C-Met as a potential target for the treatment of gastrointestinal cancer: Current status and future perspectives

J Cell Physiol. 2017 Oct;232(10):2657-2673. doi: 10.1002/jcp.25794. Epub 2017 Apr 10.

Abstract

Aberrant activation of the HGF/c-Met signalling pathways is shown to be related with cell proliferation, progression, metastasis, and worse prognosis in several tumor types, including gastrointestinal cancers, suggesting its value as a stimulating-target for cancer-therapy. Several approaches have been developed for targeting HGF and/or c-Met, and one of them, crizotinib (dual c-Met/ALK inhibitor), is recently been approved by FDA for lung-cancers with ALK-rearrangement. The main aim of current review is to give an overview on the role of c-Met/HGF pathway in gastrointestinal cancer, in preclinical and clinical trials. Although several important matters is still remained to be elucidated on the molecular pathways underlying the antitumor effects of this therapy in gastrointestinal-cancers. Further investigations are warranted to recognize the main determinants of the activity of c-Met inhibitors, for parallel targeting signalling pathway associated/activated via MET/HGF pathway or in response to the cell resistance to anti-c-Met agents. Additionally, identification of patients that might benefit from therapy could help to increase the selectivity and efficacy of the therapy.

Keywords: c-Met inhibitors; c-Met/HGF pathway; resistance to targeted agents; upper gastrointestinal cancers.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / therapeutic use*
  • Digestive System Neoplasms / drug therapy*
  • Digestive System Neoplasms / enzymology
  • Digestive System Neoplasms / pathology
  • Drug Resistance, Neoplasm
  • Hepatocyte Growth Factor / metabolism
  • Humans
  • Molecular Targeted Therapy
  • Protein Kinase Inhibitors / therapeutic use*
  • Proto-Oncogene Proteins c-met / antagonists & inhibitors*
  • Proto-Oncogene Proteins c-met / metabolism
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents
  • HGF protein, human
  • Protein Kinase Inhibitors
  • Hepatocyte Growth Factor
  • MET protein, human
  • Proto-Oncogene Proteins c-met