Chimeric Heteromultimer Adhesins
    5.
    发明申请
    Chimeric Heteromultimer Adhesins 有权
    嵌合Heteromultimer粘附素

    公开(公告)号:US20100135957A1

    公开(公告)日:2010-06-03

    申请号:US12639822

    申请日:2009-12-16

    Abstract: Novel chimeric heteromultimer adhesins that bind the ligand of natural heteromultimeric receptors and uses therefor are disclosed. The chimeric molecules of the heteromultimer adhesins comprise an extracellular domain of a heteromultimeric receptor monomer and a multimerization domain for the stable interaction of the chimeric molecules in the adhesin. Specifically disclosed are heteromultimeric adhesins comprising the extracellular domains of ErbB2 and ErbB3 or ErbB2 and ErbB4. The chimeric ErbB heteromultimer adhesins of the present invention are useful as competitive antagonists or agonists of a neuregulin for the treatment of diseases such as various cancers.

    Abstract translation: 公开了结合天然异源多聚体受体的配体的新型嵌合杂多聚体粘附素及其用途。 杂多聚体粘附素的嵌合分子包含异源多聚体受体单体的细胞外结构域和用于粘附素中嵌合分子的稳定相互作用的多聚化结构域。 具体公开的是包含ErbB2和ErbB3或ErbB2和ErbB4的细胞外结构域的异源多聚体粘附素。 本发明的嵌合ErbB异源多聚体粘附素可用作神经调节蛋白的竞争性拮抗剂或激动剂用于治疗各种癌症等疾病。

    γ-heregulin
    9.
    发明授权
    γ-heregulin 有权
    γ-asgulin

    公开(公告)号:US07585673B2

    公开(公告)日:2009-09-08

    申请号:US11173893

    申请日:2005-07-01

    Abstract: A novel member of the heregulin superfamily has been identified which is designated “γ-HRG”. This molecule, secreted by human breast cancer MDA-MB-175 cells, leads to the formation of a constitutive active receptor complex and stimulates the growth of these cells in an autocrine manner. γ-HRG polypeptide and nucleic acid are disclosed, together with various uses therefor (e.g. use of γ-HRG nucleic acid for the recombinant production of γ-HRG). γ-HRG antagonists (e.g. neutralizing antibodies and antisense nucleic acid molecules) as well as uses therefor are also described.

    Abstract translation: 已经鉴定了一个被称为“γ-HRG”的蛋白质超家族的新成员。 这种由人乳腺癌MDA-MB-175细胞分泌的分子导致组成型活性受体复合物的形成,并以自分泌的方式刺激这些细胞的生长。 公开了γ-HRG多肽和核酸,以及其各种用途(例如,使用γ-HRG核酸进行γ-HRG的重组生产)。 还描述了γ-HRG拮抗剂(例如中和抗体和反义核酸分子)及其用途。

    ErbB4 antagonists
    10.
    发明申请
    ErbB4 antagonists 审中-公开
    ErbB4拮抗剂

    公开(公告)号:US20070092513A1

    公开(公告)日:2007-04-26

    申请号:US11581221

    申请日:2006-10-13

    Abstract: The present invention concerns methods and means for controlling excessive proliferation and/or migration of smooth muscle cells, and in particular for treating stenosis, by using antagonists of a native ErbB4 receptor. The invention further concerns a method for the identification of ErbB4 agonists and antagonists capable of inhibiting or enhancing the proliferation or migration of smooth muscle cells.

    Abstract translation: 本发明涉及通过使用天然ErbB4受体的拮抗剂来控制平滑肌细胞的过度增殖和/或迁移,特别是用于治疗狭窄的方法和手段。 本发明还涉及鉴定能够抑制或增强平滑肌细胞增殖或迁移的ErbB4激动剂和拮抗剂的方法。

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