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GENOMIC REARRANGEMENTS ASSOCIATED WITH PROSTATE CANCER AND METHODS OF USING THE SAME

机译:与前列腺癌相关的基因组重排和使用相同的方法

摘要

The present disclosure provides methods of identifying or characterizing prostate cancer comprising detecting in a biological sample the presence or absence of a genomic rearrangement that results in a deletion of an LSAMP gene and detecting in a biological sample the presence or absence of a genomic rearrangement that results in a deletion of a CHD1 gene. In certain embodiments, the patient self-identifies as being of African descent. Also disclosed herein are methods of testing for the presence of genomic rearrangements in an LSAMP gene and a CHD1 gene in a biological sample. The LSAMP and CHD1 genomic rearrangements serves as a biomarker for prostate cancer and can be used to stratify prostate cancer based on ethnicity or the severity or aggressiveness of prostate cancer and/or identify a patient for prostate cancer treatment. Also provided are kits for diagnosing and prognosing prostate cancer and methods of selecting a targeted prostate cancer treatment for a patient.
机译:本公开提供了鉴定或表征前列腺癌的方法,包括在生物样品中检测基因组重排的存在或不存在,导致揭示液体样品并在生物样品中检测结果或不存在基因组重排的结果 在缺失CHD1基因。 在某些实施方案中,患者将自我识别为非洲血统。 本文还公开了用于在生物样品中存在基因组和CHD1基因的基因组重排的测试的方法。 LSAMP和CHD1基因组重排用作前列腺癌的生物标志物,可用于基于种族或前列腺癌的严重程度或严重程度或侵略性分析前列腺癌和/或鉴定前列腺癌治疗的患者。 还提供了用于诊断和预先诊断和预先诊断前列腺癌的试剂盒及选择针对患者的靶向前列腺癌治疗的方法。

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