Method of treatment of cancers characterized by ligand-dependent activating mutations in FGFR2 with FGFR1 ECD proteins
    2.
    发明授权
    Method of treatment of cancers characterized by ligand-dependent activating mutations in FGFR2 with FGFR1 ECD proteins 有权
    以FGFR2与FGFR1 ECD蛋白的配体依赖性激活突变为特征的癌症治疗方法

    公开(公告)号:US09169313B2

    公开(公告)日:2015-10-27

    申请号:US14079742

    申请日:2013-11-14

    CPC classification number: C07K14/71 A61K38/179 A61K38/1825

    Abstract: The present invention relates to the use of Fibroblast Growth Factor Receptor I (FGFR1) extracellular domain (ECD) polypeptides for treatment of cancers characterized by ligand dependent activating mutations in Fibroblast Growth Factor Receptor 2 (FGFR2). For example, the present invention relates to the treatment of endometrial cancers and other cancers wherein tumor cells express FGFR2 mutants in the IgII-IgIII hinge region or IgIII domain of the protein, such as at amino acid positions 252 and/or 253.

    Abstract translation: 本发明涉及成纤维细胞生长因子受体I(FGFR1)细胞外结构域(EGFR)多肽用于治疗以成纤维细胞生长因子受体2(FGFR2)中配体依赖性激活突变为特征的癌症的用途。 例如,本发明涉及治疗子宫内膜癌和其它癌症,其中肿瘤细胞在蛋白质的IgII-IgIII铰链区或IgIII结构域中表达FGFR2突变体,例如在氨基酸位置252和/或253。

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