Prioritizing genes associated with prostate cancer development
- Ivan P Gorlov1Email author,
- Kanishka Sircar†2,
- Hongya Zhao†1, 5,
- Sankar N Maity1,
- Nora M Navone1,
- Olga Y Gorlova3,
- Patricia Troncoso2,
- Curtis A Pettaway4,
- Jin Young Byun1 and
- Christopher J Logothetis1
© Gorlov et al; licensee BioMed Central Ltd. 2010
Received: 25 March 2010
Accepted: 2 November 2010
Published: 2 November 2010
The genetic control of prostate cancer development is poorly understood. Large numbers of gene-expression datasets on different aspects of prostate tumorigenesis are available. We used these data to identify and prioritize candidate genes associated with the development of prostate cancer and bone metastases. Our working hypothesis was that combining meta-analyses on different but overlapping steps of prostate tumorigenesis will improve identification of genes associated with prostate cancer development.
A Z score-based meta-analysis of gene-expression data was used to identify candidate genes associated with prostate cancer development. To put together different datasets, we conducted a meta-analysis on 3 levels that follow the natural history of prostate cancer development. For experimental verification of candidates, we used in silico validation as well as in-house gene-expression data.
Genes with experimental evidence of an association with prostate cancer development were overrepresented among our top candidates. The meta-analysis also identified a considerable number of novel candidate genes with no published evidence of a role in prostate cancer development. Functional annotation identified cytoskeleton, cell adhesion, extracellular matrix, and cell motility as the top functions associated with prostate cancer development. We identified 10 genes--CDC2, CCNA2, IGF1, EGR1, SRF, CTGF, CCL2, CAV1, SMAD4, and AURKA--that form hubs of the interaction network and therefore are likely to be primary drivers of prostate cancer development.
By using this large 3-level meta-analysis of the gene-expression data to identify candidate genes associated with prostate cancer development, we have generated a list of candidate genes that may be a useful resource for researchers studying the molecular mechanisms underlying prostate cancer development.
Ample gene-expression data are publicly available. Two major databases are Oncomine http://www.oncomine.org and the Gene Expression Omnibus (GEO; http://www.ncbi.nlm.nih.gov/geo/). Oncomine is a rapidly growing compendium of more than 20,000 cancer transcriptomes. Version 3.6, as accessed on January 5, 2010, comprised 35 datasets related to different aspects of prostate tumorigenesis. The GEO database is part of the open National Center for Biotechnology Information (NCBI) resources. GEO, the largest publicly available repository of gene-expression data , was established in 2000 to house and distribute those data to researchers . This resource, however, is not generally used efficiently because it is not obvious how to combine data from different sources. Meta-analysis has the potential to reduce the biases of individual studies and may identify a reproducible set of genes [12–14].
A tumor's ability to invade distant sites may develop during relatively early stages of tumorigenesis and may be associated with the gene-expression signature in normal tissue, although the genes associated with metastatic progression would be expected to have their highest level of up-regulation or down-regulation during the later stages. Therefore, it should be beneficial to use data from different stages of prostate tumorigenesis to identify genes associated with prostate cancer development. We hypothesized that combining the gene-expression data from studies targeting different stages of prostate tumorigenesis can reliably identify those genes associated with prostate cancer development.
Our approach is based on the ideas that tumorigenesis is a continuous process and that the gene-expression signature underlying the development of bone metastases starts to form in the early stages of prostate tumorigenesis and becomes well developed in the later stages. We have assumed that combining meta-analyses of different steps of prostate carcinogenesis and assigning greater weight to more-specific data might improve identification of genes associated with prostate tumorigenesis, especially those involved in the development of bone metastases; therefore, we have up-weighted the third level of meta-analysis.
First level of the meta-analysis
The tendency of prostate tumor to metastasize to bone is a hallmark of prostate tumorigenesis. Breast and lung cancer also often metastasize to bone, although not as frequently as prostate cancer does. Bone-metastasizing cancers may share a gene-expression signature that predisposes them to form bone metastases. On the basis of this hypothesis, the first level of our meta-analysis focused on comparing bone-metastasizing and non-bone metastasizing cancers. Bone-metastasizing cancers included breast and lung cancers. Non-bone metastasizing cancers included colorectal and ovarian cancers, which very rarely metastasize to bone. The studies we used are listed in Additional file 1; all of them were aimed at identifying genes differently expressed between normal tissue and localized tumor tissues.
For the meta-analysis, we used Rosenthal's extension of Stouffer's method . The choice of the method was dictated by the available data: for many studies, the individual gene-expression data points were not available, although the t test results and corresponding p values were readily accessible. In Z score-based meta-analysis, the individual p value p ij of gene i in study j will be converted to deviate: z ij = F -1(1-p ij ), where F is the standard normal cumulative distribution function. Z scores can then be summed across studies: , where Z i is the combined Z score for the ith gene and N is the number of studies (datasets). The Z score is positive when the gene is up-regulated in a more adverse phenotype and negative when it is down-regulated in a more adverse phenotype. We used the information on the direction of the changes in gene expression (up- or down-regulated from the original studies). If the gene was down-regulated, we directly converted the p value into a Z score to produce negative Z values. If the gene was up-regulated, we used 1 - p to obtain corresponding positive Z values.
The number of studies varied for the different cancers; e.g., 4 studies were used for breast and 9 for lung cancer. To correct for the differences, we adjusted individual Z scores to make the average absolute values the same across all types of cancer. For example, the average of the absolute values of the Z scores for breast cancer is 1.87, and that for lung cancer is 2.85. That difference is likely a result of the difference in sample size, i.e., 4 vs. 9 studies. To correct for the difference in sample size, we needed to adjust the Z scores for each probe so that the average absolute Zs will be the same and equal to (1.87 + 2.85)/2 = 2.36. Then the adjustment factor will be 2.36/1.87 = 1.26 for breast and 2.36/2.85 = 0.83 for lung cancer. The adjustment ensured equal contributions of individual cancer types to the global Z scores. This adjustment guarantees that differences between bone-metastasizing and non-bone metastasizing cancers are not driven by a single cancer type (e.g., lung cancer). Similar adjustments were made for the datasets used in the second and third levels of the meta-analysis. The sample size in individual studies is also an important factor that directly influences the p value: assuming the same effect size, the p value will be smaller for studies that have a larger sample size. Since smaller p values are transformed to larger Z scores, larger studies contribute more strongly to the global Z score than smaller studies do.
We subtracted the Z scores for the non-bone metastasizing cancers from those for the bone-metastasizing cancers. This subtraction takes away the genes that are common in the transition from normal tissue to localized tumor in bone-metastasizing and non-bone metastasizing cancer and simultaneously allows identification of genes that are up-regulated or down-regulated in the bone-metastasizing cancers.
Second level of the meta-analysis
Studies used for the second and third levels of our meta-analysis: genes expressed differently in the transition from normal prostate and localized prostate cancer to metastatic disease (Oncomine datasets)
Primary author's name
Tissue type (no. of samples) Class 1 Class 2
Total no. of genes
Normal prostate (22)
Primary prostate cancer (59)
Normal adjacent prostate (12)
Prostate cancer (25)
Normal prostate (4)
Prostate cancer (23)
Normal prostate (41)
Prostate carcinoma (62)
Benign hyperplasia (9)
Prostate carcinoma (16)
Normal prostate (3)
Prostate carcinoma (22)
Benign prostate (22)
Prostate carcinoma (30)
Normal prostate (8)
Prostate adenocarcinoma (27)
Benign prostate (6)
Prostate carcinoma (7)
Normal prostate (9)
Prostate carcinoma (25)
Normal prostate (23)
Prostate carcinoma (64)
Primary prostate cancer (59)
Metastatic prostate cancer (20)
Prostate cancer (25)
Metastatic prostate cancer (6)
Prostate carcinoma (30)
Metastatic prostate cancer (19)
Prostate carcinoma (64)
Metastatic prostate cancer (25)
Prostate adenocarcinoma (27)
Metastatic prostate cancer (5)
Prostate cancer (23)
Metastatic prostate cancer (9)
Prostate carcinoma (23)
Metastatic prostate cancer (9)
Third level of the meta-analysis
Table 1 also lists the studies we used for meta-analysis of genes expressed differently in localized and primary metastatic prostate cancers. All datasets for localized vs. metastatic prostate cancer comparisons are from the Oncomine database. We followed Oncomine's definition of analysis that compared localized vs. metastatic samples. Localized samples were from primary prostate tumor, and metastatic samples, from metastatic tumors (bone, lung, liver, and others). For clinical details, see the original publications indicated in Table 1. We computed average Z scores by using the scores from the second-level meta-analysis and those from meta-analysis of gene expression in localized vs. metastatic prostate cancer.
For functional annotation, we used the Database for Annotation, Visualization, and Integrated Discovery (DAVID; http://david.abcc.ncifcrf.gov/) . DAVID tests the null hypothesis that genes are uniformly distributed across pathways and biologic functions. P values characterize the strength of statistical evidence for clustering: the lower the p value, the stronger the evidence that the genes are overrepresented in a specific pathway. Because our previous analyses [17, 18] demonstrated that separate functional annotation of up-regulated and down-regulated genes tends to produce lower p values than joint analysis does, we separately annotated the 250 top down-regulated and the 250 top up-regulated genes.
Proof of principle: Zscores of the genes with published evidence of an association with prostate cancer development
If our approach is methodologically sound, relative Z scores for the known prostate cancer-related genes are expected to rise from the first level to the third level. We used 2 sets of known prostate cancer-related genes--those identified by the KnowledgeNet approach  and those identified in the Gene Ontology (GO; http://www.geneontology.org/) database--for the functions and pathways that are known to be involved in prostate tumorigenesis: androgen receptor signaling, tumor growth factor beta (TGF-β) signaling, components of the extracellular matrix, cell adhesion, the Wnt signaling pathway, and bone development. The genes from those pathways are listed in Additional files 2 and 3.
In silico validation: primary tumors vs. distant prostate metastases
The results of 2 studies comparing gene expression in primary tumors and distant metastases were recently published (GEO dataset GDS2547) [20, 21]. We estimated the overlap between the genes expressed differently in primary tumors vs. distant metastases and the candidate genes our analysis identified.
Experimental validation of the candidates: clinically advanced prostate cancer vs. benign prostatic hypertrophy
We used in-house gene-expression data to further validate the candidates identified by our meta-analysis. The tissue samples were frozen surgical specimens obtained using a protocol approved by the institutional review board of The University of Texas MD Anderson Cancer Center. The samples were from men undergoing cystoprostatectomies (n = 6) and pelvic exenterations (n = 3) for clinically advanced prostate cancer (CAPC). Seven of those 9 patients had had metastasis at the time of surgery; the other 2 patients had developed metastatic disease shortly after surgery. As controls, we used prostate tissues from 5 men with benign prostatic hypertrophy (BPH).
The tumor tissue samples were macrodissected from the frozen sections, and the RNA was extracted by using a mirVana miRNA isolation kit from Ambion, Inc. (Austin, TX). Microarray experiments were carried out using whole-human genome oligoarrays with 44,000 60-mer probes (with 500 ng of total RNA starting material) according to the manufacturer's protocol (Agilent Technologies, Inc., Santa Clara, CA). Hybridized arrays were scanned with Agilent's dual laser-based scanner, as described previously .
After the quality control procedure, we had 36,549 probes for analysis. The gene-expression data were normalized by using the limma package in R language http://www.bioconductor.org. The number of unique genes was 24,829. The mean expression values were calculated across all spots on the condition that they were mapped to the same gene. A standard t test with equal variance was used for calculating p values for the comparison of the tumor and normal samples. The raw data were normalized within and between arrays by using the composite method of Yang et al. . The false-discovery rate was computed by using Significance Analysis of Microarrays software http://www-stat.stanford.edu/~tibs/SAM/.
Gene-expression profile of bone-metastasizing cancers (breast plus lung) is similar to that of prostate cancer
Z scores characterize both the direction (a positive score means that the gene is up-regulated) and the strength of statistical evidence (the higher the absolute value of the Z score, the stronger the evidence). We found that the Z scores derived from the comparison of normal and localized tumor tissue of bone-metastasizing cancers (breast plus lung) were much more strongly correlated with those of the prostate cancers (normal prostate vs. localized prostate tumor) than they were with those of the non-bone metastasizing cancers (colon plus ovarian): Pearson's correlation coefficients for breast vs. prostate cancer were 0.29, n = 9,824; for lung vs. prostate cancer, 0.36, n = 10,824; for colon vs. prostate cancer, 0.21, n = 12,756; and for ovarian vs. prostate cancer, 0.22, n = 11,984. The difference in correlation coefficients between any bone-metastasizing and any non-bone metastasizing cancer was significant (minimal Z test = 8.1, p < 10-6). This supports the ideas that breast and lung cancers have a gene-expression signature in common with that of prostate cancer.
The genes and their corresponding Z scores from the third level of analysis are listed in Additional file 6. Functional annotation of down-regulated genes from the third level of the analysis identified cytoskeleton, cell adhesion, actin binding, and extracellular matrix as the top functional categories (Additional file 7). The associations between those genes and functions remained statistically significant after application of Bonferroni's adjustment for multiple testing. For the up-regulated genes, cell cycle and ATP binding were the most significant functional categories.
Zscore for known prostate cancer genes
Average absolute Z scores for genes from pathways and biologic functions associated with the development of bone metastases
Function and gene categorya
No. of genesb
Absolute Z score (SE)
Degrees of freedom
AR signaling pathway
Components of EC matrix
Wnt signaling pathway
Primary prostate tumor vs. distant metastasis
Clinically advanced prostate cancer vs. benign prostatic hypertrophy
We used Spearman's correlation coefficient testing to assess for overall consistency between the results of the comparison of CAPC and BPH and the results of the third-level meta-analysis. The genes shared by the 2 studies were ranked on the basis of (a) Z scores from the third-level meta-analysis and (b) the log ratio of their expression values in the CAPC vs. BPH analysis. A positive significant correlation between the ranks was noted (r = 0.18, n = 15,503, p < 10-6).
Our meta-analysis integrated data from studies targeting a number of phenotypes related to prostate cancer development. The question is, does our meta-analysis perform better than analysis of a single phenotype, e.g., localized vs. metastatic primary tumors? It is impossible to answer this question directly because we do not have a "correct" list of genes associated with prostate cancer development. Indirect tests suggest that the 3-level meta-analysis does a better job of identifying candidate genes than the analysis of a single phenotype does. The top genes from our meta-analysis showed stronger functional clustering than did the top genes from individual meta-analyses. For example, the average -Log(p) value for the top 10 GO molecular functions identified by the 3-level meta-analysis was 4.1, whereas it was 1.9 in the comparison of localized and metastatic disease (the difference was statistically significant by the nonparametric sign test: Z = 2.9, p = 0.004). We also found that the relative Z score for the known prostate cancer genes increased from the first-level to the third-level meta-analysis. The top candidates from our meta-analysis strongly overlap with those genes that are (a) expressed differently in primary tumors and distant metastases, (b) involved in cancer development, and (c) expressed differently in CAPC and BPH. Taken together, these results suggest that our 3-level meta-analysis of the gene-expression data is an effective tool to identify the genes associated with prostate cancer development.
Recently Nakagawa et al.  published the results of a large retrospective case-control study of systemic progression of prostate cancer (GEO dataset ID GSE10645). Those authors identified 68 genes that are significantly up-regulated or down-regulated in patients with relapse defined by prostate-specific antigen concentration and systemic progression (detected on positive bone or computed-tomographic scanning) compared with those genes in patients with prostate-specific antigen concentration-defined relapse and no systemic progression. We found that our candidate genes overlapped with genes identified in Nakagawa's study: the correlation coefficient between the degree of change from Nakagawa's study and the Z scores from our analysis was 0.62, n = 58, p < 10-6. Genes that were significantly up-regulated after Bonferroni correction for multiple testing in both studies included TOP2A, MKI67, CDC2, TPX2, SEC14L1, EIF2C2, THBS2, EZH2, CDKN3, BUB1, PGK1, CCNB1, HPRT1, MSR1, WDR67, CTHRC1, BIRC5, TAF2, YY1, RAD21, RAP2B, FAM49B, SQLE, F2R, CHRAC1, INHBA, SDHC, and NOX4. Significantly down-regulated genes in both studies included PAGE4, SRD5A2, and AZGP1. We hypothesize that these 31 genes may be used to predict tumor progression after surgery.
One would expect that strong functional clustering of the top candidates might be a result of gene-gene interactions. To investigate this, we used Pathway Studio software  to construct the network of interactions of the top 200 genes. Only direct interactions--direct regulation of gene expression, protein-protein binding, or promoter binding--were used. We found that 96 genes formed the network of interactions. We then selected the genes that interacted with at least 5 other genes from the network and whose local connectivity was at least 2 times higher than the overall connectivity of the gene. This method identified 10 genes: CDC2, CCNA2, IGF1, EGR1, SRF, CTGF, CCL2, CAV1, SMAD4, and AURKA. Since those genes have a large number of downstream targets, they likely drive prostate cancer development and consequently are the best candidates for experimental verification.
A major limitation of this study is rooted in the available data and the fact that the genes assessed in the different studies only partially overlap. The studies we used were conducted for various purposes and, as a result, they are not absolutely homogeneous in terms of phenotype. This is especially relevant to the comparison of localized and metastatic cancer. Metastatic cancer included a variety of phenotypes possessing a gene-expression signature associated with the development of metastases. It is likely that the genes identified in our analysis do not completely reflect the diversity of genetic mechanisms underlying prostate cancer development but instead represent only the most common universal players in prostate tumorigenesis.
Another limitation is related to the fact that different studies use different platforms with the different sets of genes. Because of that, in our meta-analysis, different genes were assessed in a different number of the studies. One can expect a higher absolute Z score for a gene whose expression was assessed in a larger number of studies. In accord with this expectation, we found that the absolute Z scores positively correlated with the number of studies we used in the meta-analysis. However, our assessments demonstrate that this correlation is unlikely to explain more than 10% of the observed variation in Z scores (data not shown).
In conclusion, our multilevel meta-analysis efficiently combined almost all publicly available gene-expression data on prostate cancer and allowed identification of candidate genes associated with prostate tumor development. The results of several in silico validation tests of the top candidate genes suggest that they are enriched by genes associated with prostate cancer development. The list of candidate genes we have generated may be a useful resource for researchers studying the molecular mechanisms underlying prostate cancer development.
Abbreviations and acronyms
Gene Expression Omnibus database
Gene Ontology database
transforming growth factor beta
clinically advanced prostate cancer
benign prostatic hypertrophy
This study was supported by the David H. Koch Center for Applied Research of Genitourinary Cancers, the National Institutes of Health Prostate SPORE grant 1 P50 CA140388-01, and the National Institutes of Health Cancer Center Support Grant 5 P30 CA16672. The work was also supported by institutional funds from UTMDACC (KS).
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