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FAM150A and FAM150B are activating ligands for anaplastic lymphoma kinase

机译:FAM150A和FAM150B是间变性淋巴瘤激酶的活化配体

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摘要

Aberrant activation of anaplastic lymphoma kinase (ALK) has been described in a range of human cancers, including non-small cell lung cancer and neuroblastoma (). 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.>DOI:
机译:已在多种人类癌症中描述了间变性淋巴瘤激酶(ALK)的异常激活,包括非小细胞肺癌和神经母细胞瘤()。脊椎动物ALK被认为是孤儿受体,而ALK配体的身份是一个关键问题。在这里,我们显示FAM150A和FAM150B是与ALK胞外域结合的人ALK的有效配体,除了激活野生型ALK之外,还可以驱动成神经细胞瘤激活的ALK突变体的“超激活”。总之,我们的数据表明,ALK被FAM150A / B配体牢固激活,并为在全长受体的情况下ALK被过度表达/激活或突变的情况下提供了开发ALK靶向疗法的机会。> DOI :

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