TMPRSS2-ERG fusions linked to prostate cancer racial health disparities : a focus on Africa

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dc.contributor.author Blackburn, James
dc.contributor.author Vecchiarelli, Stefano
dc.contributor.author Heyer, Erin E.
dc.contributor.author Patrick, Sean Mark
dc.contributor.author Lyons, Ruth J.
dc.contributor.author Jaratlerdsiri, Weerachai
dc.contributor.author Van Zyl, Smit
dc.contributor.author Bornman, Maria S. (Riana)
dc.contributor.author Mercer, Tim R.
dc.contributor.author Hayes, Vanessa M.
dc.date.accessioned 2020-03-23T15:31:35Z
dc.date.available 2020-03-23T15:31:35Z
dc.date.issued 2019-07
dc.description.abstract BACKGROUND : The androgen‐regulated gene TMPRSS2 to the ETS transcription factor gene ERG fusion is the most common genomic alteration acquired during prostate tumorigenesis and biased toward men of European ancestry. In contrast, African American men present with more advanced disease, yet their tumors are less likely to acquire TMPRSS2‐ERG. Data for Africa is scarce. METHODS : RNA was made available for genomic analyses from 181 prostate tissue biopsy cores from Black South African men, 94 with and 87 without pathological evidence for prostate cancer. Reverse transcription polymerase chain reaction was used to screen for the TMPRSS2‐ERG fusion, while transcript junction coordinates and isoform frequencies, including novel gene fusions, were determined using targeted RNA sequencing. RESULTS : Here we report a frequency of 13% for TMPRSS2‐ERG in tumors from Black South Africans. Present in 12/94 positive versus 1/87 cancer negative prostate tissue cores, this suggests a 92.62% predictivity for a positive cancer diagnosis (P = 0.0031). At a frequency of almost half that reported for African Americans and roughly a quarter of that reported for men of European ancestry, acquisition of TMPRSS2‐ERG appears to be inversely associated with aggressive prostate cancer. Further support was provided by linking the presence of TMPRSS2‐ERG to low‐grade disease in younger patients (P = 0.0466), with higher expressing distal ERG fusion junction coordinates. CONCLUSIONS : Only the second study of its kind for the African continent, we support a link between TMPRSS2‐ERG status and prostate cancer racial health disparity beyond the borders of the United States. We call for urgent evaluation of androgen deprivation therapy within Africa. en_ZA
dc.description.department School of Health Systems and Public Health (SHSPH) en_ZA
dc.description.librarian am2020 en_ZA
dc.description.sponsorship The Cancer Association of South Africa (CANSA) and National Research Foundation (NRF) South Africa for funds to support and maintain the SAPCS (to MSRB. and VMH). The project was further supported by a University of Sydney Bridging Support Grant to V.M.H. (#G199756), with additional support from the Australian Prostate Cancer Research Centre (APCRC) NSW. National Health and Medical Research Council (NHMRC) grants support JB (#APP1108254 and APP1114016) and EEH (#APP1103685), while VMH is supported by the University of Sydney Foundation and Petre Foundation, Australia. en_ZA
dc.description.uri http://wileyonlinelibrary.com/journal/pros en_ZA
dc.identifier.citation Blackburn, J., Vecchiarelli, S., Heyer, E.E. et al. 2019, 'TMPRSS2-ERG fusions linked to prostate cancer racial health disparities : a focus on Africa', Prostate, vol. 79, pp. 1191-1196. en_ZA
dc.identifier.issn 0270-4137 (print)
dc.identifier.issn 1097-0045 (online)
dc.identifier.other 10.1002/pros.23823
dc.identifier.uri http://hdl.handle.net/2263/73817
dc.language.iso en en_ZA
dc.publisher Wiley en_ZA
dc.rights © 2019 The Authors. The Prostate Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution License. en_ZA
dc.subject African ancestry en_ZA
dc.subject Early‐onset en_ZA
dc.subject Fusion gene en_ZA
dc.subject Prostate cancer en_ZA
dc.subject Racial health disparity en_ZA
dc.subject TMPRSS2‐ERG en_ZA
dc.title TMPRSS2-ERG fusions linked to prostate cancer racial health disparities : a focus on Africa en_ZA
dc.type Article en_ZA


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