Brazilian Journal of Pharmaceutical Sciences · 2011 · 18 citations · 24 references
Life SciencesHematologyMolecular BiologyApoptosisGene ExpressionImmunogeneticsApoptosis RegulationApoptotic SignalingBcl-2 Family ProteinsApoptotic BiomarkersBcl-2 Family DysregulationBcl-2 Protein ExpressionJak2 MutationsJak2 V617f MutationMutationProapoptotic Bcl-2 ProteinsProtein Expression Biomarkers
Apoptosis deregulation might have a role in the pathophysiology of polycythemia vera (PV). This study evaluated Bcl-2 molecule expression in CD34+ cells and leukocytes in 12 PV patients. Gene expression was investigated by real time PCR using SybrGreen Quantitect kit and protein expression was evaluated by western-blotting. JAK2 V617F mutation was detected according to Baxter et al (2005). CD34+ cells from PV patients presented higher levels of A1 and Mcl-1 expression (median: 22.6 and 5.2, respectively) in comparison with controls (0.9 and 0.5, p=0.004 and p=0.020); while Bcl-2 and Bcl-xL expression decreased in PV patients (0.18 and 1.19) compared with controls (1.39 and 2.01, p=0.006 and p=0.020). CD34+ cells in PV patients showed an elevated Bid expression (14.4) in comparison with healthy subjects (1.0; p=0.002). Patients' leukocytes showed an A1 augmentation (7.41, p=0.001) and a reduced expression of Bax (0.19; p=0.040) and Bad (0.2; p=0.030). There was no correlation between JAK2 V617F allele burden and molecular expression. PV patients showed alterations in Bcl-2 members' expression, which may interfere with control of apoptotic machinery and contribute to disease pathogenesis.
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A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
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