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Authordc.contributor.authorCampolina Silva, Gabriel 
Authordc.contributor.authorWerneck Gomes, Hipacia 
Authordc.contributor.authorBruna T., María 
Authordc.contributor.authorBarata, María C. 
Authordc.contributor.authorTorres, María José 
Authordc.contributor.authorContreras Muñoz, Héctor 
Authordc.contributor.authorMahecha, Germana 
Authordc.contributor.authorOliveira, Cleida 
Admission datedc.date.accessioned2020-04-01T23:02:20Z
Available datedc.date.available2020-04-01T23:02:20Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationLife Sciences Volume 242, 1 February 2020es_ES
Identifierdc.identifier.issn0024-3205
Identifierdc.identifier.other10.1016/j.lfs.2019.117149
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/173798
Abstractdc.description.abstractAims: The purpose of this study was to describe a suitable experimental model for studying aging-related prostate disorders including cancer. Materials and methods: 12-month old Wistar rats were kept in control conditions (n = 12) or treated (n = 16) for 6 months with Silastic implants filled with testosterone (T) and estradiol (E-2). After the experiment period (at 18 months of age), animals were euthanized and the prostate and other organs were harvested, dissected, weighed, and processed for morphological, ultrastructural and molecular analyses. Key findings: We demonstrated that male rats of Wistar strain nicely recapitulate the carcinogenesis process taking place in the aging prostate through the arising of benign, precancerous and malignant lesions, and above all yields a modest incidence of spontaneous PCa (similar to 36%). Moreover, our results highlight that 100% incidence of PCa and precancerous lesions such as prostatic intraepithelial neoplasia and proliferative inflammatory atrophy were achieved in this rat strain after T + E-2 treatment, without changing the broad spectrum of changes that naturally emerge in the prostate at advanced ages. Such enhancement of precancerous lesions and tumors was linked to a decreased expression of E-cadherin and beta-catenin in parallel with an increase in Vimentin and N-cadherin, hallmark modifications of epithelial-mesenchymal transition. Significance: Our findings provide solid evidence that aged Wistar rats may be an excellent model for studies regarding human prostate biology and related disorders including canceres_ES
Patrocinadordc.description.sponsorshipNational Council for Scientific and Technological Development (CNPq) Minas Gerais State Research Foundation (FAPEMIG) CAPESes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevieres_ES
Sourcedc.sourceLife Scienceses_ES
Keywordsdc.subjectProstate lesionses_ES
Keywordsdc.subjectAdenocarcinomaes_ES
Keywordsdc.subjectAginges_ES
Keywordsdc.subjectAndrogen:estrogen imbalancees_ES
Keywordsdc.subjectWistar rates_ES
Títulodc.titleTargeting wistar rat as a model for studying benign, premalignant and malignant lesions of the prostatees_ES
Document typedc.typeArtículo de revistaes_ES
dcterms.accessRightsdcterms.accessRightsAcceso a solo metadatoses_ES
Catalogueruchile.catalogadorapces_ES
Indexationuchile.indexArtículo de publicación ISI
Indexationuchile.indexArtículo de publicación SCOPUS


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