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    • 3. 发明申请
    • Inhibition of Tumorigenesis by Inhibition of a6b4 Integrin
    • 抑制a6b4整合素抑制肿瘤发生
    • US20080317752A1
    • 2008-12-25
    • US10596364
    • 2006-04-18
    • Filippo G. Giancotti
    • Filippo G. Giancotti
    • A61K39/395A61K31/7088A61P35/00
    • C07K16/2839
    • Inhibitors of a6b4 integrin that target beta 4 are used as therapeutic agents to inhibit tumorigensis in individuals, including humans, of tumors that express a6b4 integrin. The therapeutic agent may be an antibody or a small molecule, for example a laminin-5 analog, which binds to a6b4 integrin and inhibits its normal function. The therapeutic agent may also be a chemical species that interferes with the production of beta 4, including for example an antisense or RNAi species. The therapeutic agent is administered to the tissue or patient in a therapeutically effective amount. The therapeutic agent may be used as a single agent or in combination with other therapies, especially those directed toward suppressing the activity of RPTKs known to cooperate with a6b4, including but not limited to ErbB2, EGF-R, Met, and Ron.
    • 靶向β4的a6b4整联蛋白的抑制剂用作治疗剂以抑制表达一种6b4整联蛋白的肿瘤的个体(包括人)的肿瘤发生。 治疗剂可以是抗体或小分子,例如层粘连蛋白-5类似物,其结合a6b4整联蛋白并抑制其正常功能。 治疗剂也可以是干扰β4产生的化学物质,包括例如反义或RNAi物种。 治疗剂以治疗有效量施用于组织或患者。 治疗剂可以用作单一药剂或与其它治疗剂组合使用,特别是那些旨在抑制已知与db4(包括但不限于ErbB2,EGF-R,Met和Ron)配合的RPTK的活性的治疗剂。