EVALUATING PROTEIN EXPRESSION IN PATIENT STRATIFICATION AND OTHER THERAPEUTIC, DIAGNOSTIC AND PROGNOSTIC METHODS FOR CANCER
    3.
    发明申请
    EVALUATING PROTEIN EXPRESSION IN PATIENT STRATIFICATION AND OTHER THERAPEUTIC, DIAGNOSTIC AND PROGNOSTIC METHODS FOR CANCER 审中-公开
    评估患者分娩中的蛋白质表达和其他治疗,诊断和预后方法

    公开(公告)号:WO2012129517A3

    公开(公告)日:2014-05-01

    申请号:PCT/US2012030398

    申请日:2012-03-23

    CPC classification number: G01N33/574 G01N33/573 G01N2333/96494

    Abstract: Provided are compositions and methods for quantifying the expression or activity of MMP-14, MMP-9, TIMP-I, and/or MMP-2 and other biomarkers of cancer, for example, osteotropic cancer, breast cancer, lung cancer, melanoma, pancreatic cancer, colon cancer or prostate cancer, which may be used diagnostically (e.g., to identify patients who have cancer, or a particular subclass of cancer) and prognostically (e.g., to identify patients who are likely to develop cancer or respond well to a particular therapeutic for treating cancer). Kits for detecting MMP-14 and other biomarkers and for the practice of the methods incorporating such detection are also described herein. Specifically, in certain embodiments, provided are methods of utilizing expression of and/or expression ratios of any two of MMP-14, MMP-2, TIMP (e.g., TIMP-I), and MMP-9 in tumors and other cancer cells in order to stratify patients and identify those who would benefit from MMP-14 inhibitor treatment.

    Abstract translation: 提供了用于定量MMP-14,MMP-9,TIMP-1和/或MMP-2和其它癌症生物标志物的表达或活性的组合物和方法,例如骨性癌,乳腺癌,肺癌,黑素瘤, 胰腺癌,结肠癌或前列腺癌,其可以在诊断上使用(例如,鉴定患有癌症的患者或癌症的特定亚类)和预后(例如,鉴定可能发展为癌症或对 特别治疗癌症)。 本文还描述了用于检测MMP-14和其他生物标志物的试剂盒以及结合这种检测的方法的实践。 具体地,在某些实施方案中,提供了利用肿瘤和其它癌细胞中MMP-14,MMP-2,TIMP(例如TIMP-1)和MMP-9中任意两种的表达和/或表达比例的方法 命令分层患者,并确定谁将受益于MMP-14抑制剂治疗。

    DIAGNOSIS AND RISK STRATIFICATION OF BLADDER CANCER
    4.
    发明申请
    DIAGNOSIS AND RISK STRATIFICATION OF BLADDER CANCER 审中-公开
    乳腺癌的诊断和风险分析

    公开(公告)号:WO2014060753A1

    公开(公告)日:2014-04-24

    申请号:PCT/GB2013/052705

    申请日:2013-10-16

    Abstract: The invention provides amethod of defining the likelihood of a subject having bladder cancer, comprising the steps of: (A) assessing the subject's likelihood of having bladder cancer by:i. identifying at least one sub-population group appropriate to the subject;ii. determining the level of one or more biomarkers selected according to the sub- population group in a sample obtained from the subject;iii. inputting each of the biomarker values into an algorithm to produce an output value; and iv. correlating the output value with the likelihood of the subject having bladder cancer, wherein the sub-population group is selected according to smoking habits, gender, presence/absence of stone disease, historyof benign prostate enlargement (BPE) or prescription ofanti-hypertensive, anti-platelet and/or anti- ulcer medication, and (B) determining the subject's stratified risk levelof serious disease by:v. determining the level of one or more biomarkers specific for one or more risk classifiers defined using Random Forest Classifiers (RFC), logistic regression or another appropriate systems biology or statistical approach in a sample obtained from the subject,vi. inputting each of the biomarker values into an algorithm or algorithms to produce an output value; and vii. correlating the output value with a stratified risk level of underlying serious disease, wherein the likelihoodof having bladder cancer is combined with the stratified risk level of having serious disease, wherein the risk of having bladder cancer and/or serious disease is categorised as: high-risk bladder cancer requiring immediate cystoscopy; low-risk bladder cancer requiring urgent cystoscopy; high- risk control requiring close evaluation and further investigation; or low-risk control requiring primary care monitoring.

    Abstract translation: 本发明提供了定义具有膀胱癌的受试者的可能性的方法,其包括以下步骤:(A)通过以下方式评估受试者患膀胱癌的可能性:i。 识别适合该受试者的至少一个亚群体群体; ii。 确定从受试者获得的样品中根据亚群体组选择的一种或多种生物标志物的水平; iii。 将每个生物标记值输入到算法中以产生输出值; 和iv。 将输出值与患有膀胱癌的患者的可能性相关联,其中根据吸烟习惯,性别,存在/不存在石头疾病,良性前列腺增生(BPE)或抗高血压症, 血小板和/或抗溃疡药物,和(B)通过以下方式确定受试者的分层危险性严重疾病: 确定使用随机森林分类器(RFC)定义的一个或多个风险分类器特定的一个或多个生物标志物的水平,逻辑回归或从受试者获得的样本中的其他适当系统生物学或统计学方法。 将每个生物标记值输入算法或算法以产生输出值; 和vii。 将输出值与潜在严重疾病的分层风险水平相关联,其中将膀胱癌的可能性与具有严重疾病的分层风险水平相结合,其中将膀胱癌和/或严重疾病的风险分类为: 膀胱癌需要立即膀胱镜检查的风险; 低危膀胱癌需要紧急膀胱镜检查; 高风险控制需要进行密切的评估和进一步的调查; 或需要初级保健监测的低风险控制。

    ラテックス凝集法によるマトリックスメタロプロテイナーゼ-3の検出方法
    7.
    发明申请
    ラテックス凝集法によるマトリックスメタロプロテイナーゼ-3の検出方法 审中-公开
    通过LATEX AGGLUTINATION方法检测基质金属蛋白酶-3的方法

    公开(公告)号:WO2013077332A1

    公开(公告)日:2013-05-30

    申请号:PCT/JP2012/080097

    申请日:2012-11-20

    Abstract:  低値領域において反応性が高く、かつ、MMP-10等の他のMMPファミリーとの交差反応性が認められない、MMP-3に対するモノクローナル抗体を用いた、迅速な測定が可能であり検体処理能力が高いLTIA法に基づくMMP-3の検出方法を提供することを課題とし、モノクローナル抗体14B1が担持されたラテックス粒子、及び、モノクローナル抗体3D3が担持されたラテックス粒子、を血液検体と接触させることによる抗原抗体反応による凝集をシグナルとして、当該血液検体におけるヒトマトリックスメタロプロテイナーゼ-3を検出するラテックス凝集法による検出方法、並びに、当該検出方法を行うための検出試薬と検出キットを提供することにより、上記の課題を解決することを見出した。

    Abstract translation: 本发明的目的是提供一种通过LTIA方法检测基质金属蛋白酶-3(MMP-3)的方法,该方法利用在低值区具有高反应性的抗MMP-3单克隆抗体, 与其他MMP家族成员(如MMP-10)的反应能够快速测定,样品通量较高。 发现目的可以通过以下方式来实现:通过乳胶凝集法检测血液样品中的人体基质金属蛋白酶-3的检测方法,作为信号,使用作为抗原的结果的凝集的发生 通过使各自具有单体抗体14B1的胶乳颗粒和其上承载有单克隆抗体3D3的胶乳颗粒与血液样品接触进行的 - 抗体反应; 以及可以用于检测方法的检测试剂和检测试剂盒。

    N-TERMINALLY CONJUGATED POLYPEPTIDES FOR TARGETED THERAPY AND DIAGNOSIS
    9.
    发明申请
    N-TERMINALLY CONJUGATED POLYPEPTIDES FOR TARGETED THERAPY AND DIAGNOSIS 审中-公开
    用于定向治疗和诊断的N-末端连接的多聚体

    公开(公告)号:WO2011094671A2

    公开(公告)日:2011-08-04

    申请号:PCT/US2011/023140

    申请日:2011-01-31

    Inventor: SAFAVY, Ahmad

    Abstract: The present disclosure provides polypeptide conjugates comprising a polypeptide moiety and an agent, wherein the polypeptide moiety is linked to the agent through the -amino group of the polypeptide moiety. The present disclosure also provides methods for the manufacture of polypeptide conjugates comprising a polypeptide moiety and an agent, wherein the polypeptide moiety is linked to the agent through the -amino group of the polypeptide moiety. The methods disclosed provide for the selective attachment of the agent to the polypeptide moiety. Furthermore, the method of attachment utilizes mild conditions to link the polypeptide moiety and the agent, thereby maintaining the overall molecular structure of the polypeptide moiety so that is biological activity and/or binding activity is maintained. Such conjugates have many uses, for example in targeting specific cell types, treating disease, preventing disease, and diagnosing disease.

    Abstract translation: 本公开提供了包含多肽部分和试剂的多肽缀合物,其中所述多肽部分通过多肽部分的氨基与所述试剂连接。 本公开还提供了制备包含多肽部分和试剂的多肽缀合物的方法,其中多肽部分通过多肽部分的氨基与试剂连接。 所公开的方法提供了将试剂选择性连接到多肽部分。 此外,附着方法利用温和的条件来连接多肽部分和试剂,从而维持多肽部分的总体分子结构,从而保持生物活性和/或结合活性。 这样的缀合物具有许多用途,例如靶向特定细胞类型,治疗疾病,预防疾病和诊断疾病。

    BIOMARKERS FOR ATHEROSCLEROSIS
    10.
    发明申请
    BIOMARKERS FOR ATHEROSCLEROSIS 审中-公开
    生物标志物的ATHEROSCLEROSIS

    公开(公告)号:WO2010064147A3

    公开(公告)日:2010-12-29

    申请号:PCT/IB2009007986

    申请日:2009-12-04

    Abstract: The invention provides compositions and methods for defining the state of atherosclerotic degeneration processes for the purposes of detection, severity assessment, monitoring and treatment. The states of atherosclerotic degeneration processes are identified by means of a biomarker panel particularly suited for detecting atherosclerotic degeneration processes. The simultaneous use of multiple markers with independent classification power will increase the performance of the panel in identifying atherosclerosis compared to other panels.

    Abstract translation: 本发明提供了用于定义动脉粥样硬化变性过程的状态以用于检测,严重性评估,监测和治疗的组合物和方法。 通过特别适用于检测动脉粥样硬化变性过程的生物标志物鉴定动脉粥样硬化变性过程的状态。 与其他面板相比,同时使用具有独立分类能力的多个标记物将增加面板识别动脉粥样硬化的性能。

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