- Research article
- Open Access
Dependence receptor UNC5A restricts luminal to basal breast cancer plasticity and metastasis
Breast Cancer Research volume 20, Article number: 35 (2018)
The majority of estrogen receptor-positive (ERα+) breast cancers respond to endocrine therapies. However, resistance to endocrine therapies is common in 30% of cases, which may be due to altered ERα signaling and/or enhanced plasticity of cancer cells leading to breast cancer subtype conversion. The mechanisms leading to enhanced plasticity of ERα-positive cancer cells are unknown.
We used short hairpin (sh)RNA and/or the CRISPR/Cas9 system to knockdown the expression of the dependence receptor UNC5A in ERα+ MCF7 and T-47D cell lines. RNA-seq, quantitative reverse transcription polymerase chain reaction, chromatin immunoprecipitation, and Western blotting were used to measure the effect of UNC5A knockdown on basal and estradiol (E2)-regulated gene expression. Mammosphere assay, flow cytometry, and immunofluorescence were used to determine the role of UNC5A in restricting plasticity. Xenograft models were used to measure the effect of UNC5A knockdown on tumor growth and metastasis. Tissue microarray and immunohistochemistry were utilized to determine the prognostic value of UNC5A in breast cancer. Log-rank test, one-way, and two-way analysis of variance (ANOVA) were used for statistical analyses.
Knockdown of the E2-inducible UNC5A resulted in altered basal gene expression affecting plasma membrane integrity and ERα signaling, as evident from ligand-independent activity of ERα, altered turnover of phosphorylated ERα, unique E2-dependent expression of genes effecting histone demethylase activity, enhanced upregulation of E2-inducible genes such as BCL2, and E2-independent tumorigenesis accompanied by multiorgan metastases. UNC5A depletion led to the appearance of a luminal/basal hybrid phenotype supported by elevated expression of basal/stem cell-enriched ∆Np63, CD44, CD49f, epidermal growth factor receptor (EGFR), and the lymphatic vessel permeability factor NTN4, but lower expression of luminal/alveolar differentiation-associated ELF5 while maintaining functional ERα. In addition, UNC5A-depleted cells acquired bipotent luminal progenitor characteristics based on KRT14+/KRT19+ and CD49f+/EpCAM+ phenotype. Consistent with in vitro results, UNC5A expression negatively correlated with EGFR expression in breast tumors, and lower expression of UNC5A, particularly in ERα+/PR+/HER2− tumors, was associated with poor outcome.
These studies reveal an unexpected role of the axon guidance receptor UNC5A in fine-tuning ERα and EGFR signaling and the luminal progenitor status of hormone-sensitive breast cancers. Furthermore, UNC5A knockdown cells provide an ideal model system to investigate metastasis of ERα+ breast cancers.
The luminal subtypes that express the estrogen receptor (ER)α represent approximately 70% of breast cancers, and the majority of these tumors respond to endocrine therapy . However, resistance to endocrine therapy resulting in relapse is seen in approximately 30% of patients . ERα+ breast cancers are heterogeneous with at least two subtypes, luminal A and luminal B . Luminal A tumors are estradiol (E2)-dependent and responsive to antiestrogens, whereas luminal B tumors display either intrinsic or acquired resistance to antiestrogens with an outcome almost similar to triple negative breast cancers (TNBCs) . A subgroup of luminal A tumors, particularly those that have metastasized despite expressing luminal A biomarkers (ERα and progesterone receptor (PR)), do not respond to antiestrogen therapies and approximately 55% of these metastases have converted to a different subtype through an unknown mechanism .
Multiple mechanisms of antiestrogen resistance have been documented . Most of the prior work focused on mechanisms that confer E2-independent activity to ERα, including kinases that phosphorylate ERα, co-activator molecules that enhance ERα activity, pioneer factors that govern chromatin binding of ERα, and growth factor receptor–ERα crosstalk [6,7,8]. However, to our knowledge, there have been limited attempts to decipher negative regulatory loops that may restrict ERα signaling subsequent to ligand-activated induction and deregulation of these negative regulatory loops leading to prolonged/sustained activation of ERα.
To identify luminal cell-expressed genes that may play a role in restricting E2-dependent proliferation, we scanned gene expression array datasets for E2-inducible genes with ERα binding sites and that have a growth inhibitory activity . From this search, we focused on the dependence receptor (DR) pathways for their potential role in a negative feedback loop. Under physiological conditions, unliganded DRs elicit cell death and/or growth inhibition but elicit cell survival and proliferation when coupled with their ligands such as Netrin-1 (NTN1) . DRs are direct transcriptional targets of p53 and integral to p53-dependent apoptotic pathways, particularly in the absence of ligands . NTN1 belongs to the evolutionary conserved netrin family secreted proteins and is well characterized for its role in the nervous system . Both netrins and DRs also play crucial roles in other systems, including development of the mammary gland, inner ear, lungs, and pancreas [12, 13]. Loss of heterozygosity and homozygous deletion of DRs and upregulation of netrins are observed in a variety of cancers including breast cancer [11, 13]. These aberrations in DR–netrin pathways are believed to confer resistance to p53-dependent apoptosis and enhance proliferation of cancer cells.
In the present study, we show that UNC5A is an E2-inducible gene. Knockdown of UNC5A in ERα+/PR+ cells resulted in defective turnover of phosphorylated ERα, enhanced E2 signaling, cell proliferation, and tumorigenesis independent of E2 supplementation accompanied with multiorgan metastases in xenograft models. Furthermore, UNC5A knockdown cells acquired a hybrid basal/luminal phenotype including elevated expression of epidermal growth factor receptor (EGFR). Thus, UNC5A could serve as a negative feedback molecule in ERα signaling, the deregulation of which could lead to breast cancer progression through enhanced plasticity.
Immunohistochemistry of tissue microarray (TMA)
Tissue samples were collected with Indiana University Institutional Review Board approval, informed patient consent, and HIPAA compliance. UNC5A and EGFR immunostaining was performed at the CLIA certified Indiana University Health Pathology Laboratory and scoring has been described previously . H scores were calculated using stain intensity (0 to 3) multiplied by percent positive pixels (for UNC5A) or a formula based on stain intensity and number of weak, moderate, or strong positive pixels (for EGFR). For subjects with multiple tumor samples, only those with the highest H score were considered. Statistical analysis was performed on samples from 221 breast cancer patients, but only 196 patient samples (89%) had UNC5A values available. The log-rank test was used to compare patient and tumor variables between those with UNC5A H scores versus those without. The correlations between UNC5A and EGFR were determined by Spearman’s correlation coefficient. For modeling the outcomes of overall survival and disease-free survival, the multivariate covariates used in the multivariate models from the individual reports for EGFR and UNC5A were included. Additionally, the H score information for EGFR and UNC5A were handled in three ways. First, the EGFR and UNC5A were dichotomized using the same optimal cut-points as used in their individual reports. Secondly, the EGFR and UNC5A were dichotomized using their individual medians and cut-points. Finally, the continuous values were used in the models. Since EGFR was not linear, the natural log of EGFR was used in the models. For the models with continuous values, hazard ratios were calculated at the 25th, 50th, and 75th percentile of EGFR. Subgroup analyses were performed where the number of patients available was sufficient.
MCF7 and T-47D cells were obtained from American Tissue Culture Collection and cultured in minimum essential media (MEM) media as described previously . TMCF7 cells correspond to cell lines derived from tumors developed in the mammary fat pad of nude mice implanted with MCF7 cells . Cell lines were authenticated using Short Tandem Repeat Profiling Systems for cell line identification by a commercial vendor (DNAcenter.com) in August 2012 and cell lines recreated from xenograft tumors were authenticated by Genetica (Burlington, NC, USA).
Short hairpin (sh)RNA and CRISPR constructs
The human shRNA lentiviral transduction particles for sh5-UNC5A and pLKO.1-puro vector control plasmids (sh-Control) were purchased from Sigma (cat. nos. SHCLNV-NM_133369 and SHC 001, respectively). The lentivector for sh2-UNC5A was obtained from Applied Biological Materials (cat. no. i026703g). CRISPR plasmids to target UNC5A were obtained from Sigma-Aldrich (HS0000509914).
Treatments consisted vehicle, heregulin-β1 (HRG-β1, R&D systems), E2, 4-hydroxy-tamoxifen (OHT), or ICI-182,780 (Sigma-Aldrich). The immunoblotting has been previously described  and details of antibodies are provided in Additional file 1. Although the majority of immunoblots were reprobed with antibodies against ACTB (β-actin) as a loading control, only representative data per batch of cell lysates are shown.
RNA-seq and quantitative reverse transcription polymerase chain reaction (qRT-PCR)
cDNA was synthesized from 1 to 2 μg of total RNA using the cDNA Synthesis Kit (Bio-Rad). qRT-PCR in duplicates from at least two biological replicates was performed with either Sybr-Green or TaqMan Universal PCR master mix and transcripts were analyzed in StepOnePlus and TaqMan 7900HT instruments (Applied Biosystems) with β-ACTIN as the normalization control. Fold-change was calculated by the ∆∆Ct method, whereas statistical analysis was performed on ΔCt values. Primers (Integrated DNA Technologies) and TaqMan probe details are shown in Additional file 1. RNA-seq of sh-Control and sh5-UNC5A cells treated for 3 h with vehicle or E2 was performed in triplicate as previously described , and raw sequencing data have been submitted to the gene expression omnibus (GEO; accession number GSE89700).
We used STAR RNA-Seq aligner to map all sequence libraries to the human genome (UCSC hg19)  followed by the assignment of uniquely mapped reads to individual genes based on annotation of hg19 refGene by featureCounts . After trimmed mean of M values (TMM) normalization, gene expression profiling was summarized on the base-2 logarithmic scale. Genes with an average expression level lower than 1 for all phenotypes in MCF7 and T-47D cells, respectively, were excluded for further analysis. Differential expression (DE) analysis was performed using edgeR [21, 22] for special group comparisons in the study. All p values were corrected by multiple testing false discovery rate (FDR) adjustments. Genes with FDR < 0.05 and absolute value of fold change (FC) larger than 2 were determined as differentially expressed genes (DEGs).
Gene function enrichment analysis was performed using DAVID (http://david.abcc.ncifcrf.gov/home.jsp v6.8) [23, 24]. Significantly overrepresented gene ontology (GO) terms were selected if their q values (p values after FDR multiple test correction) were less than 0.05.
Promoter luciferase assay
Cells transfected with luciferase constructs were allowed to grow overnight in charcoal-dextran treated fetal calf serum (CCS) containing media followed by a 12-h E2 treatment. The Dual-Luciferase® Reporter assay (Promega) was performed according to the manufacturer’s protocol.
Chromatin immunoprecipitation (ChIP) assay
ChIP assays for ERα binding on UNC5A and BCL2 were performed under vehicle or E2 treatment for 45 min and 2 h as described previously .
Cell proliferation and mammosphere assays
After 24-h plating in regular media, the media was changed to CCS-containing media for 3 days and cells were treated with the indicated drug combinations. Cell proliferation was determined using the bromodeoxyuridine-incorporation enzyme-linked immunosorbent assay (ELISA) kit from Calbiochem after 5–6 days of plating with one media/drug change. Mammosphere assays with 5000 cells were performed as described previously .
Cells grown on 35-mm glass-bottom culture dishes were fixed with 4% (w/v) paraformaldehyde for 10 min and permeabilized in phosphate-buffered saline (PBS) containing 0.15% (v/v) Triton X-100, 5% (v/v) donor goat serum (Gibco), and 1% (w/v) bovine serum albumin (Sigma-Aldrich) for 1 h. Cells were incubated with primary antibodies (Additional file 1) diluted in Dako antibody diluent (Dako; Agilent Technologies) for 90 min followed by 1-h incubation with the Alexa Fluor® 488 and 555 conjugated secondary antibodies (ThermoFisher Scientific). Nuclei was counterstained with Hoechst® 33,342.
The Indiana University Animal Care and Use Committee approved the use of animals in this study and all procedures were performed as per NIH guidelines. sh-Control, sh2-UNC5A, and sh5-UNC5A TMCF7 cells (2 × 106 in 100 μl serum-free HBSS) were implanted into the mammary fat pad of 7-week-old female nude mice with or without a 60-day slow-release E2 pellet. Tumor growth was measured weekly and tumor volume was calculated as described previously . After 12 weeks, the lungs and primary tumors were collected and processed for hematoxylin and eosin (H&E) and PECAM1 (CD31) staining. The whole slide digital imaging system of Aperio (ScanScope CS) was used for imaging of PECAM1-stained tumors. For the metastatic model, mice were inoculated with 2 × 105 TMCF7 cells into the left cardiac ventricle. Ovaries, spleen, and adrenal glands were collected within 17 weeks and processed as described above.
Statistical analyses were performed in GraphPad Prism® (6.02 version) or Statistical Analysis System (SAS; version 9.4) software with p < 0.05 considered as significant.
UNC5A is a luminal cell-enriched gene and is E2 inducible
To determine E2-inducible signaling molecules that may dampen the E2 response or gene-specific E2 regulation and that are expressed at higher levels in luminal breast cancers compared with TNBCs, we first searched our previous microarray data of E2-regulated genes in MCF7 cells for known growth suppressive roles and then determined whether E2 directly regulated their expression by integrating E2-inducible gene expression with ERα ChIP-on-chip and ChIP-seq datasets. UNC5A suited these criteria as its expression was E2 inducible and ERα binding sites for this gene was detectable in ChIP-on-chip and ChIP-seq datasets [9, 27] (Fig. 1a). Furthermore, in 11 out of 12 studies in publicly available Nuclear Receptor Signaling Atlas web resources showed 2- to 35-fold E2-inducible expression of UNC5A in MCF7 cells, uterus, and vagina (Additional file 2). We further confirmed E2-inducible expression of UNC5A in MCF7 cells by qRT-PCR (Fig. 1b) and Western blotting (see below), although induction at mRNA levels in our MCF7 cells was modest. Interestingly, the antiestrogen tamoxifen (OHT) failed to overcome the effect of E2 on UNC5A levels (Fig. 1b) suggesting unique effects of E2 on the expression of UNC5A. We used ChIP assay to verify ERα binding to one of the ERα binding sites (Fig. 1c). R2 Genomic and Visualization Platform (http://r2.amc.nl) analyses revealed a positive correlation between UNC5A and ESR1 mRNA levels in breast cancer cell lines (Fig. 1d). Also, analyses of The Cancer Genome Atlas (TCGA) dataset for the relationship between UNC5A expression and breast cancer subtypes using the UALCAN program  revealed highest UNC5A expression in luminal breast cancers, which are usually ERα-positive, compared with TNBCs (Fig. 1e). In contrast, NTN1 expression was higher in TNBCs compared with normal breast or luminal breast cancers (Fig. 1f).
Low UNC5A expression in primary breast cancers is associated with poor outcome
To obtain additional support for our hypothesis that a protein that attenuates ERα signaling has prognostic relevance, we performed immunohistochemical analyses of UNC5A in our previously described breast TMA in which 196 out of 221 tumors had measurable UNC5A expression  (Additional file 3). A representative staining pattern of UNC5A in breast tumor is shown in Fig. 2a. Tumor cells were moderate in staining in many of the cases with little to no background staining in the other tissues in the core (vascular endothelial cells, smooth muscle cells, fibroblasts, macrophages, and/or scattered lymphocytes infiltrating the tumor region). In both univariate and multivariate analyses, low UNC5A H score was associated with poor overall survival (Fig. 2b and Additional file 4). In subgroup analyses, in ER+/PR+/HER2−, lower UNC5A H score showed a trend of poor overall survival (p = 0.055) (Fig. 2c). UNC5A had no prognostic relevance when tumors were subgrouped broadly into ER+ or ER− subgroups (Fig. 2d, e). Thus, UNC5A is a potential biomarker of outcome in a subgroup of breast cancer patients whose tumors express luminal A markers.
UNC5A knockdown results in enhanced ERα signaling
To model low UNC5A levels in cells with intact ERα-dependent signaling, we created shRNA-UNC5A MCF7 and T-47D cells, which express ERα and PR at different levels (Fig. 3a, b). MCF7 cells are more responsive to E2 than T-47D cells and, therefore, most of the experiments were performed in MCF7 cells with a few validation experiments in T-47D cells. UNC5A knockdown did not have an effect on ERα levels and the receptor underwent activation-coupled degradation upon E2 treatment in both sh-Control and sh-UNC5A cells (Fig. 3a, b). Note that E2 increased UNC5A protein in sh-Control but not in sh-UNC5A MCF7 cells (Fig. 3a). We note that this is the only commercially available antibody (Abcam, ab81165) that recognized protein of expected size but showed variability in potency between batches. In transient transfection assay, estrogen response element (ERE)-driven luciferase-reporter gene showed elevated activity in vehicle-treated sh-UNC5A cells compared with sh-Control cells (Fig. 3c). In T-47D cells, which express higher levels of PR than MCF7 cells , UNC5A knockdown enhanced E2-inducible expression of PGR (Fig. 3d). In both MCF7 and T-47D cells, UNC5A knockdown substantially increased both basal (vehicle-treated) and, consequently, E2-inducible expression of BCL2 mRNA and protein (Fig. 3e, f). The enhanced BCL2 expression in sh-UNC5A cells correlated with increased E2-independent binding of ERα to the enhancer element of BCL2 to which ERα and JMJD3 bind to create a poised chromatin  (Fig. 3g). To determine whether enhanced ERα activity in UNC5A-knockdown cells is due to altered phosphorylation of ERα, we used phospho-specific antibodies to determine the levels of ERα phosphorylated at S118 and S167. Phosphorylation of ERα at these residues is known to confer ligand-independent activity to the receptor . Although we did not find any differences in basal phosphorylation status between sh-Control and sh-UNC5A cells, phosphorylated ERα underwent ligand-coupled degradation in sh-Control cells but not in sh-UNC5A cells (Fig. 3h). As a consequence, there was a modest difference in the rate of degradation of total ERα between clones. These results suggest the need for signaling events downstream of UNC5A in turnover of phosphorylated ERα.
To determine whether the above observations of altered phospho-ERα turnover upon UNC5A knockdown show any relationship with cell proliferation, we measured cell proliferation under vehicle control and E2 ± OHT-treated conditions. In MCF7 cells, sh-UNC5A increased proliferation under vehicle control, E2-, OHT-, and OHT plus E2-treated conditions compared with sh-Control to levels similar to E2-treated sh-Control cells (Fig. 3i, j). Although OHT reduced E2-inducible proliferation of sh-UNC5A cells, the overall proliferation rate of these cells under various treatments remained elevated compared with sh-Control cells. Collectively, these results suggest that UNC5A restricts the proliferation of ERα-positive cells.
To investigate whether enhanced the baseline proliferation of sh-UNC5A cells compared with sh-Control cells is ERα-dependent, we treated cells with ICI-182,780 (Fulvestrant) which degrades ERα. While ICI-182,780 reduced E2-induced proliferation of these cells, it had a minimal effect on baseline proliferation of all cell types (Additional file 5). These negative results can be interpreted in two ways: enhanced basal proliferation of sh-UNC5A cells compared with sh-Control cells is independent of ERα, or ERα in sh-UNC5A cells is less sensitive to ICI-182780-mediated degradation. Surprisingly, although ICI-182,780 caused degradation of total ERα in sh-Control and sh-UNC5A cells to a similar extent, ICI-182,780 increased the levels of ERα phosphorylated at S118 (Additional file 5). This unique effect of ICI-182,780 on phospho-ERα could explain the lack of its effects on the baseline proliferation rate of sh-UNC5A cells. Additional work is needed to clarify the role of ERα in the baseline proliferation rate of sh-UNC5A cells.
The dramatic effect of UNC5A on BCL2 expression was puzzling. To ensure that this increase in BCL2 expression is not due to aberrant integration of shRNAs into the genome, we used the CRISPR/Cas9 system to reduce UNC5A expression and selected single cell clones (Additional file 5). UNC5A protein levels were partially reduced in these single cell clones with an accompanying increase in BCL2 expression. Thus, even a modest decrease in UNC5A protein levels was sufficient to trigger BCL2 expression. We also observed stable BCL2 overexpression in both UNC5A shRNA and CRISPR clones cultured for a prolonged time despite these clones regaining UNC5A protein expression as measured using the available antibody. Thus, it appears that even transient knockdown of UNC5A leads to robust/permanent activation of BCL2, which is similar to previously reported stable activation of cancer germline genes upon transient knockdown of DNA methyltransferase 1 (DNMT1) .
Changes in gene expression associated with UNC5A knockdown
We performed RNA-seq of sh-Control and sh5-UNC5A MCF7 and T-47D cells treated with vehicle (basal) or E2 for 3 h and did pairwise comparisons to determine the effect of UNC5A on basal and E2-regulated gene expression (Fig. 4a). Genes were determined as DEGs for comparison if their FDR was < 0.05 and absolute value of fold change |FC| was > 2 (Fig. 4a and Additional file 6). Under basal growth conditions, UNC5A knockdown notably affected the expression of approximately 20% and 7% of genes in MCF7 and T-47D cells, respectively, potentially indicating its role in regulating the transcriptional machinery. For example, APOBEC3B, which is integral to ERα signaling , was one of the genes differentially expressed in sh-UNC5A cells compared with sh-Control MCF7 and T-47D cells (Additional file 6). We confirmed elevated expression of APOBEC3B in sh-UNC5A compared with sh-Control MCF7 cells (Fig. 4b). Based on the gene functional analysis using DAVID, genes differentially expressed in UNC5A knockdown MCF7 and T47-D cells were an integral part of the plasma membrane and extracellular region (Fig. 4c and Additional file 7). It is interesting to note that 167 DEGs in MCF7 cells were significantly overrepresented in sequence-specific transcription factor DNA binding activity (Fig. 4c). UNC5A knockdown also had a significant effect on E2-regulated gene expression, particularly in MCF7 cells. A total of 434 genes were recognized as undergoing significant changes in gene expression by E2 in sh-UNC5A MCF7 cells, whereas only 21 genes were identified as DEGs in sh-UNC5A T-47D cells (Fig. 4a and Additional file 6). In sh-UNC5A MCF7 cells but not in sh-Control cells, E2-targeted genes were associated with negative regulation of cell proliferation, extracellular region, and histone demethylase activity (Fig. 4c). For example, E2 induced the expression of histone demethylases KDM4B and KDM7A but reduced the levels of UTY and ARID5B in sh-UNC5A but not in sh-Control MCF7 cells  (Additional file 6). JARID2, which regulates the polycomb complex and histone methyltransferases , was E2 inducible in sh-UNC5A but not in sh-Control MCF7 cells (Additional file 6). Furthermore, we found that 109 out of these 434 genes (Fig. 4d) were not regulated by E2 in sh-Control MCF7 cells (FDR > 0.5 and |FC| < 1.15), whereas their expression was under E2 control in sh-UNC5A MCF7 cells. These 109 genes are associated with positive regulation of gene expression and affect transcriptional regulation by RNA polymerase II (Fig. 4c). By contrast, no specific GO functions could be assigned to uniquely E2-regulated genes in sh-UNC5A T-47D cells. We note that the effect of UNC5A on E2-regulated genes is gene-specific since sh-Control and sh-UNC5A MCF7 cells showed similar levels of E2-regulated expression of TFF1 and only a modest effect on E2-regulated expression of GREB1, two commonly used genes to measure E2-inducible genes (Fig. 4e). Collectively, these results indicate a cell type-dependent role of UNC5A in controlling basal and E2-regulated gene expression with potential downstream effects ranging from plasma membrane composition to transcriptional output from RNA polymerase II.
UNC5A knockdown results in nonclassical luminal/basal hybrid gene expression pattern
UNC5A knockdown increased the levels of oncogenic ΔNp63 isoform mRNA while simultaneously lowering the expression of tumor suppressive TAp63 isoform  (Fig. 5a, b). TP63 is an E2-repressed gene and ERα failed to repress ΔNp63 in sh-UNC5A clones with efficient UNC5A knockdown (sh5-UNC5A clones of MCF7 and T-47D; Fig. 5a, b). Overall, ΔNp63 levels ± E2 treatment remained elevated in sh-UNC5A cells compared with sh-Control cells. RNA-seq studies showed lower expression of luminal/alveolar differentiation-associated ELF5 but elevated expression of the pro-oncogenic MECOM (EVI-1) and lymphangiogenic NTN4 [36,37,38] in sh-UNC5A cells compared with sh-Control cells (Additional file 6). Indeed, ELF5 levels were significantly lower and NTN4 levels were higher in sh-UNC5A cells compared with sh-Control cells (Fig. 5c, d). MECOM protein was undetectable in MCF7 cells but elevated in sh-UNC5A T-47D cells compared with sh-Control cells (Fig. 5e). In addition, while sh-Control cells expressed mainly KRT19, sh-UNC5A cells expressed either KRT14, KRT19, or both KRT14 and KRT19 (basal and luminal cytokeratins, respectively)  (Fig. 5f and Additional file 8). Bipotent luminal progenitor cells are KRT14 and KRT19 double-positive . Note that UNC5A knockdown did not result in the morphologic features of epithelial to mesenchymal transition (EMT), nor did it result in the expression of EMT-associated genes such as SNAI1, SNAI2, ZEB1, or ZEB2 (Additional file 6 and data not shown). However, we observed elevated expression of ITGB6 (Integrin β6) in sh-UNC5A cells compared with sh-Control cells (Additional file 6); ITGB6 is pro-oncogenic and is induced during EMT of colon cancer cells .
Since ΔNp63 maintains stem cell phenotype and cancer cells with hybrid luminal/basal/mesenchymal characteristics display enhanced cancer stem cell (CSC) properties [35, 42], we used mammosphere assays and flow cytometry to characterize sh-Control and sh-UNC5A MCF7 cells for stemness. While mammospheres of sh-Control were well organized, sh-UNC5A cells formed irregular mammospheres (Fig. 5g). In addition, while sh-Control cells were predominantly CD49f (ITGA6)−/EPCAM+, a subpopulation of sh-UNC5A cells showed CD49f+/EPCAM+ phenotype (Fig. 5h). CD49f+/EPCAM−, CD49f+/EPCAM+, and CD49f−/EPCAM+ cells display stem/basal, luminal progenitor, and differentiated/mature features, respectively . Sh-Control cells showed CD44−/CD24+ non-CSC phenotype whereas sh-UNC5A cells acquired the features of CSCs as evident from the presence of CD44+/CD24+ and CD44+/CD24− cells . Furthermore, sh-UNC5A MCF7 cells expressed significantly higher levels of stemness-associated SOX2  (Additional file 6).
UNC5A knockdown results in elevated EGFR expression and AKT activity
Two of our observations and one prior report prompted us to investigate whether UNC5A knockdown is associated with altered activity of EGFR, which could explain the effects of UNC5A on E2-regulated gene expression. First, we observed enhanced basal ERE-luciferase activity in sh-UNC5A cells, suggesting ligand-independent activity of ERα which typically involves growth factor receptor–ERα crosstalk . EGFR is forefront in this crosstalk as it can alter ERα cistrome and ERα-regulated gene expression . Second, sh-UNC5A cells showed luminal/basal hybrid phenotype, and EGFR activation is common in cells with basal phenotype . Third, a recent study showed that NTN1, in the absence of UNC5A, increases EGFR at the post-translational level . We first measured EGFR levels in sh-Control and UNC5A knockdown cells. EGFR protein but not mRNA levels were significantly higher in sh-UNC5A cells compared with sh-Control cells (Fig. 6a and data not shown). AKT and ERK are the two major kinases activated downstream of EGFR that can increase ligand-independent activity of ERα . We determined whether UNC5A knockdown had an effect on vehicle, E2-regulated, and HRGβ1-induced activation of these kinases. sh-UNC5A cells showed robust activation of AKT as measured by pAKT-S473 levels but not ERK (Fig. 6b). We recently reported that AKT1 but not AKT2 is active in MCF7 cells . Immunoblotting using isoform-specific phospho-antibodies showed upregulation of pAKT1 but not pAKT2 in sh-UNC5A cells compared with sh-Control cells (Fig. 6c). These results indicate a negative relationship between EGFR and UNC5A expression in cell line models. Similarly, UNC5A and EGFR expression showed negative correlation in breast tumor samples when the analyses included all samples or only ER+ samples (Fig. 6d).
We next investigated the role of ERα in negative crosstalk between UNC5A and EGFR/TP63. Treatment of cells with ICI-182,780 results in degradation of ERα and, consequently, elevated expression of genes typically repressed by ERα. Indeed, treatment of sh-Control MCF7 and T-47D cells caused degradation of ERα with a concomitant increase in TP63 (Fig. 6e). Interestingly, ICI-182,780 treatment did not have an effect on EGFR but reduced the level of TP63 in sh-UNC5A cells (Fig. 6e). Similar to TP63, elevated expression of BCL2 upon UNC5A knockdown is ERα-dependent as its levels were lower in ICI-182,780-treated cells compared with untreated sh-UNC5A cells (Fig. 6e). Thus, while elevated EGFR levels in sh-UNC5A cells are ERα-independent, ΔNp63 and BCL2 upregulation in these cells is at least partially ERα-dependent.
sh-UNC5A cells form metastatic tumors independent of E2 supplementation
MCF7 cells form nonmetastatic tumors in female nude mice when injected with matrigel or when supplemented with E2 pellets, although there is less uniformity between the sizes of tumors between animals . We had previously reported in the MDA-MB-231 model that cell lines derived from tumors that develop in the mammary fat pad upon implantation of parental cells show enhanced and uniform tumorigenicity upon re-implantation . We used this approach to increase uniformity in tumorigenicity and generated TMCF7 sh-Control, sh2-UNC5A, and sh5-UNC5A cells. As with MCF7 cells, sh-UNC5A TMCF7 cells showed elevated BCL2 and ΔNp63 compared with sh-Control cells (Additional file 8). sh-UNC5A but not sh-Control TMCF7 cells displayed KRT14/KRT19 double-positive phenotype (Additional file 8). A large subpopulation of sh-UNC5A TMCF7 cells was of the CD44+/CD24+ and CD49f+/EPCAM+ phenotype compared with sh-Control cells (Additional file 8), and mammospheres formed by these cells were irregular compared to mammospheres from sh-Control cells (Additional file 8). In addition, sh-UNC5A TMCF7 cells expressed significantly higher levels of SOX2 despite maintaining ERα expression (Additional file 8). Consistent with RNA-seq data (Additional file 6), a large subpopulation of sh-UNC5A TMCF7 cells were ITGB6+ compared with sh-Control cells (Additional file 8).
A significant number of mice injected with sh-UNC5A cells but not sh-Control cells developed tumors in the absence of E2 pellets (Fig. 7a). The size of these tumors was larger than tumors in animals injected with sh-Control cells in the presence of E2 pellet (Fig. 7b). While none of the animals injected with sh-Control cells developed lung metastasis, consistent with our previous study with TMCF7 cells , animals that received sh-UNC5A cells showed lung metastasis (Fig. 7c). We next examined whether sh-Control cell- and sh-UNC5A cell-derived tumors differ in angiogenesis because of the differences in NTN4 expression between sh-Control and sh-UNC5A cells noted in Fig. 5. sh-UNC5A cell-derived tumors contained higher numbers of PECAM1+ cells compared with sh-Control cell-derived tumors (Fig. 7d), suggesting enhanced angiogenesis in the absence of UNC5A.
To determine whether UNC5A knockdown enhanced the multiorgan homing capacity of tumor cells, sh-Control and sh-UNC5A cells were injected via the intracardiac route into animals supplemented with E2 pellets. Autopsies within 17 weeks of injection revealed growth of tumor cells in ovaries and adrenal glands at a higher frequency in animals injected with sh-UNC5A cells compared with sh-Control cells (Fig. 7e). Histological analysis revealed a severe disruption of the normal architecture of both organs (Fig. 7f). Ovaries were devoid of follicles and corpora lutea, and the very few remaining were undergoing atresia and degeneration. Likewise, adrenals lost a clear differentiation between the cortex and medulla zones with hemorrhagic areas and high vacuolization even in areas where the capsule is still preserved. Spleens of animals that received sh-UNC5A cells showed extramedullary hematopoiesis with enhanced myeloid and erythroid elements and megakaryocytes causing distention of the spleen in the red pulp area (data not shown). Overall, the results presented above clearly indicate the role of UNC5A in regulating the metastasis of ER+ tumors and its loss of expression leading to E2-independent growth both in vitro and in vivo.
UNC5A is a transmembrane receptor that generates cell survival or death signals in a ligand-dependent manner . UNC5A and NTN1 are described as tumor suppressor and oncogene, respectively, in breast cancer [51, 52]. However, signaling pathways that control their expression to alter the balance between UNC5A and NTN1 are unknown. Analyses of TCGA dataset showed elevated expression of UNC5A in luminal breast cancers, and NTN1 overexpression in TNBCs and E2 could further enhance luminal expression of UNC5A (Fig. 1). Thus, the UNC5A–NTN1 signaling axis is likely tilted more towards UNC5A-activated signals in ERα+/PR+ breast cancers and NTN1-generated signals in TNBC/ER− tumors. Consistent with this possibility, UNC5A expression was prognostic in ER+/PR+/HER2− breast cancers but not in ER− tumors, suggesting its critical role in ER+/PR+/HER2− breast cancers. A subgroup of women with ER+/PR+ breast cancers develop recurrence, and molecular assays such as the Recurrence Score and Breast Cancer Index are helping to identify ER+/PR+ breast cancer patients requiring hormonal and/or chemotherapy . UNC5A, possibly in combination with EGFR, could be developed as a biomarker to identify such patients .
Molecular events causing variable UNC5A expression in ER+ tumors are unknown. UNC5A is a TP53-inducible gene, and TP53 is infrequently mutated in ER+/PR+ breast cancer [2, 54]. Deregulated p53 activity instead of mutations may lead to loss of UNC5A expression in ER+/PR+ tumors, although this remains to be investigated. In addition, there is potential for p53 to control UNC5A activity since we noted a differential effect of UNC5A knockdown on proliferation in wild-type p53 containing MCF7 cells compared with mutant p53 containing T-47D cells, although knockdown had a similar effect on BCL2 and TP63 expression in both cell lines. cBioPortal analyses revealed frequent missense and truncating mutations in UNC5A . Additionally, UNC5A expression is regulated through allele-specific DNA methylation . Thus, mutations and DNA methylation could be other mechanisms leading to inactivation/silencing of UNC5A during breast cancer progression.
One of the consequences of reduced UNC5A expression is significant changes in basal gene expression and altered ERα signaling. GO analyses revealed a specific effect of UNC5A knockdown on a network of transcription factors including the stem cell-associated transcription factor SOX2, which may be a reason for the altered expression of 20% of genes in sh-UNC5A MCF7 cells and 7% in sh-UNC5A T-47D cells compared with sh-Control cells (Fig. 4). It is interesting that, in both cell lines, UNC5A knockdown affected the expression of genes linked to the plasma membrane and extracellular region composition (Fig. 4), which can explain the aggressive growth characteristics of sh-UNC5A compared with sh-Control MCF7 cells in vivo. We also observed a distinct effect of UNC5A on E2-regulated gene expression, with several genes gaining E2-regulated gene expression (Fig. 4). These results suggest a role for UNC5A in restricting the activity of unliganded ERα in a gene-specific manner, which could involve the following mechanisms. One possibility is the direct effect of UNC5A-activated signals on chromatin organization since we observed an effect of UNC5A knockdown on the histone demethylation network in E2-treated cells (Fig. 4). UNC5A knockdown increased the E2-inducible expression of KDM4B, which is a master regulator of ERα activity . Elevated KDM4B in sh-UNC5A cells could further amplify the E2 signaling axis as evident from more than 400 genes gaining E2-regulated expression in sh-UNC5A cells. Robustness at which UNC5A knockdown altered BCL2 expression further suggests a direct link between UNC5A and chromatin organization. This drastic effect of UNC5A knockdown on BCL2 expression is reminiscent of permanent gene expression changes observed upon transient knockdown of DNMT1 . However, we did not observe an effect of UNC5A knockdown on the expression of any DNMTs, although there was a modest but statistically significant effect on TET1 and TET3 which antagonize DNMTs (Additional file 6). UNC5A knockdown may have an effect on histone acetylation/deacetylation since sh-UNC5A MCF7 cells expressed significantly higher levels of the epigenetic regulator HDAC9 compared with sh-Control cells (Additional files 6). The second possibility is the involvement of ELF5. ELF5 suppresses E2 sensitivity by reducing the expression of ESR1 and the pioneer factors FOXA1 and GATA3 . ERα, FOXA1, and GATA3 constitute a positive lineage-restricted hormone responsive regulatory loop in luminal cells . We observed the effect of UNC5A knockdown on ELF5 expression, and reduced ELF5 expression in sh-UNC5A MCF7 cells correlated with elevated GATA3 expression (Additional file 6). The third possibility is the involvement of AKT. UNC5A knockdown caused upregulation of activated AKT, which confers ligand-independent activity to ERα . The fourth possibility involves ERα–EGFR crosstalk since UNC5A knockdown cells contained higher levels of EGFR protein (Fig. 7), and EGF through EGFR has been shown to alter ERα cistrome and transcriptome .
UNC5A knockdown in MCF7 cells resulted in a hybrid phenotype with cells expressing luminal (ER, PGR), myoepithelial (TP63), and stem cell markers (SOX2), which in part is due to altered ERα signaling. Recent studies have identified similar hybrid cells in primary breast cancers, potentially generated through Notch-Jagged signaling [42, 61]. Based on cell surface marker profiles and KRT14/KRT19 expression patterns in sh-UNC5A cells, we propose that the gradual loss of UNC5A results in cancer cells acquiring hybrid phenotype without expressing classic markers of EMT. Since there is still a controversy related to in-vivo detection of cancer cells with EMT features, it is possible that primary tumors contain cells with hybrid phenotype which functionally behave like cancer cells with EMT features. Characterizing primary tumors for ER, PR, UNC5A, EGFR, and additional basal cell markers would allow the detection of such hybrid cells. Collectively, results presented in this study provide novel insights into pathways that restrict ERα signaling and metastatic progression of ERα+ breast cancer, which potentially involves luminal to luminal/basal hybrid conversion due to an aberrant DR pathway.
In this study, we demonstrate an unexpected role for the dependence receptor UNC5A in regulating ERα activity and restricting the expression of basal cell-enriched genes in luminal cells. Progressive loss of UNC5A expression could result in ERα-positive luminal cells acquiring basal features including the expression of ΔNp63, SOX2, and EGFR, while maintaining ERα expression. These results describe the role of UNC5A in controlling plasticity of luminal breast cancer. Therefore, UNC5A, ERα, and EGFR could be developed as markers to identify luminal breast cancers with a potential for subtype conversion.
v-AKT murine thymoma viral oncogene
Apolipoprotein B mRNA-editing enzyme
B cell leukemia/lymphoma 2
Charcoal-dextran treated fetal calf serum
Cancer stem cell
Differentially expressed gene
DNA methyltransferase 1
Epidermal growth factor receptor
Enzyme-linked immunosorbent assay
Epithelial to mesenchymal transition
Estrogen response element
Extracellular signal-regulated kinase
False discovery rate
Gene expression omnibus
Hematoxylin and eosin
Minimum essential media
Quantitative reverse transcription polymerase chain reaction
Short hairpin RNA
The Cancer Genome Atlas
Triple negative breast cancer
Unc-5 netrin receptor A
Ali S, Coombes RC. Endocrine-responsive breast cancer and strategies for combating resistance. Nat Rev Cancer. 2002;2(2):101–12.
Sorlie T, Perou CM, Tibshirani R, Aas T, Geisler S, Johnsen H, Hastie T, Eisen MB, van de Rijn M, Jeffrey SS, et al. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications. Proc Natl Acad Sci U S A. 2001;98(19):10869–74.
Ades F, Zardavas D, Bozovic-Spasojevic I, Pugliano L, Fumagalli D, de Azambuja E, Viale G, Sotiriou C, Piccart M. Luminal B breast cancer: molecular characterization, clinical management, and future perspectives. J Clin Oncol. 2014;32(25):2794–803.
Cejalvo JM, Martinez de Duenas E, Galvan P, Garcia-Recio S, Burgues Gasion O, Pare L, Antolin S, Martinello R, Blancas I, Adamo B, et al. Intrinsic subtypes and gene expression profiles in primary and metastatic breast cancer. Cancer Res. 2017;77:2213–21.
Ellis MJ, Tao Y, Young O, White S, Proia AD, Murray J, Renshaw L, Faratian D, Thomas J, Dowsett M, et al. Estrogen-independent proliferation is present in estrogen-receptor HER2-positive primary breast cancer after neoadjuvant letrozole. J Clin Oncol. 2006;24(19):3019–25.
Zaret KS, Carroll JS. Pioneer transcription factors: establishing competence for gene expression. Genes Dev. 2011;25(21):2227–41.
Badve S, Turbin D, Thorat MA, Morimiya A, Nielsen TO, Perou CM, Dunn S, Huntsman DG, Nakshatri H. FOXA1 expression in breast cancer correlation with luminal subtype A and survival. Clin Cancer Res. 2007;13(15):4415–21.
Ma CX, Reinert T, Chmielewska I, Ellis MJ. Mechanisms of aromatase inhibitor resistance. Nat Rev Cancer. 2015;15(5):261–75.
Bhat-Nakshatri P, Wang G, Appaiah H, Luktuke N, Carroll JS, Geistlinger TR, Brown M, Badve S, Liu Y, Nakshatri H. AKT alters genome-wide estrogen receptor alpha binding and impacts estrogen signaling in breast cancer. Mol Cell Biol. 2008;28(24):7487–503.
Mehlen P, Bredesen DE. Dependence receptors: from basic research to drug development. Sci Signal. 2011;4(157):mr2.
Arakawa H. Netrin-1 and its receptors in tumorigenesis. Nat Rev Cancer. 2004;4(12):978–87.
Cirulli V, Yebra M. Netrins: beyond the brain. Nat Rev Mol Cell Biol. 2007;8(4):296–306.
Mehlen P, Delloye-Bourgeois C, Chedotal A. Novel roles for Slits and netrins: axon guidance cues as anticancer targets? Nat Rev Cancer. 2011;11(3):188–97.
Perkins SM, Bales C, Vladislav T, Althouse S, Miller KD, Sandusky G, Badve S, Nakshatri H. TFAP2C expression in breast cancer: correlation with overall survival beyond 10 years of initial diagnosis. Breast Cancer Res Treat. 2015;152(3):519–31.
McCune K, Bhat-Nakshatri P, Thorat M, Nephew KP, Badve S, Nakshatri H. Prognosis of hormone-dependent breast cancers: implications of the presence of dysfunctional transcriptional networks activated by insulin via the immune transcription factor T-bet. Cancer Res. 2010;70:685–96. PMID:20068169.
Kumar S, Kishimoto H, Chua HL, Badve S, Miller KD, Bigsby RM, Nakshatri H. Interleukin-1 alpha promotes tumor growth and cachexia in MCF-7 xenograft model of breast cancer. Am J Pathol. 2003;163(6):2531–41.
Bhat-Nakshatri P, Goswami CP, Badve S, Magnani L, Lupien M, Nakshatri H. Molecular insights of pathways resulting from two common PIK3CA mutations in breast cancer. Cancer Res. 2016;76(13):3989–4001.
Miller DF, Yan PS, Buechlein A, Rodriguez BA, Yilmaz AS, Goel S, Lin H, Collins-Burow B, Rhodes LV, Braun C, et al. A new method for stranded whole transcriptome RNA-seq. Methods. 2013;63(2):126–34.
Dobin A, Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, Batut P, Chaisson M, Gingeras TR. STAR: ultrafast universal RNA-seq aligner. Bioinformatics. 2013;29(1):15–21.
Liao Y, Smyth GK, Shi W. featureCounts: an efficient general purpose program for assigning sequence reads to genomic features. Bioinformatics. 2014;30(7):923–30.
Robinson MD, McCarthy DJ, Smyth GK. edgeR: a bioconductor package for differential expression analysis of digital gene expression data. Bioinformatics. 2010;26(1):139–40.
McCarthy DJ, Chen Y, Smyth GK. Differential expression analysis of multifactor RNA-Seq experiments with respect to biological variation. Nucleic Acids Res. 2012;40(10):4288–97.
Huang DW, Sherman BT, Tan Q, Collins JR, Alvord WG, Roayaei J, Stephens R, Baseler MW, Lane HC, Lempicki RA. The DAVID gene functional classification tool: a novel biological module-centric algorithm to functionally analyze large gene lists. Genome Biol. 2007;8(9):R183.
Huang da W, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc. 2009;4(1):44–57.
Bhat-Nakshatri P, Goswami CP, Badve S, Sledge GW Jr, Nakshatri H. Identification of FDA-approved drugs targeting breast cancer stem cells along with biomarkers of sensitivity. Sci Rep. 2013;3:2530.
Nakshatri H, Anjanappa M, Bhat-Nakshatri P. Ethnicity-dependent and -independent heterogeneity in healthy normal breast hierarchy impacts tumor characterization. Sci Rep. 2015;5:13526.
Welboren WJ, van Driel MA, Janssen-Megens EM, van Heeringen SJ, Sweep FC, Span PN, Stunnenberg HG. ChIP-Seq of ERalpha and RNA polymerase II defines genes differentially responding to ligands. EMBO J. 2009;28(10):1418–28.
Chandrashekar DS, Bashel B, Balasubramanya SAH, Creighton CJ, Ponce-Rodriguez I, Chakravarthi B, Varambally S. UALCAN: a portal for facilitating tumor subgroup gene expression and survival analyses. Neoplasia. 2017;19(8):649–58.
Dressing GE, Knutson TP, Schiewer MJ, Daniel AR, Hagan CR, Diep CH, Knudsen KE, Lange CA. Progesterone receptor-cyclin D1 complexes induce cell cycle-dependent transcriptional programs in breast cancer cells. Mol Endocrinol. 2014;28(4):442–57.
Svotelis A, Bianco S, Madore J, Huppe G, Nordell-Markovits A, Mes-Masson AM, Gevry N. H3K27 demethylation by JMJD3 at a poised enhancer of anti-apoptotic gene BCL2 determines ERalpha ligand dependency. EMBO J. 2011;30(19):3947–61.
Cannuyer J, Van Tongelen A, Loriot A, De Smet C. A gene expression signature identifying transient DNMT1 depletion as a causal factor of cancer-germline gene activation in melanoma. Clin Epigenetics. 2015;7:114.
Periyasamy M, Patel H, Lai CF, Nguyen VT, Nevedomskaya E, Harrod A, Russell R, Remenyi J, Ochocka AM, Thomas RS, et al. APOBEC3B-mediated cytidine deamination is required for estrogen receptor action in breast cancer. Cell Rep. 2015;13(1):108–21.
Hyun K, Jeon J, Park K, Kim J. Writing, erasing and reading histone lysine methylations. Exp Mol Med. 2017;49(4):e324.
Vizan P, Beringer M, Ballare C, Di Croce L. Role of PRC2-associated factors in stem cells and disease. FEBS J. 2015;282(9):1723–35.
Melino G, Memmi EM, Pelicci PG, Bernassola F. Maintaining epithelial stemness with p63. Sci Signal. 2015;8(387):re9.
Kalyuga M, Gallego-Ortega D, Lee HJ, Roden DL, Cowley MJ, Caldon CE, Stone A, Allerdice SL, Valdes-Mora F, Launchbury R, et al. ELF5 suppresses estrogen sensitivity and underpins the acquisition of antiestrogen resistance in luminal breast cancer. PLoS Biol. 2012;10(12):e1001461.
Singh S, Pradhan AK, Chakraborty S. SUMO1 negatively regulates the transcriptional activity of EVI1 and significantly increases its co-localization with EVI1 after treatment with arsenic trioxide. Biochim Biophys Acta. 2013;1833(10):2357–68.
Larrieu-Lahargue F, Welm AL, Thomas KR, Li DY. Netrin-4 induces lymphangiogenesis in vivo. Blood. 2010;115(26):5418–26.
Malzahn K, Mitze M, Thoenes M, Moll R. Biological and prognostic significance of stratified epithelial cytokeratins in infiltrating ductal breast carcinomas. Virchows Arch. 1998;433(2):119–29.
Villadsen R, Fridriksdottir AJ, Ronnov-Jessen L, Gudjonsson T, Rank F, LaBarge MA, Bissell MJ, Petersen OW. Evidence for a stem cell hierarchy in the adult human breast. J Cell Biol. 2007;177(1):87–101.
Bates RC, Bellovin DI, Brown C, Maynard E, Wu B, Kawakatsu H, Sheppard D, Oettgen P, Mercurio AM. Transcriptional activation of integrin beta6 during the epithelial-mesenchymal transition defines a novel prognostic indicator of aggressive colon carcinoma. J Clin Invest. 2005;115(2):339–47.
Grosse-Wilde A, Fouquier d'Herouel A, McIntosh E, Ertaylan G, Skupin A, Kuestner RE, del Sol A, Walters KA, Huang S. Stemness of the hybrid epithelial/mesenchymal state in breast cancer and its association with poor survival. PLoS One. 2015;10(5):e0126522.
Visvader JE, Stingl J. Mammary stem cells and the differentiation hierarchy: current status and perspectives. Genes Dev. 2014;28(11):1143–58.
Al-Hajj M, Wicha MS, Benito-Hernandez A, Morrison SJ, Clarke MF. Prospective identification of tumorigenic breast cancer cells. Proc Natl Acad Sci U S A. 2003;100(7):3983–8.
Sarkar A, Hochedlinger K. The sox family of transcription factors: versatile regulators of stem and progenitor cell fate. Cell Stem Cell. 2013;12(1):15–30.
Osborne CK, Schiff R. Mechanisms of endocrine resistance in breast cancer. Annu Rev Med. 2011;62:233–47.
Lupien M, Meyer CA, Bailey ST, Eeckhoute J, Cook J, Westerling T, Zhang X, Carroll JS, Rhodes DR, Liu XS, et al. Growth factor stimulation induces a distinct ER(alpha) cistrome underlying breast cancer endocrine resistance. Genes Dev. 2010;24(19):2219–27.
Valentin MD, da Silva SD, Privat M, Alaoui-Jamali M, Bignon YJ. Molecular insights on basal-like breast cancer. Breast Cancer Res Treat. 2012;134(1):21–30.
Plissonnier ML, Lahlali T, Michelet M, Lebosse F, Cottarel J, Beer M, Neveu G, Durantel D, Bartosch B, Accardi R, et al. Epidermal growth factor receptor-dependent mutual amplification between Netrin-1 and the hepatitis C virus. PLoS Biol. 2016;14(3):e1002421.
Sweeney CJ, Mehrotra S, Sadaria MR, Kumar S, Shortle NH, Roman Y, Sheridan C, Campbell RA, Murry DJ, Badve S, et al. The sesquiterpene lactone parthenolide in combination with docetaxel reduces metastasis and improves survival in a xenograft model of breast cancer. Mol Cancer Ther. 2005;4(6):1004–12.
Fitamant J, Guenebeaud C, Coissieux MM, Guix C, Treilleux I, Scoazec JY, Bachelot T, Bernet A, Mehlen P. Netrin-1 expression confers a selective advantage for tumor cell survival in metastatic breast cancer. Proc Natl Acad Sci U S A. 2008;105(12):4850–5.
Thiebault K, Mazelin L, Pays L, Llambi F, Joly MO, Scoazec JY, Saurin JC, Romeo G, Mehlen P. The netrin-1 receptors UNC5H are putative tumor suppressors controlling cell death commitment. Proc Natl Acad Sci U S A. 2003;100(7):4173–8.
Sestak I, Zhang Y, Schroeder BE, Schnabel CA, Dowsett M, Cuzick J, Sgroi D. Cross-stratification and differential risk by breast cancer index and recurrence score in women with hormone receptor-positive lymph node-negative early-stage breast cancer. Clin Cancer Res. 2016;22(20):5043–8.
Miyamoto Y, Futamura M, Kitamura N, Nakamura Y, Baba H, Arakawa H. Identification of UNC5A as a novel transcriptional target of tumor suppressor p53 and a regulator of apoptosis. Int J Oncol. 2010;36(5):1253–60.
Cerami E, Gao J, Dogrusoz U, Gross BE, Sumer SO, Aksoy BA, Jacobsen A, Byrne CJ, Heuer ML, Larsson E, et al. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer discovery. 2012;2(5):401–4.
Wang J, Valo Z, Bowers CW, Smith DD, Liu Z, Singer-Sam J. Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes. PLoS One. 2010;5(11):e13843.
Gaughan L, Stockley J, Coffey K, O'Neill D, Jones DL, Wade M, Wright J, Moore M, Tse S, Rogerson L, et al. KDM4B is a master regulator of the estrogen receptor signalling cascade. Nucleic Acids Res. 2013;41(14):6892–904.
Eeckhoute J, Keeton EK, Lupien M, Krum SA, Carroll JS, Brown M. Positive cross-regulatory loop ties GATA-3 to estrogen receptor alpha expression in breast cancer. Cancer Res. 2007;67(13):6477–83.
Campbell RA, Bhat-Nakshatri P, Patel NM, Constantinidou D, Ali S, Nakshatri H. Phosphatidylinositol 3-kinase/AKT-mediated activation of estrogen receptor alpha: a new model for anti-estrogen resistance. J Biol Chem. 2001;276(13):9817–24.
Lupien MMC, Bailey ST, Eeckhoute J, Cook J, Westerling T, Zhang X, Carroll JS, Rhodes DR, Liu XS, Brown M. Growth factor stimulation induces a distinct ERalpha cistrome underlying breast cancer endocrine resistance. Genes Dev. 2010;24:2219–27.
Boareto M, Jolly MK, Goldman A, Pietila M, Mani SA, Sengupta S, Ben-Jacob E, Levine H, Onuchic JN. Notch-Jagged signalling can give rise to clusters of cells exhibiting a hybrid epithelial/mesenchymal phenotype. J R Soc Interface. 2016;13(118). doi: https://doi.org/10.1098/rsif.2015.1106.
We thank Dr. Hitesh Appaiah for initial analysis of UNC5A expression in breast cancer cell lines, the IU Simon Cancer Center Flow Cytometry Core for flow cytometry, and the Tissue Procurement facility of IUSCC for the TMA.
Susan G. Komen for the Cure SAC110025 provided financial support for this work (HN). The Vera Bradley Foundation for Breast Cancer Scholar Program at the IU Simon Cancer Center provided support to MBP. Collaborative Care for Cancer Bioinformatics, supported by the Walther Cancer Foundation, performed the bioinformatics analyses of RNA-seq data.
Availability of data and materials
RNA-seq data has been deposited with GEO under the accession number GSE89700. All cell lines will be made available upon request.
Ethics approval and consent to participate
Tumor samples used in the tissue microarray were obtained after informed consent and the Indiana University Institutional Review Board has approved the use of human tissue. Participants have consented for publication. The article does not contain data from individual participants. All animal studies were performed as per NIH guidelines and with approval from the Institutional Animal Care and Use Committee.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Tables that describe antibodies and primers used in the study. (DOCX 121 kb)
E2-regulated expression of UNC5A in various cell types extracted from published studies using NURSA data resource. (XLSX 13 kb)
Description of patients and characteristics of their tumors (n = 221). (DOCX 98 kb)
Summary of results of overall survival: univariate and multivariate analyses on the UNC5A H score category. (DOCX 96 kb)
The effect of ICI-182,780 (Fulvestrant) treatment on UNC5A knockdown cells and Western blot showing UNC5A knockdown by CRISPR in MCF-7 cells. (PSD 3346 kb)
Summary of results of RNA-seq of sh-Control and sh5-UNC5A clones of MCF7 and T-47D cells. Various comparisons are shown. (XLSX 859 kb)
Pathways analyses using DAVID of differentially expressed genes under different conditions and in different cell types. (XLSX 139 kb)
Characterization of TMCF7 cells with and without UNC5A knockdown for stemness and luminal/basal hybrid features. (PSD 50580 kb)
About this article
Cite this article
Padua, M.B., Bhat-Nakshatri, P., Anjanappa, M. et al. Dependence receptor UNC5A restricts luminal to basal breast cancer plasticity and metastasis. Breast Cancer Res 20, 35 (2018). https://doi.org/10.1186/s13058-018-0963-5
- Breast cancer
- Estrogen receptor
- Estradiol and metastasis