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The EML4-ALK transcript but not the fusion protein can be expressed in reactive and neoplastic lymphoid tissues.

Abstract
Rearrangements involving the ALK gene define two distinct entities in the new 2008 WHO classification of lymphoid neoplasms, i.e. ALK+ anaplastic large cell lymphoma and a rare subset of ALK+ diffuse large B-cell lymphoma. Recently, rearrangements involving ALK and the echinoderm microtubule associated protein-like 4 (EML4) gene were described as a specific genetic alteration in about 6% of non-small cell lung cancer (NSCLC). We investigated the expression of EML4-ALK mRNA and protein in 51 reactive and 58 neoplastic lymphoid tissues. EML4-ALK transcripts were detected in 3/51 (5.9%) of reactive lymphoid tissues and 12/58 (20.7%) of lymphomas of different categories, including follicular lymphoma, diffuse large B-cell lymphoma and Hodgkin's disease. Notably, none of these cases expressed the EML4-ALK fusion protein at Western blotting samples and immunohistochemistry. These results indicate that EML4-ALK rearrangements are not specific of NSCLC and raise yet unsolved questions about their role in promoting human neoplasms.
AuthorsGabriella Sozzi, Maria Paola Martelli, Davide Conte, Piergiorgio Modena, Valentina Pettirossi, Stefano A Pileri, Brunangelo Falini
JournalHaematologica (Haematologica) Vol. 94 Issue 9 Pg. 1307-11 (Sep 2009) ISSN: 1592-8721 [Electronic] Italy
PMID19734424 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • EML4-ALK fusion protein, human
  • Oncogene Proteins, Fusion
Topics
  • Animals
  • Carcinoma, Non-Small-Cell Lung (genetics, metabolism)
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Lung Neoplasms (genetics, metabolism)
  • Lymphoma (genetics, metabolism)
  • Mice
  • NIH 3T3 Cells
  • Oncogene Proteins, Fusion (biosynthesis, genetics)

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