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dc.contributor.authorSnow, H
dc.contributor.authorHazell, S
dc.contributor.authorFrancis, N
dc.contributor.authorMohammed, K
dc.contributor.authorO'Neill, S
dc.contributor.authorDavies, E
dc.contributor.authorMansfield, D
dc.contributor.authorMessiou, C
dc.contributor.authorHujairi, N
dc.contributor.authorNicol, D
dc.contributor.authorHarrington, K
dc.contributor.authorSmith, M
dc.date.accessioned2020-07-09T12:05:36Z
dc.date.issued2020-12-01
dc.identifier.citationJournal of cutaneous pathology, 2020, 47 (12), pp. 1115 - 1122
dc.identifier.issn0303-6987
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3839
dc.identifier.eissn1600-0560
dc.identifier.doi10.1111/cup.13774
dc.description.abstractBACKGROUND: Prostate-specific membrane antigen (PSMA) is a prostatic epithelial protein that is used as a radiotracer (68Ga-PSMA-11) for prostate cancer staging. PSMA-PET/CT (positron emission tomography/computed tomography) performed for prostate cancer has been observed to detect melanoma metastases. The aim of this study was to investigate the performance of PSMA immunohistochemistry on resected melanoma metastases to explore its use as a diagnostic imaging biomarker for melanoma. METHODS: A total of 41 specimens with stage III/IV melanoma were stained with PSMA immunohistochemistry. All specimens required both disease and control regions. Two pathologists scored the specimens and a receiver operating characteristic (ROC) curve was plotted. Western blot and multiplex immunofluorescence were also performed. RESULTS: The area under the ROC curve was 0.82, suggesting that PSMA has excellent discriminatory power in melanoma metastases. Sensitivity is 82.9% and specificity 73.2%. Immunohistochemistry and Western blot reveal that PSMA staining in melanoma consistently and most intensely occurs in tumor neovasculature. Multiplex immunofluorescence shows that melanocytes may also weakly express PSMA. CONCLUSION: The performance of PSMA immunohistochemistry in melanoma metastases contrasts with that reported in prostate cancer studies. This study indicates that PSMA shows promise for use as a novel biomarker in melanoma and justifies further research in the clinical setting with potential as a PET/CT radiotracer and intraoperative fluorescence marker for melanoma.
dc.formatPrint-Electronic
dc.format.extent1115 - 1122
dc.languageeng
dc.language.isoeng
dc.publisherWILEY
dc.rights.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
dc.titleProstate-specific membrane antigen expression in melanoma metastases.
dc.typeJournal Article
dcterms.dateAccepted2020-05-22
rioxxterms.versionofrecord10.1111/cup.13774
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/under-embargo-all-rights-reserved
rioxxterms.licenseref.startdate2020-12
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfJournal of cutaneous pathology
pubs.issue12
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.publication-statusPublished
pubs.volume47
pubs.embargo.termsNot known
icr.researchteamTargeted Therapy
dc.contributor.icrauthorMansfield, David
dc.contributor.icrauthorHarrington, Kevin
dc.contributor.icrauthorSmith, Myles


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