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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2010-1-14
pubmed:abstractText
Ovarian carcinoma is the leading cause of death among gynecologic cancers. Although transformation of the outer ovarian epithelium was linked with ovulation, the disease is significantly more prevalent and severe in postmenopausal women. We postulated that menopause could augment ovarian cancer progression through the effects of gonadotropins on multifocal seeding to the mesothelial layer lining the peritoneum. This seeding is mediated by integrins as well as by CD44 interaction with hyaluronan (HA). Here, we report the effect of gonadotropins on HA synthesis and degradation and on peritoneal adhesion. A significant concentration- and time-dependent induction in expression levels of HA synthases (HASs) and hyaluronidases (Hyals) was observed in vitro on stimulation of human epithelial ovarian carcinoma cells by gonadotropins. Hormonal regulation of HA-mediated adhesion was manifested in vivo as well, by fluorescence microscopy of stained MLS multicellular tumor spheroids. The number of spheroids adhered to the mesothelium of ovariectomized CD-1 nude mice 9.5 hours after intraperitoneal insertion was significantly higher than in nonovariectomized mice. Inhibition of HA synthesis by 6-diazo-5-oxo-1-norleucine (DON) both in spheroids and ovariectomized mice significantly reduced the number of adhered spheroids. Thus, the change in the hormonal environment during menopause assists in HA-dependent adherence of ovarian cancer spheroids onto the peritoneum. However, HA is antiangiogenic and it can significantly suppress tumor progression. Accordingly, angiogenesis of the adhered spheroids was significantly elevated in DON-treated tumors. These results can explain the selective pressure that can lead to simultaneously increased tumor expression of both HASs and Hyals.
pubmed:grant
pubmed:commentsCorrections
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pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1476-5586
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
51-60
pubmed:dateRevised
2011-9-26
pubmed:meshHeading
pubmed-meshheading:20072653-Humans, pubmed-meshheading:20072653-Animals, pubmed-meshheading:20072653-Mice, pubmed-meshheading:20072653-Follicle Stimulating Hormone, pubmed-meshheading:20072653-Gonadotropins, pubmed-meshheading:20072653-Ovariectomy, pubmed-meshheading:20072653-Hyaluronoglucosaminidase, pubmed-meshheading:20072653-Peritoneum, pubmed-meshheading:20072653-Hyaluronic Acid, pubmed-meshheading:20072653-Ovarian Neoplasms, pubmed-meshheading:20072653-Female, pubmed-meshheading:20072653-Microscopy, Fluorescence, pubmed-meshheading:20072653-Luteinizing Hormone, pubmed-meshheading:20072653-Antimetabolites, Antineoplastic, pubmed-meshheading:20072653-Diazooxonorleucine, pubmed-meshheading:20072653-Neovascularization, Pathologic, pubmed-meshheading:20072653-Dose-Response Relationship, Drug, pubmed-meshheading:20072653-Cell Adhesion, pubmed-meshheading:20072653-Glucuronosyltransferase, pubmed-meshheading:20072653-Cell Line, Tumor
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