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Comprehensive immunohistochemical analysis of PD-L1 shows scarce expression in castration-resistant prostate cancer.
Fankhauser, Christian D; Schüffler, Peter J; Gillessen, Silke; Omlin, Aurelius; Rupp, Niels J; Rueschoff, Jan H; Hermanns, Thomas; Poyet, Cedric; Sulser, Tullio; Moch, Holger; Wild, Peter J.
Afiliação
  • Fankhauser CD; Department of Urology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Schüffler PJ; Department of Computer Science, ETH Zurich, Zurich, Switzerland.
  • Gillessen S; Department of Medical Physics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Omlin A; Department of Medical Oncology and Hematology, Cantonal Hospital, St. Gallen, Switzerland.
  • Rupp NJ; Department of Medical Oncology and Hematology, Cantonal Hospital, St. Gallen, Switzerland.
  • Rueschoff JH; Department of Pathology and Molecular Pathology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Hermanns T; Department of Pathology and Molecular Pathology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Poyet C; Department of Urology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Sulser T; Department of Urology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Moch H; Department of Urology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Wild PJ; Department of Pathology and Molecular Pathology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Oncotarget ; 9(12): 10284-10293, 2018 Feb 13.
Article em En | MEDLINE | ID: mdl-29535806
BACKGROUND: We aimed to analyze the frequency and distribution of PD-L1 expression in specimens from prostate cancer (PC) patients using two different anti-PD-L1 antibodies (E1L3N, SP263). MATERIALS AND METHODS: PD-L1 immunohistochemistry was performed in a tissue microarray consisting of 82 castration-resistant prostate cancer (CRPC) specimens, 70 benign prostate hyperplasia (BPH) specimens, 96 localized PC cases, and 3 PC cell lines, using two different antibodies (clones E1L3N, and SP263). Staining images for CD4, CD8, PD-L1, and PanCK of a single PD-L1 positive case were compared, using a newly developed dot-wise correlation method for digital images to objectively test for co-expression. RESULTS: Depending on the antibody used, in tumor cells (TC) only five (E1L3N: 6%) and three (SP263: 3.7%) samples were positive. In infiltrating immune cells (IC) 12 (SP263: 14.6%) and 8 (E1L3N: 9.9%) specimens showed PD-L1 expression. Two PC cell lines (PC3, LnCaP) also displayed membranous immunoreactivity. All localized PCs or BPH samples tested were negative. Dot-wise digital correlation of expression patterns revealed a moderate positive correlation between PD-L1 and PanCK expression, whereas both PanCK and PD-L1 showed a weak negative Pearson correlation coefficient between CD4 and CD8. CONCLUSIONS: PD-L1 was not expressed in localized PC or BPH, and was only found in a minority of CRPC tumors and infiltrating immune cells. Protein expression maps and systematic dot-wise comparison could be a useful objective way to describe the relationship between immuno- and tumor-related proteins in the future, without the need to develop multiplex staining methods.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2018 Tipo de documento: Article