Serum Biomarkers for Colorectal Cancer Detection
Serum Biomarkers for Colorectal Cancer Detection
批准号:
7586435
负责人:
MICHAEL A TAINSKY
金额:
$21.19万
依托单位:
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:
2009-05-05 至 2011-04-30
关键词:
AntibodiesAntigensBenignBindingBiological AssayBiological MarkersBiological Neural NetworksBlood TestsCancer DetectionCancer PatientCancerousCharacteristicsClinicalColon CarcinomaColorectal CancerComorbidityComplementary DNADNA SequenceDataDatabasesDetectionDevelopmentDiagnosisDiagnosticDiagnostic Neoplasm StagingDiagnostic testsDifferentiation AntigensEarly DiagnosisFamily history ofGastrointestinal DiseasesGenerationsGoalsImmunoglobulin GIndividualInflammatory Bowel DiseasesLaboratoriesLungMachine LearningMalignant NeoplasmsMethodsNon-MalignantPatientsPopulation StudyPrevention strategyPrintingProteinsPublic HealthResearchSamplingScreening procedureSensitivity and SpecificitySerumSubgroupSurvival RateSymptomsTechniquesTechnologyTestingTimeWorkclinical practicecohortdemographicsgastrointestinalimprovednew technologyracial and ethnictherapeutic targettumor
中文摘要
描述(由申请人提供):当癌症在早期阶段被发现时,癌症的存活率会急剧增加,因此可以发现早期癌症的诊断筛选测试至关重要。我们研究的总体目标是开发这样一种早期检测筛选测试。我们打算前瞻性地积累一个大型的定义明确的独立的结直肠癌(CRC)病例队列,在诊断时收集该队列的广泛数据。我们将建立一个全面的数据库,包括人口统计数据、个人和家族史、肿瘤特征和合并症。我们的初步研究工作是开发一种检测方法,利用我们发现的CRC患者和健康对照者的血清。我们已经开发了一种高通量的方法来分离抗原的cDNA克隆,这种克隆可以通过检测测试对象血清中肿瘤蛋白自身抗体的存在来用于识别癌症病例。我们的第一个目标是利用我们最初的发现队列,确定在区分结直肠癌患者和健康对照血清中至关重要的抗原克隆的最小数量。我们将从我们发现的3800个克隆中剔除与其他癌症、良性胃肠道疾病、重复或不与任何CRC血清反应的抗原克隆。我们的第二个目标是确定这些新选择的抗原标记物的测试特征(敏感性,特异性,准确性),用于区分结直肠癌病例,使用新获得的血清样本,而不是以前用于开发标记集。最后,我们打算确定这些抗原标记物在大肠癌患者和健康对照者的大型独立定义队列中的测试特征。此外,由于研究人群的规模、种族/民族构成和捕获的患者数据,我们将能够评估这些标志物与重要亚组的关系。
英文摘要
DESCRIPTION (provided by applicant): When cancer is identified at the earliest stages, cancer survival rates dramatically increase and therefore diagnostic screening tests that can detect early stage cancer are crucial. The overall goal of our research is to develop such an early detection screening test. We intend to prospectively accrue a large well-defined independent cohort of colorectal cancer (CRC) cases where we collect extensive data on this cohort at the time of diagnosis. We will generate a comprehensive database that includes data on demographics, personal and family history, tumor characteristics, and comorbidities. Our preliminary research efforts have been to develop a detection assay utilizing the sera of our discovery cohort of CRC patients and healthy controls. We have developed a high throughput method to isolated cDNA clones of antigens which can be used to identify cancer cases by detecting the presence of auto-antibodies to tumor proteins in the serum of the test subject. Our first aim is to identify the minimal number of antigen clones that are critical in distinguishing sera from patients with colorectal cancer from healthy controls utilizing our initial discovery cohort. We will eliminate antigen clones from our discovery set of 3800 clones that react with sera from patients with other cancers, benign gastrointestinal conditions, duplicates or do not react with any CRC sera. Our second aim is to determine the test characteristics (sensitivity, specificity, accuracy) on these newly selected antigen markers for distinguishing colorectal cancer cases using newly acquired sera samples not previously used in the development of the marker set. Lastly, we intend to determine the test characteristics of these antigen markers on a large independent well-defined cohort of colorectal cancer patients and healthy controls. In addition, due to the size, racial/ethnic makeup of the study population, and captured patient data, we will be able to evaluate the expression of these markers in relationship to important subgroups.
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专著(0)
科研奖励(0)
会议论文
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依托单位:
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批准号:7826919
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财政年份:2005
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依托单位:
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国内基金
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