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    • 1. 发明申请
    • IDENTIFICATION AND USE OF PROGNOSTIC AND PREDICTIVE MARKERS IN CANCER TREATMENT
    • 癌症治疗中预防和预防标记的鉴定与使用
    • WO2009148593A1
    • 2009-12-10
    • PCT/US2009/003382
    • 2009-06-02
    • NSABP FOUNDATION, INC.PAIK, SoonmyungKIM, Chungyeul
    • PAIK, SoonmyungKIM, Chungyeul
    • C12Q1/68A61K39/395A61P35/00
    • A61K31/704A61K31/337A61K31/675A61K39/39558C12Q1/6841C12Q1/6886C12Q2600/106A61K2300/00
    • The present invention provides a method of screening for markers useful in predicting the efficacy of a specified cancer that includes: (a) constructing a tissue microarray from a tissue bank comprising multiple tissue samples that are annotated with clinical follow up data; (b) labeling polynucleic acid probes specific for oncogenes or cancer associated genes known to be potential amplicons; (c) performing fluorescent in situ hybridization analysis on the tissue microarray; and (d) correlating the result of the fluorescent in situ hybridization with the clinical follow up data. The present disclosure also provides methods of treating breast cancer that include screening a breast cancer patient for amplification of one or more of the genes disclosed herein, and treating a patient having amplification of one or more of these genes with a therapeutically effective amount of a compound that interferes with HER2 signaling.
    • 本发明提供筛选用于预测特定癌症功效的标志物的方法,其包括:(a)从包含多个组织样本的组织库构建组织微阵列,所述多个组织样本用临床跟踪数据注释; (b)标记针对致癌基因或已知为潜在扩增子的癌症相关基因特异性的多核酸探针; (c)对组织微阵列进行荧光原位杂交分析; 和(d)将荧光原位杂交的结果与临床随访数据相关联。 本公开还提供了治疗乳腺癌的方法,其包括筛选乳腺癌患者以扩增本文公开的一种或多种基因,并用治疗有效量的化合物治疗具有这些基因中的一种或多种的扩增的患者 这干扰了HER2信号。
    • 4. 发明申请
    • METHODS OF WHOLE GENOME OR MICROARRAY EXPRESSION PROFILING USING NUCLEIC ACIDS
    • 使用核酸的全基因组或微阵列表达谱的方法
    • WO2007127458A3
    • 2007-12-27
    • PCT/US2007010392
    • 2007-04-30
    • NSABP FOUNDATION INCPAIK SOONMYUNGPOGUE-GEILE KATHERINE LEAKIM CHUNGYEUI
    • PAIK SOONMYUNGPOGUE-GEILE KATHERINE LEAKIM CHUNGYEUI
    • C12P19/34
    • C12Q1/6806C12N15/1003C12Q1/6837C12Q2565/515
    • The present invention provides novel methods for analyzing gene expression levels from fresh or aged (more than one year old) formalin-fixed, paraffin-embedded tissue ("FFPET") samples that comprise pre-hybridizing a labeled nucleic acid sample prepared from the formalin-fixed, paraffin-embedded tissue sample with a first microarray, hybridizing the unbound labeled nucleic acid sample with a second microarray, and detecting the labeled nucleic acid sample bound to the second microarray. The pre-hybridization step results in an increase in the specific gene signals in subsequent hybridizations with high density gene expression arrays. The first microarray used for the pre-hybridization step can be either a new or used microarray. Importantly, from a cost-savings perspective, the inventors determined that when the first microarray used for the pre-hybridization step is a previously used microarray, the results of the subsequent hybridization on a second microarray are nearly identical to the results obtained when the pre-hybridization was carried out using a new or previously unused microarray.
    • 本发明提供用于分析来自新鲜或老化(一岁以上)福尔马林固定的石蜡包埋组织(“FFPET”)样品的基因表达水平的新方法,其包括将从福尔马林制备的标记的核酸样品预先杂交 固定的石蜡包埋的组织样品与第一微阵列,将未结合的标记的核酸样品与第二微阵列杂交,并检测结合到第二微阵列的标记的核酸样品。 预杂交步骤导致随后与高密度基因表达阵列杂交的特异性基因信号的增加。 用于预杂交步骤的第一个微阵列可以是新的或使用过的微阵列。 重要的是,从成本节约的角度来看,发明人确定当用于预杂交步骤的第一微阵列是先前使用的微阵列时,第二微阵列上的随后杂交的结果几乎与当预先 - 使用新的或以前未使用的微阵列进行杂交。
    • 7. 发明申请
    • IDENTIFICATION AND USE OF PROGNOSTIC AND PREDICTIVE MARKERS IN CANCER TREATMENT
    • 在癌症治疗中识别和使用预测性和预测性标志物
    • WO2006065940A2
    • 2006-06-22
    • PCT/US2005/045322
    • 2005-12-15
    • NSABP FOUNDATION, INC.PAIK, SoonmyungKIM, Chungyeul
    • PAIK, SoonmyungKIM, Chungyeul
    • C12Q1/68G01N33/574
    • G01N33/5082C12Q1/6886C12Q2600/106C12Q2600/158G01N33/574G01N33/57415G01N33/57492G01N33/6845G01N2500/00
    • The present invention provides a method of screening for markers useful in predicting the efficacy of a specified cancer that includes: (a) constructing a tissue microarray from a tissue bank comprising multiple tissue samples that are annotated with clinical follow up data; (b) labeling polynucleic acid probes specific for oncogenes or cancer associated genes known to be potential amplicons; (c) performing fluorescent in situ hybridization analysis on the tissue microarray; and (d) correlating the result of the fluorescent in situ hybridization with the clinical follow up data. In addition, the present invention provides a method of treating breast cancer that includes measuring the expression levels or amplification of HTPAP in a patient having breast cancer and then providing a patient having increased levels of HTPAP expression or HTPAP amplification with therapeutic quantities of at least one compound that interferes with the phosphatidic acid phosphatase activity of HTPAP. The present invention also encompasses a method of treating breast cancer that includes screening a breast cancer patient for amplification of the cMYC gene and then treating a patient having amplification of the cMYC gene with therapeutic quantities of a compound that interferes with HER2 signaling.
    • 本发明提供筛选可用于预测特定癌症功效的标志物的方法,所述方法包括:(a)从包含多个组织样本的组织库构建组织样本,所述组织样本用临床 跟进数据; (b)标记对已知为潜在扩增子的致癌基因或癌症相关基因特异性的多核苷酸探针; (c)对组织微阵列进行荧光原位杂交分析; 和(d)将荧光原位杂交的结果与临床随访数据相关联。 此外,本发明提供了治疗乳腺癌的方法,其包括测量患有乳腺癌的患者中的HTPAP的表达水平或扩增,然后提供具有增加水平的HTPAP表达或HTPAP扩增的患者,其治疗量为至少一种 干扰HTPAP的磷脂酸磷酸酶活性的化合物。 本发明还包括治疗乳腺癌的方法,包括筛选乳腺癌患者扩增cMYC基因,然后用治疗量的干扰HER2信号传导的化合物治疗患有cMYC基因扩增的患者。