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dc.contributor.authorZaldumbide Dueñas, Laura
dc.contributor.authorErramuzpe Aliaga, Asier
dc.contributor.authorGuarch, Rosa
dc.contributor.authorPulido Murillo, Rafael
dc.contributor.authorCortés Díaz, Jesús María
dc.date.accessioned2016-05-12T14:34:14Z
dc.date.available2016-05-12T14:34:14Z
dc.date.issued2016-03-08
dc.identifier.citationBMC Cancer 16 : (2015) // Article ID 194es
dc.identifier.issn1471-2407
dc.identifier.urihttp://hdl.handle.net/10810/18243
dc.description.abstractBackground: Intratumor heterogeneity may be responsible of the unpredictable aggressive clinical behavior that some clear cell renal cell carcinomas display. This clinical uncertainty may be caused by insufficient sampling, leaving out of histological analysis foci of high grade tumor areas. Although molecular approaches are providing important information on renal intratumor heterogeneity, a focus on this topic from the practicing pathologist' perspective is still pending. Methods: Four distant tumor areas of 40 organ-confined clear cell renal cell carcinomas were selected for histopathological and immunohistochemical evaluation. Tumor size, cell type (clear/granular), Fuhrman's grade, Staging, as well as immunostaining with Snail, ZEB1, Twist, Vimentin, E-cadherin, beta-catenin, PTEN, p-Akt, p110 alpha, and SETD2, were analyzed for intratumor heterogeneity using a classification and regression tree algorithm. Results: Cell type and Fuhrman's grade were heterogeneous in 12.5 and 60 % of the tumors, respectively. If cell type was homogeneous (clear cell) then the tumors were low-grade in 88.57 % of cases. Immunostaining heterogeneity was significant in the series and oscillated between 15 % for p110a and 80 % for Snail. When Snail immunostaining was homogeneous the tumor was histologically homogeneous in 100 % of cases. If Snail was heterogeneous, the tumor was heterogeneous in 75 % of the cases. Average tumor diameter was 4.3 cm. Tumors larger than 3.7 cm were heterogeneous for Vimentin immunostaining in 72.5 % of cases. Tumors displaying negative immunostaining for both ZEB1 and Twist were low grade in 100 % of the cases. Conclusions: Intratumor heterogeneity is a common event in clear cell renal cell carcinoma, which can be monitored by immunohistochemistry in routine practice. Snail seems to be particularly useful in the identification of intratumor heterogeneity. The suitability of current sampling protocols in renal cancer is discussed.es
dc.description.sponsorshipThe authors thank the excellent immunohistochemical work of Mar Gonzalez, Alicia Esteve, Aida Larranaga and Maria Cruz Andreu, Lab Technicians at the Department of Pathology, Cruces University Hospital, Barakaldo, Bizkaia, Spain. This work was partially funded by grant SAF2013-48812-R from Ministerio de Economia y Competitividad (Spain).es
dc.language.isoenges
dc.publisherBiomed Centrales
dc.relationinfo:eu-repo/grantAgreement/MINECO/SAF2013-48812-R
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.subjectclear cell renal cell carcinomaes
dc.subjectintratumor heterogeneityes
dc.subjectepithelial to mesenchymal transitiones
dc.subjectimmunohistochemistryes
dc.subjectsnailes
dc.subjecttumor samplinges
dc.subjectepithelial mesenchymal transitiones
dc.subjectbeta-catinines
dc.subjectprognostic-significancees
dc.subjectindependent predictores
dc.subjectcancer invasiones
dc.subjectpoor-prognosises
dc.subjectexpressiones
dc.subjectpathwayes
dc.subjectimpactes
dc.titleSnail heterogeneity in clear cell renal cell carcinomaes
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2016 Zaldumbide et al. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise statedes
dc.relation.publisherversionhttp://bmccancer.biomedcentral.com/articles/10.1186/s12885-016-2237-x#Abs1es
dc.identifier.doi10.1186/s12885-016-2237-x
dc.departamentoesBiología celular e histologíaes_ES
dc.departamentoeuZelulen biologia eta histologiaes_ES
dc.subject.categoriaGENETICS AND HEREDITY
dc.subject.categoriaONCOLOGY


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