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COMBINATION THERAPIES INCLUDING INHIBITORS OF THE EXTRACELLULAR DOMAIN OF E-CADHERIN

机译:联合疗法包括E-钙粘蛋白的胞外域抑制剂

摘要

The present invention is based on our work with E-cadherin, including soluble portions of this integral membrane glycoprotein. The compositions of the present invention include therapeutically effective amounts of a first agent that targets epitopes within one or more of the EC2-EC5 subdomains of the ectodomain of E-cadherin (including these domains in the shed sEcad fragment) and a second agent that inhibits one or more of: endothelial tube formation; angiogenesis; the human epidermal growth factor receptor family (i.e. HER1-4); an insulin-like growth factor 1 receptor (IGF-1R); any other receptor tyrosine kinase receptor family member; the P13K-MAPK pathway; and the P13K/Akt/mTOR pathway. The compositions can be used in the treatment of epithelial cancers and can be used to inhibit tumor growth and metastasis. The invention also features methods in which cancer is staged.
机译:本发明基于我们对E-钙粘着蛋白的研究,包括该完整膜糖蛋白的可溶部分。本发明的组合物包括治疗有效量的靶向E-钙粘蛋白的胞外域的一个或多个EC2-EC5亚域(包括脱落的sEcad片段中的这些域)的一个或多个EC2-EC5亚域内的表位的第一药物和抑制该药物的第二药物。一种或多种:内皮管形成;血管生成;人表皮生长因子受体家族(即HER1-4);胰岛素样生长因子1受体(IGF-1R);任何其他受体酪氨酸激酶受体家族成员; P13K-MAPK途径;以及P13K / Akt / mTOR途径。该组合物可以用于治疗上皮癌,并且可以用于抑制肿瘤的生长和转移。本发明的特征还在于癌症分期的方法。

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