Matches in SemOpenAlex for { <https://semopenalex.org/work/W2184178464> ?p ?o ?g. }
- W2184178464 abstract "Background: In order to unravel the interactions between the epithelium and the extra cellular matrix (ECM) in breast tissue progressing to cancer, it is necessary to understand the relevant interactions in healthy tissue under normal physiologic settings. Proteoglycans in the ECM play an important role in the signaling between the different tissue compartments. The proteoglycan decorin is abundant in the breast stroma. Decreased expression in breast cancer tissue is a sign of a poor tumor prognosis. The heparane sulphate proteoglycans syndecan-1 and syndecan-4 promote the integration of cellular adhesion and proliferation. The aim of this study was to investigate the gene expression and location of decorin, syndecan-1 and syndecan-4 in the healthy breast during the menstrual cycle. Methods: Tissue from healthy women undergoing breast reduction plastic surgery was examined using immunohistochemistry (n = 38) and Real-Time RT-PCR (n = 20). Both parous and nulliparous women were eligible and the mean age of the women was 34(+/- 10 years) with regular menstrual cycles (28 +/- 7 days). None of the women had used hormonal treatment the last three months. The women were randomized to needle biopsy two months before the operation in the follicular or luteal menstrual phase and for another biopsy at the operation in the opposite phase. Serum samples were obtained to characterize the menstrual phase. The Wilcoxon signed rank test and Mann Whitney test were used for statistical analyses. Results: By real time-RT-PCR the gene signal for all three proteoglycans; decorin (p = 0.02) and syndecan-1 (p = 0.03) and syndecan-4 (p = 0.02) was significantly lower among parous women in the luteal phase than in the follicular phase. Immunohistochemistry confirmed the identification of the proteins but no significant difference between menstrual phases was observed. Serum samples verified the menstrual phase. Conclusions: Our study shows, for the first time in the healthy breast, a significantly lower expression of the genes for the three proteoglycans, decorin, syndecan-1 and syndecan-4 in the luteal phase during the menstrual cycle. These changes were registered under normal physiologic conditions. Since ECM molecules appear to be involved in tumor progression, these findings in the normal breast could constitute a base for further studies in women receiving hormonal therapy or those with breast cancer." @default.
- W2184178464 created "2016-06-24" @default.
- W2184178464 creator A5001622608 @default.
- W2184178464 creator A5033525822 @default.
- W2184178464 creator A5067455186 @default.
- W2184178464 creator A5087791278 @default.
- W2184178464 date "2010-01-01" @default.
- W2184178464 modified "2023-09-27" @default.
- W2184178464 title "decorin in healthy human breast tissue during the menstrual cycle" @default.
- W2184178464 cites W1765183309 @default.
- W2184178464 cites W1779232475 @default.
- W2184178464 cites W178734214 @default.
- W2184178464 cites W1804236737 @default.
- W2184178464 cites W1968428572 @default.
- W2184178464 cites W1970855600 @default.
- W2184178464 cites W1974531415 @default.
- W2184178464 cites W2009219948 @default.
- W2184178464 cites W2021467798 @default.
- W2184178464 cites W2046153681 @default.
- W2184178464 cites W2047384838 @default.
- W2184178464 cites W2061273916 @default.
- W2184178464 cites W2063797073 @default.
- W2184178464 cites W2067552124 @default.
- W2184178464 cites W2069788438 @default.
- W2184178464 cites W2070072418 @default.
- W2184178464 cites W2083106832 @default.
- W2184178464 cites W2084578643 @default.
- W2184178464 cites W2087307762 @default.
- W2184178464 cites W2089924725 @default.
- W2184178464 cites W2101886409 @default.
- W2184178464 cites W2161742564 @default.
- W2184178464 cites W2163592418 @default.
- W2184178464 cites W2167629024 @default.
- W2184178464 cites W2169829977 @default.
- W2184178464 cites W2414496327 @default.
- W2184178464 hasPublicationYear "2010" @default.
- W2184178464 type Work @default.
- W2184178464 sameAs 2184178464 @default.
- W2184178464 citedByCount "0" @default.
- W2184178464 crossrefType "journal-article" @default.
- W2184178464 hasAuthorship W2184178464A5001622608 @default.
- W2184178464 hasAuthorship W2184178464A5033525822 @default.
- W2184178464 hasAuthorship W2184178464A5067455186 @default.
- W2184178464 hasAuthorship W2184178464A5087791278 @default.
- W2184178464 hasConcept C105702510 @default.
- W2184178464 hasConcept C121608353 @default.
- W2184178464 hasConcept C126322002 @default.
- W2184178464 hasConcept C143228043 @default.
- W2184178464 hasConcept C1491633281 @default.
- W2184178464 hasConcept C187785154 @default.
- W2184178464 hasConcept C2775934546 @default.
- W2184178464 hasConcept C2779058012 @default.
- W2184178464 hasConcept C2779335624 @default.
- W2184178464 hasConcept C2779794767 @default.
- W2184178464 hasConcept C2780550940 @default.
- W2184178464 hasConcept C530470458 @default.
- W2184178464 hasConcept C54355233 @default.
- W2184178464 hasConcept C65001120 @default.
- W2184178464 hasConcept C71315377 @default.
- W2184178464 hasConcept C71924100 @default.
- W2184178464 hasConcept C86803240 @default.
- W2184178464 hasConceptScore W2184178464C105702510 @default.
- W2184178464 hasConceptScore W2184178464C121608353 @default.
- W2184178464 hasConceptScore W2184178464C126322002 @default.
- W2184178464 hasConceptScore W2184178464C143228043 @default.
- W2184178464 hasConceptScore W2184178464C1491633281 @default.
- W2184178464 hasConceptScore W2184178464C187785154 @default.
- W2184178464 hasConceptScore W2184178464C2775934546 @default.
- W2184178464 hasConceptScore W2184178464C2779058012 @default.
- W2184178464 hasConceptScore W2184178464C2779335624 @default.
- W2184178464 hasConceptScore W2184178464C2779794767 @default.
- W2184178464 hasConceptScore W2184178464C2780550940 @default.
- W2184178464 hasConceptScore W2184178464C530470458 @default.
- W2184178464 hasConceptScore W2184178464C54355233 @default.
- W2184178464 hasConceptScore W2184178464C65001120 @default.
- W2184178464 hasConceptScore W2184178464C71315377 @default.
- W2184178464 hasConceptScore W2184178464C71924100 @default.
- W2184178464 hasConceptScore W2184178464C86803240 @default.
- W2184178464 hasLocation W21841784641 @default.
- W2184178464 hasOpenAccess W2184178464 @default.
- W2184178464 hasPrimaryLocation W21841784641 @default.
- W2184178464 hasRelatedWork W1685023024 @default.
- W2184178464 hasRelatedWork W1980036776 @default.
- W2184178464 hasRelatedWork W1980164142 @default.
- W2184178464 hasRelatedWork W2037516070 @default.
- W2184178464 hasRelatedWork W2046153681 @default.
- W2184178464 hasRelatedWork W2075872572 @default.
- W2184178464 hasRelatedWork W2104159239 @default.
- W2184178464 hasRelatedWork W2117730961 @default.
- W2184178464 hasRelatedWork W2128541210 @default.
- W2184178464 hasRelatedWork W2186568933 @default.
- W2184178464 hasRelatedWork W2397326594 @default.
- W2184178464 hasRelatedWork W2406940520 @default.
- W2184178464 hasRelatedWork W2465562314 @default.
- W2184178464 hasRelatedWork W2744055111 @default.
- W2184178464 hasRelatedWork W2949470442 @default.
- W2184178464 hasRelatedWork W3142859624 @default.
- W2184178464 hasRelatedWork W3163811744 @default.
- W2184178464 hasRelatedWork W3211002271 @default.
- W2184178464 hasRelatedWork W3214070997 @default.