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Experimental approaches to hypothetical hormones: detection of a candidate ligand of the neu protooncogene.

机译:假设激素的实验方法:检测新原癌基因的候选配体。

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摘要

There is a growing list of oncogenes encoding transmembrane tyrosine kinases that have structures reminiscent of growth factor receptors. In most cases, the ligands for these putative receptors are unknown. Using the neu oncogene as a model system, we have developed several experimental approaches for the detection of such hypothetical ligands. The following lines of evidence collectively imply that a candidate ligand of the neu-encoded oncoprotein is secreted by ras-transformed fibroblasts: Medium conditioned by ras transformants is able to induce down-modulation of the neu-encoded p185 and to activate its intrinsic tyrosine kinase activity in vitro. In addition, a rapid increase in the phosphorylation in vivo of tyrosine residues of the neu-encoded protein is induced by the conditioned medium. Finally, transfer of the neu gene into hematopoietic cells renders them mitogenically responsive to the conditioned medium. The possibility of indirect activation of the oncoprotein through other known receptors, especially the receptor for the epidermal growth factor, was experimentally excluded.
机译:编码跨膜酪氨酸激酶的致癌基因列表不断增加,其结构让人联想到生长因子受体。在大多数情况下,这些推定受体的配体是未知的。使用neu癌基因作为模型系统,我们已经开发了几种检测这种假设配体的实验方法。以下证据共同暗示了neu编码癌蛋白的候选配体由ras转化的成纤维细胞分泌:受ras转化子调节的培养基能够诱导neu编码的p185的下调并激活其固有的酪氨酸激酶。体外活性。另外,条件培养基诱导了neu编码蛋白的酪氨酸残基的体内磷酸化的快速增加。最后,neu基因转移到造血细胞中使它们对条件培养基有丝分裂反应。通过实验排除了癌蛋白通过其他已知受体,特别是表皮生长因子受体间接激活的可能性。

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