The potential role of HGF-MET signaling and autophagy in the war of Alectinib versus Crizotinib against ALK-positive NSCLC

J Exp Clin Cancer Res. 2018 Feb 20;37(1):33. doi: 10.1186/s13046-018-0707-5.

Abstract

Non-small-cell lung cancer (NSCLC) is currently the leading cause of cancer-related death. Accumulating evidences suggest that overcoming the therapeutic resistance in NSCLC is a big challenge. Recently, the outcomes of two independent phase 3 trials regarding Alectinib versus Crizotinib in ALK-positive NSCLC are encouraging. However, given the potential relevance of HGF-MET signaling and especially autophagy to the war against ALK-positive NSCLC between Alectinib and Crizotinib, it's too early to reach a convincing conclusion. Therefore, to further improve the therapeutic efficacy of ALK-positive NSCLC, this commentary highlights the negligence in design of relevant clinical trials, emphasizes the importance of molecular characteristics investigation, and discusses the prospect of combination therapy.

Keywords: ALK-targeted therapy; Alectinib; Autophagy; Combined treatment; Crizotinib; HGF-MET signaling; LIR motif; NSCLC; Therapeutic resistance.

Publication types

  • Letter

MeSH terms

  • Anaplastic Lymphoma Kinase / metabolism*
  • Autophagy / drug effects*
  • Carbazoles / pharmacology*
  • Carbazoles / therapeutic use
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / metabolism*
  • Crizotinib / pharmacology*
  • Crizotinib / therapeutic use
  • Hepatocyte Growth Factor / metabolism*
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / genetics
  • Lung Neoplasms / metabolism*
  • Piperidines / pharmacology*
  • Piperidines / therapeutic use
  • Proto-Oncogene Proteins c-met / metabolism*
  • Signal Transduction / drug effects*

Substances

  • Carbazoles
  • HGF protein, human
  • Piperidines
  • Crizotinib
  • Hepatocyte Growth Factor
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • MET protein, human
  • Proto-Oncogene Proteins c-met
  • alectinib