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Logo of bmccancBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Cancer
BMC Cancer. 2007; 7: 182.
Published online Sep 25, 2007. doi:  10.1186/1471-2407-7-182
PMCID: PMC2077336

Pathway analysis of gene signatures predicting metastasis of node-negative primary breast cancer



Published prognostic gene signatures in breast cancer have few genes in common. Here we provide a rationale for this observation by studying the prognostic power and the underlying biological pathways of different gene signatures.


Gene signatures to predict the development of metastases in estrogen receptor-positive and estrogen receptor-negative tumors were identified using 500 re-sampled training sets and mapping to Gene Ontology Biological Process to identify over-represented pathways. The Global Test program confirmed that gene expression profilings in the common pathways were associated with the metastasis of the patients.


The apoptotic pathway and cell division, or cell growth regulation and G-protein coupled receptor signal transduction, were most significantly associated with the metastatic capability of estrogen receptor-positive or estrogen-negative tumors, respectively. A gene signature derived of the common pathways predicted metastasis in an independent cohort. Mapping of the pathways represented by different published prognostic signatures showed that they share 53% of the identified pathways.


We show that divergent gene sets classifying patients for the same clinical endpoint represent similar biological processes and that pathway-derived signatures can be used to predict prognosis. Furthermore, our study reveals that the underlying biology related to aggressiveness of estrogen receptor subgroups of breast cancer is quite different.


Microarray technology has become a popular tool to classify breast cancer patients into histological subtypes, subgroups with a different prognosis, different site of relapse, and different types of response to treatment [1-9]. A major challenge for application of gene expression profiling is stability of the gene list as a signature [10]. Considering that many genes have correlated expression on a gene expression array, especially for genes involved in the same biological process, it is quite possible that different genes may be present in different signatures when different training sets of patients and different statistical tools are used. Furthermore, genes are usually included in a classifier applying stringent statistical criteria. At these strict significance levels, there is only a small chance for any specific gene to be included. Reproducibility in gene signatures identified in different datasets is thus unlikely [11]. To our knowledge, so far prognostic gene signatures were identified based on the performance of individual genes, regardless of their biological functions. We and others have previously suggested that it might be more appropriate to interrogate the gene lists for biological themes, rather than individual genes [8,12-19]. Moreover, identification of the distinct biological processes between subtypes of cancer patients is more relevant to understand the mechanism of the disease development and for targeted drug development.

In this study we associated biological processes with the tumor's metastatic capability. We re-sampled our data set numerous times to get multiple gene lists whose expression correlated with patients' survival. Based on these gene lists, over-represented pathways defined in Gene Ontology Biological Process (GOBP) were identified for estrogen receptor (ER)-positive or ER-negative breast cancer patients, separately. One step further, we compared the pathways represented by different published prognostic gene signatures with the over-represented pathways associated with metastatic capability. This study also demonstrated it is feasible to construct a gene signature from the key pathways to predict clinical outcomes.


Patient population

The study was approved by the Medical Ethics Committee of the Erasmus MC Rotterdam, The Netherlands (MEC 02.953), and was performed in accordance to the Code of Conduct of the Federation of Medical Scientific Societies in the Netherlands [20]. A cohort of 344 breast tumor samples from our tumor bank at the Erasmus Medical Center (Rotterdam, Netherlands) was used in this study. All these samples were from patients with lymph node-negative breast cancer who had not received any adjuvant systemic therapy, and had more than 70% tumor content. Among them, 286 samples had been used to derive a 76-gene signature to predict distant metastasis [8]. Fifty-eight additional ER-negative cases were included to increase the numbers in this subgroup. According to our previous study [21], array-measured ER status and clinical ER status have the best correlation when the cutoff is set at 1000, after scaling the average intensity of probe sets on an Affymetrix HG-U133A chip to 600. Using array-based ER status allows us to avoid the variations of the measures of ER by either immunohistochemistry or biochemical assays, as well as including tumors whose ER status is undetermined. Therefore, ER status for a patient was determined based on the expression level of the ER gene on the chip in this study. A sample is considered ER-positive if its ER expression level is higher than 1000. Otherwise, the sample is ER-negative [21]. As a result, there are 221 ER-positive and 123 ER-negative patients in the 344-patient population. The mean age of the patients was 53 years (median 52, range 26–83 years), 197 (57%) were premenopausal and 147 (43%) postmenopausal. T1 tumors (≤ 2 cm) were present in 168 patients (49%), T2 tumors (> 2–5 cm) in 163 patients (47%), T3/4 tumors (> 5 cm) in 12 patients (3%), and 1 patient had unknown tumor stage. Pathological examination was carried out by regional pathologists as described previously [22] and the histological grade was coded as poor in 184 patients (54%), moderate in 45 patients (13%), good in 7 patients (2%), and unknown for 108 patients (31%). During follow-up 103 patients showed a relapse within 5 years and were counted as failures in the analysis for DMFS. Eighty two patients died after a previous relapse. The median follow-up time of patients still alive was 101 months (range 61–171 months).

RNA isolation and hybridization

Total RNA was extracted from 20–40 cryostat sections of 30 um thickness with RNAzol B (Campro Scientific, Veenendaal, Netherlands). After being biotinylated, targets were hybridized to Affymetrix HG-U133A chips as described [8]. Gene expression signals were calculated using Affymetrix GeneChip analysis software MAS 5.0. Chips with an average intensity less than 40 or a background higher than 100 were removed. Global scaling was performed to bring the average signal intensity of a chip to a target of 600 before data analysis. For the validation dataset [23], quantile normalization was performed and ANOVA was used to eliminate batch effects from different sample preparation methods, RNA extraction methods, different hybridization protocols and scanners.

Multiple gene signatures

For ER-positive and ER-negative patients, 80 samples were randomly selected as a training set and univariate Cox proportional-hazards regression was performed to identify genes whose expression patterns were most correlated to patients' DMFS time. Our previous analysis suggested that 80 patients represent a minimum size of the training set for producing a prognostic gene signature with stable performance [8]. Because the majority of the published gene expression signatures had less than 100 genes, the top 100 genes from the Cox regression were used as a signature to predict tumor recurrence for the remaining patients. A relapse score for a patient was used to calculate a patient's risk of distant metastasis and was defined as the linear combination of logarithmically transformed gene expression levels weighted by the standardized Cox regression coefficient as described [8]. ROC analysis with distant metastasis within 5 years as a defining point was conducted. Patients who did not have 5-year follow-up were excluded from ROC analysis. The AUC of the ROC plots was used as a measure of the performance of a signature in the test set. The above procedure was repeated 500 times (Figure (Figure1).1). Thus, 500 signatures of 100 genes each were obtained for both the ER-positive and ER-negative subgroups. The frequency of the selected genes in the 500 signatures was calculated and the genes were ranked based on the frequency.

Figure 1
Work flow of data analysis for deriving core genes and over-represented pathways.

As a control, the patient survival data for the ER-positive patients or ER-negative patients was permuted randomly and re-assigned to the chip data. As described above, 80 chips were then randomly selected as a training set and the top 100 genes were selected using the Cox modeling based on the permuted clinical information. The clinical information was permuted 10 times. For each permutation of the survival data, 50 training sets of 80 patients were created. For each training set, the top 100 genes were obtained as a control gene list based on the Cox modeling. Thus, a total of 500 control signatures were obtained. The predictive performance of the 100 genes was examined in the remaining patients. A ROC analysis was conducted and AUC was calculated in the test set.

Mapping signatures to GOBP and identification of over-represented pathways

To identify over-representation of biological pathways in the signatures, genes on Affymetrix HG-U133A chip were mapped to the categories of GOBP based on the annotation table downloaded from [24]. Categories that contained at least 10 probe sets from the HG-U133A chip were retained for subsequent pathway analysis. As a result, 304 categories were used for following pathway analysis. The 100 genes of each signature were mapped to GOBP. Hypergeometric distribution probabilities for all included GOBP categories were calculated for each signature to evaluate its statistical significance. A pathway that had a hypergeometric distribution probability < 0.05 and was hit by two or more genes from the 100 genes was considered an over-represented pathway in a signature. The total number of times a pathway occurred in the 500 signatures was considered as the frequency of over-representation.

To evaluate the relationship between a pathway as a whole and the clinical outcome, each of the top 20 over-represented pathways that have the highest frequencies in the 500 signatures were subjected to Global Test program [12,14]. The Global Test examines the association of a group of genes as a whole to a specific clinical parameter such as DMFS. The contribution of individual genes in the top over-represented pathways to the association was also evaluated.

Building pathway-based signatures

To explore the possibility of using the genes from over-represented pathways as a signature to predict distant metastasis, the top two pathways for ER-positive and ER-negative tumors that were in the top 20 list based on frequency of over-representation and had the smallest p values with the Global Test program were chosen to build a gene signature. First, genes in the pathway were selected if their z-score was greater than 1.96 from the Global Test program. A z-score greater than 1.96 indicates that the association of the gene expression with DMFS time is significant (p < 0.05) [12,14]. To determine the optimal number of genes in a given pathway used for building the signature, combinations of gene markers were tested by adding one gene at a time according to their z-scores. The number of significant genes that gave the highest AUC value of the ROC analysis with distant metastasis within 5 years as the defining point was considered optimal and used to build a pathway-based signature.

The relapse score for a given patient was calculated as the difference between the linear combination of the logarithmically transformed expression signals weighted by their z-scores for negatively correlated genes and that for positively correlated genes. The predicting performance of the gene signature was evaluated by ROC and Kaplan-Meier survival analysis in an independent patient group [23] for ER-positive patients and ER-negative patients both separately and combined.

Comparing multiple gene signatures

To compare the genes from various prognostic signatures for breast cancer, five gene signatures were selected [3,8,23,25,26]. Identity of the genes between the signatures was determined by BLAST program. To examine the representation of the top 20 pathways in the signatures, genes in each of the signatures were mapped to GOBP.

Data availability

The microarray data analyzed in this paper have been submitted to the NCBI/Genbank GEO database (series entry GSE2034 for the first 286 patients, and GSE5327 for the additional 58 patients). The microarray and clinical data used for the independent validation testing set analysis were obtained from the GEO database with accession number GSE2990.


Multiple gene signatures

Using re-sampling, we constructed a total of 1,000 prognostic gene signatures derived from different patient groups aiming to improve understanding of the underlying biological processes of breast cancer metastasis. Since gene expression patterns of ER-subgroups of breast tumors are quite different [1-4,8,27] data analysis to derive gene signatures and subsequent pathway analysis were conducted separately [8]. For both ER-positive and ER-negative patients, 80 samples were randomly selected as a training set and the 100 genes most significantly associated with distant metastasis-free survival (DMFS) were used as a signature to predict tumor recurrence for the remaining ER-positive and ER-negative patients, respectively (Figure (Figure1).1). The area under the curve (AUC) of receiver operating characteristic (ROC) analysis with distant metastasis within 5 years as a defining point was used as a measure of the performance of a signature in a corresponding test set. The above procedure was repeated 500 times. The average of AUCs for the 500 signatures in the ER-positive test sets was 0.70 (95% confidence interval (CI): 0.61–0.77) whereas the average of AUCs for 500 random gene lists was 0.50 (95% CI: 0.33–0.66), indicating a non-random prediction for the true test sets (Figure (Figure2A).2A). For ER-negative datasets, these values of average AUCs were 0.67 (95% CI: 0.53–0.80) and 0.51 (95% CI: 0.31–0.76), respectively (Figure (Figure2B).2B). The results demonstrate that depending on the training set different gene signatures can be identified with comparable performance. This could explain the results obtained by earlier studies, which reported different gene signatures with similar power to predict risk groups. The 20 most frequently found genes in the 500 signatures for ER-positive and ER-negative tumors are listed in Table Table1.1. The most frequent genes were KIAA0241 protein (KIAA0241) for ER-positive tumors, and zinc finger protein multitype 2 (ZFPM2) for ER-negative tumors. There was no overlap between genes of the ER-positive and -negative core gene lists suggesting that different molecular mechanisms are associated with the subtypes of breast cancer disease.

Table 1
Genes with highest frequencies in 500 signatures
Figure 2
Evaluation of the 500 gene signatures. Each of the 100-gene signatures for 80 randomly selected tumors in the training set was used to predict relapsed patients in the corresponding test set. Its performance was measured by the AUC of the ROC analysis. ...

Over-represented pathways in gene signatures and Global Test

The 100 genes in each of the 500 signatures for ER-positive and ER-negative tumors were mapped to the categories of GOBP. For a given gene signature, a pathway (or category) that had a hypergeometric distribution probability smaller than 0.05 and included two or more genes was considered an over-represented pathway. The "inclusion of 2 or more genes" as a selection criterion in addition to the statistical significance was to avoid selecting statistically significant pathways containing only one gene in the signature. The frequency of over-representation of GOBP in the 500 signatures for ER-positive and ER-negative dataset was calculated. Like the observation of most frequently found genes, the biological pathways over-represented in the gene signatures are distinct for ER-positive and ER-negative tumors (Table (Table2).2). For ER-positive tumors, cell division-related processes and immune-response-related pathways are frequently found in the top 20 over-represented pathways. All of the 20 pathways had a significant association with DMFS as analyzed by the Global Test program [12,14], with the 2 most significant being "apoptosis" (mainly containing genes of the extrinsic apoptotic pathway) and "regulation of cell cycle" (Table (Table2).2). For ER-negative tumors, many of the top 20 pathways are related with RNA processing, transportation and signal transduction. Eighteen of the top 20 pathways demonstrated a significant association with DMFS in the Global Test, the 2 most significant being "regulation of cell growth" and "regulation of G-protein coupled receptor signaling" (Table (Table22).

Table 2
Top 20 pathways in the 500 signatures of ER-positive and ER-negative tumors evaluated by Global Test

The contribution and significance of individual genes in the top over-represented pathways to the association with DMFS were determined for ER-positive [see Additional files 1 and 2] and ER-negative tumors [see Additional files 3 and 4]. Genes can either show a positive association with DMFS, indicating a higher expression in tumors without metastatic capability, or a negative association, indicative of a higher expression in metastatic tumors. In ER-positive tumors, pathways with a mixed association include the 2 most significant pathways "apoptosis" and "regulation of cell cycle" (Figure (Figure3A).3A). There were also a number of pathways that had a predominant positive or negative correlation with DMFS. For example, the pathway "immune response" is associated with 379 probe sets, of which the majority showed positive correlation to DMFS (Figure (Figure3A).3A). Similarly in the biological processes "cellular defense response" and "chemotaxis", most genes displayed a strong positive correlation with DMFS [see Additional file 1]. On the other hand, genes in "mitosis" (Figure (Figure3A),3A), "mitotic chromosome segregation" and "cell cycle" showed a predominant negative correlation with DMFS [see Additional file 1].

Figure 3
Association of the expression of individual genes with DMFS time for selected over-represented pathways. The Geneplot function in the Global Test program [12, 14] was applied and the contribution of the individual genes in each selected pathway is plotted. ...

In ER-negative tumors (Figure (Figure3B),3B), examples of pathways with genes that had both positive and negative correlation to DMFS include "regulation of cell growth", the most significant pathway, and "cell adhesion". Of the top 20 pathways in ER-negative tumors, none showed a dominant positive association with DMFS. Although for some pathways most genes correlated negatively with DMFS [see Additional file 3], including "regulation of G-protein coupled receptor signaling" and "skeletal development" (Figure (Figure3B),3B), ranked among the top 3 pathways in significance (Table (Table2).2). Of the top 20 core pathways 4 overlapped between ER-positive and -negative tumors, i.e., "regulation of cell cycle", "protein amino acid phosphorylation", "protein biosynthesis", and "cell cycle" (Table (Table22).

Pathway-derived gene expression profiles as a predictor

In an attempt to use gene expression profiles in the most significant biological processes to predict distant metastases we used the genes of the top 2 significant pathways in both ER-positive (Table (Table3,3, Table Table4)4) and -negative tumors (Table (Table5,5, Table Table6)6) to construct a gene signature for the prediction of distant recurrence. A 50-gene signature was constructed by combining the 38 genes from the top 2 ER-positive pathways ("apoptosis", "regulation of cell cycle") and 12 genes for the top 2 ER-negative pathways ("regulation of cell growth", "regulation of G-coupled receptor signaling"). This signature was further validated using an independent 152-patient cohort [23], which consisted of 125 ER-positive tumors and 27 ER-negative tumors (after removing 36 lymph node positive patients and a patient who died 15 days after surgery). When the 38 genes was applied to the 125 ER-positive patients, a ROC analysis gave an AUC of 0.782 (95% CI: 0.681–0.883) (Figure (Figure4A,4A, left), and Kaplan-Meier analysis for DMFS showed a clear separation in risk groups (p < 0.001, HR: 3.36 and 95% CI: 1.68–6.70) (Figure (Figure4A,4A, right). For the 12 genes for the 27 ER-negative patients, an AUC of 0.872 (95% CI: 0.719–1) (Figure (Figure4B,4B, left) and separation between risk groups with a p < 0.001 and a HR of 19.8 (95% CI: 2.41–163) (Figure (Figure4B,4B, right) was obtained. The combined 50-gene signature for ER-positive and ER-negative patients gave an AUC of 0.795 (95% CI: 0.705–0.878) (Figure (Figure4C,4C, left) and a p < 0.001 and a HR of 4.44 (95% CI: 2.31–8.54) for separation between risk groups (Figure (Figure4C,4C, right).

Table 3
Significant genes in the Apoptosis pathway in ER-positive tumors
Table 4
Significant genes in the Regulation of cell cycle pathway in ER-positive tumors
Table 5
Significant genes in the Regulation of cell growth pathway in ER-negative tumors
Table 6
Significant genes in the Regulation of G-protein coupled receptor signaling pathway in ER-negative tumors
Figure 4
Validation of pathway-based breast cancer classifiers constructed from the optimal significant genes. To find the optimal number of genes as a signature, ROC analyses, with 5-year DMFS as defining point, with an increasing number of genes were conducted ...

Pathway analysis of published prognostic gene signatures

To compare genes from various prognostic signatures for breast cancer, five published gene signatures were selected [3,8,23,25,26]. We first compared the gene sequence identity between each pair of the gene signatures and found, consistent with previous reports, very few overlapping genes (Table (Table7).7). The grade index gene expression signature comprising 97 genes, of which most are associated with cell cycle regulation and proliferation [23], showed the highest number of overlapping genes between the various signatures ranging from 5 of the 16 genes of Genomic Health [25] to 10 with Yu's 62 genes [26]. The other 4 gene signatures showed only 1 gene overlap in a pair-wise comparison, and there was no common gene for all signatures. In spite of the low number of overlapping genes across signatures, we hypothesized that the representation of common pathways in the various signatures may underlie their individual prognostic value [8]. Therefore, we examined the representation of the core prognostic pathways (Table (Table2)2) in the 5 signatures. The Genomic Health 16-gene signature mapped to 10 of the 36 distinct core pathways (20 for both ER-positive and -negative tumors but counting the 4 overlapping pathways once) whereas it mapped to a total of 25 out of 304 GOBPs. The statistical significance for the enrichment of GOBP, as computed by hypergeometric distribution probability was 2 × 10-5. Each of the other 4 signatures have 62 or more genes and were mapped to 19 (53%) distinct prognostic pathways and their statistical significance of enrichment was 1 × 10-7 for Wang and van 't Veer, 1 × 10-6 for Sotiriou and 6 × 10-11 for Yu's signature (Table (Table8).8). Of these 19 pathways, 9 were identical for all 4 signatures, i.e., "mitosis", "apoptosis", "regulation of cell cycle", "DNA repair", "cell cycle", "protein amino acid phosphorylation", "DNA replication", "intracellular signaling cascade", and "cell adhesion".

Table 7
Number of common genes between different gene signatures for breast cancer prognosis
Table 8
Mapping various gene signatures to core pathways


Gene-expression profiling for separating patients into different subtypes and risk groups have been focused on the identification of differential expression of individual genes rather than obtaining biological insight. In the present study we have used an alternative approach to identify in ER-positive and ER-negative populations of breast cancer patients the underlying biological processes associated with metastasis. Using a stringent re-sampling and permutation methodology we were able to show that indeed multiple signatures can be identified showing similar prognostic power while the genes from these different samplings have similar functions. Similar observations were made when we mapped the core prognostic pathways to 5 published prognostic signatures [3,8,23,25,26]. Thus, we showed that in spite of the low number of overlapping genes between the various published gene signatures, the signatures had many pathways in common, implying that different prognostic gene signatures represent common biology. In a recent study, comparing the prognostic performance of different gene-signatures, agreement in outcome predictions were found as well [28]. However, in contrast to our present approach, the underlying pathways were not investigated. Instead, the performance of various gene signatures on a single patient cohort, heterogeneous with respect to nodal status and adjuvant systemic therapy [29], was compared [28]. It is important to note, however, that although similar pathways are represented in various signatures, it does not necessarily mean the individual genes in a pathway are equally significant or are all similarly associated with tumor aggressiveness [see Additional files 1 and 3].

The fact that none of the 20 genes most frequently present in the 500 signatures for the ER-positive tumors were among in the top 20 core gene list of the ER-negative tumors, was not surprising and is in line with the fact that ER-subgroups of tumors are biologically very different entities [1-4,8,27]. Furthermore, although among the top 20 over-represented pathways, 4 were common for ER-positive tumors and ER-negative tumors, there were in total only 2 shared genes pointing into the same direction with respect to metastatic capability of the tumors. Both genes, KIAA0256 in the "protein biosynthesis" pathway and CCNT2 in the "cell cycle pathway", were associated with an aggressive tumor behavior. These results imply that the underlying biological processes between ER-subgroups of tumors with respect to their metastatic behavior have little if any in common. Of the top 20 core prognostic pathways for the ER-positive tumors many biological processes are related to cell division activities, immunity, signal transduction, and extrinsic apoptosis-related biological processes. The cell division-related pathways have predominantly negative correlation with survival time, while immune-related pathways have predominantly positive correlation. This indicates that ER-positive tumors with metastatic capability tend to have higher cell division rates, are more resistant to external apoptotic stimuli, and induce a poor immune reaction in the host body. In ER-positive tumors, one or more of these pathways, or genes in these pathways, have also been described to be associated with the efficacy of tamoxifen therapy in recurrent breast cancer [7], in the various prognostic signatures described in the present paper [8,23,25,26], as well as in other published signatures not specifically designed for ER-positive tumors, such as the 70-gene prognostic signature [3], the stromal signatures [30], and the hypoxia signature [31]. The differences in metastatic behavior between ER-subgroups of tumors is further substantiated by the finding that in ER-negative tumors other pathways showed the strongest involvement, including those related with cell growth regulation, possibly through JAK/STAT signaling, and modulation of G-protein receptor signal transduction, RNA splicing or processing, and ion transport. No comparison can be made with the literature since no other studies so far have described prognostic of predictive pathways specifically in ER-negative breast cancer.

We were able to construct a 50-gene signature by combining the genes from the 2 most significant ER-positive and ER-negative pathways. This signature was validated and performed well on an independent published patient cohort [23], herewith showing the feasibility to derive a gene signature from biological pathways. Although further methodology and analysis would be required to optimize the selection of such a pathway-based prognostic signature, our example provides not only a new way to derive gene signatures for cancer prognosis, but also gives insight into the distinct biological processes between subgroups of tumors.


Our study for the first time applied a method that systematically evaluated the biological pathways related to patient outcomes of breast cancer and showed that various published prognostic gene signatures providing similar outcome predictions are based on the representation of largely overlapping biological processes. Identification of the key biological processes, rather than the assessment of signatures based on individual genes, allows not only to build a biological meaningful gene signature from functionally related genes, but also provides insight into the mechanism of the disease development and, as spin off, potential targets for future drug development. In this respect, as pharmacologic inhibitors for specific pathways become available for the clinic, the signatures that define tumors according to their vital pathways may provide crucial guidance for designing appropriate drug combinations [32].


AUC, area under the curve; DMFS, distant metastasis-free survival; ER, estrogen receptor. GOBP, gene ontology biological process; ROC, receiver operating characteristic.

Competing interests

Regarding conflict of interest, three co-authors are employed by Veridex LLC, a Johnson & Johnson company (Jack Yu, Yi Zhang, Yixin Wang). Johnson & Johnson is a healthcare company that is in the business of commercialising diagnostic products. The Erasmus Medical Center (Anieta Sieuwerts, John Martens, Marcel Smid, Jan Klijn, John Foekens) was financially supported by Veridex LLC for tissue processing and isolating RNA for microarray analysis.

Authors' contributions

JXY assisted in the study design study, carried out the data analysis and drafted the manuscript; AMS processed the tumor tissues, isolated the RNA and did the quality control; YZ JXY assisted in the study design study and carried out the data analysis; JWMM assisted in the study design and contributed to the drafting of the manuscript; MS contributed to the data analysis; JGMK assisted in the collection of the clinical data and the study design; YW assisted in the study design, data analysis and drafting of the manuscript; JAF assisted in the study design, provided the clinical samples with the follow-up data, and contributed to the drafting of the manuscript. All authors have read and approved the final paper.

Pre-publication history

The pre-publication history for this paper can be accessed here:


Supplementary Material

Additional file 1:

Top 20 prognostic pathways in ER-positive tumors. The data provided represent the results of the Geneplot function in the Global test program. The contribution of each individual gene in the top 20 prognostic pathways with distant metastasis-free survival in ER-positive tumors is plotted.

Additional file 2:

Significant genes in the top 20 prognostic pathways for ER-positive tumors. The data provided represent the contribution, standard deviation, and z-scores of each individual gene with distant metastasis-free survival in ER-positive tumors in the top 20 prognostic pathways.

Additional file 3:

Top 20 prognostic pathways in ER-negative tumors. The data provided represent the results of the Geneplot function in the Global test program. The contribution of each individual gene in the top 20 prognostic pathways with distant metastasis-free survival in ER-negative tumors is plotted.

Additional file 4:

Significant genes in the top 20 prognostic pathways for ER-negative tumors. The data provided represent the contribution, standard deviation, and z-scores of each individual gene with distant metastasis-free survival in ER-negative tumors in the top 20 prognostic pathways.


This work was supported in part by the by a research grant from the Netherlands Genomics Initiative/Netherlands Organization for Scientific Research (M.S, J.G.M.K., J.A.F.). The Netherlands Genomics Initiative had no role in the design and conduct of the study, in the collection, analysis, and interpretation of the data, in the writing of the mansucript and the decision to submit the manuscript for publication.


  • Perou CM, Sorlie T, Eisen MB, van de Rijn M, Jeffrey SS, Rees CA, Pollack JR, Ross DT, Johnsen H, Akslen LA, Fluge O, Pergamenschikov A, Williams C, Zhu SX, Lonning PE, Borresen-Dale AL, Brown PO, Botstein D. Molecular portraits of human breast tumours. Nature. 2000;406:747–752. doi: 10.1038/35021093. [PubMed] [Cross Ref]
  • Sorlie T, Perou CM, Tibshirani R, Aas T, Geisler S, Johnsen H, Hastie T, Eisen MB, van de Rijn M, Jeffrey SS, Thorsen T, Quist H, Matese JC, Brown PO, Botstein D, Eystein Lonning P, Borresen-Dale AL. Gene expression patterns of breast carcinomas distinguish tumor subclasses with clinical implications. Proc Natl Acad Sci USA. 2001;98:10869–10874. doi: 10.1073/pnas.191367098. [PMC free article] [PubMed] [Cross Ref]
  • Van 't Veer LJ, Dai H, van de Vijver MJ, He YD, Hart AA, Mao M, Peterse HL, van der Kooy K, Marton MJ, Witteveen AT, Schreiber GJ, Kerkhoven RM, Roberts C, Linsley PS, Bernards R, Friend SH. Gene expression profiling predicts clinical outcome of breast cancer. Nature. 2002;415:530–536. doi: 10.1038/415530a. [PubMed] [Cross Ref]
  • Sorlie T, Tibshirani R, Parker J, Hastie T, Marron JS, Nobel A, Deng S, Johnsen H, Pesich R, Geisler S, Demeter J, Perou CM, Lønning PE, Brown PO, Børresen-Dale AL, Botstein D. Repeated observation of breast tumor subtypes in independent gene expression data sets. Proc Natl Acad Sci USA. 2003;100:8418–8423. doi: 10.1073/pnas.0932692100. [PMC free article] [PubMed] [Cross Ref]
  • Sotiriou C, Neo SY, McShane LM, Korn EL, Long PM, Jazaeri A, Martiat P, Fox SB, Harris AL, Liu ET. Breast cancer classification and prognosis based on gene expression profiles from a population-based study. Proc Natl Acad Sci USA. 2003;100:10393–10398. doi: 10.1073/pnas.1732912100. [PMC free article] [PubMed] [Cross Ref]
  • Brenton JD, Carey LA, Ahmed AA, Caldas C. Molecular classification and molecular forecasting of breast cancer: ready for clinical application? J Clin Oncol. 2005;23:7350–7360. doi: 10.1200/JCO.2005.03.3845. [PubMed] [Cross Ref]
  • Jansen MP, Foekens JA, van Staveren IL, Dirkzwager-Kiel MM, Ritstier K, Look MP, Meijer-van Gelder ME, Sieuwerts AM, Portengen H, Dorssers LC, Klijn JG, Berns EM. Molecular classification of tamoxifen-resistant breast carcinomas by gene expression profiling. J Clin Oncol. 2005;23:732–740. doi: 10.1200/JCO.2005.05.145. [PubMed] [Cross Ref]
  • Wang Y, Klijn JG, Zhang Y, Sieuwerts AM, Look MP, Yang F, Talantov D, Timmermans M, Meijer-van Gelder ME, Yu J, Jatkoe T, Berns EM, Atkins D, Foekens JA. Gene-expression profiles to predict distant metastasis of lymph-node-negative primary breast cancer. Lancet. 2005;365:671–679. [PubMed]
  • Smid M, Wang Y, Klijn JG, Sieuwerts AM, Zhang Y, Atkins D, Martens JW, Foekens JA. Genes associated with breast cancer metastatic to bone. J Clin Oncol. 2006;24:2261–2267. doi: 10.1200/JCO.2005.03.8802. [PubMed] [Cross Ref]
  • Michiels S, Koscielny S, Hill C. Prediction of cancer outcome with microarrays: a multiple random validation strategy. Lancet. 2005;365:488–492. doi: 10.1016/S0140-6736(05)17866-0. [PubMed] [Cross Ref]
  • Simon R. Development and evaluation of therapeutically relevant predictive classifiers using gene expression profiling. J Natl Cancer Inst. 2006;98:1169–1171. [PubMed]
  • Goeman JJ, van de Geer SA, de Kort F, van Houwelingen HC. A global test for groups of genes: testing association with a clinical outcome. Bioinformatics. 2004;20:93–99. doi: 10.1093/bioinformatics/btg382. [PubMed] [Cross Ref]
  • Vogelstein B, Kinzler KW. Cancer genes and the pathways they control. Nat Med. 2004;10:789–799. doi: 10.1038/nm1087. [PubMed] [Cross Ref]
  • Goeman JJ, Oosting J, Cleton-Jansen AM, Anninga JK, van Houwelingen HC. Testing association of a pathway with survival using gene expression data. Bioinformatics. 2005;21:1950–1957. doi: 10.1093/bioinformatics/bti267. [PubMed] [Cross Ref]
  • Segal E, Friedman N, Kaminski N, Regev A, Koller D. From signatures to models: understanding cancer using microarrays. Nat Genet. 2005:S38–45. doi: 10.1038/ng1561. [PubMed] [Cross Ref]
  • Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA, Paulovich A, Pomeroy SL, Golub TR, Lander ES, Mesirov JP. Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci USA. 2005;102:15545–15550. doi: 10.1073/pnas.0506580102. [PMC free article] [PubMed] [Cross Ref]
  • Tian L, Greenberg SA, Kong SW, Altschuler J, Kohane IS, Park PJ. Discovering statistically significant pathways in expression profiling studies. Proc Natl Acad Sci USA. 2005;102:13544–13549. doi: 10.1073/pnas.0506577102. [PMC free article] [PubMed] [Cross Ref]
  • Adler AS, Lin M, Horlings H, Nuyten DS, van de Vijver MJ, Chang HY. Genetic regulators of large-scale transcriptional signatures in cancer. Nat Genet. 2006;38:421–430. doi: 10.1038/ng1752. [PMC free article] [PubMed] [Cross Ref]
  • Tinker AV, Boussioutas A, Bowtell DD. The challenges of gene expression microarrays for the study of human cancer. Cancer Cell. 2006;9:333–339. doi: 10.1016/j.ccr.2006.05.001. [PubMed] [Cross Ref]
  • http://www.fmwv.nl
  • Foekens JA, Atkins D, Zhang Y, Sweep FC, Harbeck N, Paradiso A, Cufer T, Sieuwerts AM, Talantov D, Span PN, Tjan-Heijnen VC, Zito AF, Specht K, Hoefler H, Golouh R, Schittulli F, Schmitt M, Beex LV, Klijn JG, Wang Y. Multicenter validation of a gene expression-based prognostic signature in lymph node-negative primary breast cancer. J Clin Oncol. 2006;24:1665–1671. doi: 10.1200/JCO.2005.03.9115. [PubMed] [Cross Ref]
  • Foekens JA, Portengen H, van Putten WL, Trapman AM, Reubi JC, Alexieva-Figusch J, Klijn JGM. Prognostic value of receptors for insulin-like growth factor 1, somatostatin, and epidermal growth factor in human breast cancer. Cancer Res. 1989;49:7002–7009. [PubMed]
  • Sotiriou C, Wirapati P, Loi S, Harris A, Fox S, Smeds J, Nordgren H, Farmer P, Praz V, Haibe-Kains B, Desmedt C, Larsimont D, Cardoso F, Peterse H, Nuyten D, Buyse M, van de Vijver MJ, Bergh J, Piccart M, Delorenzi M. Gene expression profiling in breast cancer: understanding the molecular basis of histologic grade to improve prognosis. J Natl Cancer Inst. 2006;98:262–272. [PubMed]
  • http://www.affymetrix.com
  • Paik S, Shak S, Tang G, Kim C, Baker J, Cronin M, Baehner FL, Walker MG, Watson D, Park T, Hiller W, Fisher ER, Wickerham DL, Brynat J, Wolmark N. A multigene assay to predict recurrence of tamoxifen-treated, node-negative breast cancer. N Engl J Med. 2004;351:2817–2826. doi: 10.1056/NEJMoa041588. [PubMed] [Cross Ref]
  • Yu K, Lee CH, Tan PH, Hong GS, Wee SB, Wong CY, Tan P. A molecular signature of the Nottingham prognostic index in breast cancer. Cancer Res. 2004;64:2962–2968. doi: 10.1158/0008-5472.CAN-03-2430. [PubMed] [Cross Ref]
  • Gruvberger S, Ringner M, Chen Y, Panavally S, Saal LH, Borg A, Ferno M, Peterson C, Meltzer PS. Estrogen receptor status in breast cancer is associated with remarkably distinct gene expression patterns. Cancer Res. 2001;61:5979–5984. [PubMed]
  • Fan C, Oh DS, Wessels L, Weigelt B, Nuyten DS, Nobel AB, van't Veer LJ, Perou CM. Concordance among gene-expression-based predictors for breast cancer. N Engl J Med. 2006;355:560–569. doi: 10.1056/NEJMoa052933. [PubMed] [Cross Ref]
  • van de Vijver MJ, He YD, van't Veer LJ, Dai H, Hart AA, Voskuil DW, Schreiber GJ, Peterse JL, Roberts C, Marton MJ, Parrish M, Atsma D, Witteveen A, Glas A, Delahaye L, van der Velde T, Bartelink H, Rodenhuis S, Rutgers ET, Friend SH, Bernards R. A gene-expression signature as a predictor of survival in breast cancer. N Engl J Med. 2002;347:1999–2009. doi: 10.1056/NEJMoa021967. [PubMed] [Cross Ref]
  • West RB, Nuyten DS, Subramanian S, Nielsen TO, Corless CL, Rubin BP, Montgomery K, Zhu S, Patel R, Hernandez-Boussard T, Goldblum JR, Brown PO, van de Vijver M, van de Rijn M. Determination of stromal signatures in breast carcinoma. PLoS Biol. 2005;3:e187. doi: 10.1371/journal.pbio.0030187. [PMC free article] [PubMed] [Cross Ref]
  • Winter SC, Buffa FM, Silva P, Miller C, Valentine HR, Turley H, Shah KA, Cox GJ, Corbridge RJ, Homer JJ, Musgrove R, Slevin N, Sloan P, Price P, West CM, Harris AL. Relation of a hypoxia metagene derived from head and neck cancer to prognosis of multiple cancers. Cancer Res. 2007;67:3441–3449. doi: 10.1158/0008-5472.CAN-06-3322. [PubMed] [Cross Ref]
  • Massague J. Sorting out breast-cancer gene signatures. N Engl J Med. 2007;356:294–297. doi: 10.1056/NEJMe068292. [PubMed] [Cross Ref]

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