Awardee OrganizationUT SOUTHWESTERN MEDICAL CENTER
Description
Abstract Text
The Pharmacology Core facility will be responsible for the design, execution, and analysis of experiments
that address metabolic stability, general in i//Vo toxicity, pharmacokinetics, and in vivo efficacy of anti-cancer
compounds generated by this Program Project Grant (PPG). In addition, they will maintain the cell lines,
animal resources, and equipment that support these functions. It is anticipated that all four projects of this
PPG may potentially have need for the services provided by this Core facility. In addition, the Core will serve
as a resourcefor members of the UT Southwestern Medical Center (UTSWMC) Comprehensive Cancer
Center needing assistance with pharmacological assays. Since there are no other facilities here that can
provide in-depth analysis of the behavior of novel small molecules in an in vivo setting, the creation of such a
shared resource has the potential to impact the future development of translational cancer research at
UTSWMC. The services provided by the Core facility will include: in vitro screening of compounds against a
broad tumor panel; characterization of the metabolic stability of individual compounds in vitro and
identification of metabolites as necessary; assessment of the solubility, plasma protein binding, and
absorption characteristics of compounds in vitro; determination of the maximum in vivo tolerated dose and a
preliminary assessment of toxicity; assessment of the distribution of compounds in small rodent models
(pharmacokinetics); and development of mouse xenograft or other appropriate models for assessment of
compound efficacy in vivo. The Pharmacology Core facility will work closely with PPG chemists to refine the
structure of individual compounds so that characteristics that favor optimal efficacy in vivo will be maximized.
There is an urgent need for new therapeutics to fight cancer, which in 2005 was responsible for over 500,000
deaths. The overall goal of this Program Project grant (PPG) is to discover and characterize synthetic, small
molecule compounds that may be effective in the treatment of this disease. The Pharmacology Core facility
will perform in vitro and in vivo measurements of compound concentration, toxicity, and efficacy in animal
models. The overall goal of the Core is to guide chemical synthesis efforts of PPG projects in such a way
that novel molecules with the best chance of clinical success in cancer patients are generated.
Public Health Relevance Statement
Data not available.
NIH Spending Category
BiotechnologyCancer
Project Terms
AddressAnimal ModelBehaviorBiologicalBiological AssayCancer CenterCancer PatientCell Culture TechniquesCell LineCessation of lifeCharacteristicsChemicalsChemistryClinicalCommitCommunitiesComprehensive Cancer CenterCore FacilityDevelopmentDiseaseDoseDrug KineticsEnsureEquipmentEvaluationExperimental DesignsFutureGoalsIn VitroIndividualIrelandMalignant NeoplasmsMeasurementMedical centerMetabolicMetabolismModelingMolecularMonitorMycoplasmaNCI-Designated Cancer CenterPatientsPharmacologyPlasma ProteinsPositioning AttributeProcessProgram Research Project GrantsPropertyProtein BindingResearchResearch PersonnelResource SharingResourcesRodent ModelScreening procedureServicesSolubilityStandardizationStructureTestingTimeToxic effectUniversitiesUniversity HospitalsWorkXenograft procedureabsorptionanimal colonyanimal resourceanticancer researchbasechemical synthesisdesignexperiencefightingin vivoliquid chromatography mass spectrometrymembermouse developmentnovelnovel therapeuticsoperationpathogenprogramsresearch studysmall moleculesuccesstumor
No Sub Projects information available for 5P01CA095471-10 9002
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Patents
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Outcomes
The Project Outcomes shown here are displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed are those of the PI and do not necessarily reflect the views of the National Institutes of Health. NIH has not endorsed the content below.
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Clinical Studies
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