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FGF2 Signaling as a Clinically Relevant Resistance Mechanism to TKIs in GIST

FGF2 Signaling as a Clinically Relevant Resistance Mechanism to TKIs in GIST
FGF2 信号传导作为 GIST 中 TKI 的临床相关耐药机制
批准号:
8900749
负责人:
Nathalie R Javidi-Sharifi
金额:
$4.81万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-08-01 至 2017-07-31
关键词:
AccountingAddressAdverse effectsAutomobile DrivingAwardBiological AssayCell LineCellsCo-ImmunoprecipitationsCombined Modality TherapyCycloheximideCytostaticsDNA RepairDataDevelopmentDimerizationDiseaseDisease ProgressionDisease ResistanceDoseDrug TargetingExhibitsExposure toFGFR3 geneFaceFibroblast Growth Factor 2Fibroblast Growth Factor Receptor 2FluorescenceGastrointestinal Stromal TumorsGastrointestinal tract structureGeneticGenetic TranscriptionGoalsHalf-LifeImageImaging TechniquesImatinibImmuneImmunohistochemistryIn VitroIndividualLabelLigandsLinkLiteratureLuciferasesMalignant NeoplasmsMediatingMesenchymalMesenchymal Cell NeoplasmMicroscopyModelingMutationNuclearOutcomePDGFRA geneParaffin EmbeddingParentsPathway interactionsPatientsPharmaceutical PreparationsPhosphorylationProgression-Free SurvivalsProgressive DiseaseProliferatingProtein Synthesis InhibitionProteinsQuality of lifeReceptor Protein-Tyrosine KinasesRecurrenceRefractory DiseaseResearchResistanceResistance developmentResolutionRoleSamplingSignal PathwaySignal TransductionSiteSmall Interfering RNASolid NeoplasmStaining methodStainsStratificationStromal NeoplasmTestingTissue SampleTranscriptional RegulationTranslational RegulationTumor Cell LineTumor TissueTyrosine Kinase InhibitorUp-RegulationXenograft procedureautocrinecancer typeclinically relevanthigh riskimprovedinhibitor/antagonistmacrophagemouse modelneoplastic cellneutrophilnew therapeutic targetnovelnovel markeroverexpressionpromoterprotein complexpublic health relevancereceptorresearch studyresistance mechanismsmall moleculestandard of caretargeted treatmenttumor

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DESCRIPTION (provided by applicant): Gastrointestinal Stromal Tumor is the most common mesenchymal tumor of the GI tract. The current standard of care for metastatic or inoperable GIST, therapy with small molecule inhibitors targeting the receptor tyrosine kinase KIT, has vastly improved the outcome for patients with this disease. However, many patients who initially respond to therapy exhibit refractory disease within a few years. In these cases, options are still limited, and patients face therapy choices with more severe side effects. GIST is also a paradigm for targeted treatment in solid tumors, and findings in this disease may well be extrapolated to other types of cancer. The goal of the project described in this application is t investigate how Fibroblast Growth Factor 2 (FGF2) contributes to the development of imatinib resistance in Gatrointestinal Stromal Tumor (GIST). Under this goal, aims drawing from preliminary data will be to 1) Characterize a potential direct interaction between the receptor tyrosine kinases KIT and Fibroblast Growth Factor Receptor 3 using Bimolecular Fluorescence Complementation (BiFC) microscopy, 2) Determine the mechanism of FGF2 upregulation in a novel imatinib-resistant GIST cell line, and evaluate the clinical relevance of this mechanism in GIST patient samples, and 3) Determine whether there is a statistically significant correlation and a functional link between tumor-intrinsic expression of FGF2 and resistance to targeted therapy in GIST. The thesis research will contribute to the mechanistic understanding of GIST cell signaling and resistance. Findings have the potential to provide new markers for the stratification of GIST patients, and/or rationale for the use of new targeted therapeutics or combination therapies, with the ultimate aim of anticipating or overcoming resistance to targeted therapy in this disease. Thus, this project addresses the most pressing question in the GIST field, which has a large impact on patients' quality of life and overall survival.
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FGF2 Signaling as a Clinically Relevant Resistance Mechanism to TKIs in GIST
  • 批准号:
    8716290
  • 项目类别:
  • 资助金额:
    $4.77万
  • 财政年份:
    2014
  • 负责人:
    Nathalie R Javidi-Sharifi
  • 依托单位:
海外基金