Abstract
The biological function of inhibin-α subunit (INHα) in prostate cancer (PCa) is currently unclear. A recent study associated elevated levels of INHα in PCa patients with a higher risk of recurrence. This prompted us to use clinical specimens and functional studies to investigate the pro-tumourigenic and pro-metastatic function of INHα. We conducted a cross-sectional study to determine a link between INHα expression and a number of clinicopathological parameters including Gleason score, surgical margin, extracapsular spread, lymph node status and vascular endothelial growth factor receptor-3 expression, which are well-established prognostic factors of PCa. In addition, using two human PCa cell lines (LNCaP and PC3) representing androgen-dependent and -independent PCa respectively, we investigated the biological function of elevated levels of INHα in advanced cancer. Elevated expression of INHα in primary PCa tissues showed a higher risk of PCa patients being positive for clinicopathological parameters outlined above. Over-expressing INHα in LNCaP and PC3 cells demonstrated two different and cell-type-specific responses. INHα-positive LNCaP demonstrated reduced tumour growth whereas INHα-positive PC3 cells demonstrated increased tumour growth and metastasis through the process of lymphangiogenesis. This study is the first to demonstrate a pro-tumourigenic and pro-metastatic function for INHα associated with androgen-independent stage of metastatic prostate disease. Our results also suggest that INHα expression in the primary prostate tumour can be used as a predictive factor for prognosis of PCa.
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Main
Inhibins A and B are members of the transforming growth factor-β (TGFβ) superfamily. Inhibins are heterodimers of an 18 kDa α-subunit disulphide linked to one of two 13 kDa β-subunits (βA and βB) resulting in inhibin A (αβA) and B (αβB) respectively. Primarily of gonadal origin, inhibins regulate pituitary follicle-stimulating hormone secretion by feedback inhibition. In humans, women produce both inhibin A and inhibin B (Welt et al, 1999; Welt and Schneyer, 2001), whereas in adult men inhibin B is the primary form (Marchetti et al, 2003). Inhibins have also been shown to be expressed in adrenal cortex, pituitary and prostate (reviewed in Risbridger et al, 2001). Other endocrine and paracrine functions of inhibins involve regulating members of the TGFβ superfamily, such as TGFβ itself, activins and bone morphogenic protein (BMP), by competing for their receptors (Wiater and Vale, 2003; Farnworth et al, 2007). This antagonistic effect of inhibin is amplified in the presence of the inhibin receptor, TGFβ receptor III (TGFβRIII), also known as betaglycan.
The first study that linked inhibin to reproductive cancers showed that serum inhibin increased in women with granulosa cell tumours of the ovary (Lappohn et al, 1989) and inhibin currently serves as a robust biomarker for this cancer. A direct biological function for inhibin in carcinogenesis was demonstrated by Matzuk et al (1992) when they created the inhibin-α subunit (INHα) knockout mouse. Both sexes developed gonadal sex-cord stromal tumours with high penetrance and developed tumours in their adrenal glands after castration, showing that INHα can act as a tumour suppressor. Subsequent mouse model studies revealed a complex network of interactions involving inhibin, activin and other modifiers in the development and progression of gonadal and adrenal tumours in INHα-deficient mice (reviewed in Risbridger et al, 2001). Although it is clear that total inhibin as a serum test has utility in the initial detection and prognosis of certain types of ovarian cancers, the biological function of inhibin in tumourigenesis is far from clear.
We have observed both up- and down-regulation of INHα expression in prostate cancer (PCa) tissues dependent on the stage of disease. Studies from our laboratory on metastatic PCa epithelial cell lines demonstrated that high concentrations (400 ng ml−1) of recombinant inhibin A inhibited growth of androgen-responsive LNCaP cells, but not androgen-independent DU145 cells, suggesting that the effect of inhibin may be dependent on cell phenotypes related to specific stages of PCa (McPherson et al, 1997). Furthermore, we have shown loss of heterozygosity or epigenetically regulated loss or down-regulation of INHα in PCa patient samples and LNCaP, DU145 and PC3 cell lines (Mellor et al, 1998; Schmitt et al, 2002; Balanathan et al, 2004). Collectively, these data suggest a tumour suppressive function for INHα in the prostate. In contrast, new insights into the role of INHα in the prostate came from a recent study using a large cohort of PCa patient tissues that showed that INHα was frequently over-expressed in high-grade PCa (Risbridger et al, 2004a, 2004b). The intensity of INHα immunoreactivity was associated with a higher risk of recurrence of PCa. These variable clinical and experimental observations provide equivocal evidence for a role of INHα in PCa. Thus it was proposed that like TGFβ (Roberts and Wakefield, 2003), INHα has tumour suppressive activity in normal epithelial cells, which changes to tumour promoting in cancer cells (Ball et al, 2004; Risbridger et al, 2004a).
To date there is no proof that INHα can increase tumourigenesis and metastasis. Thus the primary aim of this study was to examine the pro-tumourigenic and pro-metastatic function of INHα in advanced PCa. Specifically, the expression profile of INHα and clinicopathological parameters were examined in primary PCa tissues including specimens from patients with organ-confined disease and those with metastasis to the lymph nodes. In addition, human metastatic PCa cell lines, LNCaP and PC3, were used in in vitro and in vivo functional studies to determine the biological function of elevated levels of INHα on migration, invasion, tumour growth and metastasis.
Materials and methods
Analysis of clinical material
Relationship between INHα expression and clinicopathological parameters in primary prostate adenocarcinomas
This study was conducted in accordance with Australian National Health and Medical Research Council (NHMRC) guidelines. Archival formalin-fixed paraffin-embedded tissue blocks were retrieved from 37 patients with prostate carcinoma who underwent radical prostatectomy. The clinicopathological characteristics, vascular endothelial growth factor-C (VEGF-C) expression, lymphatic vessel density (LVD) and lymph node status of this cohort have been described previously (Zeng et al, 2004, 2005). We conducted a cross-sectional study to determine whether INHα expression was associated with clinicopathological parameters (Gleason score, surgical margins, extracapsular spread, VEGF receptor-3 (VEGFR-3) expression and lymph nodes status) and/or linked to well-established prognostic factors in prostatic adenocarcinoma. The PO 12 antibody (kindly provided by Dr Nigel Groome) was used to determine the expression pattern of INHα in primary prostate tissues as previously described (Risbridger et al, 2004b). Each immunostained tissue section was assessed and staining intensity in benign epithelial, cancer (Gleason grade G3/G4) and stromal regions was scored from 0 to 4 with 0 representing negative staining and 4 representing very strong positive staining. The relative risk of PCa patients being positive for the respective parameters was determined.
Stable transfection of LNCaP and PC3 cell lines
LNCaP and PC3 were obtained from American Type Culture Collection (Rockville, MD, USA) and routinely cultured as described previously (Balanathan et al, 2004). Expression vectors pcDNA3.1 (empty vector, EV) and human INHα cDNA subcloned into pcDNA3.1 (pcDNA3.1 (INHα)) were purchased from Invitrogen (Mount Waverley, Victoria, Australia) and prepared for transfection according to the manufacturer's instructions. LNCaP and PC3 cells were transfected using Lipofectamine plus (Invitrogen) and Superfect (Qiagen, Doncaster, Victoria, Australia) respectively according to the manufacturer's instructions. Individual colonies surviving after 2–3 weeks selection were picked and propagated for analysis.
Confirmation of mRNA expression in INHα-transfected LNCaP and PC3 cell lines
Total RNA was extracted using RNeasy Mini Kit (Qiagen) according to the manufacturer's instructions. Reverse transcription (RT) was performed as previously described (Balanathan et al, 2004). β2-microglobulin (β2mg) was used as a housekeeping gene for block PCR. Primer sequences were: INHA, forward: CCTGTTCTTGGATGCCTTG; reverse: AGCTGGGCTGAAGTCACCT and β2 mg, forward: CCGTGTGAACCATGTGACTT; reverse: CAAACATGGAGACAGCACTC. Absolute quantitative real-time analysis was used to assess the levels of TGFβRIII mRNA expression in the clones. The analysis was performed on a LightCycler real-time PCR machine (Roche Diagnostic, Mannheim, Germany) using LightCycler Fast Start DNA Master SYBR Green 1 (Roche Diagnostic) according to the manufacturer's instructions. All experiments were carried out twice and duplicate readings were taken for each replicate. The quantity of mRNA was determined using a standard curve and all values were normalised using the housekeeping gene, hypoxanthine ribosyl transferase (HPRT). Primer sequences were: TGFβRIII, forward: TTCCCTGTTCACCCGACCTGAAAT; reverse: CGTCAGGAGGCACACATTA and HPRT, forward: TGTAATGACCAGTCAACAGGG; reverse: TGGCTTATATCCAACACTTCG.
Confirmation of protein expression by ELISA
Cell lysates and conditioned media (conditioned for 24 h) were prepared from EV- and INHα-transfected clones. Total protein (1 μg μl−1) was used for further analysis. Inhibin A and B and activin A concentrations were measured in triplicate using specific ELISA according to the manufacturer's instructions (Diagnostic Systems Laboratories, Webster, TX, USA). VEGF-A and VEGF-C ELISAs were measured in duplicate using specific ELISA according to the manufacturer's instructions (R&D Systems, Minneapolis, MN, USA). Two biological replicates were examined.
Direct cell counting: proliferation assay
LNCaP and PC3 cells were seeded at a density of 1 × 105 cells per well and 5 × 103 cells per well, respectively, in 24-well plates and incubated at 37°C. Triplicate wells were harvested by trypsinisation on days 1, 2, 3, 4 and 5, and numbers of cells per well were counted using haemocytometer. Each experiment was repeated twice. The results obtained from individual clones (EV and INHα) were pooled for each treatment.
Scratch wound assay: motility assay
Cells were plated in triplicate in 6- or 12-well plates and grown until approximately 70–80% confluence. The cell monolayer was then wounded and analysed over time as previously described (Sharp et al, 2004). Each experiment was repeated twice. The results obtained from individual clones (EV and INHα) were pooled for each treatment.
Intra-prostatic inoculation of LNCaP and PC3 cells
The experiments were in accordance with NHMRC of Australia guidelines. LNCaP (2 × 106) or PC3 (5 × 105) clones were injected orthotopically into the ventral lobe of the prostate gland (10 animals per clone) of male SCID mice as previously described (Zeng et al, 2006). After 7–9 weeks, mice were killed and primary prostate tumours were removed and weighed. In addition, regional lymph nodes were removed for analysis. Monoclonal human mitochondria antibody (1 : 100; Chemicon, Temecula, CA, USA) was used to determine the presence of human cells in the tumours as previously described (McCulloch et al, 2005). The monoclonal R1 antibody (7.5 μg ml−1), kindly provided by Dr Nigel Groome, was used to determine INHα expression in tumours as previously described (Balanathan et al, 2004).
Lymph node volumes were determined using stereological analysis as previously described (McPherson et al, 2001). The lymph nodes were serially sectioned at 5 μm thickness and using a random sampling scheme, every 20th section was chosen for analysis. Briefly, the computer program newCAST component (version 2.14; Visiopharm, Hørsholm, Denmark) was used to generate a point grid, and volumes of the lymph nodes were determined. Each section was examined using × 20 magnification and tissue sections were mapped to define tissue boundaries and were sampled at predetermined intervals along x- and y-axes using a single grid-counting frame. The volume was then determined using the equation=no of points for each tissue × area per point × distance; in this case the distance was defined by thickness of the sections (5 μm) plus (5 μm × 20 for every 20th section).
LVD in the intra-prostatic tumours
Lymphatic vessels were identified using lymphatic vascular endothelial hyaluronan receptor (LYVE-1), a marker of lymphatic endothelium (Banerji et al, 1999). Invasion of tumour cells into lymphatics was monitored by the presence of human mitochondrial protein-stained cancer cells in lymph vessels. Double immunostaining for LYVE-1 and mitochondria was performed on a Dako Autostainer (Dako, Glostrup, Denmark). The sections were incubated with LYVE-1 antibody (Fitzgerald, Boston, MA, USA) diluted at 0.5 μg ml−1 for 2 h. LYVE-1 was detected by incubation with Envision polymer-anti-rabbit-HRP (Dako) for 15 min and visualised with diaminobenzidine (Dako). Sections were then incubated with Double Staining Enhancer (Zymed, San Francisco, CA, USA) for 15 min and exposed to mitochondrial antibody (Chemicon) diluted at 1 : 200 for 2 h. Secondary antibody, biotinylated rabbit anti-mouse IgG1 (Zymed) was applied and the immunoreactivity was detected by ExtrAvidin-Alkaline phosphatase (Sigma, St Louis, MO, USA) and visualised by reaction with Vector Red (Vector Laboratories, Burlingame, CA, USA). The sections were counterstained with hematoxylin (Dako) and immunolocalisation was examined using an Olympus BX-60 microscope (Tokyo, Japan).
Lymphatic vessels were counted using stereological methods as previously described (Balanathan et al, 2004). Lymphatic vessels were counted within tissue sections (of randomly selected INHA-positive prostate tumours, n=15 and EV tumours, n=11; using n=2 randomly selected sections per tumour) to assess the LVD within the tumour (intra-tumoural) region, the region in contact with both the tumour and the stroma (peritumoural) and the region away from tumour. LVD was expressed as the number of lymph vessels per mm2.
Statistical analyses
All statistical analyses were performed and results were analysed by ANOVA or t-tests as specified. The relationships between INHα expression and clinicopathological parameters were evaluated by Fisher's exact test. The mean staining intensity of patients positive for each of the respective clinicopathological parameter was compared to the mean staining intensity (reference) of those patients who were negative. The relative risks and 95% confidence intervals (CI) were estimated.
Results
Relationship between INHα expression and clinicopathological parameters in primary prostate adenocarcinomas
Immunostaining revealed differential expression of INHα in benign epithelial, G3/G4 cancer regions as well as in the stroma of primary PCa tissues from patients with organ-confined disease (Figure 1A–D) and those with metastasis to the lymph nodes (Figure 1E–H). Association between clinicopathological prognostic factors and INHα expression is shown in Table 1. Elevated expression of INHα in the benign epithelial regions of the primary PCa tissues showed a higher relative risk in PCa patients positive for extracapsular spread (P=0.01). Similarly, elevated expression of INHα in the stroma of the primary PCa tissues showed a higher risk of PCa patients positive for extracapsular spread (P=0.0011), surgical margins (P=0.0006), VEGFR-3 expression (P=0.00067) and lymph node metastasis (P<0.0001). Further analysis showed that there was a significant increase in INHα staining in benign epithelial (P=0.018) and stromal (P<0.0001) regions but not in G3/G4 cancer regions in tissues from patients with lymph node metastasis compared to patients with organ-confined disease (data not shown).
Isolation and characterisation of cells over-expressing INHα
The INHα expression profile in clinical specimens suggests pro-tumourigenic and pro-metastatic function for INHα in advanced PCa. Thus, to elucidate the effect of elevated levels of INHα expression on PCa cells, we stably transfected LNCaP and PC3 cell lines with an expression vector containing an INHα cDNA or with a control EV and confirmed the expression of the transgene by PCR (Supplementary Figure 1). Expression of dimeric proteins (inhibin A, inhibin B and activin A) was examined by ELISA. Analysis of cell lysates and conditioned media identified an increase in expression of inhibin B, but not inhibin A in INHα-transfected LNCaP cells and both inhibin A and inhibin B in the INHα-transfected PC3 cell lines (Table 2). There was no change in activin A level in the transfected cells. The expression of INHα protein was also validated by western blot and immunohistochemistry (data not shown). Immunohistochemistry of antibiotic selected clones revealed that the selected INHα-transfected clones were a heterogeneous population of INHα-positive and -negative cells. Because primary PCa cells are known for their heterogeneity and the aim of this study was to determine the effect of elevated levels of INHα in cancer, it was concluded the heterogeneous population was not going to bias the outcomes of the functional assays.
Growth characteristics of INHα-transfected LNCaP and PC3 clones in vitro
To evaluate the effect of over-expression of INHα on the growth of LNCaP and PC3 cell lines, we examined the proliferative capacity and motility of the various clones. Direct cell count demonstrated reduced proliferation of INHα over-expressing LNCaP cells (Figure 2A) and increased proliferation of PC3 cells (Figure 2B) when compared to their respective EV clones in the later stages of the growth curve. Monolayer wound healing assays showed INHα over-expressing LNCaP cells had a reduced rate of wound closure at earlier time points (Figure 2C) whereas INHα over-expressing PC3 cells demonstrated a trend towards increased rate of wound closure (Figure 2D). Because the significant changes in proliferation and motility observed in this study occur at different time points, it suggests that they are independent from each other.
Effect of INHα over-expression on tumour growth and metastasis
The influence of INHα on tumour growth and metastasis was determined in vivo. The clones were injected at the orthotopic site (prostate) and after 7–9 weeks primary prostate tumours as well as the adjacent lymph nodes were harvested. Primary prostate tumour size was determined and the incidence of lymph node metastasis was scored. Positive immunostaining for human mitochondrial protein confirmed that the primary and secondary tumours originated from intra-prostatic injection of human cells. INHα immunostaining was used to confirm INHα expression in tumours (Figure 3A–D, left). Immunostaining in the INHα tumours showed that INHα expression was not uniform within the tumour, which is consistent with a heterogeneous population of INHα-positive and -negative cells in the INHα-transfected clones we had observed previously. INHα immunostaining of the lymph nodes showed INHα-positive LNCaP cells to be distributed throughout the lymph node tumours whereas INHα-positive PC3 cells were confined to the outer tumour regions (Figure 3C and D, left). INHα over-expression in LNCaP cells did not affect orthotopic tumour take but significantly reduced the size of the primary tumour (P=0.0029) compared to the EV-transfected clones (Figure 3A, middle and right). Furthermore, INHα over-expression in LNCaP cells did not change the incidence of lymph node metastasis or the size of the lymph node tumours (Figure 3C, middle and right). INHα over-expression in PC3 cells had no effect on orthotopic tumour take but a significant increase in the primary prostate tumour size (P=0.005) was observed (Figure 3B, middle and right). INHα over-expression in PC3 significantly increased the incidence of lymph node tumours (P=0.0341) and lymph node tumour size (P=0.0047) compared to the EV-transfected clones (Figure 3D, middle and right). The altered tumour size following INHα over-expression may have influenced the formation of metastasis.
LVD and invasion of tumour cells into lymphatics in INHα over-expressing primary prostate tumours
Changes to LVD and lymphangiogenesis are often associated with metastatic spread of cancer cells to the lymph nodes (Mattila et al, 2002; Zeng et al, 2005). To understand the mechanisms and to provide proof of metastatic spread observed in the mice injected with INHα-positive cells, we stained LNCaP and PC3 INHα and EV orthotopic tumours for LYVE-1, and human mitochondrial antibody to determine LVD and the degree of invasion of tumour cells into lymphatic vessels (lymphatic invasion) in the tissues. Consistent with our previous study (Zeng et al, 2006), the analysis of LNCaP tumours in the present study was complicated by the significantly larger size of the tumours compared to PC3 tumours. This larger size resulted in numerous necrotic areas in the LNCaP tumours, making it difficult to consistently define the different tumour peripheries and the intra- and inter-tumoural regions. For this reason stereological analysis of the LNCaP tumours was not possible. However, histological evaluation of the LNCaP tumours demonstrated no LYVE-1-positive lymphatic vessels within the tumour with lymphatic vessels only present in the regions away from the tumour (Figure 4A and B). In contrast, PC3 tumours had lymphatic vessels distributed throughout the tumour (Figure 4C and D). Stereological analysis of the PC3 tumours revealed a significant increase (P=0.0023) in total LVD in the intra-tumoural regions with no difference in LVD in peritumoural regions and regions away from tumour in INHα-positive tumours compared to the controls (Figure 4E). A significant increase in lymphatic invasion in the intra-tumoural (P=0.0002), peritumoural (P=0.0225) and regions away from tumour (P=0.0077) in INHα-positive tumour tissues compared to the controls was evident (Figure 4F).
Factors inducing tumour growth and metastasis in INHα over-expressing PC3 tumours
The observed increase in LVD in INHα-positive PC3 tumours suggests that the metastatic spread of the cancer cells from the primary tumour site to the lymph nodes occurs through the process of lymphangiogenesis. Because VEGF-A and VEGF-C have been implicated in inducing/promoting metastasis to the lymph nodes in PCa (Karkkainen et al, 2002; Weis and Cheresh, 2005; Zeng et al, 2006), we went on to determine the expression of VEGF-A and VEGF-C proteins by ELISA (Table 3) in INHα- and EV-transfected clones in vitro. There was no significant change in the amount of VEGF-A and VEGF-C secreted by the different LNCaP clones. VEGF-C protein was significantly increased (P=0.0011) in the INHα over-expressing PC3 clones compared to their EV clones, however there was no significant change in secreted VEGF-A levels.
Expression of TGFβRIII in LNCaP and PC3 transfected clones
Although being a receptor for TGFβ, TGFβRIII is also a receptor for inhibins (Wiater and Vale, 2003), and recent studies have reported loss of TGFβRIII as a common and important event in human PCa (Turley et al, 2007; Sharifi et al, 2007a). Down-regulation of TGFβRIII in PCa has been suggested to reflect loss of sensitivity to tumour suppressive inhibin by the PCa cells. To test this hypothesis, we determined the levels of TGFβRIII mRNA expression in the clones. Consistent with a recent study (Sharifi et al, 2007a), real-time analysis of PCa cell lines revealed LNCaP cells to have more TGFβRIII mRNA expression compared to PC3 cells. There was no change in TGFβRIII expression in INHα-transfected LNCaP or PC3 clones compared to EV-transfected clones (Figure 5).
Discussion
Although inhibin is used as a biomarker for ovarian cancer, the biological function of elevated levels of INHα expression in PCa and certain types of ovarian cancer is unclear. This study is the first functional study to link up-regulation of INHα expression in androgen-independent prostate disease and progression of primary prostate and secondary tumours and metastasis.
We conducted a cross-sectional study to determine a link between INHα expression and a number of clinicopathological parameters: Gleason score, surgical margin status, extracapsular spread, lymph node status and VEGFR-3 expression, which are well-established prognostic factors of PCa (Wheeler et al, 1998; Cheng et al, 1999, 2001, 2005; Li et al, 2004). This study showed that an elevated level of INHα expression in the primary prostate tumour can be used as a predictive factor for prognosis in PCa. Univariate analysis showed a significant association between elevated levels of INHα in primary PCa tissues and extracapsular spread, surgical margins, VEGFR-3 expression and lymph node status. This finding is supported by our previous study that reported elevated levels of INHα in PCa patients to be associated with a higher risk of recurrence, although this association was not statistically significant (Risbridger et al, 2004b). The proposed cellular site for INHα expression and action is epithelial cells, however our immunostaining and analysis of the primary prostate tumour showed a significant association of elevated levels of INHα in both benign epithelial cells and stromal cells to extracapsular spread. There is increasing evidence that the surrounding microenvironment also has a major function in cancer cell growth, survival, invasion and metastatic progression, further supporting the pro-tumourigenic and pro-metastatic function of INHα in advanced PCa (reviewed in Chung et al, 2005; Alberti, 2006; Taylor and Risbridger, 2008). Likewise, Wheeler et al (1998) reported that invasion into or through the capsule of the prostate is strongly associated with both the ability of PCa to metastasise and with recurrence of cancer after radical prostatectomy. Our data link INHα expression in both epithelial and stromal cells with extracapsular spread, which suggests a role for INHα in advanced PCa. In addition, the observed up-regulation of INHα in benign epithelium and stromal regions in the primary prostate tumours in patients with lymph node metastasis suggests an association with VEGF-C-linked metastasis. Further analysis of our clinical data showed that INHα expression is stronger in benign epithelium and stroma but not the G3/G4 regions of the prostate in patients with lymph node metastasis compared to those with organ-confined disease. In PCa, Tsurusaki et al (1999) found that VEGF-C mRNA levels were significantly higher in lymph-node-positive tumours and that VEGFR-3-positive vessels were increased in the stroma of VEGF-C-positive tumours. Also, VEGF-C has been shown to promote growth of lymphatic vessels into and around tumours in animal models and this was associated with metastatic spread to the lymph nodes and sometimes to distant organs (Mandriota et al, 2001; Skobe et al, 2001; Mattila et al, 2002). Collectively, our analysis of INHα expression in primary prostate tumour tissues and the association to well-established prognostic factors strongly supports a pro-tumourigenic and pro-metastatic function for INHα in PCa.
Because the proposed cellular site for pro-tumourigenic and pro-metastatic action of INHα is cancer epithelial cells, we over-expressed INHA in metastatic epithelial PCa cell lines, LNCaP and PC3, to evaluate functionally the effect of elevated levels of INHα in PCa. A key event in the progression of PCa is the transition from an androgen-dependent to -independent stage, where subpopulations of tumour cells either gain resistance to, or adapt to, an androgen-depleted environment, and begin to proliferate resulting in the progression to highly aggressive and metastatic androgen-independent disease. Furthermore, when PCa is advanced or metastatic it is usually incurable and tends to metastasise to bone and lymph nodes. LNCaP cells, originally isolated from a lymph node metastasis (Horoszewicz et al, 1980, 1983), have retained their ability to respond to androgens, whereas PC3 cells, originally derived from a bone metastasis (Kaighn et al, 1979), are androgen independent. Thus these cell lines represent early and late stages of metastatic prostate disease.
INHα over-expression in LNCaP cells demonstrated reduced cell proliferation, migration and primary prostate tumour growth whereas INHα over-expression in these cells did not change the cells’ ability to metastasise to the lymph nodes nor did it influence the growth of the lymph node tumours. The lack of change in VEGF-C expression in INHα-transfected LNCaP cells is consistent with the unchanged metastatic ability of LNCaP cells in vivo. In contrast, INHα over-expression PC3 cells demonstrated increased cell proliferation, migration, primary prostate tumour and lymph node tumour growth. These cells showed increased metastasis to the lymph node, which was accompanied by an elevation of LVD and tumour cell invasion into lymphatics. These effects were associated with up-regulation of VEGF-C. Similarly, Karpanen et al (2001) reported that VEGF-C expression in a mouse tumour model strongly promoted the growth of tumour-associated lymphatic vessels, which in the tumour periphery were commonly infiltrated with the tumour cells. Although limited to the use of only two cell lines, the current study is the first to functionally show a pro-tumourigenic and pro-metastatic function for INHα in an androgen-independent model of metastatic prostate disease.
Another explanation for the different effects of INHα observed in the current study is the loss or gain of a yet-to-be-identified signalling pathway for INHα in either tumour suppression or promotion. We have shown that LNCaP cells express more TGFβRIII mRNA expression compared to PC3 cells and that the level of TGFβRIII mRNA expression is maintained after INHα over-expression. Loss of TGFβRIII during PCa progression has been suggested to be a reason for loss of sensitivity to the tumour suppressive effect of inhibin in prostate disease (Turley et al, 2007; Sharifi et al, 2007a, 2007b). Whether androgen status, different cell types and/or levels of TGFβRIII expression are responsible for the different effects of inhibin observed in the present study is an important area of future investigation.
Inhibins are known to be involved with regulating members of the TGFβ superfamily, including TGFβ itself, as well as activins and BMP, by competing for their receptors or co-receptors (Wiater and Vale, 2003; Farnworth et al, 2006, 2007). However, unlike other members of the TGFβ superfamily (Pangas and Woodruff, 2000; Shi and Massagué, 2003), the signalling pathway(s) for inhibin have not yet been defined. Although it remains unclear how INHα mediates downstream cellular events leading to prostate disease, the observed effect of INHα in the present study suggests and supports an effect of inhibin which is independent of TGFβ/activin in PCa. Owing to the presence of both βA and βB subunits in LNCaP and PC3 cells, the clones were able to produce dimeric inhibin A and inhibin B. The presence of inhibin B in both LNCaP and PC3 cells is significant as inhibin B is the pre-dominant form of inhibin in men and therefore more relevant to the study of PCa. Although the presence of inhibin A in PC3 may be of relevance to the observed phenotypes of PC3 cells, further investigation into the functional difference resulting from inhibin A vs inhibin B production in these cells was beyond the scope of this project. The level of inhibin A and inhibin B produced by the cells reflects the level of the β-subunits expressed and secreted by the respective cell lines (McPherson et al, 1999). Our study showed no change in the levels of activin A (βAβA), which indicates that observed effects are specific to inhibin and not a response to activin levels. Therefore, although TGFβ/activins have been shown to induce expression of angiogenic/lymphangiogenic factors through P13K and/or SMAD2 pathways (Wagner et al, 2004; Kang, 2006) and TGFβ/activins inhibit growth of PCa cells (Wilding et al, 1989; Wang et al, 1996; McPherson et al, 1997), the different responses of the PCa cell lines to elevated levels of INHα we have observed cannot be simply explained by abrogation of TGFβ/activin signalling. Thus, the effect of inhibin on LNCaP cells observed in this study supports a role for inhibin in PCa independent of TGFβ/activin. Also, the increased metastatic ability of INHα observed in INHα over-expressing PC3 cells cannot be due to antagonism of activin action because of the simultaneous expression of follistatin in these cells (McPherson et al, 1999). Follistatin is an activin-binding protein that binds to activin with a high affinity thereby inhibiting activin bioactivity (Phillips and de Kretser, 1998). Taken together, the current study demonstrates a direct action of INHα in PCa that is context and/or cell-type dependent.
In summary, this study showed both benign epithelial and stromal regions of primary prostate tumours to be the sites of INHα expression. We have also demonstrated a strong association of elevated levels of INHα to well-established prognostic factors of PCa. This finding has identified INHα as a very important predictive factor that can be used to identify patients at increased risk for disease progression and cancer death after radical prostatectomy, so that appropriate therapy can be selected. Finally, the current study has shown a pro-tumourigenic and pro-metastatic role for INHα in an androgen-independent model of metastatic prostate disease. This suggests that in the absence of androgens, elevated levels of inhibin may be driving the more aggressive and metastatic phenotypes of PCa tumour.
Change history
16 November 2011
This paper was modified 12 months after initial publication to switch to Creative Commons licence terms, as noted at publication
References
Alberti C (2006) Prostate cancer progression and surrounding microenvironment. Int J Biol Markers 21: 88–95
Balanathan P, Ball EMA, Wang H, Harris SE, Shelling AN, Risbridger GP (2004) Epigenetic regulation of inhibin α-subunit gene in prostate cancer cell lines. J Mol Endocrinol 32: 55–67
Ball EM, Mellor SL, Risbridger GP (2004) Cancer progression: is inhibin alpha from Venus or Mars? Cytokine Growth Factor Rev 15: 291–296
Banerji S, Ni J, Wang SX, Clasperm S, Su J, Tammi R, Jones M, Jackson DG (1999) LYVE-1, a new homologue of the CD44 glycoprotein, is a lymph-specific receptor for hyaluronan. J Cell Biol 144: 789–801
Cheng L, Darson MF, Bergstralh EJ, Slezak J, Myers RP, Bostwick DG (1999) Correlation of margin status and extraprostatic extension with progression of prostate carcinoma. Cancer 86: 1775–1782
Cheng L, Jones TD, Lin H, Eble JN, Zeng G, Carr MD, Koch MO (2005) Lymphovascular invasion is an independent prognostic factor in prostatic adenocarcinoma. J Urol 174: 2181–2185
Cheng L, Zincke H, Blute ML, Bergstralh EJ, Scherer B, Bostwick DG (2001) Risk of prostate carcinoma death in patients with lymph node metastasis. Cancer 91: 66–73
Chung LW, Baseman A, Assikis V, Zhau HE (2005) Molecular insights into prostate cancer progression: the missing link of tumor microenvironment. J Urol 173: 10–20
Farnworth PG, Wang Y, Escalona R, Leembruggen P, Ooi GT, Findlay JK (2007) Transforming growth factor-beta blocks inhibin binding to different target cell types in a context-dependent manner through dual mechanisms involving betaglycan. Endocrinology 148: 5355–5368
Farnworth P, Stanton P, Wang Y, Escalona R, Findlay J, Ooi G (2006) Inhibins differentially antagonize activin and bone morphogenetic protein action in a mouse adrenocortical cell line. Endocrinology 147: 3462–3471
Horoszewicz J, Leong S, Chu T, Wajsman Z, Friedman M, Papsidero L, Kim U, Chai L, Kakati S, Arya S, Sandberg A (1980) The LNCaP cell line – a new model for studies on human prostatic carcinoma. Prog Clin Biol Res 37: 115–132
Horoszewicz JS, Leong SS, Kawinski EK, Rosenthal H, Chu TM, Mirand EA, Murphy GP (1983) LNCaP model of human prostatic carcinoma. Cancer Res 43: 1809–1818
Kaighn ME, Narayan KS, Ohnuki Y, Lechner JF, Jones LW (1979) Establishment and characterization of a human prostatic carcinoma cell line (PC-3). Invest Urol 17: 16–23
Kang Y (2006) Pro-metastasis function of TGFbeta mediated by the Smad pathway. J Cell Biochem 98: 1380–1390
Karkkainen MJ, Makinen T, Alitalo K (2002) Lymphatic endothelium: a new frontier of metastasis research. Nat Cell Biol 4: E2–E5
Karpanen T, Egeblad M, Karkkainen MJ, Kubo H, Yla-Herttuala S, Jaattela M, Alitalo K (2001) Vascular endothelial growth factor C promotes tumor lymphangiogenesis and intralymphatic tumor growth. Cancer Res 61: 1786–1790
Lappohn RE, Burger HG, Bouma J, Bangah M, Krans M, de Bruijn HW (1989) Inhibin as a marker for granulosa-cell tumors. N Engl J Med 321: 790–793
Li R, Younes M, Wheeler TM, Scardino P, Ohori M, Frolov A, Ayala G (2004) Expression of vascular endothelial growth factor receptor-3 (VEGFR-3) in human prostate. Prostate 58: 193–199
Mandriota SJ, Jussila L, Jeltsch M, Compagni A, Baetens D, Prevo R, Banerji S, Huarte J, Montesano R, Jackson DG, Orci L, Alitalo K, Christofori G, Pepper MS (2001) Vascular endothelial growth factor-C-mediated lymphangiogenesis promotes tumour metastasis. EMBO J 20: 672–682
Marchetti C, Hamdane M, Mitchell V, Mayo K, Devisme L, Rigot JM, Beauvillain JC, Hermand E, Defossez A (2003) Immunolocalization of inhibin and activin alpha and betaB subunits and expression of corresponding messenger RNAs in the human adult testis. Biol Reprod 68: 230–235
Mattila MM, Ruohola JK, Karpanen T, Jackson DG, Alitalo K, Harkonen PL (2002) VEGF-C induced lymphangiogenesis is associated with lymph node metastasis in orthotopic MCF-7 tumors. Int J Cancer 98: 946–951
Matzuk MM, Finegold MJ, Su JG, Hsueh AJ, Bradley A (1992) Alpha-inhibin is a tumour-suppressor gene with gonadal specificity in mice. Nature 360: 313–319
McCulloch DR, Opeskin K, Thompson EW, Williams ED (2005) BM18: a novel androgen-dependent human prostate cancer xenograft model derived from a bone metastasis. Prostate 65: 35–43
McPherson S, Wang H, Jones M, Pedersen J, Iismaa T, Wreford N, Simpson E, Risbridger G (2001) Elevated androgens and prolactin in aromatase deficient (ArKO) mice cause enlargement but not malignancy of the prostate gland. Endocrinology 142: 2458–2467
McPherson SJ, Mellor SL, Wang H, Evans LW, Groome NP, Risbridger GP (1999) Expression of activin A and follistatin core proteins by human prostate tumor cell lines. Endocrinology 140: 5303–5309
McPherson SJ, Thomas TZ, Wang H, Gurusinghe CJ, Risbridger GP (1997) Growth inhibitory response to activin A and B by human prostate tumour cell lines, LNCaP and DU145. J Endocrinol 154: 535–545
Mellor SL, Richards MG, Pedersen JS, Robertson DM, Risbridger GP (1998) Loss of the expression and localization of inhibin alpha-subunit in high grade prostate cancer. J Clin Endocrinol Metab 83: 969–975
Pangas SA, Woodruff TK (2000) Activin signal transduction pathways. Trends Endocrinol Metab 11: 309–314
Phillips DJ, de Kretser DM (1998) Follistatin: a multifunctional regulatory protein. Front Neuroendocrinol 19: 287–322
Risbridger GP, Ball EM, Wang H, Mellor SL, Peehl DM (2004a) Re-evaluation of inhibin alpha subunit as a tumour suppressor in prostate cancer. Mol Cell Endocrinol 225: 73–76
Risbridger GP, Schmitt JF, Robertson DM (2001) Activins and inhibins in endocrine and other tumors. Endocr Rev 22: 836–858
Risbridger GP, Shibata A, Ferguson KL, Stamey TA, McNeal JE, Peehl DM (2004b) Elevated expression of inhibin alpha in prostate cancer. J Urol 171: 192–196
Roberts AB, Wakefield LM (2003) The two faces of transforming growth factor beta in carcinogenesis. Proc Natl Acad Sci USA 100: 8621–8623
Schmitt JF, Millar DS, Pedersen JS, Clark SL, Venter DJ, Frydenberg M, Molloy PL, Risbridger GP (2002) Hypermethylation of the inhibin alpha-subunit gene in prostate carcinoma. Mol Endocrinol 16: 213–220
Sharifi N, Hurt EM, Kawasaki BT, Farrar WL (2007a) TGFBR3 loss and consequences in prostate cancer. Prostate 67: 301–311
Sharifi N, Lechleider RJ, Farrar WL (2007b) Transforming growth factor-b receptor III downregulation in prostate cancer: is inhibin B a tumor suppressor in prostate? J Mol Endocrinol 39: 329–332
Sharp JA, Waltham M, Williams ED, Henderson MA, Thompson EW (2004) Transfection of MDA-MB-231 human breast carcinoma cells with bone sialoprotein (BSP) stimulates migration and invasion in vitro and growth of primary and secondary tumors in nude mice. Clin Exp Metastasis 21: 19–29
Shi Y, Massagué J (2003) Mechanisms of TGF-beta signaling from cell membrane to the nucleus. Cell 113: 685–700
Skobe M, Hamberg LM, Hawighorst T, Schirner M, Wolf GL, Alitalo K, Detmar M (2001) Concurrent induction of lymphangiogenesis, angiogenesis, and macrophage recruitment by vascular endothelial growth factor-C in melanoma. Am J Pathol 159: 893–903
Taylor RA, Risbridger GP (2008) Prostatic tumor stroma: a key player in cancer progression. Curr Cancer Drug Targets 8: 490–497
Tsurusaki T, Kanda S, Sakai H, Kanetake H, Saito Y, Alitalo K, Koji T (1999) Vascular endothelial growth factor-C expression in human prostatic carcinoma and its relationship to lymph node metastasis. Br J Cancer 80: 309–313
Turley RS, Finger EC, Hempel N, How T, Fields TA, Blobe GC (2007) The type III transforming growth factor-β receptor as a novel tumor suppressor gene in prostate cancer. Cancer Res 67: 1090–1098
Wagner K, Peters M, Scholz A, Benckert C, Ruderisch HS, Wiedenmann B, Rosewicz S (2004) Activin A stimulates vascular endothelial growth factor gene transcription in human hepatocellular carcinoma cells. Gastroenterology 126: 1828–1843
Wang QF, Tilly KI, Tilly JL, Preffer F, Schneyer AL, Crowley Jr WF, Sluss PM (1996) Activin inhibits basal and androgen-stimulated proliferation and induces apoptosis in the human prostatic cancer cell line, LNCaP. Endocrinology 137: 5476–5483
Weis SM, Cheresh DA (2005) Pathophysiological consequences of VEGF-induced vascular permeability. Nat Rev 437: 497–504
Welt CK, Schneyer AL (2001) Differential regulation of inhibin B and inhibin a by follicle-stimulating hormone and local growth factors in human granulosa cells from small antral follicles. J Clin Endocrinol Metab 86: 330–336
Welt CK, Adams JM, Sluss PM, Hall JE (1999) Inhibin A and inhibin B responses to gonadotropin withdrawal depends on stage of follicle development. J Clin Endocrinol Metab 84: 2163–2169
Wheeler TM, Dillioglugil O, Kattan MW, Arakawa A, Soh S, Suyama K, Ohori M, Scardino PT (1998) Clinical and pathological significance of the level and extent of capsular invasion in clinical stage T1-2 prostate cancer. Hum Pathol 29 (8): 856–862
Wiater E, Vale W (2003) Inhibin is an antagonist of bone morphogenetic protein signaling. J Biol Chem 278: 7934–7941
Wilding G, Valverius E, Knabbe C, Gelmann EP (1989) Role of transforming growth factor-alpha in human prostate cancer cell growth. Prostate 15: 1–12
Zeng Y, Opeskin K, Baldwin ME, Horvath LG, Achen MG, Stacker SA, Sutherland RL, Williams ED (2004) Expression of vascular endothelial growth factor receptor-3 by lymphatic endothelial cells is associated with lymph node metastasis in prostate cancer. Clin Cancer Res 10: 5137–5144
Zeng Y, Opeskin K, Goad J, Williams ED (2006) Tumor-induced activation of lymphatic endothelial cells via vascular endothelial growth factor receptor-2 is critical for prostate cancer lymphatic metastasis. Cancer Res 66: 9566–9575
Zeng Y, Opeskin K, Horvath LG, Sutherland RL, Williams ED (2005) Lymphatic vessel density and lymph node metastasis in prostate cancer. Prostate 65: 222–230
Acknowledgements
We thank Dr Christopher Bulter for critically reviewing this paper and Dr Stephen McPherson for his assistance with stereological analysis. Post-doctoral training award by United States Department of Defense (PB), Cancer Council Victoria grant-in-aid (EDW), Cancer Institute of New South Wales (LGH), Senior Research Fellowship from Australian National Health and Medical Research Council (NHMRC) and the Pfizer Foundation (MGA and SAS) and by an NHMRC program grant. Principal Research Fellowship from Australian NHMRC (GPR).
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Balanathan, P., Williams, E., Wang, H. et al. Elevated level of inhibin-α subunit is pro-tumourigenic and pro-metastatic and associated with extracapsular spread in advanced prostate cancer. Br J Cancer 100, 1784–1793 (2009). https://doi.org/10.1038/sj.bjc.6605089
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DOI: https://doi.org/10.1038/sj.bjc.6605089
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