Abstract
We identified in-frame fusion transcripts of KIF5B (the kinesin family 5B gene) and the RET oncogene, which are present in 1-2% of lung adenocarcinomas (LADCs) from people from Japan and the United States, using whole-transcriptome sequencing. The KIF5B-RET fusion leads to aberrant activation of RET kinase and is considered to be a new driver mutation of LADC because it segregates from mutations or fusions in EGFR, KRAS, HER2 and ALK, and a RET tyrosine kinase inhibitor, vandetanib, suppresses the fusion-induced anchorage-independent growth activity of NIH3T3 cells.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
Adenocarcinoma / genetics*
-
Adenocarcinoma / pathology
-
Adenocarcinoma of Lung
-
Anaplastic Lymphoma Kinase
-
Animals
-
Cell Transformation, Neoplastic / drug effects
-
ErbB Receptors / genetics
-
Gene Expression Regulation, Neoplastic
-
High-Throughput Nucleotide Sequencing
-
Humans
-
Japan
-
Kinesins / genetics*
-
Lung Neoplasms / genetics*
-
Lung Neoplasms / pathology
-
Mice
-
NIH 3T3 Cells
-
Norway
-
Oncogene Proteins, Fusion / genetics*
-
Piperidines / pharmacology
-
Proto-Oncogene Proteins / genetics
-
Proto-Oncogene Proteins c-ret / antagonists & inhibitors
-
Proto-Oncogene Proteins c-ret / genetics*
-
Proto-Oncogene Proteins p21(ras)
-
Quinazolines / pharmacology
-
Receptor Protein-Tyrosine Kinases / genetics
-
Receptor, ErbB-2 / genetics
-
United States
-
ras Proteins / genetics
Substances
-
KIF5B protein, human
-
KRAS protein, human
-
Oncogene Proteins, Fusion
-
Piperidines
-
Proto-Oncogene Proteins
-
Quinazolines
-
ALK protein, human
-
Alk protein, mouse
-
Anaplastic Lymphoma Kinase
-
EGFR protein, human
-
ERBB2 protein, human
-
ErbB Receptors
-
Proto-Oncogene Proteins c-ret
-
RET protein, human
-
Receptor Protein-Tyrosine Kinases
-
Receptor, ErbB-2
-
Kinesins
-
Proto-Oncogene Proteins p21(ras)
-
ras Proteins
-
vandetanib