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FAM150A and FAM150B are activating ligands for anaplastic lymphoma kinase.

Jikui GuanGanesh UmapathyYasuo YamazakiGeorg WolfstetterPatricia MendozaKathrin PfeiferAteequrrahman MohammedFredrik HugossonHongbing ZhangAmy W HsuRobert HalenbeckBengt HallbergRuth H Palmer
Published in: eLife (2015)
Aberrant activation of anaplastic lymphoma kinase (ALK) has been described in a range of human cancers, including non-small cell lung cancer and neuroblastoma (Hallberg and Palmer, 2013). Vertebrate ALK has been considered to be an orphan receptor and the identity of the ALK ligand(s) is a critical issue. Here we show that FAM150A and FAM150B are potent ligands for human ALK that bind to the extracellular domain of ALK and in addition to activation of wild-type ALK are able to drive 'superactivation' of activated ALK mutants from neuroblastoma. In conclusion, our data show that ALK is robustly activated by the FAM150A/B ligands and provide an opportunity to develop ALK-targeted therapies in situations where ALK is overexpressed/activated or mutated in the context of the full length receptor.
Keyphrases
  • advanced non small cell lung cancer
  • endothelial cells
  • wild type
  • epidermal growth factor receptor
  • signaling pathway
  • young adults
  • tyrosine kinase
  • artificial intelligence
  • deep learning