Please use this identifier to cite or link to this item: http://hdl.handle.net/1843/60893
Type: Artigo de Periódico
Title: Intra-tumor genetic heterogeneity in wilms? tumor samples
Authors: Paulo a. Faria
Bruna m. de sá Pereira
Rafaela Montalvão de Azevedo
Joaquim Caetano de Aguirre Neto
Clarice Franco Menezes
Karla Emilia de sa Rodrigues
Beatriz de Camargo
Mariana Maschietto
Abstract: Childhood renal tumors account for ~7% of all childhood cancers, and most cases are embryonic Wilms’ tumors (WT). Children with WT are usually treated by either COG or SIOP. The later treats the children using preoperative chemotherapy, but both have around 90% of overall survival in five years. WT is a genetically heterogeneous group with a low prevalence of known somatic alterations. Only around 30% of the cases present mutation in known genes, and there is a relatively high degree of intra-tumor genetic heterogeneity (ITGH). Besides potentially having an impact on the clinical outcome of patients, ITGH may interfere with the search for molecular markers that are prospectively being tested by COG and SIOP. In this review, we present the proposal of the current UMBRELLA SIOP Study 2017/Brazilian Renal Tumor Group that requires the multi-sampling collection of each tumor to better evaluate possible molecular markers, as well as to understand WT biology
Subject: Wilms tumor
Biomarkers
Genetic Heterogeneity
language: eng
metadata.dc.publisher.country: Brasil
Publisher: Universidade Federal de Minas Gerais
Publisher Initials: UFMG
metadata.dc.publisher.department: MED - DEPARTAMENTO DE PEDIATRIA
Rights: Acesso Aberto
metadata.dc.identifier.doi: 10.1590/1806-9282.65.12.1496
URI: http://hdl.handle.net/1843/60893
Issue Date: 2019
metadata.dc.url.externa: https://doi.org/10.1590/1806-9282.65.12.1496
metadata.dc.relation.ispartof: Revista da Associação Médica Brasileira
Appears in Collections:Artigo de Periódico

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