laq824 and Multiple-Myeloma

Histone deacetylase (HDAC) inhibitors are emerging as a promising new treatment strategy in hematologic malignancies. Here we show that NVP-LAQ824, a novel hydroxamic acid derivative, induces apoptosis at physiologically achievable concentrations (median inhibitory concentration [IC50] of 100 nM at 24 hours) in multiple myeloma (MM) cell lines resistant to conventional therapies. MM.1S myeloma cell proliferation was also inhibited when cocultured with bone marrow stromal cells, demonstrating ability to overcome the stimulatory effects of the bone marrow microenvironment. Importantly, NVP-LAQ824 also inhibited patient MM cell growth in a dose- and time-dependent manner. NVP-LAQ824-induced apoptotic signaling includes up-regulation of p21, caspase cascade activation, and poly (adenosine diphosphate [ADP]) ribose (PARP) cleavage. Apoptosis was confirmed with cell cycle analysis and annexin-propidium iodide staining. Interestingly, treatment of MM cells with NVPLAQ824 also led to proteasome inhibition, as determined by reduced proteasome chymotrypsin-like activity and increased levels of cellular polyubiquitin conjugates. Finally, a study using NVP-LAQ824 in a preclinical murine myeloma model provides in vivo relevance to our in vitro studies. Taken together, these findings provide the framework for NVP-LAQ824 as a novel therapeutic in MM.

Topics: Acetylation; Animals; Cell Cycle; Cysteine Endopeptidases; Dexamethasone; Enzyme Inhibitors; Glucocorticoids; Histone Deacetylase Inhibitors; Humans; Hydroxamic Acids; Immunocompromised Host; Interleukin-6; Mice; Mice, Nude; Multienzyme Complexes; Multiple Myeloma; NF-kappa B; Poly(ADP-ribose) Polymerases; Proteasome Endopeptidase Complex; Proto-Oncogene Proteins p21(ras); Tumor Cells, Cultured; Up-Regulation; Xenograft Model Antitumor Assays