Identification and characterization of a novel SCYL3-NTRK1 rearrangement in a colorectal cancer patient
Author(s) -
Massimo Milione,
Elena Ardini,
Jason Christiansen,
Emanuele Valtorta,
Silvio Veronese,
Roberta Bosotti,
Alessio Pellegrinelli,
Adele Testi,
Filippo Pietrantonio,
Giovanni Fucá,
Wei Ge,
Danielle Murphy,
Salvatore Siena,
Antonella Isacchi,
Filippo de Braud
Publication year - 2017
Publication title -
oncotarget
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.373
H-Index - 127
ISSN - 1949-2553
DOI - 10.18632/oncotarget.19512
Subject(s) - medicine , colorectal cancer , cancer , identification (biology) , cancer research , oncology , biology , botany
In colorectal cancer patients, chromosomal rearrangements involving NTRK1 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 SCYL3-NTRK1 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 NTRK rearrangements. Therefore, screening for rearrangements involving NTRK genes may help identifying a subset of patients able to derive benefit from treatment with entrectinib or other targeted inhibitors.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom