Molecular pathogenesis of intestinal serrated polyps
Molecular pathogenesis of intestinal serrated polyps
批准号:
8160339
负责人:
SERGIO A. LIRA
金额:
$35.17万
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:
2011-09-01 至 2016-07-31
关键词:
AccountingAffectBRAF geneBiochemicalCancer EtiologyCancer ModelCarcinomaColon CarcinomaColorectal CancerCpG Island Methylator PhenotypeDTR geneDevelopmentDiseaseEnvironmental Risk FactorEpigenetic ProcessG Protein-Coupled Receptor GenesGene-ModifiedGeneticHumanIntestinesKRAS2 geneLesionMalignant NeoplasmsMicrobeMolecularMusMutationPathogenesisPathway interactionsPolypsPreventionProcessSerrated AdenomaSignal TransductionTestingTransgenic MiceUnited Statesintestinal epitheliummicrobiomemortalitymouse modelnovelpathogenresearch studysmall molecule
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Colon cancer is the third most common cancer and the third leading cause of cancer-related mortality in the United States. Approximately 10% of colorectal cancer develops within a small subset of serrated polyps, which is associated with the CpG Island Methylator Phenotype (CIMP). A number of genetic lesions have been associated with the serrated polyps, but the mechanisms that cause serrated adenomas and carcinomas to form are poorly understood. We have developed the first mouse model for serrated polyps. In HB28 mice, the combined expression of HB-EGF and an activated GPCR (US28) in the intestinal epithelium leads to development of lesions that share many morphological and biochemical similarities to the serrated polyps in humans. Strikingly, development of the serrated lesions appears to be dependent on both genetic and environmental factors. We hypothesize that the combined activity of HB-EGF and US28 induces disease development by up-regulating RAS/RAF signaling, which is seen in human serrated adenomas. We will directly test this hypothesis by comparing and contrasting HB28 mice with newly generated transgenic mice expressing activated Braf and Kras in the intestinal epithelium. Finally, we will determine if environmental factors such as microbes are required for development of serrated polyps. Together the studies outlined in this proposal should help define the molecular mechanisms accounting for development of serrated polyps.
PUBLIC HEALTH RELEVANCE: Colon cancer is the third most common cancer and the third leading cause of cancer-related mortality in the United States. A significant proportion of colorectal cancer develops within a small subset of lesions called serrated lesions. We have generated genetically modified mice that develop such lesions. The study of this novel cancer model may contribute to a better understanding of the mechanisms leading to the formation of serrated lesions and hopefully to the development of new strategies for its prevention and treatment.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Mechanisms associated with diet-induced colitis
-
批准号:9886336
-
项目类别:
-
资助金额:$58.89万
-
财政年份:2020
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with diet-induced colitis
-
批准号:10093034
-
项目类别:
-
资助金额:$58.89万
-
财政年份:2020
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with diet-induced colitis
-
批准号:10553265
-
项目类别:
-
资助金额:$58.89万
-
财政年份:2020
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with diet-induced colitis
-
批准号:10339359
-
项目类别:
-
资助金额:$58.89万
-
财政年份:2020
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with flares and remission in colitis
-
批准号:9922284
-
项目类别:
-
资助金额:$38.14万
-
财政年份:2017
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with flares and remission in colitis
-
批准号:10623214
-
项目类别:
-
资助金额:$73.42万
-
财政年份:2017
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with flares and remission in colitis
-
批准号:10438874
-
项目类别:
-
资助金额:$70.11万
-
财政年份:2017
-
负责人:SERGIO A. LIRA
-
依托单位:
Mechanisms associated with flares and remission in colitis
-
批准号:10297538
-
项目类别:
-
资助金额:$71.94万
-
财政年份:2017
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:8519092
-
项目类别:
-
资助金额:$33.06万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:8706828
-
项目类别:
-
资助金额:$34.12万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:8319298
-
项目类别:
-
资助金额:$35.17万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:8883405
-
项目类别:
-
资助金额:$35.17万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:9982797
-
项目类别:
-
资助金额:$40.26万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:9104512
-
项目类别:
-
资助金额:$40.26万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
Molecular pathogenesis of intestinal serrated polyps
-
批准号:9336799
-
项目类别:
-
资助金额:$40.26万
-
财政年份:2011
-
负责人:SERGIO A. LIRA
-
依托单位:
2010 Chemotactic Cytokines Gordon Research Conference
-
批准号:7896906
-
项目类别:
-
资助金额:$0.3万
-
财政年份:2010
-
负责人:SERGIO A. LIRA
-
依托单位:
The role of chemokines in experimental thyroiditis
-
批准号:7998757
-
项目类别:
-
资助金额:$0.77万
-
财政年份:2010
-
负责人:SERGIO A. LIRA
-
依托单位:
Epithelial TLR signaling and IgA production
-
批准号:7700340
-
项目类别:
-
资助金额:$25.43万
-
财政年份:2009
-
负责人:SERGIO A. LIRA
-
依托单位:
Epithelial TLR signaling and IgA production
-
批准号:7866496
-
项目类别:
-
资助金额:$20.98万
-
财政年份:2009
-
负责人:SERGIO A. LIRA
-
依托单位:
2008 Chemotactic Cytokines Gordon Research Conference
-
批准号:7539465
-
项目类别:
-
资助金额:$0.3万
-
财政年份:2008
-
负责人:SERGIO A. LIRA
-
依托单位:
海外基金