Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Aug. 26, 2022
Necroptosis
is
a
novel
type
of
regulated
cell
death
that
intimately
associated
with
variety
tumors.
However,
how
necroptosis
affects
the
identification
gastric
cancer
(GC)
remains
unclear.
Here
we
seek
to
find
new
potential
necroptosis-related
biomarkers
predict
GC
prognosis
and
immunotherapy
effect.
We
used
Cox
analysis
obtain
shared
prognostic
markers
related
from
five
datasets
(TCGA
four
GEO
datasets).
Then,
gene
score
(NRGPS)
system
was
constructed
using
LASSO
regression,
NRGPS
consisting
three
mRNAs
(AXL,
RAI14,
NOX4)
identified,
31
pairs
adjacent
normal
tissues
Second
Hospital
Harbin
Medical
University
were
collected
Real-Time
Quantitative
PCR
(RT-qPCR)
detect
relative
expression
levels
mRNAs,
external
validation
performed
on
(GSE84437,
GSE26901,
GSE62254
GSE15459).
In
this
study,
Overall
survival
(OS)
in
high-NRGPS
group
significantly
lower
than
low-NRGPS
group.
regression
analyses
showed
an
independent
variable.
Tumor-mutation-burden
(TMB),
tumor
microenvironment
(TME),
microsatellite
instability
(MSI),
Tumor
Immune
Dysfunction
Exclusion
(TIDE)
scoring
as
predictors
response.
A
cancer-friendly
immune
microenvironment,
high
TIDE
score,
low
TMB,
MSI
all
characteristics
group,
they
consistently
issues
seen
there
are
escape
GC.
The
combination
candidate
genes
may
be
effective
method
for
diagnostic
assessment
efficacy.
Cell Death Discovery,
Journal Year:
2022,
Volume and Issue:
8(1)
Published: Aug. 29, 2022
Gastric
cancer
is
a
gastrointestinal
tumor
with
high
morbidity
and
mortality
rates.
Several
factors
influence
its
progression,
cell
death
being
an
important
element.
In
this
review,
we
summarized
the
effects
of
necrosis,
apoptosis,
necroptosis,
pyroptosis,
ferroptosis,
eight
less
common
modalities
on
gastric
cells
microenvironment,
detailed
molecular
mechanisms
various
their
major
regulatory
pathways
in
cancer,
explored
prevalence
complexity
progression
highlighted
potentials
death-related
therapies
cancer.
Frontiers in Genetics,
Journal Year:
2022,
Volume and Issue:
13
Published: Feb. 16, 2022
Background:
Breast
invasive
carcinoma
(BRCA)
is
the
second
leading
cause
of
malignancy
death
among
women.
Necroptosis
a
newly
discovered
mechanism
cell
involved
in
progression
and
prognosis
cancer.
The
role
necroptosis-related
genes
(NRGs)
BRCA
still
mystery.
Methods:
LASSO
Cox
regression
analysis
was
performed
to
construct
prognostic
signature.
A
ceRNA
constructed
explore
potential
lncRNA-miRNA-mRNA
regulatory
axis
BRCA.
Results:
total
63
were
differentially
expressed
We
also
summarized
genetic
mutation
landscape
NRGs
patients
with
low
expression
BCL2
LEF1,
as
well
high
PLK1
BNIP3,
had
poor
OS,
DSS,
DFS.
signature
four
(BCL2,
PLK1,
BNIP3)
constructed,
it
could
serve
biomarker
BRCA,
predicting
OS
rate
medium
accuracy.
Moreover,
risk
score
correlated
immune
infiltration
Further
comprehensive
revealed
that
BCL2,
BNIP3
tumor
burden,
microsatellite
instability,
drug
sensitivity,
pathology
stage.
Previous
studies
have
been
extensively
studied.
roles
selected
for
further
analysis.
then
network,
which
identified
an
lncRNA
LINC00665/miR-181c-5p/BCL2
Conclusion:
bioinformatics
method
develop
containing
network
vivo
vitro
should
be
conducted
verify
these
results.
International Journal of Molecular Sciences,
Journal Year:
2023,
Volume and Issue:
24(11), P. 9392 - 9392
Published: May 28, 2023
Clear
cell
renal
carcinoma
(ccRCC)
is
one
of
the
most
prevalent
cancers,
and
PANoptosis
a
distinct,
inflammatory-programmed
death
regulated
by
PANoptosome.
The
essential
regulators
cancer
occurrence
progression
are
microRNAs
(miRNAs).
However,
potential
function
PANoptosis-related
(PRMs)
in
ccRCC
remains
obscure.
This
study
retrieved
samples
from
Cancer
Genome
Atlas
database
three
Gene
Expression
Omnibus
datasets.
PRMs
were
recognized
based
on
previous
reports
scientific
literature.
Regression
analyses
used
to
identify
prognosis
construct
miRNA
prognostic
signature
risk
score.
We
discovered
that
high-risk
patients
had
poorer
survival
prognoses
significantly
linked
high-grade
advanced-stage
tumors,
using
variety
R
software
packages
web
analysis
tools.
Furthermore,
we
demonstrated
low-risk
group
significant
changes
their
metabolic
pathways.
In
contrast,
was
characterized
high
immune
infiltration,
checkpoint
expression,
low
half-maximum
inhibition
concentration
(IC50)
values
chemotherapeutic
agents.
suggests
may
benefit
more
immunotherapy
chemotherapy.
conclusion,
constructed
microRNA
revealed
its
significance
clinicopathological
features
tumor
immunity,
thereby
providing
new
precise
treatment
strategies.
Frontiers in Genetics,
Journal Year:
2022,
Volume and Issue:
13
Published: Aug. 15, 2022
Background:
Colorectal
cancer
(CRC)
is
one
gastrointestinal
malignancy,
accounting
for
10%
of
diagnoses
and
cancer-related
deaths
worldwide
each
year.
Therefore,
it
urgent
to
identify
genes
involved
in
CRC
predicting
the
prognosis.
Methods:
CRC's
data
were
acquired
from
Gene
Expression
Omnibus
(GEO)
database
(GSE39582
GSE41258
datasets)
The
Cancer
Genome
Atlas
(TCGA)
database.
differentially
expressed
necroptosis-related
(DENRGs)
sorted
out
between
tumor
normal
tissues.
Univariate
Cox
regression
analysis
least
absolute
shrinkage
selectionator
operator
(LASSO)
applied
selected
DENRGs
concerning
patients'
overall
survival
construct
a
prognostic
biomarker.
effectiveness
this
biomarker
was
assessed
by
Kaplan-Meier
curve
receiver
operating
characteristic
(ROC)
analysis.
GSE39582
dataset
utilized
as
external
validation
signature.
Moreover,
using
univariate
multivariate
analyses,
independent
factors
identified
nomogram.
Next,
signaling
pathways
regulated
signature
explored
through
gene
set
enrichment
(GSEA).
single
sample
(ssGSEA)
algorithm
immune
dysfunction
exclusion
(TIDE)
used
explore
correlation
two
groups,
high-risk
low-risk
ones.
Finally,
genes'
expression
examined
dataset.
Results:
In
total,
27
filtered,
based
on
6
constructed,
which
may
better
understand
(OS)
CRC.
manifested
signature,
ROC
showed
same
result.
addition,
analyses
revealed
that
age,
pathology
T,
risk
score
factors,
nomogram
established.
Furthermore,
most
significantly
associated
with
apoptosis
pathway.
Meanwhile,
24
cells
represented
significant
differences
like
activated
B
cell.
32
checkpoints,
TIDE
scores,
PD-L1
T-cell
scores
different
groups.
6-gene
levels
samples
Conclusion:
Our
study
established
including
could
assess
prognosis
patients
Journal of Immunology Research,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 21
Published: May 5, 2022
Breast
cancer
(BRCA)
is
one
of
the
leading
causes
death
among
women
worldwide,
and
drug
resistance
often
leads
to
a
poor
prognosis.
Necroptosis
type
programmed
cell
(PCD)
exhibits
regulatory
effects
on
tumor
progression,
but
few
studies
have
focused
relationships
between
necroptosis-associated
lncRNAs
BRCA.
In
this
study,
we
established
signature
basis
7
necroptosis-related
associated
with
prognosis
divided
BRCA
patients
into
high-
low-risk
groups.
Kaplan-Meier
curves
all
showed
an
adverse
for
in
high-risk
group.
Cox
assays
confirmed
that
risk
score
was
independent
prognostic
factor
patients.
The
receiver
operating
characteristic
(ROC)
curve
proved
predictive
accuracy
area
under
(AUC)
values
reached
0.722.
nomogram
relatively
accurately
predicted
GSEA
analysis
suggested
related
signaling
pathways
biological
processes
enriched
groups
may
influence
microenvironment
(TME)
ssGSEA
difference
immune
infiltration,
pathway
activation,
checkpoint
expression
two
groups,
group
more
suitable
immunotherapy.
According
significant
IC50
can
be
guided
individualized
treatment
plan.
Overall,
authors
consisting
independently
predict
clinical
outcome
low-
populations
reason
immunotherapy
some
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: July 14, 2022
This
study
aims
to
investigate
the
immune
and
epigenetic
mutational
landscape
of
necroptosis
in
lung
adenocarcinoma
(LUAD),
identify
novel
molecular
phenotypes,
develop
a
prognostic
scoring
system
based
on
regulatory
molecules
for
better
understanding
tumor
microenvironment
(TIME)
LUAD.
Based
Cancer
Genome
Atlas
Gene
Expression
Omnibus
database,
total
29
overlapped
necroptosis-related
genes
were
enrolled
classify
patients
into
different
phenotypes
using
unsupervised
consensus
clustering.
We
systematically
correlated
with
clinical
features,
immunocyte
infiltrating
levels,
mutation
characteristics.
A
was
then
constructed,
termed
NecroScore,
quantify
LUAD
by
principal
component
analysis.
Three
distinct
confirmed.
Two
clusters
high
expression
regulators
“hot
tumors”,
while
another
phenotype
low
“cold
tumor”.
Molecular
characteristics,
including
frequency
types,
copy
number
variation,
regulon
activity
differed
significantly
among
subtypes.
The
as
an
independent
factor
(HR=1.086,
95%CI=1.040-1.133,
p<0.001),
able
predict
survival
outcomes
show
that
higher
scores
experienced
poorer
prognosis.
It
could
also
evaluate
responses
immunotherapy
chemotherapeutic
efficiency.
In
conclusion,
are
genome
diversity
pan-cancer,
playing
significant
role
forming
TIME
Necroptosis
can
distinguish
NecroScore
is
promising
biomarker
predicting
prognosis,
well
immuno-
benefits
Journal of Animal Breeding and Genetics,
Journal Year:
2024,
Volume and Issue:
141(4), P. 403 - 414
Published: Jan. 21, 2024
Abstract
Genomic
structural
variants
(SVs)
constitute
a
significant
proportion
of
genetic
variation
in
the
genome.
The
rapid
development
long‐reads
sequencing
has
facilitated
detection
long‐fragment
SVs.
There
is
no
published
study
to
detect
SVs
using
long‐read
data
from
sheep.
We
applied
mapping
approach
and
characterized
total
30,771
insertions,
deletions,
inversions
translocations.
identified
716,
916,
842
303
specific
Southdown
sheep,
Alpine
merino
Qilian
White
Tibetan
sheep
Oula
respectively.
annotated
these
found
that
SV‐related
genes
were
primarily
enriched
well‐established
pathways
involved
regulation
immune
system,
growth
environmental
adaptability.
detected
based
on
NGS
resequencing
validate
accuracy
third‐generation
detection.
Moreover,
five
candidate
verified
PCR
method
50
Our
first
use
construct
novel
map
have
completed
preliminary
exploration
potential
effects
Cell Death Discovery,
Journal Year:
2025,
Volume and Issue:
11(1)
Published: March 10, 2025
Abstract
Cell
death
is
critical
in
tumor
biology.
The
common
cancer
therapies
can
cause
cell
and
alleviate
tumor,
while
the
cells
develop
a
resistance
to
survive
from
therapies.
Thus,
not
only
observing
alternative
mechanisms
of
resistant
death,
but
also
understanding
intricate
dynamics
processes
within
microenvironment
(TME),
are
essential
for
tailoring
effective
therapeutic
strategies.
High-throughput
sequencing
technologies
have
revolutionized
research
by
enabling
comprehensive
molecular
profiling.
Recent
advances
single
unraveled
heterogeneity
TME
components,
shedding
light
on
their
complex
interactions.
In
this
review,
we
explored
interplay
between
signaling
TME,
summarised
potential
drugs
inducing
pre-clinical
stage,
reviewed
some
studies
applying
next-generation
research,
discussed
future
utilization
updated
platforms
screening
novel
treatment
methods
targeted
death.
conclusion,
leveraging
multi-omics
dissect
context
holds
great
promise
advancing
therapy
development.