Energetic Factors, Lethal Prostate Cancer, and Survivorship
Energetic Factors, Lethal Prostate Cancer, and Survivorship
批准号:
8072430
负责人:
Jing Ma
金额:
$67.78万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-07-28 至 2016-05-31
关键词:
AccountingAddressAdvanced Malignant NeoplasmBehaviorBehavior TherapyBeta CellBinding ProteinsBiological MarkersBiologyBloodBody WeightBody Weight ChangesBody mass indexC-PeptideCancer CenterCancer PatientCancer SurvivorshipCause of DeathCell physiologyCessation of lifeClinicalClinical ResearchCountryCountyDevelopmentDiagnosisDietDiet ModificationDiseaseEnergy MetabolismEnvironmentEnvironmental EpidemiologyEpidemiologic StudiesFatal OutcomeFunctional disorderGeneticGenetic MarkersGenetic RiskGleason Grade for Prostate CancerHealthHip region structureIncidenceIndividualInsulinInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor ILinkMalignant NeoplasmsMalignant neoplasm of prostateMeasuresMediatingNeighborhoodsNeoplasm MetastasisNewly DiagnosedNon-Insulin-Dependent Diabetes MellitusObesityOutcomeOutcome AssessmentParticipantPathway interactionsPatientsPhysical activityPhysiciansPlayPrevention strategyProductionProinsulinProstate-Specific AntigenPublishingQiRecurrenceResearchRiskRoleScreening procedureSomatomedinsStage at DiagnosisStagingTestingTherapeuticUnited StatesVariantWeight GainWorkadiponectinanthrax lethal factorcancer diagnosiscancer epidemiologycancer preventioncohortcost effectiveenergy balancefollow-upgenetic variantgenome wide association studyindexinginsightinsulin sensitivitymalemenmortalityneoplasticnovelnovel markernutritiontherapeutic targettumortumor progression
中文摘要
点击翻译按钮获取中文摘要
英文摘要
In the United States, prostate cancer (PCa) is the most commonly diagnosed and second-most lethal cancer in
men. Widespread prostate-specific antigen (PSA) screening has led to an increase in PCa incidence and a
shift in stage at diagnosis with 90% of tumors now being localized at diagnosis. However, the determination of
clinical features (PSA, clinical stage, and Gleason grade) alone has limited ability to identify patients at
substantially elevated risk of PCa-specific mortality. A better understanding ofthe biology of lethal PCa and
identification of novel markers of aggressive disease are urgently needed to develop effective therapeutic and
preventive strategies. Excess body weight is consistently linked to PSA recurrence in numerous clinical
studies, but its role in PCa-specific and total mortality in PCa patients remains unclear. Our intriguing
preliminary findings on the relations of body mass index (BMI), C-peptide (a marker of insulin production), and
adiponectin with fatal PCa support important roles of insulin/insulin-like growth factor (IGF) axis in pathways
connecting energy balance and obesity to cancer progression and survival. In this application, we plan to
extend this exciting work to comprehensively evaluate energetic factors and PCa-specific and all-cause
mortality in men diagnosed with PCa, accounting for competing causes of death. These factors include
adiposity (BMI, waist and hip circumference, and weight gain) and Type 2 diabetes (Aim 1), biomarkers (Cpeptide,
insulin, proinsulin, proinsulin/insulin ratio, IGF-1, IGF binding protein-3, and adiponectin; Aim 2), and
genetic variants related to beta-cell function, insulin production, insulin sensitivity, and obesity identified by
published genome-wide association studies (GWAS) (Aim 3). dietary insulin demand (assessed by the Cpeptide
score, insulin index, and insulin load; Aim 4), vigorous physical activity and the macro-level factor of
neighborhood built environment (assessed by the county sprawl index, Aim 5). This cost-effective project uses
a unique and well-characterized PCa patient cohort of U.S. male physicians with 30 years of complete followup
for outcomes and assessment of both pre- and post-cancer exposures. Findings of these studies will
provide new insights for the role of energy metabolism in PCa progression, guide the identification of novel
cancer therapeutic targets, and aid in the development of cancer prevention strategies from urban planning to
diet and lifestyle modification.
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会议论文
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批准号:10708748
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项目类别:
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资助金额:$35.83万
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财政年份:2022
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负责人:Jing Ma
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依托单位:
IRON STATUS AND RISK OF CHD AND COLON CANCER
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批准号:2668094
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项目类别:
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资助金额:$10.96万
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财政年份:1998
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负责人:Jing Ma
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依托单位:
IRON STATUS AND RISK OF CHD AND COLON CANCER
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批准号:2856501
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项目类别:
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资助金额:$11.56万
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财政年份:1998
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负责人:Jing Ma
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依托单位:
IRON STATUS AND RISK OF CHD AND COLON CANCER
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批准号:6137674
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项目类别:
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资助金额:$11.91万
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财政年份:1998
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负责人:Jing Ma
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依托单位:
IRON STATUS AND RISK OF CHD AND COLON CANCER
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批准号:6342095
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项目类别:
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资助金额:$12.26万
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财政年份:1998
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负责人:Jing Ma
-
依托单位:
IRON STATUS AND RISK OF CHD AND COLON CANCER
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批准号:6489146
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项目类别:
-
资助金额:$12.63万
-
财政年份:1998
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负责人:Jing Ma
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依托单位:
Nutritional and Biochemical/Genetic Markers of Cancer
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批准号:6910684
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项目类别:
-
资助金额:$73.59万
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财政年份:1986
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负责人:Jing Ma
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依托单位:
Nutritional and Biochemical/Genetic Markers of Cancer
-
批准号:6788182
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项目类别:
-
资助金额:$77.61万
-
财政年份:1986
-
负责人:Jing Ma
-
依托单位:
Nutiritional and Biochemical/Genetic Markers of Cancer
-
批准号:7120006
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项目类别:
-
资助金额:$73.75万
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财政年份:1986
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负责人:Jing Ma
-
依托单位:
Nutiritional and Biochemical/Genetic Markers of Cancer
-
批准号:6682585
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项目类别:
-
资助金额:$76.36万
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财政年份:1986
-
负责人:Jing Ma
-
依托单位:
Nutritional and Biochemical/Genetic Markers of Cancer
-
批准号:7249343
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项目类别:
-
资助金额:$71.44万
-
财政年份:1986
-
负责人:Jing Ma
-
依托单位:
Energetic Factors, Lethal Prostate Cancer, and Survivorship
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批准号:8382068
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项目类别:
-
资助金额:$43.91万
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财政年份:--
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负责人:Jing Ma
-
依托单位:
Energetic Factors, Lethal Prostate Cancer, and Survivorship
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批准号:8715333
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项目类别:
-
资助金额:$44.06万
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财政年份:--
-
负责人:Jing Ma
-
依托单位:
Energetic Factors, Lethal Prostate Cancer, and Survivorship
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批准号:8880140
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项目类别:
-
资助金额:$43.43万
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财政年份:--
-
负责人:Jing Ma
-
依托单位:
Energetic Factors, Lethal Prostate Cancer, and Survivorship
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批准号:8513157
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项目类别:
-
资助金额:$41.29万
-
财政年份:--
-
负责人:Jing Ma
-
依托单位:
海外基金