Open Access

Long non-coding RNA ATB promotes growth and epithelial-mesenchymal transition and predicts poor prognosis in human prostate carcinoma

  • Authors:
    • Song Xu
    • Xiao-Ming Yi
    • Chao-Peng Tang
    • Jing-Ping Ge
    • Zheng-Yu Zhang
    • Wen-Quan Zhou
  • View Affiliations

  • Published online on: May 9, 2016     https://doi.org/10.3892/or.2016.4791
  • Pages: 10-22
  • Copyright: © Xu et al. This is an open access article distributed under the terms of Creative Commons Attribution License.

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Abstract

Long non-coding RNAs (lncRNAs) have been identified to be critical mediators in various tumors associated with cancer progression. Long non-coding RNA activated by TGF-β (lncRNA-ATB) is a stimulator of epithelial-mesenchymal transition (EMT) and serves as a novel prognostic biomarker for hepatocellular carcinoma. However, the biological role and clinical significance of lncRNA-ATB in human prostate cancer have yet to be fully elucidated. The present study was designed to explore the expression of lncRNA-ATB in human prostate cancer patients and the role of lncRNA-ATB in prostate cancer cells. We showed that lncRNA-ATB expression was significantly upregulated in tumor tissues in patients with prostate cancer in comparison with adjacent non-tumor tissues. Further analysis indicted that high lncRNA-ATB expression may be an independent prognostic factor for biochemical recurrence (BCR)-free survival in prostate cancer patients. Overexpression of lncRNA-ATB promoted, and knockdown of lncRNA-ATB inhibited the growth of prostate cancer cells via regulations of cell cycle regulatory protein expression levels. In addition, lncRNA-ATB stimulated epithelial-mesenchymal transition (EMT) associated with ZEB1 and ZNF217 expression levels via ERK and PI3K/AKT signaling pathways. These results indicated that lncRNA-ATB may be considered as a new predictor in the clinical prognosis of patients with prostate cancer. Overexpression of lncRNA-ATB exerts mitogenic and EMT effects of prostate cancer via activation of ERK and PI3K/AKT signaling pathways.

Introduction

Prostate cancer is the most frequently diagnosed malignancy in males worldwide and is the second most common cause of cancer mortality in the United States (1). It accounts for 15% of all cancer diagnoses (2). The incidence of prostate cancer is robustly increasing due to increase in the life expectancy, modified diagnostic techniques and increased awareness of prostate cancer screening (3). It is reported that the 5-year survival rate of prostate cancer patients was only 29%, exerting a big burden on public health a worldwide (4). The pathogenesis of tumorigenesis and progression of prostate cancer has not been fully elucidated although intensive studies of prostate cancer have been performed. Despite the therapeutic strategies developed in prostate cancer, the annual morbidity rate has explosively increased by 14% since 1990 (5). The management of prostate cancer is recognized to be one of the most serious medical challenges (6). It is unfortunate that no implementation of a population screening program is available for early detection of prostate cancer (7).

The prostate-specific antigen (PSA) is indicated to be employed as a biomarker for early detection of prostate cancer and digital rectal examination (DRE) is also conventionally used for diagnosis of prostate cancer (8). Prostate biopsy is considered as a gold standard in patients with raised suspicion from digital rectal examination or increased PSA levels (9). However, the rate of negative biopsies is substantially high even in cases with increased PSA levels, thus greatly affecting the patient quality of life (10,11). The low specificity of PSA has been demonstrated in aggressive and indolent prostate cancer (12). The U.S. Preventive Services Task Force has proposed to quit the conventional screening by PSA testing for prostate cancer (13). Therefore, it is required to identify novel prognostic biomarkers for improvement of patient outcomes and clinical management in prostate cancer patients.

The long non-coding RNAs (lncRNAs) are defined as <200 nucleotide non-protein-coding RNA molecules and play critical roles in the biological and pathological processes of many cancers associated with regulation of cell proliferation, migration and invasion (14,15). A number of studies have clarified that lncRNAs may function as oncogenes or tumor suppressors in various types of cancers (16). It is evidenced that lncRNA DANCR is upregulated in human colorectal cancer tissues and may serve as an independent negative prognostic factor for both overall survival and disease-free survival in colorectal cancer (17). The lncRNA HOTTIP overexpression is found to be associated with increased metastasis of hepatocellular carcinoma and is suggested to be a negative prognostic factor in hepatocellular carcinoma (18). Mounting evidence highlights that the lncRNAs may be emerged as novel and improved markers or therapeutic targets in the diagnosis and treatment of cancer (19). The lncRNA-ATB is observed to be higher in hepatocellular carcinoma tissues and have a poor prognosis in hepatocellular carcinoma patients (20). To date, however, little is known about the clinical significance and role of lncRNA-ATB in human prostate cancer.

In the present study, we aimed to determine the lncRNA-ATB expression in human prostate cancer tissue and the association between lncRNA-ATB and clinicopathological factors and prognosis the prostate cancer. The role of lncRNA-ATB in proliferation and EMT of prostate cancer cells was also investigated.

Materials and methods

Ethics statement

The approval of this study protocol was obtained from the Ethics Committee of Jinling Hospital and the written informed consent was provided from all subjects. All experiments were performed in accordance with relevant guidelines and regulations.

Subjects

A total of 57 prostate cancer patients who underwent radical prostatectomy were included from Department of Urology, Jinling Hospital, School of Medicine, Nanjing University ranged from September 2001 to August 2005. All patients were diagnosed with H&E-stained tissue section and histopathological grading for each subject was confirmed by experienced pathologists. The biochemical and clinicopathological parameters pre- and post-operation were recorded and summarized. The date of prostatectomy was considered as the beginning of the follow-up period. The endpoint time of biochemical recurrence was set as the period from surgical treatment to the assay of two successive values of serum PSA level ≥0.2 ng/ml. The patients who received any treatment including chemotherapy, radiation therapy, androgen deprivation treatment before radical prostatectomy or died of unexpected events or other diseases were excluded from this study. The primary prostate cancer and paired noncancerous prostate tissues from 57 cases were collected and were frozen in liquid nitrogen and stored at −80°C prior to use.

RNA isolation and quantitative real-time PCR

The TRIzol reagent (Life Technologies, Gaithersburg, MD, USA) was used to extract the total RNA according to the manufacturer's instructions. The mRNA of lncRNA-ATB, ZEB1 and ZNF217 were analyzed by real-time PCR (SYBR Premix Ex Taq™, Takara, Otsu, Shiga, Japan) in triplicates by reacting with sequence-specific PCR primers in ABI PRISM 7500 sequence detection PCR system (Applied Biosystems, Foster City, CA, USA). GAPDH was used as an internal control for each sample. The relative quantification of gene expression was expressed as fold changes via normalization against GAPDH by using the 2−ΔΔCT method. The sequences of primers were listed as follows: lncRNA-ATB: forward: 5′-CTTCACCAGCACCCAGAGA-3′, reverse: 5′-AAGACAGAAAAACAGTTCCGAGTC-3′; ZEB1: forward: 5′-GACAGTGTTACCAGGGAGGAGCA-3′, reverse: 5′-TTCAGGTGCCTCAGGAAAAATGA-3′; ZNF21: forward: 5′-CTGAAACGGGGAAGAAGCCT-3′, reverse: 5′-CTTGCCCCGATTCCTTCACT-3′; GAPDH: forward: 5′-CAGGAGGCATTGCTGATGAT-3′, reverse: 5′-GAAGGCTGGGGCTCATTT-3′. E-cadherin: forward: 5′-GCCCCATCAGGCCTCCGTTT-3′, reverse: 5′-ACCTTGCCTTCTTTGTCTTTGTTGGA-3′; ZO-1: forward: 5′-CACGCAGTTACGAGCAAG-3′, reverse: 5′-TGAAGGTATCAGCGGAGG-3′; N-cadherin forward: 5′-TGGACCATCACTCGGCTTA-3′, reverse: 5′-ACACTGGC AAACCTTCACG-3′; Vimentin: forward: 5′-CCTGAACCTG AGGGAAACTAA-3′, reverse: 5′-GCAGAAAGGCACTTGAAAGC-3′.

Cell culture and transfection

The prostate cell lines PC-3 and DU145 were purchased from the Cell Bank of Chinese Academy of Sciences (Shanghai, China). The cells were cultured in RPMI-1640 medium supplemented with 10% FBS coupled with 1% penicillin/streptomycin and 1% non-essential amino acids and 1% (mg/ml) sodium pyruvate at 37°C in a humidified incubator with 5% CO2. The day before transfection, PC-3 and DU145 cells were seeded in 6-well plates, and the transient transfection of lncRNA-ATB siRNA (5′-CCAUGAGGAGUACUGCCAATT-3′) and non-targeting Control (5′-UUCUCCGAACGUGUCACGUtt-3′) were conducted with Lipofectamine 2000 Transfection Reagent (Invitrogen) following manufacturer's instructions.

Construction of lentivirus-mediated overexpression of lncRNA-ATB

The construction of lentiviral vector expressing human lncRNA-ATB gene was performed by Genomeditech (Shanghai, China). The primers used for lentivirus production sequences were as follows: forward: 5′-CCTCTCTCCCCAGGGGGATCCTGGCTAGTTAAGCTTGGCCCT-3′, reverse: 5′-ATCCAGAGGTTGATTGTCGACTATCTGCAGAATTCTGGTAAATg-3′ (20).

Cell proliferation assay

The Cell Counting Kit-8 (CCK-8, Dojindo, Japan) was employed to determine the proliferation of PC-3 and DU145 cells accordance with the manufacturer's instructions (21).

Western blotting

Equal amounts of protein in each sample were loaded onto an SDS gel and transferred to immobilon polyvinylidene difluoride (PVDF) membranes (Millipore, Billerica, MA, USA). The membrane was incubated with designed primary antibodies overnight at 4°C. The positive signals from HRP-coupled secondary antibodies (Santa Cruz Biotechnology; Santa Cruz, CA, USA) were visualized by enhanced chemiluminescence detection kit (Thermo Scientific, Rockford, IL, USA). The densitometric analysis of the band intensities was measured and normalized to the band intensities of GAPDH using the ImageJ softwere (NIH, Bethesda, MD, USA).

Chemicals

The primary antibodies against proliferating cell nuclear antigen (PCNA), phosphorylated histone H3 (P-H3) and GAPDH were obtained from Santa Cruz Biotechnology. The antibodies of phosphorylated Akt, phosphorylated ERK, Akt, ERK cyclin E, cyclin D1, p21 and p27 were purchased from Cell Signaling Technology Inc. (Beverly, MA, USA). The ZEB1 and ZNF217 antibodies were purchased from Abcam (Cambridge, UK). LY294002 were obtained from Selleck Chemicals (Houston, TX, USA). U0126 was purchased from Beyotime Biotechnology (Shanghai, China). The siRNA specifically targeting lncRNA-ATB and non-targeting control were synthesized by GenePharma Co. (Shanghai, China).

Statistical analysis

SPSS 17.0 software (SPSS Inc., Chicago, IL, USA) was used for statistical analysis. All data on continuous variables were expressed as mean ± SD. The test for categorical variables was made by Chi-square test, and the small cell variables were compared by Fisher's exact test. Comparisons between two groups were made by Student's t-test. One-way or two-way ANOVA followed by post hoc Bonferroni test was used when multiple comparisons were made. The receiver operating characteristic (ROC) curve was applied to calculate the area under the ROC curve (AUC) for evaluating the diagnostic efficacy of lncRNA-ATB. Survival analysis was conducted with the Kaplan-Meier method. Multivariate analysis was carried out with the Cox proportional hazards model. P-values <0.05 was considered statistically significant.

Results

Upregulation of lncRNA-ATB expression in prostate cancer tissues

The lncRNA-ATB expression in 57 pairs of prostate cancer and adjacent non-cancerous prostate tissues was measured by qRT-PCR analysis. The results showed that the expression of lncRNA-ATB was significantly increased in the prostate cancer patients in comparison with the adjacent noncancerous prostate tissues (P<0.05, Fig. 1A).

Diagnostic efficacy of lncRNA-ATB in prostate cancer patients

The diagnostic efficacy of lncRNA-ATB in prostate cancer tissues of prostate cancer patients was evaluated by calculating the area under the receiver operating characteristic curve. The ROC curve analysis revealed that AUC was 0.931 (95% CI=0.000–1.000, P<0.001). When the cutoff value=1.30, the diagnostic sensitivity (100%) and specificity (83.3%) reached their peak values (P<0.05, Fig. 1B). Thus the lncRNA-ATB expression was further classified into the low expression group (n = lncRNA-ATB expression <1.30, n=32) and high expression group (lncRNA-ATB expression ≥1.30, n=25) as the threshold ROC curve value of 1.30.

Relationship between lncRNA-ATB expression and biochemical recurrence-free survival

The Kaplan-Meier curves plotted between high or low lncRNA-ATB expression and biochemical recurrence (BCR)-free survival suggested that prostate cancer patients with a high lncRNA-ATB expression had a shorter BCR-free survival compared with low lncRNA-ATB expression (P<0.001, Fig. 1C).

Correlation of lncRNA-ATB expression with clinical features of prostate cancer patients

As seen in Table I, the high lncRNA-ATB expression in prostate cancer tissues of prostate cancer patients is closely related with aggressive clinical pathological parameters including histological grade (P=0.017), high preoperative PSA level (P=0.001), pathological stage (P=0.003), high Gleason score (P=0.045), lymph node metastasis (P=0.007), angiolymphatic invasion (P=0.008), biochemical recurrence (P=0.003). However, there was no correlation between lncRNA-ATB with age (P=0.952) and surgical margin status (P=0.257). The Cox multivariate analysis was conducted to assess the relationship of lncRNA-ATB expression with the BCR-free survival of patients with prostate cancer. The results established the significance of lncRNA-ATB expression (P<0.001), and other clinicopathological parameters including histological grade (P=0.020), preoperative PSA level (P=0.002), Gleason score (P=0.049), pathological stage (P<0.001), lymph node metastasis (P=0.025) and angiolymphatic invasion (P=0.011) for independent prognostic predictors of BCR-free survival of prostate cancer patients (Table II).

Table I

Prostate cancer patient clinicopathological characteristics and clinical features.

Table I

Prostate cancer patient clinicopathological characteristics and clinical features.

VariableAll Cases (%)lncRNA-ATB expression
χ2P-value
Low (%)High (%)
Age
 ≤7039 (68.4)22 (56.4)17 (43.6)0.0040.952
 >7018 (31.6)10 (55.6)8 (44.4)
Histological grade
 G1 + G235 (61.4)24 (68.6)11 (31.4)5.6910.017
 G322 (38.6)8 (36.4)14 (63.6)
Preoperative PSA
 <10 ng/ml21 (36.8)18 (85.7)3 (14.3)11.8110.001
 ≥10 ng/ml36 (63.2)14 (38.9)22 (61.1)
Pathological stage
 I + II37 (64.9)26 (70.2)11 (29.7)8.5500.003
 III + IV20 (35.1)6 (30.0)14 (70.0)
Gleason score
 4–622 (38.6)16 (72.7)6 (27.3)4.0030.045
 7–1035 (61.4)16 (45.7)19 (54.3)
Lymph node metastasis
 Negative49 (86.0)31 (63.3)18 (36.7)7.1980.007
 Positive8 (14.0)1 (12.5)7 (87.5)
Surgical margin status
 Negative47 (82.5)28 (59.6)19 (40.4)1.2830.257
 Positive10 (17.5)4 (40.0)6 (60.0)
Angiolymphatic invasion
 Negative40 (70.2)27 (67.5)13 (32.5)7.0290.008
 Positive17 (29.8)5 (29.4)12 (70.6)
Biochemical recurrence
 Negative43 (75.4)29 (67.4)14 (32.6)9.0810.003
 Positive14 (24.6)3 (21.4)11 (78.6)

Table II

Multivariate analysis by Cox regression model on factors related to biochemical recurrence (BCR)-free survival in 57 prostate cancer patients.

Table II

Multivariate analysis by Cox regression model on factors related to biochemical recurrence (BCR)-free survival in 57 prostate cancer patients.

VariablesBCR-free survival
Exp (B)95% CIP-value
Age (≤70 vs. >70)1.0350.336–3.1880.952
Histological grade (G1+ G2 vs. G3)3.8181.241–11.7520.020
Preoperative PSA (<10 ng/ml vs. ≥10 ng/ml)9.4292.339–38.0010.002
Pathological stage (I + II vs. III + IV)5.5151.681–18.059<0.001
Gleason score (4–6 vs. 7–10)3.1671.003–10.0010.049
Lymph node metastasis (Negative vs. Positive)12.0561.371–106.0410.025
Surgical margin status (Negative vs. Positive)2.2110.549–8.9000.264
Angiolymphatic invasion (Negative vs. Positive)4.9851.449–17.1460.011
lncRNA-ATB expression (High vs. Low)1.7492.313–14.249<0.001
Effect of lncRNA-ATB on prostate cell growth

The lncRNA-ATB-specific siRNA or lentiviral vector expressing human lncRNA-ATB gene was transfected to PC-3 and DU-145 prostate cell lines to determine its effect on the proliferation of prostate cell in vitro. The depletion of lncRNA-ATB obviously attenuated the proliferation rate of PC-3 and DU-145 prostate cell lines (Fig. 2A), but the enforced overexpression of lncRNA-ATB effectively affected the proliferation rate of PC-3 and DU-145 prostate cell lines at day 2 and 4 post-transfection (Fig. 2B). Furthermore, the proliferating markers including PCNA and phosphorylated histone H3 (P-H3) was also obviously inhibited by reduction of lncRNA-ATB (Fig. 3A and C), but further enhanced by lncRNA-ATB overexpression (Fig. 3B and D).

Effects of lncRNA-ATB on cell cycle regulatory protein expression

The increased expression levels of cyclin E and cyclin D1 and decreased expression levels of p27 and p21 in PC-3 and DU-145 prostate cell lines were significantly rescued by gene silencing of lncRNA-ATB (Fig. 4A and C). Overexpression of lncRNA-ATB further promoted the cyclin E expression in PC-3 cell line and cyclin E and cyclin D1 in DU-145 prostate cell line, but had no effect on p27 or p21 expression levels (Fig. 4B and D).

Effect of lncRNA-ATB on the mRNA expression levels of EMT markers

Knockdown of lncRNA-ATB significantly rescued the increased expression levels of E-cadherin and ZO-1 and decreased expression levels of N-cadherin and Vimentin in PC-3 and DU-145 prostate cell lines (Fig. 5A). Overexpression of lncRNA-ATB further inbibited the E-cadherin and ZO-1 expression levels, but further promoted expression levels of N-cadherin and Vimentin in PC-3 and DU-145 prostate cell lines (Fig. 5B).

Effects of lncRNA-ATB on ZEB1 and ZNF217 expression levels

We found that downregulation of lncRNA-ATB could inhibit the expression levels of ZEB1 and ZNF217 at mRNA and protein levels in PC-3 and DU-145 prostate cell lines (Fig. 6A, C and E). In contrast, upregulation of lncRNA-ATB further augmented the mRNA and protein levels of ZEB1 and ZNF217 in PC-3 and DU-145 prostate cell lines (Fig. 6B, D and F).

Effects of lncRNA-ATB on PI3K/Akt and ERK signaling pathways

The activation of PI3K/Akt and ERK signaling pathways reflected the increase in phosphorylation levels of Akt and ERK was suppressed by knockdown of lncRNA-ATB (Fig. 7A and C). The continuous lncRNA-ATB expression further stimulated the phosphorylation levels of Akt and ERK in both PC-3 and DU-145 prostate cell lines (Fig. 7B and D). Additionally, inhibition of PI3K/Akt and ERK signaling pathways prevented the proliferation of PC-3 and DU-145 prostate cell line responses to overexpression of lncRNA-ATB (Fig. 9).

PI3K/Akt and ERK signaling pathways contribute to ZEB1 and ZNF217 protein expression levels

Pretreatment with PI3K inhibitor LY294002 (Fig. 8A and C) or ERK inhibitor U0126 (Fig. 8B and D) almost abolished the effects of lncRNA-ATB overexpression on the ZEB1 and ZNF217 protein expression levels.

Discussion

Our results for the first time established that the expression of lncRNA-ATB was remarkably increased in prostate cancer tissues, and might have prognostic significance in human prostate cancer. We also showed that lncRNA-ATB may be a potential stimulator in growth and EMT of prostate cancer cells.

Prostate cancer is a common cause of malignant mortality among males all over the world and brings a huge and increasing healthy burden in China (22). The clinical outcome of patients with prostate cancer is still poor even with the aid of advanced diagnosis and adjuvant therapy (23). It is also challenging to identify the pathogenesis, and develop novel diagnosis and medical treatments of prostate cancer (24). It is recommended that the early and accurate diagnosis is helpful for improvement of therapeutic efficiency of prostate cancer patients (25). Therefore, it is urgent to identify new molecular targets of prostate cancer in order to understand the pathogenesis and prognosis of prostate cancer (26). It is estimated that 15,000 lncRNAs are identified in human genome (27) and lncRNAs have multiple roles in the carcinogenesis and cancer metastasis (28).

Several studies have disclosed the lncRNAs are possible diagnostic or prognostic biomarkers in human cancers (29). For example, it is reported that the expression of lncRNA MALAT-1 was increased in colorectal cancer tissues and is negatively correlated with the progression of colorectal cancer (30). In addition, the lncRNA HOTAIR is also progressively upregulated in colorectal cancer patients and is employed as a biomarker for clinical prognosis of human colorectal cancer (31). A recent study indicates that lncRNA SNURF-1 is upregulated in prostate cancer (32). LncRNA PCA3 is demonstrated to be a dominant-negative oncogene in human prostate cancer (33). LncRNA BX647187 is characterized to be the important mediator of mitotic regulator Hec1 in human prostate cancer (22). These results suggested that lncRNAs are emerging as potential prognostic biomarkers or useful therapeutic target in prostate cancer. LncRNA-ATB was recently identified to play a critical role in invasion of human hepatocellular carcinoma and positively associated with poor prognosis of human hepatocellular carcinoma (20).

Gastric cancer tissues exhibit overexpressed lncRNA-ATB and the gastric cancer patients with low lncRNA-ATB expression have a longer overall survival rate, and lncRNA-ATB may be an independent prognostic factor in human gastric cancer (34). However, to our knowledge, the clinical significance and biological function of lncRNAs, especially lncRNA-ATB in prostate cancer remains largely unknown. Our data in the present study showed obvious increase in lncRNA-ATB expression in prostate cancer tissues in comparison with adjacent non-cancerous prostate tissues. Further analysis showed that the upregulation of lncRNA-ATB was positively associated with the histological grade, high preoperative PSA level, pathological stage, high Gleason score, lymph node metastasis, angiolymphatic invasion and biochemical recurrence in prostate cancer patients. Moreover, it is proven that prostate cancer patients with high lncRNA-ATB expression had poor biochemical recurrence (BCR)-free survival. The multivariate analyses clarified that the loss of lncRNA-ATB expression was a potential independent prognostic factor for BCR-free survival of prostate cancer patients. These results suggested that the lncRNA-ATB may be a novel and important prognostic biomarker for prostate cancer.

The abnormal growth is closely related with tumorigenesis and tumor progression. Recent studies indicate that lncRNAs are essential modulators in tumor growth (35). Overexpression of lncRNA MVIH stimulates the proliferation and cell cycle in human breast cancer (35). Knockdown of lncRNA H9 obviously prevented the proliferation of non-small cell lung cancer cells (36). In the present study, we showed that lncRNA-ATB overexpression promoted cell proliferation of PC-3 and DU-145 prostate cancer cell lines reflected by CCK8 assay and the protein downregulations of PCNA and phosphorylated histone H3 (markers of proliferation) in response to transfection with LV-mediated lncRNA-ATB plasmid, while reduced lncRNA-ATB expression had the opposite effect. These results imply that lncRNA-ATB functions as oncogene in prostate cancer and lncRNA-ATB may be defined as a potential treatment target for prostate cancer.

Dysregulated cell cycle is considered as a crucial event in the cellular processes during cancer development (37). Emerging evidence indicates that dysregulated lncRNAs are of great importance in tumor-associated cell cycle defects (38). Herein, we found that decrease of lncRNA-ATB retarded the cell cycle-related proteins, including downregulation of cyclin E and cyclin D1, but upregulation of p21 and p27 in prostate cancer cell lines of PC-3 and DU-145, but overexpression of lncRNA-ATB had the contrary effect. These results indicated that lncRNA-ATB exerts promotion of growth of prostate cancer cells via direct stimulating effect on the cell cycle progression, suggesting a unifying mechanism whereby lncRNA-ATB overexpression might contribute to the growth in malignant prostate cancer.

In various cancers EMT has been intimately related with enhanced cell motility and invasiveness in tumor development (39). New emerging evidence indicates that EMT plays an important role in development and metastasis of prostate cancer and EMT may be a key therapeutic target in prostate cancer (40). ZEB1 is demonstrated to be a direct target of miR-200 during EMT in breast cancer cell lines (41). The reduction of miR-652 induced EMT by stimulating ZEB1 expression levels in pancreatic cancer cells (42). ZNF217 is also indicated to be an accelerator of EMT in breast cancer (42). Both ZEB1 and ZNF217 are negatively regulated in the inhibition of EMT in response to miR-200 overexpression (43). In the present study, we found that overexpression of lncRNA-ATB induced EMT reflected by increases in E-cadherin and ZO-1 and decreases in N-cadherin and Vimentin in PC-3 and DU-145 prostate cell lines, knockdown of lncRNA-ATB exerted contrary effect. In addition, downregulation of lncRNA-ATB inhibited, while upregulation of lncRNA-ATB promoted the expression levels of ZEB1 and ZNF217 at mRNA and protein levels in PC-3 and DU-145 prostate cell lines. These results indicated that lncRNA-ATB may drive EMT in prostate cancer cells via positive modulation of ZEB1 and ZNF217 expression levels.

Both MAPK/ERK pathways and PI3K-Akt pathways are essential intracellular signaling pathways involving in the proliferation and EMT during the processes of cancers (44). Herein, our results showed that the signaling pathways of PI3K/Akt and ERK were suppressed by knockdown of lncRNA-ATB, but the continuous lncRNA-ATB expression further stimulated the phosphorylation levels of Akt and ERK in both PC-3 and DU-145 prostate cell lines. It is interesting that inhibition of PI3K/Akt and ERK signaling pathways prevented the proliferation of PC-3 and DU-145 prostate cell line responses to overexpression of lncRNA-ATB. Furthermore, pretreatment with PI3K inhibitor LY294002 or ERK inhibitor U0126 almost diminished the effects of lncRNA-ATB overexpression on the ZEB1 and ZNF217 protein expression levels. These results indicated both PI3K/Akt and ERK signaling pathways involved lncRNA-ATB-mediated growth and EMT of human prostate cancer. However, studies on the role of lncRNA-ATB in the migration, invasion and tumor growth in nude mice as well as their molecular mechanisms are necessary to be further elucidated.

In conclusion, our results demonstrated that high lncRNA-ATB expression is significantly associated with a poor prognosis independently of other factors in prostate cancer. LncRNA-ATB might be considered as a novel molecular target for the diagnosis and treatment of prostate cancer.

Acknowledgments

We appreciate the co-operation of all the people, and patients who participated in this study.

References

1 

Scher HI, Solo K, Valant J, Todd MB and Mehra M: Prevalence of Prostate Cancer Clinical States and Mortality in the United States: Estimates Using a Dynamic Progression Model. PLoS One. 10:e01394402015. View Article : Google Scholar : PubMed/NCBI

2 

Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, Parkin DM, Forman D and Bray F: Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 136:E359–E386. 2015. View Article : Google Scholar

3 

Jung KW, Won YJ, Kong HJ, Oh CM, Cho H, Lee DH and Lee KH: Cancer statistics in Korea: Incidence, mortality, survival, and prevalence in 2012. Cancer Res Treat. 47:127–141. 2015. View Article : Google Scholar : PubMed/NCBI

4 

Carroll PR: Early stage prostate cancer - do we have a problem with over-detection, overtreatment or both? J Urol. 173:1061–1062. 2005. View Article : Google Scholar : PubMed/NCBI

5 

Ishizaki F, Hara N, Koike H, Kawaguchi M, Tadokoro A, Takizawa I, Nishiyama T, Takahashi K and Hohenfellner R: Prediction of pathological and oncological outcomes based on extended prostate biopsy results in patients with prostate cancer receiving radical prostatectomy: A single institution study. Diagn Pathol. 7:682012. View Article : Google Scholar : PubMed/NCBI

6 

Lopes PM, Sepúlveda L, Ramos R and Sousa P: The role of transrectal ultrasound in the diagnosis of prostate cancer: New contributions. Radiol Bras. 48:7–11. 2015. View Article : Google Scholar : PubMed/NCBI

7 

Ilic D, O'Connor D, Green S and Wilt T: Screening for prostate cancer: A Cochrane systematic review. Cancer Causes Control. 18:279–285. 2007. View Article : Google Scholar : PubMed/NCBI

8 

Pritchard CC, Morrissey C, Kumar A, Zhang X, Smith C, Coleman I, Salipante SJ, Milbank J, Yu M, Grady WM, et al: Complex MSH2 and MSH6 mutations in hypermutated micro-satellite unstable advanced prostate cancer. Nat Commun. 5:49882014. View Article : Google Scholar

9 

Merdan S, Womble PR, Miller DC, Barnett C, Ye Z, Linsell SM, Montie JE and Denton BT: Toward better use of bone scans among men with early-stage prostate cancer. Urology. 84:793–798. 2014. View Article : Google Scholar : PubMed/NCBI

10 

Morgia G, Russo GI, Tubaro A, Bortolus R, Randone D, Gabriele P, Trippa F, Zattoni F, Porena M, Mirone V, et al Members of the LUNA Foundation; Società Italiana d'Urologia: Patterns of prescription and adherence to European Association of Urology guidelines on androgen deprivation therapy in prostate cancer: An Italian multicentre cross-sectional analysis from the Choosing Treatment for Prostate Cancer (CHOICE) study. BJU Int. Aug 31–2015.Epub ahead of print. PubMed/NCBI

11 

Albertsen PC: The unintended burden of increased prostate cancer detection associated with prostate cancer screening and diagnosis. Urology. 75:399–405. 2010. View Article : Google Scholar

12 

Martin NE and D'Amico AV: Progress and controversies: Radiation therapy for prostate cancer. CA Cancer J Clin. 64:389–407. 2014. View Article : Google Scholar : PubMed/NCBI

13 

Moyer VA; U.S. Preventive Services Task Force: Screening for prostate cancer: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 157:120–134. 2012. View Article : Google Scholar : PubMed/NCBI

14 

Shi X, Sun M, Liu H, Yao Y and Song Y: Long non-coding RNAs: A new frontier in the study of human diseases. Cancer Lett. 339:159–166. 2013. View Article : Google Scholar : PubMed/NCBI

15 

Li CH and Chen Y: Targeting long non-coding RNAs in cancers: Progress and prospects. Int J Biochem Cell Biol. 45:1895–1910. 2013. View Article : Google Scholar : PubMed/NCBI

16 

Wang KC, Yang YW, Liu B, Sanyal A, Corces-Zimmerman R, Chen Y, Lajoie BR, Protacio A, Flynn RA, Gupta RA, et al: A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression. Nature. 472:120–124. 2011. View Article : Google Scholar : PubMed/NCBI

17 

Liu Y, Zhang M, Liang L, Li J and Chen YX: Over-expression of lncRNA DANCR is associated with advanced tumor progression and poor prognosis in patients with colorectal cancer. Int J Clin Exp Pathol. 8:11480–11484. 2015.PubMed/NCBI

18 

Quagliata L, Matter MS, Piscuoglio S, Arabi L, Ruiz C, Procino A, Kovac M, Moretti F, Makowska Z, Boldanova T, et al: Long noncoding RNA HOTTIP/HOXA13 expression is associated with disease progression and predicts outcome in hepatocellular carcinoma patients. Hepatology. 59:911–923. 2014. View Article : Google Scholar :

19 

Ji J, Tang J, Deng L, Xie Y, Jiang R, Li G and Sun B: LINC00152 promotes proliferation in hepatocellular carcinoma by targeting EpCAM via the mTOR signaling pathway. Oncotarget. 6:42813–42824. 2015.PubMed/NCBI

20 

Yuan JH, Yang F, Wang F, Ma JZ, Guo YJ, Tao QF, Liu F, Pan W, Wang TT, Zhou CC, et al: A long noncoding RNA activated by TGF-β promotes the invasion-metastasis cascade in hepatocellular carcinoma. Cancer Cell. 25:666–681. 2014. View Article : Google Scholar : PubMed/NCBI

21 

Sun HJ, Liu TY, Zhang F, Xiong XQ, Wang JJ, Chen Q, Li YH, Kang YM, Zhou YB, Han Y, et al: Salusin-β contributes to vascular remodeling associated with hypertension via promoting vascular smooth muscle cell proliferation and vascular fibrosis. Biochim Biophys Acta. 1852:1709–1718. 2015. View Article : Google Scholar : PubMed/NCBI

22 

Wang H, Gao X, Lu X, Wang Y, Ma C, Shi Z, Zhu F, He B, Xu C and Sun Y: The mitotic regulator Hec1 is a critical modulator of prostate cancer through the long non-coding RNA BX647187 in vitro. Biosci Rep. 35:352015. View Article : Google Scholar

23 

Zhang C, Liu Z, Wang L, Qiao B, Du E, Li L, Xu Y and Zhang Z: Prognostic significance of GPC5 expression in patients with prostate cancer. Tumour Biol. Dec 2–2015.Epub ahead of print.

24 

Ma C, Shi X, Zhu Q, Li Q, Liu Y, Yao Y and Song Y: The growth arrest-specific transcript 5 (gAS5): a pivotal tumor suppressor long noncoding RNA in human cancers. Tumour Biol. Dec 3–2015.Epub ahead of print.

25 

Mapelli P and Picchio M: Initial prostate cancer diagnosis and disease staging - the role of choline-PET-CT. Nat Rev Urol. 12:510–518. 2015. View Article : Google Scholar : PubMed/NCBI

26 

Degirmenci M, Erdogan AP, Bulut G, Atmaca H, Uzunoglu S, Karaca B, Karabulut B and Uslu R: Octreotide in combination with AT-101 induces cytotoxicity and apoptosis through up-regulation of somatostatin receptors 2 and 5 in DU-145 prostate cancer cells. Tumour Biol. Nov 3–2015.Epub ahead of print. PubMed/NCBI

27 

Walsh AL, Tuzova AV, Bolton EM, Lynch TH and Perry AS: Long noncoding RNAs and prostate carcinogenesis: The missing 'linc'? Trends Mol Med. 20:428–436. 2014. View Article : Google Scholar : PubMed/NCBI

28 

Prensner JR and Chinnaiyan AM: The emergence of lncRNAs in cancer biology. Cancer Discov. 1:391–407. 2011. View Article : Google Scholar : PubMed/NCBI

29 

Enfield KS, Pikor LA, Martinez VD and Lam WL: Mechanistic roles of noncoding RNAs in lung cancer biology and their clinical implications. Genet Res Int. 2012:7374162012.PubMed/NCBI

30 

Zheng HT, Shi DB, Wang YW, Li XX, Xu Y, Tripathi P, Gu WL, Cai GX and Cai SJ: High expression of lncRNA MALAT1 suggests a biomarker of poor prognosis in colorectal cancer. Int J Clin Exp Pathol. 7:3174–3181. 2014.PubMed/NCBI

31 

Svoboda M, Slyskova J, Schneiderova M, Makovicky P, Bielik L, Levy M, Lipska L, Hemmelova B, Kala Z, Protivankova M, et al: HOTAIR long non-coding RNA is a negative prognostic factor not only in primary tumors, but also in the blood of colorectal cancer patients. Carcinogenesis. 35:1510–1515. 2014. View Article : Google Scholar : PubMed/NCBI

32 

Zhao T, Xu J, Liu L, Bai J, Xu C, Xiao Y, Li X and Zhang L: Identification of cancer-related lncRNAs through integrating genome, regulome and transcriptome features. Mol Biosyst. 11:126–136. 2015. View Article : Google Scholar

33 

Salameh A, Lee AK, Cardó-Vila M, Nunes DN, Efstathiou E, Staquicini FI, Dobroff AS, Marchiò S, Navone NM, Hosoya H, et al: PRUNE2 is a human prostate cancer suppressor regulated by the intronic long noncoding RNA PCA3. Proc Natl Acad Sci USA. 112:8403–8408. 2015. View Article : Google Scholar : PubMed/NCBI

34 

Saito T, Kurashige J, Nambara S, Komatsu H, Hirata H, Ueda M, Sakimura S, Uchi R, Takano Y, Shinden Y, et al: A long non-coding RNA activated by transforming growth factor-β is an independent prognostic marker of gastric cancer. Ann Surg Oncol. 22(Suppl 3): S915–S922. 2015. View Article : Google Scholar

35 

Lei B, Xu SP, Liang XS, Li YW, Zhang JF, Zhang GQ and Pang D: Long non-coding RNA MVIH is associated with poor prognosis and malignant biological behavior in breast cancer. Tumour Biol. Nov 10–2015.Epub ahead of print.

36 

Zhang E, Li W, Yin D, De W, Sun S and Han L: c-Myc-regulated long non-coding RNA H19 indicates a poor prognosis and affects cell proliferation in non-small-cell lung cancer. Tumour Biol. Oct 20–2015.Epub ahead of print.

37 

Zeng XX, Chu TJ, Yuan JY, Zhang W, Du YM, Ban ZY, Lei DM, Cao J and Zhang Z: Transmembrane 7 superfamily member 4 regulates cell cycle progression in breast cancer cells. Eur Rev Med Pharmacol Sci. 19:4353–4361. 2015.PubMed/NCBI

38 

Yang L, Qiu M, Xu Y, Wang J, Zheng Y, Li M, Xu L and Yin R: Upregulation of long non-coding RNA PRNCR1 in colorectal cancer promotes cell proliferation and cell cycle progression. Oncol Rep. 35:318–324. 2016.

39 

Emadi Baygi M, Soheili ZS, Essmann F, Deezagi A, Engers R, Goering W and Schulz WA: Slug/SNAI2 regulates cell proliferation and invasiveness of metastatic prostate cancer cell lines. Tumour Biol. 31:297–307. 2010. View Article : Google Scholar : PubMed/NCBI

40 

Li P, Yang R and Gao WQ: Contributions of epithelial-mesenchymal transition and cancer stem cells to the development of castration resistance of prostate cancer. Mol Cancer. 13:552014. View Article : Google Scholar : PubMed/NCBI

41 

Gregory PA, Bert AG, Paterson EL, Barry SC, Tsykin A, Farshid G, Vadas MA, Khew-Goodall Y and Goodall GJ: The miR-200 family and miR-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1. Nat Cell Biol. 10:593–601. 2008. View Article : Google Scholar : PubMed/NCBI

42 

Vendrell JA, Thollet A, Nguyen NT, Ghayad SE, Vinot S, Bièche I, Grisard E, Josserand V, Coll JL, Roux P, et al: ZNF217 is a marker of poor prognosis in breast cancer that drives epithelial-mesenchymal transition and invasion. Cancer Res. 72:3593–3606. 2012. View Article : Google Scholar : PubMed/NCBI

43 

Bai WD, Ye XM, Zhang MY, Zhu HY, Xi WJ, Huang X, Zhao J, Gu B, Zheng GX, Yang AG, et al: MiR-200c suppresses TGF-β signaling and counteracts trastuzumab resistance and metastasis by targeting ZNF217 and ZEB1 in breast cancer. Int J Cancer. 135:1356–1368. 2014. View Article : Google Scholar : PubMed/NCBI

44 

Lui GY, Kovacevic Z, Richardson V, Merlot AM, Kalinowski DS and Richardson DR: Targeting cancer by binding iron: Dissecting cellular signaling pathways. Oncotarget. 6:18748–18779. 2015. View Article : Google Scholar : PubMed/NCBI

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July-2016
Volume 36 Issue 1

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Copy and paste a formatted citation
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Spandidos Publications style
Xu S, Yi X, Tang C, Ge J, Zhang Z and Zhou W: Long non-coding RNA ATB promotes growth and epithelial-mesenchymal transition and predicts poor prognosis in human prostate carcinoma. Oncol Rep 36: 10-22, 2016
APA
Xu, S., Yi, X., Tang, C., Ge, J., Zhang, Z., & Zhou, W. (2016). Long non-coding RNA ATB promotes growth and epithelial-mesenchymal transition and predicts poor prognosis in human prostate carcinoma. Oncology Reports, 36, 10-22. https://doi.org/10.3892/or.2016.4791
MLA
Xu, S., Yi, X., Tang, C., Ge, J., Zhang, Z., Zhou, W."Long non-coding RNA ATB promotes growth and epithelial-mesenchymal transition and predicts poor prognosis in human prostate carcinoma". Oncology Reports 36.1 (2016): 10-22.
Chicago
Xu, S., Yi, X., Tang, C., Ge, J., Zhang, Z., Zhou, W."Long non-coding RNA ATB promotes growth and epithelial-mesenchymal transition and predicts poor prognosis in human prostate carcinoma". Oncology Reports 36, no. 1 (2016): 10-22. https://doi.org/10.3892/or.2016.4791