The Genetics of Prostate Cancer

Germline mutations in prostate cancer carcinogenesis

Some of the first data to delineate the value of assessment of inherited genetic changes in prostate cancer came from Pritchard and colleagues who assessed the prevalence of mutations in 20 DNA-repair genes among 692 patients with metastatic prostate cancer8. They identified such mutations in 82 men (11.8%).

Interestingly, there is significant geographic heterogeneity, even among these recognized cancer centers with a prevalence of 8.8% in patients treated at the University of Washington and 18.5% in patients treated at Memorial Sloan Kettering, potentially reflecting referral biases. Similarly, Castro et al. found a prevalence of germline DNA damage repair gene mutations of 16.2% in patients with metastatic castrate resistance prostate cancer9.

More recently, Nicolosi and colleagues published data in JAMA Oncology assessing the prevalence of germline mutations in a diverse cohort of 3607 men with prostate cancer at various stages of the disease trajectory10. All included patients had germline genetic testing which may enrich the population for mutations. The authors identified germline variants in 620 patients (17.2%), of which BRCA1/2 comprised only a small proportion. The 10 most commonly identified variants are as follows:

10 most commonly identified mutated genes
Among a cohort of patients with metastatic castrate-resistant prostate cancer in the PROREPAIR-B cohort, Castro et al. found that, while germline mutations in ATM, BRCA1, BRCA2, or PALB2 were not significantly associated with prostate cancer-specific survival (different in survival 10 months, p=0.264) when considered in aggregate, germline BRCA2 mutations specifically were associated with significantly worse prostate cancer-specific mortality (17 months compared with 33 months, hazard ratio 2.11, p-value = 0.033)9. Further, there was a significant interaction between germline BRCA2 mutation status and treatment type with better survival among BRCA2 carriers treated with androgen axis-targeting agents such as abiraterone acetate or enzalutamide, as compared to those who received taxanes. In a cohort of 50 patients with heavily pretreated metastatic castrate-resistant prostate (100% receipt of docetaxel, 98% receipt of abiraterone or enzalutamide, 58% receipt of cabazitaxel), Mateo et al. found that patients with mutations in DNA-repair genes (including BRCA1/2, CHEK2, and Fanconi’s anemia genes) had a high response rate to the poly ADP-ribose polymerase (PARP) inhibitor olaparib11. These results were confirmed in the Phase II TOPARP-B trial and are currently being investigated in a Phase III trial.

Unlike in other disease states where commonly identified germline mutations may be actionable, Nicolosi and colleagues found that actionable mutations (ie. those due to variants in mismatch repair genes) were identified in 1.74% of the study cohort. In previous analyses, Robinson et al. reported clinically actionable pathogenic germline mutations in 8% of 150 patients with metastatic castrate-resistant prostate cancer, in contrast to clinically actionable aberrations in the androgen receptor in 63% and aberrations in other cancer-related genes in 65%12. It is likely not surprising that actionable underlying germline mutations would be more common in a cohort with more advanced prostate cancer.

Interestingly, in the cohort of Nicolosi et al., underlying germline mutations were identified more commonly in Ashkenazi Jewish patients (22.7%) and white patients (17.8%) than African American patients (10.1%) and Hispanic patients (6.4%)10. Importantly, a review of family history of 558 patients with available data demonstrated that a significant proportion of those with identified germline variants (37%) would not be eligible for genetic testing according to current guidelines. Of course, a clinical index of suspicion must have been presented in the treating clinician for these patients to have to undergo germline genetic testing and, as a result, these results may not be directly generalizable to most urologists’ practices.

In 2017, the Philadelphia Prostate Cancer Consensus Conference was convened to define the role of genetic testing in inherited prostate cancer13. The strongest conclusion of the expert panel was that patients should be engaged in the decision to pursue genetic testing. In patients with suspected hereditary prostate cancer, the panel recommended testing for HOXB13 while for those with suspected hereditary breast and ovarian cancer and for those with suspected Lynch syndrome, the panel recommended testing for BRCA1/2 and testing for DNA mismatch repair genes, respectively. In discussions regarding prostate cancer screening, the panel strongly felt that BRCA2 mutations should be considered while in men with more advanced disease, testing for BRCA1/2 and ATM should be considered. As highlighted previously, adherence to these (and other guideline recommendations) is likely to under-estimate the prevalence of germline mutations.

Somatic mutations in prostate cancer carcinogenesis

Numerous somatic genetic and epigenetic changes are associated with prostate cancer carcinogenesis. These may occur at many levels including somatic copy number alterations, structural rearrangements, point mutations, single nucleotide polymorphisms, microRNAs, and methylation changes14.

Somatic copy number alterations (SCNAs) are gains or losses in genetic material that affect a larger fraction of the cancer genome than do any other form of somatic genetic alteration14. They have an integral role in both the activation of oncogenes and the inactivation of tumor suppressor genes. SCNAs are found in nearly 90% of prostate tumors14.

As DNA unwinds, double-stranded breaks may occur. Improper repair of these can result in both intra- and inter-chromosome rearrangements. TMPRSS2:ERG is perhaps the best studied of these in prostate cancer. This rearrangement occurs in nearly 50% of all primary prostate tumors. Nam et al. showed that expression of this gene fusion confers an increased risk of disease relapse after treatment for clinically localized prostate cancer (hazard ratio 7.1, 95% confidence interval 1.1 to 45)14. A number of other rearrangements have been described in prostate cancer including ESRP1:CRAF, the ETS family and RAF kinase gene fusions14.

Prostate cancer has a somatic mutation rate between 1x10-6 and 2x10-6 which is similar to breast, renal and ovarian cancer14. With such a rate, each prostate tumor gene may have many thousand mutations although less than 20 are likely to affect protein stability or function. Examples of affected genes include HPC1/RNase L, HPC2/ELAC2, MSR1, HOXB13, and SPOP.

Genome-wide association studies have detected a wide variety of susceptibility loci (single-nucleotide polymorphisms, SNPs) that have been implicated in prostate cancer. These studies have typically been undertaken in European populations and in cases of sporadic prostate cancer14. For the most part, the implicated SNPs are found in intergenic regions and, as a result, many have no putative function. Examples of implicated SNPs include 8q24, MSMB, KLK2-3, HNF1B, JAZF1, LILRA3, 10q26, 15q21, and many more.

MicroRNAs (miRNAs) are a class of small non-coding RNA which bind to messenger RNA (mRNA) in a manner to modulate mRNA expression. For the most part, miRNA-mRNA interactions result in down-regulation though a small number cause up-regulation or complete destruction of the mRNA target. MicroRNA can either initiate carcinogenesis or drive disease progression14. Unlike germline or somatic DNA mutations, miRNA expression is dynamic and both their expression and target may vary within the same cell depending on time or circumstance. This allows for significant signal amplification as a single protein may act via a small number of miRNAs to influence many genes14. MicroRNA have been implicated in apoptosis avoidance (eg. miR-17-92 and miR-21), in cellular signaling pathways (eg. miR-221 and miR-15a), in androgen signaling (eg. miR-21 and miR-141)14.

Finally, aberrant DNA methylation is a hallmark of prostate cancer15. These changes often result in growth dysfunction. Methylation-based markers are stable and thus offer a potential for biomarker utilization16.


Prostate cancer is a highly heritable cancer. However, there is a relatively low frequency of identifiable germline mutations in patients with prostate cancer, though the prevalence increases with disease severity (from localized disease to metastatic castrate-resistant prostate cancer). While relatively infrequent, germline mutations may significantly affect decisions regarding prostate cancer screening, prognosis and treatment.

Published Date: December 2019

Written by: Zachary Klaassen, MD, MSc
References: 1. Kang ZJ, Liu YF, Xu LZ, et al. The Philadelphia chromosome in leukemogenesis. Chin J Cancer 2016; 35:48.
2. An X, Tiwari AK, Sun Y, et al. BCR-ABL tyrosine kinase inhibitors in the treatment of Philadelphia chromosome positive chronic myeloid leukemia: a review. Leuk Res 2010; 34(10):1255-68.
3. Lichtenstein P, Holm NV, Verkasalo PK, et al. Environmental and heritable factors in the causation of cancer--analyses of cohorts of twins from Sweden, Denmark, and Finland. N Engl J Med 2000; 343(2):78-85.
4. Stanford JL, Ostrander EA. Familial prostate cancer. Epidemiol Rev 2001; 23(1):19-23.
5. Carter BS, Bova GS, Beaty TH, et al. Hereditary prostate cancer: epidemiologic and clinical features. J Urol 1993; 150(3):797-802.
6. Bostwick DG, Burke HB, Djakiew D, et al. Human prostate cancer risk factors. Cancer 2004; 101(10 Suppl):2371-490.
7. Alvarez-Cubero MJ, Saiz M, Martinez-Gonzalez LJ, et al. Genetic analysis of the principal genes related to prostate cancer: a review. Urol Oncol 2013; 31(8):1419-29.
8. Pritchard CC, Mateo J, Walsh MF, et al. Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer. N Engl J Med 2016; 375(5):443-53.
9. Castro E, Romero-Laorden N, Del Pozo A, et al. PROREPAIR-B: A Prospective Cohort Study of the Impact of Germline DNA Repair Mutations on the Outcomes of Patients With Metastatic Castration-Resistant Prostate Cancer. J Clin Oncol 2019; 37(6):490-503.
10. Nicolosi P, Ledet E, Yang S, et al. Prevalence of Germline Variants in Prostate Cancer and Implications for Current Genetic Testing Guidelines. JAMA Oncol 2019; 5(4):523-528.
11. Mateo J, Carreira S, Sandhu S, et al. DNA-Repair Defects and Olaparib in Metastatic Prostate Cancer. N Engl J Med 2015; 373(18):1697-708.
12. Robinson D, Van Allen EM, Wu YM, et al. Integrative clinical genomics of advanced prostate cancer. Cell 2015; 161(5):1215-1228.
13. Giri VN, Knudsen KE, Kelly WK, et al. Role of Genetic Testing for Inherited Prostate Cancer Risk: Philadelphia Prostate Cancer Consensus Conference 2017. J Clin Oncol 2018; 36(4):414-424.
14. Wallis CJ, Nam RK. Prostate Cancer Genetics: A Review. EJIFCC 2015; 26(2):79-91.
15. Ahmad AS, Vasiljevic N, Carter P, et al. A novel DNA methylation score accurately predicts death from prostate cancer in men with low to intermediate clinical risk factors. Oncotarget 2016; 7(44):71833-71840.
16. Majumdar S, Buckles E, Estrada J, et al. Aberrant DNA methylation and prostate cancer. Curr Genomics 2011; 12(7):486-505.
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