Diabetes induces stromal remodelling and increase in chondroitin sulphate proteoglycans of the rat ventral prostate

dc.contributor.authorRibeiro, Daniele Lisboa
dc.contributor.authorTaboga, Sebastiao Roberto
dc.contributor.authorGoes, Rejane Maira [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.date.accessioned2014-05-20T14:01:03Z
dc.date.available2014-05-20T14:01:03Z
dc.date.issued2009-08-01
dc.description.abstractP>Extracellular matrix (ECM) remodelling is an important process involved in prostate cancer progression. Alterations in ECM caused by diabetes in different tissues such as kidney is well described; however, it is poorly investigated in prostate. The aim of this study was to evaluate changes in ECM of rat prostate showing gland atrophy caused by diabetes and their implications in development of malignant lesions. Diabetes was induced in Wistar rats using alloxan (45 mg/kg bw). After 90 days of diabetes onset, animals were killed and ventral prostate was removed and prepared for light microscopy following immunoreaction for fibronectin, chondroitin sulphate and Picrossirius staining for collagen fibres. Proteoglycans (PG) were identified at transmission electron microscopy after fixation with Cuprolinic Blue. Diabetes led to a thickening of 25% in the acinar basement membrane accompanied by increase and disorganization of its proteoglycans (P1). Three additional populations of prostatic stromal PGs were identified: collagen fibril linked (P2) and interstitial (P3) and (P4) PGs. Diabetes increased P3 and mainly P4 which had higher dimension and accumulated around the smooth muscle cells. In addition, an increase in chondrotin sulphate (33%, mainly in sites where P4 were noted) and collagen (44%) was noted in diabetic rats, whereas fibronectin did not change. Atrophic changes observed in rat ventral prostate after diabetes are accompanied by stromal remodelation related to increase in collagen and chondroitin sulphate proteoglycans. Thus, diabetes can promote a stromal microenvironment rich in elements that could favour cell migration, proliferation and pathological process.en
dc.description.affiliationSão Paulo State Univ, Dept Biol, Ibilce, Inst Biosci Letters & Exact Sci,Unesp, BR-15054000 São Paulo, Brazil
dc.description.affiliationUniv Estadual Campinas, UNICAMP, Dept Cell Biol, Inst Biol, São Paulo, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Dept Biol, Ibilce, Inst Biosci Letters & Exact Sci,Unesp, BR-15054000 São Paulo, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 06/07008-3
dc.format.extent400-411
dc.identifierhttp://dx.doi.org/10.1111/j.1365-2613.2009.00657.x
dc.identifier.citationInternational Journal of Experimental Pathology. Malden: Wiley-blackwell Publishing, Inc, v. 90, n. 4, p. 400-411, 2009.
dc.identifier.doi10.1111/j.1365-2613.2009.00657.x
dc.identifier.issn0959-9673
dc.identifier.lattes1445259468526188
dc.identifier.lattes0947193347312157
dc.identifier.orcid0000-0002-0970-4288
dc.identifier.orcid0000-0002-3622-460X
dc.identifier.urihttp://hdl.handle.net/11449/21571
dc.identifier.wosWOS:000268171300003
dc.language.isoeng
dc.publisherWiley-Blackwell Publishing, Inc
dc.relation.ispartofInternational Journal of Experimental Pathology
dc.relation.ispartofjcr1.938
dc.relation.ispartofsjr0,712
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectchodroitin sulphateen
dc.subjectCollagenen
dc.subjectDiabetesen
dc.subjectProstateen
dc.subjectproteoglycansen
dc.titleDiabetes induces stromal remodelling and increase in chondroitin sulphate proteoglycans of the rat ventral prostateen
dc.typeArtigo
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-406071.html
dcterms.rightsHolderWiley-blackwell Publishing, Inc
unesp.author.lattes1445259468526188
unesp.author.lattes0947193347312157[3]
unesp.author.orcid0000-0002-0970-4288[2]
unesp.author.orcid0000-0002-3622-460X[3]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Biociências Letras e Ciências Exatas, São José do Rio Pretopt

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