TY - JOUR
T1 - Identification and characterization of a novel SCYL3-NTRK1 rearrangement in a colorectal cancer patient
AU - Milione, Massimo
AU - Ardini, Elena
AU - Christiansen, Jason
AU - Valtorta, Emanuele
AU - Veronese, Silvio
AU - Bosotti, Roberta
AU - Pellegrinelli, Alessio
AU - Testi, Adele
AU - Pietrantonio, Filippo
AU - Fucà, Giovanni
AU - Wei, Ge
AU - Murphy, Danielle
AU - Siena, Salvatore
AU - Isacchi, Antonella
AU - De Braud, Filippo
PY - 2017/1/1
Y1 - 2017/1/1
N2 - 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.
AB - 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.
KW - CRC
KW - Entrectinib
KW - NTRK1
KW - Rearrangement
KW - TRKA
UR - http://www.scopus.com/inward/record.url?scp=85029101640&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85029101640&partnerID=8YFLogxK
U2 - 10.18632/oncotarget.19512
DO - 10.18632/oncotarget.19512
M3 - Article
AN - SCOPUS:85029101640
SN - 1949-2553
VL - 8
SP - 55353
EP - 55360
JO - Oncotarget
JF - Oncotarget
IS - 33
ER -