Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:dateCreated
2001-1-17
pubmed:abstractText
A key mechanism underlying the cyclical growth of the endometrium is its ability to regenerate a vascular capillary network. In normal cycling human endometrium, angiogenesis is influenced by both endocrine and paracrine factors. Hormonal manipulation of the endometrium, such as that occurring during the use of steroidal contraception, appears to result in capillary proliferation and fragility. As a consequence of these vascular changes, contraceptive users may be predisposed to unpredictable uterine bleeding, which is responsible for the high frequency of contraceptive discontinuation. In this paper we address mechanisms responsible for vascular endothelial cell proliferation in normal and contraceptive steroid-exposed endometria. We propose that regulation of endometrial angiogenesis is mediated indirectly, via steroid and cytokine actions on vascular endothelial growth factor (VEGF), and we present data indicating that VEGF expression in normal endometrial stromal cells is increased by oestrogens and progestins. Three proinflammatory cytokines with angiogenic effects in other systems (i.e. interleukin-1beta, tumour necrosis factor-alpha and interferon-gamma) do not appear to up-regulate VEGF expression in normal endometrial stromal cells. Well-characterized in-vitro models in conjunction with immunohistochemistry provide useful experimental systems to study endometrial neovascularization under physiological conditions and in those potentially perturbed via the use of contraceptive steroids.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Contraceptives, Oral, Hormonal, http://linkedlifedata.com/resource/pubmed/chemical/Cytokines, http://linkedlifedata.com/resource/pubmed/chemical/Endothelial Growth Factors, http://linkedlifedata.com/resource/pubmed/chemical/Estradiol, http://linkedlifedata.com/resource/pubmed/chemical/Estrogens, http://linkedlifedata.com/resource/pubmed/chemical/Gonadotropin-Releasing Hormone, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/Lymphokines, http://linkedlifedata.com/resource/pubmed/chemical/Medroxyprogesterone Acetate, http://linkedlifedata.com/resource/pubmed/chemical/Progestins, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A, http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factors
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0268-1161
pubmed:author
pubmed:issnType
Print
pubmed:volume
15 Suppl 3
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
67-77
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11041223-Biopsy, pubmed-meshheading:11041223-Cells, Cultured, pubmed-meshheading:11041223-Contraceptives, Oral, Hormonal, pubmed-meshheading:11041223-Cytokines, pubmed-meshheading:11041223-Endometrium, pubmed-meshheading:11041223-Endothelial Growth Factors, pubmed-meshheading:11041223-Estradiol, pubmed-meshheading:11041223-Estrogens, pubmed-meshheading:11041223-Female, pubmed-meshheading:11041223-Gonadotropin-Releasing Hormone, pubmed-meshheading:11041223-Hormone Replacement Therapy, pubmed-meshheading:11041223-Humans, pubmed-meshheading:11041223-Immunohistochemistry, pubmed-meshheading:11041223-Interleukin-1, pubmed-meshheading:11041223-Lymphokines, pubmed-meshheading:11041223-Medroxyprogesterone Acetate, pubmed-meshheading:11041223-Menstrual Cycle, pubmed-meshheading:11041223-Neovascularization, Physiologic, pubmed-meshheading:11041223-Progestins, pubmed-meshheading:11041223-RNA, Messenger, pubmed-meshheading:11041223-Stromal Cells, pubmed-meshheading:11041223-Vascular Endothelial Growth Factor A, pubmed-meshheading:11041223-Vascular Endothelial Growth Factors
pubmed:year
2000
pubmed:articleTitle
Ovarian steroid and cytokine modulation of human endometrial angiogenesis.
pubmed:affiliation
Department of Obstetrics, Gynecology and Reproductive Sciences, University of California, San Francisco 94143-0556, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.