| Literature DB >> 24200995 |
Simona Martinotti1, Elia Ranzato2, Monica Parodi3, Massimo Vitale4, Bruno Burlando1.
Abstract
Malignant mesothelioma (MMe) is a poor-prognosis tumor in need of innovative therapies. In a previous in vivo study, we showed synergistic anti-MMe properties of the ascorbate/epigallocatechin-3-gallate/gemcitabine combination. We have now focused on the mechanism of action, showing the induction of apoptosis and cell cycle arrest through measurements of caspase 3, intracellular Ca(2+), annexin V, and DNA content. StellArray™ PCR technology and Western immunoblotting revealed DAPK2-dependent apoptosis, upregulation of cell cycle promoters, downregulation of cell cycle checkpoints and repression of NFκB expression. The complex of data indicates that the mixture is synergistic in inducing cell cycle deregulation and non-inflammatory apoptosis, suggesting its possible use in MMe treatment.Entities:
Keywords: Cell cycle; Combined therapy; DAPK2; PCR array; REN mesothelioma cells
Mesh:
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Year: 2013 PMID: 24200995 DOI: 10.1016/j.taap.2013.10.025
Source DB: PubMed Journal: Toxicol Appl Pharmacol ISSN: 0041-008X Impact factor: 4.219