Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: Feb. 15, 2023
Background:
There
is
a
rapid
increase
in
lung
adenocarcinomas
(LUAD),
and
studies
suggest
associations
between
cuproptosis
the
occurrence
of
various
types
tumors.
However,
it
remains
unclear
whether
plays
role
LUAD
prognosis.
Methods:
Dataset
TCGA-LUAD
was
treated
as
training
cohort,
while
validation
cohort
consisted
merged
datasets
GSE29013,
GSE30219,
GSE31210,
GSE37745,
GSE50081.
Ten
studied
cuproptosis-related
genes
(CRG)
were
used
to
generated
CRG
clusters
cluster-related
differential
expressed
gene
(CRG-DEG)
clusters.
The
differently
lncRNA
that
with
prognosis
ability
CRG-DEG
put
into
LASSO
regression
for
signature
(CRLncSig).
Kaplan-Meier
estimator,
Cox
model,
receiver
operating
characteristic
(ROC),
time-dependent
AUC
(tAUC),
principal
component
analysis
(PCA),
nomogram
predictor
further
deployed
confirm
model's
accuracy.
We
examined
connections
other
forms
regulated
cell
death,
including
apoptosis,
necroptosis,
pyroptosis,
ferroptosis.
immunotherapy
demonstrated
by
applying
eight
mainstream
immunoinformatic
algorithms,
TMB,
TIDE,
immune
checkpoints.
evaluated
potential
drugs
high
risk
CRLncSig
LUADs.
Real-time
PCR
human
tissues
performed
verify
expression
pattern,
signature's
pan-cancer's
also
assessed.
Results:
A
nine-lncRNA
signature,
CRLncSig,
built
owning
prognostic
power
applied
cohort.
Each
confirmed
differentially
real
world
real-time
PCR.
correlated
2,469/3,681
(67.07%)
apoptosis-related
genes,
13/20
(65.00%)
necroptosis-related
35/50
(70.00%)
pyroptosis-related
238/380
(62.63%)
ferroptosis-related
genes.
Immunotherapy
suggested
status,
checkpoints,
KIR2DL3,
IL10,
IL2,
CD40LG,
SELP,
BTLA,
CD28,
linked
closely
our
potentially
suitable
targets.
For
those
high-risk
patients,
we
found
three
agents,
gemcitabine,
daunorubicin,
nobiletin.
Finally,
some
lncRNAs
play
vital
cancer
need
more
attention
studies.
Conclusion:
results
this
study
can
help
determine
outcome
effectiveness
immunotherapy,
well
better
select
targets
therapeutic
agents.
Cancers,
Journal Year:
2023,
Volume and Issue:
15(4), P. 1095 - 1095
Published: Feb. 8, 2023
Lithium,
a
trace
element
important
for
fetal
health
and
development,
is
considered
metal
drug
with
well-established
clinical
regime,
economical
production
process,
mature
storage
system.
Several
studies
have
shown
that
lithium
affects
tumor
development
by
regulating
inositol
monophosphate
(IMPase)
glycogen
synthase
kinase-3
(GSK-3).
Lithium
can
also
promote
proliferation
programmed
cell
death
(PCD)
in
cells
through
number
of
new
targets,
such
as
the
nuclear
receptor
NR4A1
Hedgehog-Gli.
may
increase
cancer
treatment
efficacy
while
reducing
side
effects,
suggesting
it
be
used
an
adjunctive
therapy.
In
this
review,
we
summarize
effects
on
progression
discuss
underlying
mechanisms.
Additionally,
lithium’s
limitations
antitumor
applications,
including
its
narrow
therapeutic
window
potential
pro-cancer
immune
Aging,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Feb. 1, 2024
Renal
cell
carcinoma
(RCC)
is
the
predominant
form
of
malignant
kidney
cancer.
Sunitinib,
a
primary
treatment
for
advanced,
inoperable,
recurrent,
or
metastatic
RCC,
has
shown
effectiveness
in
some
patients
but
increasingly
limited
by
drug
resistance.
Recently
identified
cuproptosis,
copper-ion-dependent
programmed
death,
holds
promise
combating
cancer,
particularly
drug-resistant
types.
However,
its
treating
resistant
RCC
remains
to
be
determined.
Exploring
cuproptosis's
regulatory
mechanisms
could
enhance
strategies.
Our
analysis
data
from
GEO
and
TCGA
databases
showed
that
cuproptosis-related
gene
DBT
markedly
under
expressed
tissues,
correlating
with
worse
prognosis
disease
progression.
In
our
study,
we
investigated
copper
CRGs
ccRCC,
noting
substantial
expression
differences,
advanced-stage
tumors.
We
established
connection
between
CRG
levels
patient
survival,
positioning
as
potential
therapeutic
targets
ccRCC.
cases,
found
distinct
patterns
GLS
CRGs,
linked
experiments
demonstrated
increasing
significantly
reduces
growth
spread,
underscoring
target.
This
research
sheds
new
light
on
role
ccRCC
their
impact
International Journal of Molecular Sciences,
Journal Year:
2024,
Volume and Issue:
25(8), P. 4372 - 4372
Published: April 16, 2024
Cuproptosis
and
ferroptosis
represent
copper-
iron-dependent
forms
of
cell
death,
respectively,
both
are
known
to
play
pivotal
roles
in
head
neck
squamous
carcinoma
(HNSCC).
However,
few
studies
have
explored
the
prognostic
signatures
related
cuproptosis
HNSCC.
Our
objective
was
construct
a
model
based
on
genes
associated
with
ferroptosis.
We
randomly
assigned
502
HSNCC
samples
from
The
Cancer
Genome
Atlas
(TCGA)
into
training
testing
sets.
Pearson
correlation
analysis
utilized
identify
cuproptosis-associated
set.
Cox
proportional
hazards
(COX)
regression
least
absolute
shrinkage
operator
(LASSO)
were
employed
model.
performance
internally
validated
using
single-factor
COX
regression,
multifactor
Kaplan–Meier
analysis,
principal
component
(PCA),
receiver
operating
curve
(ROC)
analysis.
Additionally,
we
obtained
97
Gene
Expression
Omnibus
(GEO)
database
for
external
validation.
constructed
model,
12
genes,
proved
be
an
independent
predictor
HNSCC
prognosis.
Among
these
increased
expression
aurora
kinase
A
(AURKA)
has
been
implicated
various
cancers.
To
further
investigate,
small
interfering
RNAs
(siRNAs)
knock
down
AURKA
conducted
functional
experiments.
results
demonstrated
that
knockdown
significantly
inhibited
proliferation
migration
cells
(Cal27
CNE2).
Therefore,
may
serve
as
potential
biomarker
Frontiers in Pharmacology,
Journal Year:
2023,
Volume and Issue:
14
Published: Feb. 15, 2023
Background:
There
is
a
rapid
increase
in
lung
adenocarcinomas
(LUAD),
and
studies
suggest
associations
between
cuproptosis
the
occurrence
of
various
types
tumors.
However,
it
remains
unclear
whether
plays
role
LUAD
prognosis.
Methods:
Dataset
TCGA-LUAD
was
treated
as
training
cohort,
while
validation
cohort
consisted
merged
datasets
GSE29013,
GSE30219,
GSE31210,
GSE37745,
GSE50081.
Ten
studied
cuproptosis-related
genes
(CRG)
were
used
to
generated
CRG
clusters
cluster-related
differential
expressed
gene
(CRG-DEG)
clusters.
The
differently
lncRNA
that
with
prognosis
ability
CRG-DEG
put
into
LASSO
regression
for
signature
(CRLncSig).
Kaplan-Meier
estimator,
Cox
model,
receiver
operating
characteristic
(ROC),
time-dependent
AUC
(tAUC),
principal
component
analysis
(PCA),
nomogram
predictor
further
deployed
confirm
model's
accuracy.
We
examined
connections
other
forms
regulated
cell
death,
including
apoptosis,
necroptosis,
pyroptosis,
ferroptosis.
immunotherapy
demonstrated
by
applying
eight
mainstream
immunoinformatic
algorithms,
TMB,
TIDE,
immune
checkpoints.
evaluated
potential
drugs
high
risk
CRLncSig
LUADs.
Real-time
PCR
human
tissues
performed
verify
expression
pattern,
signature's
pan-cancer's
also
assessed.
Results:
A
nine-lncRNA
signature,
CRLncSig,
built
owning
prognostic
power
applied
cohort.
Each
confirmed
differentially
real
world
real-time
PCR.
correlated
2,469/3,681
(67.07%)
apoptosis-related
genes,
13/20
(65.00%)
necroptosis-related
35/50
(70.00%)
pyroptosis-related
238/380
(62.63%)
ferroptosis-related
genes.
Immunotherapy
suggested
status,
checkpoints,
KIR2DL3,
IL10,
IL2,
CD40LG,
SELP,
BTLA,
CD28,
linked
closely
our
potentially
suitable
targets.
For
those
high-risk
patients,
we
found
three
agents,
gemcitabine,
daunorubicin,
nobiletin.
Finally,
some
lncRNAs
play
vital
cancer
need
more
attention
studies.
Conclusion:
results
this
study
can
help
determine
outcome
effectiveness
immunotherapy,
well
better
select
targets
therapeutic
agents.