1Amina El–Sayed Hussein, 2Nadia A. Sadek, 1Ghoneim HM, 3Nadia El-Sayed Zaki and 4Dekra El-Aghbary
Departments of 1Immunology and 2Hematology, Medical Research Institute and 3Hematology Unit, 4Internal Medicine Department, Faculty of Medicine, Alexandria University, Egypt and 4Hematology Department, Sana’a University, Yemen.
The aim of this work was to investigate the linkage between
the deregulation of apoptosis and telomerase activity in patients with acute
leukemias and evaluate the level of Bcl-2 protein and teleomerase activity as
parameters for monitoring the disease state before and after chemotherapy. The
study was carried out on 10 patients with acute lymphoplastic leukemia (ALL),
17 patients with acute myeloid leukemia (AML) and 10 healthy age and
sex-matched controls. They were subjected to history taking, clinical
examination, complete blood picture and bone marrow aspiration with
cytochemistry and/or immunophenotyping to confirm diagnosis. Estimation of
serum Bcl-2 protein was done by ELISA, while determination of telomerase
activity in mononuclear cell extracts was performed by PCR-ELISA. At initial
presentation, the Bcl-2 levels were significantly higher in both ALL
(P<0.001) and AML (P<0.001) patients compared to the controls. After
chemotherapy, the levels were still significantly higher than the
prechemotherapy in both groups of patients. Similarly, the telomerase activity,
was significantly higher in patients with ALL (P<0.05) and AML (P<0.05)
at presentation when compared to the controls. After chemotherapy,
statistically significant decrease in the mean telomerase activity was observed
in comparison to the pre-therapy mean values in both ALL (P<0.01) and AML (P<0.001)
patients. A statistically significant positive correlation (r=0.568,
P<0.001) was found between Bcl-2 protein level and telomerase activity
before chemotherapy but there was no correlation (r=0.013, P>0.05) between
the two parameters post-chemotherapy. It is
concluded that telomerase activity and Bcl-2 level are closely linked.
It is possible that Bcl-2 modulates telomerase activity in highly replicating
cells. Telomerase is a good tumour marker in acute leukemias and is of value in
monitoring treatment outcome and disease activity.