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@ARTICLE{Kahlert:276571,
author = {Kahlert, Ulf Dietrich and Koch, Katharina and Suwala,
Abigail Kora and Hartmann, Rudolf and Cheng, Menglin and
Maciaczyk, Donata and Willbold, Dieter and Eberhart, Charles
G. and Glunde, Kristine and Maciaczyk, Jarek},
title = {{T}he effect of neurosphere culture conditions on the
cellular metabolism of glioma cells},
journal = {Folia neuropathologica},
volume = {3},
issn = {1641-4640},
address = {Pozna´n [u.a.]},
publisher = {Termedia Publ. House73588},
reportid = {FZJ-2015-06936},
pages = {219 - 225},
year = {2015},
abstract = {Glioblastoma (GBM) is the most common and lethal adult
glial brain tumour, with a mean overall survival of 16-19
months after primary diagnosis under the current
standard-of-care treatment scheme [26]. Despite enormous
research efforts towards early diagnosis and more efficient
treatment, the prognosis of GBMs remains dismal.The
influence of culture conditions has been widely
investigated in the field of glioma research, suggesting
that neurosphere cultures, compared to adherent growth, more
closely resemble the original patient’s tumour [29]
showing high stem cell compartment [1] and therefore are
more suitable for testing of novel therapeutic spectras
approaches [30]. In this report we describe altered relative
concentrations of the cholines, creatine, myo-inositol, and
glycine in the human GBM cell line U87 propagated under stem
cell conditions as compared to classical monolayer culture.
Furthermore, U87 neurospheres showed significant higher
levels of the putative GBM stem cell marker CD133 as their
serum-propagated counterparts. Detection and targeting of
miss-regulated choline-, myo-inositol-, creatine-, and
glycine-metabolism has been described to have potential
utility in the diagnosis and treatment of malignant gliomas
[2-4,13,16,19].This is, to our knowledge, the hitherto first
link of changes in those oncometabolites [4,25] to
variations in cell culture conditions of glioma cells. Inter
spectral co-analysis of metabolite concentrations under the
two propagation conditions identified reductions in ratios
of phosphocholine to glycerophosphocholine (PC/GPC) and
glycine to total choline (Gly/tCho) but increases in the
quotient of total choline to total creatine (tCho/tCre) and
PC/tCre, as well as Gly/myo-inositol (Gly/myo). This work
should draw the attention of the scientific community on
possible in vitro artefacts and on the need for appropriate
models most closely resembling the in vivo biology of
investigated tumours.},
cin = {ICS-6},
ddc = {610},
cid = {I:(DE-Juel1)ICS-6-20110106},
pnm = {551 - Functional Macromolecules and Complexes (POF3-551)},
pid = {G:(DE-HGF)POF3-551},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000362463100004},
doi = {10.5114/fn.2015.54422},
url = {https://juser.fz-juelich.de/record/276571},
}