Source:http://linkedlifedata.com/resource/pubmed/id/21247731
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2011-2-21
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pubmed:abstractText |
Endometriosis is one of the most common gynecological diseases in women of reproductive age. Although cyclooxygenase (COX)-2 inhibitors are effective in the treatment of endometriosis, the adverse cardiovascular effects associated with these inhibitors have limited their use. Microsomal prostaglandin E synthase-1 (mPGES-1) is an inducible enzyme downstream of COX-2 in prostaglandin E(2) biosynthesis. Previously, we developed mPGES-1 knockout mice (mPGES-1(-/-)) and have identified for the first time the roles of ectopic lesion- and host-associated mPGES-1 in angiogenesis and the growth of endometrial tissues. When mPGES-1(-/-) endometrial fragments were implanted into wild type (WT) mice (mPGES-1(-/-)?WT), or WT fragments implanted into mPGES-1(-/-) mice (WT?mPGES-1(-/-)), the growth of the implants was suppressed at days 14 and 28 after implantation, compared toWT?WT transplantation. An even greater degree of suppression was observed in mPGES-1(-/-) endometrial fragments implanted into mPGES-1(-/-) mice (mPGES-1(-/-)?mPGES-1(-/-)). After WT-WT implantation, mPGES-1 expression was localized at the border of the implanted endometrial tissues. Microvessel density, determined by CD31 immunostaining, was markedly suppressed in the mPGES-1(-/-) endometrial fragments implanted into mPGES-1(-/-) mice, with some suppression also observed in the mPGES-1(-/-)?WT and WT?mPGES-1(-/-) groups. The expression of vascular endothelial growth factor (VEGF-A) was significantly reduced in mPGES-1(-/-) endometrial tissues implanted into mPGES-1(-/-) mice at days 14 and 28, in comparison to the WT?WT group. These results suggested that mPGES-1 enhanced angiogenesis and growth of the endometrial implant, and indicate that mPGES-1 may be a good therapeutic target for endometriosis.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cyclooxygenase 2,
http://linkedlifedata.com/resource/pubmed/chemical/Intramolecular Oxidoreductases,
http://linkedlifedata.com/resource/pubmed/chemical/Ptgs2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A,
http://linkedlifedata.com/resource/pubmed/chemical/prostaglandin-E synthase
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1950-6007
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2010. Published by Elsevier SAS.
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pubmed:issnType |
Electronic
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pubmed:volume |
65
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
77-84
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pubmed:meshHeading |
pubmed-meshheading:21247731-Animals,
pubmed-meshheading:21247731-Cyclooxygenase 2,
pubmed-meshheading:21247731-Endometriosis,
pubmed-meshheading:21247731-Endometrium,
pubmed-meshheading:21247731-Female,
pubmed-meshheading:21247731-Intramolecular Oxidoreductases,
pubmed-meshheading:21247731-Mice,
pubmed-meshheading:21247731-Mice, Inbred C57BL,
pubmed-meshheading:21247731-Models, Animal,
pubmed-meshheading:21247731-Neovascularization, Physiologic,
pubmed-meshheading:21247731-Vascular Endothelial Growth Factor A
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pubmed:year |
2011
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pubmed:articleTitle |
The inducible prostaglandin E synthase mPGES-1 regulates growth of endometrial tissues and angiogenesis in a mouse implantation model.
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pubmed:affiliation |
Department of Pharmacology, Kitasato University School of Medicine, Kanagawa 252-0374, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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