Frontiers in Immunology,
Journal Year:
2024,
Volume and Issue:
15
Published: Sept. 5, 2024
Immunotherapy
has
profoundly
changed
the
treatment
of
gastric
cancer,
but
only
a
minority
patients
benefit
from
immunotherapy.
Therefore,
numerous
studies
have
been
devoted
to
clarifying
mechanisms
underlying
resistance
immunotherapy
or
developing
biomarkers
for
patient
stratification.
However,
previous
focused
mainly
on
tumor
microenvironment.
Systemic
immune
perturbations
long
observed
in
with
and
involvement
peripheral
system
effective
anticancer
responses
attracted
much
attention
recent
years.
understanding
distinct
types
systemic
organization
cancer
will
aid
personalized
designed
pair
traditional
therapies
alleviate
their
detrimental
effects
immunity
directly
activate
response
immunity.
Herein,
this
review
aims
comprehensively
summarize
including
induced
by
therapies,
potential
clinical
applications
detection,
prediction,
prognosis
therapy
cancer.
Clinical and Experimental Medicine,
Journal Year:
2024,
Volume and Issue:
24(1)
Published: Sept. 26, 2024
Abstract
Long
non-coding
RNAs
(lncRNAs)
have
emerged
as
crucial
regulators
in
various
cellular
processes,
including
cancer
progression
and
stress
response.
Recent
studies
demonstrated
that
copper
accumulation
induces
a
unique
form
of
cell
death
known
cuproptosis,
with
lncRNAs
playing
key
role
regulating
cuproptosis-associated
pathways.
These
may
trigger
cell-specific
responses
to
stress,
presenting
new
opportunities
prognostic
markers
therapeutic
targets.
This
paper
delves
into
the
cuproptosis-mediated
cancer,
underscoring
their
potential
biomarkers
targets
for
innovative
strategies.
A
thorough
review
scientific
literature
was
conducted,
utilizing
databases
such
PubMed,
Google
Scholar,
ScienceDirect,
search
terms
like
'lncRNAs,'
'cuproptosis,'
'cancer.'
Studies
were
selected
based
on
relevance
lncRNA
regulation
cuproptosis
pathways
implications
prognosis
treatment.
The
highlights
significant
contribution
cuproptosis-related
genes
pathways,
impacting
metabolism,
mitochondrial
responses,
apoptotic
signaling.
Specific
are
breast,
lung,
liver,
ovarian,
pancreatic,
gastric
cancers.
objective
this
article
is
explore
cancers
mediated
by
cuproptosis.
Cancer Immunology Immunotherapy,
Journal Year:
2025,
Volume and Issue:
74(4)
Published: Feb. 25, 2025
Gastric
cancer
(GC)
is
one
of
the
most
common
causes
cancer-related
death
worldwide.
As
a
novel
form
programmed
cell
death,
disulfidptosis
characterized
by
excessive
cysteine
accumulation,
disulfide
stress
and
actin
destruction.
There
evidence
that
targeting
promising
anticancer
strategy.
Further
improvement
GC
risk
stratification
based
on
has
positive
clinical
significance.
We
analyzed
expression
levels
disulfidptosis-associated
genes
(DPAGs)
in
normal
tissues
molecular
subtypes
patients.
Based
characteristics
DPAG
subtypes,
differentially
expressed
prognosis-related
were
selected
LASSO-univariate
Cox
analysis
multivariate
to
establish
prognostic
model.
Using
single-cell
sequencing
reveals
subpopulation
for
GC.
The
function
target
was
verified
vitro
experimental
means,
including
siRNA,
qRT-PCR,
Western
blot,
CCK-8,
Transwell
assay.
score
be
an
independent
factor
significantly
associated
with
poor
prognosis
gastric
cancer.
Subsequent
studies
subgroup
immunoinfiltration
characteristics,
drug
sensitivity
analysis,
immunotherapy
response
somatic
mutation
comprehensively
confirmed
potential
guiding
significance
individualized
treatment
Single-cell
revealed
DPAG-related
signatures
across
subpopulations.
In
experiments
showed
APC11,
as
DPAGs,
highly
cancer,
knockdown
APC11
could
inhibit
proliferation
migration
cells,
demonstrating
reliability
bioinformatics
results.
results
this
study
provide
new
perspective
exploring
role
occurrence
development
Frontiers in Pharmacology,
Journal Year:
2024,
Volume and Issue:
15
Published: May 9, 2024
Gastric/gastroesophageal
junction
(G/GEJ)
cancer
represents
a
significant
global
health
challenge.
Radical
surgery
remains
the
cornerstone
of
treatment
for
resectable
G/GEJ
cancer.
Supported
by
robust
evidence
from
multiple
clinical
studies,
therapeutic
approaches,
including
adjuvant
chemotherapy
or
chemoradiation,
and
perioperative
chemotherapy,
are
generally
recommended
to
reduce
risk
recurrence
enhance
long-term
survival
outcomes
post-surgery.
In
recent
years,
immune
checkpoint
inhibitors
(ICIs)
have
altered
landscape
systemic
advanced
metastatic
cancer,
becoming
standard
first-line
therapy
specific
patients.
Consequently,
exploring
efficacy
ICIs
in
neoadjuvant
setting
is
worthwhile.
This
review
summarizes
current
advances
application
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
14
Published: Jan. 7, 2025
Gastrointestinal
(GI)
cancers
represent
a
significant
global
health
burden,
and
the
need
for
more
effective
treatment
options
is
exceptionally
pressing.
The
present
meta-analysis
aimed
to
explore
efficacy
safety
of
combination
nivolumab
ipilimumab
in
treating
GI
cancers.
A
systematic
search
four
databases
(PubMed,
Embase,
Web
Science,
Cochrane
Library)
was
conducted
articles
on
with
combined
ipilimumab,
published
from
2014
up
30
August
2024.
inclusion
criteria
were
designed
according
principles
Participants,
Intervention,
Control,
Outcomes,
Study
(PICOS).
control
group
chemotherapy
or
monotherapy
other
drugs.
We
extracted
data
10
randomized
controlled
trials
utilized
random
effects
model
assess
objective
response
rate
(ORR),
median
progression-free
survival
(mPFS),
overall
(mOS),
duration
(mDOR),
treatment-related
adverse
events
(TRAEs).
analysis
using
Review
Manager
version
5.4
Stata
12.0.
Overall,
demonstrated
superior
outcomes,
including
higher
ORR
(OR
=
1.69,
P
0.01),
prolonged
mOS
(MD
1.74,
0.04)
extended
mDOR
5.64,
<
0.00001)
compared
group.
Subgroup
that
1.75,
0.02)
5.02,
0.003)
significantly
improved
patients
esophageal
cancer.
Notably,
biliary
cancer
lower
0.11,
0.04).
Additionally,
NIVO1
+
IPI3group
2.82,
0.01)
NIVO3
IPI1
1.62,
0.01).
Regarding
safety,
there
no
statistically
difference
between
regimen
terms
any
grade
0.72,
0.26)
3-4
TRAEs
1.36,
0.14).
Nivolumab
(especially
cancer)
without
causing
reactions.
However,
its
still
needs
be
further
proven.
https://www.crd.york.ac.uk/prospero/,
identifier
CRD42024590994.
Research Square (Research Square),
Journal Year:
2025,
Volume and Issue:
unknown
Published: Feb. 14, 2025
Abstract
Background
DNA
methylation
alterations
play
a
crucial
role
in
rectal
cancer
development.
This
study
identifies
and
characterizes
methylation-driven
genes
the
TCGA-READ
cohort,
exploring
their
association
with
development
underlying
mechanism.
Methods
were
identified
using
MethylMix
package
subjected
to
gene
ontology
(GO)
enrichment
analysis
via
cluster
profiler
package.
Prognostic
model
involved
Lasso
regression
ten-fold
cross-validation,
followed
by
performance
evaluation
Kaplan-Meier
survival
curves,
time-dependent
ROC
calibration
decision
curve
analysis.
Cancer-promoting
mechanism
high
risk
score
group
was
clarified
through
set
(GSEA)
multi-algorithm-based
immune
infiltration
analyses.
Results
GO
highlighted
significant
functional
terms
based
on
490
genes,
implicating
Wnt
signaling
cell
fate
commitment
The
developed
prognostic
model,
consisting
of
CCNI2,
LINC00899,
ST6GALNAC1,
exhibited
predictive
accuracy.
Differential
expression
89
underexpressed
high-risk
group,
SULF1
as
hub
gene.
negative
regulation
process
malignant
tumor-associated
pathways
is
suppressed,
decreased
abundance
cytotoxic
cells,
such
NK
may
represent
potential
for
poor
prognosis
observed
group.
Conclusions
Our
findings
elucidate
landscape
cancer.
These
insights
contribute
deeper
understanding
progression
provide
targets
therapeutic
intervention.
Frontiers in Oncology,
Journal Year:
2025,
Volume and Issue:
15
Published: May 8, 2025
As
one
of
the
most
common
gastrointestinal
tumors,
Gastric
Cancer
(GC)
poses
a
serious
threat
to
human
health
due
its
high
morbidity
and
mortality.
The
current
treatment
strategy
is
comprehensive
program
mainly
based
on
surgery,
especially
for
advanced
GC
patients.
emergence
immune
checkpoint
inhibitors
has
completely
changed
this
status
quo,
synergistic
effect
neoadjuvant
immunotherapy
combined
with
chemotherapy
significantly
improved
resection
radical
rate
overall
survival
patients
local
GC.
We
present
case
locally
(cT4N0Mx)
microsatellite
instability
(MSI-H)
PD-L1
Combined
Positive
Score
(CPS)=2.
patient
received
therapy
Sintilimab
FOLFOX
(folinic
acid
(leucovorin),
5-fluorouracil
(5-FU),
oxaliplatin),
reduced
tumor
volume
after
3
cycles
treatment.
Then
she
underwent
subtotal
gastrectomy
gastrojejunostomy
D2
lymph
node
dissection.
postoperative
pathological
results
showed
that
no
cancerous
tissue
remained
in
tissue,
pathologic
complete
response
(pCR)
was
achieved.
first
cycle
adjuvant
same
protocol
surgery.
During
therapy,
experienced
side
effects
such
as
dyspepsia,
nausea
mild
myelosuppression.
Therefore,
potential
be
an
effective
option
resectable
MSI-H