The androgen receptor fuels prostate cancer by regulating central metabolism and biosynthesis

Identifying a core set of direct AR-regulated genes

To identify direct AR-regulated genes, we combined genome-wide AR binding profiles with detailed transcript profiling. We also integrated androgen-stimulated recruitment of the transcriptional machinery to identify a core set of AR binding sites, which regulate gene expression in prostate cancer cells. First, we mapped AR binding profiles in two cell lines which represent distinct molecular subtypes of prostate cancer: one harbouring an AR ligand binding domain mutation (LNCaP); one harbouring an AR gene amplification (VCaP). Using chromatin immunoprecipitation with direct Solexa sequencing (ChIP-seq), we identified 11 053 AR binding sites in LNCaP cells and 51 811 androgen-dependent AR binding sites in VCaP cells (Supplementary Tables S1 and S2). VCaP cells harbour a copy number gain of the AR gene locus resulting in elevated AR expression (Supplementary Figure S1; Makkonen et al, 2011), which may at least in part explain the larger number of AR binding sites found in VCaP compared with LNCaP cells. Despite the difference in total number of identified binding sites, over 90% of the LNCaP AR binding sites were also found in the VCaP cells (Figure 1A; Supplementary Figure S2; Supplementary Table S3), suggesting that these core binding sites are commonly occupied by the AR even in distinct molecular subtypes of prostate cancer. The common AR binding sites between LNCaP and VCaP cells included all established AR target genes (Figure 1A; Supplementary Figure S2), had significant correlations with other published data sets (Supplementary Figure S3) and identified thousands of AR targets not identified in previous AR ChIP studies (Supplementary Table S3). As a resource we have compiled all published AR ChIP-chip studies together with our data in Supplementary Table S3.

Next, we integrated the location of the transcriptional machinery on the prostate cancer genome together with detailed expression profiling. We identified 15 761 androgen-dependent RNAP II (serine 5 phosphorylated RNA polymerase II) regions in LNCaP cells using ChIP-seq (Supplementary Table S4), 1283 of which overlapped with androgen-stimulated AR binding sites (Figure 1B). The regions enriched for RNAP II alone (n=14 478) represent sites of paused, primed or active transcription (Bernstein et al, 2006; Core et al, 2008); however, sites to which the AR and RNAP II are dynamically co-recruited (n=1283) are candidate regions for androgen-stimulated transcriptional initiation (explored in detail below). Using Illumina BeadArrays, we made a detailed study of androgen-regulated gene expression with samples taken every 30 min for 4 h and then every hour up to 24 h following androgen stimulation of LNCaP cells. This detailed expression array time course made it possible to identify androgen-regulated gene expression changes based on trends with time following androgen stimulation (using autocorrelation), allowing detection of early and even small gene expression changes (see Materials and methods for details). In total, we found 3319 transcripts with altered expression in response to androgens, 1556 (47%) transcripts were upregulated and 1763 (53%) were downregulated (Supplementary Table S5).

We made a combined analysis of our treatment contrast ChIP and detailed gene expression profiling to identify AR binding sites which recruit the transcriptional machinery and direct AR-regulated genes. Such combined analyses require a predefined genomic distance between transcript factor binding sites and genes, which is often set arbitrarily. To address this issue, we took a more empirical approach using gene set enrichment analysis (GSEA) to define the optimal genomic distance between AR binding sites (peaks) and androgen-regulated genes (gene boundaries). We found that genes located within 25 kb of an AR binding site were the most significantly enriched for androgen-regulated genes; the maximal enrichment score at 25 kb suggests that smaller genomic windows would include a greater proportion of false negatives and that larger genomic windows would include a greater proportion of false positives (Figure 1C; Supplementary Figure S3; Supplementary data). Therefore, using this 25 kb window we integrated the genomic locations of AR binding sites, androgen-stimulated recruitment of the core transcriptional machinery and detailed gene expression profiling (Figure 1D). This integrated analysis revealed that loci bound by either the AR or RNAP II alone contain genes which are upregulated, downregulated or not affected by AR signalling (Figure 1D). This finding is consistent with previous studies showing that the AR can directly activate or repress transcription (Margiotti et al, 2007; Prescott et al, 2007), that only a proportion of transcription factor binding sites are active in a given cellular context (Carroll et al, 2006) and that RNAP II enriched regions of the genome include both sites of active transcription and also sites where transcription has paused or stalled (Bernstein et al, 2006; Core et al, 2008). In contrast, the core overlap of androgen-stimulated AR binding sites and RNAP II recruitment showed specific enrichment for androgen upregulated transcripts (Figure 1D). Therefore, our combined analysis has identified a core set of AR binding sites that recruit the transcriptional machinery and upregulate the transcription of adjacent genes. These core AR targets may help to identify the features of transcriptionally active AR binding sites.

Analysis of the genomic sequences underlying all AR binding sites found in LNCaP, VCaP or those identified in both cell lines revealed evolutionary conservation, enrichment of AR binding sequences and motifs for previously reported AR interacting transcription factors, including forkhead and NF-1 (Supplementary Figure S1; Supplementary Table S6) (Wang et al, 2007; Jia et al, 2008). The overlapping AR and RNAP II sites showed significant enrichment of 6 bp and 15 bp AR binding motifs (Figure 1E and F), but also showed enrichment for CREB and AHR binding motifs, in contrast to the full set of AR binding sites (Supplementary Figure S1; Supplementary Table S6). De novo motif analysis revealed an inverted-repeat 15 bp ARE similar to the in vitro-derived consensus binding motif (Roche et al, 1992) and also a 6 bp motif consisting of one half of the consensus 15 bp element, as previously reported in other AR ChIP studies (Massie et al, 2007; Wang et al, 2007) (Figure 1E; Supplementary Figure S1).

Identifying cellular processes regulated by the AR

Our combined analysis of AR, RNAP II and detailed expression profiling also identified a core set of direct androgen-regulated genes for further investigation. We defined direct AR targets as those genes induced by androgen treatment and for which there were overlapping hormone-induced AR binding sites within 25 kb of the genes. This definition identified a sufficient number of genes to allow pathway enrichment analysis and as a resource we have included a table noting these genes together with their androgen-stimulated expression profile, annotated with the location of adjacent AR and RNAP II binding sites (Supplementary Table S7). Interestingly, this core set of direct AR-regulated genes gave overlapping but distinct functional enrichment by gene ontology (GO) analysis compared with gene expression data alone (Figure 2A; Supplementary Tables S8 and S9).

While many established classes of AR target gene were represented within the data sets as a whole, including cell-cycle regulators (e.g., CDC25, CDK6 and E2F1) and signalling molecules which have been implicated in prostate cancer (e.g., WWP1, ERBB2, MEK5, SGK1 and IGF1R) (Figure 2C; Craft et al, 1999; Hellawell et al, 2002; Mehta et al, 2003; Chen et al, 2007; Sherk et al, 2008), the combined analysis of direct AR targets and androgen-regulated genes also revealed a significant enrichment of metabolic targets (Figure 2A–C; Supplementary Table S9). GO analysis highlighted central metabolism and biosynthetic pathways among the direct AR targets (Figure 2A) and GSEA also revealed significant enrichment of central metabolism and metabolic gene signatures (Mootha et al, 2003) among direct AR-regulated genes (Figure 2B). Unlike other biological processes, metabolism has been subjected to decades of detailed biochemical study and consists of a series of interlinked and well-characterized processing steps. This makes the functional consequences of changes in enzyme expression uniquely predictable for metabolic pathways and made these pathways an ideal testing ground for the linkages established by our genomics data. We found that the AR directly upregulated expression of key steps in glucose uptake and glycolysis including glucose transporter 1 (GLUT1/SLC2A1), hexokinase I and II (HK1 and HK2), phosphofructokinase (PFK2/PFKFB2) and also many anabolic enzymes at both the transcript and protein level (Figure 2C and D; Supplementary Figures S4 and S5). Based on the annotation of these direct metabolic AR target genes within well-defined metabolic pathways we predicted that the AR may facilitate cell growth by promoting glucose uptake and anabolic metabolism (Figure 2D). To test these predictions from our genomics data, we undertook comprehensive metabolomic profiling to assess the effects of AR signalling on glucose consumption and lactate production, O₂ consumption and detailed metabolite profiling of intracellular and extracellular metabolites using proton nuclear magnetic resonance (1H NMR) and glucose flux using carbon-13-labelled glucose with gas chromatography–mass spectrometry (GC/MS).

The AR regulates aerobic glycolysis and anabolism in prostate cancer cells

Androgen stimulation of prostate cancer cells increased glucose uptake and increased lactate production in normoxia, but had no effect on oxygen consumption, showing that AR signalling does indeed stimulate aerobic glycolysis (Christofk et al, 2008; Vander Heiden et al, 2009) (Figure 2E–I; Supplementary Figure S4F). Citrate levels were also increased following androgen stimulation (Figure 2G) while the levels of the tricarboxylic acid (TCA) cycle metabolite succinate remained unchanged (Figure 2H), further underscoring androgen stimulation of glycolysis and highlighting the truncated TCA cycle in prostate epithelial cells (Costello et al, 1997). We also found that AR signalling significantly stimulated anabolic synthesis, by measuring the flux from carbon-13-labelled glucose to amino acids (e.g., glutamine) and RNA (ribose) in response to androgen stimulation (Supplementary Figure S6; Figure 4F and G). Therefore by specifically upregulating these rate-limiting steps in glycolysis, the AR stimulates energy production and provides carbon needed for macromolecule synthesis. In addition, we found that the AR stimulated the expression of key anabolic enzymes, which utilize glucose metabolites (e.g., fatty acid synthase (FASN) and acetyl-CoA carboxylase α (ACACA)) and master regulators of biosynthesis (e.g., MTOR, encoded by FRAP1; Supplementary Figure S5). Therefore, AR signalling appears to coordinately regulate energy production and biosynthesis at multiple levels (Figure 2D), highlighting these metabolic pathways as potential targets to inhibit the growth of prostate cancer cells (Migita et al, 2009).

CAMKK2 is a metabolic master regulator downstream of the AR in prostate cancer cells

Identifying cancer-specific alterations that affect central metabolism is a major challenge for drug discovery in cancer biology. Therefore, we used clinical gene expression data (Rhodes et al, 2004) to assess cancer-specific expression of AR targets (Supplementary Table S7). Among the direct AR target genes, we identified calcium/calmodulin-dependent kinase kinase 2 (CAMKK2, Figure 3A) as consistently overexpressed in prostate cancer in nine independent clinical gene expression studies (Rhodes et al, 2004; Varambally et al, 2005), showing a similar pattern to the established prostate cancer marker AMACR (Jiang et al, 2001, 2002) (Figure 3B; Supplementary Figure S5). CAMKK2 was only highlighted by integrating AR genomic targets with clinical expression data, since we identified a core set of 1164 direct AR-regulated genes and on average CAMKK2 was ranked only 40th over the nine clinical studies (Figure 3B). CAMKK2 has previously been linked to central metabolism as an essential regulator of the metabolic sensor AMP kinase (AMPK) in the hypothalamus (Anderson et al, 2008), implicating CAMKK2 also as a regulator of cellular metabolism. The AR was recruited to the CAMKK2 promoter in both androgen-dependent and castrate-resistant prostate cancer cell lines (Supplementary Figure S7), suggesting that CAMKK2 is an AR target in both stages of the disease. CAMKK2 transcript and protein were upregulated early (<4 and <12 h, respectively) in response to androgen stimulation and downregulated in response to the AR antagonist bicalutamide, underscoring the direct regulation of CAMKK2 by the AR (Figure 3C and D; Supplementary Figure S7i). In clinical samples, we found CAMKK2 protein overexpression in two independent prostate cancer cohorts (Figure 3E; Supplementary Figure S7; Supplementary Table S10) and confirmed that CAMKK2 was a direct AR target in a panel of clinical prostate cancer samples using ChIP from human tissue (Figure 3F). These data highlight CAMKK2 as an AR-regulated gene in prostate cancer and in combination with the published role of CAMKK2 as a metabolic regulator (Anderson et al, 2008), prompted us to investigate the functional effects of AR-CAMKK2 signalling.

Since CAMKK2 has been shown to phosphorylate AMP activated kinase (AMPK) in the hypothalamus (Anderson et al, 2008) we tested the effects of CAMKK2 inhibition on AMPK phosphorylation in a panel of prostate cancer cell lines. Inhibition of CAMKK2 using siRNA or the specific inhibitor STO-609 (Tokumitsu et al, 2002) reduced p-AMPK without affecting total AMPK levels (Figure 4A; Supplementary Figure S8). This shows that CAMKK2 is required for AMPK phosphorylation in prostate cancer cells and confirmed that CAMKK2 was inhibited by the STO-609 compound. Androgen treatment induced AMPK phosphorylation and this was blocked by siRNA knock-down of either the AR or CAMKK2 (Figure 4B), highlighting an AR-CAMKK2-AMPK signalling pathway in prostate cancer cells. AMPK activity promotes glycolysis by phosphorylation of PFK2 and negatively regulates protein synthesis by phosphorylating the TSC1/TSC2 complex upstream of mTOR (Marsin et al, 2000; Gwinn et al, 2008). We assessed the relative impact of the AR-CAMKK2-AMPK pathway on mTOR by blotting for phospho-mTOR and for phospho-S6 kinase downstream of mTOR. These surrogates for mTOR activity were unaffected either by STO-609 or by CAMKK2 siRNA, indicating that protein synthesis is unperturbed by targeting the AR-CAMKK2-AMPK (Figure 4A; Supplementary Figure S8). By contrast glycolytic flux was significantly inhibited by these interventions (Figure 4C–E); cells treated with the CAMKK2 inhibitor STO-609 or CAMKK2 siRNA had reduced glucose uptake and produced less lactate and citrate (Figure 4C–F), suggesting a reduction in aerobic glycolysis. In addition, metabolic profiling revealed an intracellular accumulation of glucose following CAMKK2 inhibition (Figure 4C) and decreased anabolism from glucose to citrate, ribose and amino acids (Figure 4G; Supplementary Figure S6), together suggesting a metabolic block downstream of glucose uptake (Figure 5F). CAMKK2 inhibition also reduced PFK activity (Supplementary Figure S8), suggesting that AR-CAMKK2-AMPK signalling may stimulate glucose uptake and glycolysis through effects on PFK (Figure 5F). Importantly, CAMKK2 knock-down or inhibition was sufficient to block AR stimulated glucose uptake and lactate production (Figure 4E and F), highlighting CAMKK2 as an essential regulator of these metabolic effects downstream of the AR in prostate cancer cells.

Both RNAi knock-down and chemical inhibition of CAMKK2 reduced proliferation in prostate cancer cells (Figure 5A; Supplementary Figure S8), while CAMKK2 overexpression stimulated proliferation (Supplementary Figure S8). Interestingly, combining CAMKK2 inhibition with glucose depletion or the metabolic inhibitor metformin has a synergistic effect on proliferation and cell viability (Figure 5B and C). To assess the contribution of other signalling pathways downstream of CAMKK2 in prostate cancer we used phospho-protein profiler arrays from replicate CAMKK2 siRNA transfected and STO-609-treated cell lysates. These showed almost identical profiles (Pearson's correlation >0.9), highlighting the specificity of STO-609 in this context. Loss of AMPK phosphorylation was confirmed on the phospho-specific antibody array following either CAMKK2 siRNA or STO-609 treatment, interestingly both treatments resulted in loss of AMPK1a phosphorylation but no measurable change in AMPKa2 phosphorylation (Supplementary Figure S9). In addition, we observed no change in the phosphorylation of the CAMK1 and CAMK4 target CREB (Supplementary Figure S9), suggesting no gross alterations in CAMK1 or CAMK4 signalling downstream of CAMKK2 inhibition in AR-dependent prostate cancer cells. To further test the contribution of these downstream targets of CAMKK2, we used siRNA knock-down of CAMK1 and CAMK4, and the AMPK activator AICAR. Knock-down of CAMK1 and CAMK4 had marginal effects on cell proliferation, glucose consumption and lactate production (Supplementary Figure S9). These effects were significantly less than the effects of CAMKK2 inhibition in both androgen-dependent and castrate-resistant cell lines which express the AR (Supplementary Figure S9; Figure 6B). In contrast, the AMPK activator AICAR was sufficient to rescue the growth inhibitory effects of CAMKK2 RNAi knock-down or STO-609 treatment in AR expressing cell lines (Figure 5D; Supplementary Figure S8). Importantly, while CAMKK2 knock-down or chemical inhibition significantly inhibited androgen-stimulated proliferation, the AMPK activator AICAR was sufficient to rescue this effect and also to rescue the growth inhibitory effects of androgen depletion (Figure 5D and E; Supplementary Figure S8). Together, these functional studies implicate CAMKK2-AMPK signalling in prostate cancer growth and place this signalling axis downstream of the AR. Overall, our data suggest that CAMKK2 stimulates glycolysis by activating AMPK and without significant effects on biosynthesis (e.g., mTOR signalling) or other CAMKK2 substrates (Figure 5F).

CAMKK2 is functionally important in hormone-sensitive and castrate-resistant prostate cancer

In clinical samples, CAMKK2 levels were reduced following neoadjuvant hormone therapy, confirming in vivo the AR regulation of CAMKK2 (Figure 6A). Interestingly, we found that CAMKK2 levels were increased again in castrate-resistant disease (Figure 6A; Supplementary Table S10). This supports the in vitro findings that the AR binds to the CAMKK2 promoter in castrate-resistant prostate cancer cell lines (Supplementary Figure S7i) and that both glycolysis (Supplementary Figure S9) and cell proliferation (Figure 6B; Supplementary Figure S8) were sensitive to CAMKK2 inhibition or knock-down in these resistant cell lines. Collectively, these data implicate CAMKK2 in late stage drug-resistant prostate cancer where existing therapies are no longer effective. Therefore, to assess the functional importance of CAMKK2 in tumour formation we used the C4-2B xenograft model of castrate-resistant prostate cancer, a model which mirrors clinical late stage disease where AR signalling frequently remains functionally important (Snoek et al, 2009; Tran et al, 2009). Pharmacokinetic measurements showed that the CAMKK2 inhibitor STO-609 had a moderate half-life, low clearance and a low volume of distribution when administered IV or IP (Supplementary Figure S10). There was little difference in the plasma concentration of STO-609 following a single administration and after 19 sequential doses, indicating neither accumulation nor increased clearance with repeat dosing of STO-609 (Figure 6C). STO-609 was easily detected in tumour samples with a mean concentration of 2670 and 682 nM at 0.5 and 2 h, respectively (Figure 6C; Supplementary Figure S10). The tumour levels of STO-609 were approximately equal in tumour and plasma at 2 h (682 versus 663 nM, respectively), although earlier time points suggest that the tumour kinetics of STO-609 differ from plasma kinetics (Supplementary Figure S10). The growth of C4-2B prostate cancer xenografts was reduced in mice treated with the CAMKK2 inhibitor STO-609 (Figure 6D–F; Supplementary Figure S10) and we observed an additive effect with AR inhibition, in castrated mice treated with the CAMKK2 inhibitor STO-609 (Figure 6F). Interestingly, CAMKK2 inhibition had no measurable effect on normal mouse prostate size or the cytoplasmic volume of prostate epithelial cells (Supplementary Figure S10), whereas castration resulted in macroscopic loss of prostate size and atrophy of luminal epithelial cells (Supplementary Figure S10). This shows greater selective effects on cancer tissue through targeting CAMKK2 than through complete inhibition of the AR itself. Yet more significantly CAMKK2 is overexpressed in both hormone-sensitive and castrate-resistant prostate cancer, opening up the possibility of using CAMKK2 inhibitors alone or in combination with other therapies at all stages of the disease.

Chromatin immunoprecipitation

ChIP was performed as previously described (Massie et al, 2007; Schmidt et al, 2008; Wilson et al, 2008) (see Supplementary data for details). Cells were cultured in phenol red-free RPMI media supplemented with 10% charcoal dextran-stripped FBS for 72 h before adding 1 nM R1881 or 0.01% ethanol for 4 h. AR and RNAP II antibodies used for ChIP were AR N20 (SC-816X, Santa Cruz) and phospho-Ser-5 RNAP II (AB-5401, Abcam). ChIP enrichment was tested by real-time PCR and the remainder was used for single-end SOLEXA library preparation.

ChIP-seq SOLEXA library preparation

Single-end SOLEXA sequencing libraries were prepared as previously described (Schmidt et al, 2008) (see Supplementary data for details). Sequence reads were generated using an Illumina (Solexa) Genome Analyzer II and these reads were mapped back to the reference human genome before peak calling.

Sequence read analysis

Sequence reads were generated by the Illumina analysis pipeline versions 1.3.4 and 1.4.0. The two lanes of reads were combined for each sample, and aligned to the Human Reference Genome (assembly hg18, NCBI Build 36.1, March 2008) using MAQ (Li et al, 2008). Next, they were filtered by alignment quality score, removing all reads with a MAQ score <20, and exact duplicate reads were removed such that no single read start position was represented more than once. Enriched regions of the genome were identified by comparing the ChIPed samples with input samples using two independent peak calling algorithms: MACS (Zhang et al, 2008) and ChIPSeqMini (Johnson et al, 2007), taking only those regions found by both algorithms. Sites found in the androgen-stimulated condition, but not the vehicle-treated condition, were taken forward for further analysis. All ChIP-seq data have been deposited at the NCBI Short Read Archive (SRA012454.1) and identified binding sites (peaks) are available in Supplementary Tables S1, S2, S3. The ‘super-set’ of AR binding sites (Supplementary Table S3) was generated by combining the publicly available AR peak regions from previous reports (Horie-Inoue et al, 2004, 2006; Barski et al, 2007; Bolton et al, 2007; Jariwala et al, 2007; Massie et al, 2007; Takayama et al, 2007; Jia et al, 2008; Lin et al, 2009; Wang et al, 2009).

Analysis of ChIP peak regions

Overlap, subtraction, union and feature annotation of ChIP-seq enriched regions were performed using the Galaxy suite (Blankenberg et al, 2007; Taylor et al, 2007). Transcription factor motifs were identified using CEAS, de novo motif searches using MEME and Nested MICA (Bailey and Elkan, 1995; Down and Hubbard, 2005) and position weight matrix searches using RSAT matrix-scan (http://rsat.ulb.ac.be/rsat/). Motifs identified using de novo searches were aligned with known transcription factor PWMs using the motif alignment tool in the JASPAR database (http://jaspar.cgb.ki.se/). The optimal genomic distance between AR binding sites (peak boundaries) and androgen-regulated genes (gene boundaries) was defined using GSEA. Briefly, we generated gene sets by identifying all genes within 1, 2.5, 5, 25, 100, 200 and 500 kb of AR binding sites and control set were generated by identifying genes with no adjacent AR binding sites. These gene sets were tested for enrichment of the 3319 androgen-regulated genes identified in our detailed expression profiling data using GSEA (using the ‘time course’ correlation).

Illumina beadarrays

Forty-eight total RNA samples were harvested from LNCaP cells grown for 72 h in steroid depleted medium (RPMI supplemented with 10% charcoal dextran-stripped FBS). These comprised 3 time zero samples; 10 vehicle (ethanol) control samples taken at 2, 4, 8, 12 and 24 h in duplicate; 36 androgen (R1881)-treated samples taken every 30 min for 4 h then every hour until 24 h following treatment (with replicates at 1, 2, 4, 8, 12, 16, 20 and 24 h).

Autocorrelation analysis of Illumina gene expression data

The Illumina HumanWG v2 BeadArrays consist of two replicate sections that we treat as technical replicate arrays for the purposes of this analysis due to small but systematic shifts between sections that need to be addressed in the normalization. Data were analysed from the raw bead-level using the beadarray software, with spatial artefacts identified and removed automatically (BASH) and curated manually (Dunning et al, 2007; Cairns et al, 2008). The resultant, reduced, data set was then summarized in a standard manner (with outliers removed) in order to obtain a mean log-intensity and standard error for each probe/array combination. The November 2008 annotation from http://www.compbio.group.cam.ac.uk/Resources/Annotation/index.html was used to map probes to transcripts, and probes with no ‘good’ or ‘perfect’ match were discarded along with those that registered no signal above background on all 96 arrays. This resulted in 17 182 probes for which analysis proceeded.

To detect probes that showed a systematic, smooth, change over time without prescribing a form for that change we used the autocorrelation at lag 1 as a measure of activity. This measure identifies profiles where neighbouring time points are more similar than disparate time points, and so can identify all smooth and systematic gene expression changes regardless of the shapes of their profiles. To account for the uncertainty in our measurements, we simulated 100 sets of observations from the known mean values and standard errors, calculated the autocorrelation of each and took the mean. Simulations and arguments of symmetry suggested that a cutoff of autocorrelation 0.5 would lead to a low false-discovery rate and 4224 probes passed this threshold. Raw and normalized data from Illumina BeadArray experiments have been deposited at GEO (under accession GSE18684).

Functional annotation was done using the DAVID gene ontology tool, GSEA and interaction networks were generated using Cytoscape with the BiNGO and BioNetBuilder plug-ins.

Real-time PCR validation

We used SYBR-green quantitative real-time PCR to confirm AR binding sites and gene expression changes (see Supplementary data for details and primer sequences).

Immunohistochemistry

Tissue sections were stained with CAMKK2 antibody (Atlas Antibodies #HPA017389) at a 1:100 dilution (see Supplementary data for details).

Xenograft experiments

Xenograft tumours were generated with C4-2b cells that stably expressed a fusion protein of luciferase and YFP. There were four groups of mice (castration+vehicle, castration+STO-609, full+vehicle and full+STO-609), each consisting of four mice. In all, 10 μmol/kg of STO-609 (or the equivalent vehicle, 10% DMSO in PBS) was injected intraperitoneally three times per week and the growth of the tumours was monitored weekly through bioluminescence with an IVIS camera (Xenogen). See Supplementary data for details.

Pharmacokinetic/pharmacodynamic measurements

For plasma studies, mice (Supplementary Figure S10B) were injected IV or IP with 0.5 μmol/kg STO-609 and at time points (5, 15, 30, 45 min, 1, 1.5, 2, 4, 6 h) after treatment blood samples were collected into heparinized tubes. Blood was centrifuged to obtain the plasma fraction and frozen at −80°C before analysis. For tumour and parallel serum measurements (Figure 6C), mice were treated with 10 μmol/kg and samples of blood and tumour were collected at 0.5 and 2 h after treatment. Bioanalysis was carried out by protein precipitation of plasma followed by detection using an STO-609-specific LC-MS/MS method with an assay range of 1–1000 ng/ml. The plasma concentration:time profile was then constructed for PK analysis by WinNonLin. Tumour samples were homogenized 4 v/w in 50% CH₃CN (aq). An aliquot of this homogenate then processed using the same extraction procedure as plasma. The assay range for STO609 in tumour homogenate was 4–4000 ng/g.

Metabolomic profiling

LNCaP cells grown in RPMI media supplemented with 10% FBS were harvested on days 0, 1, 2 and 3 after DMSO or STO-609 treatment. LNCaP cells grown in RPMI media supplemented with 10% charcoal dextran-treated (steroid depleted) FBS were harvested on days 0, 1, 2 and 3 with and without androgen treatment (1 nM R1881). Cell culture media and cell lysates were collected from all the cell plates for NMR analysis. ¹H NMR spectroscopy data were acquired on a 600 MHz Bruker Avance NMR spectrometer. See Supplementary data for details. Metabolite concentrations were normalized to the protein content of cells.

Glucose flux experiments using 1,2-13C2-glucose and GC/MS

Cells were grown in media supplemented with charcoal dextran-treated FBS (steroid depleted conditions) and treated either with vehicle (0.01% ethanol), androgen (1 nM R1881), androgen+STO-609 (25 μM) or androgen+CAMKK2 siRNA for 72 h. Cells were harvested by scraping on ice and metabolites were obtained by methanol/chloroform extraction (Wu et al, 2008). The aqueous phase was dried using a Speedvac and derivatized by silylation (Perroud et al, 2006). RNA ribose extraction and derivatization was performed as previously described (Boren et al, 2003). The sample was injected into a GC-TOF MS (Leco Pegasus HT GC/TOFMS; Leco UK, Stockport, UK) and run according to methods described previously (Perroud et al, 2006). The obtained chromatograms were analysed using the ChromaTOF software package (Leco UK) to identify the different peaks. Mass spectral results were accepted only if the standard sample deviation was <1% of the normalized peak intensity.

PFK activity measurements

PFK activity was measured in prostate cancer cell line extracts using the method of Brand and Soling (1974), see Supplementary data for details.

Glucose and lactate measurements

Media were harvested from cells grown in RPMI supplemented with either 10% FBS or 10% charcoal dextran-treated FBS and treated for 3 days with or without androgen, bicalutamide (casodex) or ST0-609. Glucose and lactate levels were determined using commercial enzyme based kits (Abcam and BioVision Inc., USA).

Oxygen consumption

Oxygen consumption of cell suspensions was measured using a Clark-type oxygen electrode (DW1 Oxygen Electrode Chamber, Hansatech) over a 15 min time course at 37°C, according to the manufacturer's instructions (see Supplementary data for details).