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COMPOSITIONS AIMED AT THE SOLUBLE EXTRACELLULAR DOMAIN OF E-CADGERIN AND RELATED METHODS FOR TREATING ONCOLOGICAL DISEASES

机译:E-cadgerin在胞外可溶性区的生物成分及治疗肿瘤的相关方法

摘要

1. A method of treating a patient with an oncological disease, comprising administering to the patient a therapeutically effective amount of an agent that specifically targets one or more of the second, third, fourth or fifth subdomains (EC2, ECZ, EC4 and EC5, respectively) of soluble E-cadherin (sEcad ), but not on the first subdomain (EC1) sEcad. 2. A method according to claim 1, characterized in that the agent specifically targets EC4 and / or EC5.3. The method of claim 2, wherein the agent specifically targets EC4.4. The method of claim 2, wherein the agent specifically targets EC5.5. The method of claim 1, wherein the agent is a framework protein. The method of claim 5, wherein the scaffold protein is an antibody or fragment thereof that specifically binds to an epitope containing amino acid residues in one or more of the subdomains of EC2, EC3, EC4 and EC5 of the sEcad protein, but not in the EC1 sEcad subdomain .7. A method according to claim 6, characterized in that the antibody is a humanized, chimeric or human antibody. The method of claim 6, wherein the antibody is a single chain antibody. The method of claim 6, wherein the antibody is a monoclonal or polyclonal antibody. The method of claim 6, wherein the antibody is a class G immunoglobulin (IgG) or a class M immunoglobulin (IgM). A method according to claim 1, characterized in that the agent contains a detectable label. A method according to claim 1, characterized in that the agent destroys cancer cells expressing E-cadherin and does not kill cancer cells. The method according to p. 12, characterized in that the agent destroys the malignant cells
机译:1.一种治疗患有肿瘤疾病的患者的方法,包括向患者施用治疗有效量的特异性靶向第二,第三,第四或第五亚域(EC2,ECZ,EC4和EC5中的一个或多个)的试剂,分别是可溶性E-钙粘蛋白(sEcad),但不在第一个子域(EC1)sEcad上。 2.根据权利要求1所述的方法,其特征在于,所述药剂特异性地靶向EC4和/或EC5.3。 3.根据权利要求2所述的方法,其中,所述试剂特异性靶向EC4.4。 3.根据权利要求2所述的方法,其中,所述试剂特异性地靶向EC5.5。 2.权利要求1的方法,其中所述试剂是框架蛋白。 6.根据权利要求5所述的方法,其中所述支架蛋白是特异性结合至表位的抗体或其片段,所述表位包含在所述sEcad蛋白的EC2,EC3,EC4和EC5的一个或多个亚域中的氨基酸残基,但不在所述sEcad蛋白的亚域中。 EC1 sEcad子域.7。 7.根据权利要求6所述的方法,其特征在于,所述抗体是人源化,嵌合或人抗体。 7.根据权利要求6所述的方法,其中所述抗体是单链抗体。 7.根据权利要求6所述的方法,其中所述抗体是单克隆或多克隆抗体。 7.根据权利要求6所述的方法,其中所述抗体是G类免疫球蛋白(IgG)或M类免疫球蛋白(IgM)。 2.根据权利要求1所述的方法,其特征在于,所述试剂包含可检测的标记。 2.根据权利要求1所述的方法,其特征在于,所述试剂破坏表达E-钙粘蛋白的癌细胞,并且不杀死癌细胞。根据p的方法。 12,特征在于该药剂破坏了恶性细胞

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