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Inhibition of non-small cell lung cancer (NSCLC) growth by a novel small molecular inhibitor of EGFR

  • Jinsong Li
  • , Huayun Deng
  • , Meichun Hu
  • , Yuanzhang Fang
  • , Amanda Vaughn
  • , Xiaopan Cai
  • , Leqin Xu
  • , Wei Wan
  • , Zhenxi Li
  • , Shijie Chen
  • , Xinghai Yang
  • , Song Wu
  • , Jianru Xiao*
  • *Corresponding author for this work
  • Changzheng Hospital
  • East China Normal University
  • Central South University
  • University of Texas at Austin

Research output: Contribution to journalArticlepeer-review

Abstract

The epidermal growth factor receptor (EGFR) is a therapeutic target (oncotarget) in NSCLC. Using in vitro EGFR kinase activity system, we identified a novel small molecule, WB-308, as an inhibitor of EGFR. WB-308 decreased NSCLC cell proliferation and colony formation, by causing G2/M arrest and apoptosis. Furthermore, WB-308 inhibited the engraft tumor growths in two animal models in vivo (lung orthotopic transplantation model and patient-derived engraft mouse model). WB-308 impaired the phosphorylation of EGFR, AKT, and ERK1/2 protein. WB-308 was less cytotoxic than Gefitinib. Our study suggests that WB-308 is a novel EGFR-TKI and may be considered to substitute for Gefitinib in clinical therapy for NSCLC.

Original languageEnglish
Pages (from-to)6749-6761
Number of pages13
JournalOncotarget
Volume6
Issue number9
DOIs
StatePublished - 2015
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • EGFR
  • NSCLC
  • TKIs
  • Tumor growth

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