Research Papers:
Changes in programmed death-ligand 1 expression during cisplatin treatment in patients with head and neck squamous cell carcinoma
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Abstract
Chan-Young Ock1, Sehui Kim2, Bhumsuk Keam1,3, Soyeon Kim3, Yong-Oon Ahn3, Eun-Jae Chung4, Jin-Ho Kim5, Tae Min Kim1,3, Seong Keun Kwon4, Yoon Kyung Jeon2, Kyeong Chun Jung2, Dong-Wan Kim1,3, Hong-Gyun Wu5, Myung-Whun Sung4 and Dae Seog Heo1,3
1Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea
2Department of Pathology, Seoul National University Hospital, Seoul, Korea
3Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea
4Department of Otorhinolaryngology, Seoul National University Hospital, Seoul, Korea
5Department of Radiation Oncology, Seoul National University Hospital, Seoul, Korea
Correspondence to:
Bhumsuk Keam, email: [email protected]
Keywords: programmed death-ligand 1, head and neck squamous cell carcinoma, cisplatin
Received: February 22, 2017 Accepted: June 04, 2017 Published: June 16, 2017
ABSTRACT
Programmed death-ligand 1 (PD-L1) expression is regarded as a predictive marker for anti-PD-1/PD-L1 therapy. The purpose of study was to explore the changes in PD-L1 expression in head and neck squamous cell carcinoma (HNSCC) during treatment. Paired HNSCC tissues prior to and after cisplatin-based treatment were evaluated to determine PD-L1 protein expression by immunohistochemistry. Among the 35 HNSCC patient samples, PD-L1 expression status changed after treatment in 37.1% (13/35) of samples. Among the 13 patients whose baseline PD-L1 was negative, PD-L1 expression was increased in 9 cases (69.2%) and remained negative in 4 cases (30.8%, P = 0.003). Patients exposed to cisplatin generally showed PD-L1 up-regulation (83.3%, P = 0.037) compared to those not exposed to cisplatin (57.1%, P = 0.072). To validate these findings in vitro, changes in PD-L1 expression in HNSCC cell lines (Detroit-562, PCI-13, SNU-1041, SNU-1066, SNU-1076, and FaDu) were analyzed by western blotting and flow cytometry after treatment with cisplatin and interferon-gamma. In HNSCC cell lines, PD-L1 expression was significantly up-regulated after cisplatin, along with phosphor-MAPK/ERK kinase up-regulation. In conclusion, PD-L1 expression in HNSCC may be altered during cisplatin treatment, activating the MAPK/ERK kinase pathway.
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