A Model for Preclinical Biomarker Discovery in Pancreatic Ductal Adenocarcinoma
A Model for Preclinical Biomarker Discovery in Pancreatic Ductal Adenocarcinoma
批准号:
8120953
负责人:
Eric Collisson
金额:
$16.31万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-08-03 至 2015-07-31
关键词:
1-Phosphatidylinositol 3-KinaseAdenocarcinoma CellBiological MarkersBiological ModelsCancer PatientCell LineClinical TrialsCollectionConduct Clinical TrialsCouplingDataDescriptorDevelopmentDiagnosisDiseaseDrug resistanceEventFutureGenerationsGenomicsGoalsIn VitroIndividualMEKsMalignant NeoplasmsMalignant neoplasm of pancreasMedicineModelingModern MedicineMolecularMolecular AbnormalityMolecular AnalysisMusPancreatic Ductal AdenocarcinomaPathway interactionsPatientsPharmaceutical PreparationsPre-Clinical ModelPrimary NeoplasmProto-Oncogene Proteins c-aktRas InhibitorResectedResistanceSignal TransductionSystemTechnologyTestingTherapeuticTherapeutic AgentsValidationWorkXenograft procedurearmbasechemotherapydrug sensitivitydrug testingefficacy testinggemcitabinehuman FRAP1 proteinin vivoinhibitor/antagonistkinase inhibitormolecular markeroncologypancreatic neoplasmpre-clinicalpreclinical studypublic health relevanceresponsetumortumor xenograft
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Pancreatic Ductal Adenocarcinoma (PDA) is a deadly malignancy. Early systemic spread and resistance to chemotherapy combine to make PDA one of the most dismal diagnoses in modern medicine. However, hundreds of experimental anticancer medicines are now in development and could be considered for Pancreatic Ductal Adenocarcinoma (PDA). Our studies to date show that PDA can be divided into distinct subclasses that differ biologically and that may respond differently to treatment. Our goal now is to advance treatment of PDA by refining molecular descriptors of Pancreatic Ductal Adenocarcinoma (PDA), identifying therapeutic agents on the Ras pathway that are effective in specific tumors, and eventually testing these in biomarker-marker guided clinical trials. This will be accomplished through work in two aims. Aim 1 will identify and model omic determinants of response to inhibitors of the Raf-MEK-ERK and PI3 Kinase/Akt pathways in a well characterized panel of PDA cell lines. Since we suspect that combined blockade will be required, we plan to test these agents both alone and in combination. Aim 2 will validate the biomarkers of sensitivity and resistance discovered in cell lines in a selected panel of PDA xenografts resected from patients and propagated and treated in the mouse. Biomarkers identifying specific responses in both preclinical systems will be tested in biomarker-guided clinical trials with inhibitors of the Ras pathway (beyond the scope of this proposal). Overall, we expect to test the hypothesis that biomarkers identified in efficient, preclinical model system screens will prospectively identify drug responsive and drug resistant patients in clinical trials. If true, this will allow experimental drugs now under development to be quickly tested for efficacy in subclasses of PDA and then moved quickly into trials in patient subpopulations in which they are most likely to be effective. This work is 100% relevant to Pancreatic Ductal Adenocarcinoma.
PUBLIC HEALTH RELEVANCE: Clinical Trials in oncology often fail because the tested drugs do not work in patients. This project will employ molecular analysis of pancreatic tumors to predict which tumors and patients will be most sensitive to certain treatments. These studies hold promise in expanding treatment options for pancreatic cancer patients, and changing the way clinical trials are conducted.
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