ONCOLOGIE,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Sept. 2, 2024
Abstract
Objectives
Metastasis
of
tumor
cells
is
the
leading
reason
for
mortality
among
patients
diagnosed
with
gastric
cancer
(GC).
Emerging
evidence
indicated
a
strong
correlation
between
programmed
cell
death
(PCD)
and
invasion
metastasis
cells.
Therefore,
we
aimed
to
develop
signature
assess
prognosis
therapeutic
efficacy
in
GC
patients.
Methods
Here,
collected
1911
PCD-related
genes
from
19
different
PCD
patterns,
developed
an
immune-derived
multiple
index
(MPCDI)
using
integrating
machine
learning
multi-omics
analysis,
systematically
dissected
heterogeneity
Subsequently,
divided
into
two
categories,
namely
high-MPCDI
group
low-MPCDI
group,
median
MPCDI
as
threshold.
We
performed
comprehensive
analysis
clinical
characteristics,
somatic
mutations,
immune
infiltration,
drug
sensitivity,
immunotherapeutic
groups.
Results
Survival
immunotherapy
response
analyses
that
experienced
poorer
overall
survival
(p=0.018)
were
more
resistant
commonly
used
chemotherapeutic
drugs
but
benefited
compared
In
addition,
was
confirmed
standalone
risk
factor
survival,
nomograms
can
provide
precise
tool
diagnosis
Conclusions
Taken
together,
serve
robust
diagnostic
classifier
guide
medication
administration
improve
outcomes
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 15, 2025
PANoptosis
is
one
of
several
modes
programmed
cell
death
(PCD)
and
plays
an
important
role
in
many
inflammatory
immune
diseases.
The
bowel
disease
(IBD)
currently
unknown.
Differentially
expressed
PANoptosis-related
genes
(DE-PRGs)
were
identified,
pathway
enrichment
analyses
performed.
LASSO
regression
model
construction,
a
nomogram
model,
calibration
curves,
ROC
DCA
curves
used
to
evaluate
the
predictive
value
model.
Predicts
transcription
factors
(TFs)
small-molecule
drugs
DE-PRGs
analysed.
Model
immuno-infiltration
features
IBD
include
12
genes:
OGT,
TLR2,
GZMB,
TLR4,
PPIF,
YBX3,
CASP5,
BCL2L1,
CASP6,
MEFV,
GSDMB
BAX.
analysis
suggested
that
these
related
TNF
signalling,
NF-κB,
pyroptosis
necroptosis.
Machine
learning
identified
three
GZMB
CASP5.
have
strong
value.
Immuno-infiltration
revealed
infiltration
was
increased
patients
with
IBD,
closely
various
cells.
TFs
associated
RELA,
NFKB1,
HIF1A,
TP53
SP1.
In
addition,
Connectivity
Map
(CMap)
database
top
10
compounds,
including
buspirone,
chloroquine,
spectinomycin
chlortetracycline.
This
study
indicate
good
ability
for
IBD.
Moreover,
may
mediate
process
through
pyroptosis,
necroptosis
mechanisms.
These
results
present
new
horizon
research
treatment
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 11, 2025
Lung
cancer,
particularly
adenocarcinoma,
ranks
high
in
morbidity
and
mortality
rates
worldwide,
with
a
relatively
low
five-year
survival
rate.
To
achieve
precise
prognostic
assessment
clinical
intervention
for
patients,
thereby
enhancing
their
prospects,
there
is
an
urgent
need
more
accurate
stratification
schemes.
Currently,
the
TNM
staging
system
predominantly
used
practice
evaluation,
but
its
accuracy
constrained
by
reliance
on
physician
experience.
Although
biomarker
discovery
based
molecular
pathology
offers
new
perspective
assessment,
dependence
expensive
gene
panel
testing
limits
widespread
application.
Pathological
images
contain
abundant
diagnostic
information,
providing
avenue
evaluation.
In
this
study,
we
employed
advanced
Hover-Net
technology
to
accurately
quantify
abundance
of
epithelial
cells,
lymphocytes,
macrophages,
neutrophils
from
pathological
images,
delved
into
biological
significance
these
cellular
abundances.
Our
research
findings
reveal
that,
contrast
patients
classified
as
N0
stage,
those
belonging
N1
stage
demonstrated
marked
elevation
infiltration
neutrophils.
Notably,
patterns
lymphocytes
exhibited
inverse
relationship
activation
status
numerous
pivotal
pathways,
including
HALLMARK_HEME_METABOLISM
pathway.
Furthermore,
our
analysis
distinguished
FABP7
biomarker,
exhibiting
pronounced
differential
expression
between
levels
neutrophil
infiltration,
indicate
that
can
provide
cost-effective
offering
strategies
management
lung
adenocarcinoma.
PeerJ,
Journal Year:
2025,
Volume and Issue:
13, P. e18895 - e18895
Published: Feb. 10, 2025
Background
Tumor
development
involves
the
critical
role
of
programmed
cell
death
(PCD),
but
correlation
between
colon
adenocarcinoma
(COAD)
and
PCD-related
genes
is
not
clear.
Methods
Subtyping
analysis
COAD
was
performed
by
consensus
clustering
based
on
The
Cancer
Genome
Atlas
(TCGA),
with
AC-ICAM
queue
from
cBioportal
database
as
a
validation
set.
Immune
infiltration
samples
evaluated
using
CIBERSORT
Microenvironment
Cell
Populations
(MCP)-counter
algorithms.
Patients’
immunotherapy
response
predicted
TIDE
aneuploidy
scores.
Pathway
enrichment
conducted
gene
set
(GSEA).
A
RiskScore
model
established
independent
prognostic
filtered
Cox
regression
analysis.
mafCompare
function
used
to
compare
differences
in
mutation
rates
somatic
genes.
Wound
healing,
transwell
assays
Flow
cytometer
were
applied
measure
migration,
invasion
apoptosis.
Results
patients
grouped
into
S1
S2
subtypes
total
21
PCD
associated
outcomes
COAD.
Specifically,
subtype
mainly
related
pathway
activation
tumor
deterioration
had
worse
prognosis.
six
genes,
including
two
protective
(
ATOH1
,
ZG16
)
four
risk
HSPA1A
SEMA4C
CDKN2A
ARHGAP4
).
Notably,
silencing
inhibited
activity
migration
promoted
apoptosis
cells.
Based
model,
high-
low-risk
groups.
Independent
factors,
namely,
Age,
pathologic_M,
pathologic_stage,
RiskScore,
integrated
develop
nomogram
strong
good
prediction
performance.
High-risk
group
high-expressed
immune
checkpoint
higher
scores,
showing
escape
ability
less
active
response.
Compared
group,
TP53
exhibited
rate
high-risk
group.
Conclusion
We
constructed
for
assessment
COAD,
providing
valuable
insight
exploration
new
targets
improvement
Frontiers in Cell and Developmental Biology,
Journal Year:
2025,
Volume and Issue:
13
Published: Feb. 26, 2025
Lung
cancer
(LC)
is
a
highly
prevalent
and
deadly
type
of
characterized
by
intricate
molecular
pathways
that
drive
tumor
development,
metastasis,
resistance
to
conventional
treatments.
Recently,
ferroptosis,
controlled
mechanism
cell
death
instigated
iron-dependent
lipid
peroxidation,
has
gained
attention
for
its
role
in
LC
progression
treatment.
Noncoding
RNAs
(ncRNAs),
such
as
microRNAs
(miRNAs)
long
noncoding
(lncRNAs),
are
emerging
key
modulators
significantly
influencing
biology.
This
review
explores
how
ncRNAs
control
ferroptotic
affect
growth,
therapy
LC.
By
understanding
the
dual
functions
both
activating
inhibiting
we
aim
uncover
new
therapeutic
targets
strategies
These
insights
provide
promising
direction
development
ncRNA-based
treatments
designed
induce
potentially
improving
outcomes
patients
with
Frontiers in Genetics,
Journal Year:
2025,
Volume and Issue:
16
Published: April 8, 2025
Lung
cancer
has
the
highest
mortality
rate
among
all
cancers
worldwide.
Alkaliptosis
is
characterized
by
a
pH-dependent
form
of
regulated
cell
death.
In
this
study,
we
constructed
model
related
to
alkaliptosis-associated
long
non-coding
RNAs
(lncRNAs)
and
developed
prognosis-related
framework,
followed
identification
potential
therapeutic
drugs.
The
TCGA
database
was
utilized
obtain
RNA-seq-based
transcriptome
profiling
data,
clinical
information,
mutation
data.
We
conducted
multivariate
Cox
regression
analysis
identify
alkaliptosis-related
lncRNAs.
Subsequently,
employed
training
group
construct
prognostic
testing
validate
model's
accuracy.
Calibration
curves
were
generated
illustrate
discrepancies
between
predicted
observed
outcomes.
Principal
Component
Analysis
(PCA)
performed
investigate
distribution
LUAD
patients
across
high-
low-risk
groups.
Additionally,
Gene
Ontology
(GO)
Set
Enrichment
(GSEA)
conducted.
Immune
infiltration
Tumor
Mutational
Burden
(TMB)
analyses
carried
out
using
CIBERSORT
maftools
algorithms.
Finally,
"oncoPredict"
package
predict
immunotherapy
sensitivity
further
forecast
anti-tumor
immune
qPCR
used
for
experimental
verification.
identified
155
lncRNAs
determined
that
5
these
serve
as
independent
factors.
progression-free
survival
(PFS)
overall
(OS)
rates
significantly
higher
than
those
high-risk
group.
risk
signature
functions
factor
other
variables.
Different
stages
(I-II
III-IV)
effectively
lung
adenocarcinoma
(LUAD)
patients,
can
reliably
signatures.
GSEA
revealed
processes
chromosome
segregation
response
activation
enriched
in
both
exhibited
lower
fraction
plasma
cells
proportion
activated
CD4
memory
T
cells.
OS
low
TMB
compared
high
Furthermore,
drug
greater
These
may
biomarkers
treating
patients.
summary,
construction
an
lncRNA
provides
new
insights
into
diagnosis
treatment
advanced