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GSTP1 positive prostatic adenocarcinomas are more common in black than white men in the United States

dc.contributor.coauthorVidal, I.
dc.contributor.coauthorZheng, Q.
dc.contributor.coauthorHicks, J. L.
dc.contributor.coauthorChen, J.
dc.contributor.coauthorPlatz, E. A.
dc.contributor.coauthorTrock, B. J.
dc.contributor.coauthorBaena Del Valle, J. A.
dc.contributor.coauthorSfanos, K. S.
dc.contributor.coauthorErnst, S.
dc.contributor.coauthorJones, T.
dc.contributor.coauthorMaynard, J. P.
dc.contributor.coauthorGlavaris, S. A.
dc.contributor.coauthorNelson, W. G.
dc.contributor.coauthorYegnasubramanian, S.
dc.contributor.coauthorDe Marzo, A. M.
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorKulaç, İbrahim
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T12:17:05Z
dc.date.issued2021
dc.description.abstractGSTP1 is a member of the Glutathione-S-transferase (GST) family silenced by CpG island DNA hypermethylation in 90-95% of prostate cancers. However, prostate cancers expressing GSTP1 have not been well characterized. We used immunohistochemistry against GSTP1 to examine 1673 primary prostatic adenocarcinomas on tissue microarrays (TMAs) with redundant sampling from the index tumor from prostatectomies. GSTP1 protein was positive in at least one TMA core in 7.7% of cases and in all TMA cores in 4.4% of cases. The percentage of adenocarcinomas from Black patients who had any GSTP1 positive TMA cores was 14.9%, which was 2.5 times higher than the percentage from White patients (5.9%; P < 0.001). Further, the percentages of tumors from Black patients who had all TMA spots positive for GSTP1 (9.5%) was 3-fold higher than the percentage from White patients (3.2%; P<0.001). In terms of association with other molecular alterations, GSTP1 positivity was enriched in ERG positive cancers among Black men. By in situ hybridization, GSTP1 mRNA expression was concordant with protein staining, supporting the lack of silencing of at least some GSTP1 alleles in GSTP1-positive tumor cells. This is the first report revealing that GSTP1-positive prostate cancers are substantially over-represented among prostate cancers from Black compared to White men. This observation should prompt additional studies to determine whether GSTP1 positive cases represent a distinct molecular subtype of prostate cancer and whether GSTP1 expression could provide a biological underpinning for the observed disparate outcomes for Black men.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.issue6
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipUnited States Department of Health & Human Services
dc.description.sponsorshipNational Institutes of Health (NIH) USA
dc.description.sponsorshipNIH National Cancer Institute (NCI)
dc.description.sponsorshipUnited States Department of Defense
dc.description.versionPublisher version
dc.description.volume16
dc.identifier.doi10.1371/journal.pone.0241934
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR02988
dc.identifier.issn1932-6203
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85108980081
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0241934
dc.identifier.wos671698800038
dc.keywordsGlutathione-S-transferase (GST)
dc.keywordsERG
dc.keywordsProstate cancer
dc.keywordsCell staining
dc.keywordsAdenocarcinoma
dc.keywordsDNA methylation
dc.keywordsCarcinoma
dc.keywordsIn situ hybridization
dc.keywordsDU145 cells
dc.keywordsProstatectomy
dc.language.isoeng
dc.publisherPublic Library of Science
dc.relation.grantnoP50CA58236
dc.relation.grantnoU01 CA196390
dc.relation.grantnoP30 CA006973
dc.relation.grantnoW81XWH-18-2-0015
dc.relation.ispartofPLOS One
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/9636
dc.subjectScience and technology
dc.titleGSTP1 positive prostatic adenocarcinomas are more common in black than white men in the United States
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorKulaç, İbrahim
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
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