The genetic etiology of prostate cancer, the most common cancer in western men, is poorly understood. Highest incidences and mortality rates are reported for African-Americans, with 1.6x more likely than European-Americans and 2.6x more likely than Asian-Americans to develop disease. This ethnic disparity and a strong link to a family history of disease, eludes to the importance of genetics in explaining the observed health disparity (including disease risk, aggression and outcomes). We report for the first time a highly significant increase in disease aggression in non-migrant Africa, compared with African-Americans and European-Americans, and hypothesize that a genetic link to Africa plays a fundamental role in unraveling the prostate cancer disparities. The mitochondrial genome is not only a critical target for inherited disparity (due to ethnic-based diversity, which is greatest wihin Africa), but is also an important target for acquired tumor-causing somatic mutations. Mitochondria play a central role not only in generating cellular energy, but also cell death (apoptosis), cell growth and differentiation, signaling and cell cycle control, making the mitochondrial genome an essential target for carcinogenic variation. The high mutation rate and copy number of the mitochondrial compared to the nuclear genome, further impacts on its unique potential for pathogenesis and as a disease marker. This project will provide the first known analysis of the role and extent of acquired mitochondrial genome variation (somatic mutations with functional predictive relevance) on a backbone of inherited variation (polymorphic variants) in defining the increased severity of prostate cancer within Africa. Using a unique study resource of non-admixed Southern African ancestry, combined with whole mitochondrial genome analysis using next generation sequencing technology, will provide an opportunity to identify genetic-based non- invasive biomarkers of aggressive versus indolent prostate cancer disease (a major clinical limitation in the management of prostate cancer), as well as the tools to detect low levels of somatic heteroplasmy (mutant to wild-type mtDNA environment) for early-disease detection and monitoring. This study addresses an important biological explanation for the observed ethnic- based disparities in prostate cancer.

Public Health Relevance

Ones genetics background has been speculated to be a key contributor to the observed disparity in prostate cancer risk and disease status, with increased severity in men of African ancestry compared with European and Asian men. In this study we report for the first time 'extremely'aggressive prostate cancer disease in non-migrant Africans and utilize this unique resource to determine the likely contribution of mitochondrial genome variation (both inherited and somatic) in explaining this disparity. Our study provides a rational biological explanation for this disparity based on the essential role of the mitochondrial genome in carcinogenesis and its ideal application for non-invasive testing, providing the potential for early detection of aggressive versus indolent disease.

National Institute of Health (NIH)
National Cancer Institute (NCI)
Exploratory/Developmental Grants (R21)
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Special Emphasis Panel (ZRG1-OBT-A (55))
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Banez, Lionel L
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J. Craig Venter Institute, Inc.
United States
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McCrow, John P; Petersen, Desiree C; Louw, Melanie et al. (2016) Spectrum of mitochondrial genomic variation and associated clinical presentation of prostate cancer in South African men. Prostate 76:349-58
Tindall, Elizabeth A; Monare, L Richard; Petersen, Desiree C et al. (2014) Clinical presentation of prostate cancer in black South Africans. Prostate 74:880-91