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- W1858593325 abstract "Targeting of essential growth drivers represents an ideal approach to cancer treatment. To identify such molecules in clinical specimens, we developed a highly sensitive functional screening system based on the preparation of retroviral cDNA expression libraries. By screening such a library of lung adenocarcinoma with a focus formation assay, we discovered the EML4-ALK fusion-type oncogene. A small chromosomal inversion thus leads to fusion of the amino-terminal portion of the microtubule-associated protein EML4 to the intracellular kinase domain of ALK, a receptor-type protein tyrosine kinase. Constitutive dimerization of EML4-ALK mediated by a dimerization motif of EML4 results in kinase activation. Specific inhibitors of the kinase activity of ALK have been developed as therapeutic drugs for EML4-ALK-positive lung cancer, three of which (crizotinib, ceritinib, and alectinib) have already been approved for clinical use. An overall clinical response rate of 93.5% for alectinib has shown that agents that target essential growth drivers can become magic bullets for cancer treatment." @default.
- W1858593325 created "2016-06-24" @default.
- W1858593325 creator A5090560513 @default.
- W1858593325 date "2015-01-01" @default.
- W1858593325 modified "2023-10-01" @default.
- W1858593325 title "The <i>EML4-ALK</i> oncogene: targeting an essential growth driver in human cancer" @default.
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- W1858593325 doi "https://doi.org/10.2183/pjab.91.193" @default.
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