FAM150A and FAM150B are activating ligands for anaplastic lymphoma kinase

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...

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Veröffentlicht in:eLife 2015-09, Vol.4, p.e09811-e09811
Hauptverfasser: Guan, Jikui, Umapathy, Ganesh, Yamazaki, Yasuo, Wolfstetter, Georg, Mendoza, Patricia, Pfeifer, Kathrin, Mohammed, Ateequrrahman, Hugosson, Fredrik, Zhang, Hongbing, Hsu, Amy W, Halenbeck, Robert, Hallberg, Bengt, Palmer, Ruth H
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Sprache:eng
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Zusammenfassung: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.
ISSN:2050-084X
2050-084X
DOI:10.7554/elife.09811