An Unbiased Functional Genetics Screen Identifies Rare Activating ERBB4 Mutations

无偏功能遗传学筛查可识别罕见的 ERBB4 激活突变

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作者:Deepankar Chakroborty #, Veera K Ojala #, Anna M Knittle, Jasmin Drexler, Mahlet Z Tamirat, Regina Ruzicka, Karin Bosch, Johanna Woertl, Susanne Schmittner, Laura L Elo, Mark S Johnson, Kari J Kurppa, Flavio Solca, Klaus Elenius

Significance

ERBB4 is a member of the ERBB family of oncogenes that is frequently mutated in different cancer types but the functional impact of its somatic mutations remains unknown. Here, we have analyzed the function of over 8,000 randomly mutated ERBB4 variants in an unbiased functional genetics screen. The data indicate the presence of rare activating ERBB4 mutations in cancer, with potential to be targeted with clinically approved pan-ERBB inhibitors.

Statement of significance

ERBB4 is a member of the ERBB family of oncogenes that is frequently mutated in different cancer types but the functional impact of its somatic mutations remains unknown. Here, we have analyzed the function of over 8,000 randomly mutated ERBB4 variants in an unbiased functional genetics screen. The data indicate the presence of rare activating ERBB4 mutations in cancer, with potential to be targeted with clinically approved pan-ERBB inhibitors.

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