Discordant results in preclinical and clinical trials have raised questions over the effectiveness of antioxidants in prostate cancer chemoprevention. Results from the large-scale Selenium and Vitamin E Cancer Prevention Trial (SELECT) showed that antioxidants failed to prevent, and in some cases promoted, prostate cancer formation in men without a history of the disease. One possible explanation for these alarming results is the notion that the effects of antioxidant treatment on the prostate are modified by specific, intrinsic genetic risk factors, causing some men to respond negatively to antioxidant treatment. Loss of expression of the homeobox transcription factor NKX3.1 in the prostate is frequently associated with human prostate cancer. Nkx3.1 mutant mice display prostatic hyperplasia and dysplasia and are used as a model of the early stages of prostate cancer initiation. While the mechanisms by which Nkx3.1 loss promotes prostate tumorigenicity are not completely understood, published data have suggested that elevated reactive oxygen species (ROS) associated with Nkx3.1 loss may be a causative factor. Here we have tested this hypothesis by treating Nkx3.1 mutant mice with the antioxidant N-acetylcysteine (NAC) for 13 weeks post-weaning. Surprisingly, while NAC treatment decreased ROS levels in Nkx3.1 mutant mouse prostates, it failed to reduce prostatic epithelial hyperplasia/dysplasia. Rather, NAC treatment increased epithelial cell proliferation and promoted the expression of a pro-proliferative gene signature. These results show that ROS do not promote proliferation in the Nkx3.1-null prostate, but instead inhibit proliferation, suggesting that antioxidant treatment may encourage prostate epithelial cell proliferation early in prostate tumorigenesis. Our findings provide new insight that may help explain the increased prostate cancer risk observed with vitamin E treatment in the SELECT trial and emphasize the need for preclinical studies using accurate models of cancer.
Citation: Martinez EE, Anderson PD, Logan M, Abdulkadir SA (2012) Antioxidant Treatment Promotes Prostate Epithelial Proliferation in Nkx3.1 Mutant Mice. PLoS ONE 7(10): e46792. https://doi.org/10.1371/journal.pone.0046792
Editor: Bharat B. Aggarwal, The University of Texas M. D. Anderson Cancer Center, United States of America
Received: May 31, 2012; Accepted: September 6, 2012; Published: October 15, 2012
Copyright: © Martinez et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by grant R01 CA094858 from the National Cancer Institute (NCI) to SAA and Vanderbilt Ingram Cancer Center Support Grant P30 CA068485. PDA was supported by Department of Defense Postdoctoral Fellowship Award W81XWH-11-1-0230. ML was supported by 2T32H007735-17 from the National Heart, Lung, and Blood Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Due to the high prevalence and significant treatment-related morbidity associated with human prostate cancer, there is a strong interest in preventive approaches. In order to accomplish this, a more thorough understanding of the relationship between oxidative stress and the steps of prostate tumor progression is needed. In recent years, extensive research has been devoted to the relationship between oxidative stress and the etiology of prostate cancer , , , . In addition, the prostate gland has been associated with chronic inflammation , a condition linked to elevated oxidative stress. Many studies have proposed a positive correlation between elevated oxidative stress and prostate cancer progression and have argued the value of antioxidants in preventing prostate cancer (reviewed in ). However, it is notable that the majority, if not all, of these studies have employed models of late stage, aggressive disease, focusing on later steps in carcinogenesis rather than prevention of prostate cancer initiation , , , , , , , .
The Selenium and Vitamin E Cancer Prevention Trial (SELECT) was initiated in 2001 to conduct a large, randomized controlled clinical trial on the efficacy of the antioxidants selenium and vitamin E in the prevention of prostate cancer . Results from two previously published clinical trials ,  suggested that these two antioxidants could prevent prostate cancer development. However, initial results published in 2009  showed that neither selenium, vitamin E, nor their combination significantly prevented prostate cancer in the study population. Follow-up results published in late 2011  showed that vitamin E treatment increased rather than decreased the risk of development of prostate cancer. This concerning finding highlights the importance of understanding the role of ROS in prostate tumorigenesis. In fact, one of the lead authors of the SELECT trial has suggested that any success in future chemoprevention may reside in the identification of specific risk factors in individuals that will help determine the effect any agent may have on their tumor development .
NKX3.1 is a homeodomain transcription factor whose loss of expression correlates with human prostate cancer progression , , . NKX3.1 expression is lost early in tumorigenesis, suggesting that it is an early step in the progression to malignant disease. While several studies have investigated the role Nkx3.1 loss plays in prostate cancer , , , , , , , , , , , much remains unknown. Nkx3.1−/− mice are a model of the early stages of prostate tumorigenesis, exhibiting hyperplasia and dysplasia at 8 weeks of age and progressing to prostatic intraepithelial neoplasia (PIN), a precursor lesion to prostate cancer, later in life , , . With additional genetic lesions, such as the loss of one allele of the Pten tumor suppressor gene , these mice develop prostate cancer. Ouyang et al. showed that prostates of Nkx3.1−/− mice show dysregulation of several antioxidant and pro-oxidant control enzymes, accompanied by elevated oxidative stress . They and others have suggested that increased oxidative stress may be an important way in which Nkx3.1 loss promotes prostate tumor initiation , . However, the ability of oxidative stress to mediate the hyperplasia of the Nkx3.1−/− mouse prostate has not been examined.
In this study, we tested the ability of antioxidant treatment to prevent the prostate pathology of Nkx3.1−/− mice. Interestingly, we found that antioxidant treatment did not inhibit, but instead promoted, the hyperplastic phenotype of the Nkx3.1−/− prostate. NAC treatment of Nkx3.1−/− prostate also induced expression of a pro-proliferative gene signature, as demonstrated by Genome Set Enrichment Analysis (GSEA). This suggests that ROS restrain the proliferative potential of the prostate epithelium in the setting of Nkx3.1-loss. Our studies give new insight into the failure of antioxidants to prevent prostate cancer in healthy men.
Materials and Methods
Nkx3.1−/− mice have been described . Mice were maintained at Vanderbilt University Medical Center in compliance with national and institutional animal welfare standards. For NAC treatment, Nkx3.1+/+ and Nkx3.1−/− pups were weaned at 3 weeks of age and littermates were divided between NAC treatment cages or vehicle cages. Mice received vehicle or 5 mM NAC (Sigma) in drinking water ad lib beginning at weaning for 13 weeks. The pH of NAC solution was adjusted to that of regular drinking water. Analysis of water intake and weight data after the conclusion of the experiment showed that the NAC dosage achieved was 158.5 mg/kg/day in Nkx3.1+/+ mice and 140.7 mg/kg/day in Nkx3.1−/− mice. At the end of 13 weeks of treatment, the mice were euthanized following BrdU intraperitoneal injection (50mg/kg) for prostate histological analysis. Animal protocol M/08/047 was approved by Vanderbilt's Institutional Animal Care and Use Committee.
Quantitative reverse transcription-PCR (qRT-PCR)
Total RNA was extracted from snap-frozen mouse anterior prostate tissue according to the Trizol® manufacturer's protocol. RNA was treated with RQ1 Rnase-free DNAse (Promega) according to manufacturer's protocol and incubated at 37°C for 20 minutes, followed by purification using the RNA Clean Up protocol from the RNeasy Mini Kit (Qiagen). 1 ug RNA was subjected to reverse transcription using M-MLV Reverse Transcriptase (Invitrogen). Quantitative real time PCR was performed using SYBR® Green and the Applied Biosystems 7300 Real Time PCR system with gene-specific primers designed using Applied Biosystems Primer Express® software. The following primers were used: 18s forward (5′-CGCCGCTAGAGGTGAAATTCT-3′), 18s reverse (5′-CGAACCTCCGACTTTCGTTCT-3′), Gpx2 forward (5′-TGACCCGTTCTCCCTCATG-3′), Gpx2 reverse (5′-GCGCACGGGACTCCATAT-3′), Prdx6 forward (5′-TCTGGCAAAAAATACCTCCGTTA-3′), Prdx6 reverse (5′-GCCCCAATTTCCGCAAAG-3′), Qsox1 forward (5′-GGCTGGGAGGGTGACAGTT-3′), and Qsox1 reverse (5′-std 18 GCCCCTACCACCAAGCAA-3′), The expression of each mRNA was normalized to 18s rRNA expression.
ChIP-qPCR of Nkx3.1 binding sites in LNCaP cells
Chromatin immunoprecipitation (ChIP) was performed using the ChIP Assay kit (Millipore) as described by the manufacturer with the following modifications. LNCaP cells (ATCC) were grown in RPMI medium supplemented with 10% fetal bovine serum (FBS) and 1 nM dihydrotestosterone (DHT) for 48 hours. Cells were fixed in 1% formaldehyde at 37°C for 10 minutes to crosslink protein-DNA complexes. Next, cells were thoroughly washed with ice-cold PBS, pelleted, and resuspended in SDS lysis buffer [1% SDS, 10 mM EDTA, 50 mM Tris at pH 8.1]. Chromatin was sheared to a size of ∼300–500 base pairs and diluted 1∶10 with ChIP dilution buffer. An aliquot of the diluted sample (1%) was saved as input. Samples were precleared and precipitated overnight at 4°C with anti-NKX3.1 (Santa Cruz Biotechnology) or normal goat IgG (Santa Cruz Biotechnology) antibodies. Antibody complexes were collected with Protein A Agarose/Salmon Sperm DNA (Millipore) for 2 h and washed extensively per manufacturer's instructions. Samples were reverse cross-linked at 65°C overnight with 0.3 M NaCl and 30 µg of RNase A (Qiagen). Input and bound DNA were purified with a PCR Purification kit (Qiagen) and analyzed by qPCR (Applied Biosystems 7300) using SYBR Green. The following primers were used for qPCR: QSOX1 forward (5′-CCTTCATTGCTATTCACTGGCTAA-3′), QSOX1 reverse (5′-TCCCCAACTGCAATGCAAA-3′), PRDX6 forward (5′- GGTGGCCGAAAGACTTTTTG-3′), PRDX6 reverse (5′- TGGCTCTTCCTAAAGCTGTTATCA-3′), GPX2 forward (5′- GAATCAGTCTAGCAAAGGATCAAACA-3′), and GPX2 reverse (5′-GCATAGAGGGTGTAGTTACTGAGAACA-3′). Immunoprecipitated DNA was normalized to 1% input. Results are presented as mean ± SD.
DHE staining was performed on anterior prostate tissue frozen in Tissue Tek® OCT embedding medium. 10 µm sections were cut and stained with 10 µM dihydroethidium (Molecular Probes) for 30 minutes in a 5% CO2 incubator and visualized on a Zeiss fluroescent microscope. Fluorescence intensity of each image was scanned and scored using Bio Rad GS-700 Imaging Densitometer and BioRad Quantity One® software.
Histology and immunohistochemistry
Tissue was fixed overnight in 10% formalin solution and washed in 70% ethanol. Tissue processing and hematoxalin and eosin (H&E) staining was performed by the Vanderbilt Translational Pathology Shared Resource. For immunohistochemistry, paraffin embedded sections were deparaffinized, rehydrated, and steam/pressure antigen retrieval was performed. The following antibodies were used: anti-BrdU (mouse, 1∶200, Santa Cruz Biotechnology), anti-phospho histone H3 (rabbit, 1∶500, Millipore), anti-cleaved caspase-3 (rabbit, 1∶200, Cell Signaling), anti-smooth muscle actin (mouse, 1∶2000, Sigma), anti-p63 (PIN cocktail, Biocare Medical), anti-AR (rabbit, 1∶600 Santa Cruz Biotechnology), anti-p16 (rabbit, 1∶1000, Santa Cruz Biotechnology), anti-8-Hydroxydeoxyguanosine (8-OHdG) (mouse, 1∶1000, QED Bioscience), anti-p27 (mouse, 1∶2000, BD Transduction Laboratories), and anti-p21 (mouse, 1∶50, Santa Cruz Biotechnology). Horseradish peroxidase (HRP) conjugated secondary antibodies (BioRad) were used to detect primary antibodies and 3, 3′-diaminobenzidine (Sigma) or Nova Red (Vector Laboratories) were used as the chromogenic substrates. Counterstain was performed with hematoxylin.
Three independent fields of anterior prostate at 60× were observed for 8-OHdG immunohistochemical staining in one year old Nkx3.1+/+ and Nkx3.1−/− mice and for BrdU, pHH3, and/or activated caspase 3 staining in the Nkx3.1+/+ and Nkx3.1−/− vehicle and NAC-treated mice. Number of total cells and cells staining positive for each of the markers were recorded and data was reported as percent cells positive for the marker. In all cases, at least 500 total cells were counted per mouse.
Statistical analysis for immunohistochemisrty, qRT-PCR, and fluorescence intensity image data was performed using two tailed Student's t-Test, with two samples of unequal variance. All results are presented as mean ± Standard Deviation. P values≤0.05 are considered significant.
Microarray and Genome Set Enrichment Analysis (GSEA)
Total RNA from four vehicle and four NAC-treated Nkx3.1−/− mice was extracted from snap-frozen mouse anterior prostate tissue according to the Trizol® manufacturer's protocol. RNA was treated with RQ1 Rnase-free DNAse (Promega) according to manufacturer's protocol, followed by purification using the RNA Clean Up protocol from the RNeasy Mini Kit (Qiagen). RNA was processed and microarray analysis was performed by the Vanderbilt Genome Sciences Resource Core. Briefly, RNA was quantified using the Qubit RNA assay and RNA quality was assessed with the Agilent Bioanalyzer. cDNA was generated using the Ambion® WT Expression Kit. After fragmentation, the cDNA was labelled and hybridized to Affymetrix Mouse Gene 1.0 ST arrays. Arrays were scanned with Affymetrix Gene Chip Scanner [version 3.2.2]. CEL files were imported to R [version 2.15.1] for quality control and pre-processing. Arrays for three vehicle and four NAC-treated mice passed quality control. Using the Affy package [version 1.34.0] , raw intensity scores for probes were normalized by quantiles, background corrected with RMA , and summarized by median polish using PM-only probes. The C2 (curated) gene sets of MSigDB [version 3.0] were queried using GSEA [version 2.07]  to test for differences between vehicle and NAC-treated prostates. Relationships between functional terms were visualized in Cytoscape [version 2.8.3]  with the Enrichment Map package [version 1.2] . All microarray and GSEA analysis was performed on a node running Debian Linux [version 6.0.5].
Nkx3.1 directly regulates antioxidant and pro-oxidant genes in the prostate
Previous gene expression analyses studies have revealed mis-expression of antioxidant and pro-oxidant genes in the Nkx3.1 null mouse prostate, including Glutathione peroxidase (Gpx2), Peroxiredoxin 6 (Prdx6), and quiescin Q6 sulfhydryl oxidase 1 (Qsox1 or Qscn6) , , . We performed qRT-PCR analysis on anterior prostates to confirm these gene expression changes. Expression of the antioxidant genes Gpx2 and Prdx6 was decreased in 10–11-week-old and 16–17-week-old Nkx3.1−/− mice, while expression of the pro-oxidant gene Qsox1 was elevated in these mice (Figure 1A). Examination of chromatin immunoprecipitation coupled to massively parallel sequencing (ChIP-seq) analysis for Nkx3.1 in mouse prostate  and the human prostate cancer cell line LNCaP (PDA, ML and SAA, manuscript in preparation) performed by our laboratory revealed binding sites for Nkx3.1 in both human and mouse tissue at all three genes (Figure 1B, 1C). Therefore, Gpx2, Prdx6 and Qsox1 are direct target genes of the Nkx3.1 transcription factor.
(A) Quantitative reverse transcriptase-PCR analysis of RNA from 10–11-week and 16–17-week-old Nkx3.1+/+ and Nkx3.1−/− mouse anterior prostate for the expression of Gpx2, Prdx6, and Qsox1. Expression levels are relative to 18s rRNA. (10–11 weeks: n = 4 Nkx3.1+/+, n = 2 Nkx3.1−/−; 16–17 weeks: n = 3 Nkx3.1+/+, n = 5 Nkx3.1−/−) (B) ChIP-seq screen shots from Integrative Genomics Viewer (IGV) displays direct binding of Nkx3.1 to the gene loci of Gpx2, Prdx6 and Qsox1 in mouse prostate, (C) and to GPX2, PRDX6 and QSOX1 in the human prostate cancer cell line LNCaP. (D) ChIP-qPCR analysis for Nkx3.1 binding sites in GPX2, PRDX6, and QSOX1. Results are presented for each binding site primer set with anti-NKX3.1 antibody and IgG control. Immunoprecipitated DNA was normalized to 1% input. (E) Percent positive stained anterior prostate epithelial cells from immunohistochemical staining for 8-OHdG in one-year-old Nkx3.1+/+ and Nkx3.1−/− anterior prostate. (n = 5 in each group) Student's t-Test * = p≤0.05.
Nkx3.1−/− mouse prostate displays increased oxidative stress
The most common oxidative DNA base lesion, 8-OHdG, is commonly used as a marker of persistent oxidative stress . Immunohistochemical staining of one-year-old mouse anterior prostate showed significantly increased staining in Nkx3.1−/− mice (Figure 1D). These results confirm earlier findings of increased oxidative DNA damage in the prostates of independently generated Nkx3.1−/− mice .
NAC treatment of Nkx3.1−/− mice does not inhibit hyperplastic prostate phenotype
To determine if increased oxidative stress plays a causative role in the hyperplasia and dysplasia observed in the Nkx3.1−/− mouse prostate, we treated Nkx3.1−/− mice with 5 mM NAC in their drinking water from 3 weeks of age until mice were sacrificed at 16 weeks of age (Figure 2A). The 5 mM NAC concentration was chosen to achieve a dosage of approximately 125 mg/kg/day for 13 weeks, a dosage and treatment duration shown to inhibit plasma ROS, decrease oxidative DNA and protein lesions in the prostate, and decrease the incidence of prostate anterior lobe hyperplasia in the Transgenic Adenocarcinoma Mouse Prostate (TRAMP) model , . Examination of water intake and weight data revealed that the achieved dosage for the Nkx3.1−/− mice was approximately 140 mg/kg/day. The 13 week NAC treatment decreased ROS levels in the anterior prostate as shown by decreased staining for superoxide using the fluorescent dye dihydroethidium (DHE) (Figure 2B, 2C).
(A) Nkx3.1−/− mice were treated with 5 mM N-acetylcysteine (NAC) ad lib in their drinking water postweaning for 13 weeks. Mice were sacrificed for analysis at the end of treatment (16 weeks of age). (B) Dihydroethidium (DHE) staining of frozen anterior prostate from Nkx3.1−/− vehicle or NAC-treated mice. (C) Quantification of DHE staining density. (n = 3 in each group) Student's t-Test * = p≤0.05.
Histological analysis of Nkx3.1−/− anterior prostate, the prostatic lobe which displays the severest Nkx3.1−/− phenotype, showed that the NAC treatment did not reverse the Nkx3.1−/− phenotype. Observation of 23 control and 24 NAC-treated Nkx3.1−/− prostates revealed that the NAC-treated prostates did not have less hyperplasia or dysplasia than the control prostates (Figure 3A). Immunohistochemical staining for smooth muscle actin was unchanged between treated and untreated mice, suggesting the prostate epithelial cells did not alter gland structure or invade the stromal compartment (Figure 4B). Immunostaining for p63 (basal cell marker) and androgen receptor (AR) remained unchanged with treatment, showing no major histological alterations of the prostate epithelium after NAC treatment (Figure 3B).
(A) Hematoxalin and eosin stained sections of Nkx3.1−/− anterior prostate do not display significant histological changes with NAC treatment. (B) Immunohistochemical staining of anterior prostate for smooth muscle actin (SMA), p63, and androgen receptor (AR) do not have significant changes in staining pattern. Scale bar = 0.1 mm.
(A), (C), (E) Representative images from immunohistochemical staining of Nkx3.1−/− vehicle and NAC-treated anterior prostate with antibodies specific to BrdU (A), pHH3 (C), and activated caspase-3 (E). (B), (D), (F) Quantification of immunohistochemical stains. p values for a Student's t-Test are shown.
NAC treatment of Nkx3.1−/− mouse prostate promotes increased proliferation
To assess cell proliferation in the prostate after NAC treatment, mice were injected with BrdU three hours prior to sacrifice to label cells undergoing DNA synthesis, indicating the proportion of cells progressing though the cell cycle. Surprisingly, the percentage of anterior prostate epithelial cells staining positive for BrdU was increased by 60% in the NAC-treated Nkx3.1−/− mice (p = 0.02, n = 10 in each group, Figures 4A, 4B). Staining for the mitotic cell marker pHH3 was also increased by 30% in the NAC-treated animals (p = 0.05, n = 15 vehicle, n = 16 NAC, Figures 4C, 4D). However, activated caspase-3 staining revealed that apoptosis was unchanged with NAC treatment (p = 0.59, n = 10 in each group, Figures 4E, 4F). The observed increase in proliferation without a concurrent decrease in apoptosis suggests NAC treatment increases prostate epithelial cell numbers in the Nkx3.1−/− prostate.
NAC treatment of Nkx3.1+/+ mouse prostate does not affect proliferation
To determine if NAC treatment affects prostate epithelial cell proliferation in the absence of Nkx3.1-loss and elevated oxidative stress, we treated Nkx3.1+/+ mice with NAC in the same manner as was used for the Nkx3.1−/− mice. The dosage achieved in the Nkx3.1+/+ mice was comparable to the Nkx3.1−/− mice at approximately 160 mg/kg/day. The NAC treatment did not alter overall prostate histology in the Nkx3.1+/+ mice (Figure 5A). BrdU and pHH3 immunohistochemical analyses showed that NAC treatment did not alter the proliferation index of the Nkx3.1+/+ anterior prostate (Figure 5B, 5C).
(A) H&E sections of Nkx3.1+/+ vehicle and NAC-treated anterior prostate show no change in histology. Scale bar = 0.1 mm. (B) Quantification of BrdU immunohistochemical staining in Nkx3.1+/+ vehicle and NAC-treated anterior prostate. (C) Quantification of pHH3 immunohistochemical staining in Nkx3.1+/+ vehicle and NAC-treated anterior prostate. p value for a Student's t-Test is shown.
NAC treatment of the Nkx3.1−/− mouse prostate promotes expression of a pro-proliferative gene signature
ROS have been shown to induce senescence and quiescence in human and mouse models of disease . Because quenching of prostatic ROS with NAC increased epithelial cell proliferation, we hypothesized that oxidative stress in the Nkx3.1-null prostate induces cell cycle arrest. We performed immunohistochemical staining for well-defined markers of senescence (p16, p21) and quiescence (p27) in Nkx3.1−/− vehicle and NAC-treated prostates. Expression of these markers remains unchanged with NAC treatment (Figure 6).
Immunohistochemical staining of Nkx3.1−/− vehicle and NAC-treated anterior prostate for p16, p27, and p21. p16 inset: positive control for p16 staining from PbCre4; Ptenf/f prostate . p21 inset: positive control for p21 staining from PbCre4; Ptenf/f; p53f/+ prostate . Scale bar = 0.1 mm.
In order to analyze global gene expression changes associated with NAC treatment of the Nkx3.1−/− prostate, we performed Affymetrix microarray analysis on total RNA extracted from three Nkx3.1−/− vehicle and four Nkx3.1−/− NAC-treated anterior prostates. Genome Set Enrichment Analysis (GSEA) , is used to determine if the expression of a priori defined gene sets, relating to biological pathways or experimental conditions, is significantly altered in the experimental tissue of interest. GSEA allows for detection of modest gene expression changes of many genes in one pathway that as a group may have a functional biological effect. The GSEA Molcular Signatures Database (MSigDB) collections consist of sets of human genes. We compared our mouse gene expression data to the human gene sets using the human genes orthologous to the mouse genes. Using the C2 (curated) gene sets collection, we identified many gene sets that were significantly enriched or depleted in NAC-treated Nkx3.1−/− prostates, including several that are associated with proliferation control and quiescence (Tables S1 and S2).
To obtain a broader picture of the relationships between the significantly altered gene sets in NAC-treated Nkx3.1−/− prostates, we performed Enrichment Map analysis . This is a method for GSEA interpretation and visualization which constructs networks from gene sets (nodes) containing overlapping genes. Analysis of identified networks using Enrichment Map can yield important information about the broad biological processes altered in a treatment group. Enrichment Map results for all networks containing ≥5 nodes are presented in Figure 7A. The first network we term “proliferation control” and consists of 7 nodes. One of these upregulated “proliferation control” gene sets (GRAHAM_NORMAL_QUIESCENT_VS_NORMAL_DIVIDING_DN) is a gene set consisting of transcripts that are downregulated during quiescence of hemopoetic stem cells (HSCs) and another is a set upregulated in dividing leukemia stem cells compared to quiescent HSCs (GRAHAM_CML_DIVIDING_VS_NORMAL_QUIESCENT_UP) (Figure 7B,). Another upregulated “proliferation control” gene set is ROSTY_CERVICAL_CANCER_PROLIFERATION_CLUSTER, consisting of genes controlling cell division and proliferation and associated with an increased severity and early relapse in cervical cancer (Figure 7B, ). Enrichment of this network in the NAC-treated prostate serves as further quantitative evidence of increased proliferation in Nkx3.1−/− prostate upon NAC treatment. Another network upregulated in the NAC-treated Nkx3.1−/− prostates contains gene sets comprised in a large part by chemokine/growth factor genes such as REACTOME_G_ALPHA_I_SIGNALLING_EVENTS (Figure 7A, 7B). A network consisting of sets involved in immune regulation was depleted in NAC-treated Nkx3.1−/− prostates (Figure 7A).
(A) Enrichment Map  analysis for Genome Set Enrichment Analysis (GSEA) C2 (curated) gene set data obtained from vehicle and NAC-treated Nkx3.1−/− anterior prostate. Map displays the related gene networks containing ≥5 gene sets with a false discovery rate (FDR) q value <0.25. Node size corresponds to gene set size. Hue designates which manner in which the gene sets are altered (red = enriched in NAC-treatment, blue = depleted in NAC-treatment). Color intensity represents significance by enrichment p value. Line thickness connecting the gene set nodes represents the degree of gene overlap between the two sets. (B) GSEA Enrichment plots ,  for selected gene sets from the “proliferation control” network and the “chemokines/growth factors” network. Nominal p value (statistical significance of the enrichment) and the FDR are presented. (C) Potential model for Nkx3.1-loss associated ROS and NAC treatment in prostate tumor initiation.
The ‘leading edge’ is the subset of genes within a specific MSigDB gene set which drives the observed association in GSEA. Analysis of the leading edge genes may help to determine which changes in gene expression are responsible for a given phenotype. Leading edge genes from the “proliferation control” network (Table 1) include many classic pro-proliferative genes such Ccna2 (CCNA2 in human), Cdc6, Tk1, and Gmnn. Leading edge genes in the “chemokines/growth factors” network (Table 2) include many involved in pathways that have proven links to prostate cancer, including chemokines/chemokine receptors (Ccl2, Cxcl5, Cxcr1, Cxcr2) ,, the endothelin axis (Ednrb, Ednra) , and neuropeptides (Npy, Npy1r, Npy5r, Pyy) .
Our study has displayed novel evidence of prostate tumor promotion by antioxidant treatment. Using Nkx3.1-null mice, we have modeled antioxidant chemoprevention in the early stages of prostate tumorigenesis and shown an increase in prostate epithelial proliferation upon NAC treatment. These results suggest that ROS can be anti-tumorigenic in the early stages of prostate cancer and that antioxidant chemoprevention may be ineffective or harmful in many circumstances.
In this report we have confirmed that Nkx3.1−/− mice display increased prostatic oxidative stress. The hyperproliferative state of the Nkx3.1−/− prostate may promote increased oxidative stress through one of many indirect mechanisms. However, we have shown that the oxidative stress regulatory genes Gpx2, Prdx6, and Qsox1 are dysregulated in the mutant mice and are shown to be direct targets of the the Nkx3.1 transcription factor in both the mouse and human prostate. Therefore, we propose that loss of Nkx3.1 expression may directly affect oxidative stress maintenance through dysregulation of these target genes.
To determine if elevated oxidative stress is a causative mechanism for the hyperplasia observed in the Nkx3.1−/− prostate, we treated Nkx3.1−/− mice with the antioxidant NAC. NAC is a precursor for the most prevalent antioxidant molecule in cells, glutathione (GSH). NAC has been safely used for many years in mice and humans and has been shown in previous studies to increase GSH concentration, decrease oxidative stress, and have beneficial clinical effects , . While NAC treatment did decrease ROS levels in the Nkx3.1−/− prostate, it did not alter the hyperplastic phenotype. Upon immunohistochemical staining with BrdU and pHH3, we observed that NAC treatment promoted proliferation in the Nkx3.1−/− prostate. Surprisingly, rather than inhibit the hyperplastic phenotype, NAC treatment promotes hyperplasia in the Nkx3.1−/− prostate. In the Nkx3.1+/+ prostate, NAC treatment did not increase proliferation, suggesting that the mechanism by which NAC increases proliferation in the Nkx3.1−/− prostate is related to elevated oxidative stress.
Because we observed increased proliferation in the NAC-treated Nkx3.1−/− prostate, we hypothesized that elevated ROS in the Nkx3.1−/− prostate is activating an anti-proliferative pathway or inhibiting a pro-proliferative pathway, reducing the proliferative potential of the prostate epithelial cells. Antioxidant treatment would suppress this ROS-mediated effect, allowing for the epithelial cells to proliferate more. To first test this hypothesis, we performed immunoshistochemical analysis of well-established senescence and quiescence markers. This did not reveal any changes with NAC treatment of the Nkx3.1−/− prostate. To further investigate the possible mechanism behind the increased proliferation upon NAC treatment, we performed global gene expression analysis on vehicle and NAC-treated Nkx3.1−/− prostate. Analysis of the gene expression data with GSEA and Enrichment Map revealed a significant enrichment in expression of gene sets involved in proliferation control and chemokine/growth factor function. Increased expression of this pro-proliferative gene signature, consisting of classic proliferation genes (i.e. cyclins) and chemokines/growth factors, many of which have been implicated in prostate cancer , , , , may explain the increase in proliferation seen upon NAC treatment of the Nkx3.1−/− prostate.
Based upon our findings, we propose a potential model for Nkx3.1-loss associated ROS and NAC treatment in prostate tumor initiation (Figure 7C). Loss of Nkx3.1 expression in the prostate causes dysregulation of antioxidant and pro-oxidant direct target genes, resulting in elevated ROS in the hyperplastic Nkx3.1−/− prostate. These ROS may actually limit proliferation in the Nkx3.1−/− prostate by inhibiting expression of pro-proliferative genes. ROS have been shown to induce cell cycle arrest or decrease proliferation in several models of non-cancerous and cancerous cells , , , , and, in some of these cases, antioxidant treatment has been explicitly shown to reverse these ROS-induced effects. Thus, NAC may be increasing proliferation of the Nkx3.1-null prostate by decreasing ROS-mediated inhibition of pro-proliferative genes. Alternatively, NAC may promote proliferation by an alternative mechanism independent of prostatic ROS inhibition.
Results from this study emphasize the need for a deeper understanding of the role reactive oxygen species play in prostate tumor progression. The effect of ROS on cells is not always pro-tumorigenic. The level of ROS present in a tissue can influence the effect seen, with high levels of ROS promoting senescence or cell death, but lower levels promoting DNA mutations or activating pro-proliferative signaling. The cell type with which ROS interacts also determines its effect. In a normal cell, a certain level of ROS may kill the cell or cause a cell to undergo cell cycle arrest, while in a cancer cell the same level of ROS may promote proliferation and invasion.
Despite the ability of antioxidants to inhibit cancer in several mouse models, we have shown that the antioxidant NAC promotes proliferation in the Nkx3.1−/− prostate. We propose that the Nkx3.1−/− mouse is a good model for antioxidant chemoprevention, exhibiting early lesions similar to those of cancer-naïve men in whom clinicians desire to prevent malignant disease. Indeed, antioxidants may function to inhibit tumor progression at later stages, effectively treating cancer in some settings. However, at early stages, ROS may actually slow or prevent tumor progression from occurring , . In addition, different antioxidant compounds may affect the prostate in unique ways. Alternatively, ROS may have different effects on prostate tumor progression based on the genetic lesions or gene expression changes present.
The recent alarming results from the SELECT trial, in which “antioxidant chemoprevention” increased prostate cancer risk, can be informed by our study. While the proliferation upon NAC treatment is not increased to an extremely large degree, it is nevertheless a significant increase and could become more pronounced with long term treatment. NAC was not the specific antioxidant used in the SELECT trial; however, the results can yield important information due to the fact that NAC should decrease the overall oxidative state and possibly reflect possible results seen by other antioxidants. In fact, a recently published study using selenium and vitamin E in a rat model of prostate tumorigenesis showed a similar finding, that vitamin E treatment showed a marginally significant increase in prostate tumor formation .
In the setting of certain genetic lesions or expression changes, such as Nkx3.1-loss, depleting ROS may actually allow cells to escape a ROS-mediated inhibition of proliferation, increasing the chance of transformation of the prostate epithelium. The increased prostate cancer risk in the SELECT study population may indeed be driven by a subset of participants with an inherited polymorphism in Nkx3.1 (rs11781886) that is associated with increased prostate cancer risk . Depletion of ROS by vitamin E may have modified the risk from the levels normally associated with the polymorphism, producing the surprising detrimental effect with vitamin E chemoprevention. Oxidative stress and antioxidant levels have been shown in previous studies to modify cancer risk associated with inherited polymorphisms , , , , . Studies are ongoing using the SELECT biorepository to determine if antioxidant treatment increased the prostate cancer risk associated with the functional Nkx3.1 variant (rs11781886) .
Our report provides valuable insight into the inconsistent results among preclinical and clinical studies on the efficacy of prostate cancer antioxidant chemoprevention . We suggest that investigation of prostate cancer chemoprevention specifically in physiologically relevant models, with analysis of the complexities of specific gene expression changes, is critically needed if clinically applicable results are desired. Caution should be taken when using antioxidants for prostate cancer prevention, because the effect which they have, beneficial or harmful, may lie in the makeup of the prostate gland of each unique individual.
Top gene sets enriched in NAC-treated Nkx3.1−/− anterior prostate. GSEA analysis results for top gene sets enriched in NAC-treated Nkx3.1−/− anterior prostate as ranked by Normalized Enrichment Score. Gene set size, Enrichment Score, Normalized Enrichment Score, Nominal p-value, and FDR q-value are provided. Enriched gene sets with a FDR q-value<0.25 are provided (99 gene sets).
Top gene sets depleted in NAC-treated Nkx3.1−/− anterior prostate. GSEA analysis results for top gene sets depleted in NAC-treated Nkx3.1−/− anterior prostate as ranked by Normalized Enrichment Score. Gene set size, Enrichment Score, Normalized Enrichment Score, Nominal p-value, and FDR q-value are provided. Enriched gene sets with a FDR q-value<0.25 are provided (29 gene sets).
We would like to greatly thank Bill Valentine for assistance with microscopy and image analysis. We appreciate the technical assistance provided by Irina Doubinskaia and Gabriela Algarroba and helpful discussions with the Abdulkadir lab. We are grateful to Anthony Frazier, Cindy Lowe, Regina Hentz, and the rest of the members of Vanderbilt Translational Pathology Shared Resource Core for their expertise. We thank Vicki Amann and the Vanderbilt GenomeSciences Resource staff for their assistance throughout the microarray analysis.
Conceived and designed the experiments: SAA EEM. Performed the experiments: EEM PDA ML. Analyzed the data: EEM PDA ML SAA. Contributed reagents/materials/analysis tools: SAA. Wrote the paper: EEM SAA.
- 1. Fleshner NE, Klotz LH (1998) Diet, androgens, oxidative stress and prostate cancer susceptibility. Cancer Metastasis Rev 17: 325–330.
- 2. Pathak SK, Sharma RA, Steward WP, Mellon JK, Griffiths TRL, et al. (2005) Oxidative stress and cyclooxygenase activity in prostate carcinogenesis: targets for chemopreventive strategies. Eur J Cancer 41: 61–70
- 3. Khandrika L, Kumar B, Koul S, Maroni P, Koul HK (2009) Oxidative stress in prostate cancer. Cancer Lett 282: 125–136
- 4. Ozten-Kandaş N, Bosland MC (2011) Chemoprevention of prostate cancer: Natural compounds, antiandrogens, and antioxidants - In vivo evidence. J Carcinog 10: 27
- 5. Sfanos KS, De Marzo AM (2012) Prostate cancer and inflammation: the evidence. Histopathology 60: 199–215
- 6. Thapa D, Ghosh R (2012) Antioxidants for prostate cancer chemoprevention: challenges and opportunities. Biochem Pharmacol 83: 1319–1330
- 7. Nyska A, Suttie A, Bakshi S, Lomnitski L, Grossman S, et al. (2003) Slowing tumorigenic progression in TRAMP mice and prostatic carcinoma cell lines using natural anti-oxidant from spinach, NAO–a comparative study of three anti-oxidants. Toxicol Pathol 31: 39–51.
- 8. Tam NNC, Nyska A, Maronpot RR, Kissling G, Lomnitski L, et al. (2006) Differential attenuation of oxidative/nitrosative injuries in early prostatic neoplastic lesions in TRAMP mice by dietary antioxidants. Prostate 66: 57–69
- 9. Shiota M, Song Y, Takeuchi A, Yokomizo A, Kashiwagi E, et al. (2012) Antioxidant therapy alleviates oxidative stress by androgen deprivation and prevents conversion from androgen dependent to castration resistant prostate cancer. J Urol 187: 707–714
- 10. Adhami VM, Ahmad N, Mukhtar H (2003) Molecular targets for green tea in prostate cancer prevention. J Nutr 133: 2417S–2424S.
- 11. Venkateswaran V, Fleshner NE, Sugar LM, Klotz LH (2004) Antioxidants block prostate cancer in lady transgenic mice. Cancer Res 64: 5891–5896
- 12. Barve A, Khor TO, Nair S, Reuhl K, Suh N, et al. (2009) Gamma-tocopherol-enriched mixed tocopherol diet inhibits prostate carcinogenesis in TRAMP mice. Int J Cancer 124: 1693–1699
- 13. Narayanan NK, Nargi D, Randolph C, Narayanan BA (2009) Liposome encapsulation of curcumin and resveratrol in combination reduces prostate cancer incidence in PTEN knockout mice. Int J Cancer 125: 1–8
Khan N, Adhami VM, Afaq F, Mukhtar H (2012) Butein Induces Apoptosis and Inhibits Prostate Tumor Growth In Vitro and In Vivo. Antioxidants & Redox Signaling. Available:http://www.ncbi.nlm.nih.gov/pubmed/22114764. Accessed 2012 Mar 15.
- 15. Klein EA, Thompson IM, Lippman SM, Goodman PJ, Albanes D, et al. (2001) SELECT: the next prostate cancer prevention trial. Selenum and Vitamin E Cancer Prevention Trial. J Urol 166: 1311–1315.
- 16. Duffield-Lillico AJ, Dalkin BL, Reid ME, Turnbull BW, Slate EH, et al. (2003) Selenium supplementation, baseline plasma selenium status and incidence of prostate cancer: an analysis of the complete treatment period of the Nutritional Prevention of Cancer Trial. BJU Int 91: 608–612.
- 17. Heinonen OP, Albanes D, Virtamo J, Taylor PR, Huttunen JK, et al. (1998) Prostate cancer and supplementation with alpha-tocopherol and beta-carotene: incidence and mortality in a controlled trial. J Natl Cancer Inst 90: 440–446.
- 18. Lippman SM, Klein EA, Goodman PJ, Lucia MS, Thompson IM, et al. (2009) Effect of selenium and vitamin E on risk of prostate cancer and other cancers: the Selenium and Vitamin E Cancer Prevention Trial (SELECT). JAMA 301: 39–51
- 19. Klein EA, Thompson IM Jr, Tangen CM, Crowley JJ, Lucia MS, et al. (2011) Vitamin E and the risk of prostate cancer: the Selenium and Vitamin E Cancer Prevention Trial (SELECT). JAMA 306: 1549–1556
- 20. Klein EA (2009) Selenium and vitamin E: interesting biology and dashed hope. J Natl Cancer Inst 101: 283–285
- 21. Bowen C, Bubendorf L, Voeller HJ, Slack R, Willi N, et al. (2000) Loss of NKX3.1 expression in human prostate cancers correlates with tumor progression. Cancer Res 60: 6111–6115.
- 22. Asatiani E, Huang W-X, Wang A, Rodriguez Ortner E, Cavalli LR, et al. (2005) Deletion, methylation, and expression of the NKX3.1 suppressor gene in primary human prostate cancer. Cancer Res 65: 1164–1173
- 23. He WW, Sciavolino PJ, Wing J, Augustus M, Hudson P, et al. (1997) A novel human prostate-specific, androgen-regulated homeobox gene (NKX3.1) that maps to 8p21, a region frequently deleted in prostate cancer. Genomics 43: 69–77
- 24. Chen H, Nandi AK, Li X, Bieberich CJ (2002) NKX-3.1 interacts with prostate-derived Ets factor and regulates the activity of the PSA promoter. Cancer Res 62: 338–340.
- 25. Abdulkadir SA (2005) Mechanisms of prostate tumorigenesis: roles for transcription factors Nkx3.1 and Egr1. Ann N Y Acad Sci 1059: 33–40
- 26. Magee JA, Abdulkadir SA, Milbrandt J (2003) Haploinsufficiency at the Nkx3.1 locus. A paradigm for stochastic, dosage-sensitive gene regulation during tumor initiation. Cancer Cell 3: 273–283.
- 27. Tan PY, Chang CW, Chng KR, Wansa KDSA, Sung W-K, et al. (2012) Integration of regulatory networks by NKX3-1 promotes androgen-dependent prostate cancer survival. Mol Cell Biol 32: 399–414
- 28. Bowen C, Gelmann EP (2010) NKX3.1 activates cellular response to DNA damage. Cancer Res 70: 3089–3097
- 29. Wang X, Kruithof-de Julio M, Economides KD, Walker D, Yu H, et al. (2009) A luminal epithelial stem cell that is a cell of origin for prostate cancer. Nature 461: 495–500
- 30. Song H, Zhang B, Watson MA, Humphrey PA, Lim H, et al. (2009) Loss of Nkx3.1 leads to the activation of discrete downstream target genes during prostate tumorigenesis. Oncogene 28: 3307–3319
- 31. Muhlbradt E, Asatiani E, Ortner E, Wang A, Gelmann EP (2009) NKX3.1 activates expression of insulin-like growth factor binding protein-3 to mediate insulin-like growth factor-I signaling and cell proliferation. Cancer Res 69: 2615–2622 .
- 32. Zhang H, Muders MH, Li J, Rinaldo F, Tindall DJ, et al. (2008) Loss of NKX3.1 favors vascular endothelial growth factor-C expression in prostate cancer. Cancer Res 68: 8770–8778
- 33. Bowen C, Stuart A, Ju J-H, Tuan J, Blonder J, et al. (2007) NKX3.1 homeodomain protein binds to topoisomerase I and enhances its activity. Cancer Res 67: 455–464
- 34. Lei Q, Jiao J, Xin L, Chang C-J, Wang S, et al. (2006) NKX3.1 stabilizes p53, inhibits AKT activation, and blocks prostate cancer initiation caused by PTEN loss. Cancer Cell 9: 367–378
- 35. Bhatia-Gaur R, Donjacour AA, Sciavolino PJ, Kim M, Desai N, et al. (1999) Roles for Nkx3.1 in prostate development and cancer. Genes Dev 13: 966–977.
- 36. Abdulkadir SA, Magee JA, Peters TJ, Kaleem Z, Naughton CK, et al. (2002) Conditional loss of Nkx3.1 in adult mice induces prostatic intraepithelial neoplasia. Mol Cell Biol 22: 1495–1503.
- 37. Kim MJ, Bhatia-Gaur R, Banach-Petrosky WA, Desai N, Wang Y, et al. (2002) Nkx3.1 mutant mice recapitulate early stages of prostate carcinogenesis. Cancer Res 62: 2999–3004.
- 38. Kim MJ, Cardiff RD, Desai N, Banach-Petrosky WA, Parsons R, et al. (2002) Cooperativity of Nkx3.1 and Pten loss of function in a mouse model of prostate carcinogenesis. Proc Natl Acad Sci USA 99: 2884–2889
- 39. Ouyang X, DeWeese TL, Nelson WG, Abate-Shen C (2005) Loss-of-function of Nkx3.1 promotes increased oxidative damage in prostate carcinogenesis. Cancer Res 65: 6773–6779
- 40. Bethel CR, Faith D, Li X, Guan B, Hicks JL, et al. (2006) Decreased NKX3.1 protein expression in focal prostatic atrophy, prostatic intraepithelial neoplasia, and adenocarcinoma: association with gleason score and chromosome 8p deletion. Cancer Res 66: 10683–10690
- 41. Khalili M, Mutton LN, Gurel B, Hicks JL, De Marzo AM, et al. (2010) Loss of Nkx3.1 expression in bacterial prostatitis: a potential link between inflammation and neoplasia. Am J Pathol 176: 2259–2268
- 42. Gautier L, Cope L, Bolstad BM, Irizarry RA (2004) affy–analysis of Affymetrix GeneChip data at the probe level. Bioinformatics 20: 307–315
- 43. Irizarry RA, Hobbs B, Collin F, Beazer-Barclay YD, Antonellis KJ, et al. (2003) Exploration, normalization, and summaries of high density oligonucleotide array probe level data. Biostatistics 4: 249–264
- 44. Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, et al. (2005) Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci USA 102: 15545–15550
- 45. Smoot ME, Ono K, Ruscheinski J, Wang P-L, Ideker T (2011) Cytoscape 2.8: new features for data integration and network visualization. Bioinformatics 27: 431–432
- 46. Merico D, Isserlin R, Stueker O, Emili A, Bader GD (2010) Enrichment map: a network-based method for gene-set enrichment visualization and interpretation. PLoS ONE 5: e13984
- 47. Anderson PD, McKissic SA, Logan M, Roh M, Franco OE, et al. (2012) Nkx3.1 and Myc crossregulate shared target genes in mouse and human prostate tumorigenesis. J Clin Invest 122: 1907–1919
- 48. Kondo S, Toyokuni S, Iwasa Y, Tanaka T, Onodera H, et al. (1999) Persistent oxidative stress in human colorectal carcinoma, but not in adenoma. Free Radic Biol Med 27: 401–410.
- 49. Pan J-S, Hong M-Z, Ren J-L (2009) Reactive oxygen species: a double-edged sword in oncogenesis. World J Gastroenterol 15: 1702–1707.
- 50. Mootha VK, Lindgren CM, Eriksson K-F, Subramanian A, Sihag S, et al. (2003) PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. Nat Genet 34: 267–273
- 51. Graham SM, Vass JK, Holyoake TL, Graham GJ (2007) Transcriptional analysis of quiescent and proliferating CD34+ human hemopoietic cells from normal and chronic myeloid leukemia sources. Stem Cells 25: 3111–3120
- 52. Rosty C, Sheffer M, Tsafrir D, Stransky N, Tsafrir I, et al. (2005) Identification of a proliferation gene cluster associated with HPV E6/E7 expression level and viral DNA load in invasive cervical carcinoma. Oncogene 24: 7094–7104
- 53. Vindrieux D, Escobar P, Lazennec G (2009) Emerging roles of chemokines in prostate cancer. Endocr Relat Cancer 16: 663–673
- 54. Singh RK, Sudhakar A, Lokeshwar BL (2010) Role of Chemokines and Chemokine Receptors in Prostate Cancer Development and Progression. J Cancer Sci Ther 2: 89–94
- 55. Nelson J, Bagnato A, Battistini B, Nisen P (2003) The endothelin axis: emerging role in cancer. Nat Rev Cancer 3: 110–116
- 56. Ruscica M, Dozio E, Motta M, Magni P (2007) Role of neuropeptide Y and its receptors in the progression of endocrine-related cancer. Peptides 28: 426–434
- 57. De Flora S, Izzotti A, D'Agostini F, Balansky RM (2001) Mechanisms of N-acetylcysteine in the prevention of DNA damage and cancer, with special reference to smoking-related end-points. Carcinogenesis 22: 999–1013.
- 58. Aitio M-L (2006) N-acetylcysteine—passe-partout or much ado about nothing? Br J Clin Pharmacol 61: 5–15
- 59. Kim TH, Oh S, Kim SS (2005) Recombinant human prothrombin kringle-2 induces bovine capillary endothelial cell cycle arrest at G0-G1 phase through inhibition of cyclin D1/CDK4 complex: modulation of reactive oxygen species generation and up-regulation of cyclin-dependent kinase inhibitors. Angiogenesis 8: 307–314
- 60. Chen C-Y, Chen C-H, Lo Y-C, Wu B-N, Wang H-M, et al. (2008) Anticancer activity of isoobtusilactone A from Cinnamomum kotoense: involvement of apoptosis, cell-cycle dysregulation, mitochondria regulation, and reactive oxygen species. J Nat Prod 71: 933–940
- 61. Li M, Zhao L, Liu J, Liu A-L, Zeng W-S, et al. (2009) Hydrogen peroxide induces G2 cell cycle arrest and inhibits cell proliferation in osteoblasts. Anat Rec (Hoboken) 292: 1107–1113
- 62. Chaudhuri L, Sarsour EH, Kalen AL, Aykin-Burns N, Spitz DR, et al. (2010) Polychlorinated biphenyl induced ROS signaling delays the entry of quiescent human breast epithelial cells into the proliferative cycle. Free Radic Biol Med 49: 40–49
- 63. DeNicola GM, Karreth FA, Humpton TJ, Gopinathan A, Wei C, et al. (2011) Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis. Nature 475: 106–109
- 64. Gao P, Tchernyshyov I, Chang T-C, Lee Y-S, Kita K, et al. (2009) c-Myc suppression of miR-23a/b enhances mitochondrial glutaminase expression and glutamine metabolism. Nature 458: 762–765
- 65. McCormick DL, Rao KVN, Johnson WD, Bosland MC, Lubet RA, et al. (2010) Null activity of selenium and vitamin e as cancer chemopreventive agents in the rat prostate. Cancer Prev Res (Phila) 3: 381–392
- 66. Akamatsu S, Takata R, Ashikawa K, Hosono N, Kamatani N, et al. (2010) A functional variant in NKX3.1 associated with prostate cancer susceptibility down-regulates NKX3.1 expression. Hum Mol Genet 19: 4265–4272
- 67. Mikhak B, Hunter DJ, Spiegelman D, Platz EA, Wu K, et al. (2008) Manganese superoxide dismutase (MnSOD) gene polymorphism, interactions with carotenoid levels and prostate cancer risk. Carcinogenesis 29: 2335–2340
- 68. Quick SK, Shields PG, Nie J, Platek ME, McCann SE, et al. (2008) Effect modification by catalase genotype suggests a role for oxidative stress in the association of hormone replacement therapy with postmenopausal breast cancer risk. Cancer Epidemiol Biomarkers Prev 17: 1082–1087
- 69. Abe M, Xie W, Regan MM, King IB, Stampfer MJ, et al. (2011) Single-nucleotide polymorphisms within the antioxidant defence system and associations with aggressive prostate cancer. BJU Int 107: 126–134
- 70. Zhang J, Dhakal IB, Greene G, Lang NP, Kadlubar FF (2010) Polymorphisms in hOGG1 and XRCC1 and risk of prostate cancer: effects modified by plasma antioxidants. Urology 75: 779–785
- 71. Li H, Kantoff PW, Giovannucci E, Leitzmann MF, Gaziano JM, et al. (2005) Manganese superoxide dismutase polymorphism, prediagnostic antioxidant status, and risk of clinical significant prostate cancer. Cancer Res 65: 2498–2504
- 72. McNeil C (2011) Vitamin E and prostate cancer: research focus turns to biologic mechanisms. J Natl Cancer Inst 103: 1731–1734
- 73. Kim J, Eltoum I-EA, Roh M, Wang J, Abdulkadir SA (2009) Interactions between cells with distinct mutations in c-MYC and Pten in prostate cancer. PLoS Genet 5: e1000542
- 74. Kim J, Roh M, Doubinskaia I, Algarroba GN, Eltoum I-EA, et al. (2012) A mouse model of heterogeneous, c-MYC-initiated prostate cancer with loss of Pten and p53. Oncogene 31: 322–332