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Use of non-clonal chromosomal aberrations for cancer research and clinical diagnosis

机译:非克隆染色体畸变在癌症研究和临床诊断中的应用

摘要

A diagnostic method of determining tumorigenicity of a tissue specimen includes the steps of determining a magnitude of genome diversity in the tissue specimen, and diagnosing a likelihood of cancer in response to said step of determining the magnitude of genome diversity. The magnitude of genome diversity includes the determination of karyotypic heterogeneity in the tissue specimen, illustratively by detecting non-clonal chromosome aberrations (NCCAs). The detection of NCCAs includes the detection the frequency of NCCAs, and the diagnosis is responsive to the step of detecting the frequency of NCCAs. Detection of NCCAs advantageously includes the further step of screening lymphocytes. Also, the step of determining the presence of elevated genome diversity includes the step of applying Spectral Karyotyping to detect translocations throughout the genome. The diagnostic method is useful to determine drug resistance of a patient.
机译:确定组织样本的致癌性的诊断方法包括确定组织样本中基因组多样性的幅度的步骤,以及响应于所述确定基因组多样性的幅度的步骤来诊断癌症的可能性。基因组多样性的大小包括确定组织样本中核型异质性的方法,例如,通过检测非克隆染色体畸变(NCCA)。 NCCA的检测包括检测NCCA的频率,并且诊断响应于检测NCCA的频率的步骤。 NCCA的检测有利地包括筛选淋巴细胞的进一步步骤。同样,确定存在的基因组多样性升高的步骤包括应用光谱核型分析以检测整个基因组易位的步骤。该诊断方法可用于确定患者的耐药性。

著录项

  • 公开/公告号US2010086934A1

    专利类型

  • 公开/公告日2010-04-08

    原文格式PDF

  • 申请/专利权人 HENRY H. HENG;CHRISTINE YE;

    申请/专利号US20090583194

  • 发明设计人 HENRY H. HENG;CHRISTINE YE;

    申请日2009-08-14

  • 分类号C12Q1/68;

  • 国家 US

  • 入库时间 2022-08-21 18:51:43

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