Core B: Pathology and High-resolution Imaging Core
Core B: Pathology and High-resolution Imaging Core
批准号:
8794373
负责人:
Majd Zayzafoon
金额:
$19.81万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-09-17 至 2020-02-29
关键词:
AccelerationAlabamaAnimal ModelAnimalsArchivesAutopsyBenignBiological MarkersBiologyBone ResorptionBone TissueCancer DiagnosticsCell Culture TechniquesCell NucleusCellsClinicalCommunicationCountryCryoelectron MicroscopyDataDatabasesDecalcificationDevelopmentDiagnosticEnsureEpitheliumEvaluationExperimental Animal ModelExpert OpinionFluorescence MicroscopyFluorescence Resonance Energy TransferFreezingFrozen SectionsGrantHistocytochemistryHistologyHumanImageImage AnalysisImageryImmunohistochemistryIn Situ HybridizationIndividualInstitutionLaboratoriesLaser MicroscopyLasersLeadLightLos AngelesMalignant NeoplasmsMalignant neoplasm of prostateMeasurementMedical centerMetabolic Bone DiseasesMetastatic Neoplasm to the BoneMethacrylatesMicrodissectionMicroscopeMicroscopicMicroscopyMissionMolecularMolecular AnalysisMorphologyMusOsteogenesisParaffinPathologicPathologyPatientsPlastic EmbeddingPositioning AttributePreparationPrimary NeoplasmProceduresProcessProductivityProstateProstaticProstatic TissueQuality ControlResearchResearch PersonnelResearch Project GrantsResolutionResourcesRodentSamplingServicesSiteSpecial Histology Staining MethodSpecimenStaining methodStainsStandardizationTechniquesTissue BanksTissue MicroarrayTissue SampleTissuesTranslational ResearchTransmission Electron MicroscopyTumor BurdenUniversitiesValidationVeterinary PathologyWorkanimal tissuebiobankbonedigitaldigital imaginghigh throughput analysishuman tissueinstrumentationlight microscopymolecular pathologymorphometrynovelprogramsprostate cancer cell lineresponsescreeningtissue processingtumor
中文摘要
项目摘要-核心B
病理学和高分辨率成像核心是支持各种研究的有效核心
通过提供从P01中收集的充分表征和高度注释的存档病理样本,
不同的前列腺癌(PC)细胞系,人类和动物模型实验组织,并通过执行
常规和先进的软组织和硬组织的组织学程序。核心还提供临床
人和小鼠的组织切片和免疫组化解释的诊断评价
前列腺组织和PC骨转移。P01使用动物尸检的研究者还可以访问
先进的技术,如透射电子显微镜,图像分析/形态测量和激光
显微解剖可用的技术包括组织学(特殊染色,冷冻,石蜡和塑料包埋
切片)和免疫组织化学。核心的一个关键优势是,它是嵌入在中心,
代谢性骨疾病在伯明翰的亚拉巴马大学,并与
Cedars-Sinai医学中心(CSMC)和西洛杉矶的生物库和转化研究核心
洛杉矶VA医疗中心这种伙伴关系为核心提供了一个独特的地位,
P01研究者在PC骨转移的分子和细胞机制研究中的需求,
包括:a)获取新鲜前列腺和骨转移组织:原发性肿瘤、肿瘤相关的
基质、良性上皮、转移性骨标本和临床标本中与肿瘤无关的基质
在使用激光捕获显微镜的直接形态可视化下进行分子分析; B)作为
形态学核心,为临床标本和动物模型提供PC诊断专业知识,冷冻
切片和光镜设备,组织化学,免疫组织化学,原位杂交和
定量组织形态计量学;和c)提供良好表征的存档病理样品,和
组织微阵列(TMAs)用于筛选具有潜在机制重要性的候选分子,
验证细胞培养和动物模型实验数据,发现新的生物标志物,包括高
吞吐量分析正在进行的集中执行程序的开发解放了P01研究者
避免基本工作的重复,使他们能够利用现有资源提高生产力,
实验时间表它还允许调查人员之间的结果进行比较,并保证
技术准备条件不负责观察到的差异。总之,核心B将继续
为P01提供常规和先进的技术准备,并对两者进行专家解释
对来自人类和动物的细胞和组织样本进行诊断和分子分析。标准化
质量控制程序将最终导致更大的技术统一性,并允许直接
项目之间的数据比较。
英文摘要
Project Summary - Core B
The Pathology and High Resolution Imaging Core is an effective nucleus that supports the various studies
of the P01 by providing well-characterized, and highly annotated archival pathological samples collected from
different prostate cancer (PC) cell lines, human and animal model experimental tissue and by performing
routine and advanced histological procedures on soft and hard tissues. The Core also provides clinical
diagnostic evaluation of histological sections and immunohistochemical interpretation of human and murine
prostatic tissue and PC bone metastases. P01 investigators utilizing animal necropsies also have access to
sophisticated techniques, such as transmission electron microscopy, image analysis/morphometry and laser
microdissection. Techniques available include histology (special stains, frozen, paraffin- and plastic-embedded
sections) and immunohistochemistry. A key advantage of the Core is that it is embedded within the Center for
Metabolic Bone Disease at the University of Alabama at Birmingham and works in close partnership with the
Biobank and Translational Research Core at Cedars-Sinai Medical Center (CSMC) and with the West Los
Angeles VA Medical Center. This partnership provides the Core with a unique position to serve the research
needs of P01 investigators in their studies of the molecular and cellular mechanisms of PC bone metastasis,
including: a) procurement of fresh prostatic and bone metastatic tissue: primary tumor, tumor-related
stroma, benign epithelium, metastatic bone specimens, and stroma unrelated to tumor from clinical specimens
under direct morphologic visualization using laser capture microscopy for molecular analyses; b) service as the
morphology core, providing PC diagnostic expertise for both clinical specimens and animal models, frozen
section and light microscopic facilities, histochemistry, immunohistochemistry, in situ hybridization and
quantitative histomorphometry; and c) providing well-characterized, archived pathologic samples and
tissue microarrays (TMAs) for screening of candidate molecules of potential mechanistic importance,
validation of cell culture and animal model experimental data and discovery of novel biomarkers, including high
throughput analysis. The ongoing development of centrally performed procedures frees the P01 investigators
from duplication of basic work, allowing them greater productivity with available resources and acceleration of
experimental timetables. It also allows comparison of results between investigators with assurance that
technical preparatory conditions are not responsible for observed differences. In summary, Core B will continue
to provide the P01 with routine and advanced technical preparations and expert interpretation of both
diagnostic and molecular analysis of cell and tissue samples from humans and animals. The standardization of
the quality-controlled procedures will ultimately lead to greater technical uniformity and allow for direct
comparisons of data between projects.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
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海外基金