Activation of α-diacylglycerol kinase is critical for the mitogenic properties of anaplastic lymphoma kinase

Roberta Bacchiocchi, Gianluca Baldanzi, Damiano Carbonari, Catia Capomagi, Emanuela Colombo, Wim J. Van Blitterswijk, Andrea Graziani, Francesca Fazioli

Research output: Contribution to journalArticlepeer-review

Abstract

Oncogenic rearrangements of the tyrosine kinase receptor anaplastic lymphoma kinase (ALK), most commonly represented by the nucleophosmin/ALK fusion protein (NPM/ALK), are involved in the pathogenesis of anaplastic large-cell lymphomas (ALCLs). In an effort to identify new intracellular transducers operative in ALK-positive malignancies, we have investigated the potential involvement of diacylglycerol kinase (DGK). Here we show that αDGK is constitutively activated in the NPM/ALK-positive ALCL-derived cell line Karpas 299 and in NPM/ ALK-infected 32D hematopoietic cells. These results were further validated in fibroblastic NIH-3T3 cells expressing a previously described chimeric epidermal growth factor receptor (EGFR)/ALK molecule that allows dissection of ALK enzymatic function under conditions of controlled ligand-induced activation. In this cell system, we also show that ALK-mediated. αDGK activation is dependent on p60src tyrosine kinase, with which αDGK forms a complex. The specific inhibition of αDGK, obtained by cell treatment with R59949, significantly reduced cellular growth in all cell lines. This result was further confirmed in Karpas 299 cells following specific down-regulation of αDGK by RNA interference. Overall, our data indicate that αDGK activation is involved in the control of ALK-mediated mitogenic properties.

Original languageEnglish
Pages (from-to)2175-2182
Number of pages8
JournalBlood
Volume106
Issue number6
DOIs
Publication statusPublished - Sep 15 2005

ASJC Scopus subject areas

  • Hematology

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