Androgen deprivation induces neuroendocrine phenotypes in prostate cancer cells through CREB1/EZH2-mediated downregulation of REST

Although effective initially, prolonged androgen deprivation therapy (ADT) promotes neuroendocrine differentiation (NED) and prostate cancer (PCa) progression. It is incompletely understood how ADT transcriptionally induces NE genes in PCa cells. CREB1 and REST are known to positively and negatively regulate neuronal gene expression in the brain, respectively. No direct link between these two master neuronal regulators has been elucidated in the NED of PCa. We show that REST mRNA is downregulated in NEPC cell and mouse models, as well as in patient samples. Phenotypically, REST overexpression increases ADT sensitivity, represses NE genes, inhibits colony formation in culture, and xenograft tumor growth of PCa cells. As expected, ADT downregulates REST in PCa cells in culture and in mouse xenografts. Interestingly, CREB1 signaling represses REST expression. In studying the largely unclear mechanism underlying transcriptional repression of REST by ADT, we found that REST is a direct target of EZH2 epigenetic repression. Finally, genetic rescue experiments demonstrated that ADT induces NED through EZH2’s repression of REST, which is enhanced by ADT-activated CREB1 signaling. In summary, our study has revealed a key pathway underlying NE gene upregulation by ADT, as well as established novel relationships between CREB1 and REST, and between EZH2 and REST, which may also have implications in other cancer types and in neurobiology.


INTRODUCTION
Prostate cancer stands as the second most prevalent cancer and the second leading contributor to cancer-related mortality among men in the United States.The American Cancer Society estimates about 299,010 new cases and about 35,250 deaths from prostate cancer in the United States in 2024.Androgen deprivation therapies (ADT) focusing on the androgen receptor (AR) remain the cornerstone treatments for prostate cancer (PCa).Though ADT initially displays effectiveness, the majority of tumors inevitably experience recurrence and evolve into castration-resistant prostate cancer (CRPC).The process of lineage plasticity has gained prominence as a pivotal mechanism driving the progression of CRPC [1][2][3].
CREB1 and REST are two established master activator and repressor of neuronal genes in the brain, respectively [12][13][14].In epithelial cancer cells, REST has been reported to act as a tumor suppressor [15].REST represses NE gene expression in prostate cancer cells [16][17][18][19].We and others have demonstrated that activation of CREB1 signaling is critical for ADT-induction of NE markers [20][21][22][23].It is still unclear how CREB1 activation induces NE markers, and there has been no direct link established between CREB1 and REST in the context of ADT-induced NED.
REST and EZH2 are partners in transcriptional repression in mammalian cells [45][46][47].REST has been shown to physically interact with EZH2, which can lead to the recruitment of PRC2 complex to repress REST targets, such as neuronal genes [48][49][50].In addition to recruitment by REST, EZH2 has been shown to methylate REST, which stabilizes REST when bound to the RE1 sites of target genes [51].
Previously, we reported that CREB1 signaling acts through EZH2's PRC2 activity to induce NE markers [20].However, the critical link between ADT-CREB1-EZH2 pathway and NE induction is still missing.As an epigenetic repressor in this NED context, as we and others have shown [20,40], EZH2 is expected to repress some transcription regulators that in turn suppress NE marker expression.
To better understand the mechanisms of NED in prostate cancer cells, here we investigated the links between ADT, CREB1, EZH2, and REST.We found that CREB1 activation leads to the downregulation of REST, and ADT induces NED through the CREB1/ EZH2/REST pathways.Intriguingly, REST itself is an epigenetic target of EZH2 in NEPC cells.Our study has thus provided critical new information regarding how ADT, CREB1, and EZH2 induce NED, and also revealed a direct repression of REST by CREB1 signaling and by EZH2's epigenetic regulation.

REST is downregulated in NEPC
To determine the expression patterns of REST in adenocarcinoma and neuroendocrine prostate cancer (NEPC), we analyzed its expression patterns in a panel of androgen-dependent prostate cancer and NEPC cell lines, and patient samples.In line with the literature, REST mRNA and protein levels are lower, while NE markers are higher, in NE+ PCa cell lines NE1.3, LNCaP-AI, LASCPC-01, and 144-13 than in NE-cell lines C4-2 and LNCaP (Fig. 1A).Similar expression patterns were found in prostate cancer patient samples.Upon examining the Beltran_NM2016 RNA-seq dataset [39], we found that REST is significantly lower, while NE markers are significantly higher, in 15 NEPC samples compared to 34 CRPCadenocarcinoma samples (Fig. 1B, P = 1.05E-06).In another wellcited prostate cancer dataset (SU2C-PCF_PCa [52]), based on the NE scores provided in the dataset, we compared the cases in the NE score top 25% versus those in the NE score bottom 25%.As shown in Fig. 1C, REST mRNA expression is significantly lower in the top 25% of samples (P = 0.001).As expected, REST expression negatively correlates with NE markers in prostate cancer patient samples (Fig. 1D and Supplementary Fig. S1).Overall, these results confirm that REST expression is downregulated in NEPC.

REST inhibits NE marker expression, ADT resistance, and tumor progression
To investigate the role of REST in prostate cancer progression, we modulated REST expression via cDNA over-expression and shRNAs knock-down systems in prostate cancer cells, followed by examining NE marker expression and phenotypes of prostate cancer cells in vitro and in vivo.Silencing REST in C4-2 (NE-/AR+) adenocarcinoma cells leads to induction of NE markers (Fig. 2A).Conversely, overexpressing REST in PC3 cells (NE + /AR-) [53] downregulates NE markers (Fig. 2B).Phenotypically, REST overexpression dramatically reduced colony formation of PC3 cells (Fig. 2C).Moreover, REST silencing increased (Fig. 2D), while its overexpression decreased (Fig. 2E), the viability of LNCaP cells under treatment with ADT drug MDV3100 (Enzalutamide).To examine REST's role in regulating prostate tumor growth in mouse xenografts, PC3-EV (empty vector) and PC3-REST cells were implanted subcutaneously (s.c.) in NOD/SCID male mice for 24 days.Xenograft tumors from PC3-REST cells are significantly smaller than tumors from PC3-EV cells (Fig. 2F).Additionally, the expression of NE marker SYP was reduced in xenograft tumor tissues exhibiting REST overexpression (Fig. 2G).These results demonstrated that REST is a tumor suppressor gene in prostate cancer.

ADT downregulates REST both in vitro and in vivo
We and others have reported that ADT promotes NE phenotypes in prostate cancer cells [3,20,[54][55][56][57][58].However, the exact mechanism underlying the induction of neuroendocrine differentiation by ADT is still incompletely understood.We speculated that ADT induces NE markers, at least in part, through downregulating REST, which is a well-established master repressor of NE phenotypes.Indeed, treatment of ADT drug MDV3100 in androgen-dependent LNCaP cells downregulates REST (Fig. 3A).Interestingly, treating LNCaP cells with androgen Dihydrotestosterone (DHT) induces REST (Fig. 3A).Similarly, REST is reduced by MDV3100 in CRPC cells C4-2, and this reduction was rescued by adding DHT along with MDV3100 (Fig. 3B).Culturing prostate cancer cells in media with charcoal-stripped serum (CSS), which is hormone deprived, is another common method to introduce ADT in culture.REST expression is also downregulated when C4-2 cells were cultured in media with CSS (Fig. 3C).Correspondingly, C4-2 cells exhibited cell morphology changes that are reminiscent of NE phenotypes, such as extended neurite spikes and size-reduced cell bodies (Fig. 3D).To examine the impact of ADT on REST expression in vivo, we carried out REST RT-PCR on LNCaP xenograft tumors growing in uncastrated vs castrated male NOD/SCID mice [20].Castration, i.e., surgical removal of the major androgen-producing organ testis, is a common method of ADT in vivo.As shown in Fig. 3E, REST expression is downregulated by castration.Altogether, these results clearly show that ADT downregulates REST expression.

Activated CREB1 signaling represses REST
We next investigated how ADT downregulates REST transcription in prostate cancer cells.CREB1 signaling and REST are known to antagonize each other in controlling neuronal gene expression in neurobiology [12][13][14].Their relationship in prostate cancer cells is unknown.We previously showed that ADT activates CREB1 signaling, which is critical for NED of prostate cancer cells [20].We speculated that CREB1 signaling downregulates REST expression.To test this hypothesis, we first treated prostate cancer cells with known compounds that either enhance or inhibit CREB1 signaling, followed by examining REST and NE marker expression.Isoproterenol (ISO), an analog of adrenaline, acts as an agonist for beta-adrenergic receptor, enhancing PKA/ CREB1 signaling [59,60].Additionally, the combination of Forskolin and IBMX (Fsk+IBMX) also activates PKA/CREB1 pathway [61].Conversely, beta-adrenergic receptor antagonist ICI-118,551 (ICI) and synthetic peptide inhibitor of PKA (PKI) are two known inhibitors of PKA/CREB1 signaling.We found that REST levels are reduced, while p-S133-CREB1 (an indicator of CREB1 activation) and NE markers are increased, when prostate cancer cells are treated with ISO or Fsk+IBMX (Fig. 4A, Supplementary Fig. S2A, B).On the contrary, REST is induced, while p-S133-CREB and NE markers are reduced by ICI or PKI (Fig. 4B).When CREB1 signaling is enhanced by overexpressing a constitutively activated form of CREB1 cDNA (i.e., CREB1-Y134F [62]), REST is downregulated while NE markers ENO2 and CHGA are induced in PC3 cells (Fig. 4C and Supplementary Fig. S2C).
To evaluate this CREB1-repression of REST in vivo, we measured protein levels of REST and ENO2 in LNCaP cell-derived xenografts from NOD/SCID male mice treated with saline or 10 mg/kg ISO twice a day for 21 days [63].As shown in Fig. 4D, REST is downregulated and NE marker ENO2 is induced in LNCaP tumors from the mice treated with ISO.Moreover, we found that REST cDNA overexpression in PC3 cells reversed NE marker induction by the activation of CREB1 signaling by Fsk+IBMX (Fig. 4E), which suggests that REST downregulation is essential for CREB1's induction of NE markers in prostate cancer cells.Concordantly, the NE-like cell morphology induced by CREB1 activation was abrogated by REST overexpression in PC3 and LNCaP cells (Fig. 4F and Supplementary Fig. S2D respectively).All these results together indicate that CREB1 signaling induces NE markers through repressing REST expression in prostate cancer cells.

REST is a novel epigenetic target of EZH2 and it reverses EZH2-induction of NE markers
In the literature, there have been several elegant studies documenting the repression of REST function in prostate cancer through the mechanisms of alternative splicing and protein degradation [64][65][66][67].The transcriptional regulation responsible for REST downregulation in NEPC is still obscure, despite the observation that REST mRNA level is pronouncedly reduced in NEPC (Fig. 1).Therefore, we considered that REST can be downregulated by transcriptional repressors, specifically epigenetic modulators.In a recent study surveying 147 epigenetic regulators in multiple patient datasets, Clermont et al. found that several PRC2 complex proteins, such as EZH2 and CBX2, are among the most upregulated epigenetic regulators in NEPC [41].We and others have recently implicated the role of EZH2 in regulating NE phenotype in prostate cancer cells [20,39,40,68].However, the mechanism underlying EZH2's induction of NE markers is still unclear.We hypothesized that REST downregulation in NEPC is at least partially influenced by the increased activity of the PRC2 complex, and REST is a target of EZH2.Indeed, treating several prostate cancer cell lines with GSK126, an inhibitor of EZH2, resulted in REST induction and reduced NE marker ENO2 expression (Fig. 5A and Supplementary Fig. S3A).Similarly, REST was induced and ENO2 was downregulated upon silencing EZH2 with shRNA (Fig. 5B).In line with these results, overexpressing EZH2 cDNA in PC3 cells downregulated REST expression (Fig. 5C), and this downregulation was rescued by additional expression of Fig. 1 REST is downregulated in NEPC.A qPCR and Western blotting for expression patterns of the indicated genes and proteins in panels of human prostate cancer cell lines.LNCaP and C4-2 cells represent NE-/low cell models, while other cells represent NE + /high cell models.Y-axis shows relative fold changes in mRNA expression, normalized to GAPDH.Error bars in PCR results represent standard deviation (s.d).Beta actin was examined as the loading control in Western blotting.B REST mRNA is significantly lower in NEPC (CRPC-NE) than in adenocarcinoma CRPC (CRPC-adeno) (Beltran_NM2016) [39].C REST mRNA in the top 25% NE-high samples versus the bottom 25% NE-low samples of CRPC in the SU2C-PCF dataset [52].D Expression of NE marker SYP negatively correlates with that of REST in the SU2C-PCF dataset.REST correlations for additional NE markers (ENO2, CHGA, CHGB, and TUBB3) are presented in Supplementary Fig. S1.shEZH2.NE maker SYP was induced by EZH2 cDNA, which was reversed by additional expression of shEZH2, as expected (Fig. 5C).
To determine whether REST is a direct target of EZH2, we first examined ENCODE ChIP-seq datasets.We found that EZH2 binds to the REST promoter in multiple cell lines and under several conditions (Supplementary Fig. S3B), which suggests that REST is an epigenetic target of EZH2.To confirm this in NEPC cells, we performed chromatin immunoprecipitation (ChIP) using antibodies against H3K27me3, a histone repressive mark primarily catalyzed by EZH2.We carried out H3K27me3 ChIP and qPCR of the DNA sequence on REST promotor in NEPC 144-13 cells treated with DMSO control or EZH2 inhibitor GSK126.As shown in Fig. 5D, there is a clear H3K27me3 mark on the REST promoter in DMSOtreated cells, which is reduced by GSK126.To confirm a direct role of EZH2 protein in binding to REST promoter, we also carried out ChIP using EZH2 antibody.EZH2 binding to REST promoter is reduced by GSK126 in NEPC cells (Fig. 5E).Consistently with REST being a novel EZH2-repressed target in NEPC, they have a significantly negative correlation of expression in two well-cited advanced prostate cancer datasets (Beltran_NatMed [39] in Fig. 5F and SU2C-PCF [52] in Supplementary Fig. S3C).Finally, we set out to determine whether REST downregulation is essential for EZH2's induction of NE markers, by performing an epistasis experiment (genetic rescue).Of note, overexpression of REST reversed the induction of NE marker ENO2 by EZH2 overexpression in LNCaP cells (Fig. 5G).These results establish that REST is a novel epigenetic target of EZH2, whose repression is critical for EZH2's induction of NE markers.

ADT induces NE by downregulating REST through CREB1activated EZH2 epigenetic repression
We previously reported that CREB1 signaling leads to the activation of EZH2 which subsequently induces NE markers [20].
Here we confirmed this conclusion, by showing that expressing activated CREB1 cDNA (Y134F), or treatment of CREB1 signaling activator Forskolin or ISO, increases H3K27me3 epigenetic mark in LNCaP and PC3 prostate cancer cells (Fig. 6A, B).Conversely, CREB1 signaling inhibitor PKI or ICI reduces H3K27me3 level in 144-13 and NE1.3 NEPC cells (Fig. 6C).ISO treatment also induces a bulk level of H3K27me3 histone mark in LNCaP mouse xenograft tumors (Fig. 6D).
Given that we have illustrated that REST is a direct target of EZH2 in NEPC cells, next, we set out to determine the genetic relations of the three proteins on this CREB1-EZH2-REST pathway in the context of ADT-induction of NE markers in prostate cancer cells.First, repression of REST by CREB1 activators Forskolin+IBMX is reversed by EZH2 inhibitor GSK126 (Fig. 7A, left) or shEZH2 (Fig. 7B), suggesting that EZH2 is key to the CREB1-mediated repression of REST.
A similar result was observed when CREB1 signaling was activated by expressing constitutively active CREB1 cDNA (Y134F) (Fig. 7A, right).Second, as shown by ChIP-PCR in Fig. 7C, the H3K27me3 histone mark on REST promoter is evidently lower in NE1.3 cells treated with propranolol (PROP), another betaadrenergic antagonist and an inhibitor of CREB1 signaling [20,58,63].Concordantly, the H3K27me3 histone mark on the REST promoter is induced by CREB1 signaling activator ISO, which is reversed by additional treatment with PROP (Fig. 7D).Similar observations could be made when directly examining EZH2's binding to REST promoter in these conditions, by performing the ChIP with EZH2 antibody (Fig. 7E, F).Third, when EZH2 activity is inhibited by its inhibitors DZNeP and EPZ-6438 in C4-2 and LNCaP cells respectively, ADT (induced by growing cells in CSS media and treated with MDV300) no longer represses REST expression (Fig. 7G, H).Of note, EZH2 protein's binding to REST promoter is induced by ADT in AR + C4-2 and 22Rv1 cells (Fig. 7I and Supplementary Fig. S3D).Taken together, these results indicate that ADT induces NE by downregulating REST through CREB1activated EZH2 epigenetic repression.
In summary, in this study, we have delineated a new critical pathway of CREB1-EZH2-REST, which underlies NE induction by ADT.We showed that REST is downregulated in NEPC cells and patient samples.As expected, REST represses NE markers and prostate cancer progression.Furthermore, ADT downregulates REST both in vitro and in vivo.Notably, ADT-activated CREB1 signaling enhances EZH2's epigenetic repression of REST, which in turn induces NE markers in prostate cancer cells.

DISCUSSION
It has been shown by numerous studies that ADT induces NE markers in prostate cancer cells.However, the mechanisms underlying NE induction by ADT are incompletely understood.
Here we first showed that ADT induces NE markers by downregulating REST, the master NE repressor.The majority of studies on the regulations of REST expression in cancer have been on its protein degradation or alternative splicing [64][65][66][67].We found that REST mRNA level is pronouncedly reduced in NEPC (Fig. 1).The transcriptional regulation responsible for REST downregulation in NEPC is less clear.We further reported that REST is transcriptionally downregulated by EZH2, which is upregulated in NEPC and activated by CREB1 signaling.REST and CREB1 have been reported to functionally antagonize each other in regulating neurogenesis [12][13][14].For example, Laneve et al. showed that CREB1 induces, while REST reduces, neuronal miRNA miR-9-2 in neuroblastoma cells [12].However, as far as we know, a direct repression between these two master regulators has not been reported.Our study provides evidence that CREB1 signaling represses REST mRNA and protein expression during neuroendocrine differentiation of prostate cancer cells (Fig. 4).It is worth examining whether this CREB1 repression of REST transcription also occurs in neurobiology.
As to how CREB1 downregulates REST expression, we demonstrated that CREB1 signaling enhances EZH2 activity, which in turn epigenetically represses REST.Interestingly, Laneve et al further showed a negative feedback regulation between miR-9-2 and REST [12].It warrants further investigation to determine whether miR-9-2 induction also contributes to REST repression by CREB1 signaling, besides EZH2's epigenetic regulation that we demonstrated in this study.
Our study also reveals a surprising relationship between REST and EZH2.EZH2 and REST have been viewed as partners in transcriptional repression in several contexts.It has been reported that REST physically interacts with PRC2 complex proteins EZH2 and SUZ12 [48][49][50].Furthermore, ENCODE ChIP datasets showed a significant overlap of target genes between REST and EZH2 or SUZ12.In addition to recruitment by REST, the enzymatic PRC2 core component EZH2 can methylate REST, which leads to the stabilization of REST when bound to the RE1 sites of REST target genes [51].Therefore, it is counterintuitive that EZH2 represses REST expression, as we have shown in Fig. 5. EZH2 and REST clearly have opposite functions and expression patterns in NEPC compared to prostate adenocarcinoma [20,39,40,68] (Figs. 1, 2 and 5).Therefore, our study introduces a conceptual innovation and context- dependence in the relationship between EZH2 and REST.It remains an interesting question for future investigation regarding how the EZH2-REST relationship evolves during prostate cancer progression, from REST being an EZH2 partner in prostate adenocarcinoma cells to REST becoming an EZH2 target in NEPC cells.
To summarize, we have demonstrated that REST is a novel epigenetically repressed target of EZH2 in NEPC and this EZH2-REST axis is essential for ADT-induced NED.Our results provide critical new insights into the mechanisms underlying NED that is induced by ADT and EZH2 activity.In addition, our findings have revealed a direct antagonistic relationship between two master regulators of neuronal genes in neurobiology, CREB1 and REST.These results not only expand our understanding of prostate cancer progression, they will also forge links among multiple disciplines, including cancer progression, drug resistance, cellular differentiation, epigenetic regulation, and neurobiology.

Cell culture
LNCaP cells and 293 T cells were originally purchased from ATCC.The PC3 prostate cancer cells used in this study represent a poorly metastatic PC3 variant that was kindly provided by Dr. Isaiah Fidler [69] and was matched to PC3 cells from ATCC by DNA STR fingerprinting (Biosynthesis Inc).LNCaP and PC3 cells were maintained in RPMI 1640 media (Mediatech), supplemented with 10% FBS (Gibco) and 1% penicillin-streptomycin. 293 T cells were cultured in DMEM media (Mediatech), supplemented with 10% FBS and 1% penicillin-streptomycin. NEPC NE1.3 cells were derived in Dr. Ming-Fong Lin's lab from LNCaP cells after long term culturing in charcoal striped serum (CSS) medium [70] and they are cultured in phenol red-free RPMI 1640 medium supplemented with 5% CSS (Gibco) and 1% penicillin and streptomycin.We generated LNCaP-AI (androgen independent) cells in house by culturing LNCaP cells in RPMI 1640 media with CSS for >12 months and are maintained in the same CSS media.LN3 is a LNCaP derivative isolated from in vivo selection of LNCaP cells metastasizing to Fig. 5 REST is a novel epigenetic target of EZH2, and it reverses EZH2-induction of NE markers.A C4-2 and 144-13 cells were treated with DMSO or 10 µM GSK126 for 48 h.Whole cell lysate was analyzed by Western blotting.B Western blotting of indicated proteins in C4-2 and NE1.3 cells expressing scramble shRNA or shEZH2.C RT-qPCR showing that EZH2-mediated REST downregulation and SYP upregulation was reversed by shEZH2 in PC3 cells (genetic rescue).NEPC cells were treated with DMSO or 10 µM GSK126 for 48 h, followed by ChIP with control IgG, or anti-H3K27me3 antibody (D, in 144-13 cells) or anti-EZH2 antibody (E, in LASCPC-01 cells), and qPCR of REST's promoter region near its transcriptional starting site.Y-axis represents % of ChIPed DNA relative to input.F Scatter plots showing negative correlation of the expression of EZH2 and REST in the Beltran_NM2016 CRPC genomic dataset.The plot, Pearson correlation coefficient R and P value were directly downloaded from the cBioPortal genomics interface.G A genetic rescue experiment and subsequent RT-qPCR in LNCaP cells indicate that the induction of NE marker ENO2 by EZH2 was reversed by additional overexpression of REST.

cDNA/shRNA transduction and transfection
All shRNA constructs are in pLKO.1 vector [72] and were purchased from Sigma-Aldrich (St. Louis, MO).For stable knockdown, cells were transduced with lentiviral particles of Scramble control shRNA: CCTAAGGT-TAAGTCGCCCTCG; EZH2 shRNA: CGGAAATCTTAAACCAAGAAT [42,73]; shREST: GCCTCTAATCAACATGAAGTA.These shRNAs were packaged into viral particles using 293 T cells according to previously described method [72].Briefly, 293 T cells were seeded in 6-well plates at 1.5-million cells/well.Lentiviral vector carrying shRNA was transfected, together with packaging plasmids VSVG and Delta 8.9, into 293 T cells by TransIT-LT1, followed by centrifugation at 1100 × g for 30 min.After initial medium change around 16 h post-transfection, the virus supernatant was collected 48 and 72 h after transfection, aliquoted and stored at −80 °C for subsequent experiments.Cells were infected with the lentivirus supernatant in the presence of 8 μg/ml polybrene and subsequently selected with 1 μg/ml of puromycin.For overexpression of EZH2, cells were infected with retrovirus for human EZH2 cDNA or pBABE-puro vector control [74], and subsequently selected with 1 μg/ml of puromycin.For expressing constitutively active CREB1 mutant, PC3 cells were transfected with pcDNA3-Flag-empty vector (EV), or pcDNA3-CREB-Y134F (YF, constitutively active [62]), kindly provided by Dr. Rebecca Berdeaux, using TransIT-LT1 transfection reagent (Mirus) and selection with 400 μg/ml of G418 for 2 weeks.REST overexpression was achieved by LT1-mediated transfection of pcDNA3-EV, or pcDNA3-REST vector (a generous gift from Dr. Hsing-Jien Kung [18]) and selection with 400 μg/ml of G418 for 2 weeks.

Western blotting analysis
Cells were washed in ice-cold PBS and lysed in lysis buffer (30 mM Tris, 200 mM NaCl, 1.5 mM MgCl 2 , 0.4 mM EDTA, 20% Glycerol, 1% NP-40, 1 mM DTT) with Complete mini protease inhibitor cocktail and PhosSTOP phosphatase inhibitor cocktail (Roche Applied Science).Protein concentrations were determined using Pierce BCA protein assay kit (Thermo Scientific).The samples were then separated by SDS-PAGE and transferred to PVDF membrane (Bio-Rad).The membrane was blocked with 5% skimmed milk in TBST for 1 h at room temperature, followed by incubation of a primary antibody overnight at 4 °C.The dilutions and catalog numbers of primary antibodies used are listed in Supplementary Table 1.After washes, the membrane was incubated with HRP-conjugated secondary antibodies for 1 h at room temperature.The blots were then detected by Pierce ECL Western Blotting Substrate (Thermo Scientific) on Blue Basic Autoradiography Films (Thomas Scientific).

Chromatin Immunoprecipitation (ChIP)
DNA binding proteins in cells were cross-linked to DNA by 1% formaldehyde for 10 min at room temperature, which was quenched with glycine.Cells were then lysed in SDS Lysis Buffer (1% SDS, 10 mM EDTA, 50 mM Tris-HCl, pH 8.1 and freshly added protease/phosphatase inhibitors) and sonicated to shear DNA to 300-500 bp fragments using Branson Low Power Ultrasonic Systems 2000 LPt/LPe sonicator (Fisher Scientific).50 µl of supernatant was diluted in 450 µl dilution buffer (1% Triton X-100, 2 mM EDTA, 20 mM Tris-HCl pH 8.1, 150 mM NaCl supplemented with 0.1% NP40, protease and phosphatase inhibitors).Samples were pre-cleared with protein A/G agrose beads for 2 h.20 μl of the post-cleared supernatant was kept as input.The remaining supernatants were incubated overnight with 2 µg anti-H3K27me3 (Cell Signaling), EZH2 (Active Motif) or anti-IgG antibody, followed by 1 h incubation with protein A/G agarose beads at 4 °C.The immunoprecipitates were subjected to multiple washes for 5 min each at 4 °C in low salt buffer with 150 mM NaCl, high salt buffer with 500 mM NaCl, LiCl buffer with 250 mM LiCl and finally the TE buffer.DNA was recovered after reversion of the protein-DNA cross-links with 0.2 M NaCl and proteinase K. Subsequently, DNA was extracted with phenol-chloroform and precipitated with ethanol.5 µl of DNA was subjected to real time PCR.Primers used to measure the enrichment of REST promoter DNA sequence containing H3K27me3 marks are: F (5′-GTGGAAGGGTCTGAAATGGC-3′), and R (5′-GAACTCCCGACTTCTGGTGA-3′).

Fig. 2
Fig. 2 REST inhibits NE marker expression, ADT resistance and tumor progression.Western blotting and qPCR for REST and NE markers in NE-/low C4-2 cells upon REST silencing (A) and in NE + PC3 cells upon overexpressing REST cDNA (B).Y-axis shows relative fold changes in mRNA expression, normalized to beta actin.Error bars in PCR results represent standard deviation (s.d).Western blotting was carried on whole cell lysates from the indicated cell lines and for the indicated proteins.C Colony formation assay of PC3 cells carrying empty vector (EV) or REST cDNA.The two cell lines were seeded in triplicates in a 6-well plate, at 1000 cells/well and cultured for 14 days, followed by staining with crystal violet.D Viability and proliferation of LNCaP cells expressing either scramble shRNA or shREST, upon treatments of 40 µM or 80 µM of ADT drug MDV3100 for 3 days.E Cell viability and proliferation of LNCaP cells carrying either empty vector or REST cDNA, upon treating with a series doses of ADT drug MDV3100 for 3 days.Y-axis shows relative cell viability and proliferation, normalized to DMSO control.The experiment was carried out in quadruplicates each time, twice with similar results.Insert: Western blotting shows REST overexpression in PC3-REST cells.F Subcutaneous xenograft tumor growth of PC3 cells carrying either EV or REST cDNA in NOD/SCID male mice.Left: tumor weights at euthanization (P = 0.038) 8 weeks after implantation.Right: images of the xenograft tumors at euthanization (5 mice for each cell line, n = 10 tumors).G Western blotting for REST and NE marker SYP protein levels in xenograft tumors from PC3-EV and PC3-REST cells.

Fig. 3
Fig. 3 ADT downregulates REST in vitro and in vivo.A, B Western blotting of REST in LNCaP and C4-2 cells treated with ADT drug MDV3100 (10 µM, 72 h), androgen DHT (25 nM, 24 h) or both.C Western blotting of whole cell lysates from C4-2 cells growing in media with regular FBS or CSS (charcoal stripped serum) for 7 days.Culturing in CSS media that is deprived of hormones is another common ADT approach in vitro.D Morphology of C4-2 cells growing in media with regular FBS or CSS.E RT-PCR and DNA gel electrophoresis of REST and loading control RPS18 in LNCaP xenograft tumors growing in uncastrated or castrated NOD/SCID male mice.

Fig. 4
Fig. 4 Activated CREB signaling represses REST.Western blotting for REST, p-CREB1 (pS133, indicator of activation) and NE markers in prostate cancer cells upon treatments of CREB1 signaling activator 15 µM isoproterenol (ISO) or 10 µM Forskolin+ 0.5 mM IBMX for 24 h (A), or CREB1 signaling inhibitor ICI-118,551 (ICI, 10 µM) or synthetic peptide inhibitor of PKA (PKI, 10 µM) for 24 h (B).UT: untreated control, because ISO, ICI and PKI were dissolved in water.C Western blotting for REST, pS133-CREB1 and NE markers in PC3 cells carrying either an empty vector or CREB1-Y134F cDNA, a constitutively activated form of CREB1.D Western blotting for REST, pS133-CREB1, NE markers, EZH2 catalytic product H3K27me3 histone mark, loading controls histone 3 (H3) and beta actin in LNCaP cell-derived xenografts from NOD/SCID male mice, treated with saline or 10 mg/kg ISO for 54 days.E, F PC3-EV or PC3-REST cells were treated with DMSO control or CREB1 signaling activator combo 10 µM Forskolin (Fsk) + 0.5 mM IBMX for 24 h.mRNA levels of indicted genes were normalized to GAPDH control.F Morphology of PC3-EV and PC3-REST cells treated with DMSO or Fsk+IBMX.

Fig. 7
Fig.7ADT induces NE by downregulating REST through CREB1-activated EZH2 epigenetic repression.A Western blotting on PC3 cells shows that REST is downregulated by CREB1 signaling activator forskolin (10 µM, left) or by overexpressing activated CREB1 cDNA (right), which is reversed by EZH2 inhibitor GSK126 (10 µM).B Western blotting shows that, when EZH2 is silenced by shEZH2, forskolin could no longer repress REST and induce NE marker ENO2 and H3K27me3 in PC3 cells.ChIP-qPCR measuring H3K27me3 histone mark levels on REST promoter, after treating with indicated CREB1 signaling modulators: propranolol (PROP, 15 µM) for 24 h in NE1.3 (C) and PC3 (D).ChIP-qPCR measuring EZH2 protein binding on REST promoter upon treating with these CREB1 signaling modulators in PC3 (E) and NE1.3 (F).G C4-2 cells were grown in FBS or CSS media for 7 days, then treated with DMSO or 10 µM MDV3100 for 3 days, followed by treatments of DMSO or 5 µM EZH2 inhibitor DZNeP for 2 days, and then Western blotting of REST and loading control GAPDH.H LNCaP cells were grown in FBS or CSS media for 5 days, then treated with DMSO or 10 µM EZH2 inhibitor EZP-6438 for 2 days.Whole cell lysates were collected and analyzed by western blotting for REST and loading control GAPDH.I C4-2 and 22Rv1 cells were grown in FBS or CSS media for 7 days and then EZH2 protein binding on the REST promoter region were measured by EZH2 ChIP-qPCR.The quantifications and graphs for these ChIP-PCRs are in Supplementary Fig.S3D.