% 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{Katzke:176891,
author = {V. Katzke$^*$ and C. Le Cornet$^*$ and R. Mahfouz and B.
Brauer and T. S. Johnson$^*$ and F. Canzian$^*$ and V.
Rebours and M.-C. Boutron-Ruault and G. Severi and M. B.
Schulze and A. Olsen and A. Tjoenneland and K. Overvad and
M. Crous-Bou and E. Molina-Montes and P. Amiano and J. M.
Huerta and E. Ardanaz and A. Perez-Cornago and G. Masala and
V. Pala and R. Tumino and C. Sacerdote and S. Panico and B.
Bueno-de-Mesquita and R. Vermeulen and M. Sund and O.
Franklin and S. Christakoudi and L. Dossus and E. Weiderpass
and S. Olek and R. Kaaks$^*$},
title = {{A}re circulating immune cells a determinant of pancreatic
cancer risk? {A} prospective study using epigenetic cell
count measures.},
journal = {Cancer epidemiology, biomarkers $\&$ prevention},
volume = {30},
number = {12},
issn = {1538-7755},
address = {Philadelphia, Pa.},
publisher = {AACR},
reportid = {DKFZ-2021-02133},
pages = {2179-2187},
year = {2021},
note = {#EA:C020#LA:C020# / 2021 Dec;30(12):2179-2187},
abstract = {Evidence is accumulating that immune cells play a prominent
role in pancreatic cancer aetiology but prospective
investigations are missing.We conducted a nested
case-control study within the European Prospective
Investigation into Cancer and Nutrition (EPIC) study with
502 pairs of incident pancreatic cancer cases and matched
controls. Relative counts of circulating immune cells
(neutrophils and lymphocyte sub-lineages: total CD3+, CD8+,
CD4+, and FOXP3+ regulatory T cells (Tregs) relative to
nucleated cells, (white blood cells) were measured by
qRT-PCR. Odds ratios with $95\%$ Confidence Intervals were
estimated using logistic regressions, modelling relative
counts of immune cells on a continuous scale.Neither
relative counts of immune cell types taken individually, nor
mutually adjusted for each other were associated with
pancreatic cancer risks. However, in sub-group analyses by
strata of lag-time, higher relative counts of Tregs and
lower relative counts of CD8+ were significantly associated
with an increased pancreatic cancer risks in participants
diagnosed within the first 5 years of follow-up.These
results might reflect reverse causation, due to higher
relative counts of Tregs and lower counts of CD8+ cells
among individuals with more advanced stages of latent
pancreatic cancer, who are closer to the point of developing
clinical manifest disease.We have shown, for the first time,
that increased relative counts of regulatory T-cells and
lower relative counts of CD8+, cytotoxic T cells may be
associated with pancreatic cancer risk or relatively
late-stage tumor development.},
cin = {C020 / C055},
ddc = {610},
cid = {I:(DE-He78)C020-20160331 / I:(DE-He78)C055-20160331},
pnm = {313 - Krebsrisikofaktoren und Prävention (POF4-313)},
pid = {G:(DE-HGF)POF4-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34548327},
doi = {10.1158/1055-9965.EPI-21-0169},
url = {https://inrepo02.dkfz.de/record/176891},
}