| Literature DB >> 26757822 |
Roslyn N Crowder1, David T Dicker2, Wafik S El-Deiry3.
Abstract
TNF-related apoptosis-inducing ligand (TRAIL) is a potential cancer therapy that selectively targets cancer cell death while non-malignant cells remain viable. Using a panel of normal human fibroblasts, we characterized molecular differences in human foreskin fibroblasts and WI-38 TRAIL-resistant cells and marginally sensitive MRC-5 cells compared with TRAIL-sensitive human lung and colon cancer cells. We identified decreased caspase-8 protein expression and protein stability in normal fibroblasts compared with cancer cells. Additionally, normal fibroblasts had incomplete TRAIL-induced caspase-8 activation compared with cancer cells. We found that normal fibroblasts lack the ubiquitin modification of caspase-8 required for complete caspase-8 activation. Treatment with the deubiquitinase inhibitor PR-619 increased caspase-8 ubiquitination and caspase-8 enzymatic activity and sensitized normal fibroblasts to TRAIL-mediated apoptosis. Therefore, posttranslational regulation of caspase-8 confers resistance to TRAIL-induced cell death in normal cells through blockade of initiation of the extrinsic cell death pathway.Entities:
Keywords: TRAIL; caspase; cell death; deubiquitylation (deubiquitination); fibroblast
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Year: 2016 PMID: 26757822 PMCID: PMC4786729 DOI: 10.1074/jbc.M115.713545
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157