Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 855, Issue -, Pages 10-19Publisher
ELSEVIER
DOI: 10.1016/j.ejphar.2019.04.016
Keywords
Schizandrin A; Gefitinib; IKK beta/NF-kappa B signal; NSCLC
Categories
Funding
- Special fund project for technology innovation of Foshan City [2014AG10003]
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The emergence of resistance to EGF receptor (EGFR) inhibitor therapy is a significant challenge for patients with non-small cell lung cancer (NSCLC). During the past few years, a correlation between EGFR TKIs resistance and dysregulation of IKK beta/NF-kappa B signaling has been increasingly suggested. However, few studies have focused on the effects of combining IKK/NF-kappa B and EGFR inhibitors to overcome EGFR TKIs resistance. In this study, we discovered that Schizandrin A (Sch A), a lignin compound isolated from Schisandra chinesnesis, could synergize with the EGFR receptor inhibitor Gefitinib to inhibit cell growth, induce cell cycle arrest and apoptosis of HCC827/GR cells. Sch A effectively suppressed the phosphorylation of IKK beta and I kappa B alpha, as well as the nuclear translocation of NF-kappa B p65, and showed high and selective affinity for IKK beta in surface plasmon resonance (SPR) experiments, indicating that Sch A was a selective IKK beta inhibitor. Molecular modeling between IKK beta and Sch A suggested that Sch A formed key hydrophobic interactions with IKK beta, which may contribute to its potent IKK beta inhibitory effect. These findings suggest a novel approach to improve poor clinical outcomes in EGFR TKIs therapy, by combining it with Sch A.
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