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Increased expression of programmed death ligand 1 (PD-L1) in human pituitary tumors
Author(s) -
Yu Mei,
Wenya Linda Bi,
Noah F. Greenwald,
Ziming Du,
Nathalie Y.R. Agar,
Ursula B. Kaiser,
Whitney W. Woodmansee,
David A. Reardon,
Gordon J. Freeman,
Peter E. Fecci,
Edward R. Laws,
Sandro Santagata,
Gavin P. Dunn,
Ian F. Dunn
Publication year - 2016
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.12088
Subject(s) - immunotherapy , immune checkpoint , pituitary tumors , pituitary adenoma , cancer research , medicine , immune system , pituitary neoplasm , immunohistochemistry , tumor infiltrating lymphocytes , pd l1 , null cell , pituitary gland , adenoma , endocrinology , biology , immunology , hormone , cell culture , genetics
Subsets of pituitary tumors exhibit an aggressive clinical courses and recur despite surgery, radiation, and chemotherapy. Because modulation of the immune response through inhibition of T-cell checkpoints has led to durable clinical responses in multiple malignancies, we explored whether pituitary adenomas express immune-related biomarkers that could suggest suitability for immunotherapy. Specifically, programmed death ligand 1 (PD-L1) has emerged as a potential biomarker whose expression may portend more favorable responses to immune checkpoint blockade therapies. We thus investigated the expression of PD-L1 in pituitary adenomas.

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