Wdr66 is a novel marker for risk stratification and involved in epithelial-mesenchymal transition of esophageal squamous cell carcinoma
© Wang et al.; licensee BioMed Central Ltd. 2013
Received: 6 September 2012
Accepted: 11 March 2013
Published: 21 March 2013
We attempted to identify novel biomarkers and therapeutic targets for esophageal squamous cell carcinoma by gene expression profiling of frozen esophageal squamous carcinoma specimens and examined the functional relevance of a newly discovered marker gene, WDR66.
Laser capture microdissection technique was applied to collect the cells from well-defined tumor areas in collaboration with an experienced pathologist. Whole human gene expression profiling of frozen esophageal squamous carcinoma specimens (n = 10) and normal esophageal squamous tissue (n = 18) was performed using microarray technology. A gene encoding WDR66, WD repeat-containing protein 66 was significantly highly expressed in esophageal squamous carcinoma specimens. Microarray results were validated by quantitative real-time polymerase chain reaction (qRT-PCR) in a second and independent cohort (n = 71) consisting of esophageal squamous cell carcinoma (n = 25), normal esophagus (n = 11), esophageal adenocarcinoma (n = 13), gastric adenocarcinoma (n = 15) and colorectal cancers (n = 7). In order to understand WDR66’s functional relevance siRNA-mediated knockdown was performed in a human esophageal squamous cell carcinoma cell line, KYSE520 and the effects of this treatment were then checked by another microarray analysis.
High WDR66 expression was significantly associated with poor overall survival (P = 0.031) of patients suffering from esophageal squamous carcinomas. Multivariate Cox regression analysis revealed that WDR66 expression remained an independent prognostic factor (P = 0.042). WDR66 knockdown by RNA interference resulted particularly in changes of the expression of membrane components. Expression of vimentin was down regulated in WDR66 knockdown cells while that of the tight junction protein occludin was markedly up regulated. Furthermore, siRNA-mediated knockdown of WDR66 resulted in suppression of cell growth and reduced cell motility.
WDR66 might be a useful biomarker for risk stratification of esophageal squamous carcinomas. WDR66 expression is likely to play an important role in esophageal squamous cell carcinoma growth and invasion as a positive modulator of epithelial-mesenchymal transition. Furthermore, due to its high expression and possible functional relevance, WDR66 might be a novel drug target for the treatment of squamous carcinoma.
KeywordsWD repeat-containing protein Esophageal squamous cell carcinoma Epithelial-mesenchymal transition
Esophageal squamous cell carcinoma (ESCC) is one of the most lethal malignancies of the digestive tract and in most cases the initial diagnosis is established only once the malignancy is in the advanced stage . Poor survival is due to the fact that ESCC frequently metastasizes to regional and distant lymph nodes, even at initial diagnosis.
Treatment of cancer using molecular targets has brought promising results and attracts more and more attention [2–5]. Characterization of genes involved in the progression and development of ESCC may lead to the identification of new prognostic markers and therapeutic targets.
By whole genome-wide expression profiling, we found that WD repeat-containing protein 66 (WDR66), located on chromosome 12 (12q24.31), might be a useful biomarker for risk stratification and a modulator for epithelial-mesenchymal transition of ESCC.
WD-repeat protein family is a large family found in all eukaryotes and is implicated in a variety of functions ranging from signal transduction and transcription regulation to cell cycle control, autophagy and apoptosis . These repeating units are believed to serve as a scaffold for multiple protein interactions with various proteins . According to whole-genome sequence analysis, there are 136 WD-repeat proteins in humans which belong to the same structural class . Among the WD-repeat proteins, endonuclein containing five WD-repeat domains was shown to be up regulated in pancreatic cancer . The expression of human BTRC (beta-transducing repeat-containing protein), which contains one F-box and seven WD-repeats, targeted to epithelial cells under tissue specific promoter in BTRC deficient (−/−) female mice, promoted the development of mammary tumors . WDRPUH (WD repeat-containing protein 16) encoding a protein containing 11 highly conserved WD-repeat domains was also shown to be up regulated in human hepatocellular carcinomas and involved in promotion of cell proliferation . The WD repeat-containing protein 66 contains 9 highly conserved WD40 repeat motifs and an EF-hand-like domain. A genome-wide association study identified a single-nucleotide polymorphism located within intron 3 of WDR66 associated with mean platelet volume .
WD-repeat proteins have been identified as tumor markers that were frequently up-regulated in various cancers [11, 13, 14]. Here, we report for the first time that WDR66 might be an important prognostic factor for patients with ESCC as found by whole human gene expression profiling. Moreover, to our knowledge, the role of WDR66 in esophageal cancer development and progression has not been explored up to now. To this end we examined the effect of silencing of WDR66 by another microarray analysis.
In addition, the effect of WDR66 on epithelial-mesenchymal transition (EMT), cell motility and tumor growth was investigated.
Tissue samples from individuals of the first set (n = 28) were obtained from the tumor bank of Charité Comprehensive Cancer Center. Gene expression was examined by whole-human-genome microarrays (Affymetrix, Santa Clara, CA, USA). Ten esophageal squamous cell carcinoma (ESCC) and 18 normal esophageal (NE) biopsies were randomly collected. Normal healthy esophageal biopsies were collected from patients with esophageal pain but diagnosed as normal squamous without pathological changes. Surgical specimens of chemotherapy-naïve patients with known ESCC of histological grading G1, UICC stage II and III, had undergone esophagectomy. Patients’ age ranged from 22 to 83 years, with a median age of 59 years.
A second panel (n = 71) consisting of ESCC (n = 25), NE (n = 11), esophageal adenocarcinoma (EAC) (n = 13), gastric adenocarcinoma (GAC) (n = 15) and colorectal cancers (CRC) (n = 7) was used for qRT-PCR validation. Patients’ age ranged from 24 to 79 years, with a median age of 63 years.
All samples were snap-frozen in liquid nitrogen and stored at −80°C. We obtained tissue specimens from all subjects with informed written consent (approved by the local ethics committee of the Charité-Universitätsmedizin, Berlin). Each single specimen included in this study was histopathologically approved according to grade and stage by an experienced pathologist ( MV, University Bayreuth).
Laser capture microdissection and microarray
Laser Capture Microdissection (Cellcut, MMI AG and Nikon TE300 microscope) was used for isolating desired cells from sections. After transferring 5 μm sections onto MMI membrane slides, these were fixed in 70% isopropyl alcohol and then stained with the MMI basic staining kit. Desired tumor cell or NE areas were selected, cut and collected. Preparation of labeled cRNA and hybridization were done using the gene chip hybridization, wash, and stain kit (Affymetrix, Santa Clara, CA, USA), as described previously . Two cycle labeling was applied to all samples. In total 28 chip-data were collected using Gene Chip Operation Software (GCOS, Affymetrix). The 28 specimens analyzed consists 10 ESCC and 18 NE. To obtain the relative gene expression measurements, probe set-level data extraction was performed with the GCRMA (Robust Multiarray Average) normalization algorithm implemented in GeneSpring GX10.2 (Agilent). All data were log2 transformed. A list of all the genes included in these microarrays and the normalized data have been deposited in the Gene Expression Omnibus database (http://www.ncbi.nlm.nih.gov/geo/info/linking.html) under GEO accession number GSE26886. For gene-by-gene statistical testing, parametric tests were used to compare differences between groups. The False Discovery Rate (FDR) was employed using Benjamini-Hochberg procedure for multiple testing of the resulting p-value significance.
In situ hybridization
A 148 bp fragment located at the 3 terminal end of human WDR66 gene (NM144668)was subcloned into the pBluescript II vector pBS-27.16 using primer pair forward: 5’-CAACCTgCTCCgTCAAA-3’ and reverse: 5’-TAAACATTCCTggTAACTTCAC-3’. The linearized plasmid was used as a template for the synthesis of antisense probes. The probe was labeled by digoxigenin / dUTP with a DIG/RNA labelling kit (Boehringer Mannheim), according to the manufacturer’s instructions. The quality and quantity of the probe were confirmed by gel electrophoresis before used for In situ hybridization. The Digoxigenin-labeled probe was applied to 5 μm dewaxed FFPE sections and hybridized at 65°C overnight in a humid chamber. After 3 washes to remove the nonspecific binding or unbound probes, digoxigenin-labeled probe was detected using the alkaline phosphatase method.
RNA extraction and qRT-PCR
RNA extractions were carried out using the RNeasy Mini Kit (Qiagen, Valencia, CA, USA). Total RNA quality and yield were assessed using a bioanalyzer system (Agilent 2100 Bioanalyzer; Agilent Technologies, Palo Alto, CA, USA) and a spectrophotometer (NanoDrop ND-1000; NanoDrop Technologies, Wilmington, DE, USA). Only RNA with an RNA integrity number > 9.0 was used for microarray analysis.
For quantification of mRNA-expression, qRT-PCR was performed for 3 genes plus one control, using pre-designed gene-specific TaqMan® probes and primer sets purchased from Applied Biosystems (Hs01566237_m1 for WDR66, Hs00958116_m1 for VIM, Hs00170162_m1 for OCLD, and 4326317E for GAPDH). Conditions and data analysis of qRT-PCR were as described .
Cell culture and siRNA-mediated knockdown
KYSE520, OE33, SW480, Caco2, HCT116, HT29, HL60, LS174T, Daudi, HEK293, MCF7, MDA-MB-231, MDA-MB-435 and Capan-I were obtained from the American Type Culture Collection (ATCC, Manassas, VA) and cultured according to the supplier’s instructions. For siRNA-mediated knockdown of WDR66, cells were seeded in 6-well plates on the day before transfection. On day 0, cells were transfected with siRNA at 25 nmol/L concentrations using Thermo Scientific DharmaFECT transfection reagents according to manufacturer’s instructions. The siRNA sense 5’ – GuuACuAAAGGuGAGCAuA - 3’ sequence corresponding to WDR66 mRNA was chemically synthesized by sigma-Proligo (Munich, Germany). RNA was extracted at indicated time points as described.
Microarray analysis of WDR66 knock-down cells
Total RNA was extracted from 106 cell pellet using RNeasy Mini Prep Kit (Qiagen, Hilden, Germany). RNA quality was checked by Bioanalyzer (Agilent, Santa Clara, CA) Only RNA samples showing a RIN of at least 9.0 were used for labelling. Total RNA (1 μg) was labelled with Cy3 using the Low Input RNA Amplification Kit (Agilent, Santa Clara, CA). Labelled cRNAs were hybridized to Whole Human Genome 4x44K Oligonucleotide Microarrays (Agilent, Santa Clara, CA) according to the manual. Arrays were scanned by using standard Agilent protocols and a G2565AA Microarray Scanner (Agilent, Santa Clara, CA). Raw expression values were determined using Feature Extraction 9.0 software (Agilent, Santa Clara, CA).
Western blotting analysis
Total cell extracts were obtained and cell lysate containing 50 μg of protein was separated on 10% SDS-polyacrylamide gel and then blotted onto polyvinylidene difluoride (PVDF) membranes (Millipore, Bedford, MA, USA). Primary antibody for vimentin detection was mouse monoclonal anti-human vimentin antibody (Sigma-Aldrich Corporation, V5255, 1:200, approximately 54 kDa). Primary antibody for occludin detection was rabbit polyclonal anti-human occludin antibody (Invitrogen, 71–1500, 1:500, at 65 kDa). ß-actin was used as loading control (Abcam, 1:2000, ab8226). Signals were detected using ECL kit (Amersham Pharmacia Biotech, Piscataway, NJ, USA). Images were scanned by FujiFilm LAS-1000 (FujiFilm, Düsseldorf, Germany).
Cell number, cell motility and wound-healing assay
Cells were seeded in 6-well plates 24 h before transfection. Transfection was done as described above. Cells were collected at indicated time points, and cell numbers were measured using POLARstar Omega reader (BMG Labtech, Offenburg, Germany). Emission and excitation filters were 485 and 520 nm. The results were analyzed by MARS data analysis software. Cell motility was determined using 12-well Transwell Permeable Support inserts with polycarbonate filters with a pore size of 8 μm (Corning Costar, Lowell, MA), according to the manufacturer’s instructions. Wound healing assays were performed in triplicates using cytoselect 24-well wound healing assay (Cell Biolabs, Inc.).
Statistical analysis was done using GraphPad Prism version 5 for Windows (GraphPad Software) and SPSS version 13 for Windows (SPSS, Chicago, IL, USA) as follows: GraphPad Prism, Unpaired t test with Welch’s correction of quantitative real-time RT-PCR measurements of WDR66 in patient samples and of gene expression measurements in the validation cohort; nonparametric Mann–Whitney U test of cell numbers, motility assay, and cell wound assay after knockdown of WDR66; SPSS, Kaplan-Meier survival analysis and log-rank statistics, cut-point analysis of qRT-PCR measurements of WDR66 in patient samples using maximally selected rank statistics to determine the value separating a group into two groups with the most significant difference when used as a cut-point; grouping of patients according to median of qRT-PCR measurements was done as follows: WDR66 ≤ 125, WDR66 low; WDR66 > 125, WDR66 high; the stratified Cox-regression model was used to determine prognostic factors in a multivariate analysis with WDR66 dichotomized at the previously determined cut-points.
WDR66 is specifically highly expressed in esophageal squamous cell carcinoma
High expression of WDR66 correlates with poor survival outcome in ESCC
Cox regression analysis for factors possibly influencing disease-specific survival in patients with ESCC in our cohort
WDR66 (high vs low)
Gender (male vs female)
Age, y (<60 vs ≥60)
Tumor differentiation (high grade vs low or Intermediate grade)
pT factor ( pT3 or pT4 vs pT1 or pT2)
Lymph node metastasis (yes vs no)
Distant metastasis (yes vs no)
TNM stage (I or II vs III or IV)
Knockdown of WDR66 in KYSE520 effected VIM and OCLD expression in vitro
Knockdown of WDR66 in KYSE520 cells affects cell motility and results in growth suppression
By whole genome-wide expression profiling we found that WD repeat-containing protein 66 (WDR66) might be a useful biomarker for risk stratification and a modulator for epithelial-mesenchymal transition of ESCC. Among 20 normal human tissues examined by qRT-PCR, WDR66 was most abundantly expressed in the testis. Thus, our data suggest that WDR66 might be a cancer / testis antigen. Cancer-testis (CT) genes, normally expressed in germ line cells but also activated in a wide range of cancer types, often encode antigens in cancer patients . Testis is an immune-privileged site as a result of a blood barrier and lack of HLA class I expression on the surface of germ cells . Hence, if testis-specific genes are expressed in other tissues, they can be immunogenic. Expression of some cancer-testis genes in a high percentage of esophageal tumors makes them potential targets for immunotherapy, like LAGE1, MAGE-A4 and NY-ESO-1 . NY-ESO-1 is a highly immunogenic, prototypical protein marker limited in expression to a wide variety of cancer types but not in normal tissue, with the exception of the immune-privileged testes, and has been heavily investigated as target for immunotherapy in cancer patients. Recently, immunotherapy of various cancers again NY-ESO-1 showed promising clinical results [20–22]. Unfortunately, most cancer / testis antigens are expressed only in a small group of tumor patients, among 10-40%. However, we found that the expression of WDR66 was specifically enhanced in 96% of ESCC patients and also very low or absent in normal tissues. WDR66 may be a novel Immunotherapy target for ESCC.
Our experiments revealed a strong association of WDR66 expression with vimentin and occludin. Vimentin is an important mesenchymal marker and plays a central role for reversible trans-differentiation . Tumor cells undergoing EMT have an increased the ability for detachment from the main tumor bulk, which is a crucial step for tumor dissemination and metastasis . EMT is accompanied by a switch from keratin to vimentin expression . Earlier studies also demonstrated a correlation between the reduction of tight junctions and tumor metastasis. Here, we found a decreased expression of occludin, an important tight junction protein. According to a recent study comparing the risk of metastasis in ESCC and EAC, ESCC is characterized by a more aggressive behavior and tendency for early metastasis . Thus, we hypothesize that the elevated expression of WDR66 in ESCC may promote EMT through an up-regulation of vimentin expression and a down regulation of occludin and cohesion of the tumor tissue. At this point, we checked the expression of vimentin and occludin in ESCC patients of our cohort, and found that vimentin was highly expressed while occludin was less expressed in ESCC specimens in comparison to NE which supports our hypothesis. A recent study showed that low expression of the tight junction protein claudin-4 is associated with poor prognosis in ESCC . This is also in agreement with the results of our microarray study, which showed that claudin-4 was significantly less expressed in ESCC and also remarkably over expressed after WDR66 knockdown (data not shown).
In summary, we have identified WDR66 as a potential novel prognostic marker and promising target for ESCC. This result is based on our observations that (1) WDR66 is specifically highly expressed in esophageal squamous cell carcinoma and high WDR66 expression correlates with poor overall survival, (2) WDR66 regulates vimentin and occludin expression and plays a crucial role for EMT, and (3) knockdown of WDR66 suppresses cell growth and motility and decreases cell viability of ESCC cells. Therefore, we propose that WDR66 plays a major role in ESCC biology. Our functional data furthermore warrants further investigation of selective targeting of WDR66 as a novel drug target for ESCC treatment.
Esophageal squamous cell carcinoma
Epithelial to mesenchymal transition
Quantitative reverse transcription- polymerase chain reaction
Small interfering RNA
WD repeat-containing protein 66.
The authors thank Prof. Michael Vieth (Pathology, University Bayreuth, Germany) for histopathological characterization of the samples and Ms. Sabine Grigull, Ms. Gudrun Koch and Ms. Bianca Kochnowsky for excellent technical assistance.
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