发明公开
EP1705184A1 Treatment of neoplastic diseases using a combination of plasminogen activators and sulfhydryl donors
失效
使用纤溶酶原激活剂和Sulfhydryldonoren的组合肿瘤性疾病的治疗
- 专利标题: Treatment of neoplastic diseases using a combination of plasminogen activators and sulfhydryl donors
- 专利标题(中): 使用纤溶酶原激活剂和Sulfhydryldonoren的组合肿瘤性疾病的治疗
-
申请号: EP06112574.6申请日: 1997-09-17
-
公开(公告)号: EP1705184A1公开(公告)日: 2006-09-27
- 发明人: SOFF, Gerald , Gatley, Stephen T. , Twardowski, Przemyslaw
- 申请人: Northwestern University
- 申请人地址: 1801 Maple Avenue Evanston, Illinois 60201-3135 US
- 专利权人: Northwestern University
- 当前专利权人: Northwestern University
- 当前专利权人地址: 1801 Maple Avenue Evanston, Illinois 60201-3135 US
- 代理机构: TBK-Patent
- 优先权: US710305 19960917
- 主分类号: C07K14/00
- IPC分类号: C07K14/00 ; A61K38/00 ; C07K14/47 ; C12N9/68 ; A61K38/48 ; C12N9/72
摘要:
The invention provides methods of generating angiostatin in vitro comprising contacting plasminogen with a plasminogen activator and a sulfhydryl donor or contacting plasmin with a sulfhydryl donor. The invention also provides a method of treating angiogenic diseases by administering to an animal suffering from such a disease a sulfhydryl donor and, optionally, a plasminogen activator, plasminogen or plasmin. The invention further comprises a composition for generating angiostatin comprising a sulfhydryl donor and a plasminogen activator. The invention also provides a container holding a sulfhydryl donor and/or a plasminogen activator, said container having a label thereon instructing administration of the sulfhydryl donor and/or plasminogen activator to an animal suffering from an angiogenic disease. The invention further provides plasminogen fragments-whose N-terminal amino acid is the same as that of plasmin and whose C-terminal amino acid is located in kringle 5 and which inhibit angiogenesis, antibodies which bind selectively to these fragments, methods and kits for using the antibodies, methods and materials for making the fragments by recombinant DNA techniques, and a method of treating an angiogenic disease comprising administering an effective amount of one of the fragments. Finally, the invention provides a method of treating an angiogenic disease comprising administering a transgene coding for one of the fragments.
信息查询