Metastatic castration resistant prostate cancer (mCRPC) is incurable and progression after drugs that target the androgen receptor-signaling axis is inevitable. Thus, there is an urgent need to develop more effective treatments beyond hormonal manipulation. We sought to identify activated kinases in mCRPC as therapeutic targets for existing, approved agents, with the goal of identifying candidate drugs for rapid translation into proof of concept Phase II trials in mCRPC.
To identify evidence of activation of druggable kinases in these patients, we compared mRNA expression from metastatic biopsies of patients with mCRPC (n = 101) to mRNA expression in localized prostate from TCGA and used this analysis to infer differential kinase activity. In addition, we assessed the differential phosphorylation levels for key MAPK pathway kinases between mCRPC and localized prostate cancers.
Transcriptomic profiling of 101 patients with mCRPC as compared to patients with localized prostate cancer identified evidence of hyperactive ERK1, and whole genome sequencing revealed frequent amplifications of members of the MAPK pathway in 32% of this cohort. Next, we confirmed elevated levels of phosphorylated ERK1/2 in castration resistant prostate cancer as compared to untreated primary prostate cancer. We observed that the presence of detectable phosphorylated ERK1/2 in the primary tumor is associated with biochemical failure after radical prostatectomy independent of clinicopathologic features. ERK1 is the immediate downstream target of MEK1/2, which is druggable with trametinib, an approved therapeutic for melanoma. Trametinib elicited a profound biochemical and clinical response in a patient who had failed multiple prior treatments for mCRPC.
We conclude that pharmacologic targeting of the MEK/ERK pathway may be a viable treatment strategy for patients with refractory metastatic prostate cancer. An ongoing Phase II trial tests this hypothesis.
There is an unmet need for new treatments for metastatic castration resistant prostate cancer (mCRPC) that is resistant to abiraterone acetate or enzalutamide. With adequate pre-clinical and clinical rationale, targeted therapeutic strategies beyond hormonal manipulation of the androgen receptor (AR) axis might be applied in this disease state. Small molecule kinase inhibitors are effective against multiple cancers . In many cases, mutations in the kinase itself, or an upstream regulator, render these kinases constitutively active. However, identification of activating mutations in druggable kinases in mCRPCs is rare [2, 3]. Targeting of hyperactive wild-type kinases that nevertheless promote disease progression may still be a viable strategy [4,5,6]. Hyperactive kinase activity in prostate cancers can be inferred through downstream transcriptomic signatures and phosphoproteomics .
In the current study, our objective was to identify kinases activated in mCRPC that are targetable by existing, approved drugs, with the goal to identify candidate drugs for rapid translation into proof of concept Phase II trials in mCRPC. Virtual Inference of Protein-activity by Enriched Regulon (VIPER) analysis comparing mRNA expression signatures from 101 mCRPC tumors acquired as part of a multi-institutional trial [2, 7] to localized prostate adenocarcinoma (TCGA) identified ERK1 (MAPK) as a potential kinase target in mCRPC. ERK1 is druggable with trametinib, an inhibitor of MEK1/2, currently approved for melanoma. Prior reports demonstrate that ERK1/2 is phosphorylated in mCRPC at high frequencies despite a paucity of activating mutations in the principal proto-oncogenes in the pathway [8, 9]. Whole genome sequencing on this same cohort of metastatic tumors from patients with mCRPC was recently published, and consistent with prior sequencing reports of mCRPC metastases, there were infrequent activating mutations in genes within the MAPK pathway. However, we interrogated this sequencing data to detect amplification of selected MAPK pathway genes and found amplifications in 32% of this cohort. We also confirm ERK1/2 phosphorylation is characteristic of CRPC and report ERK1/2 phosphorylation in localized prostate cancers correlates with disease recurrence after surgery. In the clinic, we observed efficacy of trametinib monotherapy in a patient who failed multiple prior treatments for mCRPC. Our data suggest pharmacologic targeting of the MEK/ERK pathway may be a viable strategy for patients with refractory mCRPC. These results are rationale for an ongoing Phase II trial of MEK1/2 inhibitor trametinib in patients with mCRPC (NCT02881242).
Materials and methods
Metastatic biopsies of mCRPC, DNA, and RNA sequencing
The acquisition of mCRPC tumor biopsies, DNA whole genome, and RNA-sequencing were part of a multisite prospective IRB-approved trial (NCT02432001) described in detail elsewhere [2, 7]. Briefly, after obtaining signed informed consent, image guided biopsies were obtained from metastases (43% bone, 39% lymph node, 11% liver, 8% other site) from patients with mCRPC (27% after abiraterone, 17% after enzalutamide, 20% after both). Biopsies were embedded in OCT and snap frozen. Laser capture microdissection was used to enrich for tumor content. DNA and RNA was isolated and sequenced as previously described , with sequencing from 101 patients used in the present analysis. Amplification was defined as copy number ≥ 3 through methods as previously described [2, 7].
VIPER was used to identify evidence of activation of selected protein kinase pathways from RNA-seq data sets as previously described . Differential kinase activity was inferred between the two groups of samples (mCRPCs and primary prostate adenocarcinoma from TCGA) based on gene expression changes attributable to the kinases and downstream transcription factors. VIPER scores were computed and visualized using TumorMap .
Tissue microarrays (TMAs) were constructed from prostatectomy specimens from patients without prior local or hormonal therapy and included separate arrays consisting of primary tumor, benign tissue adjacent to primary tumor, and normal prostate tissue separate from tumor foci. A CRPC TMA was constructed from tissue acquired from palliative transurethral resections in patients with CRPC after prior treatment with ADT alone. TMAs were stained for phosphorylation of residues Thr202/Tyr204 with an anti-ERK antibody (Cell Signaling Technology (catalog #4376). To compare CRPC, primary prostate cancer, and benign tissue, H-scores were calculated based on intensity of cellular staining and percent positive cells  and comparisons made between groups by Kruskal–Wallis test. A separate TMA was constructed from radical prostatectomy specimens from patients with localized prostate cancer who underwent curative intent radical prostatectomy between 1994 and 1999 without prior therapy, with detailed long-term clinical follow-up. These specimens were scored as positive or negative for any phosphorylated ERK1/2 staining. Hazard ratios for biochemical failure were calculated and adjusted for clinicopathologic features known to affect risk of recurrence.
An existing, published phosphoproteomic database of mCRPC and localized treatment-naive prostate cancer tissue containing a mixture of tumor and benign gland was interrogated for known ERK1/2 kinase targets . Data were filtered for a false discovery rate cutoff of 0.05, at least a 4-fold difference between mCRPC and benign, and the presence of a known curated function on phosphosite.org.
We sought to identify kinases activated in mCRPC that could be targeted by existing, approved drugs, with the goal of identifying candidate drugs for rapid translation into proof of concept Phase II trials in mCRPC. We employed Virtual Inference of Protein-activity by Enriched Regulon (VIPER) analysis on 53 kinases to identify potential kinase targets by virtue of their inferred activation in mCRPC . VIPER scores were determined using mRNA expression signatures from 101 biopsies of CRPC metastases acquired as part of a multi-institutional trial [2, 7] to that of localized prostate cancer (TCGA) (Supplementary Table 1). This analysis identified 7 kinases with inferred activation significantly higher, and 4 lower, in mCRPC versus primary prostate cancers (Fig. 1a). Of the seven kinases with increased inferred activation, MAPK3 (ERK1) and SRC (c-SRC) are potentially actionable by approved drugs (e.g., trametinib and dasatanib, respectively). However, dasatanib, which inhibits SRC, was unsuccessful in a prior trial in mCRPC , so we focused on ERK1.
Given that point mutations in genes of MAPK pathway members have been rarely identified in patients with mCRPC [2, 3, 9], we hypothesized that amplifications of MAPK pathway genes [14, 15] or genes coding for proteins that have been shown to activate the MAPK pathway in mCRPC  would be more frequent in mCRPCs than in localized prostate cancers. The whole genome sequencing data  for the same patient cohort used to determine the VIPER scores was queried for any amplifications (focal or broad) of selected genes (Fig. 1b). Overall, more than 32% of the mCRPCs had amplifications  in one or more MAPK related genes, including amplifications of FGFR1 in 10% and BRAF in 6%.
We next sought to identify putative ERK kinase targets in mCRPC. ERK1 and ERK2 have similar substrate phosphorylation motifs . We previously reported the phosphoproteome of mCRPC using phosphopeptides isolated from benign and cancerous prostates and mCRPC tissues via label-free mass spectroscopy . We interrogated this existing dataset for known ERK1/2 substrates to identify potential phosphorylation targets of ERK1/2. Our phosphoproteomics study identified a total of 34 ERK1/2 kinase substrates and compared their phosphorylation rates in the metastatic tissues to those in the primary prostate tissues (Fig. 1c and Supplementary Table 2). Twenty proteins were found to be over-phosphorylated in metastatic tissues (Fig. 1c), of which, some were previously reported to be overexpressed in CRPC compared to hormone-sensitive tumors.
Prior reports demonstrated that ERK1 and 2 are phosphorylated in mCRPC at high frequencies [8, 9]. Phosphorylation of residues Thr202 and Tyr204 was evaluated as detected by immunohistochemistry on tissue comprised of normal prostate tissue controls, localized primary prostate cancer, benign tissue adjacent to the primary prostate cancer, and CRPC. Epithelial staining of phosphorylated ERK1/2 was significantly higher in CRPC compared to primary prostate tumors and benign tissue (Fig. 2a). Given the difference in ERK hyperactivation in CRPC compared to primary prostate cancer tissue, we postulated that ERK1/2 activation in primary tumors correlates with risk for biochemical failure after radical prostatectomy. TMAs consisting of 147 radical prostatectomy specimens from patients with localized prostate cancer and a median of 7.2 years follow-up were stained for phosphorylated ERK1/2 (Table 1). Specimens were scored as positive or negative by immunohistochemistry. Phosphorylated ERK1/2 in the prostatectomy specimens was associated with biochemical recurrence, both adjusted (HR 1.66, p = 0.047) for clinicopathologic features (PSA, age, Gleason grade, race, year, margins status, T stage) and unadjusted (HR 1.79, p = 0.013) (Fig. 2b).
A patient with mCRPC complicated by transfusion dependent anemia who had previously progressed on abiraterone, sipuleucel-T, enzalutamide, and radium-223, was initiated on trametinib therapy at 2 mg daily and had a serum PSA reduction of 85 and 93% at three and five months, respectively (Fig. 3a). His hemoglobin stabilized and he was no longer transfusion dependent after initiation of trametinib. The patient remained on trametinib without radiographic or clinical progression until the patient experienced a lethal stroke approximately 18 months after treatment initiation. A bone biopsy prior to treatment initiation in this patient did not yield tissue sufficient for targeted gene or RNA sequencing.
Sequencing of mCRPCs has not revealed frequent recurrent gain-of-function mutations in kinases, including the MAP kinases [2, 3]. However, our data suggest that ERK1/2 may be a potential kinase target in mCRPCs based on the clinical proteomic and transcriptomic data. Taken alone, the ERK activation signature inferred from the transcriptome of mCRPC by VIPER analysis could be explained by mechanisms independent of ERK itself. For example, Ets variant transcription factors can activate a MAPK transcriptional program in the absence of ERK activation in prostate cancer cell models . However, the clinical phosphoproteomic data demonstrates intense and frequent phosphorylation of ERK1/2 in mCRPC and is consistent with direct activation of this kinase.
To our knowledge, the overall frequency of 32% that we report for amplifications of MAPK pathway members within mCRPCs has not previously been reported. Importantly, this observed frequency of amplifications of these genes does not imply a proximal mechanism of activation for MAPK activation within mCRPCs. Notably, prior publications have reported increased expression of MAPK pathway members [8, 9, 19, 20] and high levels of phosphorylated ERK1/2 within mCRPCs . Compensatory activation of PI3 kinase and MAPK can occur in the context of suppressed androgen receptor signaling [8, 21]. Mechanistic studies in models of castration resistant, AR null prostate cancers demonstrate hyperactive MAPK signaling activated by paracrine and autocrine FGF/FGFR activation . AR null prostate cancer xenografts were also shown to be sensitive to inhibitors of MAPK or FGFR .
Our finding that CRPC tissue has phosphorylated ERK1/2 far exceeding that of most primary prostate tumors and benign prostate tissue is consistent with prior reports . The association of ERK1/2 phosphorylation in the primary tumor with biochemical recurrence has not been previously reported. However, an earlier study of sixty-three primary prostate tumors found a positive correlation between ERK1/2 phosphorylation and both T stage and Gleason Grade , and with rapid progression to CRPC .
A large number of kinase inhibitors have been tested in clinical trials for mCRPC, including dasatanib (multiple targets including SRC) , cabozantinib (MET and VEGFR2) , buparlisib (PI3 kinase) , MLN0128 (mTOR) , and sorafenib (multiple targets including RAF) , with largely disappointing results . Given these prior negative trials of single agent kinase inhibitors in combination with hormone suppression, any prospective trial of yet another kinase inhibitor for patients with mCRPC is approached with cautious optimism at best.
Prior studies in the PTEN deletion mouse model system found overexpression of members of the MAPK signaling pathway ARAF, BRAF, and CRAF (along with MERTK and NTRK2) promotes metastases . Positive staining for these kinases in 69%, 15%, and 26% in mCRPC suggests these kinases may also be viable targets . However, the multi-target kinase inhibitor sorafenib, which inhibits BRAF and CRAF, performed unimpressively in Phase II trials in mCRPC [28, 30]. Targeting the MAPK downstream, for example MEK1/2 or ERK, may be more successful than BRAF or CRAF due to activation of ERK signaling by RAF inhibitors in the context of wild-type BRAF , which is a characteristic of most mCRPCs [2, 3].
Our data support an ongoing single-arm proof of concept phase II study of single agent trametinib in men with mCRPC who have progressed on at least one prior line of therapy for mCRPC that includes abiraterone and/or enzalutamide (Fig. 3b). ERK1 activation status may represent a potential molecular selection marker for inclusion on this study; however, the fact that the most mCRPC specimens manifest increased ERK activation suggests that factors independent of ERK activation status may predict for response to trametinib. It is possible that signaling redundancies and activation of reciprocal pathways may frustrate or limit efficacy of MEK inhibition alone, potentially necessitating co-targeting of additional pathways activated in mCRPC, a strategy that has been explored in model systems (Mulholland et al.). Exomic and transcriptomic analyses of study biopsies performed at baseline and at the time of progression will facilitate our understanding of the biomarkers of response and resistance to trametinib, and inform future trials of MEK inhibitors for mCRPC.
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We thank the patients and their families for participating in this study. This work was supported by Stand Up To Cancer-Prostate Cancer Foundation Prostate Cancer Dream Team Award (SU2C-AACR-DT0812), Prostate Cancer Foundation Challenge grants (to MBR), and Prostate Cancer Foundation Young Investigator Awards (to NGN and SGZ).
Conflict of interest
NGN's research work has been funded by Janssen, Varian and Bayer. He owns stock options and has consulted for Gene Sciences Inc. MBR’s research has been funded by Novartis. He has been a speaker and consultant for Johnson and Johnson. GWT's work has been funded by the NIH. He has been on the scientific advisory board of Auron Therapeutics. EJS owns stocks in Fortis Therapeutics and Harpoon Therapeutics. He has received honoraria for speaking engagements at Janssen. He is a consultant and on Advisory Board (Compensated) of Janssen and Fortis. FYF receives research funding from Zenith Epigenetics and has received compensation as a member of the scientific advisory board or as a consultant for Bayer, Blue Earth Diagnostics, Celgene, Dendreon, EMD Serono, Ferring, Janssen Oncology, Medivation/Astellas, and Sanofi. He is a co-founder of PFS Genomics and has ownership interests. ONW currently has consulting, equity, and/or board relationships with Trethera Corporation, Kronos Biosciences, Sofie Biosciences, and Allogene Therapeutics. None of these companies contributed to or directed any of the research reported in this article. SGZ has received travel expenses, and has patents filed on unrelated work with GenomeDx Biosciences. The remaining authors declare that they have no conflict of interest.
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