4.8 Article

KIF5B-RET fusions in lung adenocarcinoma

Journal

NATURE MEDICINE
Volume 18, Issue 3, Pages 375-377

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nm.2644

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Funding

  1. National Institute of Biomedical Innovation (NiBio)
  2. Ministry of Health, Labour and Welfare
  3. National Cancer Center
  4. Norwegian Cancer Society
  5. National Cancer Center, Japan
  6. Grants-in-Aid for Scientific Research [23591330, 23249052, 22134006, 24390288] Funding Source: KAKEN

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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.

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