Identification and characterization of a novel SCYL3-NTRK1 rearrangement in a colorectal cancer patient

In colorectal cancer patients, chromosomal rearrangements involving gene (encoding the TRKA protein) are shown in a small subset of patients and are associated with the constitutive activation of the kinase domain of TRKA. In turn, activated TRKA-fusion proteins are associated with proliferation and...

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Veröffentlicht in:Oncotarget 2017-08, Vol.8 (33), p.55353-55360
Hauptverfasser: Milione, Massimo, Ardini, Elena, Christiansen, Jason, Valtorta, Emanuele, Veronese, Silvio, Bosotti, Roberta, Pellegrinelli, Alessio, Testi, Adele, Pietrantonio, Filippo, Fucà, Giovanni, Wei, Ge, Murphy, Danielle, Siena, Salvatore, Isacchi, Antonella, De Braud, Filippo
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Sprache:eng
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Zusammenfassung:In colorectal cancer patients, chromosomal rearrangements involving gene (encoding the TRKA protein) are shown in a small subset of patients and are associated with the constitutive activation of the kinase domain of TRKA. In turn, activated TRKA-fusion proteins are associated with proliferation and survival in colorectal cancer tumors. Here we report the identification and functional characterization of a new fusion gene in a 61-year-old colorectal cancer patient. To our knowledge, this fusion protein has never been previously documented in oncological patients. We show that this novel fusion is oncogenic and sensitive to TRKA inhibitors. As suggested by other pieces of evidence, entrectinib - an orally available pan-TRK, ROS1 and ALK inhibitor - may have particular efficacy in patients with rearrangements. Therefore, screening for rearrangements involving genes may help identifying a subset of patients able to derive benefit from treatment with entrectinib or other targeted inhibitors.
ISSN:1949-2553
1949-2553
DOI:10.18632/oncotarget.19512