Androgen receptor promotes the migration and invasion of upper urinary tract urothelial carcinoma cells through the upregulation of MMP-9 and COX-2
- Chi-Cheng Chen
- Teng-Fu Hsieh
- Chao-Hsiang Chang
- Wen‑Lung Ma
- Xiao-Fan Hung
- Yi‑Ru Tsai
- Meng-Hsueh Amanda Lin
- Caixia Zhang
- Chawnshang Chang
- Chih-Rong Shyr
Published online on: Tuesday, May 28, 2013
- Pages: 979-985
- DOI: 10.3892/or.2013.2506
Upper urinary tract urothelial carcinoma (UUTUC) is an aggressive urologic malignancy associated with high morbidity and mortality although it is relatively rare, accounting for approximately 5–10% of all urothelial tumors (1). The natural history of upper tract UC is different from UC of the bladder with higher incidence of high-grade deeply invasive disease in the upper urinary tract than in the bladder (2). UUTUCCs that invade the muscle wall generally have a very poor prognosis with 5-year specific survival less than 50% for pT2/pT3 and less than 10% for pT4 (1,3). The median survival of pT4 patients is only 7–9 months even with radical nephroureterectomy and chemotherapy (3,4). Therefore, UUTUC presents a serious public health problem and a challenge for clinical physicians and basic scientists to find more effective systemic adjuvant therapy to improve the outcome of UUTUC patients.
UUTUC is a male-dominant disease with a male to female ratio of 2:1 to 2.5:1 (5,6). Survival of UUTUC patients was significantly influenced by the male gender, age over 80 years, a two-incision operation, location in both the pelviocaliceal system and the ureter, grade III, and stage T3 and T4 with adjusting for gender and age (7). Gender and stage of UUTUC patients were the only independent prognostic factors predictive of overall survival and female gender was associated with a better survival (7). These studies suggest that gender plays an important role in the development and progression of UUTUC. However, gender differences in malignant diseases, including UUTUC, are not fully understood and, therefore, more studies are required to elucidate their pathological mechanisms. Androgens and androgen receptor (AR) have been demonstrated to play an important role in male-dominant cancers, including liver and bladder cancer, by affecting tumor initiation and progression (8–10). Therefore, in the present study, we hypothesized that AR also plays a role in the progression of UUTUC and accounts for the high incidence and poor prognosis of UUTUC in males.
During the progression of tumors from primary sites to metastasis, specific proteins and signals are activated to enable cancer cells to detach from neighboring cells, re-orientate their polarity, invade, migrate, survive and proliferate in foreign microenvironments. These proteins include ECM-degrading enzymes, such as matrix metalloproteinases (MMPs) and cathepsins, which help the degradation of the basement membrane and extracellular matrix (ECM) (11,12). There are also signal molecules capable of inducing stress-fiber assembly and contraction for mobility, such as small G-protein Rho and its important downstream effector, the Rho-associated serine/threonine kinase (ROCK), which are also involved in tumor cell migration and invasion (13–16). In UUTUC, the mRNA levels of RhoA and RhoA protein were higher in tumors and metastatic lymph node tissues than in non-tumor tissues, suggesting that RhoA-ROCK 1 signaling is involved in the invasion and metastasis of UUTUC (17). The expression of MMP-2, MMP-9 and TIMP-1 was an independent predictor of high pT stage (18) and elevated expression levels of MMP-9 and MMP-2 were associated with poor prognosis (19).
AR has been shown to regulate MMP-2 and MMP-9 in the prostate (20) and in prostate cancer (21) and AR action in migration is mediated by RhoA-ROCK signaling axis that controls cell motility in prostate cancer (22). The upregulation of cyclooxygenase 2 (COX-2) expression occurs frequently in a variety of different tumors and COX-2, which is also shown to be an important signaling molecule that regulates cell motility (23,24). The AR agonist, dihydrotestosterone (DHT), was shown to increase levels of the vascular inflammatory mediator COX-2 (25).
However, how AR affects the above signals related to the progress of UUTUC remains unclear. In the present study, we investigated this issue by adding AR overexpression in UUTUC cells to observe the role of AR in cell migration and invasion as well as to examine possible genes involved in the regulatory role of AR in the migration and invasion in UUTUCs.
Materials and methods
Cell lines and chemicals
The UUTUC cell line BFTC 909 cells (from a UUTUC of a renal pelvis patient) were a generous gift from Dr C.C. Tzeng (26) and were cultured in Dulbecco's modified Eagle's medium, containing 10% heat-inactivated fetal bovine serum (FBS) at 37°C in an atmosphere of 5% CO2. SV-HUC cells (ureter cells immortalized by SV40, from an 11-year-old male accident victim) were obtained from ATCC and were cultured in Ham's F-12 medium, containing 10% heat-inactivated FBS at 37°C in an atmosphere of 5% CO2. To exogenously express AR in cells, a recombinant lentiviral vector containing wild-type AR (pWPI hAR) (27) and a control lentiviral vector expressing the enhanced green fluorescent protein (pWPI) were used to overexpress AR. Lentiviral PWPI-AR/PWPI-control with pMD2.G packaging and psPAX2 envelope plasmids (lentivirus:packaging:envelopeZ 2:1:1) were co-transfected into 293T cells. After 48 h of transfection, target cells were cultured in the presence of viral supernatant containing 8 mg/ml polybrene (Millipore, Billerica, MA, USA) for 6 h.
MMP-9 inhibitor I was purchased from Calbiochem (Frankfurt, Germany) and celecoxib and casodex were purchased from Sigma-Aldrich (Buchs SG, Switzerland).
Wound-healing migration assay
Cells were seeded onto 35-mm plates until confluence. The plates were scratched using a sterile pipette tip to generate a wound through the confluent monolayer. Cells were analyzed and photographed with a microscope. Images of the cell wound were captured at 0 and 24 h of migration. The relative migration was calculated by setting the percentage of wound closure in control cells after 24 h as 1.
Transwell migration assay
Cells were first harvested from the culture dish and 1.0×104 cells in 200 μl of serum-free medium were transferred to the Transwell inserts (the top compartment, 8-μm pore size) and 750 μl of medium was placed in the lower chamber. Following incubation at 37°C for 4 h in a cell culture incubator, cells on the upper surface of the filters were removed with cotton swabs, filters were washed, fixed, and stained with crystal violet. Cells that had moved to the lower surface of the filter were counted under the microscope. Migrated cells in each field were quantified. Results are presented as relative migration by setting the migrating cell number of control cells as 1.
Transwell invasion assay
Cell invasion through a three-dimensional ECM was assessed by a Matrigel invasion assay using BD Matrigel coated-Transwell with 8.0-μm filter membranes. Cells resuspended in 200 μl of serum-free medium were plated onto each filter, and 750 μl of DMEM containing 10% FBS were added into the lower compartment of the invasion chambers. After 24 h, cells on the upper surface of the filters were removed with cotton swabs, filters were washed in 4% paraformaldehyde and stained with 1% crystal violet. Cells that had invaded to the lower surface of the filter were counted under the microscope.
In vitro adhesion to fibronectin assay
Twenty-four-well culture dishes were pre-coated with 80 μl of fibronectin (2.5 mg/ml) adhesion buffer (0.25% bovine serum albumin in Hank's balanced salt solution; HBSS) for 30 min at 37°C. Cancer cells (1×105) were added to each well. After 30 min at 37°C in a CO2 incubator, non-adherent cells were removed by gentle wash with HBSS. Then, the cells were fixed with 2% paraformaldehyde in 1X PBS and the adhesive cancer cells were stained with 0.05% crystal solution. The staining intensity was quantitated with a spectrometer.
Quantitative real-time RT-PCR
Total RNA was extracted from cells using TRIzol (Invitrogen, Carlsbad, CA, USA) and used for first-strand cDNA synthesis. The mRNA levels were measured using CFX96™ Real-Time system (Bio-Rad Laboratories) using KAPA SYBR® Fast qPCR kits (Kapa Biosystems, Inc., Woburn, MA, USA). Specific primers for MMP-2, MMP-9, RhoA, Rock1, COX-2 and β-actin were: MMP-2, F: 5′-CCCCAGACAGGTGATCTTGAC-3′ and R: 5′-GCTTGCGAGGGAAGAAGTTG-3′; MMP-9, F: 5′-CGC TGGGCTTAGATCATTCC-3′ and R: 5′-AGGTTGGATAC ATCACTGCATTAGG-3′; RhoA, F: 5′-TCAAGCCGGAGGT CAACAAC-3′ and R: 5′-ACGAGCTGCCCATAGCAGAA-3′; Rock1, F: 5′-ATGAGTTTATTCCTACACTCTACCACT TTC-3′ and R: 5′-TAACATGGCATCTTCGACAC TCTAG-3′; COX-2, F: 5′-CCCTTGGGTGTCAAAGGTAA-3′ and R: 5′-GCCCTCGCTTATGATCTGTC-3′; and β-actin, F: 5′-TCA CCCACACTGTGCCCATCTACGA-3′ and R: 5′-CAG CGGAACCGCTCATTGCCAATGG-3′. PCR cycling conditions were: 3 min at 95°C for 1 cycle followed by 40 amplification cycles at 95°C for 10 sec and 52°C (MMP-2, MMP-9, Rock-1, COX-2 and β-actin), or 62°C (RhoA) for 30 sec. Expression levels were normalized to β-actin mRNA level determined by the 2−ΔΔCT method.
Western blot analysis
Cell lysates were resolved by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE), transferred to a nitrocellulose membrane and incubated with specific primary antibodies. Protein bands were visualized using horseradish peroxidase (HRP)-conjugated secondary antibodies and enhanced chemiluminescence reagent (Millipore, Bedford, MA, USA) with the Bio-Rad imaging system.
Experiments were repeated at least three independent times. Results are expressed as the means ± SD. Two-tailed unpaired t-test was used to compare the results between the two groups. A P-value of <0.05 was considered to indicate a statistically significant difference.
Addition of AR in BFTC 909 and SV-HUC cells increases cell migration
To determine the role of AR in the migration of UUTUC cells, we used different UUT urothelial cells, including established UUTUC cells, BFTC 909, and transformed UUTUC cells, SV-HUC. Since these cells express a very low amount of AR, we exogenously expressed AR with viral infection into these cells to examine how AR affects cell migration. As shown in Fig. 1A, contrast-phase images show that the wound area was significantly reduced in BFTC 909-hAR cells with the addition of AR compared to BFTC 909-pWPI cells. Transwell migration assay also showed that SV-HUC-hAR cells migrated more than SV-HUC-pWPI cells (Fig. 1B). These results indicate that AR stimulates UUTUC cell migration either in cancer cells or transformed UC cells.
The cell migration assay of UUTUC cells infected with pWPI or hAR by lentiviral system to overexpress AR. For the wound-healing migration assay, cells were plated at high density for 24 h, and then the cell monolayer was scratched and incubated for an additional 24 h for cell migration into the wound area. Images of the wounds were captured and the recovered areas were calculated. Wound healing was analyzed by comparing the wound healing rate [% wound healing = (Initial wound width - current wound width)/Initial wound width] at 2 different intervals. (A) The quantitative relative migration data and representative microscopic images for BFTC 909-pWPI and BFTC 909-hAR cells. (B) Quantitative relative migration data for SV-HUC-pWPI and SV-HUC-hAR cells by Transwell migration assay. Data represent the means ± SD. *P<0.05 from at least 3 independent experiments and analyzed by t-test.
Addition of AR in BFTC 909 cells increases cell migration
The metastatic process involves several critical steps such as invasion and adhesion (28). We further determined the ability of AR to enhance invasion of UUTUC cells. Consistent with findings in Fig. 1, the addition of AR in BFTC 909-hAR cells increased the number of cells invading through Matrigel-coated Transwell filters (Fig. 2A). Adhesion to ECM is an important ability of cancer cells to anchor on the matrix for invasion. Therefore, we also examined the adhesion ability of BFTC 909 cells with or without AR addition. We coated fibronectin, an important component of ECM, on culture plates to investigate the effect of AR on BFTC 909 cell adhesiveness to fibronectin. The addition of AR significantly enhanced the adhesion of BFTC 909-hAR cells compared to BFTC 909-pWPI cells (Fig. 2B). Collectively, our results suggest that AR not only stimulates the invading ability of urothelial cancer cells but also the ability of cells to adhere to cell matrix to promote cell invasion.
Matrigel invasion and adhesion assay of BFTC 909 cells infected with pWPI or hAR by lentiviral system to overexpress AR. The bottoms of the top well in Transwell setting were all coated with a thin layer of Matrigel and only the cells in the top well with invasive capacity could migrate through the Matrigel layer and 8.0 μm pores. The cells with invasion potential through Matrigel-coated Transwells were monitored by crystal violet staining. (A) The quantitative relative migration data and representative microscopic images for BFTC 909-pWPI and BFTC 909-hAR cells. Relative invasion of BFTC 909 hAR cells was normalized to vector-infected cells, set at 1. (B) For the adhesion assay, BFTC 909-pWPI and BFTC 909-hAR cells were seeded on the culture dishes that were pre-coated with 80 μl of fibronectin (2.5 mg/ml) for 4 h and then washed with PBS. The adhesive cancer cells stained with 0.05% crystal solution and the staining intensity was quantitated with a spectrometer. Data represent the means ± SD of at least 3 independent experiments and were analyzed by t-test. *P<0.05 vs. vector control cells.
Genes related to migration and invasion expression changed by AR
To investigate which signaling pathways are activated by AR to increase cell migration and invasion, we examined the several genes which are involved in the migration and invasion of tumor cells. Previous studies have shown that AR stimulates MMP-2 expression in human prostate cancer, which is involved in cell migration (29). AR action in migration is mediated by RhoA-ROCK signaling axis that controls cell motility in prostate cancer (22), which regulates the cytoskeleton and cell migration and is frequently overexpressed in tumors (15). COX-2 is another important signal molecule which regulates cell motility, and AR agonist DHT was shown to increase levels of the vascular inflammatory mediator COX-2 (25). Therefore, we assessed the expression of these genes by qRT-PCR and immunoblot analysis in BFTC 909 cells with or without AR addition. In mRNA levels, the expression of MMP-9, RhoA and Rock-1 was increased, while the expression of MMP-2 and COX-2 was not changed in BFTC 909-hAR cells, when compared with BFTC 909-pWPI cells (Fig. 3A). Furthermore, in protein levels, BFTC 909-hAR cells had higher expression of MMP-9, Rock-1 and COX-2 than BFTC 909-pWPI cells (Fig. 3B). These results suggest that AR may upregulate these genes at the RNA and protein level to enhance cell migration and invasion.
(A) The expression of pro-invasion/metastasis genes on BFTC 909-pWPI and BFTC 909-hAR cells. RNAs from BFTC 909-pWPI and BFTC 909-hAR cells were analyzed by qRT-PCR on mRNA levels of pro-invasion/metastasis genes, MMP-2, MMP-9, Rho, ROCK1 and COX-2. Each transcript level from BFTC 909 pWPI cells was set as 1. Data represent the means ± SD of 3 independent experiments and were analyzed by t-test. **P<0.01 and ***P<0.001 vs. vector-infected control cells. (B) The expression of proteins related to migration and invasion changed by AR expression. BFTC 909-pWPI and BFTC 909-hAR cells. The cells were lysed. Equal amounts of protein were analyzed by SDS-PAGE and immunoblotted with anti-ROCK1, anti-AR, anti-COX-2, anti-MMP-9 and anti-β-actin antibodies. Representative blots of more than 3 independent studies are shown.
Inhibitor effects on AR-enhanced cell migration and invasion in UUTUC cells
To further determine the role of MMP-9 and COX-2 in AR-enhanced migration and invasion, we tested whether MMP-9 and COX-2 activities were required for enhancing migration and invasion of BFTC 909-hAR cells by performing the same experiments as above, but in the presence of MMP-9 inhibitor I, a cell-permeable, potent, selective, and reversible MMP-9 inhibitor, or selective COX-2 inhibitor (celecoxib). In the migration assay, as expected, AR-enhanced cell migration in BFTC 909-hAR cells was suppressed by the anti-androgen, casodex (Fig. 4A). Furthermore, MMP-9 and COX inhibitors also showed the ability to suppress AR-enhanced cell migration (Fig. 4B). In the invasion assay, BFTC 909-hAR cells that invaded Matrigel to the lower surface of the filter were decreased by casodex (Fig. 4C) and MMP-9 and COX-2 inhibitors also had the same effect (Fig. 4D). The finding that both migration and invasion were markedly reduced in the presence of casodex, MMP-9 inhibitor and celecoxib, indicate that AR, MMP-9, COX-2 signaling are involved in the ability of AR to promote migration and invasion of BFTC 909 cells.
Inhibitor effects on AR-enhanced cell migration and invasion in BFTC 909 cells. The inhibitory effect of (A) casodex and (B) MMP-9-I inhibitor or COX-2 on the AR-enhanced migration of BFTC 909-hAR cells was assessed by wound healing assay. BFTC 909-hAR cells were incubated with casodex, MMP-9-I and COX-2 inhibitors for 24 h. Relative quantification of wound repair of each inhibitor treatment group was quantified by setting the migration rate of no treatment BFTC 909-hAR cell group as 1. The inhibitory effect of (C) casodex, (D) MMP-9-I inhibitor, or COX-2 inhibitor on the AR-enhanced invasion of BFTC 909-hAR cells was assessed by Transwell invasion assay. BFTC 909-hAR cells were incubated with casodex, MMP-9-I or COX-2 inhibitors for 24 h in Transwell plates coated with a thin layer of Matrigel. Relative quantification of cell invasion of each inhibitor treatment group was quantified by setting invading cell number of no treatment BFTC 909-hAR cell group as 1. Values are the means ± SD from at least 3 independent experiments. *P<0.05, **P<0.001 vs. untreated BFTC 909-hAR cells.
The present study indicated that AR plays a role in the migration and invasiveness of UUTUC cells, based on the results that there is increased cell migration and invasion following AR addition in UUTUC cells (Figs. 1 and 2). Our findings may aid in clarifying the clinical implications of androgen and AR signaling in the progression of UUTUC, which may explain the higher male ratio in invasive UUTUC. Although our previous study showed that approximately 40% of invasive UUTUCs were AR positive (30), the correlation of AR status with relapse and metastasis following radical nephroureterectomy, and survival of patients with invasive UUTUC, has not been investigated. Whether AR is critical in influencing UUTUC progress and survival outcome requires further investigation. In the present study, we provided evidence that AR promotes UUTUC metastasis involving induction of MMP-9 and COX-2 in UUTUC cells, all of which have well established roles in cancer metastasis (6,11,12).
AR expression levels in the tumor and/or its microenvironment affect prostate cancer metastasis (31,32). Exogenous expression of AR in AR-negative PC-3 prostate cancer cells decreased their invasive properties, and treatment with androgen further reduced invasion of these cells (33), but AR functions in prostate stromal cells as a promoter for prostate cancer proliferation and metastasis (34). Although the role of AR in UUTUC has not been investigated, in UC of bladder, AR was shown to promote BBN-induced bladder cancer in mice (9) and bladder cancer cell migration and invasion (35), suggesting AR also plays an important role in urothelial carcinoma. Our study is the first to show the role of AR in increasing UUTUC cell migration and invasion, which is in contrast to the effect of AR on prostate cancer, although others also reported that AR promotes the invasiveness of prostate cancer cells (21,29). These studies indicate that AR may have diverse effects on molecules involved in cancer invasion and metastasis by suppressing or stimulating cancer cell migration and invasion, which may be due to the tumor microenvironment, coregulators of AR and alterations of growth factors and their receptors in tumors (36). The exact mechanisms by which AR exerts its effects in different cancer cells requires further investigation in order to dissect the multiple roles of AR in cancer progression and metastasis.
In delineating the molecules regulated by AR in affecting UUTUC metastasis, we examined the genes including MMPs involved in the degradation of the ECM, which is a key step in the process of cancer invasion and metastasis. Our results showed that among different MMPs, MMP-2 and MMP-9, AR increased MMP-9 expression both at the mRNA and protein level, but not MMP-2 in UUTUC cells (Fig. 3A). In prostate cancer cells, regulation of MMP-2 or MMP-9 by AR signaling has different results from different groups. Some studies have reported that androgen stimulates pro-MMP-2 expression but not pro-MMP-9 in LNCaP cells (29) and both MMP-2 and MMP-9 are stimulated by AR signaling in MDA-I cells (21). However, Miyamoto et al reported that androgen decreases MMP-9 secretion in PC-3 cells stably expressing AR (37). Therefore, the molecular mechanism on the upregulation of MMP-9 expression of AR requires further analysis, but the inhibitors of MMP-9 were shown able to block AR-enhanced cell migration and invasion. Since MMP inhibitors have been proposed as promising targets for cancer therapy (38), the combination of AR antagonists is likely to increase treatment efficacy in AR positive UUTUC cells.
To metastasize, tumor cells need to increase motility by remodelling the cytoskeletons and cell contacts with the ECM, which is regulated by RhoA and ROCK-1 kinase (15). Although we have demonstrated the increase of RhoA and ROCK-1 expression in BFTC 909 cells with addition of AR, the inhibitors of ROCK-1 failed to block AR-enhanced migration and invasion (data not shown), suggesting that RhoA and ROCK-1 may not significantly affect AR function. The higher expression level of COX-2 has been shown to increase invasiveness in colon cancer and prostate cancer cells (24,39). For UUTUC, overexpressed COX-2 was also found in patients and was associated with the pathologic stage and grade, indicating that COX-2 may be involved in UUTUC carcinogenesis and development (40,41). The effect of the specific COX-2 inhibitor on AR-enhanced migration and invasion clearly demonstrated the essential role of COX-2 in cell migration and invasion (Fig. 4B and D).
Inhibition of COX-2 and MMP-9 suppressed AR-enhanced cell migration and invasion in UUTUC (Fig. 4B and D). This finding provides the rationale to develop new therapeutic treatment by combining AR blockade and chemotherapy or target therapy, which may produce better efficacy. Since COX-2 and MMP-9 are also associated with tumor progression, inhibition of the COX-2 and MMP-9 pathways could be an effective therapeutic approach for advanced UUTUCs. The combined therapy of androgen deprivation and other anti-AR therapies with inhibition of the COX-2 and MMP-9 pathways may have improved therapeutic efficacy on advanced UUTUCs. Therefore, our study has several important clinical implications; first, our data proved that the expression of AR is linked to tumor cell migration and invasion, although whether AR overexpression in UUTUCs is associated with higher clinical stage and poor clinical outcome requires further investigation. Second, our study suggested that the addition of AR blockade in therapeutic regimens combined with targeted drugs may have better responses in UUTUC patients who have AR positive tumors. Adjuvant chemotherapy following surgery is currently used in UUTUC patients to prevent cancer relapse and metastasis, but adjuvant chemotherapy only achieves a 5-year recurrence-free rate of up to 50 % with minimal impact on survival (42,43). Since AR blockade has been commonly used and has been shown to improve survival of men with locally advanced and high-grade prostate cancer (44), the combination of AR blockade with either traditional chemotherapy or target therapy may increase the efficacy of therapeutic regimens on advanced UUTUCs.
This study was supported by the grant (TTCRD-10110) from Buddhist Tzu Chi General Hospital, Taichung, Taiwan. This study was also supported in part by Taiwan Department of Health Clinical Trial and Research Center of Excellence (DOH100-TD-B-111-004).