Hunting ALK to feed targeted cancer therapy

Nat Med. 2011 Mar;17(3):290-1. doi: 10.1038/nm0311-290.

Abstract

Neuroblastoma is a fatal childhood cancer, but lack of knowledge about the underlying causative genes has hampered the development of effective therapies. The identification of anaplastic lymphoma kinase (ALK) mutations as drivers of neuroblastoma has indicated that targeted therapy with ALK inhibitors might be a valuable strategy in the fight against this lethal cancer.

Publication types

  • News

MeSH terms

  • Anaplastic Lymphoma Kinase
  • Humans
  • Neuroblastoma / drug therapy
  • Neuroblastoma / enzymology*
  • Neuroblastoma / pathology
  • Protein Kinase Inhibitors / therapeutic use*
  • Protein-Tyrosine Kinases / antagonists & inhibitors*
  • Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases

Substances

  • Protein Kinase Inhibitors
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Protein-Tyrosine Kinases
  • Receptor Protein-Tyrosine Kinases