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    • 2. 发明申请
    • Susceptibility to HSP90-Inhibitors
    • 对HSP90抑制剂的敏感性
    • US20110319415A1
    • 2011-12-29
    • US13059557
    • 2009-08-17
    • Roman ThomasKathrin MaringThomas ZanderPeter FrommoltKwok-kin Wong
    • Roman ThomasKathrin MaringThomas ZanderPeter FrommoltKwok-kin Wong
    • A61K31/395C12Q1/68G01N33/567A61K31/5377A61P35/00A61P35/02C40B30/04C12Q1/02
    • G01N33/574C12Q1/6886C12Q2600/106C12Q2600/136C12Q2600/156G01N2800/52
    • The present invention relates to a method of selecting (a) cell(s), (a) tissue(s) or (a) cell culture(s) with susceptibility to an HSP90 inhibitor. Also a method for determining the responsiveness of a mammalian tumor cell or cancer cell to treatment with an HSP90 inhibitor is described herein. In particular, the present invention provides for an in vitro method for the identification of a responder for or a patient sensitive to an HSP90 inhibitor and uses of an oligo- or polynucleotide capable of detecting (an) activating mutation(s) in the KRAS gene are provided. The present invention also relates to a method of monitoring the efficacy of a treatment of a cancer characterized by the presence of at least one activating mutation in the KRAS gene, and. optionally, in the EGFR gene and/or the BRAF gene. In addition, a method of predicting the efficacy of a cancer treatment is described, in particular in a cancer that is characterized by the presence of at least one activating mutation in the KRAS gene. and. optionally, in the EGFR gene and/or the BRAF gene. Also the use of a (transgenic) non-human animal or a (transgenic) cell having at least one activating mutation in the KRAS gene, and, optionally, in the EGFR gene and/or the BRAF gene for screening and/or validation of a medicament for the treatment of said cancer is described and a kit useful for carrying out the methods described herein is provided.
    • 本发明涉及一种选择(a)对HSP90抑制剂具有敏感性的细胞,(a)组织或(a)细胞培养物的方法。 本文还描述了确定哺乳动物肿瘤细胞或癌细胞对用HSP90抑制剂进行治疗的反应性的方法。 特别地,本发明提供了用于鉴定对HSP90抑制剂敏感的或对其敏感的患者的体外方法,以及能够检测(或)激活KRAS基因突变的寡核苷酸或多核苷酸的用途 被提供。 本发明还涉及一种监测癌症治疗功效的方法,其特征在于在KRAS基因中存在至少一种激活突变。 任选地,在EGFR基因和/或BRAF基因中。 此外,描述了预测癌症治疗功效的方法,特别是在KRAS基因中存在至少一种激活突变的癌症中。 和。 任选地,在EGFR基因和/或BRAF基因中。 另外,在KRAS基因和/或任选地在EGFR基因和/或BRAF基因中具有至少一个激活突变的(转基因)非人动物或(转基因)细胞也用于筛选和/或验证 描述了用于治疗所述癌症的药物,并提供了可用于实施本文所述方法的试剂盒。
    • 3. 发明申请
    • SUSCEPTIBILITY TO SELECTIVE CDK9 INHIBITORS
    • 选择性CDK9抑制剂的缺点
    • US20140287454A1
    • 2014-09-25
    • US14240315
    • 2012-08-22
    • Axel ChoidasBert KleblPeter HabenbergerJan EickhoffRoman ThomasJohannes Heuckmann
    • Axel ChoidasBert KleblPeter HabenbergerJan EickhoffRoman ThomasJohannes Heuckmann
    • G01N33/50
    • G01N33/5011C12Q1/6881C12Q1/6886C12Q2600/106G01N2800/52
    • The present invention relates to a method of selecting (a) cell(s), (a) tissue(s) or (a) cell culture(s) with susceptibility to a selective CDK9 inhibitor. Also a method for determining the responsiveness of a mammalian tumor cell or cancer cell to treatment with a selective CDK9 inhibitor is described herein. In particular, the present invention provides for an in vitro method for the identification of a responder for or a patient sensitive to a selective CDK9 inhibitor, whereby the patient is suspected to suffer from NUT midline carcinoma (NMC). The present invention also relates to a method of monitoring or predicting the efficacy of a treatment of NUT midline carcinoma (NMC), wherein treatment with a selective CDK9 inhibitor is in particular envisaged. Also the use of a (transgenic) non-human animal or a (transgenic) cell having at least one rearrangement in the NUT gene for screening and/or validation of a medicament for the treatment NUT midline carcinoma (NMC) is described. Furthermore, a kit useful for carrying out the methods described herein as well as an oligo- or polynucleotide capable of detecting rearrangements in the NUT gene are provided.
    • 本发明涉及一种选择(a)对选择性CDK9抑制剂具有易感性的细胞,(a)组织或(a)细胞培养物的方法。 本文还描述了确定哺乳动物肿瘤细胞或癌细胞对用选择性CDK9抑制剂进行治疗的反应性的方法。 特别地,本发明提供了用于鉴定对选择性CDK9抑制剂敏感的患者或患者的体外方法,由此患者怀疑患有NUT中线癌(NMC)。 本发明还涉及监测或预测NUT中线癌(NMC)治疗功效的方法,其中特别设想用选择性CDK9抑制剂进行治疗。 还描述了在NUT基因中具有至少一个重排的(转基因)非人动物或(转基因)细胞用于筛选和/或验证用于治疗NUT中线癌(NMC)的药物的用途。 此外,提供了可用于实施本文所述方法的试剂盒以及能够检测NUT基因重排的寡核苷酸或多核苷酸。