Object. Glioblastomas multiforme (GBMs) grow rapidly and are highly resista
nt to treatment compared with other glioma types and grades. Consequently,
it is of major interest to identify markers of aggressiveness in these tumo
rs that could represent new therapeutic targets. Interleukin (IL)-6 is freq
uently produced in gliomas and, given its manifold properties, could be con
sidered as a candidate marker. Expression of IL-6 may be involved in cell g
rowth, resistance to chemotherapy and radiotherapy (via an antiapoptotic pa
thway), and angiogenesis. This study was conducted to test this hypotheses
and to evaluate the suitability of IL-6 as a target in the treatment of GBM
s.
Methods. The authors studied the relationship between the level of IL-6 gen
e expression as assessed using semiquantitative reverse transcription-polym
erase chain reaction and by determining various histological types and grad
es in a series of 59 gliomas. It was found that GBMs displayed a significan
tly higher level of IL-6 expression than other types of glioma (p < 0.001).
Immunohistochemical analysis revealed that IL-6 was produced mainly by mal
ignant cells and a few vascular endothelial cells. Conclusions. It can be i
nferred from these findings that IL-6 gene expression is related to glioma
aggressiveness and that IL-6 may play a central role in GEM behavior. Inter
leukin-6, therefore, could be considered as a new potential target in the t
reatment of GBMs.