EXPRESSION OF SOME ONCOGENES, MACROMOLECULAR-SYNTHESIS, APOPTOSIS ANDCLONOGENICITY OF LEUKEMIC-CELLS MODIFIED BY MOLECULES PRESENT IN HEMATOPOIETIC-TISSUE
Ai. Svirnovski et al., EXPRESSION OF SOME ONCOGENES, MACROMOLECULAR-SYNTHESIS, APOPTOSIS ANDCLONOGENICITY OF LEUKEMIC-CELLS MODIFIED BY MOLECULES PRESENT IN HEMATOPOIETIC-TISSUE, Eksperimental'naa onkologia, 18(1), 1996, pp. 19-25
To investigate a possible interrelationship of some fundamental proces
ses in leukemic cells, preparations of natural origin have been used a
s the tools for manipulation of cellular properties. Lyophylised crude
extract from regenerating spleen and its purified fraction added to m
ouse leukemia cell cultures rapidly and almost entirely inhibited DNA
synthesis in a dose-dependent manner. Total RNA moderate synthesis inh
ibition was seen at 4 h and this inhibition increased with time. Prote
in synthesis inhibition being minimal at 4 h was observed at 24 h. C-m
yc expression was maintained at the same level in the treated and cont
rol cells during incubation period and was slightly decreased in treat
ed cells at 24 h in comparison with uneffected cells. There were no no
ticable changes in c-fos or c-jun expression both in treated and contr
ol cells. The level of DNA fragmentation was more pronounced in the tr
eated cells after 1 h incubation and coincided with the dissociation o
f stopped proliferation and lasting c-myc expression. But later on the
re was no discrepancy in the expression of apoptotic process measured
by means of apoptotic ladder in treated and uneffected cultures, may b
e because of the beginning of RNA and protein synthesis suppression in
the former. In contrast, clonogenic potential of leukemic cells was m
arkedly reduced after their 24 h treatment. This seemed contradiction
may be partially overcome on the basis of understanding of the presenc
e of non-clonogenic cells in the analysed cell populations and some pe
culiarities of apoptotic process in cultured cells. In any case, regul
atory molecules present in repairing hematopoietic tissue may influenc
e leukemic cell properties.