KIF5B-RET fusions in lung adenocarcinoma

The authors report a new type of genetic alteration in lung adenocarcinoma. Fusions of KIF5B with RET kinase are found in 1–2% of lung cancer patients, segregate from other known alterations and can potentially be targeted using RET kinase inhibitors. We identified in-frame fusion transcripts of KIF...

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Veröffentlicht in:Nature medicine 2012-03, Vol.18 (3), p.375-377
Hauptverfasser: Kohno, Takashi, Ichikawa, Hitoshi, Totoki, Yasushi, Yasuda, Kazuki, Hiramoto, Masaki, Nammo, Takao, Sakamoto, Hiromi, Tsuta, Koji, Furuta, Koh, Shimada, Yoko, Iwakawa, Reika, Ogiwara, Hideaki, Oike, Takahiro, Enari, Masato, Schetter, Aaron J, Okayama, Hirokazu, Haugen, Aage, Skaug, Vidar, Chiku, Suenori, Yamanaka, Itaru, Arai, Yasuhito, Watanabe, Shun-ichi, Sekine, Ikuo, Ogawa, Seishi, Harris, Curtis C, Tsuda, Hitoshi, Yoshida, Teruhiko, Yokota, Jun, Shibata, Tatsuhiro
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Sprache:eng
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Zusammenfassung:The authors report a new type of genetic alteration in lung adenocarcinoma. Fusions of KIF5B with RET kinase are found in 1–2% of lung cancer patients, segregate from other known alterations and can potentially be targeted using RET kinase inhibitors. 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.
ISSN:1078-8956
1546-170X
DOI:10.1038/nm.2644