Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 29, 2024
Abstract
Several
E3
ligases
have
been
found
to
affect
the
immune
microenvironment
of
hepatocellular
carcinoma
(HCC)
and
lead
resistance
immunotherapy.
In
this
study,
genes
are
screened
based
on
The
Cancer
Genome
Atlas
(TCGA)
dataset.
Through
cytometry
by
time
flight
(CyTOF),
flow
cytometry,
further
experiments,
Deltex
ubiquitin
ligase
2
(DTX2)
in
HCC
cells
is
identified
promote
infiltration
polarization
tumor‐associated
neutrophils
(TANs)
with
a
protumor
phenotype,
thus
attenuating
cytotoxicity
CD8+
T
partially
through
C‐X‐C
motif
chemokine
(CXCL2)
6
(CXCL6).
Mechanistically,
DTX2
can
interact
histone
H2B
its
monoubiquitination
at
lysine120
(H2BK120ub1),
thereby
increasing
CXCL2
CXCL6
transcription
epigenetic
regulation.
Different
tumor
models
vivo
demonstrated
that
inhibitor
treatment
inhibited
growth
sensitized
therapeutic
effects
programmed
cell
death
protein
1
(PD‐1)
antibody.
summary,
study
identifies
as
potential
target
for
European Journal of Pharmacology,
Journal Year:
2024,
Volume and Issue:
987, P. 177154 - 177154
Published: Dec. 2, 2024
Kawasaki
disease
(KD)
primarily
affects
the
pediatric
population
and
exhibits
a
notable
incidence
of
drug
resistance,
resulting
in
coronary
artery
damage
thrombosis.
This
study
aimed
to
identify
innovative
therapeutic
targets
for
KD
treatment.
By
harnessing
single-cell
data
derived
from
peripheral
blood
mononuclear
cells,
we
identified
differentially
expressed
genes.
Through
integration
eQTL
Mendelian
randomization
analysis,
FCGR3B
S100A12
were
causally
linked
KD.
The
DrugBank
database
showed
their
potential
as
target
candidates.
GSEA
further
elucidated
roles
on
Furthermore,
have
confirmed
that
ligand-FCGR3B
complex
enhances
intracellular
calcium
concentration
(Ca
Advanced Science,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 29, 2024
Abstract
Several
E3
ligases
have
been
found
to
affect
the
immune
microenvironment
of
hepatocellular
carcinoma
(HCC)
and
lead
resistance
immunotherapy.
In
this
study,
genes
are
screened
based
on
The
Cancer
Genome
Atlas
(TCGA)
dataset.
Through
cytometry
by
time
flight
(CyTOF),
flow
cytometry,
further
experiments,
Deltex
ubiquitin
ligase
2
(DTX2)
in
HCC
cells
is
identified
promote
infiltration
polarization
tumor‐associated
neutrophils
(TANs)
with
a
protumor
phenotype,
thus
attenuating
cytotoxicity
CD8+
T
partially
through
C‐X‐C
motif
chemokine
(CXCL2)
6
(CXCL6).
Mechanistically,
DTX2
can
interact
histone
H2B
its
monoubiquitination
at
lysine120
(H2BK120ub1),
thereby
increasing
CXCL2
CXCL6
transcription
epigenetic
regulation.
Different
tumor
models
vivo
demonstrated
that
inhibitor
treatment
inhibited
growth
sensitized
therapeutic
effects
programmed
cell
death
protein
1
(PD‐1)
antibody.
summary,
study
identifies
as
potential
target
for