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Published on: October 19, 2014
[Relation between Bcl-2 protein expression and results of therapy in patients with acute myeloblastic leukemia]
E Tóthová1, N Stecová, A Kafková
1Klinika hematológie Lekárskej fakulty UPJS a FNsP, Kosice, Slovenská republika.
Insights
High Bcl-2 protein expression in acute myeloblastic leukemia (AML) correlates with poorer treatment outcomes. This finding suggests Bcl-2 and CD34 expression are key prognostic factors for complete remission in AML patients.
Area of Science:
- Hematology
- Immunology
- Molecular Biology
Context:
- Acute myeloblastic leukemia (AML) is a heterogeneous hematologic malignancy.
- Understanding the molecular markers associated with AML prognosis is crucial for effective treatment strategies.
- Bcl-2 protein plays a significant role in apoptosis and cell survival.
Purpose:
- To investigate the expression levels of Bcl-2 protein in newly diagnosed AML patients.
- To correlate Bcl-2 expression with French-American-British (FAB) subtypes, CD34 expression, and clinical outcomes.
- To identify potential prognostic factors for achieving complete remission (CR) in AML.
Summary:
- Flow cytometry analysis of 67 AML patients revealed heterogeneous Bcl-2 protein expression (mean 81%).
- Higher Bcl-2 expression and Mean Fluorescence Index (MFI) were observed in M0 and M1 FAB subtypes compared to M4 and M5.
- Bcl-2 MFI significantly correlated with CD34 positivity and MFI.
- High Bcl-2 expression (≥20% positive cells) was associated with a lower complete remission rate (40.4%) compared to low expression (<20% positive cells, 72%).
Impact:
- Bcl-2 protein expression and CD34 positivity are identified as independent prognostic factors for achieving complete remission in AML.
- These findings may aid in risk stratification and personalized treatment approaches for AML patients.
- Further research into targeting Bcl-2 pathways could offer new therapeutic avenues for AML.
Abstract:
Flow cytometric expression of Bcl-2 protein was analyzed in 67 newly diagnosed acute myeloblastic leukemia (AML) patients using an anti-Bcl-2 monoclonal antibody by direct immunofluorescence technique and result were correlated with FAB subtype, CD34 expression and clinical outcome. The number of Bcl-2+ cells in each sample was heterogenous (range, 19% to 96%), with mean of 81%. The percentage of Bcl-2+ cells was higher in M0 and M1 types according French-American-British classification. The mean fluorescence index (MFI), expressed as the ratio of sample channel: control mean channel was significantly higher (p < 0.01) in M0 (19.0) and M1 (17.6) than M4 (11.7) and M5 (8.9) cytotypes. In addition, Bcl-2 MFI significantly correlated both with CD34 positivity and with CD34 MFI. High percentage expression of Bcl-2 and MFI index of Bcl 2 was associated with a low complete remission rate after intensive chemotherapy (40.4% in cases with 20% and more positive cells vs 72% in cases with less than 20% positive cells). By statistical analysis we also demonstrated that both Bcl-2 high MFI (> 16) and CD34 expression are independent prognostic factors for achieving CR in AML.
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