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    • 2. 发明申请
    • COMPOSITIONS AND METHODS FOR DETERMINING THE REPLICATION CAPACITY OF A PATHOGENIC VIRUS
    • 用于确定致病病毒的复制能力的组合物和方法
    • WO2005076893A2
    • 2005-08-25
    • PCT/US2005003392
    • 2005-02-04
    • VIROLOGIC INCPARKIN NEIL TCHAPPEY COLOMBEBATES MICHAEL
    • PARKIN NEIL TCHAPPEY COLOMBEBATES MICHAEL
    • C12Q1/68C12Q1/70G01N33/48G01N33/50G01N33/569G06F19/00
    • G01N33/56988C12Q1/703
    • This invention relates to methods for predicting replication capacity of a virus based on genotype and identifying targets for antiviral therapy by identifying mutations associated with altered replication capacity. The methods are useful, for example, for identifying previously unknown interactions among viral molecules or between viral molecules and host cell molecules that are essential to viral infection and/or replication. By identifying such interactions, novel targets for antiviral therapy can be identified. In another aspect, the invention provides a method for determining that an HIV has an altered replication capacity. In certain embodiments, the method comprises detecting a mutation in a codon of gag that is selected from the group consisting of 437, 439, 441, 442, 454, 478, 479, and 484. In certain embodiments, the mutation is selected from the group consisting of I437L, P439S, E454V, P478L, and I479K. In certain embodiments, the mutation is in a codon of gag that is selected from the group consisting of 418, 456, 456, 453, 418, 483, 481, 465, 429, 484, 481, 483, 484, 465, 454, 442, 479, 418, 479, and 486.
    • 本发明涉及用于基于基因型预测病毒的复制能力的方法,并且通过鉴定与改变的复制能力相关的突变来鉴定抗病毒治疗的靶标。 该方法例如用于鉴定病毒分子之间或病毒分子与病毒感染和/或复制必需的宿主细胞分子之间的先前未知的相互作用是有用的。 通过鉴定这种相互作用,可以鉴定抗病毒治疗的新靶点。 另一方面,本发明提供了确定HIV具有改变的复制能力的方法。 在某些实施方案中,该方法包括检测gag密码子中的突变,其选自437,439,441,442,454,478,479和484.在某些实施方案中,突变选自 由I437L,P439S,E454V,P478L和I479K组成的组。 在某些实施方案中,突变是gag的密码子,其选自418,456,465,463,418,483,481,465,489,484,481,483,448,465,454,448,448,448,448,448,448,448,448,448,448,448,448,448,454,454,454,454,454,454,454,454,454,454,454,454,454,454,454,454,454,454,454,454,448,454,454,454,454,454 442,479,418,479和486。
    • 3. 发明申请
    • METHODS FOR DETERMINING RESPONSIVENESS TO CANCER THERAPY
    • 确定对癌症治疗的反应的方法
    • WO2006084018A3
    • 2006-09-21
    • PCT/US2006003660
    • 2006-02-01
    • MONOGRAM BIOSCIENCES INCTANG MENGXIANGCAO LICHINGDUA RAJIVMUKHERJEE ALIPANNU HERJITPANNU JAGRUPSHI YININGTAN YUPINGSINGH SHARATCHAPPEY COLOMBE
    • TANG MENGXIANGCAO LICHINGDUA RAJIVMUKHERJEE ALIPANNU HERJITPANNU JAGRUPSHI YININGTAN YUPINGSINGH SHARATCHAPPEY COLOMBE
    • C12Q1/68G01N33/567
    • G01N33/57484G01N33/5748G01N2333/82
    • In certain aspects, the present invention provides methods and compositions for determining whether a cancer cells is likely to respond to treatment with a Her 1 -acting agent. In one aspect, the invention provides a method for determining whether a cancer cell is likely to respond to treatment with a Her 1 -acting agent, comprising detecting on the cancer cell at least about 600 Her 1 -Her 1 dimers, wherein the presence of the at least about 600 Her 1 -Her 1 dimers indicates that the cancer is likely to respond to treatment with the Her 1 -acting agent. In another aspect, the invention provides a method for determining whether a cancer cell is likely to respond to treatment with a Her 1 -acting agent, comprising detecting on a cell of the cancer at least about 600 Her 1 -Her 1 dimers, at least about 1000 Herl-Her2 dimers, and fewer than about 1000 Her2-Her3 dimers, wherein the presence of the at least about 600 Her 1 -Her 1 dimers, the at least about 1000 Herl-Her2 dimers, and the fewer than about 1000 Her2-Her3 dimers indicates that the cancer cell is likely to respond to treatment with the Her 1 -acting agent. Preferably, methods of the invention are implemented by using sets of binding compounds having releasable molecular tags that are specific for multiple components of one or more types of receptor dimers. After binding, molecular tags are released and separated from the assay mixture for analysis.
    • 在某些方面,本发明提供了用于确定癌细胞是否可能响应Her 1作用剂治疗的方法和组合物。 在一个方面,本发明提供了用于确定癌细胞是否可能对用Her 1作用剂治疗有反应的方法,包括在癌细胞上检测至少约600个Her 1 --Her 1二聚体,其中存在 该至少约600个Her 1 -Her 1二聚体表明癌症可能对用Her 1作用剂治疗有反应。 另一方面,本发明提供了用于确定癌细胞是否可能响应用Her 1作用剂治疗的方法,包括在癌细胞上检测至少约600个Her 1 --Her 1二聚体,至少 约1000个Her1-Her2二聚体和少于约1000个Her2-Her3二聚体,其中所述至少约600个Her1-Her1二聚体,所述至少约1000个Her1-Her2二聚体和少于约1000个Her2 -Her3二聚体表明癌细胞可能对Her-1作用剂的治疗有反应。 优选地,本发明的方法通过使用具有对一种或多种类型的受体二聚体的多种组分特异的可释放分子标签的结合化合物组来实施。 结合后,分子标签被释放并从测定混合物中分离出来用于分析。
    • 4. 发明申请
    • METHODS FOR DETERMINING RESPONSIVENESS TO CANCER THERAPY
    • 用于确定对癌症治疗的反应的方法
    • WO2006084018A2
    • 2006-08-10
    • PCT/US2006/003660
    • 2006-02-01
    • MONOGRAM BIOSCIENCES, INC.TANG, MengxiangCAO, LichingDUA, RajivMUKHERJEE, AliPANNU, HerjitPANNU, JagrupSHI, YiningTAN, YupingSINGH, SharatCHAPPEY, Colombe
    • TANG, MengxiangCAO, LichingDUA, RajivMUKHERJEE, AliPANNU, HerjitPANNU, JagrupSHI, YiningTAN, YupingSINGH, SharatCHAPPEY, Colombe
    • C12Q1/68
    • G01N33/57484G01N33/5748G01N2333/82
    • In certain aspects, the present invention provides methods and compositions for determining whether a cancer cells is likely to respond to treatment with a Her 1 -acting agent. In one aspect, the invention provides a method for determining whether a cancer cell is likely to respond to treatment with a Her 1 -acting agent, comprising detecting on the cancer cell at least about 600 Her 1 -Her 1 dimers, wherein the presence of the at least about 600 Her 1 -Her 1 dimers indicates that the cancer is likely to respond to treatment with the Her 1 -acting agent. In another aspect, the invention provides a method for determining whether a cancer cell is likely to respond to treatment with a Her 1 -acting agent, comprising detecting on a cell of the cancer at least about 600 Her 1 -Her 1 dimers, at least about 1000 Herl-Her2 dimers, and fewer than about 1000 Her2-Her3 dimers, wherein the presence of the at least about 600 Her 1 -Her 1 dimers, the at least about 1000 Herl-Her2 dimers, and the fewer than about 1000 Her2-Her3 dimers indicates that the cancer cell is likely to respond to treatment with the Her 1 -acting agent. Preferably, methods of the invention are implemented by using sets of binding compounds having releasable molecular tags that are specific for multiple components of one or more types of receptor dimers. After binding, molecular tags are released and separated from the assay mixture for analysis.
    • 在某些方面,本发明提供了用于确定癌细胞是否可能对Her 1处理剂的治疗有反应的方法和组合物。 一方面,本发明提供了一种用于确定癌细胞是否可能对Her1处理剂起反应的方法,包括在癌细胞上检测至少约600个Her 1 -Her 1二聚体,其中存在 至少约600个Her 1 -Her 1二聚体表明癌症可能对她用1代谢剂的治疗有反应。 在另一方面,本发明提供了一种用于确定癌细胞是否可能对Her 1处理剂有反应的方法,包括至少检测至少约600个Her 1 -Her 1二聚体的癌细胞 约1000个Herl-Her2二聚体和少于约1000个Her2-Her3二聚体,其中存在至少约600个Her1-Her2二聚体,至少约1000个Her1-Her2二聚体,以及少于约1000个Her2-Her2二聚体 -Her3二聚体表明癌细胞很可能对Her1处理剂有反应。 优选地,通过使用具有对一种或多种类型的受体二聚体的多种成分特异的可释放分子标签的组合化合物来实现本发明的方法。 结合后,将分子标签从测定混合物中释放并分离出来进行分析。