Linked Life Data

16524621

Source:http://linkedlifedata.com/resource/pubmed/id/16524621

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SubjectPredicateObjectContext
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pubmed-article:16524621pubmed:dateCreated2006-11-24lld:pubmed
pubmed-article:16524621pubmed:abstractTextVascular intimal carcinomatosis refers to a characteristic tumor proliferation on vascular intima that replaces normal endothelium. This pathological event of unknown cause is quite different from tumor thrombotic microangiopathy due to the absence of thrombi on the tumor cell surfaces. We analyzed renal transitional cell carcinoma cases with metastasis to the main pulmonary arteries and marked hyperfibrino(geno)lysis. The fibrinogen-derived products from patients' plasma were identified as D1A/gamma, D1/gamma, and D1/beta by immunoblotting with the NH2-terminus of the fragment D specific antibody JIF-23. In all cases, the neoplastic cells with vascular intimal carcinomatosis were stained positive for anti-human annexin 2, which is a unique cell surface co-receptor for plasminogen and tissue-type plasminogen activator. In contrast, normal renal pelvic mucosa or renal transitional cell carcinoma without vascular intimal carcinomatosis did not express any annexin 2. The isolated transitional cell carcinoma cells contained annexin 2 mRNA and expressed its protein. Anti-annexin 2 antibody and transfection of annexin 2 small interfering RNA into these carcinoma cells significantly inhibited tissue-type plasminogen activator dependent plasmin generation. These findings suggest that annexin 2 mediated fibrinolysis on the transitional cell carcinoma cells may play a role in inducing hemorrhagic disorder in vascular intimal carcinomatosis.lld:pubmed
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pubmed-article:16524621pubmed:pagination229-40lld:pubmed
pubmed-article:16524621pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:16524621pubmed:year2007lld:pubmed
pubmed-article:16524621pubmed:articleTitleAnnexin 2 and hemorrhagic disorder in vascular intimal carcinomatosis.lld:pubmed
pubmed-article:16524621pubmed:affiliationDivision of Cell and Molecular Medicine, Center for Molecular Medicine, Jichi Medical School, Shimotsuke, Tochigi, Japan.lld:pubmed
pubmed-article:16524621pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16524621pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:16524621pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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