Heliyon,
Journal Year:
2023,
Volume and Issue:
9(11), P. e22083 - e22083
Published: Nov. 1, 2023
The
increasing
evidence
suggests
that
necroptosis
mediates
many
behaviors
of
tumors,
as
well
the
regulation
tumor
microenvironment.
Long
non-coding
RNAs
(lncRNAs)
are
involved
in
a
variety
regulatory
processes
during
development
and
significantly
associated
with
patient
prognosis.
It
necroptosis-related
lncRNAs
(NRlncRNAs)
may
serve
biomarkers
for
prognosis
hepatocellular
carcinoma
(HCC).lncRNA
expression
profiles
HCC
were
obtained
from
TCGA
database.
LncRNAs
extracted
using
correlation
analysis.
Prognostic
models
constructed
based
on
least
absolute
shrinkage
selection
operator
algorithm
(LASSO)
multivariate
Cox
regression
differences
microenvironment
between
high-risk
low-risk
groups
further
analyzed.
Single-cell
RNA
sequencing
data
was
performed
to
assess
enrichment
genes
immune
cell
subsets.
Finally,
real-time
RT-PCR
used
detect
prognosis-related
different
lines.We
prognostic
signature
8
NRlncRNAs,
which
also
showed
good
predictive
accuracy.
model
patients
score
worse
than
(P
<
0.05).
Combined
clinical
characteristics
risk
HCC,
Nomogram
drawn
reference
practice.
In
addition,
infiltration
analysis
single
low
level
observed
at
high
there
significant
NRlncRNAs
macrophages.
results
RT-qPCR
highly
expressed
lines
human
liver
cancer
tissues.This
provide
meaningful
insights
immunotherapy
responses
HCC.
Frontiers in Genetics,
Journal Year:
2023,
Volume and Issue:
14
Published: Feb. 10, 2023
Background:
Cuproptosis
is
a
newly
defined
form
of
cell
death,
whether
cuproptosis
involved
in
hepatocellular
carcinoma
(HCC)
remains
elusive.
Method:
We
obtained
patients’
RNA
expression
data
and
follow-up
information
from
University
California
Santa
Cruz
(UCSC)
The
Cancer
Genome
Atlas
(TCGA).
analyzed
the
mRNA
level
Cuproptosis-related
genes
(CRGs)
performed
univariate
Cox
analysis.
Liver
(LIHC)
was
chosen
for
further
investigation.
Real-Time
quantitative
PCR
(RT-qPCR),
Western
blotting
(WB),
Immunohistochemical
(IHC),
Transwell
assays
were
used
to
determine
patterns
functions
CRGs
LIHC.
Next,
we
identified
CRGs-related
lncRNAs
(CRLs)
differentially
expressed
CRLs
between
HCC
normal
cases.
Univariate
analysis,
least
absolute
shrinkage
selection
operator
(LASSO)
analysis
regression
construct
prognostic
model.
multivariate
assess
risk
model
can
act
as
an
independent
factor
overall
survival
duration.
Different
groups
immune
correlation
tumor
mutation
burden
(TMB),
Gene
Set
Enrichment
Analysis
(GSEA)
different
groups.
Finally,
assessed
performance
predictive
drug
sensitivity.
Results:
levels
have
significant
differences
tissues.
High
Dihydrolipoamide
S-Acetyltransferase
(
DLAT
)
correlated
metastasis
cells
indicated
poor
prognosis
patients.
Our
consisted
four
cuproptosis-related
lncRNA
(AC011476.3,
AC026412.3,
NRAV,
MKLN1-AS).
well
predicting
rates.
results
suggested
that
score
serve
element
durations.
Survival
revealed
low
patients
extended
periods
compared
with
those
high
risk.
has
positive
B
CD4
+
T
Th2,
while
negative
relationship
endothelial
hematopoietic
cells.
Besides,
checkpoint
higher
folds
high-risk
set
than
low-risk
set.
group
had
rates
genetic
having
shorter
time.
GSEA
signaling
pathways
enriched
mostly
immune-related,
metabolic-related
group.
Drugs
sensitivity
our
ability
predict
efficacy
clinical
treatment.
Conclusion:
formula
novel
predictor
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
Biochemistry and Biophysics Reports,
Journal Year:
2023,
Volume and Issue:
37, P. 101600 - 101600
Published: Dec. 7, 2023
Cancer
growth
is
significantly
influenced
by
processes
such
as
pyroptosis,
apoptosis,
and
necroptosis
that
underlie
PANoptosis,
a
proinflammatory
programmed
cell
death.
Several
studies
have
examined
the
long
non-coding
RNAs
(lncRNAs)
associated
with
pancreatic
adenocarcinoma
(PAAD).
However,
predictive
value
of
lncRNAs
related
to
PANoptosis
for
PAAD
has
not
been
established.
Scientific Reports,
Journal Year:
2023,
Volume and Issue:
13(1)
Published: March 6, 2023
Abstract
Pancreatic
ductal
adenocarcinoma
(PDAC)
is
one
of
the
lethal
malignancies,
with
limited
biomarkers
identified
to
predict
its
prognosis
and
treatment
response
immune
checkpoint
blockade
(ICB).
This
study
aimed
explore
predictive
ability
T
cell
marker
genes
score
(TMGS)
their
overall
survival
(OS)
ICB
by
integrating
single-cell
RNA
sequencing
(scRNA-
seq
)
bulk
RNA-
data.
Multi-omics
data
PDAC
were
applied
in
this
study.
The
uniform
manifold
approximation
projection
(UMAP)
was
utilized
for
dimensionality
reduction
cluster
identification.
non-negative
matrix
factorization
(NMF)
algorithm
molecular
subtypes
clustering.
Least
Absolute
Shrinkage
Selection
Operator
(LASSO)-Cox
regression
adopted
TMGS
construction.
prognosis,
biological
characteristics,
mutation
profile,
function
status
between
different
groups
compared.
Two
via
NMF:
proliferative
(C1)
(C2).
Distinct
prognoses
characteristics
observed
them.
developed
based
on
10
(TMGs)
through
LASSO-Cox
regression.
an
independent
prognostic
factor
OS
PDAC.
Enrichment
analysis
indicated
that
cycle
proliferation-related
pathways
are
significantly
enriched
high-TMGS
group.
Besides,
related
more
frequent
KRAS
,
TP53
CDKN2A
germline
mutations
than
low-TMGS
Furthermore,
associated
attenuated
antitumor
immunity
reduced
infiltration
compared
However,
high
correlated
higher
tumor
burden
(TMB),
a
low
expression
level
inhibitory
molecules,
dysfunction
score,
thus
having
rate.
On
contrary,
favorable
rate
chemotherapeutic
agents
targeted
therapy.
By
combining
scRNA-
data,
we
novel
biomarker,
TMGS,
which
has
remarkable
performance
predicting
guiding
pattern
patients
Frontiers in Genetics,
Journal Year:
2022,
Volume and Issue:
13
Published: Aug. 23, 2022
Background:
Hepatocellular
carcinoma
(HCC)
remains
the
most
prevalent
gastrointestinal
malignancy
worldwide,
with
robust
drug
resistance
to
therapy.
N7-methylguanosine
(m7G)
mRNA
modification
has
been
significantly
related
massive
human
diseases.
Considering
effect
of
m7G-modified
long
non-coding
RNAs
(lncRNAs)
in
HCC
progression
is
unknown,
study
aims
at
investigating
a
prognostic
signature
improve
clinical
outcomes
for
patients
HCC.
Methods:
Two
independent
databases
(TCGA
and
ICGC)
were
used
analyze
RNAseq
data
patients.
First,
co-expression
analysis
was
applied
obtain
m7G-related
lncRNAs.
Moreover,
consensus
clustering
employed
divide
into
clusters.
Then,
using
least
absolute
shrinkage
selection
operator-Cox
regression
analysis,
lncRNA
(m7G-LPS)
first
tested
training
set
then
confirmed
both
testing
ICGC
sets.
The
expression
levels
nine
lncRNAs
further
via
real-time
PCR
cell
lines,
principal
component
receiver
operating
characteristic
curve.
m7G-LPS
could
two
different
risk
groups
optimal
score.
Kaplan-Meier
curves,
tumor
mutation
burden
(TMB),
therapeutic
effects
chemotherapy
agents,
expressions
immune
checkpoints
performed
enhance
availability
immunotherapeutic
treatments
Results:
A
total
1465
associated
m7G
genes
finally
selected
from
TCGA
database,
through
univariate
Cox
regression,
22
concerning
patients'
overall
survival
(OS).
whole
grouped
subgroups,
OS
Cluster
1
longer
than
that
2.
Furthermore,
identified
conduct
m7G-LPS,
which
verified.
nomogram
combined
age,
gender,
grade,
stage,
showed
strong
reliability
accuracy
predicting
Finally,
checkpoint
expression,
TMB,
several
agents
remarkably
scores.
More
importantly,
TMB-high
worst
among
four
groups.
Conclusion:
model
we
established
validated
by
abundant
algorithms,
provided
new
perspective
on
tumorigenesis
thus
improved
individualized
Computational and Mathematical Methods in Medicine,
Journal Year:
2022,
Volume and Issue:
2022, P. 1 - 26
Published: June 21, 2022
As
an
iron-dependent
type
of
programmed
cell
death,
ferroptosis
plays
important
role
in
the
pathogenesis
and
progression
hepatocellular
carcinoma
(HCC).
Long
noncoding
RNAs
(lncRNAs)
have
been
linked
to
prognosis
patients
with
HCC
a
number
studies.
Nevertheless,
predictive
value
lncRNAs
(FRLs)
associated
has
not
fully
elucidated.
Download
RNA
sequencing
data
clinical
profiles
from
The
Cancer
Genome
Atlas
(TCGA)
database.
FRLs
were
determined
by
Pearson's
correlation
analysis.
After
that,
prognostic
signature
for
was
established
using
Cox
LASSO
regression
analyses.
Meanwhile,
survival
analysis,
analysis
clinicopathological
features,
regression,
receiver
operating
characteristic
(ROC)
curve,
nomogram
used
analyze
FRL
signature's
capacity.
relationship
between
risk
score,
immune
infiltration,
chemotherapy
drug
sensitivity
is
further
studied.
In
total,
93
found
be
HCC.
A
five-FRL
comprising
AC015908.3,
LINC01138,
AC009283.1,
Z83851.1,
LUCAT1
created
order
enhance
prediction
patients.
demonstrated
good
potency,
according
Kaplan-Meier
ROC
curves.
factor
independent
various
factors
stratified
high-risk
group
shown
enriched
tumorigenesis
immune-related
pathways
GSEA
Additionally,
checkpoint
molecules,
half-inhibitory
concentrations
differed
considerably
groups,
implying
that
this
could
evaluate
efficacy
immunotherapy.
helpful
assessing
improving
therapy
options,
so
it
can
applied
clinically.
Journal of Clinical Laboratory Analysis,
Journal Year:
2022,
Volume and Issue:
36(11)
Published: Oct. 3, 2022
Recently,
a
new
type
of
programmed
cell
death,
cuproptosis,
has
been
identified
to
play
important
role
in
the
progression
tumors.
We
constructed
cuproptosis-related
long
non-coding
RNA
(lncRNA)
signature
predict
prognostic
significance
for
head
and
neck
squamous
carcinoma
(HNSCC).The
risk
model
was
developed
based
on
differentially
expressed
lncRNAs
associated
with
cuproptosis.
Principal
component
analysis
used
assess
validity.
The
Kaplan-Meier
curves
were
analyzed
compare
overall
survival
(OS),
disease-specific
(DSS),
progression-free
(PFS)
values.
multivariate
univariate
Cox
regression
analyses
evaluate
efficiency.
Furthermore,
functional
enrichment,
immune
infiltration,
tumor
mutation
burden
(TMB),
sensitivity
toward
chemotherapy
also
explored.Six
(AL109936.2,
CDKN2A-DT,
AC090587.1,
KLF3-AS1,
AL133395.1,
LINC01063)
construct
independent
predictor
HNSCC.
area
under
curve
C-index
values
obtained
using
higher
than
corresponding
clinical
factors.
Analysis
indicated
that
OS,
PFS,
DSS
time
recorded
patients
low-risk
group
belonging
high-risk
group.
By
enrichment
analysis,
we
observed
genes
enriched
response
tumor-associated
pathways.
characterized
by
score
exhibited
better
infiltration
other
individuals
chemotherapeutic
agents
(cisplatin,
docetaxel,
paclitaxel)
those
group.A
lncRNA-based
functioned
as
an
prognosis
HNSCC
constructed.
chemosensitivity
individual
can
be
potentially
predicted
this
signature.
Anti-Cancer Drugs,
Journal Year:
2024,
Volume and Issue:
unknown
Published: March 11, 2024
Anoikis
is
a
programmed
cell
death
process
triggered
when
cells
are
dislodged
from
the
extracellular
matrix.
Numerous
long
noncoding
RNAs
(lncRNAs)
have
been
identified
as
significant
factors
associated
with
anoikis
resistance
in
various
tumor
types,
including
glioma,
breast
cancer,
and
bladder
cancer.
However,
relationship
between
lncRNAs
prognosis
of
hepatocellular
carcinoma
(HCC)
has
received
limited
research
attention.
Further
needed
to
investigate
this
potential
link
understand
role
progression
HCC.
We
developed
prognostic
signature
based
on
differential
expression
implicated
A
co-expression
network
anoikis-related
mRNAs
was
established
using
data
obtained
The
Cancer
Genome
Atlas
(TCGA)
for
Cox
regression
analyses
were
conducted
formulate
an
lncRNA
(ARlncSig)
training
cohort,
which
subsequently
validated
both
testing
cohort
combined
dataset
comprising
two
cohorts.
Receiver
operating
characteristic
curves,
nomograms,
decision
curve
ARlncSig
score
clinical
characteristics
demonstrated
robust
predictive
ability.
Moreover,
gene
set
enrichment
analysis
revealed
several
immune
processes
high-risk
group
compared
low-risk
group.
Furthermore,
differences
observed
subpopulations,
checkpoint
genes,
response
chemotherapy
immunotherapy
high-
groups.
Lastly,
we
levels
five
included
quantitative
real-time
PCR.
In
conclusion,
our
model
holds
substantial
value
regarding
HCC
patients
provide
guidance
individualized
immunotherapy.
study,
36
genes
Gene
Ontology
Set
Enrichment
Analysis
databases.
also
22
differentially
expressed
that
correlated
these
TCGA.
Using
analyses,
then
Additionally,
collected
eight
pairs
liver
cancer
tissues
adjacent
Affiliated
Tumor
Hospital
Nantong
University
further
analysis.
aim
study
biomarker
prognosis.
risk
stratification
system
called
ARlncSig,
uses
categorize
into
low-
Patients
exhibited
significantly
lower
overall
survival
rates
those
model’s
performance
supported
by
receiver
curve,
nomogram
calibration,
correlation
analysis,
curve.
function,
checkpoint,
chemotherapy,
subpopulations
Finally,
PCR
lncRNAs.
demonstrates
critical
may
personalized