Frontiers in Oncology,
Journal Year:
2024,
Volume and Issue:
14
Published: Dec. 5, 2024
Stomach
cancer
is
considered
the
fifth
most
common
worldwide.
This
study
utilized
bibliometric
analysis
to
construct
a
visualization
map
of
relationship
between
stomach
and
exosomes,
aiming
reveal
research
trends
emerging
themes,
provide
direction
for
future
research.
BMC Cancer,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Feb. 21, 2024
Abstract
Background
The
benefit
of
adding
Zolbetuximab
to
the
treatment
in
patients
with
Claudin-18
isoform
2
(CLDN18.2)-positive,
human
epidermal
growth
factor
receptor
2-negative,
locally
advanced
unresectable
or
metastatic
gastric
gastro-oesophageal
junction
adenocarcinoma
(GC/GEJ)
is
not
yet
fully
elucidated.
Methods
We
searched
PubMed,
Embase
and
Cochrane
databases
for
randomized
controlled
trials
(RCTs)
that
investigated
plus
chemotherapy
versus
alone
GC
GEJ
adenocarcinoma.
computed
hazard-ratios
(HRs)
odds-ratios
(ORs)
binary
endpoints,
95%
confidence
intervals
(CIs).
Results
Three
studies
1,233
were
included.
Comparing
alone,
progression-free
survival
(PFS)
rate
(HR
0.64;
CI
0.49–0.84;
p
<
0.01)
overall
(OS)
0.72;
0.62–0.83;
significant
favor
group.
Regarding
effectiveness,
Objective
Response
Rate
(ORR)
was
(OR
1.15;
0.87–1.53;
=
0.34).
Conclusions
In
this
comprehensive
systematic
review
meta-analysis
RCTs,
incorporation
alongside
offers
a
promising
prospect
reshaping
established
paradigms
diagnosed
CLDN18.2-positive
GC/GEJ
cancer.
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: Jan. 31, 2024
P66Shc
and
Rac1
proteins
are
responsible
for
tumor-associated
inflammation,
particularly
in
brain
tumors
characterized
by
elevated
oxidative
stress
increased
reactive
oxygen
species
(ROS)
production.
Quercetin,
a
natural
polyphenolic
flavonoid,
is
well-known
redox
modulator
with
anticancer
properties.
It
has
the
capacity
to
cross
blood–brain
barrier
and,
thus,
could
be
possible
drug
against
tumors.
In
this
study,
we
explored
effect
of
quercetin
on
Rac1/p66Shc-mediated
tumor
cell
which
principal
pathway
generation
ROS
cells.
Glioma
cells
transfected
Rac1,
p66Shc,
or
both
were
treated
varying
concentrations
different
time
points.
Quercetin
significantly
reduced
viability
migration
an
ROS-dependent
manner
concomitant
inhibition
Rac1/p66Shc
expression
production
naïve
Rac1/p66Shc-transfected
lines,
suggestive
preventing
activation.
Through
molecular
docking
simulations,
observed
that
showed
best
binding
compared
other
known
inhibitors
specifically
blocked
GTP-binding
site
A-loop
prevent
GTP
We
conclude
exerts
its
effects
via
modulation
Rac1-p66Shc
signaling
inhibiting
activation,
thus
restraining
growth.
Abstract
Gastric
cancer
(GC)
represents
a
prevalent
malignancy
globally,
often
diagnosed
at
advanced
stages
owing
to
subtle
early
symptoms,
resulting
in
poor
prognosis.
Exosomes
are
extracellular
nano-sized
vesicles
and
secreted
by
various
cells.
Mounting
evidence
indicates
that
exosomes
contain
wide
range
of
molecules,
such
as
DNA,
RNA,
lipids,
proteins,
play
crucial
roles
multiple
cancers
including
GC.
Recently,
with
the
rapid
development
mass
spectrometry-based
detection
technology,
researchers
have
paid
increasing
attention
exosomal
cargo
proteins.
In
this
review,
we
discussed
origin
diagnostic
prognostic
proteins
Moreover,
summarized
biological
functions
GC
processes,
proliferation,
metastasis,
drug
resistance,
stemness,
immune
response,
angiogenesis,
traditional
Chinese
medicine
therapy.
summary,
review
synthesizes
current
advancements
associated
GC,
offering
insights
could
pave
way
for
novel
therapeutic
strategies
foreseeable
future.
Discover Oncology,
Journal Year:
2025,
Volume and Issue:
16(1)
Published: March 16, 2025
Cisplatin
chemotherapy
is
an
important
treatment
for
advanced
ovarian
cancer
(OC).
However,
the
development
of
cisplatin
resistance
greatly
limits
survival
time
OC
patients.
Endothelial
cell-specific
molecule
1
(ESM1)
has
been
found
to
be
proto-oncogene
promoting
OC,
but
its
mediating
remains
unknown.
We
used
quantitative
polymerase
chain
reaction
(qPCR)
measure
transcription
levels
ESM1,
Growth
arrest
specific
transcript
5
(GAS5),
miR-23a-3p,
and
Phosphatase
And
Tensin
Homolog
(PTEN).
A
double
luciferase
reporter
gene
assay
confirmed
direct
binding
GAS5
miR-23a-3p
PTEN
mRNA.
The
effects
GAS5,
on
were
tested
with
Half
Maximal
Inhibitory
Concentration
(IC50)
assay.
Flow
cytometry
was
assess
cisplatin-induced
apoptosis.
Changes
in
apoptosis-related
proteins
PI3K/AKT-related
analyzed
western
blot
(WB).
ESM1
inhibits
increases
miR-23a-3p.
promote
resistance.
sensitivity
cells.
Moreover,
main
molecular
mechanism
ESM1/GAS5/miR-23a-3p/PTEN/PI3K/Akt
signaling
axis.
promotes
by
activating
Phosphoinositide-3-Kinase
(PI3K)/AKT
Serine/Threonine
Kinase
(Akt)
pathway
through
GAS5/miR-23a-3p/PTEN
This
suggests
that
prescriptive
regulates
key
downstream
mechanisms
via
non-coding
RNA
can
before
neoadjuvant
initiated.
Cancer Cell International,
Journal Year:
2025,
Volume and Issue:
25(1)
Published: April 13, 2025
Platinum
was
the
first
drug
with
proven
activity
against
gastric
cancer
(GC),
combination
fluoropyrimidine
is
standard
first-line
systemic
therapy
for
patients
of
GC.
However,
a
major
cause
treatment
failure
still
existence
resistance.
The
purpose
this
study
to
identify
and
validate
platinum-related
genes
in
GC
construct
multi-gene
joint
signature
predicting
prognosis
patients.
Based
on
326
from
GeneCards,
GO
KEGG
analysis
were
applied
differentially
expressed
GC,
UniCox
regression
used
select
effective
Lasso-Cox
utilized
model.
Stratified
analysis,
CNV
landscape,
TMB
MSI
status,
HLA
gene
expression,
GSEA
GSVA
immune
activities,
immunotherapy
sensitivities
evaluated
resistant
high
low
groups.
Drug
cell
lines,
PDO
PDX
models
signature.
140
involved
many
processes
pathways
enriched
platinum
resistance
cancer.
screened
out
21
conducted
scoring
indicated
that
score
had
good
predictive
value
subgroups
divided
by
T-stage,
age
race.
changes
more
occurred
score-high
group,
most
model
negatively
correlated
TMB,
expression.
group
significantly
higher,
within
mast
cell,
regulatory
T
dendritic
infiltrated
in.
In
vitro
vivo
showed
varying
degrees
upregulation
under
CDDP
chemotherapy
pressure.
gene-signature
developed
predict
response
It
worthwhile
further
evaluate
molecular
biology
clinical
applications
European Journal of Medicinal Chemistry,
Journal Year:
2024,
Volume and Issue:
274, P. 116528 - 116528
Published: May 23, 2024
Herein,
we
present
a
comprehensive
review
focusing
on
synthetic
strategies,
detailed
structural
analysis,
and
anticancer
activity
investigations
of
complexes
following
the
general
formula
[L