Počet záznamů: 1  

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

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    SYSNO ASEP0387575
    Druh ASEPJ - Článek v odborném periodiku
    Zařazení RIVJ - Článek v odborném periodiku
    Poddruh JČlánek ve WOS
    NázevSensitization of (colon) cancer cells to death receptor related therapies A report from the FP6-ONCODEATH research consortium
    Tvůrce(i) Pintzas, A. (GR)
    Zhivotovsky, B. (SE)
    Workman, P. (GB)
    Clarke, P.A. (GB)
    Linardopoulos, S. (GB)
    Martinou, J.C. (CH)
    Lacal, J.C. (ES)
    Robine, S. (FR)
    Nasioulas, G. (GR)
    Anděra, Ladislav (UMG-J) RID
    Zdroj.dok.Cancer Biology & Therapy - ISSN 1538-4047
    Roč. 13, č. 7 (2012), s. 458-466
    Poč.str.9 s.
    Jazyk dok.eng - angličtina
    Země vyd.US - Spojené státy americké
    Klíč. slovacancer ; death receptors ; kinase inhibitors ; mitochondria ; targeted therapies
    Vědní obor RIVEB - Genetika a molekulární biologie
    Institucionální podporaUMG-J - RVO:68378050
    UT WOS000303927700002
    DOI10.4161/cbt.19600
    AnotaceThe 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 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.
    PracovištěÚstav molekulární genetiky
    KontaktNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Rok sběru2013
Počet záznamů: 1  

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