Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants

• Verfasst von: Wegert, Jenny [VerfasserIn]
• Verfasst von: Jones, David T. W. [VerfasserIn]
• Verfasst von: Kölsche, Christian [VerfasserIn]
• Verfasst von: Pfister, Stefan [VerfasserIn]
• Titel: Recurrent intragenic rearrangements of EGFR and BRAF in soft tissue tumors of infants
• Verf.angabe: Jenny Wegert, Christian Vokuhl, Grace Collord, Martin Del Castillo Velasco-Herrera, Sarah J. Farndon, Charlotte Guzzo, Mette Jorgensen, John Anderson, Olga Slater, Catriona Duncan, Sabrina Bausenwein, Heike Streitenberger, Barbara Ziegler, Rhoikos Furtwängler, Norbert Graf, Michael R. Stratton, Peter J. Campbell, David Tw Jones, Christian Koelsche, Stefan M. Pfister, William Mifsud, Neil Sebire, Monika Sparber-Sauer, Ewa Koscielniak, Andreas Rosenwald, Manfred Gessler & Sam Behjati
• E-Jahr: 2018
• Jahr: 18 June 2018
• Umfang: 6 S.
• Fussnoten: Gesehen am 01.07.2019
• Titel Quelle: Enthalten in: Nature Communications
• Ort Quelle: [London] : Nature Publishing Group UK, 2010
• Jahr Quelle: 2018
• Band/Heft Quelle: 9(2018), Artikel-ID 2378, Seite 1-6
• ISSN Quelle: 2041-1723
• DOI: doi:10.1038/s41467-018-04650-6
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Female
• Sach-SW: Fibrosarcoma
• Sach-SW: Gene Rearrangement
• Sach-SW: Genes, erbB-1
• Sach-SW: Humans
• Sach-SW: Infant
• Sach-SW: Infant, Newborn
• Sach-SW: Kidney Neoplasms
• Sach-SW: Male
• Sach-SW: Nephroma, Mesoblastic
• Sach-SW: Proto-Oncogene Proteins B-raf
• K10plus-PPN: 1668179415

Abstract

Soft tissue tumors of infancy encompass an overlapping spectrum of diseases that pose unique diagnostic and clinical challenges. We studied genomes and transcriptomes of cryptogenic congenital mesoblastic nephroma (CMN), and extended our findings to five anatomically or histologically related soft tissue tumors: infantile fibrosarcoma (IFS), nephroblastomatosis, Wilms tumor, malignant rhabdoid tumor, and clear cell sarcoma of the kidney. A key finding is recurrent mutation of EGFR in CMN by internal tandem duplication of the kinase domain, thus delineating CMN from other childhood renal tumors. Furthermore, we identify BRAF intragenic rearrangements in CMN and IFS. Collectively these findings reveal novel diagnostic markers and therapeutic strategies and highlight a prominent role of isolated intragenic rearrangements as drivers of infant tumors.