EFFECTS OF STEM-CELL FACTOR AND OTHER BONE-MARROW-DERIVED GROWTH-FACTORS ON THE EXPRESSION OF ADHESION MOLECULES AND PROLIFERATION OF HUMANNEUROBLASTOMA-CELLS
D. Beck et al., EFFECTS OF STEM-CELL FACTOR AND OTHER BONE-MARROW-DERIVED GROWTH-FACTORS ON THE EXPRESSION OF ADHESION MOLECULES AND PROLIFERATION OF HUMANNEUROBLASTOMA-CELLS, European journal of cancer, 31A(4), 1995, pp. 467-470
Metastasis in children with neuroblastoma (NB) is a poor prognostic fa
ctor despite intensive therapy. In the near future, stem cell factor (
SCF) is likely to be used clinically to accelerate bone marrow (BM) re
covery after high-dose chemotherapy in patients with advanced NE. The
high frequency of BM metastases in NE could be secondary to BM-derived
human growth factors (HGF) modulating the adhesion, secondary growth
(or both) of circulating metastatic NE cells. To test this hypothesis,
we studied the in vitro effects on NE cell lines grown in chemically
defined medium of SCF, interleukin (IL)-1 beta, IL-3, IL-6, basic fibr
oblast growth factor (bFGF), transforming growth factor-beta (TGF-beta
) used alone or in combination. The antigenic expression of NB-associa
ted cell adhesion molecules (CAM) HLA class 1, intercellular CAM-1, ne
ural-CAM and CD44 were assayed by monoclonal antibodies and flow cytom
etry, and DNA synthesis by H-3-thymidine uptake. The expression of CAM
was not modulated by SCF or other HGFs. An increase in thymidine upta
ke was induced by bFGF alone in IMR-32 cells, while SCF and other HGFs
had no notable effect. Our results indicate that SCF and other BM-der
ived HGFs are unlikely to have a generalised effect on the expression
of adhesion molecules by NE cells or proliferation. The clinical admin
istration of recombinant human SCF to children with NE should be safe.