Molecular Differences Predicting Tumor Progression in Colorectal Cancer (PQ #14)
Molecular Differences Predicting Tumor Progression in Colorectal Cancer (PQ #14)
批准号:
8384609
负责人:
Richard Brott Halberg
金额:
$19.64万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-09-01 至 2014-08-31
关键词:
AddressAdenocarcinomaAdvanced Malignant NeoplasmAnimal ModelAnimalsAttentionBehaviorBenignBiological MarkersBiopsyCancer EtiologyCancerousCharacteristicsChemopreventionClinicalColonColonoscopyColorectalColorectal CancerColorectal NeoplasmsControlled EnvironmentDNA Microarray ChipDisease ProgressionEligibility DeterminationEventGene ExpressionGenesGeneticGoldGray unit of radiation doseHeterogeneityHumanImageImaging TechniquesIndividualLeadLesionLifeMalignant - descriptorMalignant Lymph Node NeoplasmMalignant NeoplasmsModelingMolecularMolecular AnalysisMolecular ProfilingMonitorMusMutationNatural HistoryNeoplasm MetastasisNeoplasmsOutcomePatientsPolypectomyPopulationPrecancerous PolypPreventionPrevention strategyProceduresProtocols documentationRecommendationRiskScheduleScreening procedureStagingStratificationTestingTimeTissue SampleUnited Statesadenomaarmbasecostdesignhigh riskimprovedinterestmalignant statemortalitymouse modelnovelnovel strategiesprognosticprospectiveresearch studytumortumor progressionvirtual
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Colorectal tumors have different fates. Kim and colleagues demonstrated that early adenomas in humans could grow, remain static, or even spontaneously regress as determined by longitudinally monitoring via virtual colonography (N Engl J Med. 357(14):1403-12, 2007). We found that early adenomas in the mouse had the same fates (Acad Radiol. 16(12):1475-82, 2009). Moreover, a significant percentage of adenomas eventually progress to invasive adenocarcinomas that occasionally metastasize to regional lymph nodes (Cancer Res. 69(14):5768-75, 2009). The progression of tumors from a benign to malignant state can now be meticulously detailed because of recent advances in micro-imaging. We plan to monitor tumors as they progress, collecting biopsies for histopathological assessment and molecular analysis (Aim 1). Transcriptional changes associated with progression can then be elucidated with DNA microarrays. The profile of adenomas that progress to invasive adenocarcinomas will be compared to the profile of adenomas that do not progress (Aim 2). This type of experiment is not feasible in humans because the clinical outcome of any tumor is unknowable. Identifying predictive biomarkers in a mouse model is an important first step towards identifying genes of interest in humans. Our current understanding of the genetic events leading to human colorectal cancer (CRC) is not sufficiently detailed to allow us to provide sophisticated prognostic information to patients based
on the molecular characteristics of their tumors. More detailed information would lead to personalized risk stratification and screening recommendations for patients based on genetic changes present within their tumors. This approach would minimize the risks garnered by unnecessary screening tests, while maximizing the chances that high-risk patients undergo more appropriately timed surveillance. It could also guide novel strategies for chemoprevention and treatment of CRC.
PUBLIC HEALTH RELEVANCE: Colorectal cancer is the second leading cause of cancer-related mortality in the United States. The current gold standard for screening is colonoscopy, which identifies potentially precancerous polyps or adenomas as well as cancerous lesions. Biomarkers that predict tumor progression would be invaluable to clinicians as they design personalized screening schedules and preventive strategies for each patient.
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会议论文
Features of the early adenoma and adjacent colon that drive progression: the role of mutation burden in normal tissue, senescent cells, and tumor clonal architecture
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批准号:10707105
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项目类别:
-
资助金额:$31.15万
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财政年份:2022
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负责人:Richard Brott Halberg
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依托单位:
Features of the early adenoma and adjacent colon that drive progression: the role of mutation burden in normal tissue, senescent cells, and tumor clonal architecture
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批准号:10519075
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项目类别:
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资助金额:$39.03万
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财政年份:2022
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负责人:Richard Brott Halberg
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依托单位:
Molecular Differences Predicting Tumor Progression in Colorectal Cancer (PQ #14)
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批准号:8538333
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项目类别:
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资助金额:$15.38万
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财政年份:2012
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负责人:Richard Brott Halberg
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依托单位:
Polyclonal Intestinal Tumors: Formation, Progression, and Significance
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批准号:7766296
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项目类别:
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资助金额:$33.18万
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财政年份:2009
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负责人:Richard Brott Halberg
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依托单位:
Polyclonal Intestinal Tumors: Formation, Progression, and Significance
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批准号:7652563
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项目类别:
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资助金额:$30.81万
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财政年份:2009
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负责人:Richard Brott Halberg
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依托单位:
Polyclonal Intestinal Tumors: Formation, Progression, and Significance
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批准号:8225175
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项目类别:
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资助金额:$29.89万
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财政年份:2009
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负责人:Richard Brott Halberg
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依托单位:
Polyclonal Intestinal Tumors: Formation, Progression, and Significance
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批准号:8446525
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项目类别:
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资助金额:$28.1万
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财政年份:2009
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负责人:Richard Brott Halberg
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依托单位:
Polyclonal Intestinal Tumors: Formation, Progression, and Significance
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批准号:8033178
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项目类别:
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资助金额:$29.89万
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财政年份:2009
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负责人:Richard Brott Halberg
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依托单位:
MODIFIERS OF INTESTINAL NEOPLASIA IN MICE
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批准号:2896499
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项目类别:
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资助金额:$4.17万
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财政年份:1999
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负责人:Richard Brott Halberg
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依托单位:
MODIFIERS OF INTESTINAL NEOPLASIA IN MICE
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批准号:2642965
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项目类别:
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资助金额:$3.28万
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财政年份:1998
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负责人:Richard Brott Halberg
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依托单位:
Experimental Pathology Laboratory Shared Resource
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批准号:9772006
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项目类别:
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资助金额:$0.33万
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财政年份:--
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负责人:Richard Brott Halberg
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依托单位:
Experimental Pathology Laboratory Shared Resource
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批准号:9923031
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项目类别:
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资助金额:$4.99万
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财政年份:--
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负责人:Richard Brott Halberg
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依托单位:
国内基金
海外基金
大肠癌发生机制的adenoma-adenocarcinoma pathway同serrated pathway的关系的研究
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批准号:30840003
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项目类别:专项基金项目
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资助金额:12.0万元
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批准年份:2008
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负责人:焦宇飞
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依托单位: