ACS Applied Bio Materials,
Journal Year:
2024,
Volume and Issue:
unknown
Published: Dec. 11, 2024
Multielemental
transition
metal
compounds
represent
a
class
of
promising
candidates
for
the
biomedical
field
due
to
their
unique
structure
and
application
potential.
However,
synthesis
process
remains
challenging,
which
was
subject
high-temperature
treatment
multimetallic
elements
integrated
within
one
system.
Herein,
first
time,
we
have
fabricated
nanotripod,
Advanced Science,
Journal Year:
2024,
Volume and Issue:
11(18)
Published: March 2, 2024
Abstract
The
induction
of
cuproptosis,
a
recently
identified
form
copper‐dependent
immunogenic
cell
death,
is
promising
approach
for
antitumor
therapy.
However,
sufficient
accumulation
intracellular
copper
ions
(Cu
2+
)
in
tumor
cells
essential
inducing
cuproptosis.
Herein,
an
intelligent
cuproptosis‐inducing
nanosystem
constructed
by
encapsulating
oxide
(CuO)
nanoparticles
with
the
ionophore
elesclomol
(ES).
After
uptake
cells,
ES@CuO
degraded
to
release
Cu
and
ES
synergistically
trigger
thereby
significantly
inhibiting
growth
murine
B16
melanoma
cells.
Moreover,
further
promoted
cuproptosis‐mediated
immune
responses
reprogrammed
immunosuppressive
microenvironment
increasing
number
tumor‐infiltrating
lymphocytes
secreted
inflammatory
cytokines.
Additionally,
combining
programmed
death‐1
(PD‐1)
immunotherapy
substantially
increased
efficacy
melanoma.
Overall,
findings
this
study
can
lead
use
novel
strategy
therapy,
which
may
enhance
checkpoint
inhibitor
Advanced Functional Materials,
Journal Year:
2024,
Volume and Issue:
34(29)
Published: Feb. 23, 2024
Abstract
Autophagy,
a
lysosome‐involved
degradation
pathway,
as
self‐protective
cellular
process,
always
weakens
the
efficiency
of
tumor
therapies.
Herein,
for
first
time,
biodegradable
copper
(Cu)
ions
doped
layered
double
hydroxide
(Cu‐LDH)
nanoparticles
are
reported
cancer
immunotherapy
via
lysosomal
rupture‐mediated
“Broken
Window
Effect”.
Only
injection
Cu‐LDH
single
therapeutic
agent
achieves
various
organelles
destruction
after
rupture,
well
abnormal
aggregation
Cu
in
cells
cuproptosis
and
pyroptosis.
More
importantly,
autophagy
inhibition
caused
by
rupture
improves
overload‐mediated
pyroptosis
blocking
lysosome‐mediated
bulk
leading
to
good
anti‐tumor
immune
responses
ultimately
high‐efficiency
growth
inhibition.
This
Effect”
provides
new
paradigm
enhanced
therapy.
Cell Communication and Signaling,
Journal Year:
2024,
Volume and Issue:
22(1)
Published: May 1, 2024
Copper
plays
vital
roles
in
numerous
cellular
processes
and
its
imbalance
can
lead
to
oxidative
stress
dysfunction.
Recent
research
has
unveiled
a
unique
form
of
copper-induced
cell
death,
termed
cuproptosis,
which
differs
from
known
death
mechanisms.
This
process
involves
the
interaction
copper
with
lipoylated
tricarboxylic
acid
cycle
enzymes,
causing
protein
aggregation
death.
Recently,
growing
number
studies
have
explored
link
between
cuproptosis
cancer
development.
review
comprehensively
examines
systemic
metabolism
copper,
including
tumor-related
signaling
pathways
influenced
by
copper.
It
delves
into
discovery
mechanisms
connection
various
cancers.
Additionally,
suggests
potential
treatments
using
ionophores
that
induce
combination
small
molecule
drugs,
for
precision
therapy
specific
types.
Journal of Hematology & Oncology,
Journal Year:
2024,
Volume and Issue:
17(1)
Published: Aug. 16, 2024
Cuproptosis
is
a
newly
identified
form
of
cell
death
induced
by
excessive
copper
(Cu)
accumulation
within
cells.
Mechanistically,
cuproptosis
results
from
Cu-induced
aggregation
dihydrolipoamide
S-acetyltransferase,
correlated
with
the
mitochondrial
tricarboxylic
acid
cycle
and
loss
iron–sulfur
cluster
proteins,
ultimately
resulting
in
proteotoxic
stress
triggering
death.
Recently,
has
garnered
significant
interest
tumor
research
due
to
its
potential
as
crucial
therapeutic
strategy
against
cancer.
In
this
review,
we
summarized
cellular
molecular
mechanisms
relationship
other
types
Additionally,
reviewed
current
drugs
or
strategies
available
induce
cells,
including
Cu
ionophores,
small
compounds,
nanomedicine.
Furthermore,
targeted
metabolism
specific
regulatory
genes
cancer
therapy
enhance
sensitivity
cuproptosis.
Finally,
discussed
feasibility
targeting
overcome
chemotherapy
immunotherapy
resistance
suggested
future
directions.
This
study
that
could
open
new
avenues
for
developing
therapy.
Small,
Journal Year:
2024,
Volume and Issue:
20(25)
Published: Jan. 14, 2024
Abstract
Ferroptosis
is
a
new
form
of
regulated
cell
death
featuring
iron‐dependent
lipid
peroxides
accumulation
to
kill
tumor
cells.
A
growing
body
evidence
has
shown
the
potential
ferroptosis‐based
cancer
therapy
in
eradicating
refractory
malignancies
that
are
resistant
apoptosis‐based
conventional
therapies.
In
recent
years,
studies
have
reported
number
ferroptosis
inducers
can
increase
vulnerability
cells
by
regulating
ferroptosis‐related
signaling
pathways.
Encouraged
rapid
development
ferroptosis‐driven
therapies,
interdisciplinary
fields
combine
ferroptosis,
pharmaceutical
chemistry,
and
nanotechnology
focused.
First,
prerequisites
metabolic
pathways
for
briefly
introduced.
Then,
detail
emerging
designed
boost
ferroptosis‐induced
therapy,
including
metal
complexes,
metal‐based
nanoparticles,
metal‐free
nanoparticles
summarized.
Subsequently,
application
synergistic
strategies
with
apoptosis
other
emphasis
on
use
both
cuproptosis
induce
redox
dysregulation
intracellular
bimetallic
copper/iron
metabolism
disorders
during
treatment
discussed.
Finally,
challenges
associated
clinical
translation
future
directions
potentiating
therapies
highlighted.
The
designability
and
high
reactivity
of
nanotechnology
provide
strategies
for
antitumor
therapy
by
regulating
the
redox
state
in
tumor
cells.
Here,
we
synthesize
a
kind
vanadium
dioxide
nanoparticle
encapsulated
bovine
serum
albumin
containing
disulfide
bonds
(VSB
NPs)
photothermal-enhanced
ferroptosis
pyroptosis
effects.
Mechanism
studies
show
that
can
effectively
consume
overexpressed
glutathione
(GSH)
microenvironment,
leading
to
decrease
peroxidase
4
(GPX4)
activity.
Simultaneously,
tetravalent
induce
catalytic
reaction
H2O2,
producing
plenty
toxic
hydroxyl
radicals
(·OH)
singlet
oxygen
(1O2),
cell
ferroptosis.
In
addition,
consumption
also
lead
degradation
nanoparticles
into
high-valent
vanadates,
activating
thermal
protein
domain-associated
3
(NLRP3)
inflammasomes
causing
pyroptosis.
It
is
worth
mentioning
VSB
NPs
not
only
ablate
cells
under
near-infrared
light
irradiation
but
further
disrupt
homeostasis
thereby
enhancing
induced
biodegradable
vanadium-based
nanomaterials.
This
strategy,
based
on
biological
effects
regulate
cells,
provides
possibilities
cancer
treatment.
Journal of Materials Chemistry B,
Journal Year:
2025,
Volume and Issue:
unknown
Published: Jan. 1, 2025
This
review
discusses
the
recent
developments
in
copper-based
nanomaterials
that
utilize
copper-induced
cell
death,
categorized
by
materials
systems,
while
highlighting
limitations
of
current
cuproptosis
related
nanomaterials.
Cancer Communications,
Journal Year:
2023,
Volume and Issue:
43(10), P. 1071 - 1096
Published: Sept. 17, 2023
The
advent
of
immunotherapy
has
significantly
reshaped
the
landscape
cancer
treatment,
greatly
enhancing
therapeutic
outcomes
for
multiple
types
cancer.
However,
only
a
small
subset
individuals
respond
to
it,
underscoring
urgent
need
new
methods
improve
its
response
rate.
Ferroptosis,
recently
discovered
form
programmed
cell
death,
emerged
as
promising
approach
anti-tumor
therapy,
with
targeting
ferroptosis
kill
tumors
seen
potentially
effective
strategy.
Numerous
studies
suggest
that
inducing
can
synergistically
enhance
effects
immunotherapy,
paving
way
combined
treatment
method
in
future.
Nevertheless,
recent
research
raised
concerns
about
potential
negative
impacts
on
immunity
consequence
ferroptosis,
leading
conflicting
views
within
scientific
community
interplay
between
and
immunity,
thereby
necessity
comprehensive
review
existing
literature
this
relationship.
Previous
reviews
have
touched
related
content,
many
focusing
primarily
promoting
role
while
overlooking
evidence
inhibitory
immunity.
Others
concentrated
solely
discussing
content
either
from
perspective
cells
or
immune
ferroptosis.
Given
both
exist
tumor
microenvironment,
one-sided
discussion
cannot
comprehensively
summarize
topic.
Therefore,
perspectives
tumor-infiltrating
cells,
we
systematically
current
intending
provide
explanations
identify
work
needed
establish
translational
basis
ferroptosis-targeted
therapy
treating
tumors.
Abstract
Cuproptosis,
a
newly
identified
copper
(Cu)-dependent
form
of
cell
death,
stands
out
due
to
its
distinct
mechanism
that
sets
it
apart
from
other
known
death
pathways.
The
molecular
underpinnings
cuproptosis
involve
the
binding
Cu
lipoylated
enzymes
in
tricarboxylic
acid
cycle.
This
interaction
triggers
enzyme
aggregation
and
proteotoxic
stress,
culminating
death.
specific
has
yet
be
fully
elucidated.
recognized
sparked
numerous
investigations
into
role
tumorigenesis
cancer
therapy.
In
this
review,
we
summarized
current
knowledge
on
metabolism
link
cancer.
Furthermore,
delineated
mechanisms
roles
cuproptosis-related
genes
Finally,
offered
comprehensive
discussion
most
recent
advancements
ionophores
nanoparticle
delivery
systems
utilize
as
cutting-edge
strategy
for
treatment.