Journal of Cancer,
Journal Year:
2023,
Volume and Issue:
14(9), P. 1499 - 1514
Published: Jan. 1, 2023
Lung
squamous
cell
carcinoma
has
so
far
lacked
effective
targets
for
diagnosis
and
treatment.
In
cancer
research,
long
noncoding
RNAs
(LncRNAs)
emerge
as
novel
therapeutic
biomarkers.
Cuprophosis
is
a
new
death
type
involving
multiple
biological
processes
in
tumor
cells.
Here,
we
aimed
to
explore
whether
Cuprophosis-related
lncRNAs
could
be
used
predict
prognosis,
assess
immune
function,
test
drug
sensitivity
LUSC
patients.
The
Cancer
Genome
Map
(TCGA)
was
obtain
genome
clinical
data,
Cuprophosis-relevant
genes
were
found
the
literature.
A
cuproptosis-related
lncRNA
risk
model
built
using
co-expression
analysis,
univariate/multivariate
Cox
regression,
LASSO
analysis.
survival
analysis
model's
prognostic
value.
univariate
multivariate
regression
analyses
performed
determine
score,
age,
gender,
or
stages
independent
factors.
Gene
Set
Enrichment
Analysis
mutation
on
differentially
expressed
mRNA
between
high-risk
low-risk
groups.
(TIDE)
algorithm
conduct
immunological
functional
testing.
Five
LncRNAs
identified,
selected
constructed
prognosis
model.
According
Kaplan-Meier
overall
time
patients
group
shorter
than
those
group.
For
patients,
score
serves
an
indicator.
GO
KEGG
enrichment
revealed
that
mRNAs
high-
groups
enriched
several
immune-related
processes.
of
higher
function
pathways,
including
IFN-γ
MHC
I
pathways.
Tumor
Immune
Dysfunction
Exclusion
more
likely
experience
escape.
showed
with
ratings
respond
GW441756
Salubrinal.
contrast,
scores
responsive
dasatinib
Z-LLNIe
CHO.
5-Cuprophosis-related
signature
can
Journal of Oncology,
Journal Year:
2023,
Volume and Issue:
2023, P. 1 - 18
Published: Feb. 17, 2023
Background.
Cuproptosis,
a
recently
discovered
form
of
cell
death,
is
caused
by
copper
levels
exceeding
homeostasis
thresholds.
Although
Cu
has
potential
role
in
colon
adenocarcinoma
(COAD),
its
the
development
COAD
remains
unclear.
Methods.
In
this
study,
426
patients
with
were
extracted
from
Cancer
Genome
Atlas
(TCGA)
database.
The
Pearson
correlation
algorithm
was
used
to
identify
cuproptosis-related
lncRNAs.
Using
univariate
Cox
regression
analysis,
least
absolute
shrinkage
and
selection
operator
(LASSO)
select
lncRNAs
associated
overall
survival
(OS).
A
risk
model
established
based
on
multivariate
analysis.
nomogram
evaluate
prognostic
signature
model.
Finally,
mutational
burden
sensitivity
analyses
chemotherapy
drugs
performed
for
low-
high-risk
groups.
Result.
Ten
identified
novel
constructed.
ten
an
independent
predictor
COAD.
Mutational
analysis
suggested
that
scores
had
higher
mutation
frequency
shorter
survival.
Conclusion.
Constructing
could
accurately
predict
prognosis
patients,
providing
fresh
perspective
future
research
Journal of Oncology,
Journal Year:
2023,
Volume and Issue:
2023, P. 1 - 22
Published: Feb. 27, 2023
Background.
Hepatocellular
carcinoma
(HCC),
ranking
as
one
of
the
most
common
malignant
tumors,
is
leading
causes
cancer
death,
with
a
poor
prognosis.
Cuproptosis,
novel
programmed
cell
death
modality
that
has
just
been
confirmed
recently,
may
play
an
important
role
in
HCC
Long
noncoding
RNA
(LncRNA)
key
participant
tumorigenesis
and
immune
responses.
It
be
great
significance
to
predict
based
on
cuproptosis
genes
their
related
LncRNA.
Methods.
The
sample
data
patients
were
obtained
from
Cancer
Genome
Atlas
(TCGA)
database.
Combined
cuproptosis-related
collected
literature
search,
expression
analysis
was
carried
out
find
LncRNAs
significantly
expressed
HCC.
prognostic
model
constructed
by
least
absolute
shrinkage
selection
operator
(LASSO)
regression
multivariate
Cox
regression.
feasibility
these
signature
used
for
evaluation
overall
survival
rate
independent
factors
investigated.
profile
cuproptosis,
infiltration,
status
somatic
mutation
analyzed
compared.
Results.
A
consisting
seven
gene-related
LncRNA
signatures
constructed.
Multiple
verification
methods
have
showed
this
can
accurately
prognosis
patients.
classified
high-risk
group
under
risk
score
had
worse
status,
more
significant
function,
higher
frequency.
During
analysis,
gene
CDKN2A
found
closely
DDX11-AS1
Conclusion.
identified,
basis
which
constructed,
it
verified
potential
new
targets
disease
therapy
antagonizing
development
discussed.
Heliyon,
Journal Year:
2024,
Volume and Issue:
10(9), P. e30277 - e30277
Published: April 26, 2024
Nowadays,
effective
prognostic
models
for
esophageal
cancer
(ESCA)
are
still
lacking.
Long
noncoding
RNAs
(lncRNAs)
commonly
utilized
as
indicators
diagnosing
and
forecasting
patient
outcomes.
Cuproptosis
is
regulated
by
multiple
genes
crucial
to
the
progression
of
ESCA.
However,
it
not
yet
clear
what
role
cuproptosis-associated
lncRNAs
(CuALs)
play
in
To
tackle
this
problem,
a
signature
incorporating
three
CuALs
was
created.
This
constructed
use
least
absolute
shrinkage
selection
operator
(LASSO)
multivariate
Cox
regression.
Subsequently,
effectively
stratified
ESCA
samples
into
high-risk
group
low-risk
group.
Those
demonstrated
extended
overall
survival
(OS),
well
increased
infiltration
T
cells,
macrophages,
NK
suggesting
potentially
enhanced
response
immunotherapy.
The
ROC
curve
analysis
that
outperformed
conventional
clinical
factors
predicting
prognosis
(AUC
=
0.708).
K-M
correlation
identified
UGDH-AS1
(a
CuAL)
protective
factor
positively
associated
with
prognosis.
results
RT-qPCR
wound
healing
assays
indicated
overexpressed
could
inhibit
cell
migration.
In
general,
robust
capability
immune
environment
prognosis,
highlighting
its
potential
tool
enhancing
personalized
treatment
strategies
Journal of Cancer,
Journal Year:
2023,
Volume and Issue:
14(9), P. 1499 - 1514
Published: Jan. 1, 2023
Lung
squamous
cell
carcinoma
has
so
far
lacked
effective
targets
for
diagnosis
and
treatment.
In
cancer
research,
long
noncoding
RNAs
(LncRNAs)
emerge
as
novel
therapeutic
biomarkers.
Cuprophosis
is
a
new
death
type
involving
multiple
biological
processes
in
tumor
cells.
Here,
we
aimed
to
explore
whether
Cuprophosis-related
lncRNAs
could
be
used
predict
prognosis,
assess
immune
function,
test
drug
sensitivity
LUSC
patients.
The
Cancer
Genome
Map
(TCGA)
was
obtain
genome
clinical
data,
Cuprophosis-relevant
genes
were
found
the
literature.
A
cuproptosis-related
lncRNA
risk
model
built
using
co-expression
analysis,
univariate/multivariate
Cox
regression,
LASSO
analysis.
survival
analysis
model's
prognostic
value.
univariate
multivariate
regression
analyses
performed
determine
score,
age,
gender,
or
stages
independent
factors.
Gene
Set
Enrichment
Analysis
mutation
on
differentially
expressed
mRNA
between
high-risk
low-risk
groups.
(TIDE)
algorithm
conduct
immunological
functional
testing.
Five
LncRNAs
identified,
selected
constructed
prognosis
model.
According
Kaplan-Meier
overall
time
patients
group
shorter
than
those
group.
For
patients,
score
serves
an
indicator.
GO
KEGG
enrichment
revealed
that
mRNAs
high-
groups
enriched
several
immune-related
processes.
of
higher
function
pathways,
including
IFN-γ
MHC
I
pathways.
Tumor
Immune
Dysfunction
Exclusion
more
likely
experience
escape.
showed
with
ratings
respond
GW441756
Salubrinal.
contrast,
scores
responsive
dasatinib
Z-LLNIe
CHO.
5-Cuprophosis-related
signature
can