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Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma

PURPOSE: The purpose of this study was to investigate the potential effect of activation of epidermal growth factor receptor (EGFR) signaling pathway on the expression of programmed death-ligand 1 (PD-L1) in esophageal squamous cell carcinoma (ESCC) cells with EGFR overexpression. METHODS: Flow cyto...

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Autores principales: Zhang, Wencheng, Pang, Qingsong, Yan, Cihui, Wang, Qifeng, Yang, Jingsong, Yu, Shufei, Liu, Xiao, Yuan, Zhiyong, Wang, Ping, Xiao, Zefen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315340/
https://www.ncbi.nlm.nih.gov/pubmed/28243112
http://dx.doi.org/10.2147/OTT.S118982
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author Zhang, Wencheng
Pang, Qingsong
Yan, Cihui
Wang, Qifeng
Yang, Jingsong
Yu, Shufei
Liu, Xiao
Yuan, Zhiyong
Wang, Ping
Xiao, Zefen
author_facet Zhang, Wencheng
Pang, Qingsong
Yan, Cihui
Wang, Qifeng
Yang, Jingsong
Yu, Shufei
Liu, Xiao
Yuan, Zhiyong
Wang, Ping
Xiao, Zefen
author_sort Zhang, Wencheng
collection PubMed
description PURPOSE: The purpose of this study was to investigate the potential effect of activation of epidermal growth factor receptor (EGFR) signaling pathway on the expression of programmed death-ligand 1 (PD-L1) in esophageal squamous cell carcinoma (ESCC) cells with EGFR overexpression. METHODS: Flow cytometry and Western blot methods were used to assess PD-L1 expression on ESCC cells when EGFR signaling pathway was activated by epidermal growth factor (EGF) with or without EGFR-specific inhibitor AG-1478, and then EGFR signaling array was applied to analyze the potential signaling pathways involved. RESULTS: This study found that PD-L1 expression increased significantly in an EGFR-dependent manner by the activation of EGFR signaling and decreased sharply when EGFR signaling was blocked. The upregulated expression of PD-L1 was not associated with EGFR-STAT3 signaling pathway, but may be affected by EGFR–PI3K–AKT, EGFR–Ras–Raf–Erk, and EGR–PLC-γ signaling pathways. CONCLUSION: The expression of PD-L1 can be regulated by EGFR signaling activation in ESCC, which indicates an important role for EGFR-mediated immune escape and potential molecular pathways for EGFR-targeted therapy and immunotherapy.
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spelling pubmed-53153402017-02-27 Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma Zhang, Wencheng Pang, Qingsong Yan, Cihui Wang, Qifeng Yang, Jingsong Yu, Shufei Liu, Xiao Yuan, Zhiyong Wang, Ping Xiao, Zefen Onco Targets Ther Original Research PURPOSE: The purpose of this study was to investigate the potential effect of activation of epidermal growth factor receptor (EGFR) signaling pathway on the expression of programmed death-ligand 1 (PD-L1) in esophageal squamous cell carcinoma (ESCC) cells with EGFR overexpression. METHODS: Flow cytometry and Western blot methods were used to assess PD-L1 expression on ESCC cells when EGFR signaling pathway was activated by epidermal growth factor (EGF) with or without EGFR-specific inhibitor AG-1478, and then EGFR signaling array was applied to analyze the potential signaling pathways involved. RESULTS: This study found that PD-L1 expression increased significantly in an EGFR-dependent manner by the activation of EGFR signaling and decreased sharply when EGFR signaling was blocked. The upregulated expression of PD-L1 was not associated with EGFR-STAT3 signaling pathway, but may be affected by EGFR–PI3K–AKT, EGFR–Ras–Raf–Erk, and EGR–PLC-γ signaling pathways. CONCLUSION: The expression of PD-L1 can be regulated by EGFR signaling activation in ESCC, which indicates an important role for EGFR-mediated immune escape and potential molecular pathways for EGFR-targeted therapy and immunotherapy. Dove Medical Press 2017-02-13 /pmc/articles/PMC5315340/ /pubmed/28243112 http://dx.doi.org/10.2147/OTT.S118982 Text en © 2017 Zhang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Zhang, Wencheng
Pang, Qingsong
Yan, Cihui
Wang, Qifeng
Yang, Jingsong
Yu, Shufei
Liu, Xiao
Yuan, Zhiyong
Wang, Ping
Xiao, Zefen
Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
title Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
title_full Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
title_fullStr Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
title_full_unstemmed Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
title_short Induction of PD-L1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
title_sort induction of pd-l1 expression by epidermal growth factor receptor–mediated signaling in esophageal squamous cell carcinoma
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5315340/
https://www.ncbi.nlm.nih.gov/pubmed/28243112
http://dx.doi.org/10.2147/OTT.S118982
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