Literature DB >> 22406997

Sensitization of (colon) cancer cells to death receptor related therapies: a report from the FP6-ONCODEATH research consortium.

Alexander Pintzas1, Boris Zhivotovsky, Paul Workman, Paul A Clarke, Spiros Linardopoulos, Jean-Claude Martinou, Juan Carlos Lacal, Sylvie Robine, George Nasioulas, Ladislav Andera.   

Abstract

The objective of the ONCODEATH consortium [EU Research Consortium "ONCODEATH" (2006-2010)] was to achieve sensitization of solid tumor cells to death receptor related therapies using rational mechanism-based drug combinations of targeted therapies. In this collaborative effort, during a period of 42 mo, cell and animal model systems of defined oncogenes were generated. Exploitation of generated knowledge and tools enabled the consortium to achieve the following research objectives: (1) elucidation of tumor components which confer sensitivity or resistance to TRAIL-induced cell death; (2) providing detailed knowledge on how small molecule Hsp90, Aurora, Choline kinase, BRAF inhibitors, DNA damaging agents, HDAC and DNMT inhibitors affect the intrinsic apoptotic amplification and execution machineries; (3) optimization of combined action of TRAIL with these therapeutics for optimum effects with minimum concentrations and toxicity in vivo. These findings provide mechanistic basis for a pharmacogenomic approach, which could be exploited further therapeutically, in order to reach novel personalized therapies for cancer patients.

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Year:  2012        PMID: 22406997     DOI: 10.4161/cbt.19600

Source DB:  PubMed          Journal:  Cancer Biol Ther        ISSN: 1538-4047            Impact factor:   4.742


  3 in total

1.  The DeISGylase USP18 limits TRAIL-induced apoptosis through the regulation of TRAIL levels: Cellular levels of TRAIL influences responsiveness to TRAIL-induced apoptosis.

Authors:  Ivana Manini; Andrea Sgorbissa; Harish Potu; Andrea Tomasella; Claudio Brancolini
Journal:  Cancer Biol Ther       Date:  2013-09-19       Impact factor: 4.742

2.  Upregulation of c-FLIP-short in response to TRAIL promotes survival of NSCLC cells, which could be suppressed by inhibition of Ca2+/calmodulin signaling.

Authors:  V O Kaminskyy; O V Surova; T Piskunova; I B Zborovskaya; E M Tchevkina; L Andera; B Zhivotovsky
Journal:  Cell Death Dis       Date:  2013-03-07       Impact factor: 8.469

3.  The probiotic Propionibacterium freudenreichii as a new adjuvant for TRAIL-based therapy in colorectal cancer.

Authors:  Fabien J Cousin; Sandrine Jouan-Lanhouet; Nathalie Théret; Catherine Brenner; Elodie Jouan; Gwénaëlle Le Moigne-Muller; Marie-Thérèse Dimanche-Boitrel; Gwénaël Jan
Journal:  Oncotarget       Date:  2016-02-09
  3 in total

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