- Research article
- Open Access
Peroxiredoxin-1 protects estrogen receptor α from oxidative stress-induced suppression and is a protein biomarker of favorable prognosis in breast cancer
Breast Cancer Research volume 16, Article number: R79 (2014)
Peroxiredoxin-1 (PRDX1) is a multifunctional protein, acting as a hydrogen peroxide (H2O2) scavenger, molecular chaperone and immune modulator. Although differential PRDX1 expression has been described in many tumors, the potential role of PRDX1 in breast cancer remains highly ambiguous. Using a comprehensive antibody-based proteomics approach, we interrogated PRDX1 protein as a putative biomarker in estrogen receptor (ER)-positive breast cancer.
An anti-PRDX1 antibody was validated in breast cancer cell lines using immunoblotting, immunohistochemistry and reverse phase protein array (RPPA) technology. PRDX1 protein expression was evaluated in two independent breast cancer cohorts, represented on a screening RPPA (n = 712) and a validation tissue microarray (n = 498). In vitro assays were performed exploring the functional contribution of PRDX1, with oxidative stress conditions mimicked via treatment with H2O2, peroxynitrite, or adenanthin, a PRDX1/2 inhibitor.
In ER-positive cases, high PRDX1 protein expression is a biomarker of improved prognosis across both cohorts. In the validation cohort, high PRDX1 expression was an independent predictor of improved relapse-free survival (hazard ratio (HR) = 0.62, 95% confidence interval (CI) = 0.40 to 0.96, P = 0.032), breast cancer-specific survival (HR = 0.44, 95% CI = 0.24 to 0.79, P = 0.006) and overall survival (HR = 0.61, 95% CI = 0.44 to 0.85, P = 0.004). RPPA screening of cancer signaling proteins showed that ERα protein was upregulated in PRDX1 high tumors. Exogenous H2O2 treatment decreased ERα protein levels in ER-positive cells. PRDX1 knockdown further sensitized cells to H2O2- and peroxynitrite-mediated effects, whilst PRDX1 overexpression protected against this response. Inhibition of PRDX1/2 antioxidant activity with adenanthin dramatically reduced ERα levels in breast cancer cells.
PRDX1 is shown to be an independent predictor of improved outcomes in ER-positive breast cancer. Through its antioxidant function, PRDX1 may prevent oxidative stress-mediated ERα loss, thereby potentially contributing to maintenance of an ER-positive phenotype in mammary tumors. These results for the first time imply a close connection between biological activity of PRDX1 and regulation of estrogen-mediated signaling in breast cancer.
Molecular classification of breast cancer cases using biomarkers in tumor cells provides an opportunity for the implementation of effective targeted treatment modalities, such as the expression of estrogen receptor (ER) and responses to endocrine therapy. However, despite the benefits gained by endocrine treatment, the long-term effectiveness of such targeted approaches is still unsatisfactory. Identifying novel biomarkers predictive of clinical outcome is desirable in order to guide clinicians in selecting new treatment options and monitoring the treatment response of patients, as well as potentially identifying new mechanisms that could lead to combinations with hormonal therapy.
Peroxiredoxins are a ubiquitous family of antioxidant enzymes, known to catalyze peroxide reduction to balance cellular hydrogen peroxide (H2O2) levels, which is essential for cell signaling and metabolism [1, 2]. Of particular interest is the mammalian isoform, peroxiredoxin 1 (PRDX1), which is a multifunctional protein originally identified as an intracellular scavenger of H2O2. It has been also shown to act as a molecular chaperone with the ability to modulate the actions of numerous molecules [4–8], a regulator of transcription , or as an immunomodulator . There are multiple reports of differential PRDX1 expression in human malignancies (reviewed in ). However, the diversity of PRDX1 functions makes the prediction of its role in human tumors difficult. Further validation is necessary to address the importance of PRDX1 protein expression in each cancer type.
The specific role for PRDX1 in breast cancer is controversial. In an earlier study, PRDX1 protein was found to be overexpressed in malignant versus normal tissues in 21 of 24 patients, but no significant relationship was found between PRDX1 overexpression and common clinicopathological parameters of breast cancer . In a cohort of 475 patients, it was reported that PRDX1 protein expression in breast cancer was not significantly associated with any clinicopathological parameter . However, other studies have shown that overexpression of PRDX1 mRNA in human breast carcinoma is associated with higher tumor grade , and high expression of cytoplasmic PRDX1 protein correlated with increased risk of local recurrence after radiotherapy .
Conversely, several lines of evidence suggest that PRDX1 may act as a tumor suppressor in breast cancer. Prdx1-deficient mice suffer from shortened survival due to development of hemolytic anemia and multiple tumors, including mammary carcinomas . PRDX1, acting as a chaperone, interacts with the c-Myc oncogene and suppresses its transcriptional activity . Another proposed function for PRDX1 in breast cancer is as a sensor in H2O2-mediated stress-induced senescence . Furthermore, Cao et al. have shown that PRDX1 protects the tumor suppressive function of PTEN phosphatase, likely due to the presence of a reactive oxygen species (ROS) sensitive cysteine in the catalytic domain, and reduces predisposition of genetically modified mice to develop Ras-induced mammary tumors . Accordingly, a recent study suggests that high PRDX1 expression appears to be associated with less aggressive breast cancers .
Importantly, a number of the above biomarker studies suffer from shortcomings such as lack of appropriate antibody validation, small cohort size and/or the absence of a molecular explanation supporting the clinical data. Thus, there is an ongoing need for properly designed studies on the role of PRDX1 in breast cancer that follow the REMARK guidelines for prognostic biomarkers . This is especially relevant in light of PRDX1 being considered a therapeutic target in other cancer types, as well as the recent development of adenanthin as a chemical inhibitor of PRDX1/2 .
Herein, we demonstrate a robust approach for interrogating the role of PRDX1 as a putative protein biomarker in breast cancer. We identify PRDX1 expression levels as an independent marker of favorable outcome in ER-positive tumors and elucidate a unique role for PRDX1 in maintaining ERα expression in breast cancer cells subjected to oxidative stress.
ZR-75-1, T47D, MCF7 and SKBR3 cell lines were purchased from the European Collection of Cell Cultures (Wiltshire, UK). All cell lines were maintained through continuous passaging, and were confirmed to be free of contamination by Mycoplasma spp. Cells were maintained in DMEM (ZR-75-1 cell line) or RPMI-1640 (other cell lines) media (Sigma-Aldrich, St. Louis, MO, USA), with 10% FBS (Sigma-Aldrich), 100 U/mL penicillin, 100 μg/mL streptomycin (Gibco, Rockville, MD, USA) and 1.46 mg/mL L-glutamine (Gibco). Additionally, the growth medium for ZR-75-1 was supplemented with 1 nM β-estradiol (Sigma-Aldrich), and did not contain sodium pyruvate, which mediates elimination of H2O2 from the culture medium . Tissue culture experimental techniques are further described in the Supplementary Methods (Additional file 1).
Adenanthin has been generated as previously described . H2O2 and peroxynitrite were obtained from Sigma-Aldrich and Millipore (Billerica, MA, USA), respectively.
Antibody validation and immunohistochemistry
Antibody generation against PRDX1 was as described previously . The Human Protein Atlas (HPA) Consortium carried out the initial quality control of the polyclonal anti-PRDX1 antibody (HPA007730) via optimization and testing on a variety of tissues (48 normal tissues and 16 cancer tissues) . Immunoblotting and immunohistochemistry procedures are described in Supplementary Methods (Additional file 1).
Clinical materials originating from three independent cohorts of breast cancer patients were utilized in this study. Demographic and clinical characteristics for all cohorts are presented in this study are described in Supplementary Table S1 (Additional file 2).
Cohort 1 was represented on a reverse phase protein array (RPPA) containing protein extracts from 58 breast cancer cell lines and 998 human breast tumors, with available clinicopathological data for 712 cases. The clinical samples were collected at M. D. Anderson Cancer Center (MDACC) Houston, TX, USA, Hospital Clinico Universitario de Valencia, Spain, University of British Columbia, Vancouver, BC, Canada and Baylor College of Medicine, Houston, TX, USA . Complete clinical information was available for 574 patients. All tumors in this training set were collected by excision during their primary surgery, followed by freezing of the tissue. Tumor content was verified by histopathology. All tissues were collected under Institutional Review Board (IRB)-approved laboratory protocols, awarded by the M. D. Anderson Cancer Center IRB, University of British Columbia IRB, and the Hospital Clinico Universitario de Valencia IRB. Patients consented to bank their specimens. As this was a retrospective study, each IRB provided a waiver of informed consent.
Cohort 2 consisted of a tissue microarray (TMA) with 498 consecutive invasive breast cancer cases (442 in final analysis) diagnosed at the Department of Pathology, Malmö University Hospital, between 1987 and 1992 . The median age at diagnosis was 65 years (range, 27 to 96) and the median follow-up time was 11 years (range, 0 to 17). Two hundred and sixty-three patients were dead at the last follow-up (December 2004), 90 of whom were considered to be as a direct result of breast cancer (breast cancer-specific death). Complete endocrine treatment data were available for 379 patients, 160 of whom received adjuvant tamoxifen. Information on adjuvant chemotherapy was available for 382 patients, of whom 23 patients received treatment. The study has been approved by the Ethics Committee at Lund University. Informed consent was obtained for all included patients and opting out was an option.
Cohort 3 was represented on a RPPA consisting of 410 primary breast tumors collected by The Cancer Genome Atlas (TCGA) Consortium. These frozen primary tumor specimens collected from newly diagnosed patients with invasive breast adenocarcinoma undergoing surgical resection and who had received no prior treatment for their disease (chemotherapy or radiotherapy). Owing to the short median overall follow-up (20 months) and the small number of overall survival events (44 out of 410), survival analysis was not carried out on this cohort. This cohort was used solely to correlate quantitative levels of PRDX1 protein expression with expression of 180+ other proteins assessed on the same array. The TCGA project collects high-quality breast tumor samples and makes available the clinical information, molecular/genomic profiling data, and histopathology slide images on the TCGA data portal . The TCGA data is organized into two categories: one that is openly accessible to the public and one that has controlled access, available only to qualified researchers obligated to secure the data. The open access data set contains only information that is not individually unique and does not pose a risk of patient re-identification. All the data used within this manuscript was obtained from the open access data set and has passed the criteria for unrestricted publication with the following statement ‘No restrictions; all data available without limitations’ listed at the publication guidelines section of the TCGA data portal .
Reverse phase protein array analysis
Protein was extracted from tumor tissue and cell lines and probed for protein expression by reverse phase protein array (RPPA) analysis as previously described [24, 27–30]. RPPA analysis was completed independently for cohorts 1 and 3. The technique is further described in the Supplementary Methods (Additional file 1).
Evaluation of immunohistochemical staining
Slides were scanned at 20X magnification using a ScanScope XT slide scanner (Aperio Technologies, Vista, CA, USA). The Spectrum Analysis algorithm package, ImageScope analysis software and Color Deconvolution algorithm (version 9; Aperio Technologies.) were applied to quantify immunohistochemical (IHC) staining. These algorithms were used to calculate the average positive intensity (API), as well as the area of positive staining, and the percentage of weak (1+), medium (2+), and strong (3+) positive staining. The final API was subtracted from 255, as these intensity ranges on an 8-bit scale of 0 to 255 (black to white, respectively). The maximum value from both cores for each patient was used for statistical analysis.
All statistical analysis was carried out with PASW Statistics version 20 and R Project for Statistical Computing. Spearman’s rho test was used to compare protein expression across the recombinant cell line series in the immunoblotting and RPPA setting. In cohorts 1 and 2, the median PRDX1 expression level was used for stratification into high and low PRDX1 expression. Pearson’s χ2 test and Fisher’s exact test were used to evaluate associations between protein expression and clinicopathological variables. Kaplan-Meier, univariate and multivariate Cox regression analyses were used to illustrate differences between recurrence-free survival (RFS), breast cancer-specific survival (BCCS), and overall survival (OS) according to PRDX1 expression. In cohort 3, the Pearson’s correlation test was used to determine the correlation between PRDX1 and expression of other proteins, and the two-sided t test was used to identify proteins co-regulated between the lower and upper quartile of PRDX1 protein expression cases. In all experiments, a two-tailed test value of less than 0.05 was considered significant.
Validation of PRDX1 antibody across different protein quantification platforms
In light of conflicting results regarding the prognostic relevance of PRDX1 expression in breast cancer, a fundamental step for our study was comprehensive validation of the anti-PRDX1 antibody. Antibody specificity was confirmed in several breast cancer cell lines (T47D, ZR-75-1 and SKBR3), whereby PRDX1 expression was modified using short hairpin loop RNA (shRNA)-mediated gene knockdown and overexpression of cDNA encoding V5-tagged PRDX1, before antibody validation by immunoblotting (Figure 1A and C; complete gel displayed in Figure S1A in Additional file 3), RPPA analysis (Figure 1B) and IHC (Figure 1D and E). IHC performed on formalin-fixed paraffin-embedded (FFPE) SKBR3 cells revealed a decrease in staining intensity in cells expressing either of two shRNA molecules against PRDX1 (Figure 1D, lower panel) compared to non-targeting or parental cell controls. A significant decrease was seen in percentage 3,3-diaminobenzidine (DAB) positivity of these knockdown cells (Figure 1E). This observation confirmed the specificity of the antibody in the IHC setting prior to staining of clinical specimens. Figure 1F shows representative examples of different intensities of DAB staining, that is, expression of PRDX1 protein on TMA cores. PRDX1 protein expression was found to be predominantly cytoplasmic throughout the cores (Figure 1G). An automated algorithm was used to develop a quantitative scoring model of PRDX1 protein expression, with the respective mark-up image shown. To rule out the possibility of the antibody binding to PRDX2, a protein with high homology for PRDX1, cell lines overexpressing a pLenti6-PRDX2-V5 plasmid were generated. Modulation of PRDX1 expression levels did not affect PRDX2 protein expression, and vice versa (Figure S1D in Additional file 3). An additional PRDX1-targeting antibody was tested ; however, this antibody did not satisfactorily detect differential protein expression compared to mRNA expression measured in the shRNA-expressing cell lines (Figure S1B-C in Additional file 3). These extensive validation steps allow us a high level of certainty that the antibody used is specific to PRDX1 in all techniques used throughout the study.
Identification of PRDX1 protein as a biomarker of good prognosis in ER-positive breast tumors
RPPA technology is a particularly useful tool to aid in the identification and validation of protein and phosphoprotein biomarkers using limited amounts of protein from clinical samples. PRDX1 protein expression was assessed on a RPPA cohort with clinical data available for 712 primary human breast tumors. Protein expression data was dichotomized based on the median PRDX1 expression values. High PRDX1 expression was associated with low tumor grade (P <0.001), older age at diagnosis (P <0.001) and human epidermal growth factor receptor 2 (Her2) negativity (P = 0.001), while it displayed a borderline association with positive ER status (P = 0.05) (Table S2 in Additional file 2).
Kaplan-Meier analysis demonstrated that increased levels of PRDX1 protein expression were associated with improved RFS (P = 0.004), OS (P = 0.036) and BCSS (P = 0.005). Interestingly, when various subcohorts were analyzed, high PRDX1 was associated with improved RFS (P = 0.010) and BCSS (P = 0.013) only in the subgroup of ER-positive tumors (Figure 2). Univariate Cox regression analysis demonstrated that, in these ER-positive cases, PRDX1 was associated with improved RFS (hazard ratio (HR) = 0.62, 95% confidence interval (CI) = 0.43 to 0.90, P = 0.011) and BCSS (HR = 0.59, 95% CI = 0.39 to 0.90, P = 0.014) (Table 1). When evaluated by a multivariate Cox proportional hazards model, PRDX1, as assessed by RPPA, was not an independent predictor of RFS or OS (Table 1). However, high PRDX1 protein levels trended toward a significant association with improved BCSS (HR = 0.56, 95% CI = 0.31 to 1.01, P = 0.055).
PRDX1 protein levels, as assessed by IHC, is an independent predictor of prognosis in ER-positive breast tumors
Although RPPA technology is an ideal platform for initial biomarker discovery, it was necessary to validate these findings in an independent cohort using a more clinically applicable platform, namely IHC (cohort 2). Due to core loss during sectioning, tumors from 442 (88.8%) patients were suitable for analysis. IHC staining was scored on a continuous scale based on staining intensity (Figure 1F), and the median expression level was used to stratify the cohort into high and low PRDX1 protein staining. On the basis of this classification, any possible associations between protein expression and a variety of well-defined clinicopathological variables in the TMA cohort were investigated (Table S3 in Additional file 2). PRDX1 protein expression correlated with smaller tumor size (P = 0.011), low tumor grade (P = 0.002), negative Ki67 status (P = 0.004) and lobular subtype (P = 0.003), whilst there was a borderline significant correlation with positive ER status (P = 0.05).
The relationship between differential expression of PRDX1 and patient survival was subsequently examined. In the overall cohort, increased levels of PRDX1 protein trended toward an improved RFS (P = 0.061), OS (P = 0.100) and BCSS (P = 0.068), but these values were not significant. The positive correlation between high PRDX1 expression and favorable prognosis was again limited to the ER-positive subgroup of cases. Kaplan-Meier analysis demonstrated that, in the ER-positive subgroup, increased levels of PRDX1 protein were associated with an improved RFS (P = 0.011), OS (P = 0.010) and BCSS (P = 0.002) (Figure 3). To compare the prognostic impact of PRDX1 with established factors, Cox regression analysis was performed (Table 2). Univariate Cox regression analysis confirmed that, in ER-positive tumors, high PRDX1 expression associated with improved RFS (HR = 0.60, 95% CI = 0.40 to 0.89, P = 0.012), BCSS (HR = 0.69, 95% CI = 0.52 to 0.92, P = 0.010) and OS (HR = 0.44, 95% CI = 0.24 to 0.75, P = 0.003). Importantly, multivariate analysis within the ER-positive subset showed that PRDX1 was a significant independent predictor of improved RFS (HR = 0.62, 95% CI = 0.40 to 0.96, P = 0.032), BCSS (HR = 0.44, 95% CI = 0.24 to 0.79, P = 0.006) and OS (HR = 0.61, 95% CI = 0.44 to 0.85, P = 0.004), when adjusted for well-established variables such as tumor size, grade, age, nodal, progesterone receptor (PR), Her2 and Ki67 status (Table 2).
Screening for correlations between PRDX1 and cancer-related signaling proteins in clinical breast cancer samples
RPPA technology can be used to explore cellular signaling pathways activated during cancer progression, such as proteins involved in cellular functions such as growth, proliferation and apoptosis . Utilizing an independent cohort of 410 patients (cohort 3), quantitative protein and phosphoprotein expression levels (165 proteins assessed) were screened to identify alterations in response to differential PRDX1 protein expression. This cohort was stratified into ER-positive and ER-negative cohorts based on the quantitative level of ERα protein expression (Figure 4A). This analysis showed a large number of the proteins as significantly correlated with PRDX1 protein expression in the ER-positive cohort (Table S4 in Additional file 2). Thus, a more stringent approach was necessary to refine the proteins altered in response to differential PRDX1 expression levels, whereby proteins altered between the highest quartile (75th percentile and above) versus the lowest quartile (up to 25th percentile) of PRDX1 expression were selected (Figure 4B). A statistically significant positive correlation was seen between PRDX1 protein and ERα (fold change (FC) = 1.54, P = 0.017). Other proteins that were altered include Claudin-7 (FC = 1.60, P <0.001), HSP70 (FC = 0.61, P <0.001), Collagen VI (FC = 0.61, P = 0.009) and pThr202/pTyr204-MAPK (FC = 0.65, P = 0.008) (Table 3) (represented graphically in Figure 4C). Interestingly, several of the proteins which correlated with PRDX1 expression are known to be regulated by oxidative stress and/or play a role in signaling in the context of ER-positive breast cancer.
PRDX1 protects against oxidative stress-induced ERα suppression
Since the hypoxic environment of tumors is likely to contain high levels of ROS , induction of oxidative stress in cell lines may be a close mimic of intra-tumoral conditions. In addition, oxidative stress is a very well-known modulator of several oncogenic signaling pathways, including the Akt-mediated pathway, where effects of PRDX1 have been already described in mouse mammary tissue . Therefore, we examined whether breast cancer cell lines exposed to oxidative stress had altered levels of these estrogen and breast cancer signaling proteins, and if modulation of PRDX1 expression could alter any oxidative stress-induced signaling changes. Increased oxidative stress was accomplished via treatment with exogenous H2O2 or peroxynitrite. The ER-positive ductal carcinoma cell line, ZR-75-1, was primarily utilized, being a standard model of ER-positive and estrogen-dependent tumors, with low-level oncogenic signaling [32, 33]. In the previous RPPA screen, we observed that ERα and pThr202/pTyr204-MAPK were associated with PRDX1 protein expression in ER-positive tumors (cohort 3). Thus, we set about validating these findings in our model cell line. We observed that H2O2 treatment resulted in decreased ERα protein expression in parental ZR-75-1 cells with suppression of the ER activity surrogate, PR, as well as enhanced phosphorylation of serine 473 on Akt, another oncogenic signaling molecule (Figure S2A in Additional file 4).
Subsequent studies demonstrated that oxidative stress-mediated suppression of ERα can be regulated by inducing changes in PRDX1 protein expression. In two independently transduced ZR-75-1 cell lines stably expressing different PRDX1-targeting shRNAs, PRDX1 knockdown-enhanced H2O2-mediated suppression of ERα protein (suppressed at 12.5 μM H2O2), relative to parental and non-targeting control (NTC) expressing cells (50 μM H2O2). Conversely, PRDX1 overexpression rendered the cells resistant to suppression of ERα by oxidative stress (Figure 5A). PRDX1 knockdown also enhanced oxidative stress-induced Akt phosphorylation (Ser473) with phosphorylation occurring at a lower H2O2 concentration (Figure 5B). This effect was also seen when cells were treated with the reactive nitrogen species, peroxynitrite (Figure 5C), which was in accordance with previous observations in other ER-positive breast cancer cell lines . Although H2O2 induced a decrease of E-cadherin protein expression in breast cancer cells  (Figure S2A in Additional file 4), these changes were only minimally affected by changes in PRDX1 expression. Also, H2O2 induced only marginal or no changes in pThr202/pTyr204-MAPK (ERK1/2) and ERβ expression regardless of PRDX1 expression levels [36, 37] (Figure 5). This is consistent with the selectivity of the association between PRDX1 and ER expression. ER activity was also assessed using an estrogen transcriptional response element (ERE)-luciferase reporter assay, whereby PRDX1 knockdown could potentiate oxidative stress-mediated suppression of ERα activity (25 μM H2O2: P = 0.027; 50 μM: P = 0.037; 100 μM: P = 0.002) (Figure S2B in Additional file 4). In order to determine if PRDX1 expression was driven by ERα promoter activity, we assessed PRDX1 protein expression in ZR-75-1 cells with or without stimulation with the ER ligand, 17β-estradiol. No change in PRDX1 protein content was seen following 17β-estradiol stimulation, and as expected, ERα protein is suppressed upon estradiol stimulation (Figure S2C in Additional file 4). Although ESR1 mRNA expression is decreased by induction of oxidative stress (Figure S3A in Additional file 5), PRDX1 silencing does not enhance this suppression. Alternatively in PRDX1-silenced ZR-75-1 cells, an ESR1 induction is seen at lower H2O2 concentrations, which returns to baseline levels above 50 μM H2O2. Importantly, Supplementary Figure S3B (Additional file 5) demonstrates that ERα protein levels diminished in these PRDX1-silenced cells across all H2O2 concentrations used, which suggests that PRDX1 differentially regulates ERα mRNA and protein expression. ZR-75-1 cells were treated with H2O2, and a transcription inhibitor (actinomycin D) (Figure S3C in Additional file 5) or proteasome inhibitor (MG132) in order to determine if oxidative stress affects ERα protein stability rather than mRNA levels. These results showed that inhibition of proteasomal degradation using MG132 prevents oxidative stress-induced ERα suppression and this inhibition is enhanced in the absence of PRDX1 expression (Figure S3D in Additional file 5), which suggests that the proteasomal degradation of ERα via is more active under low-PRDX1 conditions. This implies that PRDX1 may protect ERα from oxidative stress-induced suppression of the protein itself, rather than transcriptional/mRNA stability regulation. In addition, silencing of PRDX1 in ZR-75-1 and T47D cells did not alter the cell proliferation and apoptosis (Figure S4A-D in Additional file 6).
As expected, PRDX1 shRNA-expressing cells showed a reduced potential to metabolize extracellular H2O2, similar to the effects of adenanthin, a chemical inhibitor of PRDX1 and PRDX2 antioxidant activity  (Figure S2C in Additional file 4). Similar to the effect of exogenous H2O2 treatment, inhibition of PRDX1 antioxidant activity using adenanthin suppressed ERα levels (Figure 5D; reducing gel). Interestingly, treatment of T47D and ZR-75-1 cell lines with adenanthin resulted in a decrease of PRDX1 dimerization with a dose-dependent increase in PRDX1 monomer levels (Figure 5D; non-reducing gel), which has not been previously reported. Silencing of PRDX1 or PRDX2 diminishes the adenanthin-induced suppression of ERα protein (Figure S5 in Additional file 7). This suggests that PRDX1 and PRDX2 might both have similar and/or partially overlapping effects in protecting ERα from degradation. Importantly for this study, however, adenanthin was initially described as a more potent inhibitor of PRDX1 than PRDX2, as adenanthin had a significantly lower half-maximum inhibitory (IC50) values for PRDX1 (1.5 μM) compared to PRDX2 (15 μM) . Indeed, MCF7 cells, which express levels of PRDX1 comparable to ZR-75-1 and T47D, but significantly more PRDX2 protein, require higher concentrations of adenanthin in order to suppress ERα (Figure S5D-E in Additional file 7). This observation suggests that PRDX1 is a primary target for adenanthin, and that PRDX2 can partially substitute for PRDX1-mediated protection of ERα. This potentially opens a new avenue for further investigation of PRDX2 in ER-positive breast cancer.
In order to improve the outcomes for patients, advances in understanding of the pathophysiology of breast cancer combined with the identification of proteins and molecular pathways that affect key proliferation and survival mechanisms are needed. The discovery and validation of these molecular biomarkers requires the integration of several platforms, and antibody-based proteomics allows high-throughput identification and validation of candidate biomarkers (reviewed in ).
The aim of this study was to elucidate the association between PRDX1 protein levels and survival in two independent breast cancer cohorts, using two orthologous methods of assessing protein expression levels, namely RPPA and TMA technology. With RPPA, protein lysates are denatured and immobilized to the slide, a similar approach to immunoblotting, and it offers a more quantitative approach for profiling protein expression levels. This proteomic technique has become extremely useful for screening tumor lysates in respect to expression of candidate protein biomarkers. TMAs allow for the IHC-based validation of protein biomarkers, where one could examine proteins in their native non-denatured state and, in particular, to assess spatial pattern of expression which is lost in the RPPA approach. Therefore, both techniques used in this study complement and support each other.
After initially screening a large cohort of breast cancer patients to assess the prognostic potential of PRDX1, we observed that in the ER-positive subset of tumors, high PRDX1 protein expression was associated with improved survival. While RPPA analysis is useful for testing the prognostic ability of biomarkers on limited amounts of tissue, we set about validating these findings using IHC in an independent cohort. Once again, high PRDX1 expression was associated with improved RFS, OS and BCSS in ER-positive patients. In this case, PRDX1 was also an independent predictor of improved survival when adjusted for other clinicopathological variables.
This is the first report showing a functional connection between expression of PRDX1 and ERα in breast cancer. As PRDX1 is a natural antioxidant enzyme, we were interested in further elucidating the links between PRDX1, ROS and regulation of ERα levels in breast cancer. ROS are endogenously produced in all metazoan organisms as a result of aerobic respiration. ROS are essential regulators of cell signaling pathways; however, oxidative stress can occur if ROS production exceeds the capacity of the antioxidant machinery, of which the peroxiredoxin enzymes constitute important members. It has been suggested that the role of oxidative stress in ER-positive breast cancer may be different than in other tumor types . Several studies have demonstrated in vitro that mitochondrial ROS can be induced by physiological estrogen concentrations [40, 41]. As oxidative metabolism of estrogen and subsequent formation of ROS are key estrogen-related carcinogenic mechanisms [42, 43], ROS scavenging systems are expected to play a particularly important role in ER-positive malignancies.
Utilizing an independent cohort of patients (cohort 3), we screened for cancer-related signaling proteins altered in PRDX1 positive tumors. ERα protein is upregulated in PRDX1-high tumors. Although this correlation is of modest potency, it supports our mechanistic observations in vitro, as regulation of ERα expression in cells depends on a multiplicity of factors, with PRDX1-mediated protection representing only one. This screening approach also identified other cancer progression-related proteins differentially regulated by PRDX1 in the ER-positive cohort. PRDX1 is positively correlated with the tight junction protein, Claudin-7 , while negatively correlated with several proteins involved in malignant cell transformation and epithelial-mesenchymal transition (EMT): the pro-EMT molecule, Collagen VI, ; heat shock chaperone protein, HSP-70 ; and the phosphorylated form of ERK1/2 (pT202/pY204). These results suggest that PRDX1 may interact with different intracellular ligands within ER-positive tumors, possibly explaining the association of PRDX1 to improved outcomes amongst the ER-positive tumor subtypes. Further studies may elucidate the functional role of the interactions between PRDX1 and these proteins.
Our in vitro studies suggest that PRDX1 may play a role as a regulator of the balance between ERα-mediated and oncogene-induced growth patterns in this disease. Specifically, PRDX1 helps to maintain ERα protein levels under oxidative stress, and inhibits the activation of Akt under oxidative stress. This function may be particularly interesting due to the association between PI3K pathway hyperactivity and lower ER levels and activity in ER-positive breast cancer . Although PRDX1 can regulate PTEN , the phosphatase that acts upstream of Akt, this mechanism is not relevant in ZR-75-1 cells, as these cells are PTEN-deficient . Our results suggest that PRDX1 protects ERα indirectly through scavenging of H2O2, as inhibition of antioxidant activity using adenanthin suppresses ERα expression. In addition, the oligomeric state of cellular PRDX1 is a key indicator of PRDX1 function, with dimers primarily acting as an antioxidant scavenger and decameric PRDX1 functioning as a molecular chaperone [49–51]. However, follow-up experiments using PRDX1 mutants would further tease out this mechanism. PRDX1 C51/172S mutants are unable to form dimeric the PRDX1 structures required for antioxidant activity , while the PRDX1 mutant (C83S) is incapable of producing decameric PRDX1. Treatment of both PRDX1 mutant cell lines with H2O2 would further allow the elucidation of the role of PRDX1 in the protection of ERα. Furthermore, assessment of ERα expression after adenanthin treatment in the presence and absence of H2O2 could elucidate this mechanism.
Due to high homology between PRDX1 and PRDX2, we also assessed the ability of PRDX1 in maintaining ERα protein levels in absence of PRDX2. This approach showed that both proteins can independently contribute in vitro to protecting ERα protein expression. Further in vivo studies would elucidate the functional overlap between these two peroxiredoxins in breast cancer.
Recent studies identified an oxidant-sensitive subset of estrogen/ER-responsive breast cancer genes linked to cell growth and invasion pathways that was associated with loss of progesterone receptor and earlier disease-specific mortality . Assuming that oxidative stress contributes to the development of an aggressive subset of primary ER-positive breast cancers, these findings suggest that PRDX1 may be able to protect against these oxidative stress-induced changes in cellular phenotype. It is important to notice that associations with PRDX1 and the endocrine system have been recently described in prostate cancer, including effects of PRDX1 on androgen receptor activity [8, 54] and the response to anti-androgen therapies . Along with our report, this suggests a key role for PRDX1 in regulation of the activity of steroid hormone-related pathways. Interestingly, it has been suggested that resistance to endocrine therapy may be mediated, in part, by ROS-mediated dysregulation of estrogen signaling pathways (reviewed in ).
Previous studies on PRDX1 expression did not find an association with clinicopathological features or prognosis in human breast cancer [12, 13]. Potentially, the antibodies used by these studies may lack specificity for PRDX1 or alternatively, in contrast to the large sample sets studied herein, insufficient sample numbers and power may have precluded detection of associations with outcomes. Significantly, one of the above mentioned studies reports a strong nuclear pattern of PRDX1 expression as determined by IHC staining (Figure 1A in ), compared to our observation where PRDX1 is predominantly cytoplasmic. This discrepancy underscores the need for rigorous testing of antibodies in biomarker studies. Our antibody validation model includes testing using recombinant cell lines and tumor tissues across several platforms of protein quantification (immunoblotting, RPPA, cell pellet arrays, TMAs). Altogether, this study provides a model to accelerate the validation of potential biomarkers on the translational journey to the clinic.
In conclusion, we have identified PRDX1 protein as an independent predictor of favorable prognosis in ER-positive breast carcinomas. Based on our accumulated data, we hypothesize that PRDX1 shields the dependence of mammary tumors on estrogen-mediated growth stimulation, which eventually is of benefit for the patient. In this regard, PRDX1 expression may be utilized in the therapeutic decision-making process in this disease in the future. Moreover, our results suggest that any prospective PRDX1 inhibitors should be explored with caution in ER-positive breast cancer due to the potential to convert tumor cells to a more aggressive phenotype with a worsened outcome.
2,2’-azino-bis(3-ethylbenzothiazoline-sulfonic acid) diammonium salt solution
average positive intensity
breast cancer-specific survival
Dulbecco’s modified Eagle’s medium
estrogen transcriptional response element
fetal bovine serum
green fluorescent protein
human epidermal growth factor receptor 2
Human Protein Atlas
M. D. Anderson Cancer Center
phosphate-buffered saline with 0.1% Tween-20
reactive oxygen species
reverse phase protein arrays
real-time polymerase chain reaction
sodium dodecyl sulfate
short hairpin loop RNA
tris-buffered saline with 0.1% Tween-20
The Cancer Genome Atlas
Gough DR, Cotter TG: Hydrogen peroxide: a Jekyll and Hyde signalling molecule. Cell Death Dis. 2011, 2: e213-10.1038/cddis.2011.96.
Forman HJ, Maiorino M, Ursini F: Signaling functions of reactive oxygen species. Biochemistry. 2010, 49: 835-842. 10.1021/bi9020378.
Rhee SG, Kang SW, Jeong W, Chang TS, Yang KS, Woo HA: Intracellular messenger function of hydrogen peroxide and its regulation by peroxiredoxins. Curr Opin Cell Biol. 2005, 17: 183-189. 10.1016/j.ceb.2005.02.004.
Jang HH, Lee KO, Chi YH, Jung BG, Park SK, Park JH, Lee JR, Lee SS, Moon JC, Yun JW, Choi YO, Kim WY, Kang JS, Cheong GW, Yun DJ, Rhee SG, Cho MJ, Lee SY: Two enzymes in one; two yeast peroxiredoxins display oxidative stress-dependent switching from a peroxidase to a molecular chaperone function. Cell. 2004, 117: 625-635. 10.1016/j.cell.2004.05.002.
Turner-Ivey B, Manevich Y, Schulte J, Kistner-Griffin E, Jezierska-Drutel A, Liu Y, Neumann CA: Role for Prdx1 as a specific sensor in redox-regulated senescence in breast cancer. Oncogene. 2013, 32: 5302-5314. 10.1038/onc.2012.624.
Cao J, Schulte J, Knight A, Leslie NR, Zagozdzon A, Bronson R, Manevich Y, Beeson C, Neumann CA: Prdx1 inhibits tumorigenesis via regulating PTEN/AKT activity. EMBO J. 2009, 28: 1505-1517. 10.1038/emboj.2009.101.
Kim YJ, Lee WS, Ip C, Chae HZ, Park EM, Park YM: Prx1 suppresses radiation-induced c-Jun NH2-terminal kinase signaling in lung cancer cells through interaction with the glutathione S-transferase Pi/c-Jun NH2-terminal kinase complex. Cancer Res. 2006, 66: 7136-7142. 10.1158/0008-5472.CAN-05-4446.
Park SY, Yu X, Ip C, Mohler JL, Bogner PN, Park YM: Peroxiredoxin 1 interacts with androgen receptor and enhances its transactivation. Cancer Res. 2007, 67: 9294-9303. 10.1158/0008-5472.CAN-07-0651.
Wang X, He S, Sun JM, Delcuve GP, Davie JR: Selective association of peroxiredoxin 1 with genomic DNA and COX-2 upstream promoter elements in estrogen receptor negative breast cancer cells. Mol Biol Cell. 2010, 21: 2987-2995. 10.1091/mbc.E10-02-0160.
Riddell JR, Wang XY, Minderman H, Gollnick SO: Peroxiredoxin 1 stimulates secretion of proinflammatory cytokines by binding to TLR4. J Immunol. 2010, 184: 1022-1030. 10.4049/jimmunol.0901945.
Ishii T, Warabi E, Yanagawa T: Novel roles of peroxiredoxins in inflammation, cancer and innate immunity. JCBN. 2012, 50: 91-105.
Noh DY, Ahn SJ, Lee RA, Kim SW, Park IA, Chae HZ: Overexpression of peroxiredoxin in human breast cancer. Anticancer Res. 2001, 21: 2085-2090.
Karihtala P, Mantyniemi A, Kang SW, Kinnula VL, Soini Y: Peroxiredoxins in breast carcinoma. Clin Cancer Res. 2003, 9: 3418-3424.
Cha MK, Suh KH, Kim IH: Overexpression of peroxiredoxin I and thioredoxin1 in human breast carcinoma. JECCR. 2009, 28: 93-
Woolston CM, Storr SJ, Ellis IO, Morgan DA, Martin SG: Expression of thioredoxin system and related peroxiredoxin proteins is associated with clinical outcome in radiotherapy treated early stage breast cancer. Radiother Oncol. 2011, 100: 308-313. 10.1016/j.radonc.2011.05.029.
Neumann CA, Krause DS, Carman CV, Das S, Dubey DP, Abraham JL, Bronson RT, Fujiwara Y, Orkin SH, Van Etten RA: Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression. Nature. 2003, 424: 561-565. 10.1038/nature01819.
Egler RA, Fernandes E, Rothermund K, Sereika S, de Souza-Pinto N, Jaruga P, Dizdaroglu M, Prochownik EV: Regulation of reactive oxygen species, DNA damage, and c-Myc function by peroxiredoxin 1. Oncogene. 2005, 24: 8038-8050. 10.1038/sj.onc.1208821.
Pei-Jou Chua E-HL, Chunhua G, George W-C Y, Puay-Hoon T, Boon-Huat B: Clinicopathological correlation of peroxiredoxin I in breast cancer. Proceedings of the World Medical Conference. 2011, Prague, Czech Republic
Altman DG, McShane LM, Sauerbrei W, Taube SE: Reporting recommendations for tumor marker prognostic studies (REMARK): explanation and elaboration. PLoS Med. 2012, 9: e1001216-10.1371/journal.pmed.1001216.
Liu CX, Yin QQ, Zhou HC, Wu YL, Pu JX, Xia L, Liu W, Huang X, Jiang T, Wu MX, He LC, Zhao YX, Wang XL, Xiao WL, Chen HZ, Zhao Q, Zhou AW, Wang LS, Sun HD, Chen GQ: Adenanthin targets peroxiredoxin I and II to induce differentiation of leukemic cells. Nat Chem Biol. 2012, 8: 486-493. 10.1038/nchembio.935.
Giandomenico AR, Cerniglia GE, Biaglow JE, Stevens CW, Koch CJ: The importance of sodium pyruvate in assessing damage produced by hydrogen peroxide. Free Radic Biol Med. 1997, 23: 426-434. 10.1016/S0891-5849(97)00113-5.
Uhlen M, Bjorling E, Agaton C, Szigyarto CA, Amini B, Andersen E, Andersson AC, Angelidou P, Asplund A, Asplund C, Berglund L, Bergstrom K, Brumer H, Cerjan D, Ekstrom M, Elobeid A, Eriksson C, Fagerberg L, Falk R, Fall J, Forsberg M, Bjorklund MG, Gumbel K, Halimi A, Hallin I, Hamsten C, Hansson M, Hedhammar M, Hercules G, Kampf C, et al: A human protein atlas for normal and cancer tissues based on antibody proteomics. Mol Cell Proteomics. 2005, 4: 1920-1932. 10.1074/mcp.M500279-MCP200.
Human Protein Atlas Data Portal: PRDX1/HPA007730. [http://www.proteinatlas.org/ENSG00000117450/antibody]
Gonzalez-Angulo AM, Hennessy BT, Meric-Bernstam F, Sahin A, Liu W, Ju Z, Carey MS, Myhre S, Speers C, Deng L, Broaddus R, Lluch A, Aparicio S, Brown P, Pusztai L, Symmans WF, Alsner J, Overgaard J, Borresen-Dale AL, Hortobagyi GN, Coombes KR, Mills GB: Functional proteomics can define prognosis and predict pathologic complete response in patients with breast cancer. Clin Proteomics. 2011, 8: 11-10.1186/1559-0275-8-11.
Helczynska K, Larsson AM, Holmquist Mengelbier L, Bridges E, Fredlund E, Borgquist S, Landberg G, Pahlman S, Jirstrom K: Hypoxia-inducible factor-2alpha correlates to distant recurrence and poor outcome in invasive breast cancer. Cancer Res. 2008, 68: 9212-9220. 10.1158/0008-5472.CAN-08-1135.
The Cancer Genome Atlas Data Portal. [https://tcga-data.nci.nih.gov/tcga/]
Hennessy BT, Lu Y, Poradosu E, Yu Q, Yu S, Hall H, Carey MS, Ravoori M, Gonzalez-Angulo AM, Birch R, Henderson IC, Kundra V, Mills GB: Pharmacodynamic markers of perifosine efficacy. Clin Cancer Res. 2007, 13: 7421-7431. 10.1158/1078-0432.CCR-07-0760.
Tibes R, Qiu Y, Lu Y, Hennessy B, Andreeff M, Mills GB, Kornblau SM: Reverse phase protein array: validation of a novel proteomic technology and utility for analysis of primary leukemia specimens and hematopoietic stem cells. Mol Cancer Ther. 2006, 5: 2512-2521. 10.1158/1535-7163.MCT-06-0334.
Hu J, He X, Baggerly KA, Coombes KR, Hennessy BT, Mills GB: Non-parametric quantification of protein lysate arrays. Bioinformatics. 2007, 23: 1986-1994. 10.1093/bioinformatics/btm283.
Stemke-Hale K, Gonzalez-Angulo AM, Lluch A, Neve RM, Kuo WL, Davies M, Carey M, Hu Z, Guan Y, Sahin A, Symmans WF, Pusztai L, Nolden LK, Horlings H, Berns K, Hung MC, van de Vijver MJ, Valero V, Gray JW, Bernards R, Mills GB, Hennessy BT: An integrative genomic and proteomic analysis of PIK3CA, PTEN, and AKT mutations in breast cancer. Cancer Res. 2008, 68: 6084-6091. 10.1158/0008-5472.CAN-07-6854.
Fruehauf JP, Meyskens FL: Reactive oxygen species: a breath of life or death?. Clin Cancer Res. 2007, 13: 789-794. 10.1158/1078-0432.CCR-06-2082.
Engel LW, Young NA, Tralka TS, Lippman ME, O'Brien SJ, Joyce MJ: Establishment and characterization of three new continuous cell lines derived from human breast carcinomas. Cancer Res. 1978, 38: 3352-3364.
Allegra JC, Lippman ME: Growth of a human breast cancer cell line in serum-free hormone-supplemented medium. Cancer Res. 1978, 38: 3823-3829.
Chua SH: PhD Thesis. Redox regulation of estrogen receptor alpha and sodium hydrogen exchanger 1 gene expression by hydrogen peroxide. 2011, National University of Singapore, NUS Graduate School for Integrative Sciences and Engineering
Cheng JC, Klausen C, Leung PC: Hydrogen peroxide mediates EGF-induced down-regulation of E-cadherin expression via p38 MAPK and snail in human ovarian cancer cells. Mol Endocrinol. 2010, 24: 1569-1580. 10.1210/me.2010-0034.
Lu TH, Hsieh SY, Yen CC, Wu HC, Chen KL, Hung DZ, Chen CH, Wu CC, Su YC, Chen YW, Liu SH, Huang CF: Involvement of oxidative stress-mediated ERK1/2 and p38 activation regulated mitochondria-dependent apoptotic signals in methylmercury-induced neuronal cell injury. Toxicol Lett. 2011, 204: 71-80. 10.1016/j.toxlet.2011.04.013.
Tamir S, Izrael S, Vaya J: The effect of oxidative stress on ERalpha and ERbeta expression. J Steroid Biochem Mol Biol. 2002, 81: 327-332. 10.1016/S0960-0760(02)00115-2.
Brennan DJ, O'Connor DP, Rexhepaj E, Ponten F, Gallagher WM: Antibody-based proteomics: fast-tracking molecular diagnostics in oncology. Nat Rev Cancer. 2010, 10: 605-617. 10.1038/nrc2902.
Karihtala P, Kauppila S, Soini Y, Arja Jukkola V: Oxidative stress and counteracting mechanisms in hormone receptor positive, triple-negative and basal-like breast carcinomas. BMC Cancer. 2011, 11: 262-10.1186/1471-2407-11-262.
Sastre-Serra J, Valle A, Company MM, Garau I, Oliver J, Roca P: Estrogen down-regulates uncoupling proteins and increases oxidative stress in breast cancer. Free Radic Biol Med. 2010, 48: 506-512. 10.1016/j.freeradbiomed.2009.11.025.
Felty Q, Xiong WC, Sun D, Sarkar S, Singh KP, Parkash J, Roy D: Estrogen-induced mitochondrial reactive oxygen species as signal-transducing messengers. Biochemistry. 2005, 44: 6900-6909. 10.1021/bi047629p.
Okoh V, Deoraj A, Roy D: Estrogen-induced reactive oxygen species-mediated signalings contribute to breast cancer. Biochim Biophys Acta. 1815, 2011: 115-133.
Yager JD, Davidson NE: Estrogen carcinogenesis in breast cancer. N Engl J Med. 2006, 354: 270-282. 10.1056/NEJMra050776.
Kominsky SL, Argani P, Korz D, Evron E, Raman V, Garrett E, Rein A, Sauter G, Kallioniemi OP, Sukumar S: Loss of the tight junction protein claudin-7 correlates with histological grade in both ductal carcinoma in situ and invasive ductal carcinoma of the breast. Oncogene. 2003, 22: 2021-2033. 10.1038/sj.onc.1206199.
Motrescu ER, Blaise S, Etique N, Messaddeq N, Chenard MP, Stoll I, Tomasetto C, Rio MC: Matrix metalloproteinase-11/stromelysin-3 exhibits collagenolytic function against collagen VI under normal and malignant conditions. Oncogene. 2008, 27: 6347-6355. 10.1038/onc.2008.218.
Murphy ME: The HSP70 family and cancer. Carcinogenesis. 2013, 34: 1181-1188. 10.1093/carcin/bgt111.
Creighton CJ, Fu X, Hennessy BT, Casa AJ, Zhang Y, Gonzalez-Angulo AM, Lluch A, Gray JW, Brown PH, Hilsenbeck SG, Osborne CK, Mills GB, Lee AV, Schiff R: Proteomic and transcriptomic profiling reveals a link between the PI3K pathway and lower estrogen-receptor (ER) levels and activity in ER + breast cancer. Breast Cancer Res. 2010, 12: R40-10.1186/bcr2594.
She QB, Solit DB, Ye Q, O'Reilly KE, Lobo J, Rosen N: The BAD protein integrates survival signaling by EGFR/MAPK and PI3K/Akt kinase pathways in PTEN-deficient tumor cells. Cancer Cell. 2005, 8: 287-297. 10.1016/j.ccr.2005.09.006.
Lim JC, Choi HI, Park YS, Nam HW, Woo HA, Kwon KS, Kim YS, Rhee SG, Kim K, Chae HZ: Irreversible oxidation of the active-site cysteine of peroxiredoxin to cysteine sulfonic acid for enhanced molecular chaperone activity. J Biol Chem. 2008, 283: 28873-28880. 10.1074/jbc.M804087200.
Barranco-Medina S, Lazaro JJ, Dietz KJ: The oligomeric conformation of peroxiredoxins links redox state to function. FEBS Lett. 2009, 583: 1809-1816. 10.1016/j.febslet.2009.05.029.
Poynton RA, Hampton MB: Peroxiredoxins as biomarkers of oxidative stress. Biochim Biophys Acta. 1840, 2013: 906-912.
Yau C, Benz CC: Genes responsive to both oxidant stress and loss of estrogen receptor function identify a poor prognosis group of estrogen receptor positive primary breast cancers. Breast Cancer Res. 2008, 10: R61-10.1186/bcr2120.
Chae HZ, Uhm TB, Rhee SG: Dimerization of thiol-specific antioxidant and the essential role of cysteine. Proc Natl Acad Sci U S A. 1994, 47: 7022-7026.
Chhipa RR, Lee KS, Onate S, Wu Y, Ip C: Prx1 enhances androgen receptor function in prostate cancer cells by increasing receptor affinity to dihydrotestosterone. Mol Cancer Res. 2009, 7: 1543-1552. 10.1158/1541-7786.MCR-08-0546.
Wu Y, Chhipa RR, Zhang H, Ip C: The antiandrogenic effect of finasteride against a mutant androgen receptor. Cancer Biol Ther. 2011, 11: 902-909. 10.4161/cbt.11.10.15187.
Penney RB, Roy D: Thioredoxin-mediated redox regulation of resistance to endocrine therapy in breast cancer. Biochim Biophys Acta. 1836, 2013: 60-79.
Funding is acknowledged from the Irish Research Council for Science, Engineering, and Technology (IRCSET; POL), Science Foundation Ireland through the Molecular Therapeutics for Cancer Ireland Strategic Research Cluster (award 08/SRC/B1410; PCOL, BTH, AZ, MT, KC, DPOC, JPC, WMG, RZ), the 7th European Community Framework Programme (Marie Curie International Reintegration Grant No. 224865; RZ; FP7-REGPOT-2012-CT2012-316254-BASTION; PG, RZ, DAN, MB), the Polish National Science Center (No. 2012/07/B/NZ7/04183; PG, RZ, DAN, MB), the Ministry of Science and Higher Education (IP2012 048172; DAN) and the Irish Cancer Society Collaborative Cancer Research Centre BREAST-PREDICT Grant (CCRC13GAL; WMG, BTH, JPC, DPOC). UICC provided two International Cancer Technology Transfer Fellowships (ICRETT Application No. ICR/11/002/2011: PCOL; ICR/12/017/2012: RZ). The UCD Conway Institute is funded by the Programme for Third Level Institutions (PRTLI), as administered by the Higher Education Authority (HEA) of Ireland. The authors wish to thank Dr. Tomasz Rygiel, Marta Swiech and Paulina Nadkowska of Medical University of Warsaw for their valuable technical help with the PRDX2-related experiments.
No potential conflicts of interest were disclosed.
PCOL generated the PRDX1 recombinant cell lines, carried out the PRDX1 molecular genetic studies, antibody validation, immunostaining and analysis of the cohort 2 TMA and cohort 3 RPPA, survival analysis for all cohorts, and drafted the initial copy of the manuscript. RZ, MT and MB generated the PRDX2-silenced cell lines and carried out the RT-PCR, WB and apoptosis analysis. MT carried out the adenanthin treatment study on PRDX2-silenced lines. BTH, JL, AMG and GBM participated in the collection of survival data, slide preparation, immunostaining and analysis of the cohort 1 RPPA. KC contributed to the Western blotting experiments for the manuscript revision. KJ collected all patient data and prepared the TMA for cohort 2. FP and MU provided the PRDX1 antibody and participated in initial antibody validation. PCOL, PG, MT, GBM and RZ participated in the statistical analysis of the data for cohort 3. AZ, RZ and MB produced the PRDX1 and PRDX2 overexpression vectors. HDS and JXP carried out the isolation and synthesis of the adenanthin compound. PCOL, DPOC, DJB, DN, JPC, MT, RZ and WMG were involved in the conception and design of the study. RZ and WMG participated in its coordination and helped to draft the manuscript. All authors critically revised the initial draft of the manuscript and subsequent revisions. All authors approved the manuscript in its current form.
Radoslaw Zagozdzon and William M Gallagher contributed equally to this work.
Electronic supplementary material
Additional file 2: Table S1: Clinicopathological parameters for the three cohorts of breast cancer patients utilized in this study. Table S2. Association of PRDX1 expression with clinicopathological parameters in the RPPA cohort (cohort 1). Table S3. Association of PRDX1 expression with clinicopathological parameters in the consecutive cohort (cohort 2). Table S4. Proteins that correlate with PRDX1 protein expression in the ER-positive and/or ER-negative cohort. ER, estrogen receptor; PRDX1, peroxiredoxin 1; RPPA, reverse phase protein arrays. (PDF 493 KB)
Additional file 3: Figure S1: Additional antibody validation experiments. (A) Full length immunoblotting gel shows a single discrete signal, the intensity of which correlates with PRDX1 knockdown/overexpression across recombinant ZR-75-1 cell lines (V5-tagged PRDX1 protein runs at 25 kDa, with native protein at 22 kDa). (B) Immunoblotting signal in PRDX1-silenced ZR-75-1 cell lines using independent PRDX1-targeting antibodies. (C) Protein and transcript expression were compared across three recombinant ZR-75-1 cells lines (NTC shRNA, PRDX1-sh1, PRDX1-sh2), which shows a greater correlation using the antibody from Atlas antibodies (solid line) compared to the Abcam antibody (dotted line). (D) Overexpression of PRDX1 in ZR-75-1 cells did not affect PRDX2 protein expression, while PRDX2 overexpression in T47D cells did not affect PRDX1 protein expression. NTC, non-targeting control; PRDX1, peroxiredoxin 1; shRNA, short hairpin loop RNA. (JPEG 3 MB)
Additional file 4: Figure S2: Additional in vitro Western blotting and functional assays. (A) Effect of H2O2 on ERα, pSer473-Akt and E-cadherin levels, along with respective loading controls. Parental ZR-75-1 cells were treated with increasing levels of H2O2 for 16 hours. (B) PRDX1 knockdown enhances the H2O2-mediated suppression of ER activity. Relative units of the ERE-luciferase reporter expression were normalized to Renilla-luciferase units. H2O2 treatment was 16 hours in duration. (C) PRDX1 protein expression is not driven by ER activity. Western blot analysis shows that no change in PRDX1 protein expression following stimulation of parental ZR-75-1 cells with 1 or 10 nM 17-β estradiol for 48 hours. During this experiment, these cells were cultured in DMEM containing 0.1% FBS supplemented with 17-β estradiol or vehicle control. (D) Treatment with adenanthin inhibits metabolism of H2O2 following three hours treatment with 50 μM H2O2. Knockdown of PRDX1 (sh2) is shown as a positive control. (ns: non-significant; *P <0.05; **P <0.01). DMEM, Dulbecco’s modified Eagle’s medium; ER, estrogen receptor; ERE, estrogen transcriptional response element; FBS, fetal bovine serum; H2O2, hydrogen peroxide; PRDX1, peroxiredoxin 1. (JPEG 2 MB)
Additional file 5: Figure S3: Effects on mRNA expression and protein stability after H2O2 treatment. (A) ESR1 mRNA expression is suppressed after induction of oxidative stress (16 hours H2O2 treatment) in ZR-75-1 cells. Silencing of PRDX1 does not enhance this oxidative stress-mediated suppression of ESR1 mRNA. Error bars represent the SEM from independent biological experiments (*P <0.05; **P <0.01). (B) H2O2 treatment suppresses ERα protein expression in these PRDX1-silenced ZR-75-1 cells. (C) Inhibition of transcription (1 μg/μl Actinomycin D) does not alter H2O2-mediated suppression of ERα protein. (D) Inhibition of proteasomal degradation (5 μM MG132) prevents oxidative stress-induced ERα suppression in ZR-75-1 cells. After inhibition of proteasomal degradation, PRDX1-sh2 expressing cells display a weaker H2O2-mediated suppression. All treatments were 16 hours in duration. ER, estrogen receptor; H2O2, hydrogen peroxide; PRDX1, peroxiredoxin 1. (JPEG 4 MB)
Additional file 6: Figure S4: Viability and apoptosis assays. PRDX1 knockdown does not alter cell growth or viability in ZR-75-1 and T47D breast cancer cell lines. ZR-75-1 (A) and T47D (B) cells were grown in normal medium for up to 120 hours, with cell viability (MTT assay) being measured every 24 hours. Experiments were repeated three times with six wells per experiment. Error bars represent the SEM. (C) Flow cytometry viability analysis (7-AAD viability staining solution) was also used to demonstrate this lack of change in proliferation. (D) The Apotox-Glo™ Triplex assay kit was used to measure caspase 3/7 activity in PRDX1 or PRDX2-silenced ZR-75-1 cells compared to the parental and NTC shRNA controls. Error bars represent the SD (ns: non-significant). PRDX1, peroxiredoxin 1. (JPEG 3 MB)
Additional file 7: Figure S5: PRDX2 RT-PCR and Western blotting, including adenanthin treatment of PRDX2-silenced cells. (A) PRDX2 mRNA and (B) protein expression is reduced in ZR-75-1 and T47D cells after lentiviral transduction of up to five different anti-PRDX2 shRNAs. (C) Silencing of PRDX1 or PRDX2 abrogates the adenanthin-induced suppression of ERα protein in ZR-75-1. All treatments were 16 hours in duration. Error bars represent the SEM from two independent experiments (***P <0.001). ER, estrogen receptor; PRDX1, peroxiredoxin 1; RT-PCR, real-time polymerase chain reaction; shRNA, short hairpin loop RNA. (JPEG 4 MB)
About this article
Cite this article
O’Leary, P.C., Terrile, M., Bajor, M. et al. Peroxiredoxin-1 protects estrogen receptor α from oxidative stress-induced suppression and is a protein biomarker of favorable prognosis in breast cancer. Breast Cancer Res 16, R79 (2014). https://doi.org/10.1186/bcr3691
- Breast Cancer
- Overall Survival
- Reverse Phase Protein Array
- PRDX1 Expression
- Positive Estrogen Receptor Status