Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/57719
Type: Artigo de periódico
Title: Molecular and chromosomal mutations among children with B-lineage lymphoblastic leukemia in Brazil's Federal District
Author: Mesquita, DR
Cordoba, JC
Magalhaes, IQ
Cordoba, MS
Oliveira, JRC
Goncalves, A
Ferrari, I
Martins-de-Sa, C
Abstract: Acute lymphoblastic leukemia (ALL) accounts for approximately 80% of all acute leukemias during childhood. Chromosomal anomalies resulting from gene fusion, which are frequent in leukemias, create hybrid transcripts, the great majority of which encode transcription factors. We analyzed 88 pediatric patients (median age 7.3 years) who had B-lineage acute lymphoblastic leukemia (B-ALL), using reverse transcriptase-polymerase chain reaction, to look for gene fusion transcripts of TEL/AML1, E2A/PBX1, BCR/ABL p190, and MLL/AF4. The frequencies of these transcripts were 21.21, 9.68, 3.03, and 0%, respectively. All positive cases had a common B-ALL immunophenotype. The low frequency of the TEL/AML1 transcript that is found in developing countries, such as Brazil, may be due to the low incidence of leukemia; this would support Greaves' hypothesis.
Subject: Acute lymphoblastic leukemia
Cytogenetics
Reverse transcriptase-polymerase chain reaction
Chromosomal anomalies
Hybrid transcripts
Country: Brasil
Editor: Funpec-editora
Rights: fechado
Date Issue: 2009
Appears in Collections:Unicamp - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
WOS000265578600035.pdf352.3 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.