Registro completo |
Provedor de dados: |
BJMBR
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País: |
Brazil
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Título: |
The consensus sequence of FAMLF alternative splice variants is overexpressed in undifferentiated hematopoietic cells
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Autores: |
Chen,W.L.
Luo,D.F.
Gao,C.
Ding,Y.
Wang,S.Y.
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Data: |
2015-07-01
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Ano: |
2015
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Palavras-chave: |
FAMLF
Gene expression
Leukemia
Real-time polymerase chain reaction
Alternative splicing
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Resumo: |
The familial acute myeloid leukemia related factor gene (FAMLF) was previously identified from a familial AML subtractive cDNA library and shown to undergo alternative splicing. This study used real-time quantitative PCR to investigate the expression of the FAMLF alternative-splicing transcript consensus sequence (FAMLF-CS) in peripheral blood mononuclear cells (PBMCs) from 119 patients with de novo acute leukemia (AL) and 104 healthy controls, as well as in CD34+ cells from 12 AL patients and 10 healthy donors. A 429-bp fragment from a novel splicing variant of FAMLF was obtained, and a 363-bp consensus sequence was targeted to quantify total FAMLF expression. Kruskal-Wallis, Nemenyi, Spearman's correlation, and Mann-Whitney U-tests were used to analyze the data. FAMLF-CS expression in PBMCs from AL patients and CD34+ cells from AL patients and controls was significantly higher than in control PBMCs (P<0.0001). Moreover, FAMLF-CS expression in PBMCs from the AML group was positively correlated with red blood cell count (rs =0.317, P=0.006), hemoglobin levels (rs =0.210, P=0.049), and percentage of peripheral blood blasts (rs =0.256, P=0.027), but inversely correlated with hemoglobin levels in the control group (rs =–0.391, P<0.0001). AML patients with high CD34+ expression showed significantly higher FAMLF-CS expression than those with low CD34+ expression (P=0.041). Our results showed that FAMLF is highly expressed in both normal and malignant immature hematopoietic cells, but that expression is lower in normal mature PBMCs.
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Tipo: |
Info:eu-repo/semantics/article
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Idioma: |
Inglês
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Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2015000700603
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Editor: |
Associação Brasileira de Divulgação Científica
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Relação: |
10.1590/1414-431x20154430
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Formato: |
text/html
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Fonte: |
Brazilian Journal of Medical and Biological Research v.48 n.7 2015
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Direitos: |
info:eu-repo/semantics/openAccess
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