T. Brandstetter et al., Granulocyte colony-stimulating factor (G-CSF) receptor gene expression of ovarian carcinoma does not correlate with G-CSF caused cell proliferation, CANCER, 91(7), 2001, pp. 1372-1383
BACKGROUND. Recombinant human granulocyte colony-stimulating factor (rhG-CS
F) is a growth factor commonly used to avoid leukopenia after chemotherapy.
Endogenous G-CSF is produced by macrophages and granulocytes that infiltra
te tumors. It has been reported that rhG-CSF stimulates the proliferation o
f several cell lines as well as bladder carcinoma cells. Conversely, in som
e hematopoietic cell lines such as U-937, WEHI-SB, and K-562 no effect or i
n some cases a differentiation pattern was found. Moreover, the role of rhG
-CSF on the proliferation of solid tumors is not well understood.
METHODS, In this study, 10 ovarian carcinoma biopsies were characterized fo
r the presence of G-CSF and G-CSF receptor by reverse transcription-polymer
ase chain reaction (RT-PCR) and immunohistochemical analysis. Proliferation
was analyzed by ATP viability assays.
RESULTS. Performing RT-PCR, these biopsies and four ovarian carcinoma cell
lines were analyzed for endogenous G-CSF production, which was found in som
e biopsies and in all cell lines. Despite the presence of the G-CSF recepto
r in all biopsies and cell lines, no proliferation was found after rhG-CSF
incubation of the cell lines or the tumor samples for 3 and for 6 days, res
pectively.
CONCLUSIONS. Summarizing the authors' in vitro studies, rhG-CSF does not af
fect the proliferation of ovarian carcinoma cells in vitro. (C) 2001 Americ
an Cancer Society.