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@ARTICLE{Bernardi:308493,
author = {F. Bernardi and J. Torrejon and I. Basili and R. Van
Ommeren and V. Marsaud and H. Yu and J. Talbot and J.
Souphron and E. Indersie and A. Forget and B. Bonneau and A.
Massiot and C. Alcazar and L. Figeac and E. Bonerandi and G.
Cancila and O. Sirbu and N. Yadav and D. Mohanakrishnan and
B. Lombard and D. Loew and P. Poullet and S. Liva and M.
Lovino and I.-H. Lin and T. Nakashima and T. Gharsalli and
P. A. Nicolas and N. Yubuki and R. A. Ribas and B. Colsch
and E. Chu-Van and F. Castelli and J. L. Sampaio and S.
Leboucher and C. Lasgi and L. Besse and M.-N. Soler and V.
Lo Re and N. Planque and N. Abeysundara and P. Balin and H.
Wang and H. Su and X. Wu and F. M. G. Cavalli and O.
Saulnier and E. Ficarra and L. Di Marcotullio and K.
Kumegawa and R. Maruyama and D. Kawauchi and D. Picard and
M. Remke and L. Riffaud and C. Puiseux and Y. Bouchoucha and
S. Huybrechts and M. Simbozel and F. Bourdeaut and P. Varlet
and S. Puget and T. Blauwblomme and M. Andrianteranagna and
J. M. Planchon and A. Dugourd and J. Saez-Rodriguez and E.
Barillot and N. Servant and L. Martignetti and J. Rich and
M. Kool$^*$ and S. M. Pfister$^*$ and S. Agnihotri and H.
Suzuki and M. Fanjul and W.-J. Wang and J.-W. Tsai and R. C.
Sun and K. Beccaria and C. Dufour and J.-E. Sarry and K. A.
Michealraj and M. D. Taylor and O. Ayrault},
title = {{M}ultiomic integration reveals tumoral heterogeneity of
lipid dependence within lethal group 3 medulloblastoma.},
journal = {Cancer cell},
volume = {nn},
issn = {1535-6108},
address = {Cambridge, Mass.},
publisher = {Cell Press},
reportid = {DKFZ-2026-00133},
pages = {nn},
year = {2026},
note = {#DKTKZFB26# / #NCTZFB26# / epub},
abstract = {Medulloblastoma, the most common malignant brain tumor of
childhood, exhibits significant biological complexity that
demands deeper exploration. Here, we present a large
multiomics dataset integrating data from 384 primary
medulloblastoma patient samples across five omic layers: CpG
methylome, transcriptome, proteome, phosphoproteome, and
metabolome, paired with associated clinical metadata. Data
integration revealed intertumoral heterogeneity of lipid
metabolism across proteomic subtypes. Notably, while the
MYC-FASN-SCD axis drives lipid biosynthesis, pathway
inhibition elicits a compensatory escape mechanism in vivo
through exogenous fatty acid uptake. Unexpectedly, we
demonstrated that MYC triggers lipid storage, creating a
unique dependency on lipid droplet-mitochondria
communications to sustain tumor maintenance in vivo.
Together, this comprehensive analysis reveals a targetable
vulnerability downstream of MYC that constitutes a promising
therapeutic approach to treat currently untreatable
medulloblastoma subtypes.},
keywords = {lipid biosynthesis (Other) / lipid droplets (Other) / lipid
oxidative stress (Other) / medulloblastoma (Other) /
metabolomics (Other) / multiomics integration (Other) /
pediatric cancer (Other) / phosphoproteomics (Other) /
proteomics (Other) / transcriptomics (Other)},
cin = {B062 / HD01 / HD02},
ddc = {610},
cid = {I:(DE-He78)B062-20160331 / I:(DE-He78)HD01-20160331 /
I:(DE-He78)HD02-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:41544627},
doi = {10.1016/j.ccell.2025.12.012},
url = {https://inrepo02.dkfz.de/record/308493},
}