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DEK is highly expressed in breast cancer and is associated with malignant phenotype and progression
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- Published online on: April 1, 2021 https://doi.org/10.3892/ol.2021.12701
- Article Number: 440
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Copyright: © Yang et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
Abstract
Introduction
Breast cancer is the most common cancer in the world, and in the United States breast cancer alone accounted for 30% of all new cancer diagnoses in women in 2019 (1). The 5-year survival of patients with breast cancer has been improved due to recent advances in surgical therapy, radiotherapy, hormone therapy and immunotherapy. The death rate for patients with breast cancer dropped by 40% between 1989 and 2016 (1,2). The main causes of mortality are attributed to distant metastasis and disease recurrence (3). Early diagnosis of breast cancer is crucial for effective treatment (4). Determining some novel biomarkers and targets remains therefore crucial to develop efficient therapies for breast cancer.
DEK proto-oncogene (DEK) is a highly conserved endogenous DNA-binding chromatin nuclear factor that encodes a 375 amino acid protein (5). DEK was initially described as part of the protein product of the DEK-CAN fusion oncogene generated by a t (6;9) translocation in a subset of patients with acute myelogenous leukemia (6,7). DEK is one of only two known secreted nuclear chromatin factors. Its ability to bind nucleic acids leads to the regulation of numerous cellular processes, including the regulation of hematopoiesis, global heterochromatin integrity, DNA replication, gene transcription and DNA repair (5,8–12). DEK has therefore been associated with tumor formation and development. DEK has been reported to be overexpressed in numerous types of tumor, including lung cancer, gastric adenocarcinoma, cervical cancer, pancreatic cancer, hepatocellular carcinoma, ovarian cancer and oropharyngeal squamous cell carcinoma (13–22). In addition, high expression of DEK has been associated with low overall survival in patients with lung cancer (23). Silencing of DEK and inhibitor of nuclear factor kappa B can block the cell cycle in the G0/G1 phase, with a corresponding decrease in the G2/M phase, increased apoptosis and induced cell senescence in CaSki cervical cancer cells (24). These findings indicate that DEK might have an oncogenic role in tumorigenesis and neoplastic progression; however, the protein expression and role of DEK in breast cancer have not been extensively investigated.
In the present study, the association between DEK expression and the clinicopathological characteristics of patients with breast cancer was determined. In addition, the function of DEK in the proliferative and invasive abilities of MCF7 breast cancer cells was investigated to elucidate the significance of DEK in the progression of breast cancer.
Materials and methods
Patients and clinicopathological characteristics
A total of 110 patients with invasive ductal cancer were randomly selected and included in the present study. These patients underwent surgical resection at the First Affiliated Hospital of China Medical University (Shenyang, Liaoning, China) between January 2011 and December 2016. Tissues from 50 cases of breast cancer were matched with adjacent normal breast tissues (>2-cm away from the tumor). All patients were women and none underwent chemotherapy or radiotherapy prior to surgical resection. All tissue specimens were fixed with 10% neutral formalin at room temperature after surgery for pathological examination and were diagnosed as invasive ductal cancers by pathological examination. The mean age of patients was 58 years (age range, 31–85 years). The clinicopathological characteristics of patients, including age, tumor differentiation, histological grade, lymph node metastasis, tumor-node-metastasis (TNM) stage, and expression of estrogen receptor (ER), progesterone receptor (PR), human epidermal growth factor receptor 2 (Her-2) and Ki-67, were retrospectively investigated. The TNM stage of patients with breast cancer was classified as stages I–II (n=62) and stages III–IV (n=48) according to the TNM staging system of the International Union Against Cancer (25). The research protocol was reviewed and approved by the local Institutional Review Board of the China Medical University.
Immunohistochemistry
For immunohistochemical analysis, all tumor specimens were fixed in 10% neutral formalin for 24 h at room temperature and embedded in paraffin blocks. Sections (4-µm thick) were cut and placed onto glass slides precoated with 2% 3-aminopropyl triethoxysilane for 1 h at room temperature (Fuzhou Maixin Biotech Co., Ltd.). Immunostaining was performed using the streptavidin-peroxidase complex method. The sections were deparaffinized in xylene at room temperature, rehydrated in an 85–95% anhydrous alcohol gradient series and boiled in 0.01 M citrate buffer (pH 6.0) for 2 min in an autoclave. Endogenous peroxidase activity was blocked using 0.3% hydrogen peroxide at 37°C for 10 min and sections were subsequently incubated with 10% normal goat serum (Fuzhou Maixin Biotech Co., Ltd.) at 37°C to reduce nonspecific binding. The sections were incubated with the rabbit polyclonal antibody against DEK (cat. no. 16448-1-AP; 1:150; ProteinTech Group, Inc.) or the ready-to-use primary antibodies against ER (cat. no. MAB-0062), PR (cat. no. MAB-0675), Her-2 (cat. no. MAB-0198) and Ki-67 (cat. no. MAB-0672) (ready to use; all Fuzhou Maixin Biotech Co., Ltd.) at 4°C overnight. Section stained with PBS only was considered as a negative control. After washing with PBS, the sections were incubated for 30 min at 37°C with secondary biotinylated goat anti-rabbit serum IgG antibody (cat. no. SPKIT-C2) and horseradish peroxidase-conjugated streptavidin-biotin (cat. no. SPKIT-A2) (ready to use; all Fuzhou Maixin Biotech Co., Ltd.). The staining was visualized using 3,3-diaminobenzidine (Fuzhou Maixin Biotech Co., Ltd.). Sections were then stained with hematoxylin for 10 min at 37°C and observed under ×400 magnification using a light microscope (Olympus Corporation).
The evaluation of immunostaining was performed semi-quantitatively. Nuclear staining of the tumor cells was considered to be DEK positive. In total, 10 high-power representative fields were selected per slide, and the staining intensity and positive rate of tumor cells were scored. The intensity of the staining was scored as follows: 0, negative; 1, weak; 2, intermediate; and 3, strong. The positive rate for each case was obtained by calculating the percentage of positively stained tumor cells on each slide and was scored as follows: 0, negative; 1, 1–25%; 2, 26–50%; 3, 51–75%; and 4, >75%. The scores for each tumor sample were multiplied to obtain a final score of 0 to 12. A final score ≥6 was defined as high DEK expression whereas a score <6 was defined as low DEK expression (23,26).
The Cancer Genome Atlas (TCGA) data collection and analysis
The expression data of DEK in breast cancers molecular subtypes were obtained using the online database UALCAN (http://ualcan.path.uab.edu) (TCGA dataset of breast invasive carcinoma, n=719) (27). Correlation analysis between DEK expression and Ki-67 and PCNA expression in breast cancers was retrieved from cBioPortal database (http://www.cbioportal.org/) [mRNA expression (microarray), n=1,904] (28,29). Survival curve for patients with breast cancer with high or low DEK expression (n=4,929) was obtained from Kaplan-Meier plotter (http://kmplot.com/analysis/) (30).
Cell lines and transfection
The human breast cancer cell line MCF7 (luminal A subtype) was purchased from The Cell Bank of Type Culture Collection of The Chinese Academy of Sciences. Cells were cultured in DMEM (Invitrogen, Thermo Fisher Scientific, Inc.), supplemented with 10% FBS (cat. no. FB15015; Clark Bioscience) and placed at 37°C in a humidified incubator containing 5% CO2.
For transfection, MCF7 cells were seeded into 6-well plates for 24 h at 37°C and cultured to 70–80% confluence before transfection. The plasmids containing the DEK gene (pCMV6-DEK) or DEK short hairpin RNA (shRNA) sequences (pCMV6-shDEK) were synthesized by GENECHEM (Shanghai GeneChem Co., Ltd.). The corresponding empty vector pCMV6 or plasmid containing scrambled shRNA sequences served as negative controls. The plasmids (2.5 µg) were transfected into cells using Lipofectamine™ 3000 (Invitrogen; Thermo Fisher Scientific, Inc.) according to manufacturers' instructions at 37°C. Subsequent experiments were performed 24 h after transfection.
Western blotting
Cells were lysed using RIPA lysis buffer at 4°C (Pierce; Thermo Fisher Scientific, Inc.) and proteins were quantified using the Bradford method (31). Proteins (60 µg) were separated by 10% SDS-PAGE and transferred onto PVDF membranes. Membranes were blocked in 5% non-fat milk for 1 h at room temperature. The membranes were incubated with primary antibodies against DEK (cat. no. 16448-1-AP; 1:1,000; ProteinTech Group, Inc.), glycogen synthase kinase-3β (Gsk-3β; cat. no. 5676; 1:1,000; Cell Signaling Technology, Inc.), cyclin D1 (cat. no. SC-8396; 1:100; Santa Cruz Biotechnology, Inc.), β-catenin (cat. no. 17565-1-AP), active β-catenin (cat. no. 51067-2-AP), c-Myc (cat. no. 67447-1-Ig) and GAPDH (cat. no. 60004-1-Ig) (all 1:1,000; ProteinTech Group, Inc.) overnight at 4°C. Membranes were washed with tris-buffered saline containing 0.1% Tween-20 and were incubated with IgG antibody (cat. no. SA00001-1/2; 1:2,000; ProteinTech Group, Inc.) at 37°C for 2 h. Bands were detected using enhanced chemiluminescence substrate (Pierce; Thermo Fisher Scientific, Inc.) and detected using a bioimaging system (DNR Bio-Imaging System, Ltd.). All the western blotting bands were probed from the same membrane. After each probing, the membranes were stripped using a stripping buffer (Beyotime Institute of Biotechnology) according to the manufacturers' protocol and re-probed for other proteins. Relative expression levels were normalized to endogenous control GAPDH, which were analyzed with ImageJ software (version 1.47; National Institutes of Health).
Colony formation assay
Cells were seeded in 6 cm cell culture dishes (1,000 cells per dish) 24 h after transfection and were cultured for 10 days. The medium was changed every 3 days. Cells were then washed with PBS and stained with hematoxylin for 10 min at room temperature. The number of colonies with >50 cells were counted using a bioimaging system (version 5.2.1; DNR Bio-Imaging Systems, Ltd.).
Cell proliferation assay
Cell proliferation was detected using Cell Counting Kit-8 (CCK-8; Dojindo Molecular Technologies, Inc.). Briefly, 24 h after transfection, cells were seeded into 96-well plates (3,000 cells per well) in 100 ul medium containing 10% FBS. CCK-8 reagent was added to each well (1:10, v/v) and incubated for 2 h at 37°C. Cell proliferation was assessed at days 1, 2, 3, 4 and 5. The absorbance was read at 450 nm using a microplate reader.
Cell migration and invasion assays
Cell migratory and invasive abilities were assessed using 24-well transwell chambers containing inserts of 8 µm pore size (Costar; Corning, Inc.). For the invasion assay only, the upper side of the inserts were coated with Matrigel for at least 2 h at 37°C. (1:8; BD Biosciences). MCF7 cells were seeded (1.5×105 cells/well) in the upper chambers in 100 µl medium supplemented with 2% FBS. To attract cells, the lower chambers were filled with 600 µl medium containing 20% FBS. After 20 h, cells that had migrated to the lower chambers were fixed with 4% paraformaldehyde and stained with hematoxylin for 10 min at 37°C. The non-invading cells on the upper surface were cleared using a cotton swab. A total of 10 randomly selected high-power fields were observed under light microscopy (magnification, ×200), and the numbers of migrated or invaded cells were counted (Motic Image Plus 2.0; Motic (Xiamen) Medical Diagnostic Systems Co. Ltd.) All experiments described were performed independently and in triplicate.
Statistical analysis
Statistical analysis was performed using SPSS version 17.0 (IBM Corp.). Associations between DEK expression and the clinicopathological characteristics of patients were analyzed using χ2 test and Student's t-test. Comparisons among two experimental groups were performed using two-tailed Student's t-test. The P-value threshold was adjusted using Bonferroni correction when comparing more than two groups using Student's t-test. P<0.05 was considered to indicate a statistically significant difference.
Results
DEK protein expression is higher in breast cancer tissues compared with normal breast tissues
Immunohistochemistry was performed for 110 cases of breast cancer and 50 cases of adjacent normal breast tissues. The results demonstrated that DEK protein was mainly expressed in the nuclei of cancer cells. Furthermore, high DEK expression was observed in 62.7% (69/110) of breast cancer tissues, which was significantly higher than that in normal breast tissues (12.0%; P=0.002; Table I and Fig. 1A-C).
![]() | Table I.Association between DEK expression and the clinicopathological characteristics of patients with breast cancer. |
High DEK expression is associated with certain clinicopathological characteristics and poor prognosis of patients
The expression of DEK was associated with histological grade (P=0.01), lymph node metastasis (P=0.003), TNM stage (P=0.030) and Ki-67 expression (P=0.028); however, DEK expression was not associated with ER expression (P=0.070), PR expression (P=0.510), Her-2 expression (P=0.420) or patient age (P=0.290; Table I and Fig. 1). Furthermore, according to the cBioPortal database, it was also found that DEK expression was positively correlated with the expression of Ki-67 (P<0.001; n=1,904) or proliferating cell nuclear antigen (PCNA; P<0.001; n=1,904) (Fig. 2A and B), which are both indexes of proliferation (32).
In addition, according to Kaplan-Meier analysis using the online database KM-plotter, patients with high expression of DEK presented a significant shorter overall survival compared with patients with low DEK expression (P<0.01; median survival, 163.46 months for the high expression cohort vs. 216.66 months for the low expression cohort; Fig. 2C). As seen in the UALCAN database, the expression of DEK was significantly higher in triple negative breast cancer (TNBC) compared with luminal breast cancer (P<0.001) and Her-2 positive breast cancer (P<0.001). However, the expression level of DEK was not significant different between luminal and Her2 positive subtypes of breast cancer (P=0.123; Fig. 2D).
DEK regulates the expression of β-catenin and target genes of Wnt signaling pathway
Enhanced DEK expression by DEK gene transfection in MCF7 cells (MCF7-DEK) increased the expression of active-β-catenin and inhibited the expression of Gsk-3β (P<0.05). The expression of cyclin D1 and c-Myc, which are target genes of the Wnt signaling pathway, was also significantly increased in MCF7-DEK cells (P<0.05). However, the level of total β-catenin was not markedly changed following DEK overexpression (P>0.05; Fig. 3A and B). Conversely, following DEK knockdown by shRNA interference (MCF7-ShDEK), the expression of active-β-catenin, cyclin D1 and c-Myc was significantly downregulated, whereas the expression of Gsk-3β was significantly increased in MCF7 cells (P<0.05). The level of total β-catenin was not changed following DEK knockdown (P>0.05; Fig. 3C and D).
DEK overexpression promotes the proliferation, colony formation and migratory and invasive abilities of breast cancer cells
Overexpression of DEK enhanced the proliferation rate (P<0.05 for days 1 and 2; P<0.01 for days 3 and 4) and the colony formation (P<0.05) of MCF7 cells compared with control cells. Conversely, following DEK knockdown, the proliferation rate (P<0.01 for days 3, 4 and 5) and colony formation (P<0.05) of MCF7 cells were significantly inhibited compared with control cells (Fig. 4A and B).
Furthermore, DEK overexpression promoted the migratory and invasive abilities of MCF7 cells compared with control cells (P<0.01). Conversely, DEK downregulation inhibited the migratory and invasive abilities of MCF7 cells (P<0.01; Fig. 5A and B).
Discussion
In order to accurately diagnose and treat cancers, researchers are working to determine novel effective markers to improve the clinical evaluation of outcomes and to develop targeted therapy. DEK has been reported to be overexpressed in numerous types of human cancer, including lung cancer, pancreatic cancer, gastric adenocarcinoma, ovarian cancer, cervical cancer, hepatocellular cancer and TNBC (13,15–19,21,33). DEK plays an active role in tumor initiation and maintenance. The expression of DEK has been associated with the clinicopathological characteristics of patients with hepatocellular cancers and pancreatic adenocarcinomas and described as an indicator of poor prognosis (11,16), suggesting that DEK may be considered as a potential prognostic biomarker in various types of cancer.
Although DEK overexpression has been reported in breast cancer (34–36), the expression pattern of DEK and its association with the clinicopathological characteristics of patients remain unclear. The present study demonstrated that DEK protein was present in cancer cell nucleus and that its expression was higher in breast cancer tissues compared with normal breast tissues. Furthermore, high DEK expression was associated with a high grade, advanced TNM stage and high index of proliferation, which is characterized by a high expression of Ki67 or PCNA, in patients with breast cancer. In addition, high expression of DEK could predict a poor prognosis in patients with breast cancer, suggesting that DEK may be considered as a potentially valuable prognostic marker in breast cancer. As seen in UALCAN database, DEK expression level was significantly higher in TNBC compared with luminal and Her-2 positive breast cancers; however, similar results were not observed in the population from the present study; which may be due to the limited sample size and the different types of detection methods. The present study only examined the protein expression of DEK using immunohistochemistry in paraffin embedded samples. The mRNA expression of DEK was not detected in the present study and should be investigated in the future using fresh breast cancer tissues.
DEK can regulate the proliferation, migration, invasion and apoptosis of cancer cells and be subjected to a variety of tumor-associated modifications (37,38). It has been reported that DEK knockdown can inhibit the proliferation of ovarian, lung and cervical cancers (15,23,39). The present study demonstrated that DEK overexpression promoted the proliferation, colony formation and invasive and migratory abilities of MCF7 cells, which was consistent with the results in vivo.
DEK is involved in cancer progression through the regulation of numerous signaling pathways. For example, DEK expression is regulated by the transcription factors Nuclear Factor-Y and Yin Yang-1 (40) and can be induced by high-risk human papillomavirus E7 to overcome cellular senescence (41). In addition, DEK is a regulator of the G1 to S transition and a potential target gene of the p16-pRB-E2F pathway (42). DEK regulates apoptosis in glioblastomas partly through modulating p53 by inhibiting its transcription activity and protein stability (38). Furthermore, blocking the PI3K/AKT/mammalian target of rapamycin pathway using specific inhibitors can significantly attenuate DEK-enhanced migration and angiogenesis in TNBCs (33). In cervical cancer, DEK promotes Hela cell metastasis via upregulation of the Wnt pathway and matrix metalloproteinase-9 expression (39). The results from the present study demonstrated that DEK could upregulate the expression of active β-catenin and Wnt target genes, such as cyclin D1 and c-Myc. DEK may therefore promote the proliferation and invasive ability of breast cancer by activating the Wnt signaling pathway. Taken together, these findings suggested that DEK may act as an oncogene and promote breast cancer development; however, the underlying oncogenic mechanism of DEK in breast cancer requires further investigation.
In conclusion, the results from the present demonstrated that high expression of DEK was common in breast cancer tissues. In addition, DEK overexpression promoted the proliferation and invasive ability of breast cancer cells in vitro, and was associated with high grade, advanced TNM stage and poor prognosis in patients with breast cancer.
Acknowledgements
Not applicable.
Funding
This study was supported by the Youth Scientific Research Foundation of Shenyang Medical College (grant no. 20182048) and the Natural Science Foundation of Liaoning Province (grant no. 2020-MS-179).
Availability of data and materials
The datasets used during the current study are available from the corresponding author on reasonable request.
Authors' contributions
HTX designed the study. MQY and HTX participated in drafting the manuscript. MQY, LLB, ZW, LL, YWZ, ZHL, WJH and CCL performed the experiments. MQY and HTX confirm the authenticity of all the raw data. All authors have read and approved the final manuscript.
Ethics approval and consent to participate
The research protocol was reviewed and approved by the local institutional review board at the China Medical University. Written informed consent was obtained from all patients.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Glossary
Abbreviations
Abbreviations:
ER |
estrogen receptor |
Gsk |
glycogen synthase kinase |
Her-2 |
human epidermal growth factor receptor 2 |
PR |
progesterone receptor |
TCGA |
The Cancer Genome Atlas |
TNM |
tumor-node-metastasis |
TNBC |
triple negative breast cancer |
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