Cell migration: The roles of Prostaglandins
Cell migration: The roles of Prostaglandins
批准号:
7487522
负责人:
Tina L Tootle
金额:
$4.84万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-01 至 2009-07-31
关键词:
AllelesAnimal ModelBiogenesisBiologicalBiological ModelsCell Adhesion MoleculesDefectDrosophila genusEventFatty AcidsGenesGeneticGenetic ScreeningHumanImmuneImmunityInflammationMalignant NeoplasmsMediatingMethodsMolecularMutationNeoplasm MetastasisNormal CellOogenesisPhenotypeProcessProstaglandinsReactionReproductionRoleSignal PathwaySignal TransductionSignaling MoleculeSignaling Pathway GeneSiteSomatic CellStudy modelscell motilityinsightmigrationmutantnovelnovel diagnosticsprogesterone 11-hemisuccinate-(2-iodohistamine)prostaglandin transporterresearch studytherapeutic targettooltumor progression
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): While prostaglandins (PCs), fatty acid derived signaling molecules, mediate cell migration during inflammation, immune reactions, reproduction, and cancer, the mechanisms by which PGs regulate migration remain unclear. It is likely that PGs contribute to cell migration through similar means during both normal cell migrations and those that take place during cancer metastasis. As PG synthesis and signaling components have been evolutionary conserved, one can utilize the genetic tools available in Drosophila to uncover the activities and signaling events mediated by PGs during cell migrations at a level of detail that cannot easily be obtained in other species. To establish Drosophila as a model for studying PG signaling the expression and mutant phenotypes of conserved PG synthesis and signaling components will be characterized. Then, using a genetic interaction screen the PG biogenesis genes involved in cell migration, as well as which signal transduction components and cell adhesion molecules important for PG mediated migrations will be determined. As PG synthesis is upregulated in numerous cancers, the results may reveal novel mechanisms of cancer progression and identify new diagnostic tools or therapeutic targets for cancer.
期刊论文(2)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1101/sqb.2008.73.023
发表时间:
2008
期刊:
Cold Spring Harbor symposia on quantitative biology
影响因子:
--
作者:
[A. Spradling;Todd G. Nystul;D. Lighthouse;L. Morris;Donald T. Fox;Rachel T. Cox;Tina L. Tootle;R. Frederick;Andrew D. Skora]
通讯作者:
A. Spradling;Todd G. Nystul;D. Lighthouse;L. Morris;Donald T. Fox;Rachel T. Cox;Tina L. Tootle;R. Frederick;Andrew D. Skora
Prostaglandins and actin remodeling
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批准号:10328668
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项目类别:
-
资助金额:$55.06万
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财政年份:2022
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负责人:Tina L Tootle
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依托单位:
Prostaglandins and actin remodeling
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批准号:10588140
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项目类别:
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资助金额:$38.63万
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财政年份:2022
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负责人:Tina L Tootle
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依托单位:
Prostaglandins control development by coordinating actin cytoskeletal remodeling
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批准号:9207772
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项目类别:
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资助金额:$32.79万
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财政年份:2016
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负责人:Tina L Tootle
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依托单位:
Cell migration: The roles of Prostaglandins
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批准号:7053150
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项目类别:
-
资助金额:$4.88万
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财政年份:2006
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负责人:Tina L Tootle
-
依托单位:
Cell migration: The roles of Prostaglandins
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批准号:7287377
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项目类别:
-
资助金额:$5.04万
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财政年份:2006
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负责人:Tina L Tootle
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依托单位:
海外基金