Secondary Logo

Journal Logo


The epigenetics of prostate cancer diagnosis and prognosis

update on clinical applications

Blute, Michael L. Jr.a; Damaschke, Nathan A.a; Jarrard, David F.a,b,c

Author Information
doi: 10.1097/MOU.0000000000000132
  • Free



Epigenetics refers to the stable transmission of cellular information due to a chemical modification of the DNA without disrupting the DNA sequence. Among these processes include DNA methylation, RNA interference, histone post-translational modifications (PTMs), and genomic imprinting. Changes in tissue epigenetics can alter gene expression generating malignant transformation by assisting in tumor invasion, angiogenesis, and cellular dedifferentiation and proliferation. The process of prostate carcinogenesis is not well understood and many of the molecular mechanisms contributing to its progression are poorly described. To date, in addition to genetic mutations acting as a foundation for cancer development, epigenetic changes are now included in the molecular pathogenesis of prostate cancer (PCa). Among the most common and well known epigenetic changes seen in PCa is DNA methylation, in which an addition of a methyl group to cytosine adjacent to guanine within the DNA sequence occurs. DNA methylation can be either hypomethylated or hypermethylated leading to chromosomal instability, altered gene expression, and subsequent malignant changes. Newer research developing histone modifications has been undertaken, but to date, the majority of epigenetic markers used in PCa are DNA methylation based.

Epigenetic alterations offer an explanation for prostate tumor biology. It is known that PCa develops throughout the prostate gland at multiple foci suggesting a ‘field effect’. Alterations in DNA methylation and imprinting also occur with aging in the human prostate [1] and may underlie the susceptibility of the prostate gland for developing cancer [2]. Underlying factors that promote an epigenetic field effect are comprehensive and include inflammation, diet, and other environmental insults [2]. Epigenetic as well as genetic changes clearly participate in the development and progression of PCa. In contrast to genetic changes, epigenetic alterations are reversible and are an area of increasing interest with regards to therapeutics. With the advent of the ConfirmMDx test, DNA methylation markers are being commercially used for the diagnosis of PCa, and several have prognostic potential either alone or in combination with other types of molecular markers. We describe recent epigenetic findings in PCa and focus on how these molecular changes are being utilized diagnostically in PCa management.

Box 1
Box 1:
no caption available


DNA methylation is the covalent binding of a methyl group to the dinucleotide Cytosine Guanine and is sometimes referred to as the ‘fifth base’. Dense methylation at so-called Cytosine phosphate Guanine islands leads to gene silencing by inhibiting access of transcriptional activators. This can induce chromatin condensation and an inactive state in conjunction with histone deacetylases and other chromatin remodelers. Conversely, decreased methylation throughout the genome (hypomethylation) is a hallmark of cancer and participates in genome instability and the activation of proto-oncogenes.

Correlating epigenetic changes to clinical data is essential to using these gene alterations as possible biomarkers for PCa diagnosis. An even more critical area is generating a molecular marker, from a biofluid (urine, serum) or biopsy that discriminates between indolent and clinically significant PCa prior to treatment. Roughly 2 decades ago, one of the first hypermethylated gene promoters to be discovered in PCa was glutathione S-transferase PI (GSTPI), a gene involved in the detoxification of xenobiotics and oxygen radicals [3]. This hypermethylation occurs in over 90% of primary PCa and 70% of prostatic intraepithelial neoplasia lesions [4]. A recent review on the correlation of GSTPI methylation with cancer prognosis concluded there is no convincing evidence for the use of this gene in cancer tissues for predicting early disease outcomes [5].

GSTPI assays have been developed for detecting PCa in serum and other fluid sources, such as urine, ejaculate, and expressed prostatic fluid. As a prognostic approach, serum levels of GSTPI have been recently assessed as to whether they are associated with response and survival in men with castrate-resistant PCa (CRPC) treated with docetaxel, cabazitaxel, or mitoxantrone chemotherapy [6▪]. Using PCR analysis, in a phase II cohort, increased methylated GSTP1 was a better predictor of overall survival than prostate specific antigen (PSA) changes after 3 months (P = 0.02). This may reflect increased circulating tumor burden. Of note, the study validated their findings in a phase II cohort thereby increasing support for the use of GSTP1 methylation as a marker of chemotherapy response in CRPC. Its application to other types of CRPC systemic treatments has yet to be investigated.

A comprehensive assessment of emerging candidate markers for prognosis was recently published by Strand et al.[5]. These are beyond the scope of this discussion; however, several loci warrant mentioning as being validated, widely studied, and include needle biopsy tissue. Adenomatous polyposis coli (APC), a well characterized tumor suppressor regulating Wnt signaling [7], is frequently found to be methylated in PCa and other tumors [8]. It has been extensively studied in PCa, but is one of the few loci investigated using diagnostic biopsy material and looking at death as an outcome. APC methylation was investigated using methylation-sensitive PCR or methylation specific PCR in PCa tissue samples from two large patient sets (total 462), and was a significant predictor of PCa-specific death when both cohorts were combined [Hazard ratio (HR) 1.49 95% confidence interval (CI) 1.11–2.00] [9]. A smaller study also using biopsy specimens reported that APC methylation predicted either biochemical recurrence (BCR), metastasis, and/or death in a multivariate analysis [10]. In a recent meta-analysis of RASSF1A in 19 studies [11], hypermethylation was associated with Gleason score, PSA level, and tumor stage in tissue and presented evidence for its role in predicting BCR [12]. Other genes with promising earlier data include ABDHD9, [13]PTGS2, [14]EVX1[15▪▪], and CDH13[16].

A series of methylation loci, PITX2, C1orf114, and GABRE∼miR-452∼miR-224, as well as the three-gene marker panel AOX1/C1orf114/HAPLN3 have recently been found to hold independent prognostic value for biochemical recurrence in several large multicenter studies. PITX2 encodes the paired-like homeodomain transcription factor 2, involved in the regulation of cell-type-specific proliferation and is thought to be an upstream regulator of the insulin-like growth factor 1 receptor and the androgen receptor [17]. PITX2 generated an HR of 2.39 (95% CI 1.45–3.94) in a multivariate analysis validation study of 496 US and European patients [18]. C1orf114, also known as CCDC181, has an unknown function and was identified initially on methylation arrays [19▪]. A three-gene methylation signature of C1orf114, AOX1, and HAPLN3 performed better than individual genes on recent analysis [19▪]. These validated genes hold promise, but involve retrospective radical prostatectomy specimens. As predicting tumor outcomes before treatment is the ideal goal, generating this information from biopsy specimens should ideally be the tissue source of choice.

DNA methylation profiling and next-generation sequencing have made it possible to evaluate methylation differences between PCa and benign prostate tissues at thousands of loci simultaneously. This has greatly accelerated the discovery of novel methylation markers. A recent analysis using methylation arrays applied these findings to clinical follow-up and found 69 methylation alterations that predicted biochemical tumor recurrence after radical prostatectomy [20]. The DNA methyltransferases, DNMT3B1 and DMNT3B2, were overexpressed in these tumors and represent a potential underlying drug target. In another larger study involving 238 tissue samples, [21] in a multivariate analysis adjusting for Gleason score and tumor stage, 16 genes were found in multiple statistical analyses to separate recurrence vs. nonrecurrence and several (CRIP1, FLNC, RASGRF2, RUNX3, and HS3ST2) were also among the candidates validated by pyrosequencing. In a unique analysis, Lin et al.[22] used enhanced reduced bisulfite sequencing to investigate methylation in primary and CRPC specimens with a neuroendocrine phenotype. This resulted in the identification of a panel of 13-gene-associated loci (GSTP1, GRASP, TMP4, KCNC2, TBX1, ZDHHC1, CAPG, RARRES2, SAC3D1, NKX2–1, FAM107A, SLC13A3, FILIP1L) confirmed in a small independent group that demonstrated increased DNA methylation with disease progression. Ultimately, combining genes will provide increased specificity and sensitivity over single-gene approaches and it is likely that gene panels will be the methodology of choice in the future. These newer approaches require further validation efforts, but highlight the promise of DNA methylation gene panels for predicting the prognosis of patients with PCa.


Epigenetic alteration of histones has received considerably less attention than DNA methylation in PCa. However, in recent years, there has been increased interest in the association of histone PTMs and PCa outcomes. Histone PTMs dictate chromatin structure that can promote activation or silencing of associated genes. Few studies have analyzed the association between PTM status and patient outcomes. One such study using immunohistochemistry staining showed that patients with increased H3K18Acetylation and H3K4diMethylation had a significantly higher risk of prostate tumor recurrence (Log-rank P = 0.0076) [23]. Additionally, H4K12Acetylation and H4R3diMethylation were shown to correlate with tumor stage. A more recent study by the same group further showed that H3K9diMethylation significantly identified low-grade PCa patients at risk for tumor recurrence (Log-rank P = 0.0043) [24▪]. These markers have experienced less clinical application due in part to the limitations in the technology available for analysis as immunohistochemistry is the only method used clinically at present, but provide a promising avenue for further development.

Underlying changes in PTMs are due to aberrant histone-modifying enzyme activity. Because of the reversible nature of PTMs, histone-modifying enzymes present an attractive therapeutic target. Several of these enzymes have been found to be altered in PCa including histone deacetylase 1 [25], SIRT1[26], and EZH2[27]. Synthetic and natural inhibitory drugs of these enzymes have already been identified [28]. The identification of patients with altered PTMs may serve as a guide to target specific PTM enzymes in a personalized medicine approach in the future.


Anatomically, urine comes within close proximity to the prostate gland as it passes through the prostatic urethra during micturition. Prostate cells are shed into urine and are made available for clinical analysis. When examined cytologically in urine, PCa cells are typically found only in patients who have clinically advanced disease [29]. Similarly important is that free DNA may pass through urine, in the absence of PCa cells, and also be detected in macrophages that phagocytize tumor cells [30]. Thus, it would seem intuitive to employ strategies using urinalysis to evaluate epigenetic changes that may suggest a diagnosis of PCa. As in prostate tissue, DNA methylation can be identified in urine by a number of modalities such as methylation-specific polymerase chain reaction, bisulfite sequencing, methylation-sensitive single nucleotide primer extension, and combined bisulfite restriction analysis [31]. Urine-based methods hold promise for real-time, rapid detection, and high-throughput analysis of clinical samples as well as offering a truly noninvasive way of detecting PCa [32].

The most widely studied epigenetic alteration in the urine to date is methylation of the GSTPI gene. In an early study, Gonzalgo et al.[33] assessed 45 postbiopsy urine samples in men suspected of having PCa and used PCR analysis to detect methylation at the gene promoter. GSTP1 methylation was present in 39% of patients with PCa on biopsy demonstrating a sensitivity of 58%. In a recent meta-analysis of 22 published papers on GSTP1 hypermethylation in biofluids, the gene appears to have a high specificity (88–100%), but a low sensitivity for PCa detection in urine (19–84%) and serum or plasma (13–70%) [34]. This lower sensitivity is likely due to the infrequent free cancer DNA or cells in these fluids.

Methylation of GSTPI appears to perform better in combination with PSA or other methylation biomarkers. A larger analysis of hypermethylation in urine after prostatic massage, using PCR, was performed in 10 separate genes (GSTP1, RASSF1a, ECDH1, APC, DAPK, MGMT, p14, p16, RARβ2, and TIMP3) [35]. The authors found that in 93% of patients with PCa, at least one gene was hypermethylated generating a specificity of 0.74. When distinguishing malignant from nonmalignant specimens, receiver operating characteristic analysis (0.74–0.86) demonstrated a combination of GSTP1, RARβ2, RASSF1a, and APC to be the best at discriminating cancer from noncancer. Finally, in a prospective study screening 337 urine samples, an investigational prostate cancer methylation assay analyzing GSTP1, APC, and RARβ2, had better predictive accuracy [area under the curve (AUC) 0.73] than age, digital rectal exam, family history, serum PSA, and prior negative biopsy and improved the decision-making process [36]. This assay has not been commercially developed as of yet.

There are a number of limitations and challenges when utilizing urine as a biofluid for epigenetic markers. The stability of biological markers can vary with temperature, pH, and processing time that pose a challenge to urine analysis. Urine sediments, including proteins, precipitates, and crystals, may entrap biomarkers altering their quantification. A major confounder is the variable presence of other cell types including inflammatory and bladder cells. We and other centers [32] have found that epithelial cells of prostate origin make up only 10–20% of the sample and that PCa cells are exceedingly rare leading to the low sensitivity of many cancer markers. Prostatic adenocarcinomas do not form functional ducts that connect with the urethra. A potential avenue for circumventing this reliance on the presence of cancer cells is by utilizing epigenetic changes found in normal epithelial cells associated with a cancer field effect. Urine testing for epigenetic changes has the potential to provide a biomarker that is cost-effective and noninvasive. However, clinical results to date have not led to the widespread adoption of these approaches for PCa detection in part because of the limitations mentioned.


PCa development is associated with both a peritumor response (e.g., field defect) and an apparent change in the histologically normal appearing tissue within the peripheral zone at distance from tumor foci. These findings have triggered the development of several distinct new tests based on the analysis of existing histologically negative biopsy tissue. Although these new tests are invasive, they do utilize an existing resource (i.e., biopsy tissue).

Epigenetic changes within a field of susceptibility associated with PCa development were first recognized by Jarrard et al.[37] in 1995. This study found alterations in genomic imprinting existed not only in the tumor, but were widespread in the peripheral prostate tissues [38]. A recent extension of these studies compared DNA methylation alterations utilizing methylation arrays in the peripheral prostate from men with cancer to those without cancer [39]. Hypomethylation occurred more frequently than hypermethylation and changes were found at only 0.2% of sites analyzed suggesting they occur less frequently. Several of these probes were used to map the extent of these DNA methylation changes and it was similar both adjacent and distant (>1 cm) to tumor foci suggesting a more widespread field defect. Another interesting aspect was the finding that several markers associated with higher grade tumors opening the possibility to detect lethal PCas from normal-appearing biopsy tissue.

A subsequent study used the most promising markers in a training set of 65 tissues and a multiplex model was created using multivariate logistic regression analysis [40]. This model was externally validated in a blinded fashion using a set of 50 histologically negative biopsy specimens. Individual genes were all highly significant in differentiating men with cancer. Regression models incorporated individual genes (EVX1, CAV1, and FGF1) as well as gene combinations (EVX1 and FGF1) to differentiate between nontumor-associated and tumor-associated tissues from the original training set. In external validation, uniplex models incorporating EVX1, CAV1, or FGF1 distinguished between tumor associated and nontumor associated biopsy-negative specimens (AUC of 0.702, 0.696, and 0.658, respectively; P < 0.05). A multiplex model (EVX1 and FGF1) identified PCa patients with an AUC of 0.774 (P = 0.001) and a negative predictive value (NPV) of 0.909. Thus, a widespread epigenetic field defect can be utilized to detect the existence of PCa in patients with histologically negative biopsies. With further validation, this marker combination (EVX1 and FGF1) has the potential to decrease the need for repeated prostate biopsies, a procedure associated with cost and complications.

The ConfirmMDx (quantitative methylation assay) is a currently marketed test that is Clinical Laboratory Improvement Amendments approved and marketed, but has yet to be submitted for Food and Drug Administration authorization. This tissue-based assay relies on epigenetic alterations surrounding tumor foci (i.e., the ‘halo’ effect). The test evaluates methylation in three separate genes GSTP1, APC, and RASSF1 and any abnormality in any of these genes prompts a positive test. An initial European study (MATLOC study) using negative core biopsies revealed on multivariate analysis the assay to be a significant predictor of repeat biopsy outcome (OR 3.17, 95% CI 1.81–5.53) with a NPV of 90% (95% CI 87–93) [41]. A follow-up study in the US population validated these results and demonstrated an NPV of 88% and functioned as a significant multivariate predictor (OR 2.69, CI 95% 1.60–4.51) [42▪▪]. The presence of atypia on biopsy as a multivariate predictor was found also twice as frequently in cancer cases than in controls (OR 2.11).

These tissue assays help to separate men who are free of PCa from those who are more likely to harbor the disease and reduce the number of unnecessary repeat biopsies. However, several limitations arise when using tissue-based assays including the impact of infection/inflammation, available tissue retrieved for assessment, and ability to distinguish high-grade from low-grade (clinically insignificant) lesions. APC methylation is associated with inflammation [43]. In addition, the performance of the ConfirmMDx assay over a specialized pathologists reading and finding of atypia in the specimen (which frequently prompts a recommendation of rebiopsy) does not appear to be significantly different from the ConfirmMDx assay in the recent DOCUMENT study [42▪▪]. Finally, as noted above, DNA methylation of genes changes with aging and this may have an impact on the signature being evaluated. Regardless, this application of epigenetics to diagnostics is one of the most developed and appears to be a promising area clinically.


Currently, many of the key components incorporated in the diagnostic algorithm for PCa are inaccurate and may lead to unnecessary prostate biopsies, overtreatment, and patient anxiety. In the ‘post-PSA’ era, new biomarkers are urgently needed that inform the physician and patient about not only the presence of cancer, but also the biologic potential. Epigenetics has the potential to answer both of these questions. To date, only one test is commercially widespread (ConfirmMDx), but a number of other promising approaches are in validation studies. Ultimately, the important question for any test being adopted is whether clinical decision-making is altered through use of the test. A corollary is whether the test saves healthcare dollars. In a recent model looking at the impact of a tissue-based assay on healthcare costs for a commercial health plan covering 1 million individuals, a budget model projected a reduction in 1106 biopsies and savings of over $500,000 annually [44]. Thus, there is great economic potential for the use of molecular assays in modern medicine.

Several unique challenges should be considered when analyzing epigenetic biomarkers. Age is a major risk factor for PCa and alterations in DNA methylation occur with aging [45]. We and others [46] have proposed that age-induced alterations in DNA methylation contribute to PCa development. The heterogeneous and multifocal nature of PCa poses risks, as biopsy tissue may underrepresent the clinical aggressiveness of other tumor foci in the prostate. It is hoped that the molecular analysis of biofluids (blood, urine, or other body fluids) may bypass this problem by representing multiple lesions. Techniques for the analysis of methylation are well suited to high throughput analyses needed for a commercial test, and DNA is a relatively stable biomarker source.

In the future, refining epigenetic biomarkers will help resolve common clinical dilemmas among clinicians: when, who, and how patients with PCa should be treated. An improved understanding of epigenetic alterations in PCa will not only provide new and better biomarker candidates, but have the potential to direct new therapeutic strategies given the reversibility of these processes.



Conflicts of interest

There are no conflicts of interest.


Papers of particular interest, published within the annual period of review, have been highlighted as:

  • ▪ of special interest
  • ▪▪ of outstanding interest


1. Fu VX, Dobosy JR, Desotelle JA, et al. Aging and cancer-related loss of insulin-like growth factor 2 imprinting in the mouse and human prostate. Cancer Res 2008; 68:6797.
2. Damaschke NA, Yang B, Bhusari S, et al. Epigenetic susceptibility factors for prostate cancer with aging. Prostate 2013; 73:1721.
3. Lee WH, Morton RA, Epstein JI, et al. Cytidine methylation of regulatory sequences near the pi-class glutathione S-transferase gene accompanies human prostatic carcinogenesis. Proc Natl Acad Sci U S A 1994; 91:11733.
4. Nakayama M, Gonzalgo ML, Yegnasubramanian S, et al. GSTP1 CpG island hypermethylation as a molecular biomarker for prostate cancer. J Cell Biochem 2004; 91:540.
5. Strand S, Orntoft T, Sorensen K. Prognostic DNA methylation markers for prostate cancer. Int J Mol Sci 2014; 15:16544.
6▪. Mahon KL, Qu W, Devaney J, et al. Methylated glutathione S-transferase 1 (mGSTP1) is a potential plasma free DNA epigenetic marker of prognosis and response to chemotherapy in castrate-resistant prostate cancer. Br J Cancer 2014; [Epub ahead of print].

An interesting study demonstrating that GSTPI methylation in serum predicts the response to chemotherapy.

7. Aoki K, Taketo MM. Adenomatous polyposis coli (APC): a multifunctional tumor suppressor gene. J Cell Sci 2007; 120:3327.
8. Chen Y, Li J, Yu X, et al. APC gene hypermethylation and prostate cancer: a systematic review and meta-analysis. Eur J Hum Genet 2013; 21:929.
9. Richiardi L, Fiano V, Vizzini L, et al. Promoter methylation in APC, RUNX3, and GSTP1 and mortality in prostate cancer patients. J Clin Oncol 2009; 27:3161.
10. Henrique R, Ribeiro FR, Fonseca D, et al. High promoter methylation levels of APC predict poor prognosis in sextant biopsies from prostate cancer patients. Clin Cancer Res 2007; 13:6122.
11. Ge YZ, Xu LW, Jia RP, et al. The association between RASSF1A promoter methylation and prostate cancer: evidence from 19 published studies. Tumour Biol 2014; 35:3881.
12. Sørensen KD, Abildgaard MO, Haldrup C, et al. Prognostic significance of aberrantly silenced ANPEP expression in prostate cancer. Br J Cancer 2013; 108:420.
13. Weiss G, Cottrell S, Distler J, et al. DNA methylation of the PITX2 gene promoter region is a strong independent prognostic marker of biochemical recurrence in patients with prostate cancer after radical prostatectomy. J Urol 2009; 181:1678.
14. Yegnasubramanian S, Kowalski J, Gonzalgo ML, et al. Hypermethylation of CpG islands in primary and metastatic human prostate cancer. Cancer Res 2004; 64:1975.
15▪▪. Truong M, Yang B, Livermore A, et al. Using the epigenetic field defect to detect prostate cancer in biopsy negative patients. J Urol 2013; 189:2335.

A study demonstrating the ability of a DNA methylation panel to predict the presence of prostate cancer in negative prostate biopsies. The work was performed in a primary group and external validation cohort.

16. Alumkal JJ, Zhang Z, Humphreys EB, et al. Effect of DNA methylation on identification of aggressive prostate cancer. Urology 2008; 72:1234.
17. Schayek H, Bentov I, Jacob-Hirsch J, et al. Global methylation analysis identifies PITX2 as an upstream regulator of the androgen receptor and IGF-I receptor genes in prostate cancer. Horm Metab Res 2012; 44:511.
18. Bañez LL, Sun L, van Leenders GJ, et al. Multicenter clinical validation of PITX2 methylation as a prostate specific antigen recurrence predictor in patients with postradical prostatectomy prostate cancer. J Urol 2010; 184:149.
19▪. Haldrup C, Mundbjerg K, Vestergaard EM, et al. DNA methylation signatures for prediction of biochemical recurrence after radical prostatectomy of clinically localized prostate cancer. J Clin Oncol 2013; 31:3250.

Validated, multicenter study establishing a panel of genes for predicting biochemical recurrence with an HR of 3.27. Large confirmatory population.

20. Kobayashi Y, Absher DM, Gulzar ZG, et al. DNA methylation profiling reveals novel biomarkers and important roles for DNA methyltransferases in prostate cancer. Genome Res 2011; 21:1017.
21. Mahapatra S, Klee EW, Young CY, et al. Global methylation profiling for risk prediction of prostate cancer. Clin Cancer Res 2012; 18:2882.
22. Lin PC, Giannopoulou EG, Park K, et al. Epigenomic alterations in localized and advanced prostate cancer. Neoplasia 2013; 15:373.
23. Seligson DB, Horvath S, Shi T, et al. Global histone modification patterns predict risk of prostate cancer recurrence. Nature 2005; 435:1262.
24▪. Seligson DB, Horvath S, McBrian MA, et al. Global levels of histone modifications predict prognosis in different cancers. Am J Pathol 2009; 174:1619.

Interesting article demonstrating the utility of histone alterations in predicting cancer outcomes in not only prostate cancer, but other tumor types. May be important in identifying patients who would respond to drugs that alter histone modifying enzymes

25. Halkidou K, Gaughan L, Cook S, et al. Upregulation and nuclear recruitment of HDAC1 in hormone refractory prostate cancer. Prostate 2004; 59:177.
26. Huffman DM, Grizzle WE, Bamman MM, et al. SIRT1 is significantly elevated in mouse and human prostate cancer. Cancer Res 2007; 67:6612.
27. Varambally S, Dhanasekaran SM, Zhou M, et al. The polycomb group protein EZH2 is involved in progression of prostate cancer. Nature 2002; 419:624.
28. Biancotto C, Frigè G, Minucci S. Histone modification therapy of cancer. Adv Genet 2010; 70:341.
29. Tyler KL, Selvaggi SM. Morphologic features of prostatic adenocarcinoma on ThinPrep urinary cytology. Diagn Cytopathol 2011; 39:101.
30. Ahmed H. Promoter methylation in prostate cancer and its application for the early detection of prostate cancer using serum and urine samples. Biomark Cancer 2010; 2010:17.
31. Brena RM, Huang TH, Plass C. Quantitative assessment of DNA methylation: potential applications for disease diagnosis, classification, and prognosis in clinical settings. J Mol Med (Berl) 2006; 84:365.
32. Truong M, Yang B, Jarrard DF. Toward the detection of prostate cancer in urine: a critical analysis. J Urol 2013; 189:422.
33. Gonzalgo ML, Pavlovich CP, Lee SM, et al. Prostate cancer detection by GSTP1 methylation analysis of postbiopsy urine specimens. Clin Cancer Res 2003; 90:2673.
34. Wu T, Giovannucci E, Welge J, et al. Measurement of GSTP1 promoter methylation in body fluids may complement PSA screening: a meta-analysis. Br J Cancer 2011; 105:65.
35. Rouprêt M, Hupertan V, Yates DR, et al. Molecular detection of localized prostate cancer using quantitative methylation-specific PCR on urinary cells obtained following prostate massage. Clin Cancer Res 2007; 13:1720.
36. Baden J, Green G, Painter J, et al. Multicenter evaluation of an investigational prostate cancer methylation assay. J Urol 2009; 182:1186.
37. Jarrard DF, Bussemakers MJ, Bova GS, et al. Regional loss of imprinting of the insulin-like growth factor II gene occurs in human prostate tissues. Clin Cancer Res 1995; 1:1471.
38. Bhusari S, Yang B, Kueck J, et al. Insulin-like growth factor-2 (IGF2) loss of imprinting marks a field defect within human prostates containing cancer. Prostate 2011; 71:1621.
39. Yang B, Bhusari S, Kueck J, et al. Methylation profiling defines an extensive field defect in histologically normal prostate tissues associated with prostate cancer. Neoplasia 2013; 15:399.
40. Thompson IM, Pauler DK, Goodman PJ, et al. Prevalence of prostate cancer among men with a prostate-specific antigen level < or =4.0 ng per milliliter. N Engl J Med 2004; 350:2239.
41. Stewart GD, Van Neste L, Delvenne P, et al. Clinical utility of an epigenetic assay to detect occult prostate cancer in histopathologically negative biopsies: results of the MATLOC study. J Urol 2013; 189:1110.
42▪▪. Partin AW, Van Neste L, Klein EA, et al. Clinical validation of an epigenetic assay to predict negative histopathological results in repeat prostate biopsies. J Urol 2014; 192:1081.

Validation study for the ConfirmMDx assay that detects the presence of cancer by analyzing a peritumor ‘halo’ response in adjacent cells. Reasonable performance (negative predictive value (NPV) 88%) in ruling out the presence of cancer. Does not establish whether cancer is aggressive or nonaggressive.

43. Van der Auwera I, Van Laere SJ, Van den Bosch SM, et al. Aberrant methylation of the adenomatous polyposis coli (APC) gene promoter is associated with the inflammatory breast cancer phenotype. Br J Cancer 2008; 99:1735.
44. Aubry W. Budget impact model: epigenetic assay can help avoid unnecessary repeated prostate biopsies and reduce healthcare spending. Am Health Drug Benefits 2013; 6:15.
45. Rang FJ, Boonstra J. Causes and consequences of age-related changes in DNA methylation: a role for ROS? Biology (Basel) 2014; 3:403.
46. Kwabi-Addo B, Chung W, Shen L, et al. Age-related DNA methylation changes in normal human prostate tissues. Clin Cancer Res 2007; 13:3796.
Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved.