Cells,
Год журнала:
2022,
Номер
11(21), С. 3436 - 3436
Опубликована: Окт. 31, 2022
In
terms
of
mortality
and
survival,
pancreatic
cancer
is
one
the
worst
malignancies.
Known
as
a
unique
type
programmed
cell
death,
cuprotosis
contributes
to
tumor
growth,
angiogenesis,
metastasis.
Cuprotosis
programmed-cell-death-related
lncRNAs
(CRLs)
have
been
linked
PAAD,
although
their
functions
in
microenvironment
prognosis
are
not
well
understood.
This
study
included
data
from
TCGA-PAAD
cohort.
Random
sampling
PAAD
was
conducted,
splitting
into
two
groups
for
use
training
set
test
(7:3).
We
searched
differentially
expressed
genes
that
were
substantially
using
univariate
Cox
Lasso
regression
analysis.
Through
multivariate
proportional
risk
regression,
risk-rating
system
developed.
Correlations
between
CRL
signature
clinicopathological
characteristics,
microenvironment,
immunotherapy
response,
chemotherapy
sensitivity
further
evaluated.
Lastly,
qRT-PCR
used
compare
expression
healthy
tissues
tumors.
Some
CRLs
thought
strong
correlations
with
outcomes.
These
include
AC005332.6,
LINC02041,
LINC00857,
AL117382.1.
The
CRL-based
construction
exhibited
outstanding
predictive
performance
offers
fresh
approach
evaluating
pre-immune
effectiveness,
paving
way
future
studies
precision
immuno-oncology.
Advanced Materials,
Год журнала:
2022,
Номер
34(43)
Опубликована: Сен. 2, 2022
Abstract
Cuproptosis,
a
newly
identified
form
of
regulated
cell
death
that
is
copper‐dependent,
offers
great
opportunities
for
exploring
the
use
copper‐based
nanomaterials
inducing
cuproptosis
cancer
treatment.
Here,
glucose
oxidase
(GOx)‐engineered
nonporous
copper(I)
1,2,4‐triazolate
([Cu(tz)])
coordination
polymer
(CP)
nanoplatform,
denoted
as
GOx@[Cu(tz)],
starvation‐augmented
and
photodynamic
synergistic
therapy
developed.
Importantly,
catalytic
activity
GOx
shielded
in
scaffold
but
can
be
“turned
on”
efficient
depletion
only
upon
glutathione
(GSH)
stimulation
cells,
thereby
proceeding
starvation
therapy.
The
GSH
sensitizes
cells
to
GOx@[Cu(tz)]‐mediated
cuproptosis,
producing
aggregation
lipoylated
mitochondrial
proteins,
target
copper‐induced
toxicity.
increased
intracellular
hydrogen
peroxide
(H
2
O
)
levels,
due
oxidation
glucose,
activates
type
I
(PDT)
efficacy
GOx@[Cu(tz)].
vivo
experimental
results
indicate
GOx@[Cu(tz)]
produces
negligible
systemic
toxicity
inhibits
tumor
growth
by
92.4%
athymic
mice
bearing
5637
bladder
tumors.
This
thought
first
report
cupreous
nanomaterial
capable
cuproptosis‐based
cancer,
which
should
invigorate
studies
pursuing
rational
design
efficacious
strategies
based
on
cuproptosis.
Genes,
Год журнала:
2022,
Номер
13(5), С. 851 - 851
Опубликована: Май 10, 2022
Clear
cell
renal
carcinoma
(ccRCC)
is
the
most
prevalent
subtype
of
carcinoma,
which
characterized
by
metabolic
reprogramming.
Cuproptosis,
a
novel
form
death,
highly
linked
to
mitochondrial
metabolism
and
mediated
protein
lipoylation.
However,
clinical
impacts
cuproptosis-related
genes
(CRGs)
in
ccRCC
largely
remain
unclear.
In
current
study,
we
systematically
evaluated
genetic
alterations
ccRCC.
Our
results
revealed
that
CDKN2A,
DLAT,
DLD,
FDX1,
GLS,
PDHA1
PDHB
exhibited
differential
expression
between
normal
tissues
(|log2(fold
change)|
>
2/3
p
<
0.05).
Utilizing
an
iterative
sure
independence
screening
(SIS)
method,
separately
constructed
prognostic
signature
CRGs
for
predicting
overall
survival
(OS)
progression-free
(PFS)
patients.
The
score
yielded
area
under
curve
(AUC)
0.658
0.682
prediction
5-year
OS
PFS,
respectively.
Kaplan−Meier
analysis
OS,
higher
risk
gene
was
significantly
correlated
with
worse
(HR
=
2.72
(2.01−3.68),
log-rank
1.76
×
10−7).
Patients
had
shorter
PFS
2.83
(2.08−3.85),
3.66
Two
independent
validation
datasets
(GSE40435
(N
101),
GSE53757
72))
were
collected
meta-analysis,
suggesting
CDKN2A
(log2(fold
change)
1.46,
95%CI:
1.75−2.35)
showed
while
DLAT
−0.54,
−0.93−−0.15)
FDX1
−1.01,
−1.61−−0.42)
lowly
expressed.
also
associated
immune
infiltration
levels
programmed
death
1
(PD-1)
(CDKN2A:
r
0.24,
2.14
10−8;
FDX1:
−0.17,
1.37
10−4).
conclusion,
could
serve
as
potential
predictor
patients
may
offer
insights
into
cancer
treatment.
Toxics,
Год журнала:
2023,
Номер
11(7), С. 580 - 580
Опубликована: Июль 3, 2023
Natural
and
anthropogenic
sources
of
metals
in
the
ecosystem
are
perpetually
increasing;
consequently,
heavy
metal
(HM)
accumulation
has
become
a
major
environmental
concern.
Human
exposure
to
HMs
increased
dramatically
due
industrial
activities
20th
century.
Mercury,
arsenic
lead,
chrome,
cadmium
have
been
most
prevalent
that
caused
human
toxicity.
Poisonings
can
be
acute
or
chronic
following
via
water,
air,
food.
The
bioaccumulation
these
results
variety
toxic
effects
on
various
tissues
organs.
Comparing
mechanisms
action
reveals
induce
toxicity
similar
pathways,
including
production
reactive
oxygen
species,
inactivation
enzymes,
oxidative
stress.
conventional
techniques
employed
for
elimination
deemed
inadequate
when
HM
concentration
is
less
than
100
mg/L.
In
addition,
methods
exhibit
certain
limitations,
secondary
pollutants,
high
demand
energy
chemicals,
reduced
cost-effectiveness.
As
result,
employment
microbial
bioremediation
purpose
detoxification
emerged
as
viable
solution,
given
microorganisms,
fungi
bacteria,
superior
biosorption
bio-accumulation
capabilities.
This
review
deals
with
uptake
associated
HMs,
will
increase
our
knowledge
their
body
organs,
leading
better
management
poisoning.
aims
enhance
comprehension
offer
judicious
selection
remediation
technology
HMs.
Microbial-based
solutions
sustainable
could
potentially
crucial
cost-effective
reducing
Advanced Materials,
Год журнала:
2023,
Номер
35(22)
Опубликована: Март 14, 2023
Cuproptosis
is
a
new
cell
death
that
depends
on
copper
(Cu)
ionophores
to
transport
Cu
into
cancer
cells,
which
induces
death.
However,
existing
are
small
molecules
with
short
blood
half-life
making
it
hard
enough
cells.
Herein,
reactive
oxygen
species
(ROS)-sensitive
polymer
(PHPM)
designed,
used
co-encapsulate
elesclomol
(ES)
and
form
nanoparticles
(NP@ESCu).
After
entering
ES
Cu,
triggered
by
excessive
intracellular
ROS,
readily
released.
work
in
concerted
way
not
only
kill
cells
cuproptosis,
but
also
induce
immune
responses.
In
vitro,
the
ability
of
NP@ESCu
efficiently
cuproptosis
investigated.
addition,
change
transcriptomes
treated
explored
RNA-Seq.
vivo,
found
mice
model
subcutaneous
bladder
cancer,
reprograming
tumor
microenvironment.
Additionally,
further
combined
anti-programmed
protein
ligand-1
antibody
(αPD-L1).
This
study
provides
first
report
combining
nanomedicine
can
αPD-L1
for
enhanced
therapy,
thereby
providing
novel
strategy
future
therapy.
Frontiers in Pharmacology,
Год журнала:
2022,
Номер
13
Опубликована: Июнь 28, 2022
Skin
cutaneous
melanoma
(SKCM,
hereafter
referred
to
as
melanoma)
is
the
most
lethal
skin
cancer
with
increasing
incidence.
Regulated
cell
death
plays
an
important
role
in
tumorigenesis
and
serves
target
for
almost
all
treatment
strategies.
Cuproptosis
recently
identified
copper-dependent
regulated
form
that
relies
on
mitochondria
respiration.
However,
its
remains
unknown.
The
correlation
of
cuproptosis-related
genes
tumor
prognosis
far
be
understood,
either.
In
present
study,
we
explored
between
by
accessing
analyzing
a
public
database
found
11
out
12
were
upregulated
tissues
three
(LIPT1,
PDHA1,
SLC31A1)
have
predictive
value
prognosis.
subgroup
patients
higher
gene
expression
showed
longer
overall
survival
than
those
lower
expression.
We
chose
LIPT1
further
exploration.
was
increased
biopsies
independent
favorable
prognostic
indicator
patients.
Moreover,
positively
correlated
PD-L1
negatively
associated
Treg
infiltration.
after
receiving
immunotherapy,
indicating
LIPT1.
Finally,
pan-cancer
analysis
indicated
differentially
expressed
diverse
cancers
compared
normal
multiple
immune
checkpoints,
especially
PD-L1.
It
could
serve
some
types.
conclusion,
our
study
demonstrated
genes,
LIPT1,
melanoma,
revealed
infiltration
thus
providing
new
clues
assessment
immunotherapy
melanoma.
Scientific Reports,
Год журнала:
2022,
Номер
12(1)
Опубликована: Июль 5, 2022
Abstract
Increased
intracellular
toxicity
due
to
an
imbalance
in
copper
homeostasis
caused
by
ion
accumulation
could
regulate
the
rate
of
cancer
cell
growth
and
proliferation.
The
goal
this
study
was
create
a
novel
Cuproptosis-related
lncRNA
signature
that
may
be
utilized
predict
survival
immunotherapy
HCC
patients.
Cuproptosis-associated
lncRNAs
differentially
expressed
between
tumor
tissue
normal
were
discovered
first.
By
LASSO-Cox
analysis,
overlapping
then
build
signature,
which
might
used
patient
prognosis
responsiveness
immune
checkpoint
blockade
(ICB)
therapy.
Differences
infiltration
subpopulations
high
low-risk
score
subgroups
also
analyzed.
Moreover,
nomogram
based
on
clinical
features
developed
demonstrated
have
good
predictive
potential.
Finally,
qRT-PCR
performed
HerpG2
MHCC-97H
lines
explore
whether
these
indeed
involved
process
Cuproptosis.
In
summary,
we
created
prognostic
profile
linked
Cuproptosis
forecast
response
immunotherapy,
provide
new
potential
non-apoptotic
therapeutic
perspective
for
Advanced Functional Materials,
Год журнала:
2022,
Номер
32(40)
Опубликована: Июль 30, 2022
Abstract
Cuproptosis
is
a
very
newly
recognized
regulated
cell
death
modality
that
distinct
from
known
mechanisms
and
shows
enormous
prospect
in
cancer
treatment.
However,
its
efficacy
copper‐dependent
restricted
by
strictly
copper
metabolism.
Herein,
novel
copper/iron
hybrid
hollow
amorphous
metal
organic
framework
(HaMOF)
developed
as
an
oxidative
stress
amplifier
metabolic
disrupter
for
synergistic
cuproptosis/ferroptosis/apoptosis
anticancer
therapy.
The
HaMOF
fabricated
Cu
2+
,
3,3′‐dithiobis(propionohydrazide)
Fe
3+
via
unsaturated
coordination‐etching
integration
strategy,
then
doxorubicin
loaded
followed
surface
decoration
with
hyaluronan.
obtained
DOX@Fe/CuTH
exhibits
tumor
microenvironment‐triggered
catalytic
therapeutic
property,
wherein
it
can
amplify
cellular
simultaneously
boosting
H
2
O
production
depleting
glutathione.
Moreover,
cause
mitochondrial
dysfunction
downregulate
the
expressions
of
transporter
ATP7A
iron
FPN
1,
thereby
leading
to
disorders
high
retentions
cytoplasm
•OH
generation.
overloaded
lipoylated
protein
dihydrolipoamide
S‐acetyltransferase
aggregation
lead
cuproptosis.
Collectively,
both
augmented
induce
potent
ferroptosis,
which
synergizes
cuproptosis
DOX‐mediated
apoptosis
efficiently
suppress
growth.
This
bimetallic
nanoplatform
provides
new
paradigm
boost
cuproptosis‐related
therapies.
Nature Communications,
Год журнала:
2023,
Номер
14(1)
Опубликована: Окт. 20, 2023
Abstract
Cuproptosis,
caused
by
excessively
high
copper
concentrations,
is
urgently
exploited
as
a
potential
cancer
therapeutic.
However,
the
mechanisms
underlying
initiation,
propagation,
and
ultimate
execution
of
cuproptosis
in
tumors
remain
unknown.
Here,
we
show
that
content
significantly
elevated
gastric
(GC),
especially
malignant
tumors.
Screening
reveals
METTL16,
an
atypical
methyltransferase,
critical
mediator
through
m
6
A
modification
on
FDX1
mRNA.
Furthermore,
stress
promotes
METTL16
lactylation
at
site
K229
followed
cuproptosis.
The
process
inhibited
SIRT2.
Elevated
improves
therapeutic
efficacy
ionophore–
elesclomol.
Combining
elesclomol
with
AGK2,
SIRT2-specific
inhibitor,
induce
vitro
vivo.
These
results
reveal
significance
non-histone
protein
Given
lactate
concentrations
GC,
induction
becomes
promising
strategy
for
GC.
Angewandte Chemie International Edition,
Год журнала:
2022,
Номер
62(12)
Опубликована: Дек. 31, 2022
Abstract
Cuproptosis
is
a
new
form
of
programmed
cell
death
and
exhibits
enormous
potential
in
cancer
treatment.
However,
reducing
the
undesirable
Cu
ion
release
normal
tissue
maximizing
copper‐induced
therapeutic
effect
sites
are
two
main
challenges.
In
this
study,
we
constructed
photothermally
triggered
nanoplatform
(Au@MSN‐Cu/PEG/DSF)
to
realize
on‐demand
delivery
for
synergistic
therapy.
The
released
disulfiram
(DSF)
chelated
with
2+
situ
generate
highly
cytotoxic
bis(diethyldithiocarbamate)copper
(CuET),
causing
apoptosis,
formed
+
species
promoted
toxic
mitochondrial
protein
aggregation,
leading
cuproptosis.
Synergistic
photothermal
therapy,
Au@MSN‐Cu/PEG/DSF
could
effectively
kill
tumor
cells
inhibit
growth
(inhibition
rate
up
80.1
%).
These
results
provide
promising
perspective
treatment
based
on
cuproptosis,
may
also
inspire
design
advanced
nano‐therapeutic
platforms.
International Journal of Molecular Sciences,
Год журнала:
2022,
Номер
23(22), С. 13850 - 13850
Опубликована: Ноя. 10, 2022
In
the
human
body,
copper
is
an
important
trace
element
and
a
cofactor
for
several
enzymes
involved
in
energy
production,
iron
metabolism,
neuropeptide
activation,
connective
tissue
synthesis,
neurotransmitter
synthesis.
Copper
also
necessary
cellular
processes,
such
as
regulation
of
intracellular
signal
transduction,
catecholamine
balance,
myelination
neurons,
efficient
synaptic
transmission
central
nervous
system.
naturally
present
some
foods
available
dietary
supplement.
Only
small
amounts
are
typically
stored
body
large
amount
excreted
through
bile
urine.
Given
critical
role
breadth
local
concentrations
distribution
transporter
proteins
brain
to
maintain
steady
state
internal
environment.
The
dysfunction
metabolism
or
regulatory
pathways
results
imbalance
homeostasis
brain,
which
can
lead
myriad
acute
chronic
pathological
effects
on
neurological
function.
It
suggests
unique
mechanism
linking
neuronal
activation
within
This
article
explores
relationship
between
impaired
neuropathophysiological
progress
diseases.