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    • 2. 发明申请
    • METHOD OF DIAGNOSING OR PROGNOSING EPITHELIAL OVARIAN CANCER
    • 诊断或预防上皮癌的方法
    • WO2010023458A1
    • 2010-03-04
    • PCT/GB2009/002098
    • 2009-09-01
    • IMMUNOVIA ABBORREBAECK, Carl, Arne, KristerEK, Sara, Charlotte, AnderssonBRENNAN, Donal, John
    • BORREBAECK, Carl, Arne, KristerEK, Sara, Charlotte, AnderssonBRENNAN, Donal, John
    • C12Q1/68G01N33/574
    • G01N33/57449C12Q1/6886C12Q2600/118C12Q2600/158G01N2500/00G01N2800/56
    • The present invention provides a binding moiety which selectively binds to Sox11 protein and/or mRNA for imaging, diagnosis or prognosis of epithelial ovarian cancer (EOC). Optionally, the moiety is an antibody or antigen-binding fragment thereof. Advantageously, moiety comprises a further, readily detectable moiety. The invention also provides methods of imaging EOC cells as well as methods of diagnosing or prognosing EOC in an individual. A further aspect of the present invention provides a method of identifying cells associated with EOC, the method comprising analysing the pattern of gene expression in a sample of cells to be tested and comparing it to the pattern of gene expression in a sample of known lymphomas cells. Preferably, the cells to be tested are identified as EOC cells if the expression of Sox11 is up-regulated compared to normal B-cells. Preferably EOC cells are identified as improved recurrence-free survival-associated if expression of Sox11 is up-regulated compared with non-cancerous epithelial ovarian cells. Preferably, EOC cells are identified as diminished recurrence-free survival-associated if expression of Sox11 is similar to, or down-regulated, compared with non-cancerous epithelial ovarian cells.
    • 本发明提供了选择性结合Sox11蛋白和/或mRNA用于成像,诊断或预后的上皮性卵巢癌(EOC)的结合部分。 任选地,该部分是抗体或其抗原结合片段。 有利地,部分包含另外易于检测的部分。 本发明还提供对EOC细胞进行成像的方法以及在个体中诊断或预测EOC的方法。 本发明的另一方面提供了鉴定与EOC相关的细胞的方法,所述方法包括分析待测试细胞样品中基因表达的模式,并将其与已知淋巴瘤细胞样品中基因表达的模式进行比较 。 如果与正常B细胞​​相比,如果Sox11的表达被上调,则待测试的细胞被鉴定为EOC细胞。 如果与非癌性上皮性卵巢细胞相比,如果Sox11的表达上调,则优选EOC细胞被鉴定为改善的无复发存活相关性。 优选地,与非癌性上皮性卵巢细胞相比,如果Sox11的表达与非癌性上皮性卵巢细胞相似或下调,则EOC细胞被鉴定为减少的无复发存活相关。
    • 8. 发明申请
    • METHOD,ARRAY AND USE THEREOF
    • 方法,阵列及其应用
    • WO2011154698A8
    • 2013-01-17
    • PCT/GB2011000865
    • 2011-06-09
    • IMMUNOVIA ABBORREBAECK CARL ARNE KRISTERWINGREN CHRISTER LARS BERTIL
    • BORREBAECK CARL ARNE KRISTERWINGREN CHRISTER LARS BERTIL
    • G01N33/543G01N33/574
    • 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。