Identification of recurrent FGFR3 fusion genes in lung cancer through kinome-centred RNA sequencing
Details
Publication Year 2013-07,Volume 230,Issue #3,Page 270-276
Journal Title
JOURNAL OF PATHOLOGY
Publication Type
Journal Article
Abstract
Oncogenic fusion genes that involve kinases have proven to be effective targets for therapy in a wide range of cancers. Unfortunately, the diagnostic approaches required to identify these events are struggling to keep pace with the diverse array of genetic alterations that occur in cancer. Diagnostic screening in solid tumours is particularly challenging, as many fusion genes occur with a low frequency. To overcome these limitations, we developed a capture enrichment strategy to enable high-throughput transcript sequencing of the human kinome. This approach provides a global overview of kinase fusion events, irrespective of the identity of the fusion partner. To demonstrate the utility of this system, we profiled 100 non-small cell lung cancers and identified numerous genetic alterations impacting fibroblast growth factor receptor 3 (FGFR3) in lung squamous cell carcinoma and a novel ALK fusion partner in lung adenocarcinoma. (c) 2013 The Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.
Publisher
WILEY-BLACKWELL
Keywords
SQUAMOUS-CELL CARCINOMA; ACTIVATING MUTATIONS; ADENOCARCINOMA; GLIOBLASTOMA; LANDSCAPE; EML4-ALK; BLADDER; PROFILE; GENOME; HEAD
Research Division(s)
Cancer And Haematology
Terms of Use/Rights Notice
© 2013 The Authors. Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.


Creation Date: 2013-07-01 12:00:00
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