Targeting colorectal carcinogenesis using a cinnamon-derived food factor
Targeting colorectal carcinogenesis using a cinnamon-derived food factor
批准号:
8442671
负责人:
Georg T Wondrak
金额:
$19.77万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-01-01 至 2014-12-31
关键词:
AnimalsAntioxidantsBiochemical GeneticsCellsChemicalsChemopreventionChemopreventive AgentCinnamomum cassiaCinnamon - dietaryClinical ResearchColitisColonColorectalColorectal CancerConsumptionCytoprotectionDataDevelopmentDiabetic NephropathyDietary FactorsDimensionsDiseaseDocumentationDoseEpithelialEpithelial CellsFDA approvedFlavoringFoodFood AdditivesFutureHealthHumanIncidenceInflammationInflammatoryInterventionKnockout MiceLesionModelingMolecularMolecular TargetMorbidity - disease rateMusNatureNuclearOralOral AdministrationOxidation-ReductionPowder dose formPredispositionProteinsProteomicsPublishingResearchResearch Project GrantsRoleSafetySkinSpicesSri LankaStagingStructure-Activity RelationshipTestingTimeVolatile Oilsbasebiological adaptation to stresscancer chemopreventioncarcinogenesiscinnamic aldehydedesignmetastatic colorectalmortalityoutcome forecastpreclinical studyprototypepublic health relevanceresponsetooltranscription factortumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Colorectal cancer (CRC) is a major cause of tumor-related morbidity and mortality worldwide. Recent research strongly suggests that the redox-sensitive transcription factor Nrf2 (nuclear factor-E2-related factor 2) is a promising molecular target for chemoprevention of inflammation-driven colorectal carcinogenesis. The ground bark of Cinnamomum aromaticum (cassia) and Cinnamomum verum (Ceylon cinnamon), commonly referred to as 'cinnamon', is one of the three most consumed spices in the world, yet health effects of cinnamon consumption have remained mostly unexplored at the molecular level. Recently, we have identified the cinnamon-derived food factor cinnamaldehyde as the key principle in cinnamon powder responsible for potent induction of the Nrf2-regulated antioxidant response in human colon cells, conferring cytoprotection against subsequent oxidative and genotoxic insult. We propose exploratory research that tests the overall hypothesis that cinnamaldehyde represents a potent chemopreventive dietary factor targeting colorectal carcinogenesis through modulation of Nrf2-orchestrated cytoprotective mechanisms. To test this hypothesis, the following specific aims will be pursued: Aim #1. To define the specific molecular targets involved in Nrf2-activation by cinnamaldehyde in colorectal epithelial cells. Aim #2. To test feasibility of cinnamaldehyde-based intervention targeting colorectal carcinogenesis in an accepted murine model and to determine mechanistic involvement of Nrf2 in cinnamaldehyde chemopreventive activity. Successful completion of this project will generate critical proof-of-principle data guiding the rational design of future preclinical and clinical studies that aim at developing cinnamaldehyde for chemopreventive intervention targeting human colorectal carcinogenesis.
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海外基金