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  • The objective of the ONCODEATH consortium [EU Research Consortium %22ONCODEATH%22 (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 months, 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.
  • The objective of the ONCODEATH consortium [EU Research Consortium %22ONCODEATH%22 (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 months, 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. (en)
Title
  • Sensitization of (colon) cancer cells to death receptor related therapies A report from the FP6-ONCODEATH research consortium
  • Sensitization of (colon) cancer cells to death receptor related therapies A report from the FP6-ONCODEATH research consortium (en)
skos:prefLabel
  • Sensitization of (colon) cancer cells to death receptor related therapies A report from the FP6-ONCODEATH research consortium
  • Sensitization of (colon) cancer cells to death receptor related therapies A report from the FP6-ONCODEATH research consortium (en)
skos:notation
  • RIV/68378050:_____/12:00387575!RIV13-AV0-68378050
http://linked.open...avai/riv/aktivita
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  • 167454
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  • RIV/68378050:_____/12:00387575
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  • cancer; death receptors; kinase inhibitors; mitochondria; targeted therapies (en)
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  • US - Spojené státy americké
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  • [0C17021D8133]
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  • Cancer Biology & Therapy
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  • 13
http://linked.open...iv/tvurceVysledku
  • Anděra, Ladislav
  • Pintzas, A.
  • Zhivotovsky, B.
  • Clarke, P. A.
  • Lacal, J. C.
  • Linardopoulos, S.
  • Martinou, J. C.
  • Nasioulas, G.
  • Robine, S.
  • Workman, P.
http://linked.open...ain/vavai/riv/wos
  • 000303927700002
issn
  • 1538-4047
number of pages
http://bibframe.org/vocab/doi
  • 10.4161/cbt.19600
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