How Do NSAIDs Prevent Colorectal Cancer
How Do NSAIDs Prevent Colorectal Cancer
批准号:
8545125
负责人:
Darryl K Shibata
金额:
$16.18万
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:
2012-09-13 至 2015-08-31
关键词:
A MouseAdverse effectsAlgorithmsAspirinCell CountCellsChemopreventionChronicColorectal CancerDataDoseIndividualIntestinesLife StyleMalignant NeoplasmsMeasurementMeasuresMinorityMusMutationNon-Steroidal Anti-Inflammatory AgentsPharmaceutical PreparationsRiskScheduleSignal TransductionStem cellsTestingWorkcancer chemopreventioncancer riskcytotoxicimprovedintestinal cryptmouse modelmutantprevent
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Chronic low dose aspirin use decreases colorectal cancer (CRC) risks. It is uncertain how chemoprevention by aspirin and other NSAIDs mechanistically reduce CRC risks. We propose that NSAIDs reduce CRC risks by augmenting natural "anticancer" crypt niche defenses. Crypt niches inherently reduce cancer risks with a stem cell hierarchy where stem cells are a minority of all cells. Random stem cell turnover (neutral drift) further reduces "average" numbers of stem cells per crypt and can also eliminate mutant stem cells via differentiation. Anything that increases neutral drift should decrease cancer risks by decreasing "average" stem cell numbers. We propose to test this hypothesis in a new mouse model that can measure stem cell neutral drift rates. Mutations (Apc) that predispose to cancer should slow neutral drift rates whereas NSAIDs, by modulating crypt niche signaling, should increase neutral drift rates, decreasing "average" stem cell numbers and cancer risks. Verifying that neutral drift rates correlate with cancer risks will identify the stemcell niche as a new specific chemoprevention target. A mouse model of neutral drift will facilitate the rapid testing of new drugs or dosing schedules that can effectively reduce "average" stem cell numbers with fewer side effects. Chemoprevention that augments natural crypt anticancer mechanisms is more likely to have fewer side effects than cytotoxic strategies.
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会议论文
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资助金额:$18.14万
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财政年份:2022
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Photolithographic Tumor DNA Isolation
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批准号:10495070
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Project 3: Neoplastic Cell Evolution
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"Born to be Bad": Is Abnormal Cell Mobility Already Present At Initiation?
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资助金额:$21.46万
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财政年份:2014
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依托单位:
How Do NSAIDs Prevent Colorectal Cancer
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批准号:8384151
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资助金额:$22.32万
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财政年份:2012
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负责人:Darryl K Shibata
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依托单位:
Tumor Diversity As A Biomarker For Colorectal Cancer
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批准号:7874806
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资助金额:$21.17万
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财政年份:2010
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负责人:Darryl K Shibata
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依托单位:
Tumor Diversity As A Biomarker For Colorectal Cancer
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批准号:8050151
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资助金额:$17.09万
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财政年份:2010
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依托单位:
A Cancer Evolution Space-Time Machine
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批准号:7802564
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资助金额:$26.63万
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财政年份:2009
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负责人:Darryl K Shibata
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How Do Colorectal Cancers Arise Despite Surveillance?
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批准号:6859788
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资助金额:$30.91万
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财政年份:2005
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负责人:Darryl K Shibata
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依托单位:
How Do Colorectal Cancers Arise Despite Surveillance?
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批准号:7105101
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项目类别:
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资助金额:$23.96万
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财政年份:2005
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负责人:Darryl K Shibata
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依托单位:
How Do Colorectal Cancers Arise Despite Surveillance?
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批准号:7256986
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项目类别:
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资助金额:$23.26万
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财政年份:2005
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负责人:Darryl K Shibata
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依托单位:
HUMAN COLON STEM CELL AND CRYPT DYNAMICS
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批准号:6524807
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项目类别:
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资助金额:$16.25万
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财政年份:2001
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负责人:Darryl K Shibata
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依托单位:
Fixing Fixed DNA
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批准号:6515082
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项目类别:
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资助金额:$16.25万
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财政年份:2001
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负责人:Darryl K Shibata
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依托单位:
HUMAN COLON STEM CELL AND CRYPT DYNAMICS
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批准号:6446703
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项目类别:
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资助金额:$16.25万
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财政年份:2001
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负责人:Darryl K Shibata
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依托单位:
Fixing Fixed DNA
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批准号:6334404
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项目类别:
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资助金额:$16.25万
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财政年份:2001
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负责人:Darryl K Shibata
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依托单位:
MOUSE MODELS OF EARLY INTESTINAL NEOPLASIA
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批准号:6342133
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项目类别:
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资助金额:$28.13万
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财政年份:1999
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负责人:Darryl K Shibata
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依托单位:
MOUSE MODELS OF EARLY INTESTINAL NEOPLASIA
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批准号:2742755
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项目类别:
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资助金额:$28.38万
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财政年份:1999
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负责人:Darryl K Shibata
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依托单位:
Mouse Models of Early Intestinal Neoplasia
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批准号:7046097
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项目类别:
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资助金额:$30.63万
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财政年份:1999
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负责人:Darryl K Shibata
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依托单位:
MOUSE MODELS OF EARLY INTESTINAL NEOPLASIA
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批准号:6489182
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项目类别:
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资助金额:$28.82万
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财政年份:1999
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负责人:Darryl K Shibata
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依托单位:
海外基金