ErbB Family in Pituitary Tumors
ErbB Family in Pituitary Tumors
批准号:
8537140
负责人:
Odelia Cooper
金额:
$16.87万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-15 至 2015-02-28
关键词:
Animal ModelApoptosisBindingBiological AssayBreast Cancer CellCancer cell lineCell LineCellsClinical TrialsCultured Tumor CellsDevelopmentDisease ProgressionEGF geneEpidermal Growth Factor ReceptorExcisionExtracellular DomainFamilyFluorescent in Situ HybridizationGefitinibGene AmplificationGrantGrowthHormonalHormonesHumanImmunoblottingImmunohistochemistryImmunoprecipitationImplantIn VitroLaboratoriesLeadMeasurementMeasuresMedicalMessenger RNAMonoclonal AntibodiesMusNon-Small-Cell Lung CarcinomaNude MiceOperative Surgical ProceduresPathway interactionsPatientsPeripheralPharmaceutical PreparationsPhenotypePituitary GlandPituitary HormonesPituitary NeoplasmsProlactinProlactinomaPropertyProspective StudiesProtein Tyrosine KinaseRattusReceptor Protein-Tyrosine KinasesRecurrenceRecurrent tumorReportingResistanceSerumSpecimenTdT-Mediated dUTP Nick End Labeling AssayTechniquesTestingTherapeuticTumor VolumeTyrosine Kinase InhibitorWorkabstractingadenomacapecitabineclinical effectinsightkinase inhibitorlapatinibmalignant breast neoplasmmemberneoplastic cellnoveloverexpressionprotein expressionpublic health relevancereceptorreceptor expressionresponsesmall moleculetumortumor growth
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Project Summary/Abstract:
Understanding the mechanisms of pituitary tumor growth continues to be challenging. In this proposal, we hypothesize that pituitary tumors progress from a non-invasive phenotype into a more aggressive one as a consequence of changes in the expression of erbB receptor tyrosine kinases. These changes lead to development of aggressive pituitary tumors. Our preliminary observations demonstrate differential expression of members of the erbB family in aggressive pituitary tumors in comparison to noninvasive tumors. We plan to conduct a prospective study examining changes in erbB expression from microadenomas to macroadenomas to increasingly invasive tumors using immunohistochemistry techniques, fluorescent in situ hybridization, and assays for serum EGFR and erbB2. Our laboratory will demonstrate that pituitary tumor invasiveness correlates with increasing levels of EGFR and erbB2 in animal models implanted with transfected pituitary cell lines. Next, we propose that lapatinib, a small molecule dual EGFR/erbB2 tyrosine kinase inhibitor, inhibits growth and invasion of pituitary tumor cells. We will prospectively collect human pituitary tumor surgical specimens, culture the tumor cells, and assess their response to the drug in vitro. We will use immunoprecipitation and immunoblotting to examine differential expression of erbB receptors, TUNEL assay to measure apoptosis, and prolactin measurements for prolactinomas. In addition, our laboratory will test lapatinib in animal models. Finally, we hypothesize that lapatinib will inhibit tumor growth and hormonal secretion in patients with pituitary tumors. In a proof of concept clinical trial, we plan to treat patients with recurrent nonfunctioning adenomas and prolactin-secreting adenomas resistant to standard medical therapy with lapatinib for six months prior to undergoing surgical resection and assess for stabilization of tumor size and pituitary tumor secretory profiles. The work proposed in this grant will shed insight into a new class of therapeutics in pituitary tumors that are resistant to standard therapies.
PUBLIC HEALTH RELEVANCE:
NARRATIVE: We propose to investigate how pituitary tumors become more aggressive through the epidermal growth factor receptor pathways. We will test targeted therapy against this pathway to develop novel therapies in recurrent tumors.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1007/s12020-013-0093-x
发表时间:
2014-06
期刊:
ENDOCRINE
影响因子:
3.7
作者:
[Cooper, Odelia, Mamelak, Adam, Bannykh, Serguei, Carmichael, John, Bonert, Vivien, Lim, Stephen, Cook-Wiens, Galen, Ben-Shlomo, Anat]
通讯作者:
Ben-Shlomo, Anat
ErbB receptor tyrosine kinase inhibitor therapy for aggressive prolactinomas
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批准号:8874043
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项目类别:
-
资助金额:$24.62万
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财政年份:2015
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负责人:Odelia Cooper
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依托单位:
ErbB receptor tyrosine kinase inhibitor therapy for aggressive prolactinomas
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批准号:9063059
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项目类别:
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资助金额:$18.26万
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财政年份:2015
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负责人:Odelia Cooper
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依托单位:
ErbB Family in Pituitary Tumors
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批准号:8325593
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项目类别:
-
资助金额:$16.87万
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财政年份:2009
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负责人:Odelia Cooper
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依托单位:
ErbB Family in Pituitary Tumors
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批准号:7771064
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项目类别:
-
资助金额:$16.87万
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财政年份:2009
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负责人:Odelia Cooper
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依托单位:
ErbB Family in Pituitary Tumors
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批准号:8136051
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项目类别:
-
资助金额:$16.87万
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财政年份:2009
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负责人:Odelia Cooper
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依托单位:
ErbB Family in Pituitary Tumors
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批准号:7932908
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项目类别:
-
资助金额:$16.87万
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财政年份:2009
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负责人:Odelia Cooper
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依托单位:
国内基金
海外基金
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