 Department of Medical Research, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi, Taiwan
6 Departments of Radiation Oncology, Buddhist Dalin Tzu Chi General Hospital, Chia Yi, Taiwan
* These authors have contributed equally to this work
Michael W.Y. Chan, email:
Keywords: urothelial carcinoma, DNA methylation, urine, ZNF671
Received: April 03, 2015 Accepted: July 16, 2015 Published: July 22, 2015
The molecular mechanism underlying the lethal phenomenon of urothelial carcinoma (UC) tumor recurrence remains unresolved. Here, by methylation microarray, we identified promoter methylation of the zinc-finger protein gene, ZNF671 in bladder UC tumor tissue samples, a finding that was independently validated by bisulphite pyrosequencing in cell lines and tissue samples. Subsequent assays including treatment with epigenetic depressive agents and in vitro methylation showed ZNF671 methylation to result in its transcriptional repression. ZNF671 re-expression in UC cell lines, via ectopic expression, inhibited tumor growth and invasion, in possible conjunction with downregulation of cancer stem cell markers (c-KIT, NANOG, OCT4). Clinically, high ZNF671 methylation in UC tumor tissues (n=96; 63 bladder, 33 upper urinary tract) associated with tumor grade and poor locoregional disease-free survival. Quantitative MSP analysis in a training (n=97) and test (n=61) sets of voided urine samples from bladder UC patients revealed a sensitivity and specificity of 42%-48% and 89%-92.8%, respectively, for UC cancer detection. Moreover, combining DNA methylation of ZNF671 and 2 other genes (IRF8 and sFRP1) further increased the sensitivity to 96.2%, suggesting a possible three-gene UC biomarker. In summary, ZNF671, an epigenetically silenced novel tumor suppressor, represents a potential predictor for UC relapse and non-invasive biomarker that could assist in UC clinical decision-making.
Urothelial carcinoma (UC, also known as transitional cell carcinoma, TCC) is the second most common genitourinary malignancy and the ninth most common cancer in the world [1, 2]. UC is particularly common in Taiwan, where the highest incidence occurs in the southwestern coastal region . The majority of UC tumors are found in the urinary bladder, and while upper urinary tract (ureter or renal pelvis) UC accounts for 5%-10% of all worldwide cases , its incidence in Taiwan is around 25% . Although approximately 80% of UC tumors are non-muscle invasive, 70% of those will recur with muscle invasion [6, 7]. More notably, synchronous or metachronous UC through the urinary tract are not uncommon, thus necessitating long-term, repeated follow-up with highly invasive cystoscopy to monitor patients recurrence. To avoid this unpleasant procedure (and possibly, diminished patient compliance), alternative, non-invasive UC detection methods are urgently needed. Although conventional urine cytology remains the “gold standard” for non-invasive UC detection and disease monitoring, this method suffers from poor sensitivity ( < 34%) .
Accumulation of multiple genetic and epigenetic alternations that lead to the activation of proto-oncogenes and/or inactivation of tumor-suppressor genes (TSGs) is a ubiquitous event in human carcinogensis [9-11]. The intimate association of cancer and epigenetic aberrations, such as deviant DNA methylation and histone modifications, is reflective of the indispensability of epigenetics as a gene regulatory mechanism governing multi-/pluripotent cell fate commitment [12, 13]. As loss of differentiation is an essential and omnipresent event in carcinogenesis, reversal of dedifferentiating epigenetic aberrations could be highly effective for the therapy of several tumor types [14, 15].
In addition to the potential promise of epigenetic therapies, since altered chromatin (including aberrant methylomes) is one of most common molecular aberrations in human disease, methylated DNA represents an ideal bio-molecule for clinical diagnosis, due to its stability, presence in body fluids, and ease of detection [14, 16].
Previous reports, including our own, have identified numerous cancer-associated TSGs that are transcriptionally silenced by promoter DNA methylation [17-21]. However, the role of epigenetic alterations in the tumor progression and recurrence of urothelial carcinoma remains little explored. Consequently, we herein set forth to identify epigenetically silenced genes involved in UC tumor progression and recurrence, using methylomic screening of primary normal human urothelial cells (HUCs) and bladder UC tissue samples. That screening, and other assays, revealed one DNA methylation target, ZNF671, to be epigenetically silenced by promoter methylation in bladder UC. Our results demonstrate that ZNF671 promoter methylation is frequently found in urothelial carcinoma and thus, represents a promising, non-invasive biomarker for the detection and guided therapy of urothelial carcinoma.
The promoter of the zinc-finger protein gene ZNF671 is frequently hypermethylated in bladder urothelial carcinoma
We previously identified several tumor suppressors that are epigenetically silenced by promoter methylation in bladder UC. To identify additional tumor suppressor genes in bladder UC that might associate with tumor progression, and possibly be present in body fluids, we performed Illumina 27K CpG island methylation array on DNA from HUCs (primary normal human urothelial cells) and 7 bladder UC tissue samples (three low-grade and four high-grade). There were a total of 31 probes (representing 28 genes and three redundancies) that showed low β-values (β < 0.1, see Materials and Methods) in HUC cells but high β-values in tumor tissue samples (β-values: 0.2-0.5 in low grade samples; > 0.5 in high grade samples, Figure 1A, Supplementary Table 2). Subjection of this 28-gene set of differentially methylated genes to gene ontology analysis by DAVID  revealed over-representation of genes involved in transcriptional activity (Supplementary Table 3). One identified target, the ZNF671 transcriptional repressor (Figure 1A, arrow head), caught our attention, as ZNF671 was recently found epigenetically silenced by promoter DNA methylation in renal cell and cervical cancers [23, 24]. These findings are consistent with previous reports that other ZNF family proteins can act as tumor suppressors and are frequently found down-regulated by DNA methylation in multiple human cancer types [25-27]. However, the role of ZNF671 in bladder UC has never been explored. Based on all of the above, ZNF671 was selected for further analysis of its potential role in the formation and progression of urothelial carcinoma.
We first confirmed the microarray result by bisulphite pyrosequencing that showed a linear correlation between β-values (from the array) and DNA methylation levels of the promoter region of ZNF671 in the same tumor tissue samples (Figure 1B, 1C). We also determined ZNF671 methylation levels in several bladder UC cell lines by combined bisulphite restriction analysis (COBRA; Supplementary Figure 1A)  and bisulphite pyrosequencing (Figure 1D). Those assays showed that ZNF671 promoter methylation was obvious in all bladder UC cell lines but not in normal bladder HUC cells (Supplementary Figure 1A). These results suggest that the ZNF671 promoter is hypermethylated in bladder UC patient samples and cancer cell lines.
Figure 1: Methylation microarray identification of ZNF671 promoter DNA hypermethylation in bladder UC. A. Heatmap showing DNA methylation levels (β-value) of selected probes in normal bladder urothelial (HUC, n = 1) and seven human bladder UC tissues (low-grade, n = 3; high-grade, n = 4) using an Illumina infinium 27K methylation array. One gene, ZNF671 (red arrowheads) that showed promoter hypermethylation in bladder UC tissues was selected for further analysis. B. Upper panel shows the schematic diagram depicting the genomic structure and position of the CG sites (vertical dashes) in the ZNF671 promoter region (from -271 to +290 with respect to the TSS). Right-angled arrow indicates the ZNF671 gene transcriptional start site (TSS, defined as nucleotide 0). The location of the microarray probes (red horizontal line) at the TSS and promoter, bisulphite pyrosequencing (blue) and primers (small horizontal arrows) for COBRA (solid arrows) and qMSP (dashed arrows) are indicated. Lower panel shows the DNA methylation levels (as determined by bisulphite pyrosequencing) in the ZNF671 promoter in DNA from 7 bladder UC tissues used in the microarray analysis. Numbers indicate the locations (nucleotide number with respect to the TSS) of specific CpGs examined. LG denotes low grade, while HG denotes high grade. C. Scatter plot showing the correlation between the β-value (from microarray) and methylation percentage (as determined by bisulphite pyrosequencing) of ZNF671 CG sites in 7 bladder UC tissues. There was a significant correlation between β-value and methylation percentages (r2 = 0.9625, P < 0.0001). D. Methylation levels of bladder cancer cell lines as determined by bisulphite pyrosequencing. IVD (in vitro methylated DNA) was included as positive control.
ZNF671 expression is epigenetically repressed in bladder UC cells
Next, we investigated ZNF671 expression in bladder UC cell lines using quantitative real-time RT-PCR amplification of RNA from bladder UC cell lines. Compared to HUC cells, ZNF671 expression was significantly down-regulated in all bladder UC cell lines we examined (Figure 2A). To further access whether epigenetic repression, by DNA hypermethylation, was responsible for ZNF671 transcriptional down-regulation, cells were treated with the demethylating agent, 5-aza-2’-deoxycytidine (5azaDC) (Figure 2B). Indeed, the addition of 5azaDC resulted in robust ZNF671 re-expression of in all treated UC cells.
To examine, in more detail, how ZNF671 expression is epigenetically controlled by promoter methylation, in vitro promoter methylation assays were performed. A 960-bp region (-329/631) containing the ZNF671 promoter was cloned into a pGL3 luciferase reporter plasmid (Figure 2C), showing that in vitro methylation of the ZNF671 promoter significantly (P < 0.05) decreased luciferase activity, as compared to the unmethylated control (Figure 2D).
As high ZNF671 methylation levels were observed in bladder UC cell lines, and to exclude a possible “passenger event” due to selective pressure for UC cell survival in long-term culture , we examined ZNF671 expression in several non-UC cancer cell lines including cervical, ovarian, gastric, liver, brain and oral cancer cell lines. In contrast to HUC cells, ZNF671 was down-regulated in some, but not all of those non-UC cancer cell lines (Figure 2E). COBRA also confirmed that ZNF671 promoter methylation correlated with gene down-regulation in these non-UC cells (Supplementary Figure 1B). Taken together, these results demonstrate that the zinc-finger protein gene, ZNF671, is epigenetically silenced in human urothelial carcinoma.
Figure 2: ZNF671 is epigenetically silenced in bladder UC cells. A. ZNF671 expression in two normal bladder urothelial (HUC) and bladder UC cell lines was determined by real time RT-PCR. All bladder UC cell lines, showed significant down-regulation of ZNF671 expression, as compared to HUC cells. B. ZNF671 expression in bladder UC cell lines after epigenetic treatment. Bladder UC cell lines treated with 5-aza-2’-deoxycytidine (5-azaDC) were examined for ZNF671 re-expression by qRT-PCR. Epigenetic treatment significantly restored ZNF671 expression. Each error bar represents standard deviations, as determined from triplicates assessments. C. Luciferase assay of the putative ZNF671 promoter. A 960-bp region containing the putative ZNF671 promoter (-329/631) was cloned into a pGL3 luciferase vector and transfected into 293T cells. As compared to the empty vector, the ZNF671 promoter fusion construct exhibited luciferase activity. D. In vitro methylation assay of the ZNF671 promoter. The ZNF671 promoter region, with or without DNA methylation was cloned into pGL3 luciferase vectors and transfected into 293T cells. After 48 hours of transfection, cells were lysed and luciferase activity was analyzed. In vitro methylation of the ZNF671 promoter significantly decreased luciferase activity. E. Endogenous ZNF7671 expression was examined in different types of non-UC cancer cell lines by RT-PCR, showing that ZNF671 was down-regulated in some, but not all, of the cancer cells examined.
ZNF671 ectopic expression in UC cells inhibits anchorage-dependent growth and invasion
Having demonstrated that ZNF671 is epigenetically silenced by DNA methylation, we then investigated a possible tumor suppressive role of ZNF671 in bladder UC cells. Stable transfectants were selected from UMUC3 bladder UC cells transfected with a ZNF671-expression vector (ZNF671 expression levels shown in Supplementary Figure 2). As compared to stable vector only-transfected cells, ZNF671-expressing UMUC3 bladder UC cells showed significant attenuation of anchorage-dependent growth (Figure 3A, 3B) and invasion (Figure 3C, 3D).
Restoration of ZNF671 expression inhibits tumor growth in vivo
Based on our cell culture findings, we next examined the tumor suppressive effects of ZNF671 in an in vivo xenograft mouse model. Nude mice subcutaneously injected with ZNF671-overexpressing UMUC3 cells grew tumors of significantly less tumor volume and weight, as compared to mice injected with UMUC3 cells stably transfected with the empty vector control (Figure 3E, 3F). Taken together, these in vitro and in vivo results strongly suggest ZNF671 to be a potential tumor suppressor in advanced human bladder UC.
Figure 3: Ectopic expression of ZNF671 inhibits tumor growth and invasion in UMUC3 bladder UC cells. A. Ectopic expression of ZNF671 inhibited tumor growth as determined by soft agar assays. UMUC3 bladder UC cells transfected with empty or ZNF671 expression vector (pcDNA3.1) were selected for soft agar growth assay. Cells stably overexpressing ZNF671 (Supplementary Figure 2) generated significantly fewer colonies than the controls. B. Quantitative analysis of colony formation assay showing the number of colonies in the control and ZNF671-overexpression groups. C. UMUC3 bladder UC cells stably overexpressing ZNF671 demonstrated significantly lower invasion ability than the control cells. D. Quantitative analysis of invasion assay. ZNF671 overexpression inhibited tumor invasion in bladder UC cells. E. Restored ZNF671 expression similarly inhibited tumor growth in vivo. Control or ZNF671-overexpressing cells were injected subcutaneously into nude mice. Tumor volumes, measured daily, showed significant differences between the control and ZNF671-overexpressing group upon and after day 16. F. Tumor weights were measured at the end of the experiments. Significant differences between tumor weights were noted when comparing the controls and ZNF671-overexpressing cells xenograft. *P < 0.05.
Over-expression of ZNF671 down-regulates the expression of cancer stem cell markers in bladder urothelial carcinoma
A current consensus asserts that the tumor invasion-associated epithelial-mesenchymal transition (EMT) intimately correlates with cancer stem cell (CSC) phenotypes . Such “phenotypic plasticity” that allows for transitions between different levels of cellular differentiation is governed by genome-wide epigenetic modifications [31, 32]. To assess the possibility that ZNF671 tumor suppressive activity might relate to disruption of cancer “stemness” or EMT phenotypes, we examined the effects of ZNF671 on the expression of CSC markers. Interestingly, ZNF671 overexpression significantly decreased the expression of three stem cell markers, c-KIT, NANOG, and OCT4  in UMUC3 (Figure 4A) but only one such marker (c-KIT) in TSGH8301 bladder UC cells (Figure 4B). Importantly, significant up-regulation of CDH1 (E-cadherin) was observed in both ZNF671-overexpressing UMUC3 and TSGH8301 cells (Figure 4C, 4D). Taken together, these results support the postulate that ZNF671 could inhibit tumor growth and invasion through down-regulation of determinants of dedifferentiation.
Figure 4: ZNF671 expression alters the expression of cancer stem cell markers. Expression of stem cell markers (c-KIT, NANOG and OCT4) were detected by qRT-PCR in A. UMUC3; B. TSGH8301 bladder UC cells. Relative expression of E-cadherin (CDH1) in ZNF671-overexpressing C. UMUC3 and D. TSGH8301 bladder UC cell lines. ZNF671 overexpression resulted in up-regulation of E-cadherin (CDH1) in ZNF671-overexpressing cells, as compared to (vector only-transfected) controls. *P < 0.05, **P < 0.01, ***P < 0.001.
ZNF671 is epigenetically silenced in UC patient samples
The above experiments demonstrate that ZNF671 is likely a tumor suppressor that is transcriptionally suppressed by promoter DNA methylation in bladder UC cell lines. To examine the possible clinical significance of ZNF671 methylation to UC progression, we investigated the promoter methylation and expression of ZNF671 in UC patient samples. First, we compared the relative expression of ZNF671 in nine bladder UC tissues, and their corresponding adjacent normal tissues. ZNF671 expression was significantly down-regulated in five tumor tissue samples as compared to their adjacent normal counterparts (Figure 5A). We further examined the methylation status of ZNF671 by bisulphite pyrosequencing in 63 bladder UC tissues and 9 adjacent normal tissues (Table 1). To assess possible detection of ZNF671 methylation in various UC subsites, 33 upper urinary tract UC tissue samples originating from the ureter or renal pelvis, were also procured for analysis (Table 1). ZNF671 methylation in cancer tissues was significantly higher than in adjacent non-cancerous tissues (Figure 5B, P = 0.0001). Importantly, there was no significant difference between ZNF671 methylation in UC tissue samples from the bladder vs. upper urinary tract (Figure 5B). Moreover, further analysis showed that ZNF671 methylation was significantly elevated in high-grade, but not low-grade, cancer tissues (Figure 5C, Table 2, P = 0.003). Such tumor grade trends could also be observed in bladder or upper urinary tract UC tumor tissues samples (Supplementary Figure 3A, 3B). Importantly, although not significant, there was an inverse relationship between ZNF7671 promoter methylation and expression in UC patient tumor samples (n = 60, Figure 5E, Spearman R = -0.18, P = 0.14). Interestingly, we also observed a group of patients (n = 7) showing the opposite correlation, i.e., low ZNF671 expression and concomitant with low DNA methylation, thus suggesting that other genetic or epigenetic mechanisms contribute to ZNF671 down-regulation in this specific sub-group. By removing this sub-group from the analysis, ZNF671 promoter methylation showed a statistically significant inverse relationship with expression (Supplementary Figure 4, R = -0.32, P = 0.01). Taken together, these results suggest that ZNF671 is epigenetically silenced by promoter methylation, with progressively increased methylation positively correlating with increased UC patient tumor grade.
Table 1: Summary of clinical-pathological data of UC tissue and urine samples
Table 2: Correlation between ZNF671 methylation and clinical-pathological data in 96 UC samples
ZNF671 methylation associates with shorter locoregional disease-free survival
Based on our observed relationship between increased ZNF671 hyper-methylation and tumor grade, we examined possible association of ZNF671 methylation levels with UC tumor recurrence, showing that ZNF671 methylation was significantly higher in relapsed tumor tissue samples (Figure 5D, Table 2). Further sub-group analysis yielded similar results in bladder, but not in upper urinary tract UC tumor tissue samples (Supplementary Figure 3C, 3D, Supplementary Table 4). Although recurrent tumor tissue samples tended to be of higher tumor grade (Supplementary Figure 5A, 5B), there was no difference in ZNF671 methylation between primary and recurrent samples (Supplementary Figure 5C, 5D), likely due to the relatively small sample size of recurrent cases.
The correlation between UC tumor tissue ZNF671 hypermethylation and locoregional disease-free survival was also analyzed. Kaplan-Meier analysis demonstrated that patients with higher ZNF671 methylation (a cutoff value of 11%, see Material and Methods) demonstrated shorter locoregional disease-free survival than in patients with lower methylation (Figure 5F, P < 0.05). Multivariate analysis also confirmed that ZNF671 methylation was an independent risk factor for predicting recurrence (HR, 3.742; 95% CI, 1.464 - 9.562; P < 0.01; Table 3). Importantly, subgroup analysis also showed that the above-mentioned trend could also be observed in bladder or upper urinary tract UC tissues samples (Supplementary Figure 3E, 3F; Supplementary Table 5, 6).
Table 3: Hazard ratios for recurrence according to predictive factors, in 96 UC tissue samples
Abbreviation: HR, hazard ratio; 95% CI, 95% confidence interval;
TURBT, transurethral resection of bladder tumor
ZNF671 methylation as a non-invasive UC biomarker in voided urine
Having demonstrated that the potential tumor suppressor ZNF671 is epigenetically silenced in UC, and in consideration of other cancer biomarkers found in human urine [17, 34], we assessed the feasibility of using ZNF671 methylation as a biomarker for non-invasive cancer detection in urine. We first collected voided urine from 69 recruited bladder UC patients and 28 healthy control individuals as a training set (Table 1). DNA extracted from urine sediments were subjected to quantitative real-time methylation specific PCR (qMSP) analysis. As compared to the control samples, higher ZNF671 methylation levels were detected in UC patients’ urine samples (Figure 6A, P < 0.001). Based on the cutoff value generated by the area under the receiver operating characteristic curve (ROC, AUC = 0.783, a cutoff value of 5.37%, Figure 6B), we observed methylated ZNF671 to exhibit a sensitivity of 42% and a specificity of 92.8% for UC detection in urine (Table 4).
Table 4: Sensitivity and specificity of ZNF671 methylation in cancer detection using voided urine samples
To further examine the predictive power of ZNF671 methylation for non-invasive cancer detection, we obtained another 61 urine samples (33 bladder UC and 28 non-cancer) as a test set for single-blind analysis (Table 1). Similarly, higher ZNF671 methylation levels were detected in UC urine samples, as compared to urine from the control subjects (Figure 6C, P < 0.01). Using a similar cutoff as the training set, a sensitivity of 48% and a specificity of 89% for cancer detection were obtained (Table 4). These results suggest that ZNF671 methylation may serve as a non-invasive biomarker for bladder UC detection using urine.
Figure 5: ZNF671 is epigenetically silenced by promoter hypermethylation in UC patients, and associates with tumor recurrence. A. ZNF671 relative expression in bladder UC tumor tissues, and their corresponding adjacent normal from the same patient, as determined by qRT-PCR. Down-regulation of ZNF671 was observed in five UC tumor patients, as compared to their adjacent normal tissues. *P < 0.05. ZNF671 methylation levels of in 96 UC patient tissue samples were determined by bisulfite pyrosequencing. Higher ZNF671 methylation levels were observed in B. cancer tissues from bladder or upper urinary tract neoplasms, as compared to 9 non-cancerous tissues, C. patient tissues with higher tumor grades and D. UC patients with relapse, *P < 0.05, **P < 0.01. E. Scatter plot showing the relationship between relative ZNF671 methylation and expression in 60 UC patient tissue samples (bladder, n = 38, upper urinary tract, n = 22), relative to ZNF671 methylation and expression of in HUC (which was set to 1). As shown, a trend showed an inverse relationship between ZNF671 methylation and expression in this group of patient tumor tissue samples. F. Kaplan-Meier analysis of tumor tissues ZNF671 methylation for locoregional disease-free survival of UC patients. Patients with higher ZNF671 methylation ( > 11% methylation, please refer to Material and Methods) demonstrated shorter DFS than patients with lower methylation. Log-rank test, **P < 0.01.
A multi-methylation marker panel further increases the sensitivity of bladder UC detection
Our previous study demonstrated that a combined panel of methylated markers could substantially increase the sensitivity of the bladder UC detection in urine . We therefore examined the sensitivity and specificity of cancer detection in urine by combining methylated ZNF671 with methylation of two other TSGs (IRF8 and sFRP1) using a previously published urine sample cohort (26 UCs and 19 non-cancerous controls) . While the sensitivity and specificity of cancer detection using ZNF671 methylation alone was 57.7% and 89.5% (Table 5), combining hypermethylation of ZNF671 with that of IRF8 and SFRP1 increased the sensitivity to 96.2% (Table 5). Notably, the sensitivity of this marker panel for detection of high-grade samples could be up to 100% (Table 5). Taken together, these results imply that combining ZNF671 DNA methylation with other methylated genes could represent a sensitive biomarker panel for non-invasive bladder UC detection using urine.
Table 5: Sensitivity and specificity of cancer detection using voided urine samples
Figure 6: Quantitative MSP (qMSP) analysis of ZNF671 methylation in voided urine samples from bladder UC patients. A. As a training set, methylation of ZNF671 was determined by quantitative methylation specific PCR (qMSP) in voided urine samples from non-cancerous control (n = 28) and bladder UC patients (n = 69). Compared to the non-cancerous controls, higher ZNF671 methylation levels were detected in cancer samples. ***P < 0.001. B. A receiver operating characteristic curve (ROC) of ZNF671 methylation in urine samples from 28 non-cancer controls and 69 bladder UC patients. According to the area under the curve (AUC = 0.783), methylation of ZNF671 showed excellent discrimination for bladder UC. C. The predictive power of ZNF671 methylation was determined in another set of 63 urine samples (from 28 healthy control individuals and 33 UC patients) for a single-blind qMSP analysis. Similar to above, compared to the non-cancerous controls, higher ZNF671 methylation levels were also detected in cancer samples. **P < 0.01. The sensitivity and specificity of ZNF671 methylation can be found in Table 4.
Although urothelial carcinoma (UC) patients have a low mortality rate, the high recurrence rate of this cancer type requires long-term follow-up with repeated cystoscopy for monitoring return disease. Thus, a better understanding of the molecular carcinogenesis of UC tumor progression may help in developing novel, less invasive diagnostic markers. In this study, by using various DNA methylation assessments, we identified a novel tumor suppressor gene, ZNF671 that is epigenetically silenced by promoter DNA methylation in UC.
ZNF671, which contains C2H2-type zinc fingers (ZFs) and a Krüppel associated box (KRAB) domain, is a member of the KRAB-ZF (KRAB-ZFP) family of mammalian transcriptional repressors [35-37]. Through recruitment of KRAB-associated protein-1 (KAP1) and other co-repressors, KRAB-ZFPs form heterochromatin with HP1, SETDB1, and various histone deacetylases (HDACs) to epigenetically silence their targets [37-41]. Furthermore, KRAB-ZFPs are also the largest group of transcription factors regulating cell differentiation, proliferation, apoptosis, tumor suppression, and neoplastic transformation [25, 42-44]. Previous studies demonstrated that some of these ZNF proteins are tumor suppressors that are epigenetically silenced by DNA methylation in multiple human cancers [25-27]. For example, ZNF23 can enhance the expression of p27KIP1 to inhibit cancer cell growth , while ZNF668 can enhance the stability of the p53 tumor suppressor by preventing MDM2-mediated p53 ubiquitination and its subsequent proteosomal degradation, in breast cancer . While ZNF382 and ZNF545 are frequently down-regulated by promoter methylation, their expression can inhibit colony formation, proliferation and induce apoptosis via repression of the NF-kB and AP-1 signaling pathways in multiple tumors [25, 26].
Although ZNF671 was previously found to be silenced by promoter methylation in renal cell and cervical carcinomas [23, 24], its role in UC has never been explored. In this study, we found that ZNF671 was epigenetically silenced by promoter hypermethylation in UC cell lines and patient tumor tissue samples. Moreover, ZNF671 methylation was significantly higher in tumor tissues, as compared to their adjacent normal tissues, and also significantly correlated with higher tumor grade and tumor relapse, in addition to associating with shortened locoregional disease-free survival (Figure 5). It is also noteworthy to point out that we observed a sub-group of UC patients with low ZNF671 expression and low ZNF671 methylation, suggesting that the role of other epigenetic modifications and/or genetic alterations contribute to ZNF671 gene regulation.
We also observed ZNF671 epigenetic repression in patient tumors of the upper urinary tract, which in Taiwan is a more common site for this malignancy , in addition to significant association with high tumor grade and shorter locoregional disease-free survival. Currently, the sensitivity of diagnostic tool for this UC is known to be low [47, 48]. Thus, a role for ZNF671 methylation as a non-invasive biomarker for this disease deserves further investigation.
Our functional studies additionally showed that ZNF671 overexpression inhibits UC invasion and growth both in vitro, and in vivo (in xenograft mouse models). Furthermore, recent studies showed that the transcriptionally repressive ZNF KRAB domain can recruit KAP1, another transcriptional co-repressor that cooperates in epigenetically silencing KRAB-ZNF targets [49, 50]. More recently, Lin et al. demonstrated that ZBRK1, a KRAB-ZFP could suppress tumor invasion by recruiting KAP1 in cervical cancer, as loss of ZBRK1 resulted in KAP1 up-regulation and tumor migration and invasion . Further study of the role of KAP1 in the tumor suppressive function of ZNF671, however, is needed.
Previous reports, including ours, demonstrate that detection of DNA methylation in exfoliated cells from the urine of bladder UC patients represents a useful and sensitive biomarker for cancer detection [14, 17, 52, 53]. Remarkably, a multiple methylation marker panel can greatly enhance the sensitivity of cancer detection [18, 34], and the sensitivity of methylation markers is much higher than that of urine cytology in cancer detection especially for low-grade tumors [17, 34]. For example, in one large cohort study, urine cytology exhibited an overall sensitivity of 38% for bladder UC detection, while the sensitivity for low-grade tumors was only 11.9% . In the current study, using qMSP assay, we found that ZNF671 methylation exhibited a sensitivity of around 45% (42%-48%) in detecting bladder UC in urine, and that combining methylated ZNF671, IRF8 and sFRP1 increased the overall sensitivity for cancer detection in urine, to 96.2% (overall disease), 90% (low-grade disease) and remarkably 100% for high-grade tumors (Table 5). These results suggest that combining ZNF671 with other methylation markers can result in highly sensitive methylation marker panels for possible non-invasive diagnosis of bladder urothelial carcinoma in voided urine. However, further experiments with larger sample sizes are needed to examine the predictive power of such methylation marker panels.
We must acknowledge several limitations of the current study. First, as a retrospective study, selection bias may exist and cannot be totally avoided even after multivariate analysis adjustment. Second, this sample cohort failed to demonstrate any association between tumor recurrence and tumor grade or stage, each of which are established prognostic factors for UC recurrence. This shortcoming may be attributed to the relatively small samples size of low-grade tumor samples. Therefore, prospective studies, with a more balanced sample-distribution should be conducted to confirm any hypothesized associations. Third, we have not analyzed ZNF671 methylation in any voided urine samples from upper urinary tract UC patient specimens. Thus, the possible role of ZNF671 methylation as a non-invasive biomarker for all UC sub-types requires further investigation.
In conclusion, ZNF671 is a potential tumor suppressor that is epigenetically silenced by promoter methylation in bladder urothelial carcinoma. Methylation of ZNF671 represents a novel epigenetic biomarker candidate for the non-invasive diagnosis of bladder UC. Moreover, a combination of ZNF671, IRF8, and SFRP1 represents a sensitive candidate methylation marker panel for the detection of bladder UC in urine. Such biomarkers could serve as surrogates for excluding specific patient subgroups from regular cystoscopy, and could also help guide clinical decision-making by indicating tumor grade, recurrence or therapeutic response.
MATERIALS AND METHODS
Cell culture and epigenetic treatment
Human urothelial cell (HUC) were maintained in urothelial cell medium (UCM, Sciencell Research Laboratories, Carlsbad, CA). SV-HUC-1 cells were derived by transducing simian virus 40 (SV40) into normal human uroepithelial cells (HUC), as described previously , and maintained in F12 Nutrient Mixture (GIBCO, Grand Island, NY), supplemented with 10% fetal bovine serum (FBS) (Invitrogen, Carlsbad, CA) and 50 units/ml of penicillin/streptomycin (Invitrogen). TSGH8301 and BFTC905 cells were maintained in RPMI 1640 (GIBCO) supplemented with 10% fetal bovine serum (FBS) (Invitrogen), while TCCSUP cells were cultured in DMEM (GIBCO) supplemented with 10% FBS. UMUC3 and HT1376 cells were grown in MEM (GIBCO) supplemented with 10% FBS, 1% NEAA, 1uM sodium pyruvate. The transformed human embryonic kidney cell line (293T) was maintained in DMEM (GIBCO) supplemented with 10% FBS. All cells were incubated in 37°C at 5% CO2. For demethylation treatment, cells were seeded in a 60-mm plates and treated with 0.5 μM 5’-aza-2’-deoxycytidine (5azaDC, Sigma, St. Louis, MO) for 3 days. Culture media and drugs were replenished every 24 hr. Cells were then lysed and harvested for RNA analysis by reverse transcription and PCR.
All patient samples were collected from the Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi, Taiwan. Seven bladder UC tissue samples (3 low-grade and 4 high-grade) from bladder UC patients were collected for Illumina 27K CpG island methylation array analysis. Another 63 bladder UC tissue samples and 9 cancer-adjacent normal tissues were collected for analysis. To examine whether ZNF671 methylation could also be detected in UC in the upper urinary tract, 33 UC tissue samples from the ureter or renal pelvis were also procured for analysis. The clinical-pathological data of all samples is summarized in Table 1. All tissue samples were acquired from either transurethral resection (TURBT) or radical surgery. Patients were then followed up by either cystoscopy or radiographic detection (CT or MRI) for recurrence. For biomarker assessments, voided urine samples from 69 bladder UC patients and 28 non-cancer individuals were collected as a training set. Another voided urine samples from 33 bladder UC patients and 28 non-cancer individuals comprised a blinded test set. All human subjects assessments were approved by the Institutional Review Board (IRB) of the Ditmanson Medical Foundation Chia-Yi Christian Hospital, Taiwan.
DNA was extracted from cells and frozen tissues using Genomic DNA Mini Kit (Geneaid, Taiwan), according to the manufacturer’s protocol. For urine samples, 50 ml of voided urine was centrifuged at 3,000 rpm for 10 min to obtain the sediment. The pellets were then washed 3 times with cold 1X PBS followed by centrifugation at 3,000 rpm for 10 min. DNA was then isolated using Genomic DNA Mini Kits (Geneaid), according to the manufacturer’s protocol.
Extraction of RNA and quantitative RT-PCR
RNA extraction was performed using TRizol reagent (Invitrogen) according to the manufacturer’s protocol. To remove potential contaminating DNA from the complementary DNA, 1 μg of total RNA was treated with DNase I (Amplification Grade, Invitrogen) prior to reverse transcription. First-strand cDNA synthesis was carried out using MMLV High Performance Reverse Transcriptase (Epicentre, Chicago, IL). The real-time PCR reactions were performed on an ABI Step-One real-time PCR system (Applied Biosystems, Foster City, CA) with specific primers (Supplementary Table 1). Relative gene expression was determined by comparing the threshold cycle of the test gene against the Ct value of GAPDH in a given sample (i.e., the comparative Ct method).
Bisulphite conversion and combined bisulphite restriction analysis (COBRA)
DNA was bisulphite modified using EZ DNA methylation kits (ZYMO Research, Orange, CA) according to the manufacturer’s protocol as previously described . For COBRA analysis , 4 μl of bisulphite converted DNA was first amplified using specific primers (Supplementary Table 1) targeting various ZNF671 promoter regions, followed by digestion with 20 U of AciI (GGCG) (New England Biolabs, Ipswich, MA). In-vitro methylated DNA (IVD, Merck Millipore, Billerica, MA) was used as a positive control for methylation, and water was used as a negative control. The digested products were then separated on 1.5% agarose gels for visualization.
Infinium microarray DNA methylation analysis
Bisulphite-modified DNA was subjected to methylation analysis using an Illumina Infinium Human Methylation27 microarray (Illumina, San Diego, CA), as previously described . The methylation level of each probe (β-value) was defined by the intensity of the methylated allele (M) / (intensity of the unmethylated allele (U) + intensity of the methylated allele (M) + 100). Selection of differentially methylated probes used the following inclusion criteria: 1) probes were present in “CpG islands”, regions with much higher than normal CG content; 2) probes having mean β-values of < 0.5 in HUC cells and > 0.5 for tumor samples; and 3) a minimum difference of mean β-values ≥0.2 between tumor samples and HUC were obtained.
Real-time quantitative methylation-specific PCR (qMSP) of urine sample DNA
For detection of ZNF671 methylation in urine samples, DNA was extracted (see above) and quantitative real-time methylation-specific PCR (qMSP) was performed as previously described . In brief, 4 μl of bisulphite converted DNA was subjected to real time MSP within specific promoter ZNF671 regions using distinct primer sets (Supplementary Table 1) in an ABI Step One real time PCR system (ABI). In-vitro methylated DNA (IVD) (Merck Millipore, Billerica, MA) was used as a positive control for methylation. β-actin (ACTB) was used to normalize the experimental samples to the input DNA. Methylation levels were determined by the threshold cycle number (Ct) for each sample against a standard curve generated by an IVD-MSP cloned fragment. Methylation percentages were calculated as ratios of the amount of ZNF671 versus ACTB of a sample divided by the same ratio of IVD multiplied by 100.
Bisulphite pyrosequencing of methylation analysis was performed as described previously . In brief, bisulphite-modified DNA (resulting in deamination of unmethylated cytosine to uracil) was subjected to PCR amplification strategy using a tailed reverse primer and a biotin-labeled universal primer (Supplementary Table 1). PCR and sequencing primers were designed using PyroMark Assay Design 2.0 (Qiagen GmbH, Hilden, Germany). A 228-bp fragment (-72 to 156) of the ZNF671 promoter was PCR-amplified, and pyrosequencing was performed using a PyroMark Q24 (Qiagen) and Pyro Gold Reagents (Qiagen), according to the manufacturer’s protocol. The methylation levels of 8 CpG sites, from 41 to 125 relative to the ZNF671 transcriptional start site (TSS) were measured. The methylation percentage of each cytosine was determined by their fluorescence intensities of cytosines divided by the sum of fluorescence intensity of cytosines and thymines (converted from uracil by PCR) at each CpG site. IVD (in vitro methylated DNA) was included as positive control of bisulphite pyrosequencing.
In vitro promoter DNA methylation assay
For the construction of a ZNF671 promoter plasmid, a 960-bp region of the ZNF671 promoter (-329/+631) was amplified by PCR using specific primers (Supplementary Table 1) from genomic DNA of HUC cells. The PCR products were then ligated into multiple cloning sites of the pGL3 vector, which was predigested with BglII and NheI. pGL3 vector for sequencing confirmation. For in vitro DNA methylation, the ZNF671 promoter was re-isolated from the pGL3-ZNF671 promoter by DNA digestion with BglII (New England Biolabs, Beverly, MA) and NheI (New England Biolabs), and in vitro methylated using a recombinant CpG methyltransferase (M.SssI, New England Biolabs). The excised fragment without M.SssI methylated treatment was acted as a control. DNA methylation was verified using the methylation-sensitive restriction enzyme, BstUI. Both the methylated and unmethylated promoters were re-liagted into the pGL3 promoter, and 50 ng of ligated DNA was co-transfected with 25 ng Renilla luciferase vectors (pRL-TK) into 293T cells in a 24-well plates. Cells were lysed after 48hr and luciferase activities were measured using a Dual Luciferase Reporter Assay System (Promega, Madison, WI) on a luminometer (Turner Designs, Sunnyvale, CA)
Plasmid constructs and transfection
The complete coding sequence of ZNF671 was amplified by PCR using specific primers (Supplementary Table 1) from cDNA of HUC cells which endogenously express ZNF671. The PCR products were ligated into the multiple cloning site of a pcDNA3.1 mammalian expression vector predigested with KpnI (New England Biolabs) and BamHI (New England Biolabs). ZNF671 expression or empty vectors were transfected into bladder UC UMUC3 cells using Lipofectamine 2000 transfection reagent (Invitrogen) according to the manufacturer’s protocol. Transfected cells were cultivated with fresh culture medium containing 800 μg/ml Geneticin (G418, Sigma) and replaced every 3 days. Single colonies that formed were selected for further culture.
Soft agar colony formation assay
1×104 cells were mixed and seeded in 2ml of 0.3% top agar supplemented with medium and 10% FBS. This suspension was overlaid on the 2.5ml bottom agar of agar of 0.5% agar with medium and 10% FBS in a 60-mm plate. The plates were allowed to solidify and were incubated at 37°C for 14-21 days. At the end of the experiments, colonies were stained with 1mg/ml Iodonitrotetrazolium chloride (INT stain, Sigma) for overnight at 37°C. Colony numbers were counted using Image-Pro 3D Suite software version 184.108.40.206 for Windows (Media Cybernetics, Rockville, MD).
In vitro invasion assays
To assess cell invasion, polycarbonate cell culture inserts (8.0 µm pore size, Merck Millipore, Billerica, MA) were first coated with 25 ul matrigel (25%, BD Biosciences, San Jose, CA) and incubated at 37°C for 30 minutes. 2x104 cells were seeded into the upper chamber of polycarbonate cell culture inserts containing medium with 1% FBS, and then placed into 24 well plate containing medium with 10% FBS. After 48 hours incubation, the cells at the top of the filter were removed by washing with 1X PBS. Cells attached to the bottoms of the membranes were fixed and stained with Giemsa stain (Sigma). Colonies numbers were then counted using Image-Pro 3D Suite software version 220.127.116.11 for Windows (Media Cybernetics).
In vivo tumorigenicity assay
Three athymic nude mice (BALB/cByJNarl, 4-week-old) were obtained from the National Laboratory Animal Center, Taiwan. All mice were kept under specific pathogen-free conditions using a laminar airflow rack with free access to sterilized food and autoclaved water. All experiments were performed under the approval from the Animal Experimentation Ethics Committee of the National Chung Cheng University. 2x 107 cells of UMUC3 cells stably transfected with pcDNA3.1/ZNF671 or empty vector were resuspended in 0.1ml of medium and Matrigel (BD Biosciences) mixture (1:1). The cell suspensions were then injected subcutaneously into the left and right flanks of each mouse (day 0). Tumor size was measured daily with calipers in length (L) and width (W). Tumor volumes were calculated using the formula (L x W2/2). At the end of the experiment, all mice were sacrificed by cervical dislocation.
Comparisons of non-parametric variables were assessed by Mann-Whitney tests, whenever appropriate. Locoregional disease-free survival was assessed by Kaplan-Meier analysis; curve difference between groups was estimated by the log-rank test. Locoregional disease-free time period was defined as the duration from the day of surgical resection to the day of the detection of new, recurred locoregional lesions by cystoscopy or cross section images (CT or MRI). Multivariate analysis was conducted by Cox hazard-proportional regression analysis. The 95% confidence intervals were provided in conjunction with a point to estimate an effective size. A ZNF671 methylation at 11%, which is the average ZNF671 methylation level of low grade tumor samples, was used as a cutoff. All statistical analyses, including ROC curves, were performed using SPSS software version 18.0 (SPSS, Inc., Chicago, IL) or GraphPad Prism 6 (GraphPad Software, Inc., San Diego, CA). P < 0.05 was considered statistically significant.
ACKNOWLEDGMENTS AND FUNDING
The authors would like to thank Drs. Curt Balch and Hon-Yi Lin for manuscript editing and critical reading. This study was supported by a research grant from the Ministry of Science and Technology, Taiwan (NSC99-2321-B-194-001 and MOST 103-2320-B-194-002) and the Ditmanson Medical Foundation Chia-Yi Christian Hospital (R101-10), Taiwan.
CONFLICTs OF INTEREST
The authors declare no conflict of interest.
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