Journal of Turkish Society of Obstetric and Gynecology,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 18, 2025
Transforming
growth
factor-β-activated
kinase
1
binding
protein
2
(TAB2)
plays
a
vital
role
in
inflammatory
pathways.
It
has
also
been
considered
potential
target
for
the
enhancement
of
antiestrogen
effects.
Previous
evidence
indicated
that
TAB2
gene
variants
are
associated
with
several
diseases,
whereas
their
correlation
endometrial
cancer
(EC)
is
unclear.
This
study
aims
to
initially
explore
association
between
polymorphisms
(rs237028
/AG,
rs521845
T/G,
and
rs652921
T/C)
EC.
Polymerase
chain
reaction-restriction
fragment
length
polymorphism
was
applied
determine
genotype
composition
allele
frequencies
variant
270
EC
patients
294
healthy
controls.
The
G
related
increase
risk
[p=0.08,
odds
ratio
(OR):
0.72,
95%
confidence
interval
(CI):
0.56-0.91].
Moreover,
different
genetic
models
(p=0.017,
OR:
0.63,
CI:
0.44-0.91
codominant
model;
p=0.0051,
0.61,
0.43-0.87
dominant
model).
For
rs237028,
percentage
AG
highly
differentiated
tumours
(G1)
significantly
higher
than
moderately,
poorly
(G2/G3)
(p=0.031,
0.77,
0.45-1.30).
Our
results
showed
TAB2,
risk,
suggesting
may
play
crucial
prognosis.
Cancer Letters,
Journal Year:
2024,
Volume and Issue:
593, P. 216930 - 216930
Published: May 3, 2024
Radiotherapy
(RT)
in
non-small
cell
lung
cancer
(NSCLC)
triggers
cellular
senescence,
complicating
tumor
microenvironments
and
affecting
treatment
outcomes.
This
study
examines
the
role
of
lymphocyte
immunoglobulin-like
receptor
B2
(LILRB2)
modulating
RT-induced
senescence
radiosensitivity
NSCLC.
Through
methodologies
including
irradiation,
lentivirus
transfection,
various
molecular
assays,
we
assessed
LILRB2's
expression
its
impact
on
levels
behaviors.
Our
findings
reveal
that
RT
upregulates
LILRB2,
facilitating
a
senescence-associated
secretory
phenotype
(SASP),
which
turn
enhances
proliferation
resistance
to
radiation.
Importantly,
LILRB2
silencing
attenuates
these
effects
by
inhibiting
JAK2/STAT3
pathway,
significantly
increasing
NSCLC
models.
Clinical
data
correlate
high
with
reduced
response
poorer
prognosis,
suggesting
pivotal
potential
as
therapeutic
target
improve
radiosensitivity.
Biomedicines,
Journal Year:
2024,
Volume and Issue:
12(2), P. 444 - 444
Published: Feb. 16, 2024
Sepsis
is
a
syndrome
of
organ
dysfunction
caused
by
an
uncontrolled
inflammatory
response,
which
can
seriously
endanger
life.
Currently,
there
still
shortage
specific
therapeutic
drugs.
Quercetin
and
its
natural
derivatives
have
received
lot
attention
recently
for
their
potential
in
treating
sepsis.
Here,
we
provide
comprehensive
summary
the
recent
research
progress
on
quercetin
derivatives,
with
focus
mechanisms
antioxidation
anti-inflammation.
To
obtain
necessary
information,
conducted
search
PubMed,
Web
Science,
EBSCO,
Cochrane
library
databases
using
keywords
sepsis,
anti-inflammatory,
antioxidant,
anti-infection,
quercetin,
to
identify
relevant
from
6315
articles
published
last
five
years.
At
present,
11
been
intensively
studied.
They
primarily
exert
anti-inflammation
effects
through
PI3K/AKT/NF-κB,
Nrf2/ARE,
MAPK
pathways.
The
feasibility
these
compounds
experimental
models
clinical
application
were
also
discussed.
In
conclusion,
good
treatment
Journal of Inflammation Research,
Journal Year:
2025,
Volume and Issue:
Volume 18, P. 133 - 146
Published: Jan. 1, 2025
To
explore
the
neuroprotective
effect
of
Eugenol
Acetate
(EA)
on
post-stroke
neuroinflammation
and
investigate
underlying
mechanisms.
For
in
vitro
experiments,
primary
microglia
were
pre-incubated
with
EA
for
2
hours,
followed
by
lipopolysaccharide
(LPS)
stimulation
24
hours
or
Oxygen-Glucose
Deprivation
(OGD)
treatment
4
hours.
Real-time
quantitative
PCR,
enzyme-linked
immunosorbent
assay
(ELISA)
Western
blot
performed
to
examine
expression
levels
inflammatory
cytokines
microglia.
The
activation
NF-κB
signaling
pathway
was
evaluated
immunofluorescence
staining
blot.
vivo
middle
cerebral
artery
occlusion
(MCAO)
constructed
mimic
ischemic
brain
injury
8-week-old
male
C57BL/6J
mice.
mice
continuously
injected
intraperitoneally
vehicle
after
MCAO.
Neurobehavioral
tests
TTC
conducted
estimate
neurological
deficits
infarct
area.
Moreover,
white
matter
integrity
MCAO
observed
via
staining.
significantly
reduced
pro-inflammatory
LPS
OGD
treated
microglia,
inhibited
LPS-induced
pathway.
In
addition,
alleviated
improved
neuromotor
function
Furthermore,
long-term
restored
mice,
which
might
be
associated
inhibition
Therefore,
a
promising
candidate
stroke.
Chemical Biology & Drug Design,
Journal Year:
2025,
Volume and Issue:
105(1)
Published: Jan. 1, 2025
ABSTRACT
Ischemic
stroke
(IS)
often
causes
fearful
sequela,
even
death.
Curcumin
was
beneficial
to
IS,
but
its
underlying
molecular
mechanism
is
unclear.
Mice
were
subjected
middle
cerebral
artery
occlusion
(MCAO)
surgery,
and
BV‐2
cells
treated
with
oxygen–glucose
deprivation/reoxygenation
(OGD/R)
induction
establish
IS
models
in
vivo
vitro.
Abundance
of
genes
proteins
determined
using
quantitative
real‐time
polymerase
chain
reaction
(RT‐qPCR),
immunofluorescence
(IF),
western
blot.
Interleukin‐1β
(IL‐1β),
interleukin‐6
(IL‐6),
interleukin‐10
(IL‐10)
levels
analyzed
enzyme‐linked
immunosorbent
assay
(ELISA).
Modified
neurological
severity
score
(mNSS),
corner
test,
foot
fault
adhesive
removal
2,3,5‐triphenyltetrazolium
chloride
(TTC)
staining
applied
evaluate
the
brain
injury
mice.
The
correlation
between
miR‐205‐5p
Kruppel‐like
factor
2
(KLF2)
affirmed
dual
luciferase
reporter
assay.
Our
results
revealed
that
curcumin
alleviated
damage
MCAO
mice
through
driving
microglia
M2
polarization.
Of
note,
resulted
decreased
expression
knockdown
promoted
polarization
OGD/R
conditions
achieved
similar
treatment
Moreover,
played
a
promoting
role
under
conditions,
while
overexpression
or
KLF2
abolished
these
effects.
On
mechanism,
target
curcumin,
further
interacted
inhibit
activating
transcription
(ATF2)
expression.
miR‐205‐5p,
by
suppressed
worsen
mediating
KLF2/ATF2
axis.
Materials Today Bio,
Journal Year:
2025,
Volume and Issue:
31, P. 101518 - 101518
Published: Jan. 23, 2025
Spinal
cord
injury
(SCI)
is
significantly
hampered
by
an
inflammatory
microenvironment,
prompting
continued
efforts
in
drug
development
to
address
inflammation.
Research
shows
that
quercetin
(Que)
exhibits
excellent
performance
reducing
inflammation
and
neuroprotection.
However,
its
application
limited
poor
solubility,
notable
side
effects,
the
unique
pathophysiology
of
spinal
cord.
In
this
study,
we
introduce
a
novel
multifunctional
liposome
hydrogel
delivery
system
(QLipTC@HDM),
obtained
incorporating
liposomes
with
blood-spinal
barrier
penetration
site
targeting
properties
(LipTC)
into
dual-network
viscous
(HDM).
Our
results
demonstrate
encapsulating
Que
LipTC
(QLipTC)
enhances
minimizes
toxic
facilitates
lesion
targeting,
aids
crossing
barrier.
Moreover,
encapsulation
HDM
prolongs
retention
QLipTC
at
after
local
administration.
Crucially,
our
findings
reveal
QLipTC@HDM
induces
M2
phenotype
transformation
glial
cells
mice
SCI,
thereby
mitigating
This
intervention
additionally
preserves
integrity
barrier,
optimizes
reduces
scarring,
promotes
axonal
regeneration,
motor
function
recovery
SCI
mice.
summary,
investigations
highlight
potential
disease-specific
as
promising
therapeutic
approach
for
treatment
management
SCI.