4.4 Article

Systematic Screen for Tyrosine Kinase Rearrangements Identifies a Novel C6orf204-PDGFRB Fusion in a Patient with Recurrent T-ALL and an Associated Myeloproliferative Neoplasm

期刊

GENES CHROMOSOMES & CANCER
卷 51, 期 1, 页码 54-65

出版社

WILEY-BLACKWELL
DOI: 10.1002/gcc.20930

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资金

  1. AACR-SU2C Innovative Research [SU2C-AACR-IR60109]
  2. VICC Cancer Center Core [P30-CA68485]
  3. German Ministry of Science and Education (BMBF) [01GS08100]
  4. Max Planck Society [M.I.F.A. NEUR8061]
  5. Deutsche Forschungsgemeinschaft (DFG) [SFB832]
  6. Deutsche Krebshilfe [107954]
  7. Fritz-Thyssen-Stiftung [10.08.2.175]
  8. Sequenom
  9. Sanofi-Aventis
  10. Merck
  11. Roche
  12. Infinity
  13. Boehringer-Ingelheim
  14. Johnson Johnson
  15. Atlas-Biolabs
  16. Novartis
  17. AstraZeneca
  18. NCI Cancer Center [P30-CA008748]

向作者/读者索取更多资源

Gene fusions involving the catalytic domain of tyrosine kinases (TKs) are found in a variety of hematological and solid tumor malignancies. Clinically, TK fusions have emerged as prime targets for therapy with small molecule kinase inhibitors. Unfortunately, identification of TK fusions has been hampered by experimental limitations. Here, we developed version 2.0 of a genomically based systematic kinase fusion screen and used it to detect a novel imatinib-sensitive C6orf204-PDGFRB fusion in a patient with precursor T lymphoblastic lymphoma (T-ALL) and an associated myeloproliferative neoplasm with eosinophilia. These data validate the ability of this targeted capture-sequencing approach to detect TK fusion events in small amounts of DNA extracted directly from patient samples. (C) 2011 Wiley Periodicals, Inc.

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