Aging,
Journal Year:
2022,
Volume and Issue:
14(18), P. 7587 - 7616
Published: Sept. 26, 2022
As
a
type
of
programmed
cell
death,
necroptosis
is
thought
to
play
dual
role
in
tumorigenesis.
However,
comprehensive
assessment
necroptosis-related
regulators
across
human
cancers
has
not
been
reported.
Therefore,
this
study,
we
established
quantitative
index
evaluate
the
rate
and
determine
its
correlations
with
clinical
prognosis,
signaling
pathways
molecular
features,
immune
infiltration
regulation,
immunotherapy,
chemotherapy
sensitivity
cancers.
Our
results
indicated
that
score
can
act
as
favorable
or
risky
prognostic
factor
various
cancer
types.
A
gene
set
variation
analysis
suggested
significantly
associated
immune-
inflammation-related
pathways,
growth
apoptosis,
energy
metabolism.
Furthermore,
affect
tumor
microenvironment
immunity
effect
on
different
There
crosstalk
between
components
necroptosis,
pyroptosis,
ferroptosis
autophagy
multiple
types
Finally,
be
an
indicator
immunotherapy
effectiveness
cells.
study
presents
characterization
cancers,
highlights
potential
necroptotic
effects
provides
new
insights
into
development
individualized
treatments
applications
immunotherapy.
Scientific Reports,
Journal Year:
2025,
Volume and Issue:
15(1)
Published: Jan. 10, 2025
Biological
processes
intricately
intertwine
with
tumorigenesis,
significantly
influencing
treatment
outcomes
and
prognosis.
However,
the
mechanisms
fostering
mucoepidermoid
carcinoma
(MEC)
remain
inadequately
elucidated.
This
research
utilizes
expression
profiles
of
lncRNAs
from
clinical
MEC
tissues
matched
normal
glandular
tissues,
integrating
public
data
to
explore
biological
immune
microenvironment
characteristics
tumorigenesis.
Gene
set
enrichment
analysis
identified
key
pathways,
a
customized
epithelial-mesenchymal
transition
(EMT)
score
elucidated
relationship
between
pathological
prognosis,
while
an
signature
revealed
tumor
characteristics.
MECs
exhibited
significant
in
EMT
pathway,
genes
such
as
Secretogranin
II,
tissue
factor
pathway
inhibitor
2,
periostin
contributors
process.
High
scores
correlated
upregulated
response
activity,
indicating
poor
Single-sample
gene
unveiled
tumors'
infiltration
signature,
suggesting
active
antigen
presentation
positive
for
immunotherapy.
Additionally,
SLC2A1-AS1
CERS6-AS1
were
potential
mediators
environment.
study
provides
insights
into
tumorigenesis
identifies
therapeutic
targets
future
research.
Frontiers in Immunology,
Journal Year:
2023,
Volume and Issue:
13
Published: Jan. 4, 2023
Cuproptosis
was
characterized
as
a
novel
type
of
programmed
cell
death.
Recently,
however,
the
role
cuproptosis-related
long
noncoding
RNAs
(CRLs)
in
tumors
has
not
yet
been
studied.
Identifying
predictive
CRL
signature
hepatocellular
carcinoma
(HCC)
and
investigating
its
putative
molecular
function
were
goals
this
work.
Initially,
Pearson’s
test
used
to
assess
relationship
between
lncRNAs
cuproptosis-associated
genes
obtained
from
HCC
data
The
Cancer
Genome
Atlas
(TCGA).
By
implementing
differential
expression
univariate
Cox
analysis,
61
prognostic
CRLs
subsequent
least
absolute
shrinkage
selection
operator
(LASSO)
regression
analysis.
A
risk
score
model
then
constructed
evaluate
ability
predict
patients’
survival
when
combined
with
clinicopathological
parameters
HCC.
five-lncRNA
categorized
patients
into
high-
low-risk
groups.
group
exhibited
more
sensitivity
elesclomol
than
high-risk
one.
Surprisingly,
distinct
mitochondrial
metabolism
pathways
connected
cuproptosis
pivotal
immune-related
observed
two
groups
via
gene
set
enrichment
analysis
(GSEA).
Meanwhile,
there
substantial
differences
terms
tumor-infiltrating
immune
cells
(TIICs).
Furthermore,
positive
shown
checkpoints.
Additionally,
five
confirmed
our
own
samples
lines
RT-qPCR.
Finally,
vitro
assays
that
WARS2-AS1
MKLN1-AS
knockdown
could
sensitize
elesclomol-induced
cuproptosis.
Overall,
may
prognosis
an
independent
manner,
give
better
understanding
how
work
HCC,
offer
therapeutic
reference
for
Frontiers in Immunology,
Journal Year:
2022,
Volume and Issue:
13
Published: Nov. 25, 2022
Anoikis
is
a
form
of
programmed
cell
death
or
death(PCD)
for
short.
Studies
suggest
that
anoikis
involves
in
the
decisive
steps
tumor
progression
and
cancer
metastasis
spread,
but
what
part
it
plays
bladder
remains
unclear.
We
sought
to
screen
anoikis-correlated
long
non-coding
RNA
(lncRNA)
so
we
can
build
risk
model
understand
its
ability
predict
prognosis
immune
landscape.We
screened
seven
anoikis-related
lncRNAs
(arlncRNAs)
from
The
Cancer
Genome
Atlas
(TCGA)
designed
model.
It
was
validated
through
ROC
curves
clinicopathological
correlation
analysis,
demonstrated
be
an
independent
factor
prediction
by
uni-
multi-COX
regression.
In
meantime,
Kyoto
Encyclopedia
Genes
Genomes
(KEGG)
enrichment
infiltration,
half-maximal
inhibitory
concentration
(IC50)
were
implemented
with
Moreover,
divided
patients
into
three
subtypes
consensus
clustering
analysis
further
study
differences
prognosis,
infiltration
level,
checkpoints,
drug
susceptibility.We
arlncRNAs,
proved
accuracy
using
curves.
COX
regression
indicated
might
prognosis.
KEGG
showed
enriched
tumors
immune-related
pathways
among
people
at
high
risk.
Immune
susceptibility
results
had
higher
have
better
immunotherapy
efficacy
high-risk
groups.
Of
classified
cluster
3
revealed
positive
2
highest
level
sensitive
most
chemistries.
This
helpful
us
discover
more
precise
patients.In
nutshell,
found
arlncRNAs
built
identify
different
patients.
Immune-related
sensitivity
researches
demonstrate
provide
individual
therapeutic
schedule
greater
precision
Frontiers in Oncology,
Journal Year:
2023,
Volume and Issue:
13
Published: March 29, 2023
Purpose
Bladder
cancer
(BLCA)
is
one
of
the
most
frequently
diagnosed
urological
malignancies
and
4th
common
in
men
worldwide.
Molecular
targets
expressed
bladder
are
usually
used
for
developing
targeted
drug
treatments.
However,
poor
prognosis
immunotherapy
efficacy
remain
major
challenges
BLCA.
Numerous
studies
have
shown
that
long
non-coding
RNAs
(LncRNAs)
play
an
important
role
development
cancer.
lncRNAs
related
to
inflammation
BLCA
their
prognostic
value
unclear.
Therefore,
this
study
aimed
explore
new
potential
biomarkers
can
predict
prognosis.
Methods
We
downloaded
BLCA-related
RNA
sequencing
data
from
The
Cancer
Genome
Atlas
(TCGA)
searched
inflammation-related
(lncRNAs)
by
univariate
Cox
(uniCox)
regression
co-expression
analysis.
least
absolute
shrinkage
selection
operator
(LASSO)
analysis
construct
lncRNA
risk
model.
Samples
were
divided
into
high-risk
score
(HRS)
group
low-risk
(LRS)
based
on
median
scores.
independent
variable
factors
identified
(uni-Cox)
multivariate
(multi-Cox)
analyses,
receiver
operating
characteristic
(ROC)
curves
compare
different
predicting
outcomes.
Nomogram
Calibration
Plot
generated
R
package
rms
analyze
whether
prediction
results
correct
show
good
consistency.
Correlation
coefficients
calculated
Pearson
Kaplan-Meier
method
was
assess
value.
expression
7
with
also
confirmed
qRT-PCR
cell
lines.
Kyoto
Encyclopedia
Gene
(KEGG)
pathways
significantly
enriched
(
P
<
0.05)
each
GSEA
software.
pRRophetic
IC50
chemotherapeutic
agents.
TIMER,
XCELL,
QUANTISEQ,
MCPCOUNTER,
EPIC
CIBERSORT
applied
quantify
relative
proportions
infiltrating
immune
cells.
ggpubr
evaluate
TME
scores
checkpoint
activation
LRS
HRS
populations.
GSEABase
activity
cells
or
function.
Different
clusters
principal
component
(PCA),
t-distribution
random
neighborhood
embedding
(t-SNE),
survival
analyzed
using
Rtsne’s.
ConsensesClusterPlus
class
lncRNAs.
Results
In
study,
a
model
containing
constructed.
calibration
plot
consistent
1-,
3-,
5-year
ROC
curve
(AUC)
0.699,
0.689,
respectively.
High-risk
patients
tumor
invasion
immunity,
had
higher
levels
infiltration
activation.
Hot
tumors
cold
effectively
distinguished
2
3
cluster
1,
respectively,
which
indicated
hot
more
susceptible
immunotherapy.
Conclusion
Our
showed
LncRNAs
closely
BLCA,
accurately
patient
differentiate
between
tumors,
thus
improving
individualized
patients.
provides
effective
predictive
therapeutic
target
clinical
treatment
facilitating
therapy.
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: April 10, 2023
Background:
Glioma
patients
often
experience
unfavorable
outcomes
and
elevated
mortality
rates.
Our
study
established
a
prognostic
signature
utilizing
cuproptosis-associated
long
non-coding
RNAs
(CRLs)
identified
novel
biomarkers
therapeutic
targets
for
glioma.
Methods:
The
expression
profiles
related
data
of
glioma
were
obtained
from
Cancer
Genome
Atlas,
an
accessible
online
database.
We
then
constructed
using
CRLs
evaluated
the
prognosis
by
means
Kaplan-Meier
survival
curves
receiver
operating
characteristic
curves.
A
nomogram
based
on
clinical
features
was
employed
to
predict
individual
probability
patients.
Functional
enrichment
analysis
conducted
identify
crucial
CRL-related
enriched
biological
pathways.
role
LEF1-AS1
in
validated
two
cell
lines
(T98
U251).
Results:
developed
model
with
9
CRLs.
Patients
low-risk
had
considerably
longer
overall
(OS).
CRL
may
serve
independently
as
indicator
In
addition,
functional
revealed
significant
multiple
immunological
Notable
differences
observed
between
risk
groups
terms
immune
infiltration,
function,
checkpoints.
further
four
drugs
their
different
IC50
values
groups.
Subsequently,
we
discovered
molecular
subtypes
(cluster
one
cluster
two),
subtype
exhibiting
remarkably
OS
compared
subtype.
Finally,
that
inhibition
curbed
proliferation,
migration,
invasion
cells.
Conclusion:
signatures
confirmed
reliable
therapy
response
Inhibition
effectively
suppressed
growth,
gliomas;
therefore,
presents
itself
promising
biomarker
potential
target
Oncology Letters,
Journal Year:
2022,
Volume and Issue:
24(3)
Published: July 12, 2022
Clear
cell
renal
carcinoma
(ccRCC)
are
typically
situated
in
a
complex
inflammatory
and
immune
microenvironment,
which
has
been
reported
to
contribute
the
unfavorable
prognosis
of
patients
with
ccRCC.
There
would
be
beneficial
clinical
implications
for
elucidating
roles
its
molecular
characteristics
microenvironment.
This
is
because
it
facilitate
development
reliable
biomarkers
pre-stratification
prior
designation
individualized
treatment
strategies.
In
present
study,
RNA-sequencing
data
from
607
were
retrospectively
analyzed
elucidate
profile
molecules.
Based
on
this,
an
prognostic
signature
(IPS)
was
developed
further
validated
using
ccRCC
samples.
Subsequently,
associated
mechanisms
terms
microenvironment
pathways
then
investigated.
proposed
IPS
found
exhibit
superior
accuracy
compared
criterion
good
model
prediction
patient
[area
under
receiver
operating
characteristic
curve
(AUC)=0.811]
addition
being
independent
factor
risk
stratification
[hazard
ratio:
11.73
(95%
CI,
26.98-5.10);
log-rank
test,
P<0.001].
Pathologically,
cells
identified
as
high-risk
according
their
presented
more
malignant
tumor
structure,
including
voluminous
eosinophilic
cytoplasm,
acinar/lamellar/tubular
growth
patterns
atypic
nuclei.
High-risk
also
exhibited
higher
infiltration
levels
by
four
types
cells,
T
regulatory
but
lower
mast
cells.
Pathways
immune-inflammation
interaction,
IL-17
pathway,
upregulated
IPS-identified
Furthermore,
combining
factors,
integrated
index
increasing
risk-stratification
(AUC=0.911).
conclusion,
involved
ccRCC-inflammation
coupled
potential,
systematically
elucidated
study.
may
have
important
furthering
understanding
into
underlying
this
can
turn
exploited
identifying
designing
strategy.
Current Oncology,
Journal Year:
2022,
Volume and Issue:
29(9), P. 6573 - 6593
Published: Sept. 15, 2022
Background:
Colon
adenocarcinoma
(COAD)
is
the
most
common
subtype
of
colon
cancer,
and
cuproptosis
a
recently
newly
defined
form
cell
death
that
plays
an
important
role
in
development
several
malignant
cancers.
However,
studies
cuproptosis-related
lncRNAs
(CRLs)
involved
regulating
are
limited.
The
purpose
this
study
to
develop
new
prognostic
CRLs
signature
explore
its
underlying
biological
mechanism.
Methods:
In
study,
we
downloaded
RNA-seq
profiles,
clinical
data
tumor
mutational
burden
(TMB)
from
TCGA
database,
identified
cuproptosis-associated
using
univariate
Cox,
lasso
regression
analysis
multivariate
Cox
analysis,
constructed
model
with
risk
score
based
on
these
lncRNAs.
COAD
patients
were
divided
into
high-
low-risk
subgroups
score.
was
also
used
test
whether
they
independent
factors.
accuracy
further
validated
by
receiver
operating
characteristic
curve
(ROC),
C-index
Nomogram.
addition,
lncRNA/miRNA/mRNA
competing
endogenous
RNA
(ceRNA)
network
protein–protein
interaction
(PPI)
weighted
gene
co-expression
(WGCNA).
Results:
We
15
validation
results
showed
(HR
=
1.003,
95%
CI
1.001–1.004;
p
<
0.001)
could
serve
as
factor
accurate
credible
predictive
power.
had
highest
AUC
(0.793)
among
various
factors
such
score,
stage,
gender
age,
indicating
predict
patient
survival
better
than
other
characteristics.
Meanwhile,
possible
mechanisms
explored
ceRNA
PPI
WGCNA.
Conclusion:
has
reliable
power
effectively
outcomes
patients.
Journal of Ovarian Research,
Journal Year:
2023,
Volume and Issue:
16(1)
Published: April 25, 2023
Necroptosis
is
a
novel
type
of
programmed
cell
death
distinct
from
apoptosis.
However,
the
role
necroptosis
in
ovarian
cancer
(OC)
remains
unclear.
The
present
study
investigated
prognostic
value
necroptosis-related
genes
(NRGs)
and
immune
landscape
OC.
gene
expression
profiling
clinical
information
were
downloaded
TCGA
GTEx
databases.
Differentially
expressed
NRGs
(DE-NRGs)
between
OC
normal
tissueswere
identified.
regression
analyses
conducted
to
screen
construct
predictive
risk
model.
Patients
then
divided
into
high-
low-risk
groups,
GO
KEGG
performed
explore
bioinformatics
functions
two
groups.
Subsequently,
level
status
correlations
assessed
through
ESTIMATE
CIBERSORT
algorithms.
tumor
mutation
burden
(TMB)
drug
sensitivity
also
analyzed
based
on
two-NRG
signature
Totally
42
DE-NRGs
identified
screened
out
(MAPK10
STAT4)
with
values
for
overall
survival.
ROC
curve
showed
better
ability
five-year
OS
using
score.
Immune-related
significantly
enriched
group.
Macrophages
M1,
T
cells
CD4
memory
activated,
CD8,
regulatory
infiltration
associated
lower
microenvironment
score
was
demonstrated
high-risk
TMB
group
prognosis,
TIDE
suggested
checkpoint
inhibitor
response
Besides,
cisplatin
paclitaxel
found
be
more
sensitive
MAPK10
STAT4
can
important
prognosis
factors
OC,
two-gene
performs
well
predicting
survival
outcomes.
Our
provided
ways
estimation
potential
treatment
strategy.