DNA Repair Phenotype the Missing Link in Breast Cancer Risk Assessment
DNA 修复表型是乳腺癌风险评估中缺失的一环
基本信息
- 批准号:10090052
- 负责人:
- 金额:$ 11.44万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-09-15 至 2023-06-30
- 项目状态:已结题
- 来源:
- 关键词:Academic skillsBiological MarkersBiomedical ResearchBiometryBlood specimenBreast Cancer Risk FactorCareer ChoiceCell LineCodes of EthicsCohort StudiesCommunicationCustomDNA RepairEnvironmental HealthEpidemiologyFacultyFamily StudyFreezingFutureGoalsGrantHealthHealth PolicyIndividualIndividual DifferencesLeadershipLinkMentorsModelingPeripheral Blood Mononuclear CellPersonsPhasePhenotypePositioning AttributeProspective cohort studyProtocols documentationResearchResearch PersonnelResourcesRisk AssessmentSamplingSeriesStructureTrainingTraining ProgramsTraining and EducationVariantbasecareercareer developmentcell immortalizationdesigninsightmalignant breast neoplasmmultidisciplinaryparent grantpost-doctoral trainingprospectiveresponsible research conductskills
项目摘要
This application is for a Research Supplement to promote diversity in health related research, specifically to
support Dr. Hazeem Okunola in the postdoctoral research phase of his training, with the ultimate goal of his
becoming an independent and productive environmental health researcher. In this application 1) The Parent
Grant is briefly summarized; 2) Dr. Okunola's proposed activities within the Parent Grant are described, which
will enhance the research in the grant while remaining within its approved Specific Aims; and 3) a Training and
Mentoring Plan is described, specifically tailored for Dr. Okunola, designed to provide him with the skills that
are needed for him to become an independent and productive environmental health researcher.
In Aim 1A of the Parent Grant a large prospective cohort study is being undertaken using frozen blood samples
from individuals from the Breast Cancer Prospective Family Study Cohort (ProF-SC), to assess the potential
association between phenotypically characterized DNA Repair Capacity (DRC) and Breast Cancer (BC) risk.
Dr. Okunola will be responsible for two significant enhancements of the current parent grant: 1. Beyond
PBMCs: Probing person-to-person variations in DNA repair capacity in PBMC subtypes. In summary, using our
current protocols we will not know if inter-individual differences in DNA repair capacity derive uniformly from all
the PBMC subtypes or predominantly from specific PBMC subtypes. Dr. Okunola's proposed studies should
allow a definitive answer to this question. 2. Looking to the Future: Generating cell lines from blood samples
that show either diminished or enhanced DNA repair capacity. Here the goal is for Dr. Okunola to establish
immortalized cell lines from PBMC samples from the individuals with the highest / lowest levels of DNA repair
capacities. No such set of cell lines defined by anomalous DRC currently exist, and it is anticipated that they
will become a valuable resource for future mechanistically based studies, both in our group and worldwide.
The key aspect of this Supplement will be training and Mentoring Dr. Okunola to become an independent
productive investigator who will make a significant long-term contribution in environmental-health-related
biomedical research. The Parent Grant is a highly multidisciplinary project and Dr. Okunola will interact with
faculty representing epidemiology, DNA damage / repair, biomarkers, and biostatistical modeling. Dr.
Okunola's will participate in a customized structured postdoctoral training program focusing on environmental
health policy, professionalism, leadership and management, communication, career management, and
responsible conduct of research. It will consist of multiple distinct series and minicourses that together will
enable him to gain insights into available career development options, to engage in training / education
activities focused on his preferred career track, to adhere to professional ethical codes of conduct, to hone his
leadership / managements skills, to optimize his communication skills for academic research positions, and to
transition from training to independence.
本申请为研究增刊,以促进健康相关研究的多样性,特别是
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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DAVID JONATHAN BRENNER其他文献
DAVID JONATHAN BRENNER的其他文献
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{{ truncateString('DAVID JONATHAN BRENNER', 18)}}的其他基金
Center for High-Throughput Minimally-Invasive Radiation Biodosimetry
高通量微创放射生物剂量测定中心
- 批准号:
10590249 - 财政年份:2022
- 资助金额:
$ 11.44万 - 项目类别:
DNA Repair Phenotype the Missing Link in Breast Cancer Risk Assessment
DNA 修复表型是乳腺癌风险评估中缺失的一环
- 批准号:
10267896 - 财政年份:2020
- 资助金额:
$ 11.44万 - 项目类别:
Flexible Tools for Pre-Clinical Studies to Answer Key Questions UnderlyingHeavy-Ion Radiotherapy
临床前研究的灵活工具可回答重离子放射治疗的关键问题
- 批准号:
9908061 - 财政年份:2019
- 资助金额:
$ 11.44万 - 项目类别:
Flexible Tools for Pre-Clinical Studies to Answer Key Questions UnderlyingHeavy-Ion Radiotherapy
临床前研究的灵活工具可回答重离子放射治疗的关键问题
- 批准号:
10372919 - 财政年份:2019
- 资助金额:
$ 11.44万 - 项目类别:
DNA Repair Phenotype the Missing Link in Breast Cancer Risk Assessment
DNA 修复表型是乳腺癌风险评估中缺失的一环
- 批准号:
10656666 - 财政年份:2018
- 资助金额:
$ 11.44万 - 项目类别:
DNA Repair Phenotype the Missing Link in Breast Cancer Risk Assessment
DNA 修复表型是乳腺癌风险评估中缺失的一环
- 批准号:
10215533 - 财政年份:2018
- 资助金额:
$ 11.44万 - 项目类别:
6 MeV/amu ion linac for deep-penetration microbeam and millimeter-beam charged-particle irradiations in small animals and biological tissues
6 MeV/amu 离子直线加速器,用于小动物和生物组织的深穿透微束和毫米束带电粒子照射
- 批准号:
9493886 - 财政年份:2018
- 资助金额:
$ 11.44万 - 项目类别:
DNA Repair Phenotype the Missing Link in Breast Cancer Risk Assessment
DNA 修复表型是乳腺癌风险评估中缺失的一环
- 批准号:
10440447 - 财政年份:2018
- 资助金额:
$ 11.44万 - 项目类别:
DNA Repair Phenotype the Missing Link in Breast Cancer Risk Assessment
DNA 修复表型是乳腺癌风险评估中缺失的一环
- 批准号:
10430801 - 财政年份:2018
- 资助金额:
$ 11.44万 - 项目类别:
Monochromatic 222 nm UV light: Development of a safe, cost-effective technology for the efficient reduction of bacterial and viral infection and transmission
单色 222 nm 紫外线:开发安全、经济高效的技术,有效减少细菌和病毒的感染和传播
- 批准号:
9140848 - 财政年份:2016
- 资助金额:
$ 11.44万 - 项目类别:
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