% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Ose:157754,
author = {J. Ose and A. N. Holowatyj and J. Nattenmüller and B.
Gigic and T. Lin and C. Himbert and N. Habermann and D.
Achaintre and A. Scalbert and P. Keski-Rahkonen and J. Böhm
and P. Schrotz-King$^*$ and M. Schneider and A. Ulrich and
E. Kampman and M. Weijenberg and A. Gsur and P.-M. Ueland
and H.-U. Kauczor and C. M. Ulrich},
title = {{M}etabolomics profiling of visceral and abdominal
subcutaneous adipose tissue in colorectal cancer patients:
results from the {C}olo{C}are study.},
journal = {Cancer causes $\&$ control},
volume = {31},
number = {8},
issn = {1573-7225},
address = {Dordrecht [u.a.]},
publisher = {Springer Science + Business Media B.V.},
reportid = {DKFZ-2020-01791},
pages = {723 - 735},
year = {2020},
abstract = {Underlying mechanisms of the relationship between body
fatness and colorectal cancer remain unclear. This study
investigated associations of circulating metabolites with
visceral (VFA), abdominal subcutaneous (SFA), and total fat
area (TFA) in colorectal cancer patients.Pre-surgery plasma
samples from 212 patients (stage I-IV) from the ColoCare
Study were used to perform targeted metabolomics. VFA, SFA,
and TFA were quantified by computed tomography scans.
Partial correlation and linear regression analyses of VFA,
SFA, and TFA with metabolites were computed and corrected
for multiple testing. Cox proportional hazards were used to
assess 2-year survival.In patients with metastatic tumors,
SFA and TFA were statistically significantly inversely
associated with 16 glycerophospholipids (SFA: pFDR range
0.017-0.049; TFA: pFDR range 0.029-0.048), while VFA was
not. Doubling of ten of the aforementioned
glycerophospholipids was associated with increased risk of
death in patients with metastatic tumors, but not in
patients with non-metastatic tumors (phet range:
0.00044-0.049). Doubling of PC ae C34:0 was associated with
ninefold increased risk of death in metastatic tumors
(Hazard Ratio [HR], 9.05; $95\%$ confidence interval [CI]
2.17-37.80); an inverse association was observed in
non-metastatic tumors (HR 0.17; $95\%$ CI 0.04-0.87;
phet = 0.00044).These data provide initial evidence that
glycerophospholipids in metastatic colorectal cancer are
uniquely associated with subcutaneous adiposity, and may
impact overall survival.},
keywords = {Adiposity / Adolescent / Adult / Aged / Aged, 80 and over /
Body Mass Index / Colorectal Neoplasms: diagnostic imaging /
Colorectal Neoplasms: metabolism / Colorectal Neoplasms:
pathology / Female / Humans / Intra-Abdominal Fat:
diagnostic imaging / Intra-Abdominal Fat: metabolism / Male
/ Metabolomics / Middle Aged / Neoplasm Staging /
Subcutaneous Fat, Abdominal: diagnostic imaging /
Subcutaneous Fat, Abdominal: metabolism / Tomography, X-Ray
Computed / Young Adult},
cin = {C120},
ddc = {610},
cid = {I:(DE-He78)C120-20160331},
pnm = {313 - Cancer risk factors and prevention (POF3-313)},
pid = {G:(DE-HGF)POF3-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:32430684},
pmc = {pmc:PMC7425810},
doi = {10.1007/s10552-020-01312-1},
url = {https://inrepo02.dkfz.de/record/157754},
}