Expression of CREB/Bcl-2 in bone marrow mononuclear cells of children with acute leukemia.
- Author:
Chuan WEN
1
;
Fu-Tian MA
;
Wu-Qing WAN
Author Information
- Publication Type:Journal Article
- MeSH: Acute Disease; Adolescent; Bone Marrow Cells; metabolism; Child; Child, Preschool; Cyclic AMP Response Element-Binding Protein; analysis; genetics; Female; Humans; Infant; Leukemia; metabolism; Male; Proto-Oncogene Proteins c-bcl-2; analysis; genetics; RNA, Messenger; analysis
- From: Chinese Journal of Contemporary Pediatrics 2010;12(3):177-180
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the expression and role of cyclic-AMP response binding protein (CREB) and Bcl-2 in children with acute leukemia.
METHODSNinety-two children with acute leukemia (leukemia group) and 30 children with non-hematologic malignancies (control group) were enrolled. The mRNA and protein expression of CREB and Bcl-2 in bone marrow mononuclear cells were measured by reverse transcriptase polymerase chain reaction (RT-PCR) and Western blot.
RESULTSThe mRNA and protein expression of CREB and Bcl-2 in the leukemia group was significantly higher than that in the control group (p<0.01). There were no significant differences in the expression of CREB and Bcl-2 between acute lymphoblastic leukemia and acute myeloid leukemia subgroups. At the initial diagnosis, the mRNA and protein expression of CREB and Bcl-2 in children with extramedullary infiltration was higher than that in children without (p<0.05). In the leukemia group, the mRNA and protein expression of CREB and Bcl-2 in the complete remission subgroup was significantly lower than that in the non-complete remission subgroup (p<0.01). High mRNA expression of CREB and Bcl-2 in the leukemia group was positively correlated with peripheral blood leucocyte counts (r=0.62, 0.71 respectively, p<0.05). There was a positive correlation between mRNA and protein expression of CREB and Bcl-2 (r=0.75, 0.68 respectively; p<0.05).
CONCLUSIONSThe expression of CREB and Bcl-2 may be correlated with the pathogenesis and clinical prognosis of childhood leukemia, however, their expression may not be associated with the classification of acute leukemia.