Tissue and Tumor Specific Glycosylation of Proteins
Tissue and Tumor Specific Glycosylation of Proteins
批准号:
7274405
负责人:
Matthew West
金额:
$4.68万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-01 至 2010-04-30
关键词:
AntibodiesArtsBiological AssayBiological MarkersBloodCancerousCarbohydratesCell membraneCellular MembraneDataDevelopmentDiagnosisDiseaseEarly DiagnosisEpitopesExhibitsFoundationsGamma-glutamyl transferaseGenesGlycoproteinsHigh Pressure Liquid ChromatographyHumanImmunoassayIndividualLinkLiverLiver neoplasmsMalignant NeoplasmsMalignant neoplasm of liverMass Spectrum AnalysisMonoclonal AntibodiesNon-MalignantNormal tissue morphologyNumbersOligosaccharidesPancreasPancreatic AdenocarcinomaPancreatic DiseasesPathology, OtherPatientsPatternPolysaccharidesPost-Translational Protein ProcessingPrimary carcinoma of the liver cellsProtein GlycosylationPublishingRelative (related person)ResearchResearch ProposalsScreening procedureSensitivity and SpecificitySerumSerum ProteinsSiteStagingStructureSurvival RateSymptomsTechniquesTestingTherapeuticTissuesTreatment EfficacyTumor TissueVertebral columnWorkbaseglycosylationhuman diseaseinsightnovelnovel diagnosticspancreatic neoplasmpolypeptidetumortumorigenesis
中文摘要
描述(申请人提供):蛋白质糖基化模式改变和血清蛋白质水平升高通常是人类疾病的特征。血清糖蛋白γ-谷氨酰转肽酶(GGT)水平升高通常见于肝和胰腺肿瘤患者以及非恶性形式的肝和胰腺疾病患者。越来越多的数据表明,GGT具有组织特异性和肿瘤特异性糖形式,可用于区分癌症患者和其他病理患者。我的研究将集中于GGT上组织和肿瘤特异性糖链的鉴定和表征。这项研究有三个具体目标,其中包括使用最先进的荧光高效液相色谱和质谱学技术进行糖类分析。第一个特定的目的是鉴定从正常胰腺和肝脏组织中分离的GGT上的组织特异性糖形式。第二个特异性目的是鉴定从胰腺和肝脏肿瘤分离的GGT上以及这些恶性肿瘤患者血清中GGT上的肿瘤特异性糖链种类。这项建议的第三个具体目的是开发针对GGT上组织和肿瘤特异性糖表位的抗体,并评价这些抗体用于检测来自非疾病个体和诊断为胰腺癌、肝细胞癌和胰腺和肝脏非恶性疾病患者的血清中组织和肿瘤特异性GGT物种的敏感性和特异性。这些研究还将深入了解GGT在肿瘤发生过程中从细胞膜释放到血清中的机制。胰腺癌或肝癌的及时、准确诊断对于最大限度地提高治疗效果至关重要。这项工作将为发展基于血清的免疫分析方法,利用GGT进入血清的糖表位来早期检测这些恶性肿瘤奠定基础。报告摘要:被诊断为胰腺癌或肝癌的患者存活率非常低。这在很大程度上是因为这两种形式的癌症通常不会被发现,直到患者开始出现疾病症状,而这些症状通常与疾病的晚期有关。我建议识别和表征新的血液标记物,这些标记物可以用来开发筛查试验,在癌症组织对治疗最敏感的阶段早期发现胰腺癌和肝癌。第2页在整个表格中在底部连续编号第2页
英文摘要
DESCRIPTION (provided by applicant): Altered patterns of protein glycosylation and increased levels of serum proteins are often hallmarks of human diseases. Elevated serum levels of the glycoprotein gamma-glutamyl transpeptidase (GGT) are commonly seen in patients with tumors of the liver and pancreas and in patients with non malignant forms of liver and pancreatic diseases. An accumulating body of data indicates that GGT possesses tissue-specific and tumor-specific glycoforms that could be used to distinguish patients with cancer from those with other pathologies. My study will focus on the identification and characterization of tissue- and tumor-specific glycans on GGT. This study has three specific aims, which incorporate the use of state-of-the-art fluorescent HPLC and mass spectrometric techniques for glycoanalyses. The first specific aim is to identify tissue-specific glycoforms on GGT isolated from normal pancreas and liver tissue. The second specific aim is to identify tumor-specific glycan species on GGT isolated from tumors of the pancreas and liver and on GGT shed into the serum of patients with these malignancies. The third specific aim of this proposal is to develop antibodies against tissue- and tumor-specific glycoepitopes on GGT and to evaluate the sensitivity and specificity of these antibodies for detecting tissue- and tumor-specific GGT species in sera derived from non-diseased individuals and patients diagnosed with pancreatic adenocarcinoma, hepatocellular carcinoma, and non-malignant diseases of the pancreas and liver. These studies will also provide insight into the mechanism by which GGT is released from cellular membranes into serum during tumorigenesis. The timely and accurate diagnosis of pancreatic or liver cancer is critical for maximizing the efficacy of therapeutic treatments. This work will establish a foundation for the development of a serum-based immunoassay for the early detection of these malignancies using glycoepitopes on GGT shed into the serum. Lay summary: Survival rates for patients diagnosed with either pancreatic or liver cancer are very low. This is largely due to the fact that these two forms of cancer typically go undetected until patients begin showing disease symptoms, which are most often associated with advanced stages of the disease. I propose to identify and characterize novel blood markers that can be used to develop screening tests for the early detection of pancreatic and liver cancer at a stage when the cancerous tissues are the most responsive to therapeutic treatments. Page 2 Number pages consecutively at the bottom throughout Form Page 2
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Tissue and Tumor Specific Glycosylation of Proteins
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批准号:7420934
-
项目类别:
-
资助金额:$4.96万
-
财政年份:2007
-
负责人:Matthew West
-
依托单位:
Tissue and Tumor Specific Glycosylation of Proteins
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批准号:7612086
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项目类别:
-
资助金额:$5.17万
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财政年份:2007
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负责人:Matthew West
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依托单位:
国内基金
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