Journal
CANCER LETTERS
Volume 316, Issue 2, Pages 168-177Publisher
ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2011.10.035
Keywords
Apoptosis; TRAIL; XIAP; Pancreatic cancer; Interferon; Caspase-8
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Funding
- EU-FP6 Marie-Curie Excellence Team
- EU-FP6 Marie-Curie RTN
- Science Foundation Ireland [BIM084]
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The tumour necrosis factor-related apoptosis-inducing ligand (TRAIL) is a specific and potent inducer of apoptosis in cancer cells, but the resistance of many tumour cells to TRAIL still represents a major hurdle for the clinical treatment of tumours with TRAIL As apoptosis is regulated by the balance of activities of several anti-apoptotic factors and pro-apoptotic factors, we analysed the relative contribution of the two sides and found that down-regulation of Bcl-x(L) and in particular XIAP, but not c-Flip, sensitised the TRAIL resistant pancreatic cancer cell line Panc-1. A combination of both XIAP and Bcl-x(L) knockdowns showed no substantial added benefit indicating that both act in the same pathway. Notably, the degree of sensitisation by silencing of anti-apoptotic genes was further elevated by concomitantly increasing the pro-apoptotic potential in Panc-1 cells through over-expression of TRAIL-R1 or IFN-gamma-mediated increases in caspase-8 levels. Similar sensitisation effects were obtained for another TRAIL-resistant pancreatic tumour cell line, AsPC-1. Our findings demonstrate that modulation of the balance between anti- and pro-apoptotic pathways from both sides by inhibition of apoptosis-antagonists and stimulation of pro-apoptotic factors provides the best way to enhance the anti-tumourigenic effect of TRAIL. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
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