Advanced Healthcare Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Nov. 5, 2024
Abstract
Nanomedicine
has
shown
great
anticancer
potential
by
disrupting
redox
homeostasis
and
increasing
the
levels
of
oxidative
stress,
but
therapeutic
effect
is
limited
factors
including
intrinsic
self‐protection
mechanism
tumors.
Cancer
cell
death
can
be
induced
exploration
different
mechanisms,
such
as
apoptosis,
pyroptosis,
necroptosis,
cuproptosis,
ferroptosis.
The
merging
nanotechnology
with
biomedicine
provided
tremendous
opportunities
to
construct
death‐based
nanomedicine
for
innovative
cancer
therapy.
Nanocarriers
are
not
only
used
targeted
delivery
inducers,
also
components
induce
achieve
efficient
tumor
treatment.
This
review
focuses
on
seven
modalities
mediated
nanomaterials,
ferroptosis,
cuprotosis,
immunogenic
death,
autophagy.
mechanisms
these
described
in
detail,
well
preparation
nanomaterials
that
them
they
exert
their
effects.
Finally,
this
work
describes
future
development
based
current
knowledge
related
nanomaterials.
Animals,
Journal Year:
2025,
Volume and Issue:
15(4), P. 526 - 526
Published: Feb. 12, 2025
Research
on
the
effects
of
organic
and
inorganic
Cu
sources
metabolic
processes
mechanisms
in
pigs
is
lacking.
This
study
investigated
different
copper
(Cu)
levels
hepatic
metabolism
transporter
factors
growing
pigs.
Sixty
healthy
piglets
(initial
body
weight
14.00
±
0.30
kg)
were
randomly
divided
into
four
groups
with
five
replicates
three
each.
Four
diets
(AM,
AH,
BM,
BH)
had
[Cu
sulphate
(CuSO4):
A
amino
acids
(Cu-AA):
B]
[supplemented
(120
mg/kg
DM):
M,
supplemented
(240
H].
The
pre-feeding
period
was
7
days,
followed
by
a
45-day
feeding
period.
Slaughter
sample
collection
carried
out
46th
day
formal
Significant
differences
considered
at
p
<
0.05.
final
average
daily
gain
(ADG)
Cu-AA
significantly
higher
than
those
CuSO4
groups.
Serum
increased
increasing
supplementation
days
20
40.
concentrations
muscle,
liver,
liver
subcellular
organelles
In
groups,
kidneys
faeces.
both
lysosomes
cytosol
higher,
activities
cathepsin
D
(CTSD),
β-glucosidase
(BGL),
acid
phosphatase
(ACP)
cytoplasm
higher.
Comparisons
between
showed
that
mRNA
protein
1
(CTR1),
ATPase
copper-transporting
beta
(ATP7B),
ceruloplasmin
(CP),
antioxidant
(ATOX1),
metallothionein
(MT)
lower
group
group,
best
performance
120
Cu.
mRNAs
for
alpha
(ATP7A),
cytochrome
c
oxidase
chaperone
17
(COX17),
superoxide
dismutase
(CCS)
decreasing
trend
better
deposition,
enhances
utilisation
Cu,
reduces
excretion,
promotes
expression
relevant
enzymes
transporters
liver.
npj Precision Oncology,
Journal Year:
2025,
Volume and Issue:
9(1)
Published: Feb. 24, 2025
Disulfidptosis,
a
newly
discovered
cell
death
mode
distinct
from
other
programmed
in
lung
and
kidney
cancer
cells,
is
defined
as
extensive
disulfide
bonds
to
actin
cytoskeleton
proteins,
leading
contraction
cytoskeletal
disruption
death.
New
pattern
discoveries
often
drive
advances
tumor
research.
Therefore,
the
present
study
attempted
decipher
manifestation
importance
of
disulfidptosis
pan-cancer.
Combining
Clinical
specimen
immunofluorescence
staining,
single-cell
analyses,
spatial
transcriptome
we
demonstrated
Multi-omics
analysis
has
revealed
that
genomic
variants
DNA
methylation
DRGs
can
affect
prognosis
patients
with
The
nomogram
based
on
Score
model
could
accurately
predict
PF-562271,
EHT-1864,
IPA-3
are
potential
therapeutic
agents
targeting
disulfidptosis.
Collectively,
this
deciphered
for
first
time
pan-cancer
developed
assist
clinicians
predicting
guiding
individualized
treatment
patients.
British Poultry Science,
Journal Year:
2025,
Volume and Issue:
unknown, P. 1 - 8
Published: March 12, 2025
1.
A
study
was
conducted
to
investigate
the
effect
of
spermidine
on
cuproptosis
in
granulosa
cells
goose
ovarian
follicles.
Granulosa
from
F2-F5
grade
follicles
Sichuan
white
geese
were
isolated
and
cultured.2.
Copper
sulphate,
chloroquine
administered
(GC).
The
GC
activity,
intracellular
Cu2+
content,
antioxidant
enzyme
expression
levels
genes
proteins
related
autophagy
determined.3.
results
showed
that
significantly
decreased
reactive
oxygen
species
(ROS)
levels,
mitochondrial
membrane
potential
Cu2+content
(p
<
0.05),
increased
cell
activity
0.001).
At
same
time,
ferredoxin
1
(FDX1)
gene
0.001),
lipoylated-dihydrolipoamide
S-acetyltransferase
(Lip-DLAT)
protein
LC3
After
treated
with
mixed
for
8
h,
copper
p62
FDX1
0.01)
0.05).4.
In
summary,
reduced
ROS
accumulation,
improved
activity.
It
alleviated
sulphate-induced
lipoylated
aggregation
by
inducing
autophagy.
This
suggested
has
a
broad
application
prospect
alleviating
GC.
Journal of Inflammation Research,
Journal Year:
2025,
Volume and Issue:
Volume 18, P. 4651 - 4664
Published: April 1, 2025
Oxygen
supplementation
is
essential
for
patients
with
a
multitude
of
diseases
but
can
cause
severe
hyperoxia-induced
lung
injury
(HLI),
necessitating
the
identification
therapeutic
targets
to
improve
clinical
outcomes.
Cuproptosis,
novel
copper-dependent
form
cell
death
characterized
by
proteotoxic
stress
resulting
from
lipoylated
protein
aggregation
and
loss
iron-sulfur
cluster
proteins,
distinct
other
forms
death.
However,
role
cuproptosis
in
HLI
remains
unclear.
We
established
an
model
MLE-12
cells
C57BL/6
mice
investigate
involvement
toxicity.
observed
time-dependent
increase
cuproptosis-related
gene
Fdx1
under
hyperoxia.
Moreover,
hyperoxia
activated
membrane-associated
copper
transporter
SLC31A1
significantly
elevated
levels
cells,
as
well
serum
tissue
mice.
Further
analysis
revealed
that
altered
expression
genes
without
affecting
DLAT
levels,
increased
lipoylated-DLAT
levels.
ELISA,
CCK-8
assays,
HE
staining,
wet-to-dry
weight
ratio,
bronchoalveolar
lavage
fluid
demonstrated
treatment
inhibitor
TTM
reduced
pro-inflammatory
cytokines
(TNF-α
IL-1β)
alleviated
both
Our
study
identifies
HLI,
providing
new
insights
into
pathogenesis
hyperoxic
potential
strategies.
Copper
(Cu)
has
long
been
a
concern
for
human
health.
While
previous
studies
have
explored
the
toxic
effects
of
Cu,
no
study
is
available
on
relationship
between
Cu
redox
state
transformation
and
biotoxicity
in
higher
organisms.
In
this
study,
we
gut
liver
toxicity
caused
by
overflow
Cu(I)
at
low
doses
exposure.
Here,
first
elucidated
digestive
metabolic
systems
as
main
target
sites
systematic
epidemiological
analysis.
Then,
ICP-MS
analysis
verified
that
were
top
two
Cu-high-accumulated
organs
zebrafish
exposed
to
10
100
μg/L
waterborne
72
h.
In-situ
Cu(II)
imaging
techniques
demonstrated
exogenous
was
converted
gut.
Furthermore,
transcriptomic
sequencing
revealed
high
induced
cell
cycle
arrest
G
phase.
However,
substantial
accumulation
disrupted
metabolism
energy
source
nutrients
supply,
leading
hepatic
toxicity.
This
provides
new
insights
into
mechanism
based
emphasizes
health
risks
associated
with
exposure
systems.
Frontiers in Neurology,
Journal Year:
2025,
Volume and Issue:
16
Published: April 23, 2025
Introduction
Spinal
cord
injury
(SCI)
severely
affects
the
central
nervous
system.
Copper
homeostasis
is
closely
related
to
mitochondrial
regulation,
and
cuproptosis
a
novel
form
of
cell
death
associated
with
metabolism.
This
study
aimed
explore
relationship
between
SCI
construct
prediction
models.
Methods
Gene
expression
data
patient
samples
from
GSE151371
dataset
were
analyzed.
The
differential
correlation
13
cuproptosis-related
genes
(CRGs)
non-SCI
identified,
ssGSEA
algorithm
was
used
for
immunological
infiltration
analysis.
Unsupervised
clustering
performed
based
on
differentially
expressed
CRGs,
followed
by
weighted
gene
co-expression
network
analysis
(WGCNA)
enrichment
Three
machine
learning
models
(RF,
LASSO,
SVM)
constructed
screen
candidate
genes,
Nomogram
model
verification.
Animal
experiments
carried
out
an
rat
model,
including
behavioral
scoring,
histological
staining,
electron
microscopic
observation,
qRT-PCR.
Results
Seven
CRGs
showed
samples,
there
significant
differences
in
immune
levels.
divided
38
into
two
clusters
(Cluster
C1
Cluster
C2).
WGCNA
identified
key
modules
clusters,
involvement
pathways
such
as
Ribosome
HIF-1
signaling
pathway.
Four
(SLC31A1,
DBT,
DLST,
LIAS)
obtained
models,
SLC31A1
performing
best
(AUC
=
0.958).
confirmed
decrease
scores
rats
group,
pathological
changes
tissue
sections,
model.
Discussion
revealed
close
association
cuproptosis.
Abnormal
four
function,
energy
metabolism,
oxidative
stress,
response,
which
detrimental
recovery
neurological
function
SCI.
However,
this
has
some
limitations,
unidentified
SRGs,
small
sample
size.
Future
research
requires
more
vitro
vivo
deeply
regulatory
mechanisms
develop
intervention
methods.