grant

Network-based analysis of disease-associated epigenetic changes in youth electronic cigarette users

Organization UNIVERSITY OF SOUTHERN CALIFORNIALocation Los Angeles, UNITED STATESPosted 1 Sept 2023Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY2024AddressAlgorithmsAreaBiochemicalBiologicalBiological MarkersBiological Specimen BanksBiological Substance BanksBlood leukocyteBody TissuesCaliforniaCancer Causing AgentsCarcinogensCell BodyCellsCharacteristicsCollaborationsCollectionComputer ModelsComputerized ModelsDataData SetDevelopmentDevicesDietDifferential Gene ExpressionDiseaseDisorderDoseElectronic cigaretteEpidemicEpigeneticEpigenetic ChangeEpigenetic MechanismEpigenetic ProcessFunctional RNAFundingGene Action RegulationGene ExpressionGene Expression MonitoringGene Expression Pattern AnalysisGene Expression ProfilingGene Expression RegulationGene RegulationGene Regulation ProcessGene TranscriptionGenerationsGenesGenetic TranscriptionHealthLaboratoriesLeukocytesLeukocytes Reticuloendothelial SystemLife StyleLifestyleLinkMarketingMarrow leukocyteMeasurementMeasuresMediatingMethodsModelingMolecularNIDCRNIDRNational Institute of Dental ResearchNational Institute of Dental and Craniofacial ResearchNetwork AnalysisNetwork-basedNicotineNon-CodingNon-Coding RNANon-translated RNANoncoding RNANontranslated RNAOncogensOralPathway AnalysisPopulationProcessPublic HealthRNA ExpressionRNA SeqRNA sequencingRNAseqRegulationRegulator GenesResearch SpecimenRiskRisk AssessmentSamplingSmoking StatusSourceSpecial PopulationSpecimenStudy SubjectSystems BiologyTissue-Specific Differential Gene ExpressionTissue-Specific Gene ExpressionTissuesTranscript Expression AnalysesTranscript Expression AnalysisTranscriptionTranscriptional Regulatory ElementsUntranslated RNAVulnerable PopulationsWalkingWhite Blood CellsWhite CellYouthYouth 10-21analyze gene expressionbio-markersbiologicbiologic markerbiological specimen repositorybiomarkerbiosample repositorybiospecimen bankbiospecimen repositorycomputational modelingcomputational modelscomputer based modelscomputerized modelingdemographicsdevelopmentaldietsdisease riskdisorder riske-cige-cig aerosolse-cig liquidse-cig usee-cig usere-cig vapore-cigarettee-cigarette aerosolse-cigarette liquidse-cigarette usee-cigarette usere-cigarette vapore-juicee-liquidecigecig aerosolsecig liquidsecig useecig userecig vaporecigaretteecigarette aerosolsecigarette liquidsecigarette useecigarette userecigarette vaporejuiceelectronic cigarette aerosolelectronic cigarette useelectronic cigarette userelectronic cigarette vaporelectronic liquideliquidepigeneticallygene expression analysisgene expression assayhealth assessmentinnovateinnovationinnovativeinterestmanufacturenew markernoncodingnovel biomarkernovel markeroncogenic agentperipheral bloodpreservationpublic health relevancepublic repositorypublicly accessible repositorypublicly available repositoryrecruitregulate tobaccoregulatory genespecimen bankspecimen repositorytobacco productstobacco regulationtobacco regulatory effortstoxicanttrans acting elementtranscriptional profilingtranscriptome sequencingtranscriptomic sequencingvapervapingvulnerable groupvulnerable individualvulnerable peoplewhite blood cellwhite blood corpuscle
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Full Description

The widespread use of electronic cigarettes (e-cigs) by youth is a significant public health problem in the US and
many parts of the world. To date, the long-term health effects of e-cig use in this vulnerable population are largely

unknown. Many toxicants and carcinogens present in e-cig vapor exert their biological effects through epigenetic

changes that can cause dysregulation of disease-related genes. Long non-coding RNAs (lncRNAs) are key

epigenetic regulators of gene expression in health and disease states.

Approach: To investigate lncRNA-mediated gene regulation and its association with disease development in

youth vapers, we will perform RNA-seq and network-based analyses on cells and tissues of youth e-cig users

as compared to non-users. Aim 1a: Using a systems biology approach, we will detect aberrant lncRNAs and

their interaction networks that drive gene dysregulation in youth e-cig users. The detected lncRNAs that govern

gene dysregulation in youth e-cig users can serve as novel biomarkers of exposure and effects for vaping. Aim

1b: Applying advanced prediction methods, we will identify which diseases are associated with the aberrant

lncRNAs detected in youth e-cig users. Aberrant lncRNAs in youth e-cig users that are associated with specific

diseases can be used for risk assessment of vaping. Aim 2: Using computational modeling, we will find the

associations between aberrant lncRNAs and the intensity and duration of vaping (i.e., dose) and the

characteristics of vaping products used by youth. Identifying product characteristics that influence the lncRNA-

mediated gene dysregulation in youth e-cig users can inform the FDA’s regulation of tobacco products to protect

youth and promote public health.

Responsiveness to RFA-OD-21-004: This proposal will maximize the use of existing biospecimens from our

recently completed NIDCR-funded project whose study subjects were recruited through collaboration with USC-

TCORS, which is sponsored by the FDA|CTP. This is a unique collection of biospecimens from a representative

sample of population in Southern California. No publicly available repository in the US offers similar specimens

needed for this proposal. We will generate scientific evidence on the health risks of e-cig use in youth, thus

informing the FDA’s regulation of tobacco products to protect this vulnerable population and promote public

health. We will use an innovative approach to address two scientific interest areas in this RFA, including

assessment of (1) exposure; and (2) potential harm from vaping in youth, who are a population of special

relevance. By elucidating the molecular changes that underlie the biological consequences of e-cig use in youth,

we will develop novel biomarkers of exposure and effects. These biomarkers will have significant utility for

assessing the health risks of e-cig use in this vulnerable population. By determining how vaping dose and product

characteristics can modulate the induced biological effects in youth e-cig users, we will provide urgently needed

data to inform the FDA’s regulation of tobacco products to protect youth and promote public health.

Grant Number: 5R21DA058342-02
NIH Institute/Center: NIH

Principal Investigator: AHMAD BESARATINIA

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