ASSAYS FOR CANCER PATIENT MONITORING BASED ON LEVELS OF ANALYTE COMPONENTS OF THE PLASMINOGEN ACTIVATOR SYSTEM IN BODY FLUID SAMPLES
    3.
    发明申请
    ASSAYS FOR CANCER PATIENT MONITORING BASED ON LEVELS OF ANALYTE COMPONENTS OF THE PLASMINOGEN ACTIVATOR SYSTEM IN BODY FLUID SAMPLES 失效
    基于体液活化剂体系中分子激活因子分析水平的癌症患者监测的测定

    公开(公告)号:US20080113392A1

    公开(公告)日:2008-05-15

    申请号:US11965323

    申请日:2007-12-27

    IPC分类号: G01N33/53 G01N33/48

    摘要: The present invention describes clinically and medically important methods of examining, screening over time, and monitoring the outcome of a cancer patient who is undergoing treatment or therapy for his or her disease. More specifically, the invention provides a method of monitoring the progression of disease, or the effectiveness of cancer treatment, in a cancer patient by measuring the levels of one or more analytes of the plasminogen activator (uPA) system, namely, uPA, PAI-1 and the complex of uPA:PAI-1, in a sample taken from the cancer patient, preferably, before treatment, at the start of treatment, and at various time intervals during treatment. As a result of performing the method, an increase or elevation in the levels of one or more of the PA system analytes in the cancer patient compared with the levels one or more of the respective PA system analytes in normal control individuals serves as an indicator of cancer advancement or progression and/or a lack of treatment effectiveness for the patient.

    摘要翻译: 本发明描述临床和医学上重要的随时间的检查,筛选和监测正在接受治疗或治疗他或她的疾病的癌症患者的结果的重要方法。 更具体地,本发明提供了通过测量纤溶酶原激活物(uPA)系统的一种或多种分析物的水平,即uPA,PAI-1,在癌症患者中监测疾病进展或癌症治疗的有效性的方法, 1和来自癌症患者的样品中的uPA:PAI-1的复合物,优选在治疗前,治疗开始时和治疗期间的各个时间间隔。 作为执行该方法的结果,癌症患者中的一种或多种PA系统分析物的水平的增加或升高与正常对照个体中相应的PA系统分析物中的一个或多个水平相比作为 癌症进展或进展和/或患者缺乏治疗有效性。

    Quantitative assays for PDGFR-beta in body fluids
    5.
    发明申请
    Quantitative assays for PDGFR-beta in body fluids 审中-公开
    体液中PDGFR-β的定量测定

    公开(公告)号:US20070037224A1

    公开(公告)日:2007-02-15

    申请号:US11502013

    申请日:2006-08-10

    IPC分类号: G01N33/574 G01N33/567

    摘要: The present invention is directed to the detection and quantification of total PDGFR-β in body fluids, particularly serial changes of total PDGFR-β levels in a subject's body fluids. Further, the invention is directed to detecting and quantitatiing total PDGFR-β in conjunction with one or more other proteins, such as, oncoproteins, angiogenic factors, tumor markers, inhibitors, growth factor receptors, metastasis proteins, and tumor suppressors. The disclosed methods are diagnostic/prognostic for diseases, and useful to select therapies for patients with diseases, preferably preneoplastic/neoplastic diseases. The disclosed methods are particularly useful to monitor the status of a patient's disease, and/or to monitor how a patient is responding to a therapy.

    摘要翻译: 本发明涉及体液中总PDGFR-β的检测和定量,特别是受试者体液中总PDGFR-β水平的连续变化。 此外,本发明涉及检测和定量总PDGFR-β与一种或多种其它蛋白质,例如癌蛋白,血管生成因子,肿瘤标志物,抑制剂,生长因子受体,转移蛋白和肿瘤抑制剂。 所公开的方法是疾病的诊断/预后,并且可用于选择具有疾病,优选肿瘤前/肿瘤性疾病的患者的治疗。 所公开的方法对于监测患者疾病的状态和/或监视患者如何对治疗作出反应特别有用。