| Literature DB >> 28807336 |
Reza Alaghehbandan1, Jan Stehlik2, Kiril Trpkov3, Cristina Magi-Galluzzi4, Enric Condom Mundo5, Maria Pane Foix5, Daniel Berney6, Mathilde Sibony7, Saul Suster8, Abbas Agaimy9, Delia Perez Montiel10, Kristyna Pivovarcikova2, Kvetoslava Michalova2, Ondrej Daum2, Ondrej Ondic2, Pavla Rotterova2, Martin Dusek2, Milan Hora11, Michal Michal2, Ondrej Hes12.
Abstract
Fumarate hydratase-deficient renal cell carcinoma (FH-RCC) is a rare and aggressive tumor affecting mostly younger patients. This is the first study to assess the expression of programmed death-1 (PD-1) receptor/PD-1 ligand (PD-L1) in FH-RCC. Formalin-fixed paraffin-embedded samples from 13 FH-RCCs collected in an international multi-institutional study, were evaluated by immunohistochemistry (IHC) for PD-1/PD-L1 reactivity in tumor cells and tumor infiltrating lymphocytes (TILs). PD-1/PD-L1 expression was further evaluated by qPCR. By IHC, PD-1 was negative in tumor cells in all 13 cases. PD-L1 was positive in tumor cells in 2/13 cases, weak positive in 7/13, and negative in 4/13 cases, respectively. In TILs, PD-1 was positive in 1/13, weak positive in 3/13, and negative in 9/13 cases. In TILs, PD-L1 was weak positive by IHC in 5/13, and negative in 8/13 cases, respectively. qPCR confirmed the result for 2 of 3 IHC weak positive PD-1 samples. Of 7 IHC weak positive samples (in tumor cells), PD-L1 mRNA was detected in all 7 tumors. The majority of FH-RCCs did not express PD-1/PD-L1 by IHC, which was confirmed by molecular analysis. PD-1/PD-L1 expression in FH-RCC is restricted to a proportion of cases which may benefit from targeted therapies.Entities:
Keywords: Fumarate hydratase-deficient renal cell carcinoma; Kidney; PD-1 ligand (PD-L1) receptor; Programmed death-1 (PD-1) receptor
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Year: 2017 PMID: 28807336 DOI: 10.1016/j.anndiagpath.2017.04.007
Source DB: PubMed Journal: Ann Diagn Pathol ISSN: 1092-9134 Impact factor: 2.090