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    • 2. 发明申请
    • Nucleic acid useful for triggering tumor cell lethality
    • 可用于触发肿瘤细胞致死性的核酸
    • US20070197458A1
    • 2007-08-23
    • US10576818
    • 2004-10-25
    • Marie DutreixJian-Sheng Sun
    • Marie DutreixJian-Sheng Sun
    • A61K48/00C07H21/02C07F9/6533C07F9/6512
    • C12N15/11A61K38/00C12N2310/13C12N2310/53
    • The invention relates to double-stranded nucleic acid fragments comprising a chemically modified backbone and at least 4-1000 bp, preferably 8-500 bp, and most preferably 16-200 bp. The disclosed molecules (DRIL molecules) may interfere with DNA damage signalling and repair pathways, in particular the non homologous NHEJ pathway of double-stranded break repair. The invention discloses the application of the DRIL molecules as adjuvant compositions to be used in association with a DNA breaking treatment, particularly radiotherapy or chemotherapy, in combination with a pharmaceutically acceptable carrier, in an efficient amount to be introduced in the tumoral cell nuclei in order to trigger DNA repair induced lethality (DRIL in short) of tumoral cells/tissues.
    • 本发明涉及包含化学修饰的主链和至少4-1000bp,优选8-500bp,最优选16-200bp的双链核酸片段。 所公开的分子(DRIL分子)可能干扰DNA损伤信号传导和修复途径,特别是双链断裂修复的非同源NHEJ途径。 本发明公开了将DRIL分子作为辅助组合物的应用,其与DNA破坏处理(特别是放射治疗或化疗)联合使用,与药学上可接受的载体组合使用,以有效量依次引入肿瘤细胞核 触发DNA修复诱导的细胞/组织的致死性(简称DRIL)。
    • 9. 发明授权
    • Nucleic acids useful for triggering tumor cell lethality
    • 可用于触发肿瘤细胞致死性的核酸
    • US07595302B2
    • 2009-09-29
    • US10576818
    • 2004-10-25
    • Marie DutreixJian-Sheng Sun
    • Marie DutreixJian-Sheng Sun
    • A61K31/70C07H21/04C07H21/00C12Q1/68C12P19/34
    • C12N15/11A61K38/00C12N2310/13C12N2310/53
    • The invention relates to double-stranded nucleic acid fragments comprising a chemically modified backbone and at least 4-1000 bp, preferably 8-500 bp, and most preferably 16-200 bp. The disclosed molecules (DRIL molecules) may interfere with DNA damage signaling and repair pathways, in particular the non homologous NHEJ pathway of double-stranded break repair. The invention discloses the application of the DRIL molecules as adjuvant compositions to be used in association with a DNA breaking treatment, particularly radiotherapy or chemotherapy, in combination with a pharmaceutically acceptable carrier, in an efficient amount to be introduced in the tumoral cell nuclei in order to trigger DNA repair induced lethality (DRIL in short) of tumoral cells/tissues.
    • 本发明涉及包含化学修饰的主链和至少4-1000bp,优选8-500bp,最优选16-200bp的双链核酸片段。 所公开的分子(DRIL分子)可能干扰DNA损伤信号传导和修复途径,特别是双链断裂修复的非同源NHEJ途径。 本发明公开了将DRIL分子作为辅助组合物的应用,其与DNA破坏处理(特别是放射治疗或化疗)联合使用,与药学上可接受的载体组合使用,以有效量依次引入肿瘤细胞核 触发DNA修复诱导的细胞/组织的致死性(简称DRIL)。