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@ARTICLE{Ceranski:298611,
author = {A. K. Ceranski$^*$ and M. J. Carreño-Gonzalez$^*$ and A.
C. Ehlers$^*$ and K. M. Hanssen$^*$ and N. Gmelin$^*$ and F.
H. Geyer$^*$ and Z. Kolodynska$^*$ and E. Vinca$^*$ and T.
Faehling$^*$ and P. Poeller$^*$ and S. Ohmura$^*$ and F.
Cidre-Aranaz$^*$ and A. Schulze$^*$ and T. Grünewald$^*$},
title = {{R}efined culture conditions with increased physiological
relevance uncover oncogene-dependent metabolic signatures in
{E}wing sarcoma spheroids.},
journal = {Cell reports / Methods},
volume = {5},
number = {2},
issn = {2667-2375},
address = {Cambridge, MA},
publisher = {Cell Press},
reportid = {DKFZ-2025-00311},
pages = {100966},
year = {2025},
note = {DKFZ-ZMBH Alliance / 2025 Feb 24;5(2):100966 /
#EA:B410#LA:B410#},
abstract = {Ewing sarcoma (EwS) cell line culture largely relies on
standard techniques, which do not recapitulate physiological
conditions. Here, we report on a feasible and cost-efficient
EwS cell culture technique with increased physiological
relevance employing an advanced medium composition, reduced
fetal calf serum, and spheroidal growth. Improved reflection
of the transcriptional activity related to proliferation,
hypoxia, and differentiation in EwS patient tumors was
detected in EwS cells grown in this refined in vitro
condition. Moreover, transcriptional signatures associated
with the oncogenic activity of the EwS-specific FET::ETS
fusion transcription factors in the refined culture
condition were shifted from proliferative toward metabolic
gene signatures. The herein-presented EwS cell culture
technique with increased physiological relevance provides a
broadly applicable approach for enhanced in vitro modeling
relevant to advancing EwS research and the validity of
experimental results.},
keywords = {CP: Cancer biology (Other) / CP: Metabolism (Other) / Ewing
sarcoma (Other) / fetal calf serum (Other) / modeling
adequacy (Other) / physiological media (Other) / refined
cell culture (Other) / spherioidal growth (Other) /
transcriptome (Other)},
cin = {B410 / HD01 / A410},
ddc = {610},
cid = {I:(DE-He78)B410-20160331 / I:(DE-He78)HD01-20160331 /
I:(DE-He78)A410-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39922188},
doi = {10.1016/j.crmeth.2025.100966},
url = {https://inrepo02.dkfz.de/record/298611},
}