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    • 3. 发明申请
    • METHOD,ARRAY AND USE THEREOF
    • 方法,阵列及其应用
    • WO2011154698A2
    • 2011-12-15
    • PCT/GB2011/000865
    • 2011-06-09
    • IMMUNOVIA ABSMITH, Stephen EdwardBORREBAECK, Carl Ame KristerWINGREN, Christer Lars Bertil
    • BORREBAECK, Carl Ame KristerWINGREN, Christer Lars Bertil
    • G01N33/543
    • G01N33/6893G01N33/54366G01N33/57415
    • The present invention provides a method for the prognosis of breast cancer in a subject comprising the steps of: (a) providing a first proteome sample from the subject; (b) measuring in the first proteome sample the amount of one or more biomarkers selected from the group of biomarkers listed in Table 1; (c) providing an additional (e.g. a second) proteome sample from the subject; (d) measuring in the additional proteome sample the amount of the one or more biomarkers selected from the group of biomarkers listed in Table 1 measured in step (b); and (e) determining the difference between the amount of the one or more biomarkers in the first and additional proteome samples; wherein the first proteome sample and additional proteome sample are representative of the proteome composition of the subject on different days, and wherein the difference between the amount of the one or more biomarkers in the first and additional (e.g. second) proteome samples is indicative of the risk of recurrence and/or metastasis of the breast cancer in the subject. In further embodiments, step (b) comprises measuring the amount of each the biomarkers listed in Table 1 (A) or all of the biomarkers listed in Table 1. The present invention additionally provides an array for performing the method of the invention, the use in vitro of a biomarker selected from the group of biomarkers in Table 1 as a prognostic marker for determining risk of recurrence and/or metastasis of breast cancer in a subject, and a kit for performing the method of the invention comprising one or more binding agents capable of binding to a biomarker listed in Table 1.
    • 本发明提供了一种用于对象中乳腺癌预后的方法,包括以下步骤:(a)从受试者提供第一蛋白质组样品; (b)在第一蛋白质组样品中测量选自表1所列生物标志物组的一种或多种生物标志物的量; (c)从受试者提供另外的(例如第二)蛋白质组样品; (d)在另外的蛋白质组样品中测量选自在步骤(b)中测量的表1中列出的生物标志物组的一种或多种生物标志物的量; 和(e)确定第一和另外的蛋白质组样品中一种或多种生物标志物的量之间的差异; 其中所述第一蛋白质组样品和另外的蛋白质组样品在不同天数代表所述受试者的蛋白质组组成,并且其中所述第一和另外(例如第二)蛋白质组样品中所述一种或多种生物标志物的量之间的差异指示 受试者乳腺癌复发和/或转移的风险。 在另外的实施方案中,步骤(b)包括测量表1(A)中列出的每种生物标志物的量或表1中列出的所有生物标志物的量。本发明另外提供用于实施本发明方法的阵列, 选自表1中的生物标志物组的生物标志物的体外作为用于确定受试者的乳腺癌复发和/或转移风险的预后标记物,以及用于进行本发明方法的试剂盒,其包含一种或多种结合剂 能够结合表1中列出的生物标志物。