Identification and validation of the anaplastic large cell lymphoma signature.

TitleIdentification and validation of the anaplastic large cell lymphoma signature.
Publication TypeJournal Article
Year of Publication2007
AuthorsPiva R, Pellegrino E, Inghirami G
JournalAdv Exp Med Biol
Volume604
Pagination129-36
Date Published2007
ISSN0065-2598
KeywordsAnimals, Gene Expression Profiling, Gene Expression Regulation, Gene Expression Regulation, Neoplastic, Gene Silencing, Humans, K562 Cells, Lymphoma, Large B-Cell, Diffuse, Mice, Mice, Nude, Models, Biological, RNA Interference, RNA, Messenger, Signal Transduction, Transcription, Genetic
Abstract

Anaplastic large cell lymphomas (ALCL) represent a subset of lymphomas in which the anaplastic lymphoma kinase (ALK) gene is fused to several partners, most frequently to the NPM gene. We have previously demonstrated that the constitutive expression and phosphorylation of ALK chimeric proteins is sufficient for cellular transformation, and its activity is strictly required for the survival of ALCL cells. To unravel signaling pathways required for NPM-ALK-mediated transformation and tumor maintenance, we analyzed the transcriptomes of ALK positive ALCL cell lines through experimentally controlled approaches in which ALK signaling was abrogated by an inducible ALKshRNA or by ALK inhibitors. Transcripts derived from the gene expression profiling analyses uncovered a reproducible signature, which includes a novel group of ALK-regulated genes. A functional RNAi screening identified new ALK transcriptional targets instrumental to cell transformation and/or to sustain the growth and survival of ALK positive ALCL cells. Thus, we prove that an experimentally controlled and functionally validated gene expression profiling analysis represents a powerful tool to identify novel pathogenetic networks and to validate biologically suitable target genes for therapeutic interventions.

DOI10.1007/978-0-387-69116-9_12
Alternate JournalAdv Exp Med Biol
PubMed ID17695725
Grant ListR01-CA64033 / CA / NCI NIH HHS / United States
Related Faculty: 
Giorgio Inghirami, M.D.

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