EGFR-TKI down-regulates PD-L1 in EGFR mutant NSCLC through inhibiting NF-κB - PubMed (original) (raw)
. 2015 Jul;463(1-2):95-101.
doi: 10.1016/j.bbrc.2015.05.030. Epub 2015 May 18.
Affiliations
- PMID: 25998384
- DOI: 10.1016/j.bbrc.2015.05.030
EGFR-TKI down-regulates PD-L1 in EGFR mutant NSCLC through inhibiting NF-κB
Kailong Lin et al. Biochem Biophys Res Commun. 2015 Jul.
Erratum in
- Corrigendum to "EGFR-TKI down-regulates PD-L1 in EGFR mutant NSCLC through inhibiting NF-κB" [Biochem. Biophys. Res. Commun. 463(1-2) (2015) 95-101].
Lin K, Cheng J, Yang T, Li Y, Zhu B. Lin K, et al. Biochem Biophys Res Commun. 2022 Nov 12;629:189. doi: 10.1016/j.bbrc.2022.09.023. Epub 2022 Sep 13. Biochem Biophys Res Commun. 2022. PMID: 36114047 No abstract available.
Abstract
Non-small-cell lung cancer (NSCLC) is a severe disease threatening human health. Targeted therapy of epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) has obtained potent efficacy in the treatment of NSCLC patients. However, the effects of EGFR-TKIs on tumor immune microenvironment are unclear. In this study, we show that NSCLCs with EGFR mutation express higher programmed cell death ligand 1 (PD-L1) than NSCLCs with wild type EGFR. The EGFR activation is also associated with high expression of PD-L1. The EGFR-TKI gefitinib can reduce PD-L1 expression, via inhibiting NF-κB, in EGFR mutant NSCLC in vitro and in vivo. These findings elucidate a novel anti-tumor mechanism of EGFR-TKI and provide the possibility of combined strategy of targeted therapy and immunotherapy for EGFR mutant NSCLC patients.
Keywords: EGFR-TKI; NF-κB; NSCLC; PD-L1.
Copyright © 2015 Elsevier Inc. All rights reserved.
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