METHODS OF PREDICTING CANCER CELL RESPONSE TO THERAPEUTIC AGENTS
    3.
    发明申请
    METHODS OF PREDICTING CANCER CELL RESPONSE TO THERAPEUTIC AGENTS 审中-公开
    预防癌症细胞对治疗药物的反应方法

    公开(公告)号:US20140030255A1

    公开(公告)日:2014-01-30

    申请号:US13883485

    申请日:2011-11-02

    IPC分类号: C12Q1/68

    摘要: In one aspect, methods, markers, and expression signatures are disclosed for assessing the degree to which a cell sample has epithelial cell-like properties or mesenchymal cell-like properties. In another aspect, methods are provided for predicting whether a subject with cancer will respond to treatment with an agent, based on whether the cancer is classified as having a high or low EMT Signature Score.

    摘要翻译: 一方面,公开了用于评估细胞样品具有上皮细胞样特性或间充质细胞样特性的程度的方法,标记和表达特征。 在另一方面,提供了用于基于癌症是否被分类为具有高或低EMT签名积分来预测癌症受试者是否将对药物治疗反应的方法。

    METHODS AND GENE EXPRESSION SIGNATURE FOR WNT/B-CATENIN SIGNALING PATHWAY
    4.
    发明申请
    METHODS AND GENE EXPRESSION SIGNATURE FOR WNT/B-CATENIN SIGNALING PATHWAY 审中-公开
    WNT / B-CATENIN信号通路的方法和基因表达标志

    公开(公告)号:US20100169025A1

    公开(公告)日:2010-07-01

    申请号:US12641486

    申请日:2009-12-18

    IPC分类号: G06F19/00 C12Q1/68 G06N5/02

    摘要: Methods, biomarkers, and expression signatures are disclosed for assessing the regulation status of Wnt/β-catenin signaling pathway in a cell sample or subject. More specifically, several aspects of the invention provide a set of genes which can be used as biomarkers and gene signatures for evaluating Wnt/β-catenin pathway deregulation status in a sample; classifying a cell sample as having a deregulated or regulated Wnt/β-catenin signaling pathway; determining whether an agent modulates the Wnt/β-catenin signaling pathway in sample; predicting response of a subject to an agent that modulates the Wnt/β-catenin signaling pathway; assigning treatment to a subject; and evaluating the pharmacodynamic effects of therapies designed to regulate Wnt/β-catenin pathway signaling.

    摘要翻译: 公开了方法,生物标志物和表达特征,用于评估细胞样品或受试者中Wnt / / bgr-catenin信号通路的调节状态。 更具体地,本发明的几个方面提供了一组基因,其可以用作用于评估样品中Wnt / bgr-连接蛋白通路去调节状态的生物标志物和基因特征; 将细胞样品分类为具有失调或调节的Wnt / / bgr-catenin信号通路; 确定试剂是否调节样品中的Wnt / bgr-catenin信号通路; 预测受试者对调节Wnt / bgr-catenin信号通路的药剂的反应; 为受试者分配治疗; 并评估旨在调节Wnt / bgr-catenin途径信号传导的疗法的药效学作用。

    Methods and compositions for utilizing changes of hybridization signals during approach to equilibrium
    6.
    发明申请
    Methods and compositions for utilizing changes of hybridization signals during approach to equilibrium 审中-公开
    在平衡过程中利用杂交信号变化的方法和组合物

    公开(公告)号:US20050033520A1

    公开(公告)日:2005-02-10

    申请号:US10475960

    申请日:2002-04-24

    IPC分类号: C12Q1/68 G06F19/20 G06F19/00

    摘要: The present invention provides methods for utilizing the changes of hybridization levels in time during approach to equilibrium duplex formation for identifying specific hybridization to polynucleotide probes. In the invention, the changes of hybridization levels at one or more polynucleotide probes by a sample comprising a plurality of nucleic acid molecules having different sequences are monitored during their progress towards equilibrium and the continuing increase of hybridization signals beyond cross-hybridization is used as an indication of specific binding. The invention also provides methods of comparing specificities of different polynucleotides probes. The invention further provides methods for ranking and selecting polynucleotide probes that are specific to particular nucleic acids and methods for enhancing the detection of nucleic acids. The invention further provides methods for determining the orientation of nucleotide sequences.

    摘要翻译: 本发明提供了在平衡双相形成过程中利用杂交水平随时间变化的方法,用于鉴定与多核苷酸探针的特异性杂交。 在本发明中,在包含具有不同序列的多个核酸分子的样品的一个或多个多核苷酸探针处的杂交水平的变化在其进展到平衡期间被监测,并且超越交叉杂交的杂交信号的持续增加用作 指示具体绑定。 本发明还提供了比较不同多核苷酸探针的特异性的方法。 本发明还提供了用于评估和选择对特定核酸特异性的多核苷酸探针的方法和用于增强核酸检测的方法。 本发明还提供了确定核苷酸序列取向的方法。

    Statistical combining of cell expression profiles
    8.
    发明申请
    Statistical combining of cell expression profiles 失效
    细胞表达谱的统计学结合

    公开(公告)号:US20050164273A1

    公开(公告)日:2005-07-28

    申请号:US11042654

    申请日:2005-01-24

    摘要: A method for fluorophore bias removal in microarray experiments in which the fluorophores used in microarray experiment pairs are reversed. Further, a method for calculating the individual errors associated with each measurement made in nominally repeated microarray experiments. This error measurement is optionally coupled with rank based methods in order to determine a probability that a cellular constituent is up or down regulated in response to a perturbation. Finally, a method for determining the confidence in the weighted average of the expression level of a cellular constituent in nominally repeated microarray experiments.

    摘要翻译: 用于微阵列实验对中的荧光团的微阵列实验中的荧光团偏置去除方法是相反的。 此外,一种用于计算与名义上重复的微阵列实验中进行的每个测量相关联的各个错误的方法。 该误差测量可选地与基于秩的方法耦合,以便确定响应于扰动的细胞成分向上或向下调节的概率。 最后,在名义上重复的微阵列实验中确定细胞成分的表达水平的加权平均的置信度的方法。

    Methods for diagnosis and/or prognosis of colon cancer
    9.
    发明授权
    Methods for diagnosis and/or prognosis of colon cancer 失效
    结肠癌诊断和/或预后的方法

    公开(公告)号:US08105777B1

    公开(公告)日:2012-01-31

    申请号:US12370264

    申请日:2009-02-12

    IPC分类号: C12Q1/68

    摘要: The present invention relates to genetic markers whose expression is correlated with colon cancer. In one aspect, the invention provides sets of markers whose expression can be used for classifying colon cancer patients into different prognostic categories. In another aspect, the invention provides kits containing marker sets for determining prognosis of colon cancer. In another aspect, the invention provides methods of classifying cancer patients with regard to prognosis.

    摘要翻译: 本发明涉及其表达与结肠癌相关的遗传标记。 一方面,本发明提供了一组标志物,其表达可用于将结肠癌患者分类为不同的预后类别。 另一方面,本发明提供了包含用于确定结肠癌预后的标记物组的试剂盒。 另一方面,本发明提供了关于预后的癌症患者分类方法。

    Genes associated with progression and response in chronic myeloid leukemia and uses thereof
    10.
    发明授权
    Genes associated with progression and response in chronic myeloid leukemia and uses thereof 失效
    与慢性骨髓性白血病中进展和反应相关的基因及其用途

    公开(公告)号:US08014957B2

    公开(公告)日:2011-09-06

    申请号:US11640517

    申请日:2006-12-14

    IPC分类号: G01N33/48

    摘要: The invention provides molecular markers that are associated with the progression of chronic myeloid leukemia (CML), and methods and computer systems for monitoring the progression of CML in a patient based on measurements of these molecular markers. The present invention also provides CML target genes, and methods and compositions for treating CML patients by modulating the expression or activity of these CML target genes and/or their encoded proteins. The invention also provides genes that are associated with resistance to imatinib mesylate (Gleevec™) treatment in CML patients, and methods and compositions for determining the responsiveness of a CML patient to imatinib mesylate treatment based on measurements of these genes and/or their encoded proteins. The invention also provides methods and compositions for enhancing the effect of Gleevec™ by modulating the expression or activity of these genes and/or their encoded proteins.

    摘要翻译: 本发明提供了与慢性骨髓性白血病(CML)进展相关的分子标记,以及用于基于这些分子标记物的测量来监测患者中CML进展的方法和计算机系统。 本发明还提供CML靶基因,以及通过调节这些CML靶基因和/或其编码蛋白的表达或活性来治疗CML患者的方法和组合物。 本发明还提供了与CML患者中对伊马替尼甲磺酸盐(Gleevec TM)治疗有关的基因,以及基于这些基因和/或其编码蛋白质的测量来确定CML患者对甲磺酸伊马替尼治疗的反应性的方法和组合物 。 本发明还提供了通过调节这些基因和/或其编码的蛋白质的表达或活性来增强Gleevec TM的作用的方法和组合物。