Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/43095
Title: Prognostic significance of BCR-ABL rearrangement in chronic myeloid leukemia
Authors: Colleoni, Gisele Wally Braga [UNIFESP]
Costa, F. F.
Grignolli, CRE
Silva, R. S.
Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]
Kerbauy, José [UNIFESP]
Saad, Sara Teresinha Olalla [UNIFESP]
Universidade Estadual de Campinas (UNICAMP)
Universidade Federal de São Paulo (UNIFESP)
Keywords: chronic myeloid leukemia
philadelphia chromosome
polymerase chain reaction
BCR-ABL rearrangement
Issue Date: 1-Oct-1996
Publisher: Assoc Bras Divulg Cientifica
Citation: Brazilian Journal Of Medical And Biological Research. Sao Paulo: Assoc Bras Divulg Cientifica, v. 29, n. 10, p. 1307-1310, 1996.
Abstract: Chronic myeloid leukemia (CML) is a myeloproliferative disorder characterized by the presence of a reciprocal translocation between chromosomes 9 and 22 in at least 95% of cases. At the molecular level, this translocation results in the activation of the ABL oncogene of chromosome 9, which becomes contiguous with the 5' end of the BCR gene on chromosome 22. The breakpoint usually occurs between exons 2 and 3 (b2-a2 rearrangement), or 3 and 4 (b3-a2 rearrangement) of the major breakpoint cluster region (M-BCR) of the BCR gene. The aim of the present study was to characterize the type of BCR-ABL transcript in 32 patients with CML using the reverse transcriptase-polymerase chain reaction (RT-PCR) and to determine if this type of rearrangement is related to the survival of the patients. Our results confirmed that RT-PCR is more sensitive than cytogenetic analysis for identifying the Philadelphia (Ph1) chromosome (96.9% vs 79.3%). The frequencies of b2-a2 and b3-a2 rearrangements were 28.1% and 65.7%, respectively. The survival of patients presenting the b2-a2 or the b3-a2 rearrangement was not significantly different (P = 0.27750). The data suggest that the type of transcript has no prognostic value for CML patients.
URI: http://repositorio.unifesp.br/11600/43095
ISSN: 0100-879X
Appears in Collections:Artigo

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