Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Nov. 7, 2024
Scutellarin
(SCU),
a
flavonoid
glucuronide
derived
from
Scutellaria
barbata
and
Erigeron
breviscapus
,
exhibits
broad
pharmacological
effects
with
promising
therapeutic
potential
in
treating
various
chronic
diseases.
It
has
demonstrated
efficacy
modulating
multiple
biological
pathways,
including
antioxidant,
anti-inflammatory,
anti-apoptotic,
vasodilatory
mechanisms.
These
protective
roles
make
SCU
valuable
compound
diseases
such
as
cerebrovascular
diseases,
cardiovascular
neurodegenerative
disorders,
metabolic
Despite
its
multi-targeted
effects,
faces
challenges
low
bioavailability
limited
clinical
data,
which
hinder
widespread
application.
Current
research
supports
to
prevent
oxidative
stress,
reduce
inflammatory
responses,
enhance
cell
survival
cells
rats.
However,
more
comprehensive
studies
are
required
clarify
molecular
mechanisms
develop
strategies
that
for
use.
could
emerge
potent
agent
the
treatment
of
complex
pathophysiological
This
review
examines
current
literature
on
provide
understanding
activity,
action,
Cancer Communications,
Journal Year:
2023,
Volume and Issue:
44(1), P. 23 - 46
Published: Nov. 20, 2023
Abstract
Lung
cancer
is
the
second
most
common
and
deadliest
type
of
worldwide.
Clinically,
non‐small
cell
lung
(NSCLC)
pathological
cancer;
approximately
one‐third
affected
patients
have
locally
advanced
NSCLC
(LA‐NSCLC,
stage
III
NSCLC)
at
diagnosis.
Because
its
heterogeneity,
LA‐NSCLC
often
requires
multidisciplinary
assessment.
Moreover,
prognosis
much
below
satisfaction,
efficacy
traditional
therapeutic
strategies
has
reached
a
plateau.
With
emergence
targeted
therapies
immunotherapies,
as
well
continuous
development
novel
radiotherapies,
we
entered
an
era
treatment
paradigm
for
LA‐NSCLC.
Here,
reviewed
landscape
relevant
modalities,
including
adjuvant,
neoadjuvant,
perioperative
immune
in
with
resectable
with/without
oncogenic
alterations;
combinations
chemoradiation
immunotherapy/targeted
therapy
unresectable
We
addressed
unresolved
challenges
that
remain
field,
examined
future
directions
to
optimize
clinical
management
increase
cure
rate
Advanced Science,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 21, 2025
Abstract
Metabolic
disorders
have
been
identified
as
one
of
the
causes
drug‐induced
liver
injury;
however,
direct
regulatory
mechanism
regarding
this
disorder
has
not
yet
clarified.
In
study,
a
single
small
molecule
kinase
inhibitors,
with
crizotinib
representative
drug
is
elucidated.
First,
it
discovered
that
induced
aberrant
lipid
metabolism
and
apoptosis
in
liver.
A
mechanistic
study
revealed
treatment
promoted
accumulation
squalene
epoxidase
(SQLE)
by
inhibiting
autophagosome‐lysosome
fusion
which
blocked
autophagic
degradation
SQLE.
maladaptive
increase
SQLE
led
to
disturbances
cholesterol
sphingolipid
via
an
enzymatic
activity‐dependent
manner.
Abnormal
results
both
steatosis
inflammatory
infiltration,
promote
cell
inducing
lysosomal
membrane
permeabilization.
The
restoration
level
or
activity
ameliorated
hepatocyte
injury.
autophagy
activator
known
metformin
inhibitor
terbinafine
potential
clinical
use
for
alleviating
hepatotoxicity.
Journal of Materials Chemistry B,
Journal Year:
2024,
Volume and Issue:
12(38), P. 9740 - 9759
Published: Jan. 1, 2024
Inhalable
hybrid
nano-assemblies
incorporating
the
tumor
homing
peptide
TMTP1
effectively
target
and
kill
tumors,
offering
a
promising
therapeutic
strategy
for
advanced
small
cell
lung
cancer.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
15
Published: Feb. 3, 2025
Background
The
coexistence
of
lung
cancer
and
pulmonary
tuberculosis
(TB)
makes
differential
diagnosis
even
more
complicated.
purpose
the
study
is
to
explore
superiority
[
18
F]-NOTA-FAPI-04
PET/CT
in
distinguishing
TB
from
malignant
lesions
accurately
detecting
inflammatory
lymph
nodes
than
F]-FDG
PET/CT.
Case
summary
Herein,
we
described
a
case
report
patient
with
both
underwent
Al[
positron
emission
tomography/computed
tomography
(PET/CT)
determine
staging.
Additionally,
literature
review
was
conducted
discuss
potential
clinical
applications
FAPI
We
reported
70-year-old
man
newly
diagnosed
squamous
cell
carcinoma
avid
uptake
old
right
hilar
(<1
cm)
were
not
found
on
Al
After
2
months
follow-up,
small
node
finally
confirmed
be
inflammatory.
Conclusion
may
perform
better
malignancy
offer
greater
specificity
for
nodes.
BMC Cancer,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: Feb. 21, 2025
There
is
no
consensus
regarding
whether
primary
tumour
resection
(PTR)
should
be
performed
in
non-small
cell
lung
cancer
(NSCLC)
patients
with
unexpected
pleural
dissemination
(PD)
discovered
at
thoracotomy.
Consecutive
NSCLC
surgically
confirmed
PD
were
retrospectively
enrolled
from
two
high-volume
centres
between
January
2016
and
December
2023.
Patients
divided
into
the
exploratory
thoracotomy
(ET)
group.
PTR
included
wedge
resection,
segmentectomy
lobectomy.
ET
group
received
biopsy
only.
Propensity
score
matching
(PSM)
was
used
to
reduce
selection
bias
confounding
factors.
Disease-specific
survival
(DSS)
progression-free
(PFS)
analysed
using
Kaplan‒Meier
method,
comparisons
made
log-rank
test.
Multivariate
Cox
regression
analyses
identify
independent
prognostic
A
total
of
223
identified:
167
(74.9%)
56
(25.1%)
The
median
follow-up
time
(MST)
39.0
months
49.0
months,
respectively.
MST
for
groups
44.0
60.0
respectively
(HR
0.80,
95%
CI
0.51–1.24;
p
=
0.3097).
After
PSM,
there
significant
differences
terms
disease-specific
(DSS:
vs.
61.0
0.3419)
or
(PFS:
30.0
47.0
0.5471)
groups.
analysis
revealed
that
smoking
history
a
size
≥
3
cm
risk
factors
DSS
PFS,
whereas
targeted
therapy
an
protective
factor.
Our
results
suggest
does
not
improve
long-term
It
high
re-evaluate
value
surgery
avoid
overtreatment,
especially
era
immunotherapy.
ClinicalTrials.gov
NCT06232967
(approval
date:
31,
2024).
American Journal of Translational Research,
Journal Year:
2025,
Volume and Issue:
17(2), P. 1311 - 1320
Published: Jan. 1, 2025
To
evaluate
the
efficacy
of
concurrent
chemoradiotherapy
(CCRT)
combined
with
immunotherapy
(IT)
for
locally
advanced
non-small-cell
lung
cancer
(LA-NSCLC).
Short-term
treatment
outcomes
during
two-year
follow-up
were
recorded,
and
2-year
survival
data
collected
to
analyze
prognosis
identify
factors
affecting
short-term
outcome.
Additionally,
a
predictive
model
was
developed.
We
conducted
retrospective
analysis
90
LA-NSCLC
patients
admitted
between
February
2018
2020.
Patients
grouped
according
their
regimens:
45
treated
4-6
cycles
CCRT
followed
by
1
year
Sintilimab
therapy
assigned
observation
group,
cisplatin/carboplatin
+
albumin-bound
paclitaxel
after
control
group.
adverse
reactions
recorded
both
groups.
up
IT
or
chemotherapy,
toxicity
evaluated.
During
follow-up,
overall
(OS)
progression-free
(PFS)
curves
plotted.
The
Cox
proportional
hazards
used
influencing
PFS
in
value
relevant
indicators
assessed
using
receiver
operating
characteristic
(ROC)
curves.
group
showed
superior
efficacy,
higher
objective
response
rates
(ORR)
disease
(DCR)
compared
(both
P
<
0.05).
Regarding
toxicity,
exhibited
more
severe
effects,
particularly
grade
III
gastrointestinal
reactions,
leukopenia,
thrombocytopenia,
anemia
(all
significantly
than
that
(P
incidence
pneumonia
but
it
demonstrated
better
OS
multivariate
revealed
included
distant
metastasis,
tumor
differentiation,
platelet-to-lymphocyte
ratio
(PLR),
prealbumin
(PAB).
ROC
areas
under
curve
(AUC)
predicting
based
on
PLR
PAB
0.662
0.774,
respectively,
AUC
these
0.812.
is
an
effective
LA-NSCLC,
improving
outcomes.
developed
may
help
assess
guide
early
clinical
intervention.
Attention
should
be
given
prevention
management
IT.
Moreover,
combination
enhances
prognostic
prediction
NSCLC
undergoing
plus
Oncology Letters,
Journal Year:
2025,
Volume and Issue:
29(4), P. 1 - 10
Published: March 4, 2025
The
objective
of
the
present
study
was
to
elucidate
mechanism
by
which
glycyrrhizin
enhances
antitumor
activity
cisplatin
in
non-small
cell
lung
cancer.
Initially,
A549
cells
were
treated
with
different
concentrations
(0.25-8
mM)
or
(10-160
µM)
for
48
h
investigate
effect
combined
on
vitro.
Subsequently,
divided
into
control
(untreated),
CP
(20
µM
cisplatin),
GL
(2
mM
glycyrrhizin)
and
+
2
groups
underlying
glycyrrhizin.
After
incubation,
viability
colony-forming
ability
assessed
using
MTT
colony
formation
assays.
Apoptosis
levels
cycle
progression
analyzed
flow
cytometry
western
blotting
used
evaluate
apoptosis-
cycle-related
proteins.
Additionally,
comet
assays
DNA
damage
relevant
results
demonstrated
both
individually
reduced
a
concentration-dependent
manner.
Cisplatin
lower
half-maximal
inhibitory
concentration
(IC50)
at
higher
concentrations,
an
IC50
value
~35
Furthermore,
treatment
synergistically
ability,
induced
apoptosis
arrested
G2
phase,
showing
greater
efficacy
when
compared
either
individually.
In
addition,
analysis
that,
comparison
alone,
markedly
increased
protein
expression
B-cell
lymphoma
2-associated
X
protein,
cleaved-caspase-3/caspase-3,
γH2AX,
phosphorylated-checkpoint
kinase
1
phosphorylated-p53/p53,
while
notably
reducing
2,
cyclin
D1,
cyclin-dependent
4.
findings
indicate
that
cancer
modulating
apoptosis.