EXPRESSION OF SOME APOPTOSIS-CONTROLLING PROTEINS IN PEDIATRIC
LYMPHOPROLIFERATIVE MALIGNANCIES Sallam SA1, Soliman GT1, Zaghloul MS2,
Alrayhany MA1 and Ismail AM1
1al-Minya Medical School, al-Minya, Egypt 2National Cancer Institute, Cairo
University, Cairo, Egypt. Objective: to determine the serum levels of Bcl-2 and soluble
Fas in children with lymphoproliferative malignancies and to find out their
prognostic value. Methods: Total 39 children with newly diagnosed Non-Hodgkin
Lymphoma (NHL); Hodgkin Lymphoma (HL); and Acute Lymphoblastic Leukemia (ALL)
were enrolled in the study,28 males and 11 females aged from 0.5–14 years.
Twelve healthy children of matchable age and sex served as a control group.
All cases and controls were subjected to complete blood picture and liver and
renal function tests. Cases only were subjected to bone marrow (BM)
examination; cerebrospinal fluid examination; lymph node biopsy; CT and bone
scan. For both diseased cases and controls serum levels of Bcl-2 and Fas were
determined by enzyme-linked immunosorbent assay. Results: Serum levels of Fas and Bcl-2 were significantly
elevated in different groups of patients when compared with control. In cases
with ALL, serum levels of Fas were significantly higher in group of patients
with central nervous system involvement than in group without (P<0.01),
however, serum levels of Bcl-2 showed no significant difference between those
groups. In cases with NHL, serum levels of Fas and Bcl-2 were significantly
higher in group of patients with BM infiltration than in group without
infiltration (P<0.0001). In cases with NHL and HL, but not ALL, serum
levels of Fas and Bcl-2 were significantly higher in resistant patients than
those with complete remission. There was no significant difference between
serum levels of Fas before and after treatment in all patients groups. However, serum levels of Bcl-2 were
significantly lowered after treatment in NHL, HL and ALL groups (P<0.05,
P<0.001 and P<0.001 respectively). Conclusion: High serum levels of Bcl-2 and Fas were correlated
with poor prognosis in patients with HL and NHL, while no correlation was
found with prognosis in patients with ALL. |
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