| Literature DB >> 27189785 |
Neil E Kay1, Traci Sassoon1, Charla Secreto1, Sutapa Sinha1, Tait D Shanafelt1, Asish K Ghosh2, Jack L Arbiser3.
Abstract
Here we tested impact of Tris (dibenzylideneacetone) dipalladium (Tris-DBA) on chronic lymphocytic leukemia (CLL) B-cell survival. Indeed, treatment of CLL B-cells with Tris-DBA induced apoptosis in a dose-dependent manner irrespective of IgVH mutational status. Further analyses suggest that Tris-DBA-induced apoptosis involves reduced expression of the anti-apoptotic proteins Bcl-xL, and XIAP with an upregulation of the pro-apoptotic protein BIM in CLL B-cells. Our findings also indicate that Tris-DBA targets the ribosomal protein (rp)-S6, an essential component of the Akt/mTOR signaling axis in CLL B-cells. Of interest, CLL bone marrow stromal cells were unable to protect the leukemic B cells from Tris-DBA-induced apoptosis in an in vitro co-culture system. Finally, co-administration of Tris-DBA and the purine nucleoside analog fludarabine (F-ara-A) augmented CLL B-cell apoptosis levels in vitro showing synergistic effects. In total, Tris-DBA is effective at inducing apoptosis in CLL B-cells even in the presence of stromal cells likely by targeting directly the signal mediator, rpS6.Entities:
Keywords: CLL; Tris-DBA; fludarabine
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Year: 2016 PMID: 27189785 PMCID: PMC5142299 DOI: 10.3109/10428194.2016.1161186
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022