UNBIASED DNA METHYLATION MARKERS DEFINE AN EXTENSIVE FIELD DEFECT IN HISTOLOGICALLY NORMAL PROSTATE TISSUES ASSOCIATED WITH PROSTATE CANCER: NEW BIOMARKERS FOR MEN WITH PROSTATE CANCER
    5.
    发明申请
    UNBIASED DNA METHYLATION MARKERS DEFINE AN EXTENSIVE FIELD DEFECT IN HISTOLOGICALLY NORMAL PROSTATE TISSUES ASSOCIATED WITH PROSTATE CANCER: NEW BIOMARKERS FOR MEN WITH PROSTATE CANCER 审中-公开
    未经预期的DNA甲基化标记定义了与前列腺癌相关的组织学正常前列腺组织中的广泛的现场缺陷:具有前列腺癌的男性新生物标志物

    公开(公告)号:US20140296355A1

    公开(公告)日:2014-10-02

    申请号:US14226291

    申请日:2014-03-26

    CPC classification number: C12Q1/6886 C12Q2600/154

    Abstract: A method of detecting the presence of a prostate cancer field defect in a human subject comprising the step of (a) obtaining genomic DNA from the human subject and (b) quantitating methylation in at least one target region selected from the group consisting of CAV1, EVX1, MCF2L, FGF1, NCR2 and WNT2 and EXT1 and SPAG4 target, wherein significant methylation changes indicate the presence of prostate cancer or a prostate cancer field defect, wherein the change is relative to tissue from a second human subject who does not have prostate cancer.

    Abstract translation: 一种检测人受试者中前列腺癌斑块缺陷的存在的方法,包括以下步骤:(a)从人受试者获得基因组DNA,和(b)定量至少一个靶区域中的甲基化,所述靶区域选自CAV1, EVX1,MCF2L,FGF1,NCR2和WNT2以及EXT1和SPAG4靶标,其中显着的甲基化变化表明前列腺癌或前列腺癌场缺陷的存在,其中该变化相对于不具有前列腺癌的第二人类受试者的组织 。

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