Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1782508674421358592 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5315340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhangwencheng inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT pangqingsong inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT yancihui inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT wangqifeng inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT yangjingsong inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT yushufei inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT liuxiao inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT yuanzhiyong inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT wangping inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma AT xiaozefen inductionofpdl1expressionbyepidermalgrowthfactorreceptormediatedsignalinginesophagealsquamouscellcarcinoma |