Heat Shock Protein-Induced Protection Against Cisplatin-Induced Hair Cell Death
Heat Shock Protein-Induced Protection Against Cisplatin-Induced Hair Cell Death
批准号:
8301792
负责人:
Tiffany Gray Baker
金额:
$3.55万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-28 至 2015-09-27
关键词:
AdultAdverse effectsAminoglycosidesApoptosisApoptoticBiological ModelsCell DeathCell SurvivalCellsCessation of lifeChemicalsCisplatinCochleaDNA AdductsDNA DamageDataDoseDose-LimitingEventGenotoxic StressGoalsHair CellsHeat shock proteinsHeat-Shock ResponseIn VitroKidneyKnockout MiceLabyrinthMalignant NeoplasmsMediatingMediator of activation proteinMusNeonatalPatientsPharmaceutical PreparationsPlayPreventionProductionProtein p53ProteinsProximal Kidney TubulesQuality of lifeRattusReactive Oxygen SpeciesRelative (related person)ResistanceRoleSTAT proteinSensory HairSignal TransductionSignaling MoleculeStressSystemTransgenic MiceUp-RegulationUtricle structureWestern Blottingcancer celldesignhearing impairmentimprovedin vivonephrotoxicityototoxicityoverexpressionpreconditioningpreventpro-apoptotic proteinprotective effectpublic health relevanceresearch studyresponse
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英文摘要
DESCRIPTION (provided by applicant): Cisplatin has been successfully used to treat of a variety of cancers since the 1970s. However, patients who receive cisplatin can suffer from dose-limiting side-effects which include nephrotoxicity and ototoxicity. The ototoxic effects of cisplatin involve in part the death of sensory hair cells of the inner ear. Cisplatin causes cell death by forming DNA adducts and increasing the pool of reactive oxygen species (ROS) in cells. Two pro-apoptotic proteins known to play roles in cisplatin-induced cell death are p53 and the signal transducer and activator of transcription protein-1 (STAT-1). p53 is a major mediator of cisplatin-induced death of cancer cells (reviewed by Siddik 2003). However, recent evidence indicates that p53 is not required for cisplatin-induced death of renal proximal tubule cells in the kidney (Jiang et al. 2009). The role of p53 in cisplatin-induced death of hair cells has not been determined. Cisplatin-induced hair cell death is dependent on STAT-1 activation (Schmitt et al. 2009). Heat shock preconditioning, which results in upregulation of heat shock proteins (Hsps), inhibits cisplatin-induced hair cell death (Cunningham and Brandon 2006). One of these Hsps, Hsp32, has been shown to inhibit cisplatin-induced hair cell death in neonatal rat cochlea in vitro (Kim et al. 2006). Hsp70 is the most stress-inducible Hsp, and it can protect hair cells from aminoglycoside induced death both in vitro and in vivo (Taleb et al. 2008; Taleb et al. 2009). Both Hsp70 and Hsp32 have been shown to modulate the activation of either p53 or STAT-1. The experiments in this proposal are designed to examine the role of p53 in mediating cisplatin-induced hair cell death and to elucidate the mechanism(s) underlying the protective effects of Hsp32 and Hsp70.
PUBLIC HEALTH RELEVANCE: The prevention of hearing loss as a result of cisplatin treatment is necessary in order to maintain the best possible quality of life for patients receiving this drug. This project is designed to improve our understanding of cisplatin-induced hearing loss and to advance the goal of developing a co-therapy aimed at preventing cisplatin-induced hearing loss.
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Heat Shock Protein-Induced Protection Against Cisplatin-Induced Hair Cell Death
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批准号:8727504
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项目类别:
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资助金额:$2.4万
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财政年份:2009
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负责人:Tiffany Gray Baker
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依托单位:
Heat Shock Protein-Induced Protection Against Cisplatin-Induced Hair Cell Death
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批准号:8517085
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项目类别:
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资助金额:$3.55万
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财政年份:2009
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负责人:Tiffany Gray Baker
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依托单位:
Heat Shock Protein-Induced Protection Against Cisplatin-Induced Hair Cell Death
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批准号:7804981
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项目类别:
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资助金额:$3.45万
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财政年份:2009
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负责人:Tiffany Gray Baker
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依托单位:
Heat Shock Protein-Induced Protection Against Cisplatin-Induced Hair Cell Death
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批准号:8129472
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项目类别:
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资助金额:$3.51万
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财政年份:2009
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负责人:Tiffany Gray Baker
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依托单位:
海外基金