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pubmed-article:9733598pubmed:abstractTextThe activation of the zymogen plasminogen to the serine protease plasmin by urokinase-type (uPA) and tissue-type (tPA) plasminogen activators (PA) is an important event in a variety of physiologic and pathophysiologic processes in mammals. Enhanced PA activity occurs during angiogenesis and has been correlated in vitro and in vivo with increased tumor aggressiveness and is an indicator of poor prognosis in a variety of tumors in humans. Preliminary studies suggest that the antiulcer drug irsogladine maleate (IM) diminishes PA activity in vitro and may inhibit angiogenesis in vivo. To define the precise mechanism of angiogenesis inhibition by IM in vivo, we tested the ability of IM to blunt angiogenesis in a mouse cornea neovascularization model performed in wild-type and PA-knockout mice.lld:pubmed
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pubmed-article:9733598pubmed:authorpubmed-author:RenC JCJlld:pubmed
pubmed-article:9733598pubmed:copyrightInfoCopyright 1998 Academic Press.lld:pubmed
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pubmed-article:9733598pubmed:pagination126-31lld:pubmed
pubmed-article:9733598pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:9733598pubmed:articleTitleIrsogladine maleate inhibits angiogenesis in wild-type and plasminogen activator-deficient mice.lld:pubmed
pubmed-article:9733598pubmed:affiliationDepartment of Surgery, New York University School of Medicine, New York, New York, 10016, USA.lld:pubmed
pubmed-article:9733598pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9733598pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:9733598pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed