Method of reducing the number of EMT and MET type breast cancer stem cells
    1.
    发明授权
    Method of reducing the number of EMT and MET type breast cancer stem cells 有权
    减少EMT和MET型乳腺癌干细胞数量的方法

    公开(公告)号:US09352039B2

    公开(公告)日:2016-05-31

    申请号:US14376923

    申请日:2013-02-08

    Abstract: Compositions, kits, and methods for therapeutic screening, diagnostics, and cancer treatment based on the identification or use of the different states of cancer stem cells, including cancer stem cells in the EMT (epithelial to mesenchymal transition) MET (mesenchymal to epithelial transition), and EMT-MET states are disclosed. In some methods, a subject is treated with one therapeutic that targets EMT cancer stem cells and a second therapeutic that targets MET cancers stem cells. In certain methods, the different states of cancer stem cells are distinguished based on markers CD44+CD24−, EpCam−CD49P+ (for EMT cancers stem cells), ALDH+ and EPCam+CD49r− (for MET cancers stem cells), and CD44+CD24−ALDH+ (for EMT-MET cancer stem cells). In particular methods, micro RNAs are used to transition to one particular cancer stem cell type (e.g., mir-100 for EMT and mir-93 for MET).

    Abstract translation: 基于识别或使用不同状态的癌症干细胞(包括EMT中的癌症干细胞(上皮至间质转换)MET(间质至上皮转换))的治疗筛选,诊断和癌症治疗的组合物,试剂盒和方法 ,并且公开了EMT-MET状态。 在一些方法中,使用靶向EMT癌症干细胞的一种治疗剂和靶向MET癌症干细胞的第二种治疗剂治疗受试者。 在某些方法中,基于标记物CD44 + CD24-,EpCam-CD49P +(用于EMT癌症干细胞),ALDH +和EPCam + CD49r-(对于MET癌症干细胞)和CD44 + CD24来区分不同状态的癌症干细胞 -ALDH +(用于EMT-MET癌症干细胞)。 在特定方法中,微RNA用于转变成特定的癌症干细胞类型(例如,用于EMT的mir-100和用于MET的mir-93)。

    DIFFERENT STATES OF CANCER STEM CELLS
    2.
    发明申请
    DIFFERENT STATES OF CANCER STEM CELLS 有权
    癌症干细胞的不同状态

    公开(公告)号:US20150125469A1

    公开(公告)日:2015-05-07

    申请号:US14376923

    申请日:2013-02-08

    Abstract: Compositions, kits, and methods for therapeutic screening, diagnostics, and cancer treatment based on the identification or use of the different states of cancer stem cells, including cancer stem cells in the EMT (epithelial to mesenchymal transition) MET (mesenchymal to epithelial transition), and EMT-MET states are disclosed. In some methods, a subject is treated with one therapeutic that targets EMT cancer stem cells and a second therapeutic that targets MET cancers stem cells. In certain methods, the different states of cancer stem cells are distinguished based on markers CD44+CD24−, EpCam−CD49P+(for EMT cancers stem cells), ALDH+ and EPCam+CD49r− (for MET cancers stem cells), and CD44+CD24−ALDH+ (for EMT-MET cancer stem cells). In particular methods, micro RNAs are used to transition to one particular cancer stem cell type (e.g., mir-100 for EMT and mir-93 for MET).

    Abstract translation: 基于识别或使用不同状态的癌症干细胞(包括EMT中的癌症干细胞(上皮至间质转换)MET(间质至上皮转换))的治疗筛选,诊断和癌症治疗的组合物,试剂盒和方法 ,并且公开了EMT-MET状态。 在一些方法中,使用靶向EMT癌症干细胞的一种治疗剂和靶向MET癌症干细胞的第二种治疗剂治疗受试者。 在某些方法中,基于标记物CD44 + CD24-,EpCam-CD49P +(用于EMT癌症干细胞),ALDH +和EPCam + CD49r-(对于MET癌症干细胞)和CD44 + CD24来区分不同状态的癌症干细胞 -ALDH +(用于EMT-MET癌症干细胞)。 在特定方法中,微RNA用于转变成特定的癌症干细胞类型(例如,用于EMT的mir-100和用于MET的mir-93)。

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